Alexandre Moerman

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

Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey et al. · Nature · 2011 · 474 citations · Full text

Gene Dosage, Genetics, Human Polymorphism +8

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 451 citations · Full text

Kallmann Syndrome Combines, Human Growth, Genetics +21

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

Eva M. Reinthaler, Dennis Lal, Sébastien Lebon et al. · Human Molecular Genetics · 2014 · 69 citations · Full text

Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1

Laïla El Khattabi, Fabien Guimiot, Eva Pipiras et al. · European Journal of Human Genetics · 2014 · 67 citations · Full text

Biology, Linkage Disequilibrium, Genetic Disorder +8

Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age

Sandra Mercier, Annick Toutain, Aurélie Toussaint et al. · European Journal of Human Genetics · 2013 · 63 citations · Full text

Rare Diseases, Clinical Specificity, Pediatrics +6