Elliott K - Search Results

1

Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.

Moses EK, Fitzpatrick E, Freed KA, Dyer TD, Forrest S, Elliott K, Johnson MP, Blangero J, Brennecke SP. Moses EK, et al. Among authors: elliott k. Mol Hum Reprod. 2006 Aug;12(8):505-12. doi: 10.1093/molehr/gal056. Epub 2006 Jun 29. Mol Hum Reprod. 2006. PMID: 16809377

2

Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia.

Fitzpatrick E, Johnson MP, Dyer TD, Forrest S, Elliott K, Blangero J, Brennecke SP, Moses EK. Fitzpatrick E, et al. Among authors: elliott k. Mol Hum Reprod. 2009 Mar;15(3):195-204. doi: 10.1093/molehr/gap001. Epub 2009 Jan 6. Mol Hum Reprod. 2009. PMID: 19126782 Free PMC article.

3

Genetic variation in selenoprotein S influences inflammatory response.

Curran JE, Jowett JB, Elliott KS, Gao Y, Gluschenko K, Wang J, Abel Azim DM, Cai G, Mahaney MC, Comuzzie AG, Dyer TD, Walder KR, Zimmet P, MacCluer JW, Collier GR, Kissebah AH, Blangero J. Curran JE, et al. Among authors: elliott ks. Nat Genet. 2005 Nov;37(11):1234-41. doi: 10.1038/ng1655. Epub 2005 Oct 9. Nat Genet. 2005. PMID: 16227999 Clinical Trial.

4

Identifying genes predisposing to atopic eczema.

Forrest S, Dunn K, Elliott K, Fitzpatrick E, Fullerton J, McCarthy M, Brown J, Hill D, Williamson R. Forrest S, et al. Among authors: elliott k. J Allergy Clin Immunol. 1999 Nov;104(5):1066-70. doi: 10.1016/s0091-6749(99)70090-4. J Allergy Clin Immunol. 1999. PMID: 10550754

5

Association of genetic variation within UBL5 with phenotypes of metabolic syndrome.

Bozaoglu K, Curran JE, Elliott KS, Walder KR, Dyer TD, Rainwater DL, VandeBerg JL, Comuzzie AG, Collier GR, Zimmet P, MacCluer JW, Jowett JB, Blangero J. Bozaoglu K, et al. Among authors: elliott ks. Hum Biol. 2006 Apr;78(2):147-59. doi: 10.1353/hub.2006.0033. Hum Biol. 2006. PMID: 17036923

6

The -590C/T and -34C/T interleukin-4 promoter polymorphisms are not associated with atopic eczema in childhood.

Elliott K, Fitzpatrick E, Hill D, Brown J, Adams S, Chee P, Stewart G, Fulcher D, Tang M, Kemp A, King E, Varigos G, Bahlo M, Forrest S. Elliott K, et al. J Allergy Clin Immunol. 2001 Aug;108(2):285-7. doi: 10.1067/mai.2001.117180. J Allergy Clin Immunol. 2001. PMID: 11496248

7

Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype.

de Silva MG, Elliott K, Dahl HH, Fitzpatrick E, Wilcox S, Delatycki M, Williamson R, Efron D, Lynch M, Forrest S. de Silva MG, et al. Among authors: elliott k. J Med Genet. 2003 Oct;40(10):733-40. doi: 10.1136/jmg.40.10.733. J Med Genet. 2003. PMID: 14569117 Free PMC article.

8

Conservation of CNS1 and exclusion of its role in atopic eczema susceptibility.

Elliott KS, Anney RJ, Fitzpatrick EB, Williamson R, Forrest SM. Elliott KS, et al. J Allergy Clin Immunol. 2002 Jan;109(1):176-8. doi: 10.1067/mai.2002.120561. J Allergy Clin Immunol. 2002. PMID: 11799387 No abstract available.

9

Genetic variation in BEACON influences quantitative variation in metabolic syndrome-related phenotypes.

Jowett JB, Elliott KS, Curran JE, Hunt N, Walder KR, Collier GR, Zimmet PZ, Blangero J. Jowett JB, et al. Diabetes. 2004 Sep;53(9):2467-72. doi: 10.2337/diabetes.53.9.2467. Diabetes. 2004. PMID: 15331561

10

Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.

Orozco G, Hinks A, Eyre S, Ke X, Gibbons LJ, Bowes J, Flynn E, Martin P; Wellcome Trust Case Control Consortium; YEAR consortium; Wilson AG, Bax DE, Morgan AW, Emery P, Steer S, Hocking L, Reid DM, Wordsworth P, Harrison P, Thomson W, Barton A, Worthington J. Orozco G, et al. Hum Mol Genet. 2009 Jul 15;18(14):2693-9. doi: 10.1093/hmg/ddp193. Epub 2009 May 5. Hum Mol Genet. 2009. PMID: 19417005 Free PMC article.

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