Ellen Reynders

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2

Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou et al. · Nature Genetics · 2007 · 376 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Golgi function and dysfunction in the first COG4-deficient CDG type II patient

Ellen Reynders, François Foulquier, Elisa Leão Teles et al. · Human Molecular Genetics · 2009 · 138 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1–Cog8 interaction in COG complex formation

François Foulquier, Dániel Ungár, Ellen Reynders et al. · Human Molecular Genetics · 2007 · 123 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1

Renate Zeevaert, François Foulquier, Boyan Dimitrov et al. · Human Molecular Genetics · 2008 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13