Prof Claudia Langenberg
Director and Professor of Medicine and Population Health
Precision Healthcare University Research Institute (PHURI)
Queen Mary University of London
Queen Mary University of London
Research
Genomics
Interests
Claudia's research is focused on the genetic basis of metabolic control, and her team studies its effects on health through integration of molecular with clinical data in large-scale patient and population-based studies.Publications
2026
Associations of proteomic age clocks with lifestyle risk factors, incident chronic diseases and mortality in two European cohortsNature Aging, 1-15.
29-06-2026
Data-Driven Decision Support in Obesity Management Commission: enabling more equitable and personalized obesity careFranks PW, Suliman SGI, Timpson NJ, Langenberg C, le Roux CW
Nature Medicine, Springer Nature vol. 32 (6), 1959-1961.
12-05-2026
Multi-cohort proteogenomic analyses reveal genetic effects across the proteome and diseasomeKoprulu M, Smith-Byrne K, Ferolito BR, Macdonald-Dunlop E, Luan J, Hedman ÅK, Ogamba CF, Kuliesius J et al.
Cell, Elsevier vol. 189 (11), 3339-3357.e11.
01-05-2026
Data-driven prioritization of high-risk individuals for weight loss interventionsDemircan K, Carrasco-Zanini J, Williamson A, Beuchel C, Jackson L, Römisch-Margl W, Hansen AL, Finer S et al.
Nature Medicine, Springer Nature vol. 32 (6), 2117-2127.
30-04-2026
Publisher Correction: Multi-ancestry genome-wide association study of severe pregnancy nausea and vomitingFejzo M, Wang X, Tan Q, Zöllner J, Pujol-Gualdo N, Laisk T, Finer S, van Heel DA et al.
Nature Genetics, Springer Nature vol. 58 (5), 1186-1186.
28-04-2026
Glycerol-driven TNAP activation in thermogenesis and mineralizationHussain MF, Krishnan SS, Carroll BL, Samborska B, Mousa A, Williamson A, Delgado-Martin M, Srinivasu BY et al.
Nature, Springer Nature vol. 654 (8117), 198-208.
22-04-2026
The contribution of apolipoprotein E genetic variation to dementia risk in British South AsiansJacobs BM, Chandra A, Foote IF, Durrani F, Waters S, Liu Y, Proitsi P, Maher E et al.
Brain Communications, Oxford University Press (Oup) vol. 8 (3)
17-04-2026
Precision medicine in low-income settings and small island developing statesSaluja S, Mannan F, Pare G, Anand SS, Hanchard NA, Langenberg C, Anderson SG
Nature Reviews Endocrinology, Springer Nature, 1-11.
16-04-2026
Multi-ancestry genome-wide association study of severe pregnancy nausea and vomitingFejzo M, Wang X, Tan Q, Zöllner J, Pujol-Gualdo N, Laisk T, Finer S, van Heel DA et al.
Nature Genetics, Springer Nature vol. 58 (4), 810-820.
01-04-2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityKim HI, DeBoever C, Walter K, Kalantzis G, Li C, Mozaffari SV, Kundu K, Jacobs BM et al.
Nature Genetics, Springer Nature vol. 58 (4), 821-830.
27-03-2026
A predictive atlas of disease onset from retinal fundus photographs: a modelling study using data from population-based cohortsBuergel T, Loock L, Steinfeldt J, Kronenberg N, Hoffmann L, Künzel SE, Upmeier Zu Belzen J, Arnoldt L et al.
The Lancet Digital Health, Elsevier vol. 8 (3)
01-03-2026
HFpEF and MASLD: converging mechanisms and clinical implicationsCapone F, Häseli SP, Liu L, Strocchi S, Langenberg C, Lusis AJ, Pietzner M, Muoio DM et al.
Nature Reviews Cardiology, Springer Nature, 1-25.
23-02-2026
KidneyGenAfrica multi-cohort Genome-wide association study and polygenic prediction of kidney function in 110,000 AfricansKamiza AB, Chikowore T, Chen G, Ojewunmi O, Machipisa T, Zhou F, Mayanja R, Toure S et al.
Nature Communications, Springer Nature vol. 17 (1)
10-02-2026
Interactions between genetic predisposition to obesity, insulin resistance and type 2 diabetes risk, and food or beverage intake for incident type 2 diabetes: European Prospective Investigation into Cancer and Nutrition (EPIC) InterAct case–cohort studyLi SX, Imamura F, Sharp SJ, Schulze MB, Zheng J-S, Amiano P, Ardanaz E, Bergmann MM et al.
American Journal of Clinical Nutrition, Elsevier vol. 123 (3)
16-01-2026
2025
A genes and health recall study of intrahepatic cholestasis of pregnancy and cholestatic liver diseaseConstantinides M, Gafton J, Garcia ACA, Dixon PH, Williamson C, Linton K, Finer S, Gill US et al.
Communications Medicine, Springer Nature vol. 5 (1)
23-12-2025
Leveraging large-scale biobanks for therapeutic target discoveryFerolito BR, Dashti H, Giambartolomei C, Peloso GM, Golden DJ, Gravel-Pucillo K, Rasooly D, Horimoto ARVR et al.
Human Genetics and Genomics Advances, Elsevier vol. 7 (1)
09-12-2025
Associations of visceral adipose tissue with ASCVD across BMI categoriesMakhmudova U, Wild B, Steinhagen-Thiessen E, Williamson A, Langenberg C, Eils R, Landmesser U, Sannino A
European Heart Journal, Oxford University Press (Oup) vol. 46 (Supplement_1)
05-11-2025
Strengthening the reporting of observational studies in epidemiology using Mendelian randomization (STROBE-MR): a Korean translation of explanation and elaborationSkrivankova VW, Richmond RC, Woolf BAR, Davies NM, Swanson SA, VanderWeele TJ, Timpson NJ, Higgins JPT et al.
The Ewha Medical Journal, The Ewha Medical Journal, Ewha Womans University College of Medicine vol. 48 (4)
27-10-2025
Obesity due to MC4R deficiency is associated with reduced cholesterol, triglycerides and cardiovascular disease riskZorn S, Bounds R, Williamson A, Lawler K, Hanssen R, Keogh J, Henning E, Smith M et al.
Nature Medicine, Springer Nature vol. 31 (12), 4180-4188.
16-10-2025
Machine learning-guided deconvolution of plasma protein levelsPietzner M, Beuchel C, Demircan K, Hoffmann Anton J, Zeng W, Römisch-Margl W, Yasmeen S, Uluvar B et al.
Molecular Systems Biology, Springer Nature vol. 21 (12), 1822-1844.
09-10-2025
A genetic map of human metabolism across the allele frequency spectrumZoodsma M, Beuchel C, Yasmeen S, Kohleick L, Nepal A, Koprulu M, Kronenberg F, Mayr M et al.
Nature Genetics, Springer Nature vol. 57 (10), 2445-2455.
01-10-2025
Undiagnosed G6PD deficiency in Black and Asian individuals is prevalent and contributes to health inequalities in type 2 diabetes diagnosis and complicationsMartin S, Samuel M, Stow D, Ridsdale AM, Chen J, Young KG, Green HD, Hattersley AT et al.
Diabetes Care, American Diabetes Association vol. 48 (11), 1932-1941.
30-09-2025
XBP1 expression in pancreatic islet cells is associated with poor glycaemic control especially in young non-obese onset diabetes across ancestriesSiddiqui MK, Dupuis T, Anjana RM, Dawed AY, Bigossi M, Srinivasan S, Hodgson S, Adedire ET et al.
Communications Medicine, Springer Nature vol. 5 (1)
24-09-2025
Plasma Metabolite N-Formylmethionine Is Associated With Higher Blood Pressure in the Multiethnic HELIUS Cohort and Triggers Vascular DysfunctionVerhaar BJH, Romp N, Mosterd CM, Nguyen TT, Nageswaran V, Rad PR, Winkelmeijer M, Schimmel AWM et al.
Hypertension, Wolters Kluwer vol. 82 (11), 1916-1929.
17-09-2025
KidneyGenAfrica, a pan-African partnership to deliver research and training excellence in genomics of kidney diseaseFatumo S, Ojewunmi O, Camenzuli R, Kintu C, Kamiza A, Brandenburg J-T, Kalungi A, Kalyesubula R et al.
Nature Genetics, Springer Nature vol. 57 (9), 2079-2082.
20-08-2025
APOE Genotype and Statin Response: Evidence From the UK Biobank and All of Us ProgramAsiimwe IG, Jorgensen AL, Pirmohamed M, Butterworth A, Warwick A, Fernandez‐Sanles A, Henry A, Lai AG et al.
Clinical and Translational Science, Wiley vol. 18 (8)
01-08-2025
Polygenic prediction of body mass index and obesity through the life course and across ancestriesSmit RAJ, Wade KH, Hui Q, Arias JD, Yin X, Christiansen MR, Yengo L, Preuss MH et al.
Nature Medicine, Springer Nature vol. 31 (9), 3151-3168.
21-07-2025
Visceral adipose tissue, aortic distensibility and atherosclerotic cardiovascular risk across body mass index categoriesMakhmudova U, Wild B, Williamson A, Steinhagen-Thiessen E, Langenberg C, Eils R, Landmesser U, Sannino A
European Journal of Preventive Cardiology, Oxford University Press (Oup)
18-07-2025
Associations of proteomic age with mortality and incident chronic diseases in the European Prospective Investigation into Cancer and Nutrition (EPIC)Robinson O, Xiao H, Homann J, Viallon V, Ferrari P, Huerta JM, Zabala AJ, Kaaks R et al.
, Springer Nature, rs.3.rs-7087230.
15-07-2025
A computational framework for defining and validating reproducible phenotyping algorithms of 313 diseases in the UK BiobankTorralbo A, Davitte JM, Croteau-Chonka DC, Ytsma C, Tomlinson C, Fitzpatrick NK, Chung S-C, Fatemifar G et al.
Scientific Reports, Springer Nature vol. 15 (1)
09-07-2025
Sex differences in the genetic regulation of the human plasma proteomeKoprulu M, Wheeler E, Kerrison ND, Denaxas S, Carrasco-Zanini J, Orkin CM, Hemingway H, Wareham NJ et al.
Nature Communications, Springer Nature vol. 16 (1)
13-05-2025
Inherited predisposition to pneumothorax: estimating the frequency of Birt-Hogg-Dubé syndrome from genomics and population cohortsYngvadottir B, Richman L, Andreou A, Woodley J, Luharia A, Lim D, Akhtar S, Anwar M et al.
Thorax, Bmj vol. 80 (8), 553-555.
10-04-2025
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypesHenry A, Mo X, Finan C, Chaffin MD, Speed D, Issa H, Denaxas S, Ware JS et al.
Nature Genetics, Springer Nature vol. 57 (4), 815-828.
04-03-2025
Understanding the potential contribution of polygenic risk scores to the prediction of gestational and type 2 diabetes in women from British Pakistani and Bangladeshi groups: a cohort study in Genes and HealthZöllner J, Orazumbekova B, Hodgson S, van Heel DA, Team GAHR, Akhtar S, Anwar M, Asgar O et al.
Ajog Global Reports, Elsevier vol. 5 (2)
21-02-2025
Author Correction: Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threatsSteinfeldt J, Wild B, Buergel T, Pietzner M, Upmeier zu Belzen J, Vauvelle A, Hegselmann S, Denaxas S et al.
Nature Communications, Springer Nature vol. 16 (1)
10-02-2025
Large-scale multi-omics identifies drug targets for heart failure with reduced and preserved ejection fractionRasooly D, Giambartolomei C, Peloso GM, Dashti H, Ferolito BR, Golden D, Horimoto ARVR, Pietzner M et al.
Nature Cardiovascular Research, Springer Nature vol. 4 (3), 293-311.
06-02-2025
Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery diseaseYoshiji S, Lu T, Butler-Laporte G, Carrasco-Zanini-Sanchez J, Su C-Y, Chen Y, Liang K, Willett JDS et al.
Nature Genetics, Springer Nature vol. 57 (2), 345-357.
24-01-2025
Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threatsSteinfeldt J, Wild B, Buergel T, Pietzner M, Upmeier zu Belzen J, Vauvelle A, Hegselmann S, Denaxas S et al.
Nature Communications, Springer Nature vol. 16 (1)
10-01-2025
2024
Long term health outcomes in people with diabetes 12 months after hospitalisation with COVID-19 in the UK: a prospective cohort studyGharibzadeh S, Routen A, Razieh C, Zaccardi F, Lawson C, Gillies C, Heller S, Davies M et al.
Eclinicalmedicine, Elsevier vol. 79
27-12-2024
Genetic basis of early onset and progression of type 2 diabetes in South AsiansHodgson S, Williamson A, Bigossi M, Stow D, Jacobs BM, Samuel M, Gafton J, Zöllner J et al.
Nature Medicine, Springer Nature vol. 31 (1), 323-331.
26-11-2024
Altered IL-6 signalling and risk of tuberculosis: a multi-ancestry mendelian randomisation studyHamilton F, Schurz H, Yates TA, Gilchrist JJ, Möller M, Naranbhai V, Ghazal P, Timpson NJ et al.
The Lancet Microbe, Elsevier vol. 6 (1)
21-11-2024
Incidence of diabetes mellitus following hospitalisation for COVID‐19 in the United Kingdom: A prospective observational studyTyrer F, Gharibzadeh S, Gillies C, Lawson C, Routen A, Islam N, Razieh C, Zaccardi F et al.
Diabetes Obesity and Metabolism, Wiley vol. 27 (2), 767-776.
20-11-2024
Genetic architecture of routinely acquired blood tests in a British South Asian cohortJacobs BM, Stow D, Hodgson S, Zöllner J, Samuel M, Kanoni S, Bidi S, Walter K et al.
Nature Communications, Springer Nature vol. 15 (1)
16-10-2024
Disease coverage of human genome-wide association studies and pharmaceutical research and developmentGordillo-Marañón M, Schmidt AF, Warwick A, Tomlinson C, Ytsma C, Engmann J, Torralbo A, Maclean R et al.
Communications Medicine, Springer Nature vol. 4 (1)
08-10-2024
Mapping biological influences on the human plasma proteome beyond the genomeCarrasco-Zanini J, Wheeler E, Uluvar B, Kerrison N, Koprulu M, Wareham NJ, Pietzner M, Langenberg C
Nature Metabolism, Springer Nature vol. 6 (10), 2010-2023.
26-09-2024
Damaging mutations in liver X receptor-α are hepatotoxic and implicate cholesterol sensing in liver healthLockhart SM, Muso M, Zvetkova I, Lam BYH, Ferrari A, Schoenmakers E, Duckett K, Leslie J et al.
Nature Metabolism, Springer Nature vol. 6 (10), 1922-1938.
25-09-2024
Damaging mutations in LXR[alpha] uncouple lipogenesis from hepatotoxicity and implicate hepatic cholesterol sensing in human liver healthLockhart S, Muso M, Zvetkova I, Lam B, Ferrari A, Schoenmakkers E, Duckett K, Leslie J et al.
Endocrine Abstracts, Bioscientifica
16-09-2024
The genetic landscape of neuro-related proteins in human plasmaRepetto L, Chen J, Yang Z, Zhai R, Timmers PRHJ, Feng X, Li T, Yao Y et al.
Nature Human Behaviour, Springer Nature vol. 8 (11), 2222-2234.
29-08-2024
Testing for a causal role of thyroid hormone measurements within the normal range on human metabolism and diseases: a systematic Mendelian randomizationAlwan H, Luan J, Williamson A, Carrasco-Zanini J, Stewart ID, Wareham NJ, Langenberg C, Pietzner M
Ebiomedicine, Elsevier vol. 107
26-08-2024
The performance of AlphaMissense to identify genes influencing diseaseChen Y, Butler-Laporte G, Liang KYH, Ilboudo Y, Yasmeen S, Sasako T, Langenberg C, Greenwood CMT et al.
Human Genetics and Genomics Advances, Elsevier vol. 5 (4)
22-08-2024
Cognitive and psychiatric symptom trajectories 2–3 years after hospital admission for COVID-19: a longitudinal, prospective cohort study in the UKTaquet M, Skorniewska Z, De Deyn T, Hampshire A, Trender WR, Hellyer PJ, Chalmers JD, Ho L-P et al.
The Lancet Psychiatry, Elsevier vol. 11 (9), 696-708.
31-07-2024
An LGR6 frameshift variant abrogates receptor expression on select leukocyte subsets and is associated with viral infectionsGomez EA, De Matteis R, Udomjarumanee P, Team GAHR, Akhtar S, Anwar M, Arciero E, Asgar O et al.
Blood, American Society of Hematology vol. 144 (4), 420-434.
25-07-2024
Blood proteins predict the risk of many diseases years before onsetNature Medicine, Springer Nature vol. 30 (9), 2419-2420.
22-07-2024
Proteomic signatures improve risk prediction for common and rare diseasesCarrasco-Zanini J, Pietzner M, Davitte J, Surendran P, Croteau-Chonka DC, Robins C, Torralbo A, Tomlinson C et al.
Nature Medicine, Springer Nature vol. 30 (9), 2489-2498.
22-07-2024
Complex patterns of multimorbidity associated with severe COVID-19 and long COVIDPietzner M, Denaxas S, Yasmeen S, Ulmer MA, Nakanishi T, Arnold M, Kastenmüller G, Hemingway H et al.
Communications Medicine, Springer Nature vol. 4 (1)
08-07-2024
Proteomic prediction of diverse incident diseases: a machine learning-guided biomarker discovery study using data from a prospective cohort studyCarrasco-Zanini J, Pietzner M, Koprulu M, Wheeler E, Kerrison ND, Wareham NJ, Langenberg C
The Lancet Digital Health, Elsevier vol. 6 (7), e470-e479.
01-07-2024
Reporting guidelines for precision medicine research of clinical relevance: the BePRECISE checklistLim SS, Semnani-Azad Z, Morieri ML, Ng AH, Ahmad A, Fitipaldi H, Boyle J, Collin C et al.
Nature Medicine, Springer Nature vol. 30 (7), 1874-1881.
01-07-2024
SMIM1 absence is associated with reduced energy expenditure and excess weightStefanucci L, Moslemi C, Tomé AR, Virtue S, Bidault G, Gleadall NS, Watson LPE, Kwa JE et al.
Med, Elsevier vol. 5 (9), 1083-1095.e6.
20-06-2024
Identifying proteomic risk factors for overall, aggressive, and early onset prostate cancer using Mendelian Randomisation and tumour spatial transcriptomicsDesai TA, Hedman ÅK, Dimitriou M, Koprulu M, Figiel S, Yin W, Johansson M, Watts EL et al.
Ebiomedicine, Elsevier vol. 105
14-06-2024
RETRACTED ARTICLE: Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threatsSteinfeldt J, Wild B, Buergel T, Pietzner M, Upmeier zu Belzen J, Vauvelle A, Hegselmann S, Denaxas S et al.
Nature Communications, Springer Nature vol. 15 (1)
20-05-2024
Long COVID and cardiovascular disease: a prospective cohort studyLawson CA, Moss AJ, Arnold JR, Bagot C, Banerjee A, Berry C, Greenwood J, Hughes AD et al.
Open Heart, Bmj vol. 11 (1)
01-05-2024
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traitsKeaton JM, Kamali Z, Xie T, Vaez A, Williams A, Goleva SB, Ani A, Evangelou E et al.
Nature Genetics, Springer Nature vol. 56 (5), 778-791.
30-04-2024
Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancersSmith-Byrne K, Hedman Å, Dimitriou M, Desai T, Sokolov AV, Schioth HB, Koprulu M, Pietzner M et al.
Nature Communications, Springer Nature vol. 15 (1)
29-04-2024
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestriesShrine N, Guyatt AL, Erzurumluoglu AM, Jackson VE, Hobbs BD, Melbourne CA, Batini C, Fawcett KA et al.
Nature Genetics, Springer Nature vol. 56 (5), 1032-1033.
19-04-2024
Large-scale phenotyping of patients with long COVID post-hospitalization reveals mechanistic subtypes of diseaseLiew F, Efstathiou C, Fontanella S, Richardson M, Saunders R, Swieboda D, Sidhu JK, Ascough S et al.
Nature Immunology, Springer Nature vol. 25 (4), 607-621.
01-04-2024
Long-term impact of COVID-19 hospitalisation among individuals with pre-existing airway diseases in the UK: a multicentre, longitudinal cohort study – PHOSP-COVIDElneima O, Hurst JR, Echevarria C, Quint JK, Walker S, Siddiqui S, Novotny P, Pfeffer PE et al.
Erj Open Research, European Respiratory Society (Ers) vol. 10 (4), 00982-02023.
28-03-2024
Abstract 7330: Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using mendelian randomization and tumor spatial transcriptomicsDesai TA, Hedman AK, Dimitriou M, Koprulu M, Figiel S, Yin W, Johansson M, Watts EL et al.
Cancer Research, American Association For Cancer Research (Aacr) vol. 84 (6_Supplement), 7330-7330.
22-03-2024
Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood PressureGanji-Arjenaki M, Kamali Z, Pressure ICOB, Evangelou E, Warren HR, Gao H, Ntritsos G, Dimou N et al.
Kidney International Reports, Elsevier vol. 9 (6), 1849-1859.
13-03-2024
Systemic proteome adaptions to 7-day complete caloric restriction in humansPietzner M, Uluvar B, Kolnes KJ, Jeppesen PB, Frivold SV, Skattebo Ø, Johansen EI, Skålhegg BS et al.
Nature Metabolism, Springer Nature vol. 6 (4), 764-777.
01-03-2024
Genetic drivers of heterogeneity in type 2 diabetes pathophysiologySuzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A et al.
Nature, Springer Nature vol. 627 (8003), 347-357.
19-02-2024
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implicationsSterenborg RBTM, Steinbrenner I, Li Y, Bujnis MN, Naito T, Marouli E, Galesloot TE, Babajide O et al.
Nature Communications, Springer Nature vol. 15 (1)
30-01-2024
Accelerated immune ageing is associated with COVID-19 disease severityLord JM, Veenith T, Sullivan J, Sharma-Oates A, Richter AG, Greening NJ, McAuley HJC, Evans RA et al.
Immunity & Ageing, Springer Nature vol. 21 (1)
11-01-2024
2023
Genetic determinants of complement activation in the general populationNoce D, Foco L, Orth-Höller D, König E, Barbieri G, Pietzner M, Ghasemi-Semeskandeh D, Coassin S et al.
Cell Reports, Elsevier vol. 43 (1)
29-12-2023
Cohort Profile: Post-Hospitalisation COVID-19 (PHOSP-COVID) studyElneima O, McAuley HJC, Leavy OC, Chalmers JD, Horsley A, Ho L-P, Marks M, Poinasamy K et al.
International Journal of Epidemiology, Oxford University Press (Oup) vol. 53 (1)
18-12-2023
Plasma Metabolites Related to the Consumption of Different Types of Dairy Products and Their Association with New‐Onset Type 2 Diabetes: Analyses in the Fenland and EPIC‐Norfolk Studies, United KingdomTrichia E, Koulman A, Stewart ID, Brage S, Griffin SJ, Griffin JL, Khaw K, Langenberg C et al.
Molecular Nutrition & Food Research, Wiley vol. 68 (1)
06-12-2023
Estimating dose-response relationships for vitamin D with coronary heart disease, stroke, and all-cause mortality: observational and Mendelian randomisation analysesCollaboration ERFCE-CVDS, Sofianopoulou E, Kaptoge SK, Afzal S, Jiang T, Gill D, Gundersen TE, Bolton TR et al.
The Lancet Diabetes & Endocrinology, Elsevier vol. 12 (1), e2-e11.
01-12-2023
Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolismIglesias MJ, Sanchez-Rivera L, Ibrahim-Kosta M, Naudin C, Munsch G, Goumidi L, Farm M, Smith PM et al.
Nature Communications, Springer Nature vol. 14 (1)
27-11-2023
Identification of circulating proteins associated with general cognitive function among middle-aged and older adultsTin A, Fohner AE, Yang Q, Brody JA, Davies G, Yao J, Liu D, Caro I et al.
Communications Biology, Springer Nature vol. 6 (1)
03-11-2023
INTEGRATIVE PROTEOGENOMICS ANALYSIS IDENTIFIES COL6A3-DERIVED ENDOTROPHIN AS AN ACTIONABLE MEDIATOR OF THE EFFECT OF OBESITY ON CORONARY ARTERY DISEASEYoshiji S, Lu T, Butler-Laporte G, Carrasco-Zanini-Sanchez J, Chen Y, Liang K, Willett J, Su C et al.
Canadian Journal of Diabetes, Elsevier vol. 47 (7)
01-11-2023
Multi-omic prediction of incident type 2 diabetesCarrasco-Zanini J, Pietzner M, Wheeler E, Kerrison ND, Langenberg C, Wareham NJ
Diabetologia, Springer Nature vol. 67 (1), 102-112.
27-10-2023
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritizationWillems SM, Ng NHJ, Fernandez J, Fine RS, Wheeler E, Wessel J, Kitajima H, Marenne G et al.
Wellcome Open Research, F1000research vol. 8
20-10-2023
Long COVID research: an update from the PHOSP-COVID Scientific SummitBrightling CE, Evans RA, Singapuri A, Smith N, Wain LV, Brightling CE, Evans RA, Wain LV et al.
The Lancet Respiratory Medicine, Elsevier vol. 11 (11), e93-e94.
16-10-2023
ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenonHartmann S, Yasmeen S, Jacobs BM, Denaxas S, Pirmohamed M, Gamazon ER, Caulfield MJ, Hemingway H et al.
Nature Communications, Springer Nature vol. 14 (1)
12-10-2023
THU582 Actionable Circulating Proteins Mediate The Effect Of Obesity On Cardiometabolic Diseases: An Integrative Proteogenomics AnalysisYoshiji S, Lu T, Butler-Laporte G, Carrasco-Zanini-Sanchez J, Chen Y, Liang K, Willett JDS, Su C-Y et al.
Journal of The Endocrine Society, The Endocrine Society vol. 7 (Supplement_1)
05-10-2023
Performance of polygenic risk scores in screening, prediction, and risk stratification: secondary analysis of data in the Polygenic Score CatalogHingorani AD, Gratton J, Finan C, Schmidt AF, Patel R, Sofat R, Kuan V, Langenberg C et al.
Bmj Medicine, Bmj vol. 2 (1)
01-10-2023
INTEGRATIVE PROTEOGENOMICS ANALYSIS IDENTIFIES COL6A3-DERIVED ENDOTROPHIN AS AN ACTIONABLE MEDIATOR OF THE EFFECT OF OBESITY ON CORONARY ARTERY DISEASEYoshiji S, Lu T, Butler-Laporte G, Carrasco-Zanini-Sanchez J, Chen Y, Liang K, Willett J, Su C et al.
Canadian Journal of Cardiology, Elsevier vol. 39 (10), s209-s210.
01-10-2023
Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease riskFethnou E, Qafoud F, Alkhayat E, Afifi N, Tomei S, Liu W, Lorenz S, Syed N et al.
Nature Genetics, Springer Nature vol. 55 (10), 1778-1779.
25-09-2023
Multiorgan MRI findings after hospitalisation with COVID-19 in the UK (C-MORE): a prospective, multicentre, observational cohort studyBrightling CE, Evans RA, Wain LV, Chalmers JD, Harris VC, Ho LP, Horsley A, Marks M et al.
The Lancet Respiratory Medicine, Elsevier vol. 11 (11), 1003-1019.
22-09-2023
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratificationLagou V, Jiang L, Ulrich A, Zudina L, González KSG, Balkhiyarova Z, Faggian A, Maina JG et al.
Nature Genetics, Springer Nature vol. 55 (9), 1448-1461.
01-09-2023
176 A genome-wide association screening of complement activation from a general population studyNoce D, Foco L, Orth-Höller D, König E, Barbieri G, Pietzner M, Coassin S, Fuchsberger C et al.
Immunobiology, Elsevier vol. 228 (5)
01-09-2023
Testing for a causal role of thyroid hormone measurements within the normal range: a systematic mendelian randomization studyAlwan H, Luan J, Williamson A, Steward I, Wareham N, Langenberg C, Pietzner M
Endocrine Abstracts, Bioscientifica
24-08-2023
Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseasesCarland C, Png G, Malarstig A, Kho PF, Gustafsson S, Michaelsson K, Lind L, Tsafantakis E et al.
Clinical Proteomics, Springer Nature vol. 20 (1)
07-08-2023
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome‐Wide Association Meta‐Analysis Followed by Mendelian RandomizationZheng J, Wheeler E, Pietzner M, Andlauer TFM, Yau MS, Hartley AE, Brumpton BM, Rasheed H et al.
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Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locusMathieson I, Day FR, Barban N, Tropf FC, Brazel DM, Vaez A, van Zuydam N, Bitarello BD et al.
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Development and validation of a metabolite score for red meat intake: an observational cohort study and randomized controlled dietary interventionLi C, Imamura F, Wedekind R, Stewart ID, Pietzner M, Wheeler E, Forouhi NG, Langenberg C et al.
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Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational studyEvans RA, Leavy OC, Richardson M, Elneima O, McAuley HJC, Shikotra A, Singapuri A, Sereno M et al.
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Genetic Associations and Architecture of Asthma-COPD OverlapJohn C, Guyatt AL, Shrine N, Packer R, Olafsdottir TA, Liu J, Hayden LP, Chu SH et al.
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Evidence for Shared Genetic Aetiology Between Schizophrenia, Cardiometabolic, and Inflammation-Related Traits: Genetic Correlation and Colocalization AnalysesPerry BI, Bowker N, Burgess S, Wareham NJ, Upthegrove R, Jones PB, Langenberg C, Khandaker GM
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Understanding Disease Mechanisms: From Genome to Phenome via the ProteomeKoprulu M, Carrasco-Zanini J, Wheeler E, Kerrison N, Wareham N, Pietzner M, Langenberg C
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GENOME-WIDE STUDIES REVEAL FACTORS ASSOCIATED WITH CIRCULATING UROMODULIN AND ITS RELATIONS WITH COMPLEX DISEASESLi Y, Cheng Y, Consolato F, Schiano G, Chong M, Pietzner M, Nguyen NQ, Scherer N et al.
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Synergistic insights into human health from aptamer- and antibody-based proteomic profilingPietzner M, Wheeler E, Carrasco-Zanini J, Kerrison ND, Oerton E, Koprulu M, Luan J, Hingorani AD et al.
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Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex DisordersLigthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T et al.
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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetesBonàs-Guarch S, Guindo-Martínez M, Miguel-Escalada I, Grarup N, Sebastian D, Rodriguez-Fos E, Sánchez F, Planas-Fèlix M et al.
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Elevated Plasma Levels of 3-Hydroxyisobutyric Acid Are Associated With Incident Type 2 DiabetesMardinoglu A, Gogg S, Lotta LA, Stančáková A, Nerstedt A, Boren J, Blüher M, Ferrannini E et al.
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Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart DiseaseYaghootkar H, Lotta LA, Tyrrell J, Smit RAJ, Jones SE, Donnelly L, Beaumont R, Campbell A et al.
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Association of Multiple Biomarkers of Iron Metabolism and Type 2 Diabetes: The EPIC-InterAct StudyPodmore C, Meidtner K, Schulze MB, Scott RA, Ramond A, Butterworth AS, Di Angelantonio E, Danesh J et al.
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New loci for body fat percentage reveal link between adiposity and cardiometabolic disease riskLu Y, Day FR, Gustafsson S, Buchkovich ML, Na J, Bataille V, Cousminer DL, Dastani Z et al.
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Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levelsKilpeläinen TO, Carli JFM, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW et al.
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Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysisWhite J, Sofat R, Hemani G, Shah T, Engmann J, Dale C, Shah S, Kruger FA et al.
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The interaction of insulin resistance and genetically-determined pancreatic response shapes the time trajectories of insulin secretion and glucose toleranceLuca LA, Scott RA, Sharp SJ, Day FR, Luan J, Wareham NJ, Langenberg C
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Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in DiabetesTeumer A, Tin A, Sorice R, Gorski M, Yeo NC, Chu AY, Li M, Li Y et al.
Diabetes, American Diabetes Association vol. 65 (3), 803-817.
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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociGaulton KJ, Ferreira T, Lee Y, Raimondo A, Mägi R, Reschen ME, Mahajan A, Locke A et al.
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Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA RepairDay FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK et al.
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Definitions of Metabolic Health and Risk of Future Type 2 Diabetes in BMI Categories: A Systematic Review and Network Meta-analysisLotta LA, Abbasi A, Sharp SJ, Sahlqvist A-S, Waterworth D, Brosnan JM, Scott RA, Langenberg C et al.
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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction StudyWinkler TW, Justice AE, Graff M, Barata L, Feitosa MF, Chu S, Czajkowski J, Esko T et al.
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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repairDay FR, Ruth KS, Thompson DJ, Lunetta KL, Pervjakova N, Chasman DI, Stolk L, Finucane HK et al.
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panelHuang J, Howie B, McCarthy S, Memari Y, Walter K, Min JL, Danecek P, Malerba G et al.
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Prevalence and Regional Distribution of Autoantibodies Against GAD65Ab in a European Population Without Diabetes: The EPIC-InterAct StudyRolandsson O, Hampe CS, Wennberg P, Radtke J, Langenberg C, Wareham N
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Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization AnalysisNead KT, Sharp SJ, Thompson DJ, Painter JN, Savage DB, Semple RK, Barker A, Group TANECS et al.
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Associations between Potentially Modifiable Risk Factors and Alzheimer Disease: A Mendelian Randomization StudyØstergaard SD, Mukherjee S, Sharp SJ, Proitsi P, Lotta LA, Day F, Perry JRB, Boehme KL et al.
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Dietary fibre and incidence of type 2 diabetes in eight European countries: the EPIC-InterAct Study and a meta-analysis of prospective studiesThe InterAct Consortium
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A Mendelian Randomization Study of Circulating Uric Acid and Type 2 DiabetesSluijs I, Holmes MV, van der Schouw YT, Beulens JWJ, Asselbergs FW, Huerta JM, Palmer TM, Arriola L et al.
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Genetically Determined Height and Coronary Artery DiseaseNelson CP, Hamby SE, Saleheen D, Hopewell JC, Zeng L, Assimes TL, Kanoni S, Willenborg C et al.
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Erratum: Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosisBenyamin B, Esko T, Ried JS, Radhakrishnan A, Vermeulen SH, Traglia M, Gögele M, Anderson D et al.
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Untargeted Metabolic Profiling Identifies Altered Serum Metabolites of Type 2 Diabetes Mellitus in a Prospective, Nested Case Control StudyDrogan D, Dunn WB, Lin W, Buijsse B, Schulze MB, Langenberg C, Brown M, Floegel A et al.
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Genetic studies of body mass index yield new insights for obesity biologyLocke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S et al.
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New genetic loci link adipose and insulin biology to body fat distributionShungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH et al.
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Type 2 diabetes and incidence of a wide range of cardiovascular diseases: a cohort study in 1·9 million peopleShah AD, Langenberg C, Rapsomaniki E, Denaxas S, Pujades-Rodriguez M, Gale CP, Deanfield J, Smeeth L et al.
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Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 LocusMahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N et al.
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Genetic Markers of Insulin Sensitivity and Insulin Secretion Are Associated With Spontaneous Postnatal Growth and Response to Growth Hormone Treatment in Short SGA Children: the North European SGA Study (NESGAS)Jensen RB, Thankamony A, Day F, Scott RA, Langenberg C, Kirk J, Donaldson M, Ivarsson S-A et al.
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Sixty-Five Common Genetic Variants and Prediction of Type 2 DiabetesTalmud PJ, Cooper JA, Morris RW, Dudbridge F, Shah T, Engmann J, Dale C, White J et al.
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Consumption of fatty foods and incident type 2 diabetes in populations from eight European countriesBuijsse B, Boeing H, Drogan D, Schulze MB, Feskens EJ, Amiano P, Barricarte A, Clavel-Chapelon F et al.
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Common Genetic Variants Highlight the Role of Insulin Resistance and Body Fat Distribution in Type 2 Diabetes, Independent of ObesityScott RA, Fall T, Pasko D, Barker A, Sharp SJ, Arriola L, Balkau B, Barricarte A et al.
Diabetes, American Diabetes Association vol. 63 (12), 4378-4387.
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Genetic Evidence for a Normal-Weight “Metabolically Obese” Phenotype Linking Insulin Resistance, Hypertension, Coronary Artery Disease, and Type 2 DiabetesYaghootkar H, Scott RA, White CC, Zhang W, Speliotes E, Munroe PB, Ehret GB, Bis JC et al.
Diabetes, American Diabetes Association vol. 63 (12), 4369-4377.
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Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic TraitsHerder C, Nuotio M-L, Shah S, Blankenberg S, Brunner EJ, Carstensen M, Gieger C, Grallert H et al.
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Type 2 diabetes and incidence of cardiovascular diseases: a cohort study in 1·9 million peopleShah AD, Langenberg C, Rapsomaniki E, Denaxas S, Pujades-Rodriguez M, Gale CP, Deanfield J, Smeeth L et al.
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Smoking and Long-Term Risk of Type 2 Diabetes: The EPIC-InterAct Study in European PopulationsConsortium TI, Spijkerman AMW, van der A DL, Nilsson PM, Ardanaz E, Gavrila D, Agudo A, Arriola L et al.
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Defining the role of common variation in the genomic and biological architecture of adult human heightWood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K et al.
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Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosisBenyamin B, Esko T, Ried JS, Radhakrishnan A, Vermeulen SH, Traglia M, Gögele M, Anderson D et al.
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Defining the role of common variation in the genomic and biological architecture of adult human heightWood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K et al.
Nature Genetics, Springer Nature vol. 46 (11), 1173-1186.
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Association between circulating 25-hydroxyvitamin D and incident type 2 diabetes: a mendelian randomisation studyYe Z, Sharp SJ, Burgess S, Scott RA, Imamura F, Consortium I, Langenberg C, Wareham NJ et al.
The Lancet Diabetes & Endocrinology, Elsevier vol. 3 (1), 35-42.
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HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trialsSwerdlow DI, Preiss D, Kuchenbaecker KB, Holmes MV, Engmann JEL, Shah T, Sofat R, Stender S et al.
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A systematic review and meta-analysis of 130,000 individuals shows smoking does not modify the association of APOE genotype on risk of coronary heart diseaseHolmes MV, Frikke-Schmidt R, Melis D, Luben R, Asselbergs FW, Boer JMA, Cooper J, Palmen J et al.
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Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 DiabetesNg MCY, Shriner D, Chen BH, Li J, Chen W-M, Guo X, Liu J, Bielinski SJ et al.
Plos Genetics, Public Library of Science (Plos) vol. 10 (8)
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Differences in the prospective association between individual plasma phospholipid saturated fatty acids and incident type 2 diabetes: the EPIC-InterAct case-cohort studyForouhi NG, Koulman A, Sharp SJ, Imamura F, Kröger J, Schulze MB, Crowe FL, Huerta JM et al.
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Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass IndexHoggart CJ, Venturini G, Mangino M, Gomez F, Ascari G, Zhao JH, Teumer A, Winkler TW et al.
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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarchePerry JRB, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C, Chasman DI et al.
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Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant dataHolmes MV, Dale CE, Zuccolo L, Silverwood RJ, Guo Y, Ye Z, Prieto-Merino D, Dehghan A et al.
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Dietary Protein Intake and Incidence of Type 2 Diabetes in Europe: The EPIC-InterAct Case-Cohort Studyvan Nielen M, Feskens EJM, Mensink M, Sluijs I, Molina E, Amiano P, Ardanaz E, Balkau B et al.
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Gene-Lifestyle Interaction and Type 2 Diabetes: The EPIC InterAct Case-Cohort StudyLangenberg C, Sharp SJ, Franks PW, Scott RA, Deloukas P, Forouhi NG, Froguel P, Groop LC et al.
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Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic HeterogeneityDimas AS, Lagou V, Barker A, Knowles JW, Mägi R, Hivert M-F, Benazzo A, Rybin D et al.
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A Central Role for GRB10 in Regulation of Islet Function in ManProkopenko I, Poon W, Mägi R, B RP, Salehi SA, Almgren P, Osmark P, Bouatia-Naji N et al.
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityMahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD et al.
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Mendelian randomization of blood lipids for coronary heart diseaseHolmes MV, Asselbergs FW, Palmer TM, Drenos F, Lanktree MB, Nelson CP, Dale CE, Padmanabhan S et al.
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Genetic Evidence for a Metabolically Obese, Normal Weight Phenotype That Links Insulin Resistance with Type 2 Diabetes, Hypertension, and Coronary Artery DiseaseYaghootkar H, Scott R, White CC, Zhang W, Speliotes EK, Munroe PB, Ehret GB, Bis JC et al.
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Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease MechanismsClaussnitzer M, Dankel SN, Klocke B, Grallert H, Glunk V, Berulava T, Lee H, Oskolkov N et al.
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Common Genetic Variants Highlight the Role of Insulin Resistance and Body Fat Distribution in Type 2 Diabetes, Independently of ObesityScott RA, Fall T, Pasko D, Barker A, Sharp SJ, Giedraitis V, Walker M, Semple RK et al.
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Dietary Intakes of Individual Flavanols and Flavonols Are Inversely Associated with Incident Type 2 Diabetes in European Populations 1–3Zamora-Ros R, Forouhi NG, Sharp SJ, González CA, Buijsse B, Guevara M, van der Schouw YT, Amiano P et al.
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Dietary vitamin D intake and risk of type 2 diabetes in the European Prospective Investigation into Cancer and Nutrition: the EPIC-InterAct studyAbbas S, Linseisen J, Rohrmann S, Beulens JWJ, Buijsse B, Amiano P, Ardanaz E, Balkau B et al.
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The Association Between Dietary Flavonoid and Lignan Intakes and Incident Type 2 Diabetes in European Populations The EPIC-InterAct studyZamora-Ros R, Forouhi NG, Sharp SJ, González CA, Buijsse B, Guevara M, van der Schouw YT, Amiano P et al.
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Adherence to predefined dietary patterns and incident type 2 diabetes in European populations: EPIC-InterAct StudyThe InterAct Consortium
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Common variants associated with plasma triglycerides and risk for coronary artery diseaseDo R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S et al.
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Age at Menarche and Type 2 Diabetes RiskElks CE, Ong KK, Scott RA, van der Schouw YT, Brand JS, Wark PA, Amiano P, Balkau B et al.
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Discovery and refinement of loci associated with lipid levelsWiller CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J et al.
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Common variants associated with plasma triglycerides and risk for coronary artery diseaseDo R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S et al.
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The SH2B1 obesity locus and abnormal glucose homeostasis: Lack of evidence for association from a meta-analysis in individuals of European ancestryPrudente S, Copetti M, Morini E, Mendonca C, Andreozzi F, Chandalia M, Baratta R, consortium TD et al.
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Mendelian Randomization Studies Do Not Support a Causal Role for Reduced Circulating Adiponectin Levels in Insulin Resistance and Type 2 DiabetesYaghootkar H, Lamina C, Scott RA, Dastani Z, Hivert M-F, Warren LL, Stancáková A, Buxbaum SG et al.
Diabetes, American Diabetes Association vol. 62 (10), 3589-3598.
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Population Genomics of Cardiometabolic Traits: Design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumShah T, Engmann J, Dale C, Shah S, White J, Giambartolomei C, McLachlan S, Zabaneh D et al.
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Genome-wide association study identifies three novel loci for type 2 diabetesHara K, Fujita H, Johnson TA, Yamauchi T, Yasuda K, Horikoshi M, Peng C, Hu C et al.
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Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant StatisticsHu Y-J, Berndt SI, Gustafsson S, Ganna A, Consortium GIOAT, Berndt SI, Gustafsson S, Mägi R et al.
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Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric TraitsRandall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpeläinen TO, Esko T et al.
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The association of the mitochondrial DNA OriB variant (16184–16193 polycytosine tract) with type 2 diabetes in Europid populationsYe Z, Gillson C, Sims M, Khaw K-T, Plotka M, Poulton J, Langenberg C, Wareham NJ
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Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake 1 , 2 , 3 , 4Tanaka T, Ngwa JS, van Rooij FJA, Zillikens MC, Wojczynski MK, Frazier-Wood AC, Houston DK, Kanoni S et al.
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Consumption of sweet beverages and type 2 diabetes incidence in European adults: results from EPIC-InterActThe InterAct consortium
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The shared allelic architecture of adiponectin levels and coronary artery diseaseDastani Z, Johnson T, Kronenberg F, Nelson CP, Assimes TL, März W, Consortium C, Consortium A et al.
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Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From IndiaSaxena R, Saleheen D, Been LF, Garavito ML, Braun T, Bjonnes A, Young R, Ho WK et al.
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Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disordersden Hoed M, Eijgelsheim M, Esko T, Brundel BJJM, Peal DS, Evans DM, Nolte IM, Segrè AV et al.
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Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait lociPaul DS, Albers CA, Rendon A, Voss K, Stephens J, Consortium H, van der Harst P, Chambers JC et al.
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureBerndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL et al.
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CorrigendumJournal of Internal Medicine, Wiley vol. 273 (4), 422-422.
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Age at Menopause, Reproductive Life Span, and Type 2 Diabetes Risk Results from the EPIC-InterAct studyBrand JS, van der Schouw YT, Onland-Moret NC, Sharp SJ, Ong KK, Khaw K-T, Ardanaz E, Amiano P et al.
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Seropositivity and Higher Immunoglobulin G Antibody Levels Against Cytomegalovirus Are Associated With Mortality in the Population-Based European Prospective Investigation of Cancer–Norfolk CohortGkrania-Klotsas E, Langenberg C, Sharp SJ, Luben R, Khaw K-T, Wareham NJ
Clinical Infectious Diseases, Oxford University Press (Oup) vol. 56 (10), 1421-1427.
26-02-2013
Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control studyTalmud PJ, Shah S, Whittall R, Futema M, Howard P, Cooper JA, Harrison SC, Li K et al.
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Genome-Wide Association Study for Type 2 Diabetes in Indians Identifies a New Susceptibility Locus at 2q21Tabassum R, Chauhan G, Dwivedi OP, Mahajan A, Jaiswal A, Kaur I, Bandesh K, Singh T et al.
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsKöttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D et al.
Nature Genetics vol. 45 (2), 145-154.
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Distribution and determinants of circulating complement factor H concentration determined by a high-throughput immunonephelometric assaySofat R, Mangione PP, Gallimore JR, Hakobyan S, Hughes TR, Shah T, Goodship T, D'Aiuto F et al.
Journal of Immunological Methods, Elsevier vol. 390 (1-2), 63-73.
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Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studiesSmith CE, Ngwa J, Tanaka T, Qi Q, Wojczynski MK, Lemaitre RN, Anderson JS, Manichaikul A et al.
International Journal of Obesity, Springer Nature vol. 37 (9), 1211-1220.
29-01-2013
A genetic risk score comprising common variants associated with fasting insulin is associated with OGTT- and clamp-based indices of whole body insulin sensitivityScott RA, Pasko D, Fall T, Yaghootkar H, Barker A, Sharp SJ, Walker M, Wareham NJ et al.
01-01-2013
Self-rated health and type 2 diabetes risk in the European Prospective Investigation into Cancer and Nutrition-InterAct study: a case-cohort studyWennberg P, Rolandsson O, van der A DL, Spijkerman AMW, Kaaks R, Boeing H, Feller S, Bergmann MM et al.
Bmj Open, Bmj vol. 3 (3)
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Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European AncestryAhmad S, Rukh G, Varga TV, Ali A, Kurbasic A, Shungin D, Ericson U, Koivula RW et al.
Plos Genetics, Public Library of Science (Plos) vol. 9 (7)
01-01-2013
The Association between Dietary Energy Density and Type 2 Diabetes in Europe: Results from the EPIC-InterAct Studyvan den Berg SW, van der A DL, Spijkerman AMW, van Woudenbergh GJ, Tijhuis MJ, Amiano P, Ardanaz E, Beulens JWJ et al.
Plos One, Public Library of Science (Plos) vol. 8 (5)
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Causal Relevance of Blood Lipid Fractions in the Development of Carotid AtherosclerosisShah S, Casas J-P, Drenos F, Whittaker J, Deanfield J, Swerdlow DI, Holmes MV, Kivimaki M et al.
Circulation Genomic and Precision Medicine, Wolters Kluwer vol. 6 (1), 63-72.
28-12-2012
Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsKöttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D et al.
Nature Genetics, Springer Nature vol. 45 (2), 145-154.
23-12-2012
A Genome-Wide Association Study Identifies GRK5 and RASGRP1 as Type 2 Diabetes Loci in Chinese HansLi H, Gan W, Lu L, Dong X, Han X, Hu C, Yang Z, Sun L et al.
Diabetes, American Diabetes Association vol. 62 (1), 291-298.
13-12-2012
Large-scale association analysis identifies new risk loci for coronary artery diseaseDeloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D et al.
Nature Genetics, Springer Nature vol. 45 (1), 25-33.
02-12-2012
Seventy-five genetic loci influencing the human red blood cellvan der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U et al.
Nature, Springer Nature vol. 492 (7429), 369-375.
01-12-2012
Dietary Glycemic Index, Glycemic Load, and Digestible Carbohydrate Intake Are Not Associated with Risk of Type 2 Diabetes in Eight European Countriesconsortium OBOTI, Sluijs I, Beulens JWJ, van der Schouw YT, van der A DL, Buckland G, Kuijsten A, Schulze MB et al.
Journal of Nutrition, Elsevier vol. 143 (1), 93-99.
28-11-2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypesAlbrechtsen A, Grarup N, Li Y, Sparsø T, Tian G, Cao H, Jiang T, Kim SY et al.
Diabetologia, Springer Nature vol. 56 (2), 298-310.
19-11-2012
Identification of the BCAR1-CFDP1-TMEM170A Locus as a Determinant of Carotid Intima-Media Thickness and Coronary Artery Disease RiskGertow K, Sennblad B, Strawbridge RJ, Ohrvik J, Zabaneh D, Shah S, Veglia F, Fava C et al.
Circulation Genomic and Precision Medicine, Wolters Kluwer vol. 5 (6), 656-665.
14-11-2012
Abstract B76: Evidence of a causal association between fasting insulin concentrations and endometrial cancer: A Mendelian randomization analysisNead KT, Scott RA, Sharp SA, Butterworth AS, Thompson DJ, Johnson T, Spurdle AB, Pharoah PD et al.
Cancer Prevention Research, American Association For Cancer Research (Aacr) vol. 5 (11_Supplement), b76-b76.
01-11-2012
Higher Immunoglobulin G Antibody Levels Against Cytomegalovirus Are Associated With Incident Ischemic Heart Disease in the Population-Based EPIC-Norfolk CohortGkrania-Klotsas E, Langenberg C, Sharp SJ, Luben R, Khaw K-T, Wareham NJ
Journal of Infectious Diseases, Oxford University Press (Oup) vol. 206 (12), 1897-1903.
08-10-2012
The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: the EPIC-InterAct studyThe InterAct Consortium
Diabetologia, Springer Nature vol. 56 (1), 60-69.
28-09-2012
Association between dietary meat consumption and incident type 2 diabetes: the EPIC-InterAct studyThe InterAct Consortium
Diabetologia, Springer Nature vol. 56 (1), 47-59.
16-09-2012
A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding siteNürnberg ST, Rendon A, Smethurst PA, Paul DS, Voss K, Thon JN, Lloyd-Jones H, Sambrook JG et al.
Blood, American Society of Hematology vol. 120 (24), 4859-4868.
12-09-2012
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathwaysScott RA, Lagou V, Welch RP, Wheeler E, Montasser ME, Luan J, MäGi R, Strawbridge RJ et al.
Nature Genetics vol. 44 (9), 991-1005.
01-09-2012
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathwaysScott RA, Lagou V, Welch RP, Wheeler E, Montasser ME, Luan J, Mägi R, Strawbridge RJ et al.
Nature Genetics, Springer Nature vol. 44 (9), 991-1005.
12-08-2012
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesMorris AP, Voight BF, Teslovich TM, Ferreira T, Segré AV, Steinthorsdottir V, Strawbridge RJ, Khan H et al.
Nature Genetics, Springer Nature vol. 44 (9), 981-990.
12-08-2012
Fruit and vegetable intake and type 2 diabetes: EPIC-InterAct prospective study and meta-analysisCooper AJ, Forouhi NG, Ye Z, Buijsse B, Arriola L, Balkau B, Barricarte A, Beulens JWJ et al.
European Journal of Clinical Nutrition, Springer Nature vol. 66 (10), 1082-1092.
01-08-2012
Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related TraitsBillings LK, Hsu Y-H, Ackerman RJ, Dupuis J, Voight BF, Rasmussen-Torvik LJ, Hercberg S, Lathrop M et al.
Diabetes, American Diabetes Association vol. 61 (8), 2176-2186.
17-07-2012
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populationsOkada Y, Sim X, Go MJ, Wu J-Y, Gu D, Takeuchi F, Takahashi A, Maeda S et al.
Nature Genetics, Springer Nature vol. 44 (8), 904-909.
15-07-2012
The amount and type of dairy product intake and incident type 2 diabetes: results from the EPIC-InterAct StudySluijs I, Forouhi NG, Beulens JW, van der Schouw YT, Agnoli C, Arriola L, Balkau B, Barricarte A et al.
American Journal of Clinical Nutrition, Elsevier vol. 96 (2), 382-390.
03-07-2012
Lower educational level is a predictor of incident type 2 diabetes in European countries: The EPIC-InterAct studySacerdote C, Ricceri F, Rolandsson O, Baldi I, Chirlaque M-D, Feskens E, Bendinelli B, Ardanaz E et al.
International Journal of Epidemiology, Oxford University Press (Oup) vol. 41 (4), 1162-1173.
25-06-2012
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistanceManning AK, Hivert M-F, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu C-T et al.
Nature Genetics, Springer Nature vol. 44 (6), 659-669.
13-05-2012
The prospective association between total and type of fish intake and type 2 diabetes in 8 European countries: EPIC-InterAct StudyPatel PS, Forouhi NG, Kuijsten A, Schulze MB, van Woudenbergh GJ, Ardanaz E, Amiano P, Arriola L et al.
American Journal of Clinical Nutrition, Elsevier vol. 95 (6), 1445-1453.
09-05-2012
Alcohol consumption and risk of type 2 diabetes in European men and women: influence of beverage type and body sizeThe EPIC–InterAct studyBeulens JWJ, van der Schouw YT, Bergmann MM, Rohrmann S, Schulze MB, Buijsse B, Grobbee DE, Arriola L et al.
Journal of Internal Medicine, Wiley vol. 272 (4), 358-370.
08-05-2012
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese CasesPerry JRB, Voight BF, Yengo L, Amin N, Dupuis J, Ganser M, Grallert H, Navarro P et al.
Plos Genetics, Public Library of Science (Plos) vol. 8 (5)
01-05-2012
Physical activity reduces the risk of incident type 2 diabetes in general and in abdominally lean and obese men and women: the EPIC–InterAct StudyThe InterAct Consortium
Diabetologia, Springer Nature vol. 55 (7), 1944-1952.
21-04-2012
Circulating 25-hydroxyvitamin D concentration and the risk of type 2 diabetes: results from the European Prospective Investigation into Cancer (EPIC)-Norfolk cohort and updated meta-analysis of prospective studiesForouhi NG, Ye Z, Rickard AP, Khaw KT, Luben R, Langenberg C, Wareham NJ
Diabetologia, Springer Nature vol. 55 (8), 2173-2182.
15-04-2012
No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose LevelsScott RA, Chu AY, Grarup N, Manning AK, Hivert M-F, Shungin D, Tönjes A, Yesupriya A et al.
Diabetes, American Diabetes Association vol. 61 (5), 1291-1296.
13-04-2012
Genetic determinants of glucose homeostasisBarker A, Langenberg C, Wareham NJ
Best Practice & Research Clinical Endocrinology & Metabolism, Elsevier vol. 26 (2), 159-170.
01-04-2012
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populationsImamura M, Maeda S, Yamauchi T, Hara K, Yasuda K, Morizono T, Takahashi A, Horikoshi M et al.
Human Molecular Genetics, Oxford University Press (Oup) vol. 21 (13), 3042-3049.
28-03-2012
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritisStahl EA, Wegmann D, Trynka G, Gutierrez-Achury J, Do R, Voight BF, Kraft P, Chen R et al.
Nature Genetics, Springer Nature vol. 44 (5), 483-489.
25-03-2012
Evaluation of common genetic variants identified by GWAS for early onset and morbid obesity in population-based samplesden Hoed M, Luan J, Langenberg C, Cooper C, Sayer AA, Jameson K, Kumari M, Kivimaki M et al.
International Journal of Obesity, Springer Nature vol. 37 (2), 191-196.
20-03-2012
P128 Identification de nouveaux polymorphismes génétiques associés au risque de diabète de type 2 chez les obèses et non obèses européensCauchi S, Perry J, Almgren P, Scott R, Langenberg C, Wareham N, Groop L, Frayling T et al.
01-03-2012
The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysisSwerdlow DI, Holmes MV, Kuchenbaecker KB, Engmann JEL, Shah T, Sofat R, Guo Y, Chung C et al.
The Lancet, Elsevier vol. 379 (9822), 1214-1224.
01-03-2012
Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetesBonnefond A, Clément N, Fawcett K, Yengo L, Vaillant E, Guillaume J-L, Dechaume A, Payne F et al.
Nature Genetics, Springer Nature vol. 44 (3), 297-301.
29-01-2012
Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes RiskMarquez M, Huyvaert M, Perry JRB, Pearson RD, Falchi M, Morris AP, Vivequin S, Lobbens S et al.
Diabetes, American Diabetes Association vol. 61 (2), 524-530.
17-01-2012
The association between prior infection with five serotypes of Coxsackievirus B and incident type 2 diabetes mellitus in the EPIC-Norfolk studyGkrania-Klotsas E, Langenberg C, Tauriainen S, Sharp SJ, Luben R, Forouhi NG, Khaw KT, Hyöty H et al.
Diabetologia, Springer Nature vol. 55 (4), 967-970.
10-01-2012
A Genome-Wide Association Search for Type 2 Diabetes Genes in African AmericansPalmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN et al.
Plos One, Public Library of Science (Plos) vol. 7 (1)
01-01-2012
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 IndividualsDastani Z, Hivert M-F, Timpson N, Perry JRB, Yuan X, Scott RA, Henneman P, Heid IM et al.
Plos Genetics, Public Library of Science (Plos) vol. 8 (3)
01-01-2012
Circadian Gene Variants and Susceptibility to Type 2 Diabetes: A Pilot StudyKelly MA, Rees SD, Hydrie MZI, Shera AS, Bellary S, O’Hare JP, Kumar S, Taheri S et al.
Plos One, Public Library of Science (Plos) vol. 7 (4)
01-01-2012
Genome-Wide Association for Abdominal Subcutaneous and Visceral Adipose Reveals a Novel Locus for Visceral Fat in WomenFox CS, Liu Y, White CC, Feitosa M, Smith AV, Heard-Costa N, Lohman K, Johnson AD et al.
Plos Genetics, Public Library of Science (Plos) vol. 8 (5)
01-01-2012
Mendelian Randomization Studies to Understand the Role for Reduced Adiponectin Levels in Insulin Resistance or Type 2 DiabetesYaghootkar H, Warren L, Lawlor D, Scott R, Dastani Z, Hivert M-F, Henneman P, Langenberg C et al.
01-01-2012
Tea Consumption and Incidence of Type 2 Diabetes in Europe: The EPIC-InterAct Case-Cohort Studyvan Woudenbergh GJ, Kuijsten A, Drogan D, van der A DL, Romaguera D, Ardanaz E, Amiano P, Barricarte A et al.
Plos One, Public Library of Science (Plos) vol. 7 (5)
01-01-2012
Long-Term Risk of Incident Type 2 Diabetes and Measures of Overall and Regional Obesity: The EPIC-InterAct Case-Cohort StudyLangenberg C, Sharp SJ, Schulze MB, Rolandsson O, Overvad K, Forouhi NG, Spranger J, Drogan D et al.
Plos Medicine, Public Library of Science (Plos) vol. 9 (6)
01-01-2012
Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid ConcentrationsDemirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Å et al.
Plos Genetics, Public Library of Science (Plos) vol. 8 (2)
01-01-2012
The association of the mitochondrial DNA 16184-16193 poly-C variant with type 2 diabetesLangenberg C, Ye Z, Gillson C, Plotka M, Khaw K-T, Poulton J, Wareham NJ
01-01-2012
Impact of Type 2 Diabetes Susceptibility Loci on Variation in Physiologic Glycaemic Traits in Non-Diabetic IndividualsDimas AS, Gomes VI, Knowles J, Maegi R, Barker A, Hivert M-F, Benazzo A, Rybin D et al.
01-01-2012
2011
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east AsiansCho YS, Chen C-H, Hu C, Long J, Hee Ong RT, Sim X, Takeuchi F, Wu Y et al.
Nature Genetics, Springer Nature vol. 44 (1), 67-72.
11-12-2011
New gene functions in megakaryopoiesis and platelet formationGieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U et al.
Nature, Springer Nature vol. 480 (7376), 201-208.
30-11-2011
Validity of a short questionnaire to assess physical activity in 10 European countriesThe InterAct Consortium
European Journal of Epidemiology, Springer Nature vol. 27 (1), 15-25.
17-11-2011
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Gretarsdottir S, Badger SA et al.
American Journal of Human Genetics vol. 89 (5), 619-627.
11-11-2011
Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Gretarsdottir S, Badger SA et al.
American Journal of Human Genetics, Elsevier vol. 89 (5), 619-627.
01-11-2011
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaChambers JC, Zhang W, Sehmi J, Li X, Wass MN, Van der Harst P, Holm H, Sanna S et al.
Nature Genetics, Springer Nature vol. 43 (11), 1131-1138.
16-10-2011
Mendelian Randomization Study of B-Type Natriuretic Peptide and Type 2 Diabetes: Evidence of Causal Association from Population StudiesPfister R, Sharp S, Luben R, Welsh P, Barroso I, Salomaa V, Meirhaeghe A, Khaw K-T et al.
Plos Medicine, Public Library of Science (Plos) vol. 8 (10)
01-10-2011
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 DiabetesStrawbridge RJ, Dupuis J, Prokopenko I, Barker A, Ahlqvist E, Rybin D, Petrie JR, Travers ME et al.
Diabetes, American Diabetes Association vol. 60 (10), 2624-2634.
16-09-2011
The Lin28/let-7 Axis Regulates Glucose MetabolismZhu H, Shyh-Chang N, Segrè AV, Shinoda, Shah SP, Einhorn WS, Takeuchi A, Engreitz JM et al.
Cell, Elsevier vol. 147 (1), 81-94.
01-09-2011
Total Zinc Intake May Modify the Glucose-Raising Effect of a Zinc Transporter (SLC30A8) Variant A 14-Cohort Meta-analysisKanoni S, Nettleton JA, Hivert M-F, Ye Z, van Rooij FJA, Shungin D, Sonestedt E, Ngwa JS et al.
Diabetes, American Diabetes Association vol. 60 (9), 2407-2416.
20-08-2011
Mediterranean Diet and Type 2 Diabetes Risk in the European Prospective Investigation Into Cancer and Nutrition (EPIC) Study The InterAct projectRomaguera D, Guevara M, Norat T, Langenberg C, Forouhi NG, Sharp S, Slimani N, Schulze MB et al.
Diabetes Care, American Diabetes Association vol. 34 (9), 1913-1918.
19-08-2011
Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC StudyThe InterAct Consortium
Diabetologia, Springer Nature vol. 54 (9)
30-06-2011
No evidence for a causal link between uric acid and type 2 diabetes: a Mendelian randomisation approachPfister R, Barnes D, Luben R, Forouhi NG, Bochud M, Khaw K-T, Wareham NJ, Langenberg C
Diabetologia, Springer Nature vol. 54 (10), 2561-2569.
30-06-2011
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profileKilpeläinen TO, Zillikens MC, Stančákova A, Finucane FM, Ried JS, Langenberg C, Zhang W, Beckmann JS et al.
Nature Genetics, Springer Nature vol. 43 (8), 753-760.
26-06-2011
Individual and cumulative effect of type 2 diabetes genetic susceptibility variants on risk of coronary heart diseasePfister R, Barnes D, Luben RN, Khaw K-T, Wareham NJ, Langenberg C
Diabetologia, Springer Nature vol. 54 (9), 2283-2287.
03-06-2011
Association of Genetic Loci With Glucose Levels in Childhood and Adolescence A Meta-Analysis of Over 6,000 ChildrenBarker A, Sharp SJ, Timpson NJ, Bouatia-Naji N, Warrington NM, Kanoni S, Beilin LJ, Brage S et al.
Diabetes, American Diabetes Association vol. 60 (6), 1805-1812.
21-05-2011
Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypesSmall KS, Hedman ÅK, Grundberg E, Nica AC, Thorleifsson G, Kong A, Thorsteindottir U, Shin S-Y et al.
Nature Genetics, Springer Nature vol. 43 (6), 561-564.
15-05-2011
Associations of Common Genetic Variants With Age-Related Changes in Fasting and Postload Glucose Evidence From 18 Years of Follow-Up of the Whitehall II CohortJensen AC, Barker A, Kumari M, Brunner EJ, Kivimäki M, Hingorani AD, Wareham NJ, Tabák AG et al.
Diabetes, American Diabetes Association vol. 60 (5), 1617-1623.
23-04-2011
An amino acid profile to predict diabetes?Langenberg C, Savage DB
Nature Medicine, Springer Nature vol. 17 (4), 418-420.
01-04-2011
Erratum: Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysisVoight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, Zeggini E, Huth C et al.
Nature Genetics, Springer Nature vol. 43 (4), 388-388.
29-03-2011
Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))Soranzo N, Sanna S, Wheeler E, Gieger C, Radke D, Dupuis J, Bouatia-Naji N, Langenberg C et al.
Diabetes vol. 60 (3)
01-03-2011
Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic TraitsSpeliotes EK, Yerges-Armstrong LM, Wu J, Hernaez R, Kim LJ, Palmer CD, Gudnason V, Eiriksdottir G et al.
Plos Genetics, Public Library of Science (Plos) vol. 7 (3)
01-03-2011
Mendelian Randomization Studies Do Not Support a Role for Raised Circulating Triglyceride Levels Influencing Type 2 Diabetes, Glucose Levels, or Insulin ResistanceDe Silva NMG, Freathy RM, Palmer TM, Donnelly LA, Luan J, Gaunt T, Langenberg C, Weedon MN et al.
Diabetes, American Diabetes Association vol. 60 (3), 1008-1018.
21-02-2011
ErratumDiabetes Care, American Diabetes Association vol. 34 (3), 785-786.
17-02-2011
Genetic predisposition to obesity leads to increased risk of type 2 diabetesLi S, Zhao JH, Luan J, Langenberg C, Luben RN, Khaw KT, Wareham NJ, Loos RJF
Diabetologia, Springer Nature vol. 54 (4), 776-782.
26-01-2011
Design and Cohort Description of the InterAct Project: An Examination of the Interaction of Genetic and Lifestyle Factors on the Incidence of Type 2 Diabetes in the EPIC StudyLangenberg C, Wareham NJ
01-01-2011
Are population-based carriers of a mutation associated with cystic fibrosis patients more likely to have diabetes?Adler A, Langenberg C, Sims M, Wareham NJ
01-01-2011
Long-term risk of type 2 diabetes and measures of overall and regional obesity: the European InterAct studyLangenberg C, Sharp SJ, Wareham NJ
01-01-2011
Genome-wide joint meta-analysis of SNP by BMI interaction on fasting insulin: a MAGIC studyScott RA, Manning AK, Hivert M-F, Bouatia-Naji N, Grimsby J, Liu C-T, Chen H, Bielak LF et al.
01-01-2011
The association and causal inference between circulating 25-hydroxy vitamin D concentration and the risk of type 2 diabetesForouhi NG, Ye Z, Rickard AP, Khaw K-T, Luben R, Langenberg C, Wareham NJ
01-01-2011
Large-scale replication using Metabochip array identifies additional genetic loci influencing glycaemic traitsProkopenko I, Lagou V, Scott RA, Wheeler E, Welch R, Luan J, Maegi R, Teslovich TM et al.
01-01-2011
2010
Differential White Blood Cell Count and Type 2 Diabetes: Systematic Review and Meta-Analysis of Cross-Sectional and Prospective StudiesGkrania-Klotsas E, Ye Z, Cooper AJ, Sharp SJ, Luben R, Biggs ML, Chen L-K, Gokulakrishnan K et al.
Plos One, Public Library of Science (Plos) vol. 5 (10)
18-10-2010
Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic PathwaysSoranzo N, Sanna S, Wheeler E, Gieger C, Radke D, Dupuis J, Bouatia-Naji N, Langenberg C et al.
Diabetes, American Diabetes Association vol. 59 (12), 3229-3239.
21-09-2010
Interactions of Dietary Whole-Grain Intake With Fasting Glucose– and Insulin-Related Genetic Loci in Individuals of European Descent A meta-analysis of 14 cohort studiesNettleton JA, McKeown NM, Kanoni S, Lemaitre RN, Hivert M-F, Ngwa J, van Rooij FJA, Sonestedt E et al.
Diabetes Care, American Diabetes Association vol. 33 (12), 2684-2691.
06-08-2010
Biological, clinical and population relevance of 95 loci for blood lipidsTeslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S et al.
Nature, Springer Nature vol. 466 (7307), 707-713.
01-08-2010
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysisVoight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, Zeggini E, Huth C et al.
Nature Genetics, Springer Nature vol. 42 (7), 579-589.
27-06-2010
Genetic Markers of Adult Obesity Risk Are Associated with Greater Early Infancy Weight Gain and GrowthElks CE, Loos RJF, Sharp SJ, Langenberg C, Ring SM, Timpson NJ, Ness AR, Smith GD et al.
Plos Medicine, Public Library of Science (Plos) vol. 7 (5)
25-05-2010
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskDupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL et al.
Nature Genetics, Springer Nature vol. 42 (5), 464-464.
01-05-2010
MTNR1B rs10830963 is associated with fasting plasma glucose, HbA1Cand impaired beta-cell function in Chinese Hans from ShanghaiLiu C, Wu Y, Li H, Qi Q, Langenberg C, Loos RJ, Lin X
Bmc Medical Genomics, Springer Nature vol. 11 (1)
14-04-2010
Analysis of TBC1D4 in patients with severe insulin resistanceDash S, Langenberg C, Fawcett KA, Semple RK, Romeo S, Sharp S, Sano H, Lienhard GE et al.
Diabetologia, Springer Nature vol. 53 (6), 1239-1242.
27-03-2010
O10 Une méta-analyse GWA de la glycémie après 2 h d’HGPO révèle que GIPR est associé avec la sécrétion de l’insuline en réponse au glucose et que ADCY5 est un nouveau gène de susceptibilité au diabète de type 2Bouatia-Naji N, Saxena R, Hivert MF, Langenberg C, Tanaka T, Pankow J, Vollenweider P, Lyssenko V et al.
Diabetes & Metabolism, Elsevier vol. 36
01-03-2010
Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in HumansIngelsson E, Langenberg C, Hivert M-F, Prokopenko I, Lyssenko V, Dupuis J, Mägi R, Sharp S et al.
Diabetes, American Diabetes Association vol. 59 (5), 1266-1275.
25-02-2010
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskDupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL et al.
Nature Genetics, Springer Nature vol. 42 (2), 105-116.
17-01-2010
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challengeSaxena R, Hivert M-F, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, Lyssenko V, Bouatia-Naji N et al.
Nature Genetics, Springer Nature vol. 42 (2), 142-148.
17-01-2010
Interactions of Dietary Whole-Grain Intake With Fasting Glucose- and Insulin-Related Genetic Loci in Individuals of European Descent A meta-analysis of 14 cohort studiesNettleton JA, McKeown NM, Kanoni S, Lemaitre RN, Hivert M-F, Ngwa J, van Rooij FJA, Sonestedt E et al.
Diabetes Care vol. 33 (12), 2684-2691.
01-01-2010
Age-dependent genetic effects on post-load glucose during 18 years of follow-up of the Whitehall II CohortLangenberg C, Jensen AC, Barker A, Brunner EJ, Hingorani AD, Kumari M, Kivimaeki M, Wareham NJ et al.
01-01-2010
2009
Parental origin of sequence variants associated with complex diseasesKong A, Steinthorsdottir V, Masson G, Thorleifsson G, Sulem P, Besenbacher S, Jonasdottir A, Sigurdsson A et al.
Nature, Springer Nature vol. 462 (7275), 868-874.
01-12-2009
A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin LevelsRichards JB, Waterworth D, O'Rahilly S, Hivert M-F, Loos RJF, Perry JRB, Tanaka T, Timpson NJ et al.
Plos Genetics, Public Library of Science (Plos) vol. 5 (12)
01-12-2009
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetesPerry JRB, Weedon MN, Langenberg C, Jackson AU, Lyssenko V, Sparsø T, Thorleifsson G, Grallert H et al.
Human Molecular Genetics, Oxford University Press (Oup) vol. 19 (3), 535-544.
18-11-2009
Common Genetic Determinants of Glucose Homeostasis in Healthy Children The European Youth Heart StudyKelliny C, Ekelund U, Andersen LB, Brage S, Loos RJF, Wareham NJ, Langenberg C
Diabetes, American Diabetes Association vol. 58 (12), 2939-2945.
09-09-2009
Underlying Genetic Models of Inheritance in Established Type 2 Diabetes AssociationsSalanti G, Southam L, Altshuler D, Ardlie K, Barroso I, Boehnke M, Cornelis MC, Frayling TM et al.
American Journal of Epidemiology, Oxford University Press (Oup) vol. 170 (5), 537-545.
14-07-2009
A truncation mutation in TBC1D4 in a family with acanthosis nigricans and postprandial hyperinsulinemiaDash S, Sano H, Rochford JJ, Semple RK, Yeo G, Hyden CSS, Soos MA, Clark J et al.
Proceedings of The National Academy of Sciences of The United States of America, Proceedings of The National Academy of Sciences vol. 106 (23), 9350-9355.
09-06-2009
Common genetic variation in the melatonin receptor 1B gene (MTNR1B) is associated with decreased early-phase insulin responseLangenberg C, Pascoe L, Mari A, Tura A, Laakso M, Frayling TM, Barroso I, Loos RJF et al.
Diabetologia, Springer Nature vol. 52 (8)
20-05-2009
Mendelian Randomization Studies of the Role of Biomarkers in Type 2 DiabetesPerry J, Zeggini E, Scott L, Saxena R, Voight B, Ferrucci L, Maggio M, Paolisso G et al.
01-01-2009
Childhood Phenotypes Related to Adult Obesity: The Application of Genetic Risk VariantsElks C, Loos RJF, Davey-Smith G, Dunger D, Wareham N, Ong K, Sharp S, Langenberg C et al.
01-01-2009
Novel Genetic Loci Implicated in Fasting Glucose Homeostasis and Their Impact on Related Metabolic TraitsDupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL et al.
01-01-2009
A Large Genome-wide Association Study of Glycated Hemoglobin Identifies Ten Common Variants not Mediated Through BMIWheeler E, Soranzo N, Sanna S, Gieger C, Radke D, Dupuis J, Stolerman E, Bouatia-Naji N et al.
01-01-2009
Genome-wide meta-analysis identifies novel genetic loci associated with OGTT-induced post-challenge glucoseLangenberg C, Saxena R, Hivert M-F, Tanaka T, Pankow JS, Lyssenko V, Boutia-Naji N, Kao WHL et al.
01-01-2009
Novel genetic loci implicated in fasting glucose homeostasis and their impact on related metabolic traitsProkopenko I, Dupuis J, Langenberg C, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL et al.
01-01-2009
Meta-Analyses of Genome-Wide Association Studies for 2-Hour Glucose Levels during an Oral Glucose Tolerance Test Identify Novel Genetic LociSaxena R, Hivert M-F, Dupuis J, Langenberg C, Kao WL, Tanaka T, Jackson AU, Pankow JS et al.
01-01-2009
Variants in the DGKB Gene Influence Fasting Glucose Levels in Populations of European and East Asian DescentProkopenko I, Hottenga JJ, Aulchenko YS, Thorleifsson G, Dupuis J, Florez JC, Go MJ, Jackson AU et al.
01-01-2009
2008
Variants in MTNR1B influence fasting glucose levelsProkopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJF, Manning AK et al.
Nature Genetics, Springer Nature vol. 41 (1), 77-81.
07-12-2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesZeggini E, Scott LJ, Saxena R, Voight BF, Marchini JL, Hu T, de Bakker PI, Abecasis GR et al.
Nature Genetics, Springer Nature vol. 40 (5), 638-645.
30-03-2008
Prevalence of Angina in Women Versus MenHemingway H, Langenberg C, Damant J, Frost C, Pyörälä K, Barrett-Connor E
Circulation, Wolters Kluwer vol. 117 (12), 1526-1536.
17-03-2008
Usefulness of Microalbuminuria Versus the Metabolic Syndrome as a Predictor of Cardiovascular Disease in Women and Men >40 Years of Age (from the Rancho Bernardo Study)Jassal SK, Langenberg C, von Mühlen D, Bergstrom J, Barrett-Connor E
The American Journal of Cardiology, Elsevier vol. 101 (9), 1275-1280.
07-03-2008
Pre-morbid intelligence, the metabolic syndrome and mortality: the Vietnam Experience StudyBatty GD, Gale CR, Mortensen LH, Langenberg C, Shipley MJ, Deary IJ
Diabetologia, Springer Nature vol. 51 (3), 436-443.
18-01-2008
Novel type 2 diabetes susceptibility loci and measures of glycaemic control in a population based study of healthy childrenLangenberg C, Loos RJF, Brage S, Sardinha LB, Andersen LB, Ekelund U, Wareham NJ
01-01-2008
2007
Diabetes and Coronary Heart Disease in Filipino-American Women Role of growth and life-course socioeconomic factorsLangenberg C, Araneta MRG, Bergstrom J, Marmot M, Barrett-Connor E
Diabetes Care, American Diabetes Association vol. 30 (3), 535-541.
01-03-2007
Life course body size and lipid levels at 53 years in a British birth cohortSkidmore PML, Hardy RJ, Kuh DJ, Langenberg C, Wadsworth MEJ
Journal of Epidemiology & Community Health, Bmj vol. 61 (3)
26-02-2007
2006
Household Wealth and the Metabolic Syndrome in the Whitehall II StudyPerel P, Langenberg C, Ferrie J, Moser K, Brunner E, Marmot M
Diabetes Care, American Diabetes Association vol. 29 (12), 2694-2700.
01-12-2006
Adult height and lung function as markers of life course exposures: Associations with risk factors and cause-specific mortalityBatty GD, Gunnell D, Langenberg C, Smith GD, Marmot MG, Shipley MJ
European Journal of Epidemiology, Springer Nature vol. 21 (11), 795-801.
01-11-2006
Social Circumstances and Education: Life Course Origins of Social Inequalities in Metabolic Risk in a Prospective National Birth CohortLangenberg C, Kuh D, Wadsworth MEJ, Brunner E, Hardy R
American Journal of Public Health, American Public Health Association vol. 96 (12), 2216-2221.
31-10-2006
Association of Adiponectin with Coronary Heart Disease and MortalityLaughlin GA, Barrett-Connor E, May S, Langenberg C
American Journal of Epidemiology, Oxford University Press (Oup) vol. 165 (2), 164-174.
27-09-2006
Birth weight, components of height and coronary heart disease: evidence from the Whitehall II studyFerrie JE, Langenberg C, Shipley MJ, Marmot MG
International Journal of Epidemiology, Oxford University Press (Oup) vol. 35 (6), 1532-1542.
24-08-2006
Cardiovascular Death and the Metabolic Syndrome Role of adiposity-signaling hormones and inflammatory markersLangenberg C, Bergstrom J, Scheidt-Nave C, Pfeilschifter J, Barrett-Connor E
Diabetes Care, American Diabetes Association vol. 29 (6), 1363-1369.
01-06-2006
Ghrelin and Bone: Is There an Association in Older Adults?: The Rancho Bernardo Study*Weiss LA, Langenberg C, Barrett‐Connor E
Journal of Bone and Mineral Research, Oxford University Press (Oup) vol. 21 (5), 752-757.
01-05-2006
Sex differences in angina pectoris: meta-analysis of international variations in 53 studies in 23 countriesLangenberg C, Barrett-Connor E, Damant J, Hemingway H
European Journal of Preventive Cardiology, Oxford University Press (Oup) vol. 13 (Supplement 1)
01-05-2006
Metabolic syndrome improves the prediction of coronary heart disease mortality in diabetesLangenberg C, Bergstrom J, Von Mühlen D, Barrett-Connor E
01-01-2006
Aortic and coronary calcium in diabetic and nondiabetic men and women in the Multi-Ethnic Study of Atherosclerosis (MESA)Langenberg C, Allison M, Wong N, Detrano R, Shea S, Carr J, Criqui M
01-01-2006
Albuminuria improves prediction of cardiovascular disease mortality in older women with or without metabolic syndromeJassal SK, Langenberg C, Bergstrom J, von Muhlen D, Barrett-Connor E
01-01-2006
Novel risk factors do not improve prediction of cardiovascular mortality: Evidence from the Rancho Bernardo StudyBergstrom J, Langenberg C, von Muhlen D, Barrett-Connor E
01-01-2006
2005
Adult height in relation to mortality from 14 cancer sites in men in London (UK): evidence from the original Whitehall studyBatty GD, Shipley MJ, Langenberg C, Marmot MG, Smith GD
Annals of Oncology, Elsevier vol. 17 (1), 157-166.
25-10-2005
Ghrelin, Adiponectin, and Leptin Do Not Predict Long-term Changes in Weight and Body Mass Index in Older Adults: Longitudinal Analysis of the Rancho Bernardo CohortLangenberg C, Bergstrom J, Laughlin GA, Barrett-Connor E
American Journal of Epidemiology, Oxford University Press (Oup) vol. 162 (12), 1189-1197.
19-10-2005
Ghrelin and the Metabolic Syndrome in Older AdultsLangenberg C, Bergstrom J, Laughlin GA, Barrett-Connor E
The Journal of Clinical Endocrinology & Metabolism, The Endocrine Society vol. 90 (12), 6448-6453.
04-10-2005
211-S: Household Wealth and the Metabolic Syndrome in the Whitehall II CohortPerel P, Langenberg C, Ferrie J, Moser K, Brunner E, Marmot M
American Journal of Epidemiology, Oxford University Press (Oup) vol. 161 (Supplement_1), s53-s53.
27-06-2005
Department of ErrorThe Lancet, Elsevier vol. 365 (9471)
01-05-2005
Influence of short stature on the change in pulse pressure, systolic and diastolic blood pressure from age 36 to 53 years: an analysis using multilevel modelsLangenberg C, Hardy R, Breeze E, Kuh D, Wadsworth MEJ
International Journal of Epidemiology, Oxford University Press (Oup) vol. 34 (4), 905-913.
15-04-2005
Adult Socioeconomic Position and the Association Between Height and Coronary Heart Disease Mortality: Findings From 33 Years of Follow-Up in the Whitehall StudyLangenberg C, Shipley MJ, Batty GD, Marmot MG
American Journal of Public Health, American Public Health Association vol. 95 (4), 628-632.
01-04-2005
Cardiovascular risk at age 53 years in relation to the menopause transition and use of hormone replacement therapy: a prospective British birth cohort studyKuh D, Langenberg C, Hardy R, Kok H, Cooper R, Butterworth S, Wadsworth MEJ
Bjog An International Journal of Obstetrics & Gynaecology, Wiley vol. 112 (4), 476-485.
19-02-2005
Birthweight, childhood social class, and change in adult blood pressure in the 1946 British birth cohort (vol 362, pg 1178, 2003)Hardy R, Kuh D, Langenberg C, Wadsworth MEJ
Lancet vol. 365 (9471), 1620-1620.
01-01-2005
Cardiovascular death and the metabolic syndrome: Role of inflammatory cytokines and adiposity signaling hormonesLangenberg C, Bergstrom J, Barrett-Connor E
01-01-2005
Hormonal signals of weight homeostasis and 18-year weight change in older adults: Longitudinal analysis of the Rancho Bernardo cohortLangenberg C, Bergstrom J, Laughlin GA, Barrett-Connor E
01-01-2005
2004
Birthweight, childhood growth, and blood pressure at 43 years in a British birth cohortHardy R, Wadsworth MEJ, Langenberg C, Kuh D
International Journal of Epidemiology, Oxford University Press (Oup) vol. 33 (1), 121-129.
01-02-2004
Birth Weight and Lipids in a National Birth Cohort StudySkidmore PML, Hardy RJ, Kuh DJ, Langenberg C, Wadsworth MEJ
Arteriosclerosis Thrombosis and Vascular Biology, Wolters Kluwer vol. 24 (3), 588-594.
08-01-2004
2003
Commentary: The association between height growth and cholesterol levels during puberty: implications for adult healthHardy R, Langenberg C
International Journal of Epidemiology, Oxford University Press (Oup) vol. 32 (6), 1110-1111.
01-12-2003
The life course prospective design: an example of benefits and problems associated with study longevityWadsworth MEJ, Butterworth SL, Hardy RJ, Kuh DJ, Richards M, Langenberg C, Hilder WS, Connor M
Social Science & Medicine, Elsevier vol. 57 (11), 2193-2205.
01-12-2003
Birthweight, childhood social class, and change in adult blood pressure in the 1946 British birth cohortHardy R, Kuh D, Langenberg C, Wadsworth ME
The Lancet, Elsevier vol. 362 (9391), 1178-1183.
01-10-2003
Central and total obesity in middle aged men and women in relation to lifetime socioeconomic status: evidence from a national birth cohortLangenberg C, Hardy R, Kuh D, Brunner E, Wadsworth M
Journal of Epidemiology & Community Health, Bmj vol. 57 (10)
01-10-2003
Commentary: Disentangling the association between short height and cardiovascular risk—genes or environment?Langenberg C, Marmot M
International Journal of Epidemiology, Oxford University Press (Oup) vol. 32 (4), 614-616.
01-08-2003
Influence of height, leg and trunk length on pulse pressure, systolic and diastolic blood pressureLangenberg C, Hardy R, Kuh D, Wadsworth ME
Journal of Hypertension, Wolters Kluwer vol. 21 (3), 537-543.
01-03-2003
Human organic anion transporter 3 (hOAT3) in human adrenocortical cells transports cortisolAsif AR, Grunewald RW, Langenberg C, Metten M, Jarry H, Müller GA, Burckhardt G, Hagos Y
01-01-2003
2002
Mortality in adults aged 26-54 years related to socioeconomic conditions in childhood and adulthood: post war birth cohort studyKuh D, Hardy R, Langenberg C, Richards M, Wadsworth MEJ
The Bmj, Bmj vol. 325 (7372)
09-11-2002
2001
EbM-courses for hospital and practise settings - Current models in GermanyPritsche L, Donner-Banzhoff N, Druck G, Kunz R, Langenberg C, Lelgemann M, Pientka L, Von Maxen A et al.
Zeitschrift Fur Arztliche Fortbildung Und Qualitatssicherung vol. 95 (4), 297-298.
01-12-2001
Evidence-based medicine: What kind of competencies should medical education provide?Helou A, Perleth M, Lühmann D, Langenberg C, Busse R
01-01-2001
1999
Final and causal foundations of medical practice--two achievements of evidence-based medicine.Raspe H, Langenberg C
Zeitschrift FüR Evidenz Fortbildung Und QualitäT Im Gesundheitswesen vol. 93 (4)
01-06-1999
Machine learning-guided deconvolution of plasma protein levelsPietzner M, Beuchel C, Demircan K, Anton JH, Zeng W, Römisch-Margl W, Yasmeen S, Uluvar B et al.
In Medrxiv
A genetic map of human metabolism across the allele frequency spectrumZoodsma M, Beuchel C, Yasmeen S, Kohleick L, Nepal A, Koprulu M, Kronenberg F, Mayr M et al.
In Medrxiv
Leveraging Large-Scale Biobanks for Therapeutic Target DiscoveryFerolito BR, Dashti H, Giambartolomei C, Peloso GM, Golden DJ, Gravel-Pucillo K, Rasooly D, Horimoto AR et al.
In Medrxiv
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityKim HI, DeBoever C, Walter K, Kalantzis G, Li C, Mozaffari SV, Kundu K, Jacobs BM et al.
In Medrxiv
Nanoparticle enriched mass spectrometry proteomics in British South Asians identifies novel variant-protein-disease mechanismsPietzner M, Williamson A, Hunt KA, Koprulu M, Kohleick L, Demircan K, Team GHR, Finer S et al.
In Medrxiv
Glycaemic and bodyweight effects of GIPR coding variation reflect differences in both surface expression and intrinsic functional impairmentManchanda Y, Desoki R, Gardner EJ, Perry JR, Wainscott DB, Stutsman C, Langenberg C, Coghlan M et al.
In Medrxiv
A genomic-led strategy to anticipate drug safety effectsFerolito BR, Horimoto AR, Gravel-Pucillo K, Golden DJ, Dashti H, Giambartolomei C, Rasooly D, Matty R et al.
In Medrxiv
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controlsHodgson S, Bui V, Bigossi M, Bigossi M, Bigossi M, Huerta-Chagoya A, Hu S, Blee AM et al.
In Medrxiv
Proteomic and clinical impact of human knockouts in British South AsiansZanini JC, Pietzner M, Koprulu M, Zoodsma M, Williamson A, Hunt KA, Manolias A, Walter K et al.
In Medrxiv
GWAS metanalysis of atrial fibrillation reveals significant sex-related heterogeneity effects of the PITX2 and CFL2 lociCárcel-Márquez J, Boldo P, Llucià-Carol L, Muiño E, Gallego-Fabrega C, Cullell N, Lledós M, Martín-Campos JM et al.
In Research Square
KidneyGenAfrica: A multi-cohort Genome-wide association study and polygenic prediction of kidney function in 110,000 continental and diasporan AfricansFatumo S, Kamiza A, Chikowore T, Chen G, Ojewunmi O, Machipisa T, Zhou F, Mayanja R et al.
In Research Square
Quantifying the multi-tissue response to glucose ingestion in humans by plasma proteomicsUluvar B, Williamson A, Kolnes KJ, Jeppesen PB, Kolnes AJ, Koprulu M, Zoodsma M, Beuchel C et al.
Diabetologia, Springer
Estimating excess 1- year mortality from COVID-19 according to underlying conditions and age in England: a rapid analysis using NHS health records in 3.8 million adultsBanerjee A, Pasea L, Harris S, Gonzalez-Izquierdo A, Torralbo A, Shallcross L, Noursadeghi M, Pillay D et al.
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rs641738C>T near MBOAT7 is positively associated with liver fat, ALT, and histological severity of NAFLD: a meta-analysisTeo K, Abeysekera KWM, Adams L, Aigner E, Banales JM, Banerjee R, Basu P, Berg T et al.
In Medrxiv
A Saturated Map of Common Genetic Variants Associated with Human Height from 5.4 Million Individuals of Diverse AncestriesYengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, Sakaue S, Graff M, Eliasen AU et al.
In Biorxiv
Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationMahajan A, Spracklen CN, Zhang W, Ng MC, Petty LE, Kitajima H, Yu GZ, Rüeger S et al.
In Medrxiv
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat DistributionJustice AE, Karaderi T, Highland HM, Young KL, Graff M, Lu Y, Turcot V, Auer PL et al.
In Biorxiv
Genetic insights into the biological mechanisms governing human ovarian ageingRuth KS, Day FR, Hussain J, Martínez-Marchal A, Aiken CE, Azad A, Thompson DJ, Abe H et al.
In Medrxiv
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysisKanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF et al.
In Medrxiv
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsRamdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL et al.
In Biorxiv
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failureShah S, Henry A, Roselli C, Lin H, Sveinbjörnsson G, Fatemifar G, Hedman ÅK, Wilk JB et al.
In Biorxiv
The Trans-Ancestral Genomic Architecture of Glycaemic TraitsChen J, Spracklen CN, Marenne G, Varshney A, Corbin LJ, Luan J, Willems S, Wu Y et al.
In Biorxiv
Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressureWarren H, Edwards T, Vaez A, Keaton J, Kamali Z, Xie T, Ani A, Evangelou E et al.
In Research Square
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic RegulationNg NHJ, Willems SM, Fernandez J, Fine RS, Wheeler E, Wessel J, Kitajima H, Marenne G et al.
In Biorxiv
Genetic analysis of over one million people identifies 535 novel loci for blood pressureEvangelou E, Warren HR, Mosen-Ansorena D, Mifsud B, Pazoki R, Gao H, Ntritsos G, Dimou N et al.
In Biorxiv
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetesMahajan A, Wessel J, Willems SM, Zhao W, Robertson NR, Chu AY, Gan W, Kitajima H et al.
In Biorxiv
Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibilityDay FR, Thompson DJ, Helgason H, Chasman DI, Finucane H, Sulem P, Ruth KS, Whalen S et al.
In Biorxiv
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidneyWain LV, Vaez A, Jansen R, Joehanes R, van der Most PJ, Erzurumluoglu AM, O'Reilly P, Cabrera CP et al.
In Biorxiv
Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratificationLagou V, Jiang L, Ulrich A, Zudina L, González KSG, Balkhiyarova Z, Faggian A, Chen S et al.
In Medrxiv
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factorsWarrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S et al.
In Biorxiv
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsMahajan A, Taliun D, Thurner M, Robertson NR, Torres JM, Rayner NW, Steinthorsdottir V, Scott RA et al.
In Biorxiv
STROBE-MR: Guidelines for strengthening the reporting of Mendelian randomization studiesDavey Smith G, Davies NM, Dimou N, Egger M, Gallo V, Golub R, Higgins JP, Langenberg C et al.
In Peerj Preprints
New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestriesShrine N, Guyatt AL, Erzurumluoglu AM, Jackson VE, Hobbs BD, Melbourne C, Batini C, Fawcett KA et al.
In Biorxiv
SNPs associated with HHIP expression have differential effects on lung function in males and femalesFawcett K, Obeidat M, Melbourne C, Shrine N, Guyatt A, John C, Luan J, Richmond A et al.
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9Schmidt AF, Holmes MV, Preiss D, Swerdlow D, Denaxas S, Fatemifar G, Faraway R, Finan C et al.
In Biorxiv
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failureRasooly D, Peloso GM, Pereira AC, Dashti H, Giambartolomei C, Wheeler E, Aung N, Ferolito BR et al.
In Medrxiv
Multi-ancestry genome-wide association study improves resolution of genes, pathways and pleiotropy for lung function and chronic obstructive pulmonary diseaseShrine N, Izquierdo AG, Chen J, Packer R, Hall RJ, Guyatt AL, Batini C, Thompson RJ et al.
In Medrxiv
ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenonHartmann S, Yasmeen S, Jacobs BM, Denaxas S, Pirmohamed M, Gamazon ER, Caulfield MJ, Team GHR et al.
In Medrxiv
Performance of polygenic risk scores in screening, prediction, and risk stratificationHingorani A, Gratton J, Finan C, Schmidt A, Patel R, Sofat R, Kuan V, Langenberg C et al.
In Medrxiv
From genome to phenome via the proteome: broad capture, antibody-based proteomics to explore disease mechanismsKoprulu M, Carrasco-Zanini J, Wheeler E, Lockhart S, Kerrison ND, Wareham NJ, Pietzner M, Langenberg C
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Causal effects of maternal circulating amino acids on offspring birthweight: a Mendelian randomisation studyZhao J, Stewart ID, Baird D, Mason D, Wright J, Zheng J, Gaunt TR, Evans DM et al.
In Medrxiv
Damaging missense variants in IGF1R implicate a role for IGF-1 resistance in the aetiology of type 2 diabetesGardner EJ, Kentistou KA, Stankovic S, Lockhart S, Wheeler E, Day FR, Kerrison ND, Wareham NJ et al.
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The relationship of maternal gestational mass spectrometry-derived metabolites with offspring congenital heart disease: results from multivariable and Mendelian randomization analysesTaylor K, McBride N, Zhao J, Oddie S, Azad R, Wright J, Andreassen OA, Stewart ID et al.
In Medrxiv
Estimating the Population Benefits of Blood Pressure Lowering: A Wide-Angled Mendelian Randomization Study in UK BiobankHiggins H, Mason AM, Larsson SC, Gill D, Langenberg C, Burgess S
In Medrxiv
Elucidating the genetic architecture underlying IGF1 levels and its impact on genomic instability and cancer riskStankovic S, Day FR, Zhao Y, Langenberg C, Wareham NJ, Perry JRB, Ong KK
Body mass index and heart failure risk: a cohort study in 1.5 million individuals and Mendelian randomisation analysisLumbers RT, Katsoulis M, Henry A, Mordi I, Lang C, Hemingway H, Langenberg C, Holmes MV et al.
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Regional fat depot masses are influenced by protein-coding gene variantsNeville MJ, Wittemans LB, Pinnick KE, Todorčević M, Kaksonen R, Pietiläinen KH, Luan J, Scott RA et al.
In Biorxiv
Development and validation of total and regional body composition prediction equations from anthropometry and single frequency segmental bioelectrical impedance with DEXAPowell R, De Lucia Rolfe E, Day FR, Perry JRB, Griffin SJ, Forouhi NG, Brage S, Wareham NJ et al.
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Genetic Disruption of Serine Biosynthesis is a Key Driver of Macular Telangiectasia Type 2 Etiology and ProgressionBonelli R, Ansell BRE, Lotta L, Scerri T, Clemons TE, Leung I, Consortium TM, Peto T et al.
In Biorxiv
Genome-wide scan and fine-mapping of rare nonsynonymous associations implicates intracellular lipolysis genes in fat distribution and cardio-metabolic riskLotta LA, Dong L, Li C, Patel S, Stewart ID, Lim K, Day FR, Wheeler E et al.
In Biorxiv
Characterization of missing values in untargeted MS-based metabolomics data and evaluation of missing data handling strategiesTrinh K, Wahl S, Raffler J, Molnos S, Laimighofer M, Adamski J, Suhre K, Strauch K et al.
In Biorxiv
Circulating selenium and prostate cancer risk: a Mendelian randomization analysisYarmolinsky J, Bonilla C, Haycock PC, Langdon RJ, Lotta LA, Langenberg C, Relton CL, Lewis SJ et al.
In Biorxiv
A comprehensive reanalysis of publicly available GWAS datasets reveals an X chromosome rare regulatory variant associated with high risk for type 2 diabetesBonás-Guarch S, Guindo-Martínez M, Miguel-Escalada I, Grarup N, Sebastian D, Rodriguez-Fos E, Sánchez F, Planas-Félix M et al.
In Biorxiv
Lowering of circulating sclerostin may increase risk of atherosclerosis and its risk factors: evidence from a genome-wide association meta-analysis followed by Mendelian randomizationZheng J, Wheeler E, Pietzner M, Andlauer T, Yau M, Hartley AE, Brumpton BM, Rasheed H et al.
In Medrxiv
An atlas of genetic scores to predict multi-omic traitsXu Y, Ritchie SC, Liang Y, Timmers PRHJ, Pietzner M, Lannelongue L, Lambert SA, Tahir UA et al.
In Biorxiv
Acute caloric restriction acts on the plasma proteome and reveals Apolipoprotein C1 as a signal of nutritional state and metabolic diseaseVernardis S, Demichev V, Lemke O, Grüning N-M, Messner C, White M, Pietzner M, Peluso A et al.
In Research Square
ELF5 is a respiratory epithelial cell-specific risk gene for severe COVID-19Pietzner M, Chua RL, Wheeler E, Jechow K, Radbruch H, Trump S, Heidecker B, Heppner FL et al.
In Medrxiv
Circulating proteins to predict adverse COVID-19 outcomesSu C-Y, Zhou S, Gonzalez-Kozlova E, Butler-Laporte G, Brunet-Ratnasingham E, Nakanishi T, Jeon W, Morrison D et al.
In Medrxiv
Identification of rare loss of function variation regulating body fat distributionKoprulu M, Zhao Y, Wheeler E, Dong L, Rocha N, Patel S, Van de Streek M, Glastonbury CA et al.
In Medrxiv
Mapping genetic determinants of 184 circulating proteins in 26,494 individuals to connect proteins and diseasesMacdonald-Dunlop E, Klarić L, Folkersen L, Timmers PRHJ, Gustafsson S, Zhao JH, Eriksson N, Richmond A et al.
In Medrxiv
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19Klaric L, Gisby JS, Papadaki A, Muckian MD, Macdonald-Dunlop E, Zhao JH, Tokolyi A, Persyn E et al.
In Medrxiv
Cross-platform proteomics to advance genetic prioritisation strategiesPietzner M, Wheeler E, Carrasco-Zanini J, Kerrison ND, Oerton E, Koprulu M, Luan J, Hingorani AD et al.
In Biorxiv
The systematic use of metabolomic epidemiology, biobanks, and electronic medical records for precision medicine initiatives in asthma: findings suggest new guidelines to optimize treatmentKachroo P, Stewart I, Kelly R, Stav M, Mendez K, Dahlin A, Soeteman D, Chu S et al.
In Research Square
Identifying high-risk groups for change in weight and body mass index: population cohort of 11 million measurements in 2.3 million adultsKatsoulis M, Lai AG, Diaz-Ordaz K, Gomes M, Pasea L, Banerjee A, Denaxas S, Tsilidis K et al.
In Medrxiv
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19Gaziano L, Giambartolomei C, Pereira AC, Gaulton A, Posner DC, Swanson SA, Ho Y-L, Iyengar SK et al.
In Medrxiv
A Neanderthal OAS1 isoform Protects Against COVID-19 Susceptibility and Severity: Results from Mendelian Randomization and Case-Control StudiesZhou S, Butler-Laporte G, Nakanishi T, Morrison D, Afilalo J, Afilalo M, Laurent L, Pietzner M et al.
In Medrxiv
Genetic architecture of host proteins interacting with SARS-CoV-2Pietzner M, Wheeler E, Carrasco-Zanini J, Raffler J, Kerrison ND, Oerton E, Auyeung VPW, Luan J et al.
In Biorxiv
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and womenJones G, Trajanoska K, Santanasto AJ, Stringa N, Kuo C-L, Atkins JL, Lewis JR, Duong T et al.
In Medrxiv
Weight change and the incidence of cardiovascular diseases in adults with normal weight, overweight and obesity without chronic diseases; emulating trials using electronic health recordsKatsoulis M, Stavola B, Ordaz K, Gomes M, Lai A, Lagiou P, Wannamethee G, Tsilidis K et al.
In Medrxiv
Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypesSeyres D, Cabassi A, Lambourne JJ, Burden F, Farrow S, McKinney H, Batista J, Kempster C et al.
In Biorxiv
Clinical classifiers of COVID-19 infection from novel ultra-high-throughput proteomicsMessner CB, Demichev V, Wendisch D, Michalick L, White M, Freiwald A, Textoris-Taube K, Vernardis SI et al.
In Medrxiv
High-throughput multivariable Mendelian randomization analysis prioritizes apolipoprotein B as key lipid risk factor for coronary artery diseaseZuber V, Gill D, Ala-Korpela M, Langenberg C, Butterworth A, Bottolo L, Burgess S
In Medrxiv
Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomesLotta LA, Pietzner M, Stewart ID, Wittemans LBL, Li C, Bonelli R, Raffler J, Biggs EK et al.
In Biorxiv
Diabetes mellitus, glycemic traits, and cerebrovascular disease: a Mendelian randomization studyGeorgakis MK, Harshfield EL, Malik R, Franceschini N, Langenberg C, Wareham NJ, Markus HS, Dichgans M
In Medrxiv
Genomic analysis of diet composition finds novel loci and associations with health and lifestyleMeddens SFW, de Vlaming R, Bowers P, Burik CA, Linnér RK, Lee C, Okbay A, Turley P et al.
In Biorxiv
Circulating metabolites modulated by diet are causally associated with depressionAmin N, Spek AVD, Stewart I, Kühnel B, Pietzner M, Alshehri T, Gauß F, Hysi P et al.
In Research Square
Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlapJohn C, Guyatt AL, Shrine N, Packer R, Olafsdottir TA, Liu J, Hayden LP, Chu SH et al.
In Medrxiv
Genetic risk score for intracranial aneurysms to predict aneurysmal subarachnoid hemorrhage and identify associations with patient characteristicsBakker MK, Kanning JP, Abraham G, Martinsen AE, Winsvold BS, Zwart J-A, Bourcier R, Sawada T et al.
In Medrxiv
Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scoresZhu X, Zhu L, Wang H, Cooper RS, Chakravarti A
In Medrxiv
Identification of 370 genetic loci for age at first sex and birth linked to externalising behaviourMills MC, Tropf FC, Brazel DM, van Zuydam N, Vaez A, Consortium BCE, Pers TH, Snieder H et al.
In Biorxiv
Medical history predicts phenome-wide disease onset and enables the rapid response to emerging health threatsSteinfeldt J, Wild B, Buergel T, Pietzner M, Belzen JUZ, Vauvelle A, Hegselmann S, Denaxas S et al.
In Medrxiv
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric DisordersRepetto L, Chen J, Yang Z, Zhai R, Timmers PRHJ, Li T, Twait EL, May-Wilson S et al.
In Research Square
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsSuzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A et al.
In Medrxiv
COL6A3-derived endotrophin mediates the effect of obesity on coronary artery disease: an integrative proteogenomics analysisYoshiji S, Lu T, Butler-Laporte G, Carrasco-Zanini-Sanchez J, Chen Y, Liang K, Willett JDS, Su C-Y et al.
In Medrxiv
Identifying therapeutic targets for cancer: 2,094 circulating proteins and risk of nine cancersSmith-Byrne K, Hedman Å, Dimitriou M, Desai T, Sokolov AV, Schioth HB, Koprulu M, Pietzner M et al.
In Medrxiv
Complex patterns of multimorbidity associated with severe COVID-19 and Long COVIDPietzner M, Denaxas S, Yasmeen S, Ulmer MA, Nakanishi T, Arnold M, Kastenmüller G, Hemingway H et al.
In Medrxiv
Proteomic prediction of common and rare diseasesCarrasco-Zanini J, Pietzner M, Davitte J, Surendran P, Croteau-Chonka DC, Robins C, Torralbo A, Tomlinson C et al.
In Medrxiv
Proteomic analysis of 92 circulating proteins and their effects in cardiometabolic diseasesCarland C, Png G, Malarstig A, Kho PF, Gustafsson S, Michaelsson K, Lind L, Tsafantakis E et al.
In Research Square
Physical activity and sedentary behavior; mechanistic insights and role in disease preventionHoed MD, Wang Z, Emmerich A, Pillon N, Moore T, Hemerich D, Cornelis M, Mazzaferro E et al.
In Research Square
Identifying proteomic risk factors for overall, aggressive and early onset prostate cancer using Mendelian randomization and tumor spatial transcriptomicsDesai TA, Hedman ÅK, Dimitriou M, Koprulu M, Figiel S, Yin W, Johansson M, Watts EL et al.
In Medrxiv
Mapping the aetiological foundations of the heart failure spectrum using human geneticsHenry A, Mo X, Finan C, Chaffin MD, Speed D, Issa H, Denaxas S, Ware JS et al.
In Medrxiv
Genetic architecture of routinely acquired blood tests in a UK cohort of South Asian ancestry reveals ancestry-specific causal variantsJacobs B, Stow D, Hodgson S, Zöllner J, Samuel M, Kanoni S, Bidi S, Team GAHR et al.
In Research Square
Similar and different: systematic investigation of proteogenomic variation between sexes and its relevance for human diseasesKoprulu M, Wheeler E, Kerrison ND, Denaxas S, Carrasco-Zanini J, Orkin CM, Hemingway H, Wareham NJ et al.
In Medrxiv
The performance of AlphaMissense to identify genes causing diseaseChen Y, Butler-Laporte G, Liang KYH, Ilboudo Y, Yasmeen S, Sasako T, Langenberg C, Greenwood CMT et al.
In Medrxiv
Partitioned polygenic scores highlight role of beta-cell function and unfavourable fat distribution patterns in young onset type 2 diabetes in south AsiansSiddiqui M, Hodgson S, Williamson A, Stow D, Jacobs B, Samuel M, Gafton J, Zöllner J et al.
In Research Square
A predictive atlas of disease onset from retinal fundus photographsBuergel T, Loock L, Steinfeldt J, Hoffmann L, Künzel SE, Belzen JUZ, Khawaja AP, Luben R et al.
In Medrxiv
Large-scale Mendelian randomization identifies novel pathways as therapeutic targets for heart failure with reduced ejection fraction and with preserved ejection fractionRasooly D, Giambartolomei C, Peloso GM, Dashti H, Ferolito BR, Golden D, Horimoto ARVR, Pietzner M et al.
In Medrxiv
Damaging mutations in LXRα uncouple lipogenesis from hepatotoxicity and implicate hepatic cholesterol sensing in human liver healthLockhart SM, Muso M, Zvetkova I, Lam BY, Ferrari A, Schoenmakers E, Duckett K, Leslie J et al.
In Biorxiv
Transcriptome- and proteome-wide Mendelian randomization to prioritize therapeutic targets for coronary heart diseaseGaziano L, Allara E, Giambartolomei C, Stacey D, Zhao JH, Dashti H, Jiang T, Ritchie SC et al.
In Medrxiv


