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Robert J. Bryson‐Richardson

Australian Regenerative Medicine Institute

ORCID: 0000-0002-9501-8208

147 papers and 12.3k citations.

PubIndex Score41Top 59% · seniorHow it's scored

147Publications

12.3kTotal Citations

First publication: 2003First senior author: 2007

Top publicationsby citations

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Gianina Ravenscroft, Alan H. Beggs, Satoko Miyatake et al.|The American Journal of Human Genetics|2013

Cited by 224

Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization

Gina O’Grady, Sandra T. Cooper, Tanya Stojkovic et al.|The American Journal of Human Genetics|2016

Cited by 106

Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy

Avnika A. Ruparelia, Robert J. Bryson‐Richardson|Human Molecular Genetics|2012

Cited by 45

KBTBD13 is an actin-binding protein that modulates muscle kinetics

Josine M. de Winter, Coen A. C. Ottenheijm, J. Molenaar et al.|Journal of Clinical Investigation|2019

Cited by 43

Genetic model of UBA5 deficiency highlights the involvement of both peripheral and central nervous systems and identifies widespread mitochondrial abnormalities

Rita J. Serrano, Robert J. Bryson‐Richardson|Brain Communications|2023

Cited by 9

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