Sylvie Langlois

Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental Retardation

Jan M. Friedman, Ágnes Baross, Allen Delaney et al. · The American Journal of Human Genetics · 2006 · 326 citations · Full text

Psychiatry, Genetic Disorder, Genetics +9

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Gregory M. Enns, Vandana Shashi, Matthew N. Bainbridge et al. · Genetics in Medicine · 2014 · 236 citations · Full text

Genetics, Endocytic Pathway, Protein Degradation +6

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.

Wendy P. Robinson, Irene Barrett, L.E. Bernard et al. · PubMed · 1997 · 208 citations

Parental origin of triploidy in human fetuses: evidence for genomic imprinting

Deborah E. McFadden, Linda C. Kwong, Irene Yam et al. · Human Genetics · 1993 · 197 citations

Genetics, Evolutionary Biology, Human Fetuses +7

Uniparental disomy for chromosome 16 in humans.

Dagmar K. Kalousek, Sylvie Langlois, Irene Barrett et al. · PubMed · 1993 · 191 citations