N

Nigel G. Laing

Harry Perkins Institute of Medical Research

ORCID: 0000-0001-5111-3732

1.2k papers and 28.9k citations.

PubIndex Score98Top 2%How it's scored

1.2kPublications

28.9kTotal Citations

First publication: 1982First senior author: 1989

Top publicationsby citations

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing

Beryl B. Cummings, Daniel G. MacArthur, Jamie L. Marshall et al.|Science Translational Medicine|2017

Cited by 809

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Nigel G. Laing, Duangrurdee Wattanasirichaigoon, Hans H. Goebel et al.|Nature Genetics|1999

Cited by 401

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

Katarina Pelin, Carina Wallgren‐Pettersson, Pirta Hilpelä et al.|Proceedings of the National Academy of Sciences|1999

Cited by 332

Approach to the diagnosis of congenital myopathies

Kathryn N. North, C. Bönnemann, Ching H. Wang et al.|Neuromuscular Disorders|2013

Cited by 324

Nemaline myopathy: A clinical study of 143 cases

Monique M. Ryan, Kathryn N. North, Christina Schnell et al.|Annals of Neurology|2001

Cited by 275

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