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Items: 1 to 20 of 50

1.

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers.

Abecasis GR, Wigginton JE.

Am J Hum Genet. 2005 Nov;77(5):754-67. Epub 2005 Sep 20.

2.

The International HapMap Project Web site.

Thorisson GA, Smith AV, Krishnan L, Stein LD.

Genome Res. 2005 Nov;15(11):1592-3.

3.

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.

Siepel A, Bejerano G, Pedersen JS, Hinrichs AS, Hou M, Rosenbloom K, Clawson H, Spieth J, Hillier LW, Richards S, Weinstock GM, Wilson RK, Gibbs RA, Kent WJ, Miller W, Haussler D.

Genome Res. 2005 Aug;15(8):1034-50. Epub 2005 Jul 15.

4.

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration.

Zareparsi S, Branham KE, Li M, Shah S, Klein RJ, Ott J, Hoh J, Abecasis GR, Swaroop A.

Am J Hum Genet. 2005 Jul;77(1):149-53. Epub 2005 May 13.

5.

Linkage disequilibrium: ancient history drives the new genetics.

Abecasis GR, Ghosh D, Nichols TE.

Hum Hered. 2005;59(2):118-24. Epub 2005 Apr 18. Review.

PMID:
15838181
6.

Complement factor H polymorphism in age-related macular degeneration.

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J.

Science. 2005 Apr 15;308(5720):385-9. Epub 2005 Mar 10.

7.

Complement factor H polymorphism and age-related macular degeneration.

Edwards AO, Ritter R 3rd, Abel KJ, Manning A, Panhuysen C, Farrer LA.

Science. 2005 Apr 15;308(5720):421-4. Epub 2005 Mar 10.

8.

Complement factor H variant increases the risk of age-related macular degeneration.

Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA.

Science. 2005 Apr 15;308(5720):419-21. Epub 2005 Mar 10.

9.

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.

10.

Genome-wide association studies for common diseases and complex traits.

Hirschhorn JN, Daly MJ.

Nat Rev Genet. 2005 Feb;6(2):95-108. Review.

PMID:
15716906
11.

How strong is the mutagenicity of recombination in mammals?

Huang SW, Friedman R, Yu N, Yu A, Li WH.

Mol Biol Evol. 2005 Mar;22(3):426-31. Epub 2004 Oct 20. Erratum in: Mol Biol Evol. 2005 Apr;22(4):1157.

PMID:
15496551
12.

Haplotype block structures show significant variation among populations.

Liu N, Sawyer SL, Mukherjee N, Pakstis AJ, Kidd JR, Kidd KK, Brookes AJ, Zhao H.

Genet Epidemiol. 2004 Dec;27(4):385-400.

PMID:
15389924
13.

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

Ke X, Durrant C, Morris AP, Hunt S, Bentley DR, Deloukas P, Cardon LR.

Hum Mol Genet. 2004 Nov 1;13(21):2557-65. Epub 2004 Sep 14.

PMID:
15367493
14.

The fine-scale structure of recombination rate variation in the human genome.

McVean GA, Myers SR, Hunt S, Deloukas P, Bentley DR, Donnelly P.

Science. 2004 Apr 23;304(5670):581-4.

15.

Aligning multiple genomic sequences with the threaded blockset aligner.

Blanchette M, Kent WJ, Riemer C, Elnitski L, Smit AF, Roskin KM, Baertsch R, Rosenbloom K, Clawson H, Green ED, Haussler D, Miller W.

Genome Res. 2004 Apr;14(4):708-15.

16.

Genome sequence of the Brown Norway rat yields insights into mammalian evolution.

Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, Scott G, Steffen D, Worley KC, Burch PE, Okwuonu G, Hines S, Lewis L, DeRamo C, Delgado O, Dugan-Rocha S, Miner G, Morgan M, Hawes A, Gill R, Celera, Holt RA, Adams MD, Amanatides PG, Baden-Tillson H, Barnstead M, Chin S, Evans CA, Ferriera S, Fosler C, Glodek A, Gu Z, Jennings D, Kraft CL, Nguyen T, Pfannkoch CM, Sitter C, Sutton GG, Venter JC, Woodage T, Smith D, Lee HM, Gustafson E, Cahill P, Kana A, Doucette-Stamm L, Weinstock K, Fechtel K, Weiss RB, Dunn DM, Green ED, Blakesley RW, Bouffard GG, De Jong PJ, Osoegawa K, Zhu B, Marra M, Schein J, Bosdet I, Fjell C, Jones S, Krzywinski M, Mathewson C, Siddiqui A, Wye N, McPherson J, Zhao S, Fraser CM, Shetty J, Shatsman S, Geer K, Chen Y, Abramzon S, Nierman WC, Havlak PH, Chen R, Durbin KJ, Egan A, Ren Y, Song XZ, Li B, Liu Y, Qin X, Cawley S, Worley KC, Cooney AJ, D'Souza LM, Martin K, Wu JQ, Gonzalez-Garay ML, Jackson AR, Kalafus KJ, McLeod MP, Milosavljevic A, Virk D, Volkov A, Wheeler DA, Zhang Z, Bailey JA, Eichler EE, Tuzun E, Birney E, Mongin E, Ureta-Vidal A, Woodwark C, Zdobnov E, Bork P, Suyama M, Torrents D, Alexandersson M, Trask BJ, Young JM, Huang H, Wang H, Xing H, Daniels S, Gietzen D, Schmidt J, Stevens K, Vitt U, Wingrove J, Camara F, Mar Albà M, Abril JF, Guigo R, Smit A, Dubchak I, Rubin EM, Couronne O, Poliakov A, Hübner N, Ganten D, Goesele C, Hummel O, Kreitler T, Lee YA, Monti J, Schulz H, Zimdahl H, Himmelbauer H, Lehrach H, Jacob HJ, Bromberg S, Gullings-Handley J, Jensen-Seaman MI, Kwitek AE, Lazar J, Pasko D, Tonellato PJ, Twigger S, Ponting CP, Duarte JM, Rice S, Goodstadt L, Beatson SA, Emes RD, Winter EE, Webber C, Brandt P, Nyakatura G, Adetobi M, Chiaromonte F, Elnitski L, Eswara P, Hardison RC, Hou M, Kolbe D, Makova K, Miller W, Nekrutenko A, Riemer C, Schwartz S, Taylor J, Yang S, Zhang Y, Lindpaintner K, Andrews TD, Caccamo M, Clamp M, Clarke L, Curwen V, Durbin R, Eyras E, Searle SM, Cooper GM, Batzoglou S, Brudno M, Sidow A, Stone EA, Venter JC, Payseur BA, Bourque G, López-Otín C, Puente XS, Chakrabarti K, Chatterji S, Dewey C, Pachter L, Bray N, Yap VB, Caspi A, Tesler G, Pevzner PA, Haussler D, Roskin KM, Baertsch R, Clawson H, Furey TS, Hinrichs AS, Karolchik D, Kent WJ, Rosenbloom KR, Trumbower H, Weirauch M, Cooper DN, Stenson PD, Ma B, Brent M, Arumugam M, Shteynberg D, Copley RR, Taylor MS, Riethman H, Mudunuri U, Peterson J, Guyer M, Felsenfeld A, Old S, Mockrin S, Collins F; Rat Genome Sequencing Project Consortium.

Nature. 2004 Apr 1;428(6982):493-521.

PMID:
15057822
17.

The X chromosome in population genetics.

Schaffner SF.

Nat Rev Genet. 2004 Jan;5(1):43-51. Review. No abstract available.

PMID:
14708015
18.

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data.

Li N, Stephens M.

Genetics. 2003 Dec;165(4):2213-33. Erratum in: Genetics. 2004 Jun;167(2):1039.

19.

The International HapMap Project.

International HapMap Consortium.

Nature. 2003 Dec 18;426(6968):789-96.

PMID:
14685227
20.

The UCSC Table Browser data retrieval tool.

Karolchik D, Hinrichs AS, Furey TS, Roskin KM, Sugnet CW, Haussler D, Kent WJ.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D493-6.

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