Dorothée Cailley

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey et al. · Nature · 2011 · 480 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

Éric Bieth, Sanaa Eddiry, Véronique Gaston et al. · European Journal of Human Genetics · 2014 · 180 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome

Paquita Nurden, Najet Debili, Isabelle Coupry et al. · Blood · 2011 · 164 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures

Gaëlle Thierry, Claire Bénéteau, Olivier Pichon et al. · American Journal of Medical Genetics Part A · 2012 · 105 citations

Life Sciences, Genetics, Molecular Genetics +17

Array‐CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum

Caroline Rooryck, Noui Souakri, Dorothée Cailley et al. · American Journal of Medical Genetics Part A · 2010 · 68 citations

Life Sciences, Genetics, Molecular Genetics +17