Linlea Armstrong

Clinical Associate Professor

The University of British Columbia

Canada

This profile is automatically generated from trusted academic sources.

Google Scholar

ORCID

How do Turkish students reach out?

Meet Kite AI

Contact this professor

ORCID

Google Scholar

Academic Page

Research Interests

Biostatistics

70%

Obstetrics And Gynecology

20%

Medical Science

100%

Precision Medicine

40%

Genomic

30%

Pediatric Oncology

20%

Reproductive Medicine

20%

Ask ApplyKite AI

Start chatting

How can you help me contact this professor?

What are this professor's research interests?

How should I write an email to this professor?

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

Article Link

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

Article Link

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

Article Link

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

Article Link

Year:

2022

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

Article Link

Year:

2022

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

Article Link

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

Hui-Lin Chin

Assistant Professor

National University of Singapore (NUS)

SINGAPORE

Sally Ann Lynch

IRELAND

Frederick K. Kozak

Clinical Professor

The University of British Columbia

CANADA

Rebecca Deyell

Clinical Associate Professor

The University of British Columbia

CANADA

Karen Gripp

Chief

Nemours Children's Health System

UNITED STATES

Ingrid Price

Associate Professor of Teaching

The University of British Columbia

CANADA

Jan Friedman

Professor

The University of British Columbia

CANADA

Cornelius F. Boerkoel

CANADA

Mariko Nakano-Okuno

The University of Alabama

UNITED STATES

Millan S. Patel

CANADA

How do Turkish students reach out?

Meet Kite AI