Allan M. Innes

Calgary, AB, Canada

Last Updated: 09/26/2026

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Found 160 publications

Summary of the Inaugural ReNU Hope Conference and Scientific Symposium, July 23-25, 2025, Long Island, New York.

Summary of the Inaugural ReNU Hope Conference and Scientific Symposium, July 23-25, 2025, Long Island, New York.

Journal: American journal of medical genetics. Part A

Published: January 21, 2026

Shared genetic basis and structure of syndromic and normal facial variation.

Shared genetic basis and structure of syndromic and normal facial variation.

Journal: American journal of human genetics

Published: November 07, 2025

Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritance.

Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritance.

Journal: Neurogenetics

Published: October 10, 2025

Epilepsy due to a MED25 Homozygous Pathogenic Founder Variant.

Epilepsy due to a MED25 Homozygous Pathogenic Founder Variant.

Journal: Journal of child neurology

Published: September 24, 2025

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

Journal: The Journal of clinical investigation

Published: September 11, 2025

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.

Journal: American journal of human genetics

Published: August 08, 2025

45th Annual David Smith Workshop on Malformations and Morphogenesis.

45th Annual David Smith Workshop on Malformations and Morphogenesis.

Journal: American journal of medical genetics. Part A

Published: July 06, 2025

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay.

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay.

Journal: American journal of medical genetics. Part A

Published: April 21, 2025

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes.

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes.

Journal: Genome medicine

Published: April 12, 2025

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes.

Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes.

Journal: medRxiv : the preprint server for health sciences

Published: April 08, 2025

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Journal: Journal of autism and developmental disorders

Published: March 21, 2025

Mainstreaming of clinical genetic testing: A conceptual framework.

Mainstreaming of clinical genetic testing: A conceptual framework.

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

Published: January 15, 2025

Showing 1-12 of 160

Last Updated: 09/26/2026