Marten Hofker
Marten Hofker
Professor of Molecular Genetics, UMCG, Groningen University, The Netherlands
Geverifieerd e-mailadres voor umcg.nl - Homepage
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Heart disease and stroke statistics—2017 update
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
9027*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
25611996
American heart association statistics committee and stroke statistics subcommittee
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
Heart disease and stroke statistics-2017 update: a report from the American …, 2017
2559*2017
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
18462012
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
11002007
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
7862007
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
7832016
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
6492005
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
6331992
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
5651999
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
5171985
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
5132014
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
4891993
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
4442008
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
4082015
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 Genet 6 (2), e1000841, 2010
3882010
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
3782003
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 Genet 7 (8), e1002197, 2011
3612011
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
3432016
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
3141994
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