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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)

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|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 <i>SMAD3</i> 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

1 joint publications

Elaine Suk-Ying Goh

1 joint publications

Lauren Chad

1 joint publications

Melanie Lacaria

1 joint publications

Tanya N Nelson

1 joint publications

Joe Davis Velchev

1 joint publications

Ilse Luyckx

Frequent Collaborators

1 joint publications

Neetika Gupta

1 joint publications

Elka Miller

1 joint publications

Richard I Aviv

1 joint publications

Nagwa Wilson

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