Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 67

1.

A twist on admixture mapping.

Chanock SJ.

Nat Genet. 2011 Mar;43(3):178-9. doi: 10.1038/ng0311-178.

PMID:
21350496
[PubMed - indexed for MEDLINE]
2.

Variation at 7p12.2 and 10q21.2 influences childhood acute lymphoblastic leukemia risk in the Thai population and may contribute to racial differences in leukemia incidence.

Vijayakrishnan J, Sherborne AL, Sawangpanich R, Hongeng S, Houlston RS, Pakakasama S.

Leuk Lymphoma. 2010 Oct;51(10):1870-4. doi: 10.3109/10428194.2010.511356.

PMID:
20919861
[PubMed - indexed for MEDLINE]
3.

A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping.

Tian C, Hinds DA, Shigeta R, Adler SG, Lee A, Pahl MV, Silva G, Belmont JW, Hanson RL, Knowler WC, Gregersen PK, Ballinger DG, Seldin MF.

Am J Hum Genet. 2007 Jun;80(6):1014-23.

PMID:
17557415
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Methylene tetrahydrofolate reductase gene polymorphism in Egyptian children with acute lymphoblastic leukemia.

Tantawy AA, El-Bostany EA, Adly AA, Abou El Asrar M, El-Ghouroury EA, Abdulghaffar EE.

Blood Coagul Fibrinolysis. 2010 Jan;21(1):28-34. doi: 10.1097/MBC.0b013e32833135e9. Erratum in: Blood Coagul Fibrinolysis. 2010 Mar;21(2):200.

PMID:
19923983
[PubMed - indexed for MEDLINE]
5.

A classical likelihood based approach for admixture mapping using EM algorithm.

Zhu X, Zhang S, Tang H, Cooper R.

Hum Genet. 2006 Oct;120(3):431-45. Epub 2006 Aug 5.

PMID:
16896924
[PubMed - indexed for MEDLINE]
6.

Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

Irving JA, Bloodworth L, Bown NP, Case MC, Hogarth LA, Hall AG.

Cancer Res. 2005 Apr 15;65(8):3053-8.

PMID:
15833833
[PubMed - indexed for MEDLINE]
Free Article
7.

Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia.

Yang JJ, Cheng C, Devidas M, Cao X, Fan Y, Campana D, Yang W, Neale G, Cox NJ, Scheet P, Borowitz MJ, Winick NJ, Martin PL, Willman CL, Bowman WP, Camitta BM, Carroll A, Reaman GH, Carroll WL, Loh M, Hunger SP, Pui CH, Evans WE, Relling MV.

Nat Genet. 2011 Mar;43(3):237-41. doi: 10.1038/ng.763. Epub 2011 Feb 6.

PMID:
21297632
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Polymorphisms of the gamma-glutamyl hydrolase gene and risk of relapse to acute lymphoblastic leukemia in Mexico.

Organista-Nava J, Gómez-Gómez Y, Saavedra-Herrera MV, Rivera-Ramírez AB, Terán-Porcayo MA, Alarcón-Romero Ldel C, Illades-Aguiar B, Leyva-Vázquez MA.

Leuk Res. 2010 Jun;34(6):728-32. doi: 10.1016/j.leukres.2009.11.027. Epub 2010 Mar 1.

PMID:
20197200
[PubMed - indexed for MEDLINE]
9.

A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping.

Tian C, Hinds DA, Shigeta R, Kittles R, Ballinger DG, Seldin MF.

Am J Hum Genet. 2006 Oct;79(4):640-9. Epub 2006 Aug 15.

PMID:
16960800
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Allelic association patterns for a dense SNP map.

Weir BS, Hill WG, Cardon LR; SNP Consortium.

Genet Epidemiol. 2004 Dec;27(4):442-50.

PMID:
15543640
[PubMed - indexed for MEDLINE]
11.

CYP3A genotypes and treatment response in paediatric acute lymphoblastic leukaemia.

Aplenc R, Glatfelter W, Han P, Rappaport E, La M, Cnaan A, Blackwood MA, Lange B, Rebbeck T.

Br J Haematol. 2003 Jul;122(2):240-4.

PMID:
12846892
[PubMed - indexed for MEDLINE]
12.

Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.

Durrant C, Zondervan KT, Cardon LR, Hunt S, Deloukas P, Morris AP.

Am J Hum Genet. 2004 Jul;75(1):35-43. Epub 2004 May 13.

PMID:
15148658
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Efficacy assessment of SNP sets for genome-wide disease association studies.

Wollstein A, Herrmann A, Wittig M, Nothnagel M, Franke A, Nürnberg P, Schreiber S, Krawczak M, Hampe J.

Nucleic Acids Res. 2007;35(17):e113. Epub 2007 Aug 28.

PMID:
17726055
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies.

Lee S, Epstein MP, Duncan R, Lin X.

Genet Epidemiol. 2012 May;36(4):293-302. doi: 10.1002/gepi.21621. Epub 2012 Apr 16.

PMID:
22508067
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

A genome-wide association study of sporadic ALS in a homogenous Irish population.

Cronin S, Berger S, Ding J, Schymick JC, Washecka N, Hernandez DG, Greenway MJ, Bradley DG, Traynor BJ, Hardiman O.

Hum Mol Genet. 2008 Mar 1;17(5):768-74. Epub 2007 Dec 5.

PMID:
18057069
[PubMed - indexed for MEDLINE]
Free Article
16.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

PMID:
19531258
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

ATRIUM: testing untyped SNPs in case-control association studies with related individuals.

Wang Z, McPeek MS.

Am J Hum Genet. 2009 Nov;85(5):667-78. doi: 10.1016/j.ajhg.2009.10.006.

PMID:
19913122
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Toward positional cloning with SNPs.

Morton NE, Collins A.

Curr Opin Mol Ther. 2002 Jun;4(3):259-64. Review.

PMID:
12139312
[PubMed - indexed for MEDLINE]
19.

Linkage mapping methods applied to the COGA data set: presentation Group 4 of Genetic Analysis Workshop 14.

Daw EW, Doan BQ, Elston RC.

Genet Epidemiol. 2005;29 Suppl 1:S29-34.

PMID:
16342182
[PubMed - indexed for MEDLINE]
20.

Asymptotic equivalence between two score tests for haplotype-specific risk in general linear models.

Xie R, Stram DO.

Genet Epidemiol. 2005 Sep;29(2):166-70. No abstract available.

PMID:
16025443
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk