Gabrielle T Lemire

13PUBLICATIONS
85CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingEpidemiological methodsDevelopmental genetics (incl. sex determination)Foetal development and medicine
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Publications (13)

|Oct 25, 2026
Systematic evaluation of incomplete penetrance in 4,325 rare disease families reveals divergent transcriptional networks in CHD8 pathology.

|Jan 13, 2025
Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

Maggie T Arriaga, Rodrigo Mendez, Rachel A Ungar

|Sep 04, 2024
Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection.

Shloka Negi, Sarah L Stenton, Seth I Berger

|Nov 04, 2022
The implementation of an enhanced clinical model to improve the diagnostic yield of exome sequencing for patients with a rare genetic disease: A Canadian experience.

Grace Uwaila Ediae, Gabrielle Lemire, Caitlin Chisholm

|Jun 19, 2021
Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.

Gabrielle Lemire, Bixia Zheng, Grace U Ediae

|Dec 28, 2019
Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome.

Gabrielle T Lemire, Éliane Beauregard-Lacroix, Philippe M Campeau

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Frequent Collaborators

8 joint publications

Kym M Boycott

3 joint publications

Anne O'Donnell-Luria

2 joint publications

Jialan Ma

2 joint publications

Grace Uwaila Ediae