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Parameters for reliable results in genetic association studies in common disease.
Dahlman I, Eaves IA, Kosoy R, Morrison VA, Heward J, Gough SC, Allahabadia A, Franklyn JA, Tuomilehto J, Tuomilehto-Wolf E, Cucca F, Guja C, Ionescu-Tirgoviste C, Stevens H, Carr P, Nutland S, McKinney P, Shield JP, Wang W, Cordell HJ, Walker N, Todd JA, Concannon P. Dahlman I, et al. Among authors: carr p. Nat Genet. 2002 Feb;30(2):149-50. doi: 10.1038/ng825. Epub 2002 Jan 22. Nat Genet. 2002. PMID: 11799396
Haplotype tagging for the identification of common disease genes.
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA. Johnson GC, et al. Among authors: carr p. Nat Genet. 2001 Oct;29(2):233-7. doi: 10.1038/ng1001-233. Nat Genet. 2001. PMID: 11586306
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes.
Twells RC, Mein CA, Payne F, Veijola R, Gilbey M, Bright M, Timms A, Nakagawa Y, Snook H, Nutland S, Rance HE, Carr P, Dudbridge F, Cordell HJ, Cooper J, Tuomilehto-Wolf E, Tuomilehto J, Phillips M, Metzker M, Hess JF, Todd JA. Twells RC, et al. Among authors: carr p. Hum Genet. 2003 Jul;113(2):99-105. doi: 10.1007/s00439-003-0940-6. Epub 2003 Apr 17. Hum Genet. 2003. PMID: 12700977
Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene.
Twells RC, Mein CA, Phillips MS, Hess JF, Veijola R, Gilbey M, Bright M, Metzker M, Lie BA, Kingsnorth A, Gregory E, Nakagawa Y, Snook H, Wang WY, Masters J, Johnson G, Eaves I, Howson JM, Clayton D, Cordell HJ, Nutland S, Rance H, Carr P, Todd JA. Twells RC, et al. Among authors: carr p. Genome Res. 2003 May;13(5):845-55. doi: 10.1101/gr.563703. Genome Res. 2003. PMID: 12727905 Free PMC article.
A DNA damage checkpoint response in telomere-initiated senescence.
d'Adda di Fagagna F, Reaper PM, Clay-Farrace L, Fiegler H, Carr P, Von Zglinicki T, Saretzki G, Carter NP, Jackson SP. d'Adda di Fagagna F, et al. Among authors: carr p. Nature. 2003 Nov 13;426(6963):194-8. doi: 10.1038/nature02118. Epub 2003 Nov 5. Nature. 2003. PMID: 14608368
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM, Prigmore E, Burford DC, Porter KM, Ng BL, Douglas EJ, Fiegler H, Carr P, Kalaitzopoulos D, Clegg S, Sandstrom R, Temple IK, Youings SA, Thomas NS, Dennis NR, Jacobs PA, Crolla JA, Carter NP. Gribble SM, et al. Among authors: carr p. J Med Genet. 2005 Jan;42(1):8-16. doi: 10.1136/jmg.2004.024141. J Med Genet. 2005. PMID: 15635069 Free PMC article.
Applications of combined DNA microarray and chromosome sorting technologies.
Gribble SM, Fiegler H, Burford DC, Prigmore E, Yang F, Carr P, Ng BL, Sun T, Kamberov ES, Makarov VL, Langmore JP, Carter NP. Gribble SM, et al. Among authors: carr p. Chromosome Res. 2004;12(1):35-43. doi: 10.1023/b:chro.0000009325.69828.83. Chromosome Res. 2004. PMID: 14984100
760 results