MRC Epidemiology Unit
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
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Nature. Feb 2024
(DOI : 10.1038/s41586-024-07019-6)
A saturated map of common genetic variants associated with human height.
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Nature. Oct 2022
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Nature genetics. May 2022
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The genomics of heart failure: design and rationale of the HERMES consortium.
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Nature genetics. Jun 2019
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Nature genetics. Mar 2018
(DOI : 10.1038/s41588-018-0050-y)
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Nature genetics. Mar 2018
(DOI : 10.1038/s41588-018-0082-3)
Mahajan A, Taliun D, Thurner M, Robertson NR, Torres JM, Rayner NW, Payne AJ, Steinthorsdottir V, Scott RA, Grarup N, Cook JP, Schmidt EM, Wuttke M, Sarnowski C, Mägi R, Nano J, Gieger C, Trompet S, Lecoeur C, Preuss MH, Prins BP, Guo X, Bielak LF, Below JE, Bowden DW, Chambers JC, Kim YJ, Ng MCY, Petty LE, Sim X, Zhang W, Bennett AJ, Bork-Jensen J, Brummett CM, Canouil M, Ec Kardt KU, Fischer K, Kardia SLR, Kronenberg F, Läll K, Liu CT, Locke AE, Luan J, Ntalla I, Nylander V, Schönherr S, Schurmann C, Yengo L, Bottinger EP, Brandslund I, Christensen C, Dedoussis G, Florez JC, Ford I, Franco OH, Frayling TM, Giedraitis V, Hackinger S, Hattersley AT, Herder C, Ikram MA, Ingelsson M, Jørgensen ME, Jørgensen T, Kriebel J, Kuusisto J, Ligthart S, Lindgren CM, Linneberg A, Lyssenko V, Mamakou V, Meitinger T, Mohlke KL, Morris AD, Nadkarni G, Pankow JS, Peters A, Sattar N, Stančáková A, Strauch K, Taylor KD, Thorand B, Thorleifsson G, Thorsteinsdottir U, Tuomilehto J, Witte DR, Dupuis J, Peyser PA, Zeggini E, Loos RJF, Froguel P, Ingelsson E, Lind L, Groop L, Laakso M, Collins FS, Jukema JW, Palmer CNA, Grallert H, Metspalu A, Dehghan A, Köttgen A, Abecasis GR, Meigs JB, Rotter JI, Marchini J, Pedersen O, Hansen T, Langenberg C, Wareham NJ, Stefansson K, Gloyn AL, Morris AP, Boehnke M, McCarthy MI
Nature genetics. Dec 2017
(DOI : 10.1038/s41588-018-0241-6)
Wood AM, Kaptoge S, Butterworth AS, Willeit P, Warnakula S, Sweeting M, Burgess S, Astle W, Koulman A, Verschuren WMM, Sato S, Njølstad I, Woodward M, Salomaa V, Nordestgaard BG, Yeap BB, Melander O, Kuller LH, Balkau B, Koenig W, Casiglia E, Cooper C, Arndt V, Franco OH, Wennberg P, Gallacher J, Völzke H, Dahm CC, Dale CE, Bergmann MM, Crespo CJ, van der Schouw YT, Kaaks R, Simons LA, Lagiou P, Boer JMA, Key TJ, Rodriguez B, Moreno-Iribas C, Davidson KW, Sacerdote C, Wallace RB, Quirós JR, Tumino R, Linneberg A, Panico S, Skeie G, Weiderpass E, Nietert PJ, Psaty BM, Kromhout D, Salamanca-Fernández E, Kiechl S, Grioni S, Palli D, Huerta JM, Price J, Sundström J, Arriola L, Travis RC, Karakatsani A, Trichopoulou A, Kühn T, Grobbee DE, Barrett-Connor E, Boeing H, Overvad K, Kauhanen J, Wareham NJ, Langenberg C, Forouhi N, Wennberg M, Cushman M, Cooper JA, Rodriguez CJ, Voortman T, Meisinger C, Tjønneland A, Brenner H, Dallongeville J, Brunner EJ, Assmann G, Trevisan M, Gillum RF, Ford I, Sattar N, Thompson SG, Ferrari P, Smith GD, Banks E, Di Angelantonio E, Danesh J
Lancet (London, England). Sep 2017
(DOI : 10.1016/S0140-6736(18)30134-X)
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Nature genetics. Aug 2017
(DOI : 10.1038/s41588-017-0011-x)
Exome-wide association study of plasma lipids in >300,000 individuals.
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Nature genetics. Jan 2017
(DOI : 10.1038/ng.3977)
Chaker L, Baumgartner C, den Elzen WP, Collet TH, Ikram MA, Blum MR, Dehghan A, Drechsler C, Luben RN, Portegies ML, Iervasi G, Medici M, Stott DJ, Dullaart RP, Ford I, Bremner A, Newman AB, Wanner C, Sgarbi JA, Dörr M, Longstreth WT, Psaty BM, Ferrucci L, Maciel RM, Westendorp RG, Jukema JW, Ceresini G, Imaizumi M, Hofman A, Bakker SJ, Franklyn JA, Khaw KT, Bauer DC, Walsh JP, Razvi S, Gussekloo J, Völzke H, Franco OH, Cappola AR, Rodondi N, Peeters RP, Thyroid Studies Collaboration Thyroid Studies Collaboration
The Journal of clinical endocrinology and metabolism. Nov 2016
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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.
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The lancet. Diabetes & endocrinology. Oct 2016
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Nature genetics. Dec 2013
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