Camille Leroy

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 · 131 citations · Full text

Clinical Disorders, New Patients, Genetic Disorder +4

Bipolar affective disorder and early dementia onset in a male patient with SHANK3 deletion

Ksenija Vucurovic, Emilie Landais, Cécile Delahaigue et al. · European Journal of Medical Genetics · 2012 · 49 citations

Bipolar Affective Disorder, Health Sciences, Psychiatry +13

Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes

Martine Doco‐Fenzy, Camille Leroy, Anouck Schneider et al. · European Journal of Human Genetics · 2013 · 47 citations · Full text

Obesity, Metabolic Syndrome, Myt1l Genes +10

Fetal phenotype associated with the 22q11 deletion

A Noël, Fanny Pelluard, Anne‐Lise Delezoide et al. · American Journal of Medical Genetics Part A · 2014 · 47 citations

De novo deletion of <i>TBL1XR1</i> in a child with non‐specific developmental delay supports its implication in intellectual disability

Anne‐Claude Tabet, Camille Leroy, Céline Dupont et al. · American Journal of Medical Genetics Part A · 2014 · 32 citations