| 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 | 393 | 2008 |
| 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 | 322 | 2004 |
| 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 | 245 | 2012 |
| 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 | 235 | 2003 |
| 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 | 228 | 2013 |
| 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 | 194 | 2014 |
| 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 | 177 | 2013 |
| 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 | 171 | 2014 |
| 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 | 118 | 2015 |
| 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 | 117 | 2015 |
| 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 | 115 | 2015 |
| 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 | 110 | 2000 |
| 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 | 107 | 2013 |
| 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 | 95 | 2016 |
| 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 | 95 | 2013 |
| 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 | 90 | 2009 |
| 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 | 86 | 2001 |
| 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 | 84 | 2013 |
| 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 | 81 | 2004 |
| Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype FL Mastaglia, M Needham, A Scott, I James, P Zilko, T Day, L Kiers, ... Neuromuscular Disorders 19 (11), 763-765, 2009 | 69 | 2009 |
Stephan BeckUCL Cancer Institute, University College LondonVerifisert e-postadresse på ucl.ac.uk
