Vincent Marion

Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation

Vincent Marion, Corinne Stoetzel, Dominique Schlicht et al. · Proceedings of the National Academy of Sciences · 2009 · 177 citations · Full text

Metabolic Disorder, Genetics, Cellular Physiology +22

Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit <i>BBIP1</i> (<i>BBS18</i>)

Sophie Scheidecker, Christelle Etard, Nathan W. Pierce et al. · Journal of Medical Genetics · 2013 · 137 citations · Full text

Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis

Shirley Uitte de Willige, Vincent Marion, Frits R. Rosendaal et al. · Journal of Thrombosis and Haemostasis · 2004 · 129 citations · Full text

Thrombosis, Deep Venous Thrombosis, Allelic Variant +11

Exome sequencing identifies mutations in <i>LZTFL1</i>, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly

Vincent Marion, Fanny Stutzmann, Marion Gérard et al. · Journal of Medical Genetics · 2012 · 128 citations

Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease

Jean Muller, Corinne Stoetzel, M. C. Vincent et al. · Human Genetics · 2010 · 127 citations · Full text

Genetic Diseases, Bardet–biedl Syndrome Genes, Genetic Disorder +9