Linlea M. Armstrong

Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 63 publications

The Patient-reported Genetic testing Utility InDEx (P-GUIDE): A novel measure of personal utility.

The Patient-reported Genetic testing Utility InDEx (P-GUIDE): A novel measure of personal utility.

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

Published: December 16, 2025

Pilot Evaluation of a Digital Pretest Education Platform for Genomic Counseling: Perspectives of Health Care Providers and Patients.

Pilot Evaluation of a Digital Pretest Education Platform for Genomic Counseling: Perspectives of Health Care Providers and Patients.

Journal: Journal of genetic counseling

Published: August 06, 2025

How does personal utility depend on clinical setting? Evidence from 3 cohorts.

How does personal utility depend on clinical setting? Evidence from 3 cohorts.

Journal: Genetics in medicine open

Published: May 13, 2025

Research priorities in infection prevention and control in Alberta, Canada: a modified Delphi process.

Research priorities in infection prevention and control in Alberta, Canada: a modified Delphi process.

Journal: The Journal of hospital infection

Published: April 04, 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

A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.

A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.

Journal: Journal of clinical immunology

Published: June 14, 2024

Expanding the genotype-phenotype spectrum in SCN8A-related disorders.

Expanding the genotype-phenotype spectrum in SCN8A-related disorders.

Journal: Research square

Published: August 23, 2023

Expanding the genotype-phenotype spectrum in SCN8A-related disorders.

Expanding the genotype-phenotype spectrum in SCN8A-related disorders.

Journal: BMC neurology

Published: July 31, 2023

Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes.

Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes.

Journal: Journal of medical genetics

Published: May 12, 2023

Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers.

Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers.

Journal: Nature communications

Published: May 08, 2023

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Journal: American journal of medical genetics. Part A

Published: March 23, 2023

Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.

Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.

Journal: Journal of medical genetics

Published: December 27, 2022

Showing 1-12 of 63

Last Updated: 09/26/2026