Lauren Chad

13PUBLICATIONS
41CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Recommender systemsGene and molecular therapy
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Publications (13)

|Mar 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study.

Daniel Assamad, Abigail Hansen, Katharine Fooks

|Jan 10, 2026
Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencing.

Michael P Mackley, Megan A Dickson, Anna Szuto

|Jul 04, 2025
Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene.

Natasha L Rudy, Adriana Gomes, Tinatin Tkemaladze

|May 27, 2025
Canadian College of Medical Geneticists (CCMG) position statement on the storage of patient genetic and genomic information in electronic health records.

Anne-Marie Laberge, Nolan D'Souza, Lynette S Penney

|Oct 03, 2024
Canadian College of Medical Geneticists: clinical practice advisory document - responsibility to recontact for reinterpretation of clinical genetic testing.

Elaine Suk-Ying Goh, Lauren Chad, Julie Richer

|Sep 26, 2024
Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes.

Joery den Hoed, Hirokazu Hashimoto, Mubeen Khan

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Frequent Collaborators

4 joint publications

Robin Z Hayeems

2 joint publications

Wendy J Ungar

2 joint publications

Elaine Suk-Ying Goh

2 joint publications

David Chitayat