Micheil Innes

38PUBLICATIONS
272CO-AUTHORS
Aboriginal and Torres Strait Islander astronomy and cosmologyGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesCraniofacial biologyMultiphysics flows (incl. multiphase and reacting flows)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (38)

|Feb 19, 2026
Summary of the Inaugural ReNU Hope Conference and Scientific Symposium, July 23-25, 2025, Long Island, New York.

Kelsey Crocker, Jillian O'Toole, Lindsay Pearse

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

Emma H Gillesse, Miranda Wan, Setareh Ashtiani

|Nov 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Ghayda M Mirzaa, Keqin Yan, Raissa Relator

|Jul 30, 2025
45th Annual David Smith Workshop on Malformations and Morphogenesis.

Alison M Elliott, A Micheil Innes

|May 16, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.

Caroline Nava, Benjamin Cogne, Amandine Santini

|Dec 02, 2024
De novo variants in LRRC8C resulting in constitutive channel activation cause a human multisystem disorder.

Mathieu Quinodoz, Sonja Rutz, Virginie Peter

Pageof 7

Frequent Collaborators

6 joint publications

Kym M Boycott

4 joint publications

Philippe M Campeau

4 joint publications

Francois P Bernier

3 joint publications

David A Dyment