Monique N. Vergouwe

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

Channelopathies, Genetic Disorder, Genetics +5

Inhibition of NF-κB activation in macrophages increases atherosclerosis in LDL receptor–deficient mice

Edwin Kanters, Manolis Pasparakis, Marion J. Gijbels et al. · Journal of Clinical Investigation · 2003 · 312 citations · Full text

Immune Regulation, Immunology, Pathology +22

Inhibition of NF-κB activation in macrophages increases atherosclerosis in LDL receptor–deficient mice

Edwin Kanters, Manolis Pasparakis, Marion J. Gijbels et al. · Journal of Clinical Investigation · 2003 · 268 citations · Full text

Immune Regulation, Immunology, Pathology +22

Myeloid Type I Interferon Signaling Promotes Atherosclerosis by Stimulating Macrophage Recruitment to Lesions

Pieter Goossens, Marion J. Gijbels, Alma Zernecke et al. · Cell Metabolism · 2010 · 222 citations · Full text

Inflammation, Cytokine, Stimulating Macrophage Recruitment +11

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine

Gisela M. Terwindt, Roel A. Ophoff, J. Haan et al. · Neurology · 1998 · 136 citations