Richard J. N. Allcock

Author

Also Known As

R Allcock, R. Allcock, R.J. Allcock, R.J.N. Allcock, RICHARD JN ALLCOCK, Richard Allcock, Richard J N Allcock, Richard J. Allcock, Richard J. N. Allcock, Richard J.N Allcock

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

The University of Western Australia Royal Perth Hospital Pathwest Laboratory Medicine Queen Elizabeth II Medical Centre Harry Perkins Institute of Medical Research

About

Richard J. N. Allcock is an author at The University of Western Australia specializing in medicine, immunology, and autoimmune disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	23	1.4K
2	Biology	3	3	283
3	Public Health	2	2	45
4	Health Sciences	1	1	27
5	Allergy	1	1	180

Richard J. N. Allcock

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy Gianina Ravenscroft, Satoko Miyatake, Vilma‐Lotta Lehtokari, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFrequent CausePathology	2013	220
Microbial 16S rRNA Ion Tag and community metagenome sequencing using the Ion Torrent (PGM) Platform Andrew S. Whiteley, Ian Waite, Nina Kresoje, Journal of Microbiological Methods BiologyMicrobial DiversityMicrobial SystematicsIon TorrentMicrobial Ecology	2012	202
Multiple Immune Factors Are Involved in Controlling Acute and Chronic Chikungunya Virus Infection Yee Suan Poo, Penny A. Rudd, Joy Gardner, PLoS neglected tropical diseases Adaptive Immune SystemHumoral ResponseViral PathogenesisImmunologyT Cells	2014	180
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy Vandana Gupta, Gianina Ravenscroft, Ranad Shaheen, The American Journal of Human Genetics Molecular PhysiologySignal TransductionBtb-kelch-mediated UbiquitinationMolecular BiologyProtein Degradation	2013	162
Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita Gianina Ravenscroft, Flora Nolent, Sulekha Rajagopalan, The American Journal of Human Genetics Gpr126 Are ResponsibleAutoimmune DiseaseTranslational BiologyGenetic DisorderGenetics	2015	118
Combined DNA, toxicological and heavy metal analyses provides an auditing toolkit to improve pharmacovigilance of traditional Chinese medicine (TCM) Megan L. Coghlan, Garth Maker, Elly Crighton, Scientific Reports	2015	115
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, Orphanet Journal of Rare Diseases	2015	113
Comparison of faecal microbiota in Blastocystis-positive and Blastocystis-negative irritable bowel syndrome patients R Nagel, Rebecca J. Traub, Richard J. N. Allcock, Microbiome	2016	93
Scrapheap Challenge: A novel bulk-bone metabarcoding method to investigate ancient DNA in faunal assemblages Dáithí C. Murray, James Haile, Joe Dortch, Scientific Reports	2013	90
Susceptibility to severe ulcerative colitis is associated with polymorphism in the central MHC gene IKBL Emilio G. de la Concha, Miguel Fernández‐Arquero, Gontrand López-Nava, Gastroenterology	2000	88

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