Gwenaëlle Collod‐Béroud

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

François-Olivier Desmet, Dalil Hamroun, Marine Lalande et al. · Nucleic Acids Research · 2009 · 2.5K citations · Full text

Life Sciences, Bioinformatics, Molecular Biology +14

Heterozygous TGFBR2 mutations in Marfan syndrome

Takeshi Mizuguchi, Gwenaëlle Collod‐Béroud, Takushi Akiyama et al. · Nature Genetics · 2004 · 616 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study

Laurence Faivre, Gwenaëlle Collod‐Béroud, Bart Loeys et al. · The American Journal of Human Genetics · 2007 · 603 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome: Figure 1

Laurence Faivre, Robert J. Gorlin, Mary K. Wirtz et al. · Journal of Medical Genetics · 2003 · 281 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Comparison of Clinical Presentations and Outcomes Between Patients With <i>TGFBR2</i> and <i>FBN1</i> Mutations in Marfan Syndrome and Related Disorders

David Attias, Chantal Stheneur, Carine Roy et al. · Circulation · 2009 · 238 citations · Full text

Medicine, Cardiology, Genetics +16