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Richard Allcock
Richard Allcock
Verified email at uwa.edu.au
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Cited by
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Year
Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project
R Horton, R Gibson, P Coggill, M Miretti, RJ Allcock, J Almeida, S Forbes, ...
Immunogenetics 60, 1-18, 2008
3822008
Complete MHC haplotype sequencing for common disease gene mapping
CA Stewart, R Horton, RJN Allcock, JL Ashurst, AM Atrazhev, P Coggill, ...
Genome research 14 (6), 1176-1187, 2004
3192004
Microbial 16S rRNA Ion Tag and community metagenome sequencing using the Ion Torrent (PGM) Platform
AS Whiteley, S Jenkins, I Waite, N Kresoje, H Payne, B Mullan, R Allcock, ...
Journal of microbiological methods 91 (1), 80-88, 2012
2352012
The human TREM gene cluster at 6p21. 1 encodes both activating and inhibitory single IgV domain receptors and includes NKp44
RJN Allcock, AD Barrow, S Forbes, S Beck, J Trowsdale
European journal of immunology 33 (2), 567-577, 2003
2222003
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
G Ravenscroft, S Miyatake, VL Lehtokari, EJ Todd, P Vornanen, KS Yau, ...
The American Journal of Human Genetics 93 (1), 6-18, 2013
2132013
Multiple immune factors are involved in controlling acute and chronic chikungunya virus infection
YS Poo, PA Rudd, J Gardner, JAC Wilson, T Larcher, MA Colle, TT Le, ...
PLoS neglected tropical diseases 8 (12), e3354, 2014
1772014
Identification of KLHL41 mutations implicates BTB-Kelch-mediated ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathy
VA Gupta, G Ravenscroft, R Shaheen, EJ Todd, LC Swanson, M Shiina, ...
The American Journal of Human Genetics 93 (6), 1108-1117, 2013
1682013
SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy
PB Agrawal, CR Pierson, M Joshi, X Liu, G Ravenscroft, ...
The American Journal of Human Genetics 95 (2), 218-226, 2014
1652014
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth
EJ Todd, KS Yau, R Ong, J Slee, G McGillivray, CP Barnett, G Haliloglu, ...
Orphanet Journal of Rare Diseases 10, 1-14, 2015
1152015
Susceptibility to severe ulcerative colitis is associated with polymorphism in the central MHC gene IKBL
G Emilio, M Fernandez–Arquero, G Lopez–Nava, E Martin, RJ Allcock, ...
Gastroenterology 119 (6), 1491-1495, 2000
1112000
Combined DNA, toxicological and heavy metal analyses provides an auditing toolkit to improve pharmacovigilance of traditional Chinese medicine (TCM)
ML Coghlan, G Maker, E Crighton, J Haile, DC Murray, NE White, ...
Scientific reports 5 (1), 17475, 2015
1102015
Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
G Ravenscroft, F Nolent, S Rajagopalan, AM Meireles, KJ Paavola, ...
The American Journal of Human Genetics 96 (6), 955-961, 2015
1022015
16th IHIW : Review of HLA typing by NGS
D De Santis, D Dinauer, J Duke, HA Erlich, CL Holcomb, C Lind, ...
International journal of immunogenetics 40 (1), 72-76, 2013
1022013
Comparison of faecal microbiota in Blastocystis-positive and Blastocystis-negative irritable bowel syndrome patients
R Nagel, RJ Traub, RJN Allcock, MMS Kwan, H Bielefeldt-Ohmann
Microbiome 4, 1-9, 2016
882016
Polymorphisms of the CRP gene inhibit inflammatory response and increase susceptibility to depression: The Health in Men Study
OP Almeida, PE Norman, R Allcock, F Bockxmeer, GJ Hankey, K Jamrozik, ...
International journal of epidemiology 38 (4), 1049-1059, 2009
862009
Scrapheap challenge: a novel bulk-bone metabarcoding method to investigate ancient DNA in faunal assemblages
DC Murray, J Haile, J Dortch, NE White, D Haouchar, MI Bellgard, ...
Scientific reports 3 (1), 3371, 2013
852013
The central MHC gene, BAT1, may encode a protein that down‐regulates cytokine production
RJN Allcock, JH Williams, P Price
Genes to Cells 6 (5), 487-494, 2001
842001
Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA‐DR3
P Price, L Santoso, F Mastaglia, M Garlepp, CC Kok, R Allcock, N Laing
Tissue antigens 64 (5), 575-580, 2004
802004
Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia
P Gaignard, M Menezes, M Schiff, A Bayot, M Rak, HO de Baulny, CH Su, ...
The American Journal of Human Genetics 93 (2), 384-389, 2013
792013
Susceptibility to multiple sclerosis mediated by HLA-DRB1 is influenced by a second gene telomeric of the TNF cluster
RJN Allcock, EG de la Concha, M Fernandez-Arquero, P Vigil, L Conejero, ...
Human Immunology 60 (12), 1266-1273, 1999
681999
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