Mehdi Zarrei
Rm. 139715, 686 Bay St, M5G 0A4
Toronto, ON, Canada
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 53 publications
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.
Journal: Scientific reports
Published: August 12, 2024
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing.
Journal: NPJ genomic medicine
Published: July 29, 2024
Increased burden of rare protein-truncating variants in constrained, brain-specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder.
Journal: Genes, brain, and behavior
Published: May 19, 2023
Genetic overlap between idiopathic scoliosis and schizophrenia in the general population.
Journal: Spine deformity
Published: April 20, 2023
Gene copy number variation and pediatric mental health/neurodevelopment in a general population.
Journal: Human molecular genetics
Published: March 09, 2023
Three generation families: Analysis of de novo variants in autism.
Journal: European journal of human genetics : EJHG
Published: September 19, 2022
The Phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.
Journal: Journal of medical genetics
Published: July 21, 2022
Disruption of DDX53 coding sequence has limited impact on iPSC-derived human NGN2 neurons.
Journal: BMC medical genomics
Published: June 07, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Journal: Cell
Published: May 05, 2022
Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder.
Journal: Translational psychiatry
Published: February 14, 2022
Last Updated: 09/26/2026