The EPIC-Norfolk Study
The genomics of heart failure: design and rationale of the HERMES consortium.
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ESC heart failure. Jun 2021
(DOI : 10.1002/ehf2.13517)
Malik R, Chauhan G, Traylor M, Sargurupremraj M, Okada Y, Mishra A, Rutten-Jacobs L, Giese AK, Van Der Laan SW, Gretarsdottir S, Anderson CD, Chong M, Adams HHH, Ago T, Almgren P, Amouyel P, Ay H, Bartz TM, Benavente OR, Bevan S, Boncoraglio GB, Brown RD, Butterworth AS, Carrera C, Carty CL, Chasman DI, Chen WM, Cole JW, Correa A, Cotlarciuc I, Cruchaga C, Danesh J, de Bakker PIW, DeStefano AL, den Hoed M, Duan Q, Engelter ST, Falcone GJ, Gottesman RF, Grewal RP, Gudnason V, Gustafsson S, Haessler J, Harris TB, Hassan A, Havulinna AS, Heckbert SR, Holliday EG, Howard G, Hsu FC, Hyacinth HI, Ikram MA, Ingelsson E, Irvin MR, Jian X, Jiménez-Conde J, Johnson JA, Jukema JW, Kanai M, Keene KL, Kissela BM, Kleindorfer DO, Kooperberg C, Kubo M, Lange LA, Langefeld CD, Langenberg C, Launer LJ, Lee JM, Lemmens R, Leys D, Lewis CM, Lin WY, Lindgren AG, Lorentzen E, Magnusson PK, Maguire J, Manichaikul A, McArdle PF, Meschia JF, Mitchell BD, Mosley TH, Nalls MA, Ninomiya T, O'Donnell MJ, Psaty BM, Pulit SL, Rannikmäe K, Reiner AP, Rexrode KM, Rice K, Rich SS, Ridker PM, Rost NS, Rothwell PM, Rotter JI, Rundek T, Sacco RL, Sakaue S, Sale MM, Salomaa V, Sapkota BR, Schmidt R, Schmidt CO, Schminke U, Sharma P, Slowik A, Sudlow CLM, Tanislav C, Tatlisumak T, Taylor KD, Thijs VNS, Thorleifsson G, Thorsteinsdottir U, Tiedt S, Trompet S, Tzourio C, van Duijn CM, Walters M, Wareham NJ, Wassertheil-Smoller S, Wilson JG, Wiggins KL, Yang Q, Yusuf S, AFGen Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, International Genomics of Blood Pressure (iGEN-BP) Consortium, INVENT Consortium, STARNET STARNET, Bis JC, Pastinen T, Ruusalepp A, Schadt EE, Koplev S, Björkegren JLM, Codoni V, Civelek M, Smith NL, Trégouët DA, Christophersen IE, Roselli C, Lubitz SA, Ellinor PT, Tai ES, Kooner JS, Kato N, He J, van der Harst P, Elliott P, Chambers JC, Takeuchi F, Johnson AD, BioBank Japan Cooperative Hospital Group, COMPASS Consortium, EPIC-CVD Consortium, EPIC-InterAct Consortium, International Stroke Genetics Consortium (ISGC), METASTROKE Consortium, Neurology Working Group of the CHARGE Consortium, NINDS Stroke Genetics Network (SiGN) NINDS Stroke Genetics Network (SiGN), UK Young Lacunar DNA Study, MEGASTROKE Consortium, Sanghera DK, Melander O, Jern C, Strbian D, Fernandez-Cadenas I, Longstreth WT, Rolfs A, Hata J, Woo D, Rosand J, Pare G, Hopewell JC, Saleheen D, Stefansson K, Worrall BB, Kittner SJ, Seshadri S, Fornage M, Markus HS, Howson JMM, Kamatani Y, Debette S, and Dichgans M
Nature genetics. Jun 2019
(DOI : 10.1038/s41588-019-0449-0)
Malik R, Chauhan G, Traylor M, Sargurupremraj M, Okada Y, Van Der Laan SW, Chong M, Almgren P, Amouyel P, Bartz TM, Bevan S, Butterworth AS, Chasman DI, Chen WM, Correa A, Cruchaga C, Danesh J, de Bakker PIW, den Hoed M, Duan Q, Gudnason V, Gustafsson S, Haessler J, Harris TB, Havulinna AS, Heckbert SR, Holliday EG, Hsu FC, Ikram MA, Ingelsson E, Irvin MR, Jukema JW, Keene KL, Kooperberg C, Kubo M, Lange LA, Langefeld CD, Langenberg C, Launer LJ, Lin WY, Magnusson PK, Maguire J, Manichaikul A, McArdle PF, Mitchell BD, Nalls MA, Psaty BM, Reiner AP, Rice K, Rich SS, Ridker PM, Rotter JI, Sale MM, Salomaa V, Schmidt R, Schmidt CO, Schminke U, Taylor KD, Thorleifsson G, Thorsteinsdottir U, Trompet S, Tzourio C, van Duijn CM, Wareham NJ, Wassertheil-Smoller S, Wilson JG, Wiggins KL, Yang Q, Yusuf S, Bis JC, Ruusalepp A, Schadt EE, Björkegren JLM, Smith NL, Trégouët DA, Lubitz SA, Ellinor PT, Tai ES, Kooner JS, Kato N, van der Harst P, Elliott P, Chambers JC, Takeuchi F, Johnson AD, Sanghera DK, Melander O, Pare G, Hopewell JC, Saleheen D, Stefansson K, Worrall BB, Kittner SJ, Seshadri S, Fornage M, Markus HS, Howson JMM, Kamatani Y, Debette S, and Dichgans M
Nature genetics. May 2017
(DOI : 10.1038/s41588-018-0058-3)
Genetic loci for retinal arteriolar microcirculation.
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PLoS ONE. Feb 2013
(DOI : 10.1371/journal.pone.0065804)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
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Nature. Aug 2010
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