Zoha Kibar

Montreal, QC H3T1C5, Canada

Last Updated: 09/26/2026

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Found 35 publications

Traffic Jams in the Brain: How Kinesin Dysfunction Shapes Neurodevelopmental Disorders.

Traffic Jams in the Brain: How Kinesin Dysfunction Shapes Neurodevelopmental Disorders.

Journal: Current issues in molecular biology

Published: June 26, 2026

Correction: Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.

Correction: Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.

Journal: Development (Cambridge, England)

Published: February 06, 2025

Risk of meningomyelocele mediated by the common 22q11.2 deletion.

Risk of meningomyelocele mediated by the common 22q11.2 deletion.

Journal: Science (New York, N.Y.)

Published: May 02, 2024

Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.

Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis.

Journal: Development (Cambridge, England)

Published: February 26, 2024

The contribution of de novo coding mutations to meningomyelocele.

The contribution of de novo coding mutations to meningomyelocele.

Journal: Nature

Published: February 24, 2024

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.

Journal: Thyroid : official journal of the American Thyroid Association

Published: March 11, 2022

A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.

A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia.

Journal: Blood advances

Published: March 04, 2021

Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.

Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention.

Journal: Journal of the Endocrine Society

Published: August 16, 2020

Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects.

Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects.

Journal: Cells

Published: September 03, 2019

Whole exome sequencing identifies novel predisposing genes in neural tube defects.

Whole exome sequencing identifies novel predisposing genes in neural tube defects.

Journal: Molecular genetics & genomic medicine

Published: June 19, 2018

Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2.

Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2.

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: August 22, 2017

A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels.

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

Showing 1-12 of 35

Last Updated: 09/26/2026