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Items: 1 to 20 of 30

1.

A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.

Takahashi Y, Kou I, Takahashi A, Johnson TA, Kono K, Kawakami N, Uno K, Ito M, Minami S, Yanagida H, Taneichi H, Tsuji T, Suzuki T, Sudo H, Kotani T, Watanabe K, Chiba K, Hosono N, Kamatani N, Tsunoda T, Toyama Y, Kubo M, Matsumoto M, Ikegawa S.

Nat Genet. 2011 Oct 23;43(12):1237-40. doi: 10.1038/ng.974.

PMID:
22019779
2.

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets.

Jostins L, Morley KI, Barrett JC.

Eur J Hum Genet. 2011 Jun;19(6):662-6. doi: 10.1038/ejhg.2011.10. Epub 2011 Mar 2.

3.

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.

Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR.

Genet Epidemiol. 2010 Dec;34(8):816-34. doi: 10.1002/gepi.20533.

4.

Rare variant association analysis methods for complex traits.

Asimit J, Zeggini E.

Annu Rev Genet. 2010;44:293-308. doi: 10.1146/annurev-genet-102209-163421. Review.

PMID:
21047260
5.

A map of human genome variation from population-scale sequencing.

1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA.

Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534. Erratum in: Nature. 2011 May 26;473(7348):544. Xue, Yali [added]; Cartwright, Reed A [added]; Altshuler, David L [corrected to Altshuler, David]; Kebbel, Andrew [corrected to Keebler, Jonathan]; Koko-Gonzales, Paula [corrected to Kokko-Gonzales, Paula]; Nickerson, Debbie A [corrected to Nickerson, Deborah A].

6.

Statistical analysis strategies for association studies involving rare variants.

Bansal V, Libiger O, Torkamani A, Schork NJ.

Nat Rev Genet. 2010 Nov;11(11):773-85. doi: 10.1038/nrg2867. Epub 2010 Oct 13. Review.

7.

Integrating common and rare genetic variation in diverse human populations.

International HapMap 3 Consortium, Altshuler DM, Gibbs RA, Peltonen L, Altshuler DM, Gibbs RA, Peltonen L, Dermitzakis E, Schaffner SF, Yu F, Peltonen L, Dermitzakis E, Bonnen PE, Altshuler DM, Gibbs RA, de Bakker PI, Deloukas P, Gabriel SB, Gwilliam R, Hunt S, Inouye M, Jia X, Palotie A, Parkin M, Whittaker P, Yu F, Chang K, Hawes A, Lewis LR, Ren Y, Wheeler D, Gibbs RA, Muzny DM, Barnes C, Darvishi K, Hurles M, Korn JM, Kristiansson K, Lee C, McCarrol SA, Nemesh J, Dermitzakis E, Keinan A, Montgomery SB, Pollack S, Price AL, Soranzo N, Bonnen PE, Gibbs RA, Gonzaga-Jauregui C, Keinan A, Price AL, Yu F, Anttila V, Brodeur W, Daly MJ, Leslie S, McVean G, Moutsianas L, Nguyen H, Schaffner SF, Zhang Q, Ghori MJ, McGinnis R, McLaren W, Pollack S, Price AL, Schaffner SF, Takeuchi F, Grossman SR, Shlyakhter I, Hostetter EB, Sabeti PC, Adebamowo CA, Foster MW, Gordon DR, Licinio J, Manca MC, Marshall PA, Matsuda I, Ngare D, Wang VO, Reddy D, Rotimi CN, Royal CD, Sharp RR, Zeng C, Brooks LD, McEwen JE.

Nature. 2010 Sep 2;467(7311):52-8. doi: 10.1038/nature09298.

8.

Genotype imputation for genome-wide association studies.

Marchini J, Howie B.

Nat Rev Genet. 2010 Jul;11(7):499-511. doi: 10.1038/nrg2796. Review.

PMID:
20517342
9.

Genome-wide patterns of population structure and admixture in West Africans and African Americans.

Bryc K, Auton A, Nelson MR, Oksenberg JR, Hauser SL, Williams S, Froment A, Bodo JM, Wambebe C, Tishkoff SA, Bustamante CD.

Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):786-91. doi: 10.1073/pnas.0909559107. Epub 2009 Dec 22.

10.

Practical considerations for imputation of untyped markers in admixed populations.

Shriner D, Adeyemo A, Chen G, Rotimi CN.

Genet Epidemiol. 2010 Apr;34(3):258-65. doi: 10.1002/gepi.20457.

11.

Genotype imputation.

Li Y, Willer C, Sanna S, Abecasis G.

Annu Rev Genomics Hum Genet. 2009;10:387-406. doi: 10.1146/annurev.genom.9.081307.164242. Review.

12.

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.

Howie BN, Donnelly P, Marchini J.

PLoS Genet. 2009 Jun;5(6):e1000529. doi: 10.1371/journal.pgen.1000529. Epub 2009 Jun 19.

13.

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.

14.

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA.

Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9362-7. doi: 10.1073/pnas.0903103106. Epub 2009 May 27.

15.

The genetic structure and history of Africans and African Americans.

Tishkoff SA, Reed FA, Friedlaender FR, Ehret C, Ranciaro A, Froment A, Hirbo JB, Awomoyi AA, Bodo JM, Doumbo O, Ibrahim M, Juma AT, Kotze MJ, Lema G, Moore JH, Mortensen H, Nyambo TB, Omar SA, Powell K, Pretorius GS, Smith MW, Thera MA, Wambebe C, Weber JL, Williams SM.

Science. 2009 May 22;324(5930):1035-44. doi: 10.1126/science.1172257. Epub 2009 Apr 30.

16.

Use of weighted reference panels based on empirical estimates of ancestry for capturing untyped variation.

Egyud MR, Gajdos ZK, Butler JL, Tischfield S, Le Marchand L, Kolonel LN, Haiman CA, Henderson BE, Hirschhorn JN.

Hum Genet. 2009 Apr;125(3):295-303. doi: 10.1007/s00439-009-0627-8. Epub 2009 Jan 28.

17.

A comprehensive evaluation of SNP genotype imputation.

Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A.

Hum Genet. 2009 Mar;125(2):163-71. doi: 10.1007/s00439-008-0606-5. Epub 2008 Dec 17.

PMID:
19089453
18.

Imputation of missing genotypes: an empirical evaluation of IMPUTE.

Zhao Z, Timofeev N, Hartley SW, Chui DH, Fucharoen S, Perls TT, Steinberg MH, Baldwin CT, Sebastiani P.

BMC Genet. 2008 Dec 12;9:85. doi: 10.1186/1471-2156-9-85.

19.

Practical aspects of imputation-driven meta-analysis of genome-wide association studies.

de Bakker PI, Ferreira MA, Jia X, Neale BM, Raychaudhuri S, Voight BF.

Hum Mol Genet. 2008 Oct 15;17(R2):R122-8. doi: 10.1093/hmg/ddn288.

20.

Ethnic differences in cardiovascular drug response: potential contribution of pharmacogenetics.

Johnson JA.

Circulation. 2008 Sep 23;118(13):1383-93. doi: 10.1161/CIRCULATIONAHA.107.704023. Review. No abstract available.

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