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Marten Hofker
Marten Hofker
Professor of Molecular Genetics, UMCG, Groningen University, The Netherlands
Verified email at umcg.nl - Homepage
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Cited by
Year
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
254022017
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
29091996
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
25822012
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
17682016
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
12622007
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
8632007
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
8272014
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
7942005
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
7832016
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
7802015
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
7601992
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
6892015
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
6891999
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
5951993
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
5741985
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
5622008
Gut microbiota composition and functional changes in inflammatory bowel disease and irritable bowel syndrome
A Vich Vila, F Imhann, V Collij, SA Jankipersadsing, T Gurry, Z Mujagic, ...
Science translational medicine 10 (472), eaap8914, 2018
4872018
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
4582010
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
4402003
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
4382011
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