Marten Hofker

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Louis HavekesTNO Metabolic Health Research and Prof. Leiden University Medical Center, Leiden, the NetherlandsVerified email at tno.nl
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theVerified email at umcg.nl
Ko Willems van DijkLeiden University Medical CenterVerified email at lumc.nl
Menno de WintherProfessor of Vascular Immune Cell BiologyVerified email at amc.uva.nl
Gertjan van OmmenProfessor in Human Genetics, Leiden University Medical CentreVerified email at lumc.nl
Jingyuan Fu, PhDProfessor, University Medical Center Groningen, NetherlandsVerified email at umcg.nl
Debby Koonen, PhDAssistant Professor, University Medical Center Groningen, The NetherlandsVerified email at umcg.nl
Bart van de Sluis, PhDProfessor of Molecular Genetics (Department of Pediatrics), University of GroningenVerified email at umcg.nl
Peter PearsonVisiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao PauloVerified email at ib.usp.br
Kristiaan WoutersMaastricht UniversityVerified email at maastrichtuniversity.nl
Alexandra (Sasha) ZhernakovaProfessor of Human Genome and Exposome, University Medical Centre Groningen, The NetherlandsVerified email at umcg.nl
Lude FrankeProfessor of Functional Genomics, University Medical Centre GroningenVerified email at cleverfranke.com
Bart StaelsProfesseur Université LilleVerified email at pasteur-lille.fr
Christoph J. BinderMedical University of ViennaVerified email at meduniwien.ac.at
Jana van Vliet-OstaptchoukPhDVerified email at umcg.nl
Jan Albert KuivenhovenUniversity Medical Center GroningenVerified email at umcg.nl
Roel A. OphoffProfessor of Psychiatry and Human Genetics, University of California Los AngelesVerified email at ucla.edu
Folkert KuipersProfessor of Pediatrics, University Medical Center GroningenVerified email at umcg.nl
Marc Jan BonderPostdoc & Team-leader, DKFZVerified email at dkfz.de
Fareeba Sheedfar, DVM, PhD.Digestive System Diseases Unit, University Medical Center Groningen, The NetherlandsVerified email at umcg.nl

Marten Hofker

Professor of Molecular Genetics, UMCG, Groningen University, The Netherlands

Verified email at umcg.nl - Homepage

atherosclerosis metabolism genetics inflammation Diabetes


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Heart disease and stroke statistics—2017 update: a report from the American Heart Association EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ... circulation 135 (10), e146-e603, 2017	14443	2017
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 RA Ophoff, GM Terwindt, MN Vergouwe, R van Eijk, PJ Oefner, ... Cell 87 (3), 543-552, 1996	2797	1996
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ... The Lancet 380 (9841), 572-580, 2012	2327	2012
Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity A Zhernakova, A Kurilshikov, MJ Bonder, EF Tigchelaar, M Schirmer, ... Science 352 (6285), 565-569, 2016	1400	2016
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes V Steinthorsdottir, G Thorleifsson, I Reynisdottir, R Benediktsson, ... Nature genetics 39 (6), 770-775, 2007	1206	2007
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes J Gudmundsson, P Sulem, V Steinthorsdottir, JT Bergthorsson, ... Nature genetics 39 (8), 977-983, 2007	833	2007
Nuclear factor κB signaling in atherogenesis MPJ De Winther, E Kanters, G Kraal, MH Hofker Arteriosclerosis, thrombosis, and vascular biology 25 (5), 904-914, 2005	738	2005
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy C Wijmenga, JE Hewitt, LA Sandkuijl, LN Clark, TJ Wright, HG Dauwerse, ... Nature genetics 2 (1), 26-30, 1992	728	1992
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data MV Holmes, CE Dale, L Zuccolo, RJ Silverwood, Y Guo, Z Ye, ... Bmj 349, g4164, 2014	718	2014
Mendelian randomization of blood lipids for coronary heart disease MV Holmes, FW Asselbergs, TM Palmer, F Drenos, MB Lanktree, ... European heart journal 36 (9), 539-550, 2015	655	2015
Role of ApoCs in lipoprotein metabolism: functional differences between ApoC1, ApoC2, and ApoC3 MC Jong, MH Hofker, LM Havekes Arteriosclerosis, thrombosis, and vascular biology 19 (3), 472-484, 1999	648	1999
The effect of host genetics on the gut microbiome MJ Bonder, A Kurilshikov, EF Tigchelaar, Z Mujagic, F Imhann, AV Vila, ... Nature genetics 48 (11), 1407-1412, 2016	603	2016
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit JCTV Deutekom, C Wljmenga, EAEV Tlenhoven, AM Gruter, JE Hewitt, ... Human molecular genetics 2 (12), 2037-2042, 1993	556	1993
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome U Francke, HD Ochs, B de Martinville, J Giacalone, V Lindgren, ... American journal of human genetics 37 (2), 250, 1985	546	1985
The gut microbiome contributes to a substantial proportion of the variation in blood lipids J Fu, MJ Bonder, MC Cenit, EF Tigchelaar, A Maatman, JAM Dekens, ... Circulation research 117 (9), 817-824, 2015	532	2015
Dietary cholesterol, rather than liver steatosis, leads to hepatic inflammation in hyperlipidemic mouse models of nonalcoholic steatohepatitis K Wouters, PJ van Gorp, V Bieghs, MJ Gijbels, H Duimel, D Lütjohann, ... Hepatology 48 (2), 474-486, 2008	529	2008
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ... PLoS genetics 6 (2), e1000841, 2010	440	2010
Inhibition of NF-κB activation in macrophages increases atherosclerosis in LDL receptor–deficient mice E Kanters, M Pasparakis, MJJ Gijbels, MN Vergouwe, I Partouns-Hendriks, ... The Journal of clinical investigation 112 (8), 1176-1185, 2003	421	2003
Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA RSN Fehrmann, RC Jansen, JH Veldink, HJ Westra, D Arends, ... PLoS genetics 7 (8), e1002197, 2011	411	2011
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystropothhy JE Hewitt, R Lyle, LN Clark, EM Valleley, TJ Wright, C Wijmenga, ... Human molecular genetics 3 (8), 1287-1295, 1994	358	1994

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