Linlea Armstrong at University of British Columbia - Research Interests, Publications & Academic Profile

Linlea Armstrong

Clinical Associate Professor

The University of British Columbia

Canada

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Research Interests

Biostatistics

70%

Obstetrics And Gynecology

20%

Medical Science

100%

Precision Medicine

40%

Genomic

30%

Pediatric Oncology

20%

Reproductive Medicine

20%

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Articles15

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

Article Link

Year:

2023

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

Article Link

Year:

2023

The practice of genomic medicine: A delineation of the process and its governing principles

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Year:

2023

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

Article Link

Year:

2023

Characterization of Switch/Sucrose Nonfermenting Complex Proteins and Nestin Expression in a Cohort of Pediatric Central Nervous System Tumors

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Year:

2023

Impact of Variation in Practice in the Prenatal Reporting of Variants of Uncertain Significance by Commercial Laboratories: Need for Greater Adherence to Published Guidelines

Article Link

Year:

2023

The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice

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Year:

2022

Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study

Article Link

Year:

2022

Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines

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Year:

2022

Primary cutaneous follicle center lymphoma of the medial canthus of the eye in an 11-year old

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Year:

2022

Crizotinib response in a neuroblastoma patient with a constitutional mosaic anaplastic lymphoma kinase I1170N‐activating mutation

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Year:

2021

Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation

Article Link

Year:

2021

Coaching the coaches: Employing role modeling and coaching as a faculty development strategy

Article Link

Year:

2021

Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes

Article Link

Year:

2021

Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications

Article Link

Year:

2021

Collaborators11

M. E. Suzanne Lewis

CANADA

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Hui-Lin Chin

Assistant Professor

National University of Singapore (NUS)

SINGAPORE

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Sally Ann Lynch

IRELAND

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Frederick K. Kozak

Clinical Professor

The University of British Columbia

CANADA

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Rebecca Deyell

Clinical Associate Professor

The University of British Columbia

CANADA

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Karen Gripp

Chief

Nemours Children's Health System

UNITED STATES

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Ingrid Price

Associate Professor of Teaching

The University of British Columbia

CANADA

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Jan Friedman

Professor

The University of British Columbia

CANADA

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Cornelius F. Boerkoel

CANADA

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Mariko Nakano-Okuno

The University of Alabama

UNITED STATES

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Millan S. Patel

CANADA

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