Guillaume Sillon
Montreal, QC H4A3J1, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in Quebec.
Journal: Cells
Published: July 18, 2025
Using the ancestral recombination graph to study the history of rare variants in founder populations.
Journal: American journal of human genetics
Published: March 17, 2025
The Key Features of a Genetic Nondiscrimination Policy: A Delphi Consensus Statement.
Journal: JAMA network open
Published: September 26, 2024
HYDIN Variants Are a Common Cause of Primary Ciliary Dyskinesia in French Canadians.
Journal: Annals of the American Thoracic Society
Published: September 16, 2022
A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: September 17, 2020
The incidence and carrier frequency of Tay-Sachs disease in the French-Canadian population of Quebec based on retrospective data from 24 years, 1992-2015.
Journal: Journal of genetic counseling
Published: July 30, 2019
Lexigene®: An online medical genetics translation tool to facilitate communication.
Journal: Journal of genetic counseling
Published: February 16, 2019
COL4A1/2 CNVs and cerebral small vessel disease: Narrowing in on the critical chromosomal region.
Journal: Neurology
Published: August 29, 2017
Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene.
Journal: Journal of medical genetics
Published: July 04, 2016
Online Module for Carrier Screening in Ashkenazi Jewish Individuals Compared with In-Person Genetics Education: A Randomized Controlled Trial.
Journal: Journal of genetic counseling
Published: December 04, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026