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Items: 1 to 20 of 102

1.

A HapMap harvest of insights into the genetics of common disease.

Manolio TA, Brooks LD, Collins FS.

J Clin Invest. 2008 May;118(5):1590-605. doi: 10.1172/JCI34772. Review.

2.

Perspectives on human genetic variation from the HapMap Project.

McVean G, Spencer CC, Chaix R.

PLoS Genet. 2005 Oct;1(4):e54.

3.

The HapMap and genome-wide association studies in diagnosis and therapy.

Manolio TA, Collins FS.

Annu Rev Med. 2009;60:443-56. doi: 10.1146/annurev.med.60.061907.093117. Review.

4.

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.

Conrad DF, Jakobsson M, Coop G, Wen X, Wall JD, Rosenberg NA, Pritchard JK.

Nat Genet. 2006 Nov;38(11):1251-60. Epub 2006 Oct 22.

PMID:
17057719
5.

Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations.

Teo YY, Sim X, Ong RT, Tan AK, Chen J, Tantoso E, Small KS, Ku CS, Lee EJ, Seielstad M, Chia KS.

Genome Res. 2009 Nov;19(11):2154-62. doi: 10.1101/gr.095000.109. Epub 2009 Aug 21.

6.

Sequencing complex diseases With HapMap.

Liu T, Johnson JA, Casella G, Wu R.

Genetics. 2004 Sep;168(1):503-11.

7.

Mapping genes for common diseases: the case for genetic (LD) maps.

Collins A, Lau W, De La Vega FM.

Hum Hered. 2004;58(1):2-9.

PMID:
15604559
8.

A novel statistical algorithm for enhancing the utility of HapMap data to design genomic association studies in non-HapMap populations.

Sarkar-Roy N, Mondal D, Bhattacharya P, Majumder P.

Int J Data Min Bioinform. 2011;5(6):706-16.

PMID:
22295752
9.

[Analysis and application of SNP and haplotype in the human genome].

Li J, Pan YC, Li YX, Shi TL.

Yi Chuan Xue Bao. 2005 Aug;32(8):879-89. Review. Chinese.

PMID:
16231744
10.

Linkage disequilibrium and the mapping of complex human traits.

Weiss KM, Clark AG.

Trends Genet. 2002 Jan;18(1):19-24.

PMID:
11750696
11.

Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.

Mutsuddi M, Morris DW, Waggoner SG, Daly MJ, Scolnick EM, Sklar P.

Am J Hum Genet. 2006 Nov;79(5):903-9. Epub 2006 Oct 3.

12.

Human genome-wide screen of haplotype-like blocks of reduced diversity.

Costas J, Salas A, Phillips C, Carracedo A.

Gene. 2005 Apr 11;349:219-25.

PMID:
15780967
13.

Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia.

Bonnen PE, Pe'er I, Plenge RM, Salit J, Lowe JK, Shapero MH, Lifton RP, Breslow JL, Daly MJ, Reich DE, Jones KW, Stoffel M, Altshuler D, Friedman JM.

Nat Genet. 2006 Feb;38(2):214-7. Epub 2006 Jan 22.

PMID:
16429162
14.

A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.

Zhang C, Bailey DK, Awad T, Liu G, Xing G, Cao M, Valmeekam V, Retief J, Matsuzaki H, Taub M, Seielstad M, Kennedy GC.

Bioinformatics. 2006 Sep 1;22(17):2122-8. Epub 2006 Jul 15.

15.

Genetics. Harvesting medical information from the human family tree.

Altshuler D, Clark AG.

Science. 2005 Feb 18;307(5712):1052-3. No abstract available.

PMID:
15718454
16.

Utilizing HapMap and tagging SNPs.

Haiman CA, Stram DO.

Methods Mol Med. 2008;141:37-54.

PMID:
18453083
17.

Navigating the HapMap.

Barnes MR.

Brief Bioinform. 2006 Sep;7(3):211-24. Epub 2006 Jul 28. Review.

18.

Using haplotype blocks to map human complex trait loci.

Cardon LR, Abecasis GR.

Trends Genet. 2003 Mar;19(3):135-40. Review.

PMID:
12615007
19.

Perils in the use of linkage disequilibrium for fine gene mapping: simple insights from population genetics.

Gorroochurn P.

Cancer Epidemiol Biomarkers Prev. 2008 Dec;17(12):3292-7. doi: 10.1158/1055-9965.EPI-08-0717.

20.

Transferability of tag SNPs in genetic association studies in multiple populations.

de Bakker PI, Burtt NP, Graham RR, Guiducci C, Yelensky R, Drake JA, Bersaglieri T, Penney KL, Butler J, Young S, Onofrio RC, Lyon HN, Stram DO, Haiman CA, Freedman ML, Zhu X, Cooper R, Groop L, Kolonel LN, Henderson BE, Daly MJ, Hirschhorn JN, Altshuler D.

Nat Genet. 2006 Nov;38(11):1298-303. Epub 2006 Oct 22.

PMID:
17057720
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