Fadi F. Hamdan

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 64 publications

A Physics-Inspired Approach to Improve Oligonucleotide Design and Gene Synthesis.

A Physics-Inspired Approach to Improve Oligonucleotide Design and Gene Synthesis.

Journal: Computational and structural biotechnology journal

Published: March 23, 2026

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.

Journal: American journal of medical genetics. Part A

Published: February 12, 2026

Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathy.

Mono-allelic p.R37H Dehydrodolichyl Diphosphate Synthase variants lead to protein glycosylation defects, aberrant lipid profiles and interneuron scarcity in a novel mouse model of progressive epileptic encephalopathy.

Journal: bioRxiv : the preprint server for biology

Published: September 02, 2025

CUL1 variants cause severe neurodevelopmental disorders: Insights from human genetics and a zebrafish model of microcephaly.

CUL1 variants cause severe neurodevelopmental disorders: Insights from human genetics and a zebrafish model of microcephaly.

Journal: HGG advances

Published: July 16, 2025

CertPrime: a new oligonucleotide design tool for gene synthesis.

CertPrime: a new oligonucleotide design tool for gene synthesis.

Journal: Computational and structural biotechnology journal

Published: March 17, 2025

Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder.

Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder.

Journal: Pediatric neurology

Published: May 16, 2023

Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control.

Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control.

Journal: Science advances

Published: May 12, 2023

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.

Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.

Journal: Nature genetics

Published: December 23, 2022

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta.

Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 25, 2022

Assessment of burden and segregation profiles of CNVs in patients with epilepsy.

Assessment of burden and segregation profiles of CNVs in patients with epilepsy.

Journal: Annals of clinical and translational neurology

Published: March 14, 2022

Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.

Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.

Journal: Journal of medical genetics

Published: January 28, 2022

De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus.

De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus.

Journal: Brain : a journal of neurology

Published: April 13, 2021

Showing 1-12 of 64

Last Updated: 09/26/2026