Emilie Landais

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

Microdeletions including <i>YWHAE</i> in the Miller–Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment

Sandesh C. Sreenath Nagamani, Feng Zhang, O A Shchelochkov et al. · Journal of Medical Genetics · 2009 · 170 citations

Life Sciences, Genetics, Molecular Genetics +15

The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients

Camille Leroy, Emilie Landais, Sylvain Briault et al. · European Journal of Human Genetics · 2012 · 134 citations · Full text

Life Sciences, Genetics, Psychiatry +13

Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth

Lionel Van Maldergem, Qingming Hou, Vera M. Kalscheuer et al. · Human Molecular Genetics · 2013 · 79 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Xq28 duplication including <i><scp>MECP2</scp></i> in six unreported affected females: what can we learn for diagnosis and genetic counselling?

Salima El Chehadeh, Renaud Touraine, Fabienne Prieur et al. · Clinical Genetics · 2016 · 55 citations

Life Sciences, Genetics, Molecular Genetics +17