Catherine Bianco-Fallet

Montreal, QC H3T1C5, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 37 publications

Teneurin-3 and latrophilin-2 are required for somatotopic map development and somatosensory topognosis.

Teneurin-3 and latrophilin-2 are required for somatotopic map development and somatosensory topognosis.

Journal: Current biology : CB

Published: November 27, 2025

Teneurin-3 and latrophilin-2 are required for somatotopic map formation and somatosensory topognosis.

Teneurin-3 and latrophilin-2 are required for somatotopic map formation and somatosensory topognosis.

Journal: bioRxiv : the preprint server for biology

Published: September 05, 2025

Unraveling Chylomicron Retention Disease Enhances Insight into SAR1B GTPase Functions and Mechanisms of Actions, While Shedding Light of Intracellular Chylomicron Trafficking.

Unraveling Chylomicron Retention Disease Enhances Insight into SAR1B GTPase Functions and Mechanisms of Actions, While Shedding Light of Intracellular Chylomicron Trafficking.

Journal: Biomedicines

Published: May 22, 2024

Zika virus infection during pregnancy and vertical transmission: case reports and peptide-specific cell-mediated immune responses.

Zika virus infection during pregnancy and vertical transmission: case reports and peptide-specific cell-mediated immune responses.

Journal: Archives of virology

Published: July 11, 2023

mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.

mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development: Novel Variants, Topographic Mapping, and Clinical Outcomes.

Journal: Neurology. Genetics

Published: April 21, 2023

Prenatal Diagnosis of COL4A1 Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype.

Prenatal Diagnosis of COL4A1 Mutations in Eight Cases: Further Delineation of the Neurohistopathological Phenotype.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: April 06, 2022

Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations.

Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations.

Journal: Journal of clinical immunology

Published: December 07, 2020

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.

Journal: Journal of medical genetics

Published: November 16, 2020

De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes.

De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes.

Journal: Journal of medical genetics

Published: May 08, 2020

A case report of severe tuberous sclerosis complex detected in utero and linked to a novel duplication in the TSC2 gene.

A case report of severe tuberous sclerosis complex detected in utero and linked to a novel duplication in the TSC2 gene.

Journal: BMC neurology

Published: February 27, 2020

Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder.

Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder.

Journal: American journal of medical genetics. Part A

Published: April 04, 2019

No. 365-Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities with Normal Chromosome Analysis.

No. 365-Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities with Normal Chromosome Analysis.

Journal: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

Published: November 05, 2018

Showing 1-12 of 37

Last Updated: 09/26/2026