Mylène Béri‐Dexheimer

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

Robin Walters, Sébastien Jacquemont, Armand Valsesia et al. · Nature · 2010 · 554 citations · Full text

Obesity, Metabolic Syndrome, Childhood Obesity +9

Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech

Céline Bonnet, Joris Andrieux, Mylène Béri‐Dexheimer et al. · Journal of Medical Genetics · 2010 · 107 citations · Full text

Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions

Mylène Béri‐Dexheimer, Véronique Latger‐Cannard, Christophe Philippe et al. · European Journal of Human Genetics · 2008 · 94 citations · Full text

Allelic Variant, Point Mutations, Genetic Disorder +10

Further delineation of the <i>MECP2</i> duplication syndrome phenotype in 59 French male patients, with a particular focus on morphological and neurological features

Marguerite Miguet, Laurence Faivre, Jeanne Amiel et al. · Journal of Medical Genetics · 2018 · 61 citations · Full text

Gene–gene interactions of IL13 and IL4RA variants in immediate allergic reactions to betalactam antibiotics

Rosa‐Maria Guéant‐Rodriguez, Antonino Romano, Mylène Béri‐Dexheimer et al. · Pharmacogenetics and Genomics · 2006 · 52 citations