Tim Van Damme

The 2017 international classification of the Ehlers–Danlos syndromes

Fransiska Malfait, Clair A. Francomano, Peter H. Byers et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2017 · 1.9K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

Fransiska Malfait, Ariana Kariminejad, Tim Van Damme et al. · The American Journal of Human Genetics · 2013 · 140 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa

Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed et al. · The American Journal of Human Genetics · 2017 · 113 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

Comprehensive Clinical and Molecular Analysis of 12 Families with Type 1 Recessive Cutis Laxa

Bert Callewaert, Chi-Ting Su, Tim Van Damme et al. · Human Mutation · 2012 · 83 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

<i>RNF216</i> mutations as a novel cause of autosomal recessive Huntington-like disorder

Patrick Santens, Tim Van Damme, Wouter Steyaert et al. · Neurology · 2015 · 66 citations

Life Sciences, Genetics, Molecular Genetics +17