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Items: 1 to 20 of 413

1.

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
2.

Whole-genome patterns of common DNA variation in three human populations.

Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR.

Science. 2005 Feb 18;307(5712):1072-9.

3.

Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens.

Taillon-Miller P, Saccone SF, Saccone NL, Duan S, Kloss EF, Lovins EG, Donaldson R, Phong A, Ha C, Flagstad L, Miller S, Drendel A, Lind D, Miller RD, Rice JP, Kwok PY.

Genomics. 2004 Dec;84(6):899-912.

PMID:
15533707
4.

The structure of haplotype blocks in the human genome.

Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D.

Science. 2002 Jun 21;296(5576):2225-9.

5.

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
6.

Haplotype variation and linkage disequilibrium in 313 human genes.

Stephens JC, Schneider JA, Tanguay DA, Choi J, Acharya T, Stanley SE, Jiang R, Messer CJ, Chew A, Han JH, Duan J, Carr JL, Lee MS, Koshy B, Kumar AM, Zhang G, Newell WR, Windemuth A, Xu C, Kalbfleisch TS, Shaner SL, Arnold K, Schulz V, Drysdale CM, Nandabalan K, Judson RS, Ruano G, Vovis GF.

Science. 2001 Jul 20;293(5529):489-93. Erratum in: Science 2001 Aug 10;293(5532):1048.

7.

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
8.

Patterns of genetic variation in the hypertension candidate gene GRK4: ethnic variation and haplotype structure.

Lohmueller KE, Wong LJ, Mauney MM, Jiang L, Felder RA, Jose PA, Williams SM.

Ann Hum Genet. 2006 Jan;70(Pt 1):27-41.

9.

Population-wide generalizability of genome-wide discovered associations.

Ioannidis JP.

J Natl Cancer Inst. 2009 Oct 7;101(19):1297-9. doi: 10.1093/jnci/djp298. No abstract available.

PMID:
19726754
10.

Genetic variation at the calcium-sensing receptor (CASR) locus: implications for clinical molecular diagnostics.

Yun FH, Wong BY, Chase M, Shuen AY, Canaff L, Thongthai K, Siminovitch K, Hendy GN, Cole DE.

Clin Biochem. 2007 May;40(8):551-61.

PMID:
17320849
11.

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans.

Lamason RL, Mohideen MA, Mest JR, Wong AC, Norton HL, Aros MC, Jurynec MJ, Mao X, Humphreville VR, Humbert JE, Sinha S, Moore JL, Jagadeeswaran P, Zhao W, Ning G, Makalowska I, McKeigue PM, O'donnell D, Kittles R, Parra EJ, Mangini NJ, Grunwald DJ, Shriver MD, Canfield VA, Cheng KC.

Science. 2005 Dec 16;310(5755):1782-6.

12.

Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans.

Evans PD, Gilbert SL, Mekel-Bobrov N, Vallender EJ, Anderson JR, Vaez-Azizi LM, Tishkoff SA, Hudson RR, Lahn BT.

Science. 2005 Sep 9;309(5741):1717-20.

13.

Genetic ancestry and the search for personalized genetic histories.

Shriver MD, Kittles RA.

Nat Rev Genet. 2004 Aug;5(8):611-8. No abstract available.

PMID:
15266343
14.
15.
16.

The rough guide to the genome.

Dennis C.

Nature. 2003 Oct 23;425(6960):758-9. No abstract available.

PMID:
14574376
17.

Haplotype-based association studies of IGFBP1 and IGFBP3 with prostate and breast cancer risk: the multiethnic cohort.

Cheng I, Penney KL, Stram DO, Le Marchand L, Giorgi E, Haiman CA, Kolonel LN, Pike M, Hirschhorn J, Henderson BE, Freedman ML.

Cancer Epidemiol Biomarkers Prev. 2006 Oct;15(10):1993-7.

18.

Disentangling the effects of demography and selection in human history.

Stajich JE, Hahn MW.

Mol Biol Evol. 2005 Jan;22(1):63-73.

PMID:
15356276
19.

Extended tracts of homozygosity in outbred human populations.

Gibson J, Morton NE, Collins A.

Hum Mol Genet. 2006 Mar 1;15(5):789-95.

PMID:
16436455
20.

Linkage disequilibrium patterns vary substantially among populations.

Sawyer SL, Mukherjee N, Pakstis AJ, Feuk L, Kidd JR, Brookes AJ, Kidd KK.

Eur J Hum Genet. 2005 May;13(5):677-86.

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