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Items: 1 to 20 of 68

1.

The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han population.

Tu X, Nie S, Liao Y, Zhang H, Fan Q, Xu C, Bai Y, Wang F, Ren X, Tang T, Xia N, Li S, Huang Y, Liu J, Yang Q, Zhao Y, Lv Q, Li Q, Li Y, Xia Y, Qian J, Li B, Wu G, Wu Y, Yang Y, Wang QK, Cheng X.

Am J Hum Genet. 2013 Oct 3;93(4):652-60. doi: 10.1016/j.ajhg.2013.08.009. Epub 2013 Sep 26. Erratum in: Am J Hum Genet. 2014 Feb 6;94(2):311.

2.

Hunting human disease genes: lessons from the past, challenges for the future.

Brunham LR, Hayden MR.

Hum Genet. 2013 Jun;132(6):603-17. doi: 10.1007/s00439-013-1286-3. Epub 2013 Mar 17. Review.

3.

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.

Cox HC, Lea RA, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth J, Macgregor S, Nyholt D, Chasman D, Ridker PM, Schürks M, Blangero J, Griffiths LR.

Neurogenetics. 2012 Aug;13(3):261-6. doi: 10.1007/s10048-012-0325-x. Epub 2012 Jun 8.

4.

Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip.

Fernández AI, Pérez-Montarelo D, Barragán C, Ramayo-Caldas Y, Ibáñez-Escriche N, Castelló A, Noguera JL, Silió L, Folch JM, Rodríguez MC.

BMC Genet. 2012 May 20;13:41. doi: 10.1186/1471-2156-13-41.

5.

Integrated genomic analysis of sézary syndrome.

Mao X, Chaplin T, Young BD.

Genet Res Int. 2011;2011:980150. doi: 10.4061/2011/980150. Epub 2011 Nov 24.

6.

A genome-wide homozygosity association study identifies runs of homozygosity associated with rheumatoid arthritis in the human major histocompatibility complex.

Yang HC, Chang LC, Liang YJ, Lin CH, Wang PL.

PLoS One. 2012;7(4):e34840. doi: 10.1371/journal.pone.0034840. Epub 2012 Apr 20.

7.

A powerful approach for association analysis incorporating imprinting effects.

Xia F, Zhou JY, Fung WK.

Bioinformatics. 2011 Sep 15;27(18):2571-7. doi: 10.1093/bioinformatics/btr443. Epub 2011 Jul 28.

8.

Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies.

Fridley BL, Serie D, Jenkins G, White K, Bamlet W, Potter JD, Goode EL.

Genet Epidemiol. 2010 Jul;34(5):418-26. doi: 10.1002/gepi.20494.

9.

A comparison of SNPs and microsatellites as linkage mapping markers: lessons from the zebra finch (Taeniopygia guttata).

Ball AD, Stapley J, Dawson DA, Birkhead TR, Burke T, Slate J.

BMC Genomics. 2010 Apr 1;11:218. doi: 10.1186/1471-2164-11-218.

10.

Use of supplementary phenotype to identify additional rheumatoid arthritis loci in a linkage analysis of 342 UK affected sibling pair families.

Tayo BO, Liang Y, Kelemen A, Miller A, Trevisan M, Cooper RS.

BMC Med Genet. 2009 Dec 21;10:142. doi: 10.1186/1471-2350-10-142.

11.

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.

Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV.

Epilepsy Res. 2009 Dec;87(2-3):247-55. doi: 10.1016/j.eplepsyres.2009.09.010. Epub 2009 Oct 17.

12.

Detection of parent-of-origin effects using general pedigree data.

Zhou JY, Ding J, Fung WK, Lin S.

Genet Epidemiol. 2010 Feb;34(2):151-8. doi: 10.1002/gepi.20445.

13.

Finding common susceptibility variants for complex disease: past, present and future.

Panoutsopoulou K, Zeggini E.

Brief Funct Genomic Proteomic. 2009 Sep;8(5):345-52. doi: 10.1093/bfgp/elp020. Epub 2009 Jul 1. Review.

14.

Multivariate association test using haplotype trend regression.

Pei YF, Zhang L, Liu J, Deng HW.

Ann Hum Genet. 2009 Jul;73(Pt 4):456-64. doi: 10.1111/j.1469-1809.2009.00527.x. Epub 2009 Jun 1.

15.

SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data.

Fukuda Y, Nakahara Y, Date H, Takahashi Y, Goto J, Miyashita A, Kuwano R, Adachi H, Nakamura E, Tsuji S.

BMC Bioinformatics. 2009 Apr 24;10:121. doi: 10.1186/1471-2105-10-121.

16.

Differential gene expression of peripheral blood mononuclear cells from rheumatoid arthritis patients may discriminate immunogenetic, pathogenic and treatment features.

Junta CM, Sandrin-Garcia P, Fachin-Saltoratto AL, Mello SS, Oliveira RD, Rassi DM, Giuliatti S, Sakamoto-Hojo ET, Louzada-Junior P, Donadi EA, Passos GA.

Immunology. 2009 Jul;127(3):365-72. doi: 10.1111/j.1365-2567.2008.03005.x. Epub 2008 Dec 17.

17.

Genome-wide linkage and admixture mapping of type 2 diabetes in African American families from the American Diabetes Association GENNID (Genetics of NIDDM) Study Cohort.

Elbein SC, Das SK, Hallman DM, Hanis CL, Hasstedt SJ.

Diabetes. 2009 Jan;58(1):268-74. doi: 10.2337/db08-0931. Epub 2008 Oct 7.

18.

Meta-analysis of genome-wide linkage studies across autoimmune diseases.

Forabosco P, Bouzigon E, Ng MY, Hermanowski J, Fisher SA, Criswell LA, Lewis CM.

Eur J Hum Genet. 2009 Feb;17(2):236-43. doi: 10.1038/ejhg.2008.163. Epub 2008 Sep 10.

19.

Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits.

Amos CI, Chen WV, Remmers E, Siminovitch KA, Seldin MF, Criswell LA, Lee AT, John S, Shephard ND, Worthington J, Cornelis F, Plenge RM, Begovich AB, Dyer TD, Kastner DL, Gregersen PK.

BMC Proc. 2007;1 Suppl 1:S3. Epub 2007 Dec 18.

20.

Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis.

Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A.

BMC Proc. 2007;1 Suppl 1:S160. Epub 2007 Dec 18.

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