Michael S Hanna

6PUBLICATIONS
70CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)AutoimmunityNeurology and neuromuscular diseasesEnergy generation, conversion and storage (excl. chemical and electrical)Pacific Peoples and disability
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Publications (6)

|Feb 18, 2025
Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort.

Maryke Schoonen, Mahmoud Fassad, Krutik Patel

|Dec 16, 2024
Genetic Architecture of Idiopathic Inflammatory Myopathies From Meta-Analyses.

Catherine Zhu, Younghun Han, Jinyoung Byun

|Apr 25, 2024
The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India.

Venugopalan Y Vishnu, Richard J L F Lemmers, Alisha Reyaz

|Nov 29, 2022
Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice.

Enrico Bugiardini, Andreia M Nunes, Ariany Oliveira-Santos

|Feb 17, 2022
Ageing contributes to phenotype transition in a mouse model of periodic paralysis.

Karen J Suetterlin, S Veronica Tan, Roope Mannikko

|Jun 19, 2019
Natural history of limb girdle muscular dystrophy R9 over 6 years: searching for trial endpoints.

Alexander P Murphy, Jasper Morrow, Julia R Dahlqvist

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