Concepedia

Padma Sivadorai

PS

Statistics

Publications

14

Citations

943

H-Index

13

Active since

2007

Affiliations

The University of Western Australia(Current)

Harry Perkins Institute of Medical Research

Royal Perth Hospital

Queen Elizabeth II Medical Centre

Pathwest Laboratory Medicine

Padma Sivadorai is an author at The University of Western Australia specializing in genetics, life sciences, and molecular genetics.

Publications per year

2007–2020

14

Publications

14

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

Gianina Ravenscroft, Satoko Miyatake, Vilma‐Lotta Lehtokari et al. · The American Journal of Human Genetics · 2013 · 224 citations · Full text

, , +8

Dominant Mutations in KBTBD13, a Member of the BTB/Kelch Family, Cause Nemaline Myopathy with Cores

Nyamkhishig Sambuughin, Kyle S. Yau, Montse Olivé et al. · The American Journal of Human Genetics · 2010 · 161 citations · Full text

, , +9

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Emily J. Todd, Kyle S. Yau, Royston Ong et al. · Orphanet Journal of Rare Diseases · 2015 · 118 citations · Full text

, , +17

Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics

Joshua S. Clayton, Fathimath Faiz, Padma Sivadorai et al. · Journal of Medical Genetics · 2020 · 77 citations · Full text

, , +17

Mutations in CYC1, Encoding Cytochrome c1 Subunit of Respiratory Chain Complex III, Cause Insulin-Responsive Hyperglycemia

Pauline Gaignard, Minal Menezes, Manuel Schiff et al. · The American Journal of Human Genetics · 2013 · 69 citations · Full text

, , +13

1–5 of 14