William T. Gibson

Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 77 publications

Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylation.

Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylation.

Journal: European journal of human genetics : EJHG

Published: February 10, 2026

Influence of a 12 week at-home resistance exercise program on 13C-glucose metabolism in patients with metabolic myopathies.

Influence of a 12 week at-home resistance exercise program on 13C-glucose metabolism in patients with metabolic myopathies.

Journal: Molecular genetics and metabolism

Published: October 17, 2025

Correction: Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

Correction: Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

Journal: Orphanet journal of rare diseases

Published: September 19, 2025

KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

KMT2A and KMT2B episignatures address diagnostic challenges associated with rare neurodevelopmental disorders.

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

Published: September 17, 2025

Identification of Compound Heterozygous CYP11A1 Variants via Reanalysis of Clinical Sequencing Data.

Identification of Compound Heterozygous CYP11A1 Variants via Reanalysis of Clinical Sequencing Data.

Journal: American journal of medical genetics. Part A

Published: August 27, 2025

Deep learning-based seabird detection in fisheries for seabird protection.

Deep learning-based seabird detection in fisheries for seabird protection.

Journal: Journal of the Royal Society of New Zealand

Published: August 04, 2025

Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype Study.

Identifying Rare Germline Variants Associated with Metastatic Prostate Cancer Through an Extreme Phenotype Study.

Journal: medRxiv : the preprint server for health sciences

Published: May 09, 2025

Minimally Humanized Ezh2 Exon-18 Mouse Cell Lines Validate Preclinical CRISPR/Cas9 Approach to Treat Weaver Syndrome.

Minimally Humanized Ezh2 Exon-18 Mouse Cell Lines Validate Preclinical CRISPR/Cas9 Approach to Treat Weaver Syndrome.

Journal: Human gene therapy

Published: February 18, 2025

NPAS4 Depletion in POMC Neurons Protects From Obesity and Alters the Feeding-regulated Transcriptome in Male Mice.

NPAS4 Depletion in POMC Neurons Protects From Obesity and Alters the Feeding-regulated Transcriptome in Male Mice.

Journal: Endocrinology

Published: December 20, 2024

Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

Journal: Orphanet journal of rare diseases

Published: September 16, 2024

Maintenance of thermogenic adipose tissues despite loss of the H3K27 acetyltransferases p300 or CBP.

Maintenance of thermogenic adipose tissues despite loss of the H3K27 acetyltransferases p300 or CBP.

Journal: American journal of physiology. Endocrinology and metabolism

Published: August 14, 2024

Using long-read sequencing to detect and subtype a case with Temple syndrome.

Using long-read sequencing to detect and subtype a case with Temple syndrome.

Journal: Journal of medical genetics

Published: July 19, 2024

Showing 1-12 of 77

Last Updated: 09/26/2026