Claudia M Weller

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens, Boukje de Vries, Simona Donatello et al. · Nature Genetics · 2013 · 358 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

High expression of RelA/p65 is associated with activation of nuclear factor-κB-dependent signaling in pancreatic cancer and marks a patient population with poor prognosis

W Weichert, Markus Boehm, Volker Gekeler et al. · British Journal of Cancer · 2007 · 141 citations · Full text

A metabolomic profile is associated with the risk of incident coronary heart disease

Anika A. M. Vaarhorst, Aswin Verhoeven, Claudia M Weller et al. · American Heart Journal · 2014 · 83 citations · Full text

Migraine is not associated with enhanced atherosclerosis

Anine H Stam, Claudia M Weller, A. Cecile J.W. Janssens et al. · Cephalalgia · 2012 · 70 citations

Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome

Olga S. Koutsopoulos, Christine Kretz, Claudia M Weller et al. · European Journal of Human Genetics · 2012 · 64 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8