Marten Hofker

Получаване на мой собствен потребителски профил

Позовавания

	Всички	От 2019
Позовавания	65052	35175
h-индекс	99	55
i10-индекс	246	137

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Публичен достъп

Преглед на всички

62 статии

4 статии

налични

неналични

Въз основа на изисквания при финансирането

Съавтори

Louis HavekesTNO Metabolic Health Research and Prof. Leiden University Medical Center, Leiden, the NetherlandsПотвърден имейл адрес: tno.nl
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theПотвърден имейл адрес: umcg.nl
Ko Willems van DijkLeiden University Medical CenterПотвърден имейл адрес: lumc.nl
Menno de WintherProfessor of Vascular Immune Cell BiologyПотвърден имейл адрес: amsterdamumc.nl
Jingyuan Fu, PhDProfessor, University Medical Center Groningen, NetherlandsПотвърден имейл адрес: umcg.nl
Gertjan van OmmenProfessor in Human Genetics, Leiden University Medical CentreПотвърден имейл адрес: lumc.nl
Debby Koonen, PhDAssistant Professor, University Medical Center Groningen, The NetherlandsПотвърден имейл адрес: umcg.nl
Bart van de Sluis, PhDProfessor of Molecular Genetics (Department of Pediatrics), University of GroningenПотвърден имейл адрес: umcg.nl
Peter PearsonVisiting Professor Human Genetics, Dept Genetics and Evolutionary Biology, University of Sao PauloПотвърден имейл адрес: ib.usp.br
Kristiaan WoutersMaastricht UniversityПотвърден имейл адрес: maastrichtuniversity.nl
Alexandra (Sasha) ZhernakovaProfessor of Human Genome and Exposome, University Medical Centre Groningen, The NetherlandsПотвърден имейл адрес: umcg.nl
Lude FrankeProfessor of Functional Genomics, University Medical Centre GroningenПотвърден имейл адрес: cleverfranke.com
Bart StaelsProfesseur Université LilleПотвърден имейл адрес: pasteur-lille.fr
Jana van Vliet-OstaptchoukPhDПотвърден имейл адрес: umcg.nl
Christoph J. BinderMedical University of ViennaПотвърден имейл адрес: meduniwien.ac.at
Jan Albert KuivenhovenUniversity Medical Center GroningenПотвърден имейл адрес: umcg.nl
Marc Jan BonderPostdoctoral researcher UMCGПотвърден имейл адрес: umcg.nl
Roel A. OphoffProfessor of Psychiatry and Human Genetics, University of California Los AngelesПотвърден имейл адрес: ucla.edu
Folkert KuipersProfessor of Pediatrics, University Medical Center GroningenПотвърден имейл адрес: umcg.nl
Fareeba Sheedfar, DVM, PhD.Digestive System Diseases Unit, University Medical Center Groningen, The NetherlandsПотвърден имейл адрес: umcg.nl

Следене

Marten Hofker

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

Потвърден имейл адрес: umcg.nl - Начална страница

atherosclerosis metabolism genetics inflammation Diabetes


Заглавие Сортиране по цитати Сортиране по година Сортиране по заглавие	Позовавания Позовавания	Година
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	26015	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	2923	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	2638	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	1822	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	1268	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	863	2007
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	836	2014
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	801	2016
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	800	2005
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	793	2015
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	763	1992
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	716	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	696	1999
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	598	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	576	1985
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	568	2008
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	510	2018
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	461	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	442	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	441	2011

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