Sylvie Jaillard
Inserm(FR)Université Rennes 2(FR)Institut de Recherche en Santé, Environnement et Travail(FR)CIC Rennes(FR)Laboratoire de Génétique Cellulaire(FR)Centre Hospitalier Universitaire de Rennes(FR)Université de Rennes(FR)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Reproductive Biology and Fertility, Congenital heart defects research
Most-Cited Works
- → Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus(2011)475 cited
- → MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations(2009)220 cited
- → Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases(2009)173 cited
- → Delineation of 15q13.3 microdeletions(2010)150 cited
- → National perioperative outcomes of pulmonary lobectomy for cancer: the influence of nutritional status(2013)149 cited
- → Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress(2008)129 cited