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Sylvie Jaillard | Researchclopedia

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Sylvie Jaillard

142

Works

3,477

Citations

33

h-index

55

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Affiliations

Hôpital Necker-Enfants Malades2019–2019

Centre National de la Recherche Scientifique2009–2019

Royal Children's Hospital2018–2024

Hudson Institute2019–2021

Inserm2016–2025

Top Works

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

Sébastien Jacquemont,Alexandre Reymond,et al.

2011476 citations

Reproductive Biology and Fertility

Congenital heart defects research

<i>MEF2C</i> 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

Nathalie Le Meur,Muriel Holder‐Espinasse,et al.

2009220 citations

Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases

Caroline Schluth‐Bolard,Bruno Delobel,et al.

2009173 citations

Delineation of 15q13.3 microdeletions

Alice Masurel‐Paulet,Joris Andrieux,et al.

2010150 citations

National perioperative outcomes of pulmonary lobectomy for cancer: the influence of nutritional status

P. Thomas,Julie Berbis,et al.

2013149 citations

Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress

Chloé Quēlin,Claude Bendavid,et al.

2008129 citations

Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures

Gaëlle Thierry,Claire Bénéteau,et al.

2012103 citations

Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study

Sandra Martin-Brevet,Borja Rodríguez‐Herreros,et al.

201891 citations

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci

Claude Bendavid,Lucie Rochard,et al.

200989 citations