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Positional cloning of a quantitative trait locus on chromosome 13q14 that influences immunoglobulin E levels and asthma.
Zhang Y, Leaves NI, Anderson GG, Ponting CP, Broxholme J, Holt R, Edser P, Bhattacharyya S, Dunham A, Adcock IM, Pulleyn L, Barnes PJ, Harper JI, Abecasis G, Cardon L, White M, Burton J, Matthews L, Mott R, Ross M, Cox R, Moffatt MF, Cookson WO. Zhang Y, et al. Among authors: broxholme j. Nat Genet. 2003 Jun;34(2):181-6. doi: 10.1038/ng1166. Nat Genet. 2003. PMID: 12754510 Free article.
Positional cloning of a novel gene influencing asthma from chromosome 2q14.
Allen M, Heinzmann A, Noguchi E, Abecasis G, Broxholme J, Ponting CP, Bhattacharyya S, Tinsley J, Zhang Y, Holt R, Jones EY, Lench N, Carey A, Jones H, Dickens NJ, Dimon C, Nicholls R, Baker C, Xue L, Townsend E, Kabesch M, Weiland SK, Carr D, von Mutius E, Adcock IM, Barnes PJ, Lathrop GM, Edwards M, Moffatt MF, Cookson WO. Allen M, et al. Among authors: broxholme j. Nat Genet. 2003 Nov;35(3):258-63. doi: 10.1038/ng1256. Epub 2003 Oct 19. Nat Genet. 2003. PMID: 14566338
A comparison of tagging methods and their tagging space.
Ke X, Miretti MM, Broxholme J, Hunt S, Beck S, Bentley DR, Deloukas P, Cardon LR. Ke X, et al. Among authors: broxholme j. Hum Mol Genet. 2005 Sep 15;14(18):2757-67. doi: 10.1093/hmg/ddi309. Epub 2005 Aug 15. Hum Mol Genet. 2005. PMID: 16103130
Characterization of a major modifier locus for polycystic kidney disease (Modpkdr1) in the Han:SPRD(cy/+) rat in a region conserved with a mouse modifier locus for Alport syndrome.
Bihoreau MT, Megel N, Brown JH, Kränzlin B, Crombez L, Tychinskaya Y, Broxholme J, Kratz S, Bergmann V, Hoffman S, Gauguier D, Gretz N. Bihoreau MT, et al. Among authors: broxholme j. Hum Mol Genet. 2002 Sep 1;11(18):2165-73. doi: 10.1093/hmg/11.18.2165. Hum Mol Genet. 2002. PMID: 12189169
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.
Price TS, Regan R, Mott R, Hedman A, Honey B, Daniels RJ, Smith L, Greenfield A, Tiganescu A, Buckle V, Ventress N, Ayyub H, Salhan A, Pedraza-Diaz S, Broxholme J, Ragoussis J, Higgs DR, Flint J, Knight SJ. Price TS, et al. Among authors: broxholme j. Nucleic Acids Res. 2005 Jun 16;33(11):3455-64. doi: 10.1093/nar/gki643. Print 2005. Nucleic Acids Res. 2005. PMID: 15961730 Free PMC article.
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.
Martin HC, Kim GE, Pagnamenta AT, Murakami Y, Carvill GL, Meyer E, Copley RR, Rimmer A, Barcia G, Fleming MR, Kronengold J, Brown MR, Hudspith KA, Broxholme J, Kanapin A, Cazier JB, Kinoshita T, Nabbout R; WGS500 Consortium; Bentley D, McVean G, Heavin S, Zaiwalla Z, McShane T, Mefford HC, Shears D, Stewart H, Kurian MA, Scheffer IE, Blair E, Donnelly P, Kaczmarek LK, Taylor JC. Martin HC, et al. Among authors: broxholme j. Hum Mol Genet. 2014 Jun 15;23(12):3200-11. doi: 10.1093/hmg/ddu030. Epub 2014 Jan 25. Hum Mol Genet. 2014. PMID: 24463883 Free PMC article.
46 results