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Items: 1 to 20 of 193

1.

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.

Sachidanandam R, Weissman D, Schmidt SC, Kakol JM, Stein LD, Marth G, Sherry S, Mullikin JC, Mortimore BJ, Willey DL, Hunt SE, Cole CG, Coggill PC, Rice CM, Ning Z, Rogers J, Bentley DR, Kwok PY, Mardis ER, Yeh RT, Schultz B, Cook L, Davenport R, Dante M, Fulton L, Hillier L, Waterston RH, McPherson JD, Gilman B, Schaffner S, Van Etten WJ, Reich D, Higgins J, Daly MJ, Blumenstiel B, Baldwin J, Stange-Thomann N, Zody MC, Linton L, Lander ES, Altshuler D; International SNP Map Working Group.

Nature. 2001 Feb 15;409(6822):928-33.

PMID:
11237013
2.

An SNP map of the human genome generated by reduced representation shotgun sequencing.

Altshuler D, Pollara VJ, Cowles CR, Van Etten WJ, Baldwin J, Linton L, Lander ES.

Nature. 2000 Sep 28;407(6803):513-6.

PMID:
11029002
3.

An SNP map of human chromosome 22.

Mullikin JC, Hunt SE, Cole CG, Mortimore BJ, Rice CM, Burton J, Matthews LH, Pavitt R, Plumb RW, Sims SK, Ainscough RM, Attwood J, Bailey JM, Barlow K, Bruskiewich RM, Butcher PN, Carter NP, Chen Y, Clee CM, Coggill PC, Davies J, Davies RM, Dawson E, Francis MD, Joy AA, Lamble RG, Langford CF, Macarthy J, Mall V, Moreland A, Overton-Larty EK, Ross MT, Smith LC, Steward CA, Sulston JE, Tinsley EJ, Turney KJ, Willey DL, Wilson GD, McMurray AA, Dunham I, Rogers J, Bentley DR.

Nature. 2000 Sep 28;407(6803):516-20.

PMID:
11029003
4.

The Human Genome Project--an overview.

Bentley DR.

Med Res Rev. 2000 May;20(3):189-96. Review.

PMID:
10797463
5.

Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes.

Wang X, Tomso DJ, Liu X, Bell DA.

Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):84-90. Review.

PMID:
16002116
6.

A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

Matise TC, Sachidanandam R, Clark AG, Kruglyak L, Wijsman E, Kakol J, Buyske S, Chui B, Cohen P, de Toma C, Ehm M, Glanowski S, He C, Heil J, Markianos K, McMullen I, Pericak-Vance MA, Silbergleit A, Stein L, Wagner M, Wilson AF, Winick JD, Winn-Deen ES, Yamashiro CT, Cann HM, Lai E, Holden AL.

Am J Hum Genet. 2003 Aug;73(2):271-84. Epub 2003 Jul 3.

7.

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.

PMID:
16845142
8.

A high-density SNP map for the FRAX region of the X chromosome. Single-nucleotide polymorphisms.

Brightwell G, Wycherley R, Potts G, Waghorn A.

J Hum Genet. 2002;47(11):567-75.

PMID:
12436192
9.
10.
11.

An exponential dispersion model for the distribution of human single nucleotide polymorphisms.

Kendal WS.

Mol Biol Evol. 2003 Apr;20(4):579-90. Epub 2003 Apr 2. Review.

PMID:
12679541
12.

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome.

Estivill X, Cheung J, Pujana MA, Nakabayashi K, Scherer SW, Tsui LC.

Hum Mol Genet. 2002 Aug 15;11(17):1987-95.

PMID:
12165560
13.

SNP@Promoter: a database of human SNPs (single nucleotide polymorphisms) within the putative promoter regions.

Kim BC, Kim WY, Park D, Chung WH, Shin KS, Bhak J.

BMC Bioinformatics. 2008;9 Suppl 1:S2. doi: 10.1186/1471-2105-9-S1-S2.

14.

Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21.

Olivier M, Bustos VI, Levy MR, Smick GA, Moreno I, Bushard JM, Almendras AA, Sheppard K, Zierten DL, Aggarwal A, Carlson CS, Foster BD, Vo N, Kelly L, Liu X, Cox DR.

Genomics. 2001 Nov;78(1-2):64-72.

PMID:
11707074
15.

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
16.

Alu-associated enhancement of single nucleotide polymorphisms in the human genome.

Ng SK, Xue H.

Gene. 2006 Mar 1;368:110-6. Epub 2005 Dec 27.

PMID:
16380220
17.
18.

[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
19.

Proportioning whole-genome single-nucleotide-polymorphism diversity for the identification of geographic population structure and genetic ancestry.

Lao O, van Duijn K, Kersbergen P, de Knijff P, Kayser M.

Am J Hum Genet. 2006 Apr;78(4):680-90. Epub 2006 Feb 14.

20.

Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population.

Saito S, Iida A, Sekine A, Ogawa C, Kawauchi S, Higuchi S, Nakamura Y.

J Hum Genet. 2002;47(11):576-84.

PMID:
12436193

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