Julie Richer

5PUBLICATIONS
31CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Medical molecular engineering of nucleic acids and proteinsNeonatology
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Publications (5)

|May 05, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.

|Jun 04, 2025
Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant.

Noémie Villeneuve-Cloutier, Christie A Boswell-Patterson, Lucas Bronicki

|Jan 02, 2025
Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals.

Julie Richer, Joe Davis Velchev, Sharan Goobie

|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

|Apr 04, 2024
Imaging Review of Pediatric Monogenic CNS Vasculopathy with Genetic Correlation.

Neetika Gupta, Elka Miller, Aashim Bhatia

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Frequent Collaborators

1 joint publications

Neetika Gupta

1 joint publications

Elka Miller

1 joint publications

Richard I Aviv

1 joint publications

Nagwa Wilson