Philippe Lemay
Montreal, QC H3T1C5, Canada
Last Updated: 09/26/2026
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Found 8 publications
Whole exome sequencing identifies novel predisposing genes in neural tube defects.
Journal: Molecular genetics & genomic medicine
Published: June 19, 2018
A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels.
Journal: BMC genetics
Published: July 27, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Journal: American journal of human genetics
Published: June 27, 2017
Rare deleterious variants in GRHL3 are associated with human spina bifida.
Journal: Human mutation
Published: December 30, 2016
Epistasis analysis links immune cascades and cerebral amyloidosis.
Journal: Journal of neuroinflammation
Published: August 17, 2015
Loss-of-function de novo mutations play an important role in severe human neural tube defects.
Journal: Journal of medical genetics
Published: January 16, 2015
Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs.
Journal: PloS one
Published: August 26, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026