Francois P Bernier

5PUBLICATIONS
22CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseaseGenome structure and regulationAdolescent healthEpidemiological methods
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Publications (5)

|Feb 08, 2026
Identification of an additional deep intronic splice variant prompts critical evaluation of SPG7 inheritance.

Emma H Gillesse, Miranda Wan, Setareh Ashtiani

|Apr 07, 2023
Developing a Framework of Cost Elements of Socioeconomic Burden of Rare Disease: A Scoping Review.

Gillian R Currie, Brittany Gerber, Diane Lorenzetti

|Mar 24, 2022
Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo.

Danielle L Blackwell, Sherri D Fraser, Oana Caluseriu

|Jul 19, 2019
Correction: The value of diagnostic testing for parents of children with rare genetic diseases.

Deborah A Marshall, Karen V MacDonald, Sebastian Heidenreich

|Jun 27, 2019
The value of diagnostic testing for parents of children with rare genetic diseases.

Deborah A Marshall, Karen V MacDonald, Sebastian Heidenreich

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Frequent Collaborators

4 joint publications

A Micheil Innes

3 joint publications

Deborah A Marshall

3 joint publications

Karen V MacDonald

3 joint publications

Kym M Boycott