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CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, O'Hare A, Shaw D, Simkin Z, Simonoff E, Slonims V, Watson J, Ragoussis J, Fisher SE, Seckl JR, Helms PJ, Bolton PF, Pickles A, Conti-Ramsden G, Baird G, Bishop DV, Monaco AP. Newbury DF, et al. Among authors: winchester l. Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646677 Free PMC article.
A functional genetic link between distinct developmental language disorders.
Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher SE. Vernes SC, et al. Among authors: winchester l. N Engl J Med. 2008 Nov 27;359(22):2337-45. doi: 10.1056/NEJMoa0802828. Epub 2008 Nov 5. N Engl J Med. 2008. PMID: 18987363 Free PMC article.
Variations within oxygen-regulated gene expression in humans.
Brooks JT, Elvidge GP, Glenny L, Gleadle JM, Liu C, Ragoussis J, Smith TG, Talbot NP, Winchester L, Maxwell PH, Robbins PA. Brooks JT, et al. Among authors: winchester l. J Appl Physiol (1985). 2009 Jan;106(1):212-20. doi: 10.1152/japplphysiol.90578.2008. Epub 2008 Nov 13. J Appl Physiol (1985). 2009. PMID: 19008490 Free PMC article.
Comparing CNV detection methods for SNP arrays.
Winchester L, Yau C, Ragoussis J. Winchester L, et al. Brief Funct Genomic Proteomic. 2009 Sep;8(5):353-66. doi: 10.1093/bfgp/elp017. Epub 2009 Sep 8. Brief Funct Genomic Proteomic. 2009. PMID: 19737800 Review.
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.
McRonald FE, Morris MR, Gentle D, Winchester L, Baban D, Ragoussis J, Clarke NW, Brown MD, Kishida T, Yao M, Latif F, Maher ER. McRonald FE, et al. Among authors: winchester l. Mol Cancer. 2009 Jun 3;8:31. doi: 10.1186/1476-4598-8-31. Mol Cancer. 2009. PMID: 19493342 Free PMC article.
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
Maestrini E, Pagnamenta AT, Lamb JA, Bacchelli E, Sykes NH, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri TS, Minopoli F, Reichert J, Cai G, Buxbaum JD, Korvatska O, Schellenberg GD, Dawson G, de Bildt A, Minderaa RB, Mulder EJ, Morris AP, Bailey AJ, Monaco AP; IMGSAC. Maestrini E, et al. Among authors: winchester l. Mol Psychiatry. 2010 Sep;15(9):954-68. doi: 10.1038/mp.2009.34. Epub 2009 Apr 28. Mol Psychiatry. 2010. PMID: 19401682 Free PMC article.
166 results