R
Roger Horton
Researcher at Wellcome Trust Sanger Institute
Publications - 16
Citations - 4175
Roger Horton is an academic researcher from Wellcome Trust Sanger Institute. The author has contributed to research in topics: Human leukocyte antigen & Haplotype. The author has an hindex of 13, co-authored 16 publications receiving 3957 citations.
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Journal ArticleDOI
DNA methylation profiling of human chromosomes 6, 20 and 22
Florian Eckhardt,Joern Lewin,Rene Cortese,Vardhman K. Rakyan,John Attwood,Matthias Burger,John Burton,Tony Cox,Robert L. Davies,Thomas A. Down,Carolina Haefliger,Roger Horton,Kevin L. Howe,David K. Jackson,Jan Kunde,Jan Kunde,Christoph Koenig,Jennifer Liddle,David Niblett,Thomas J. Otto,Roger Pettett,Stefanie Seemann,Christian Thompson,Tony West,Jane Rogers,Alex Olek,Kurt Berlin,Stephan Beck +27 more
TL;DR: Analysis of six annotation categories showed that evolutionarily conserved regions are the predominant sites for differential DNA methylation and that a core region surrounding the transcriptional start site is an informative surrogate for promoter methylation.
Journal ArticleDOI
Gene map of the extended human MHC
Roger Horton,Laurens G. Wilming,Vikki Rand,Ruth C. Lovering,Elspeth A. Bruford,Varsha K. Khodiyar,Michael J. Lush,Sue Povey,C. Conover Talbot,Mathew W. Wright,H Wain,John Trowsdale,Andreas Ziegler,Stephan Beck +13 more
TL;DR: A gene map of the xMHC is presented and its content in relation to paralogy, polymorphism, immune function and disease is reviewed.
Journal ArticleDOI
DNA sequence and analysis of human chromosome 9
Andrew J. Mungall,Sophie Palmer,Sarah Sims,C A Edwards,Jennifer L. Ashurst,Laurens G. Wilming,Matthew Jones,Roger Horton,Sarah E. Hunt,Carol Scott,James G. R. Gilbert,Michele Clamp,Graeme Bethel,Sarah Milne,R Ainscough,J P Almeida,K D Ambrose,T D Andrews,R I S Ashwell,A K Babbage,C L Bagguley,J Bailey,Ruby Banerjee,Darren Barker,K F Barlow,K Bates,David Beare,Helen Beasley,O. Beasley,Christine P. Bird,S. Blakey,S Bray-Allen,J Brook,A J Brown,J Y Brown,D C Burford,W Burrill,John Burton,C Carder,Nigel P. Carter,J C Chapman,S Y Clark,Graeme T Clark,C M Clee,S. M. Clegg,V. Cobley,R. E. Collier,Joanna Collins,L K Colman,N Corby,G. J. Coville,K M Culley,Pawandeep Dhami,Jim Davies,Matthew Dunn,M Earthrowl,A E Ellington,K A Evans,L M Faulkner,Matthew D. Francis,Adam Frankish,J Frankland,Lisa French,P Garner,J Garnett,Mohammed J. R. Ghori,L M Gilby,Christopher J. Gillson,Rebecca Glithero,Darren Grafham,M Grant,Susan M. Gribble,C Griffiths,Mark Griffiths,Rebekah Hall,K S Halls,S Hammond,Joanna Harley,E. Hart,Paul Heath,R Heathcott,S. Holmes,Philip Howden,Kevin L. Howe,Gareth R. Howell,Elizabeth J. Huckle,Sean Humphray,Matthew Humphries,Adrienne Hunt,Christopher M. Johnson,A Joy,M. Kay,Stephen Keenan,A M Kimberley,A. King,Gavin K. Laird,Cordelia Langford,S Lawlor,Daniel Leongamornlert,Margaret A. Leversha,Christine Lloyd,D. M. Lloyd,Jane E. Loveland,J Lovell,Sancha Martin,M Mashreghi-Mohammadi,Gareth Maslen,Lucy Matthews,O. T. McCann,S J McLaren,Kirsten McLay,Amanda McMurray,M. J F Moore,James C. Mullikin,David Niblett,T Nickerson,K L Novik,Karen Oliver,E K Overton-Larty,Anne Parker,R Patel,A. V. Pearce,A I Peck,Benjamin Phillimore,Sam Phillips,Robert W. Plumb,K M Porter,Y. Ramsey,S A Ranby,Catherine M. Rice,Mark T. Ross,S. Searle,Harminder Sehra,E Sheridan,C. D. Skuce,Sarah E. Smith,Michelle Smith,L Spraggon,S. Squares,Charles A. Steward,N Sycamore,G Tamlyn-Hall,J Tester,A J Theaker,Duncan W. Thomas,A Thorpe,Alan Tracey,A Tromans,B Tubby,Melanie M. Wall,J. M. Wallis,Anthony P. West,S S White,S. Whitehead,H Whittaker,A Wild,Dave Willey,T. E. Wilmer,Jonathan Wood,Paul Wray,J C Wyatt,L Young,R M Younger,David R. Bentley,Alan Coulson,Richard Durbin,Tim Hubbard,John Sulston,Ian Dunham,Jane Rogers,Stephan Beck +170 more
TL;DR: Analysis of the sequence reveals many intra- and interchromosomal duplications, including segmental duplications adjacent to both the centromere and the large heterochromatic block, and detects recently duplicated genes that exhibit different rates of sequence divergence, presumably reflecting natural selection.
Journal ArticleDOI
Variation analysis and gene annotation of eight MHC haplotypes: The MHC Haplotype Project
Roger Horton,Richard Gibson,Penny Coggill,Marcos Mateo Miretti,Richard J.N. Allcock,J P Almeida,Simon A. Forbes,James G. R. Gilbert,Karen Halls,Jennifer Harrow,E. Hart,Kevin L. Howe,David K. Jackson,Sophie Palmer,Anne N. Roberts,Sarah Sims,C. Andrew Stewart,James A. Traherne,Steve Trevanion,Laurens G. Wilming,Jane Rogers,Pieter J. de Jong,John F. Elliott,Stephen Sawcer,John A. Todd,John Trowsdale,Stephan Beck,Stephan Beck +27 more
TL;DR: The MHC Haplotype Project was to provide a comprehensively annotated reference sequence of a single, human leukocyte antigen-homozygous MHC haplotype and to use it as a basis against which variations could be assessed from seven other similarly homozygous cell lines, representative of the most common MHChaplotype in the European population.
Journal ArticleDOI
Complete MHC Haplotype Sequencing for Common Disease Gene Mapping
C. Andrew Stewart,Roger Horton,Richard J.N. Allcock,Jennifer L. Ashurst,Alexey Atrazhev,Penny Coggill,Ian Dunham,Simon A. Forbes,Karen Halls,Joanna M. M. Howson,Sean Humphray,Sarah E. Hunt,Andrew J. Mungall,Kazutoyo Osoegawa,Sophie Palmer,Anne N. Roberts,Jane Rogers,Sarah Sims,Yu Wang,Laurens G. Wilming,John F. Elliott,Pieter J. de Jong,Stephen Sawcer,John A. Todd,John Trowsdale,Stephan Beck +25 more
TL;DR: This paper reported 4.75 Mb of contiguous sequence for each of two common haplotypes of the major histocompatibility complex (MHC) to which susceptibility to >100 diseases has been mapped.