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Page 1
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP. Dennis MY, et al. Among authors: coggill p. PLoS Genet. 2009 Mar;5(3):e1000436. doi: 10.1371/journal.pgen.1000436. Epub 2009 Mar 27. PLoS Genet. 2009. PMID: 19325871 Free PMC article.
Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia.
Raval A, Tanner SM, Byrd JC, Angerman EB, Perko JD, Chen SS, Hackanson B, Grever MR, Lucas DM, Matkovic JJ, Lin TS, Kipps TJ, Murray F, Weisenburger D, Sanger W, Lynch J, Watson P, Jansen M, Yoshinaga Y, Rosenquist R, de Jong PJ, Coggill P, Beck S, Lynch H, de la Chapelle A, Plass C. Raval A, et al. Among authors: coggill p. Cell. 2007 Jun 1;129(5):879-90. doi: 10.1016/j.cell.2007.03.043. Cell. 2007. PMID: 17540169 Free PMC article.
Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project.
Horton R, Gibson R, Coggill P, Miretti M, Allcock RJ, Almeida J, Forbes S, Gilbert JG, Halls K, Harrow JL, Hart E, Howe K, Jackson DK, Palmer S, Roberts AN, Sims S, Stewart CA, Traherne JA, Trevanion S, Wilming L, Rogers J, de Jong PJ, Elliott JF, Sawcer S, Todd JA, Trowsdale J, Beck S. Horton R, et al. Among authors: coggill p. Immunogenetics. 2008 Jan;60(1):1-18. doi: 10.1007/s00251-007-0262-2. Epub 2008 Jan 10. Immunogenetics. 2008. PMID: 18193213 Free PMC article.
A novel system of polymorphic and diverse NK cell receptors in primates.
Averdam A, Petersen B, Rosner C, Neff J, Roos C, Eberle M, Aujard F, Münch C, Schempp W, Carrington M, Shiina T, Inoko H, Knaust F, Coggill P, Sehra H, Beck S, Abi-Rached L, Reinhardt R, Walter L. Averdam A, et al. Among authors: coggill p. PLoS Genet. 2009 Oct;5(10):e1000688. doi: 10.1371/journal.pgen.1000688. Epub 2009 Oct 16. PLoS Genet. 2009. PMID: 19834558 Free PMC article.
Complete MHC haplotype sequencing for common disease gene mapping.
Stewart CA, Horton R, Allcock RJ, Ashurst JL, Atrazhev AM, Coggill P, Dunham I, Forbes S, Halls K, Howson JM, Humphray SJ, Hunt S, Mungall AJ, Osoegawa K, Palmer S, Roberts AN, Rogers J, Sims S, Wang Y, Wilming LG, Elliott JF, de Jong PJ, Sawcer S, Todd JA, Trowsdale J, Beck S. Stewart CA, et al. Among authors: coggill p. Genome Res. 2004 Jun;14(6):1176-87. doi: 10.1101/gr.2188104. Epub 2004 May 12. Genome Res. 2004. PMID: 15140828 Free PMC article.
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.
Traherne JA, Horton R, Roberts AN, Miretti MM, Hurles ME, Stewart CA, Ashurst JL, Atrazhev AM, Coggill P, Palmer S, Almeida J, Sims S, Wilming LG, Rogers J, de Jong PJ, Carrington M, Elliott JF, Sawcer S, Todd JA, Trowsdale J, Beck S. Traherne JA, et al. Among authors: coggill p. PLoS Genet. 2006 Jan;2(1):e9. doi: 10.1371/journal.pgen.0020009. Epub 2006 Jan 27. PLoS Genet. 2006. PMID: 16440057 Free PMC article.
Generation of a genomic tiling array of the human major histocompatibility complex (MHC) and its application for DNA methylation analysis.
Tomazou EM, Rakyan VK, Lefebvre G, Andrews R, Ellis P, Jackson DK, Langford C, Francis MD, Bäckdahl L, Miretti M, Coggill P, Ottaviani D, Sheer D, Murrell A, Beck S. Tomazou EM, et al. Among authors: coggill p. BMC Med Genomics. 2008 May 30;1:19. doi: 10.1186/1755-8794-1-19. BMC Med Genomics. 2008. PMID: 18513384 Free PMC article.
37 results