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Items: 1 to 20 of 514

1.

Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populations.

De La Vega FM, Gordon D, Su X, Scafe C, Isaac H, Gilbert DA, Spier EG.

Hum Hered. 2005;60(1):43-60. Epub 2005 Sep 2.

PMID:
16137993
2.

Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus.

Veal CD, Capon F, Allen MH, Heath EK, Evans JC, Jones A, Patel S, Burden D, Tillman D, Barker JN, Trembath RC.

Am J Hum Genet. 2002 Sep;71(3):554-64. Epub 2002 Jul 29.

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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
6.

Positional cloning by linkage disequilibrium.

Maniatis N, Collins A, Gibson J, Zhang W, Tapper W, Morton NE.

Am J Hum Genet. 2004 May;74(5):846-55. Epub 2004 Mar 26.

7.

Power-based, phase-informed selection of single nucleotide polymorphisms for disease association screens.

Saccone SF, Rice JP, Saccone NL.

Genet Epidemiol. 2006 Sep;30(6):459-70.

PMID:
16685721
8.

Corneodesmosin (CDSN) gene association with psoriasis vulgaris in Caucasian but not in Japanese populations.

Ameen M, Allen MH, Fisher SA, Lewis CM, Cuthbert A, Kondeatis E, Vaughan RW, Murakami H, Nakagawa H, Barker JN.

Clin Exp Dermatol. 2005 Jul;30(4):414-8.

PMID:
15953084
9.

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern.

De La Vega FM, Isaac H, Collins A, Scafe CR, Halldórsson BV, Su X, Lippert RA, Wang Y, Laig-Webster M, Koehler RT, Ziegle JS, Wogan LT, Stevens JF, Leinen KM, Olson SJ, Guegler KJ, You X, Xu LH, Hemken HG, Kalush F, Itakura M, Zheng Y, de Thé G, O'Brien SJ, Clark AG, Istrail S, Hunkapiller MW, Spier EG, Gilbert DA.

Genome Res. 2005 Apr;15(4):454-62. Epub 2005 Mar 21.

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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.

12.

Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.

Maniatis N, Collins A, Morton NE.

Genet Epidemiol. 2007 Apr;31(3):179-88.

PMID:
17285621
13.

Association of specific haplotypes of D2 dopamine receptor gene with vulnerability to heroin dependence in 2 distinct populations.

Xu K, Lichtermann D, Lipsky RH, Franke P, Liu X, Hu Y, Cao L, Schwab SG, Wildenauer DB, Bau CH, Ferro E, Astor W, Finch T, Terry J, Taubman J, Maier W, Goldman D.

Arch Gen Psychiatry. 2004 Jun;61(6):597-606.

PMID:
15184239
14.

Genotype prediction using a dense map of SNPs.

Evans DM, Cardon LR, Morris AP.

Genet Epidemiol. 2004 Dec;27(4):375-84.

PMID:
15543641
15.

Haplotype-based localization of an alcohol dependence gene to the 5q34 {gamma}-aminobutyric acid type A gene cluster.

Radel M, Vallejo RL, Iwata N, Aragon R, Long JC, Virkkunen M, Goldman D.

Arch Gen Psychiatry. 2005 Jan;62(1):47-55.

PMID:
15630072
16.

Haplotype sharing analysis with SNPs in candidate genes: the Genetic Analysis Workshop 12 example.

Fischer C, Beckmann L, Majoram P, te Meerman G, Chang-Claude J.

Genet Epidemiol. 2003 Jan;24(1):68-73.

PMID:
12508257
17.

Haplotype-based analysis of alpha 2A, 2B, and 2C adrenergic receptor genes captures information on common functional loci at each gene.

Belfer I, Buzas B, Hipp H, Phillips G, Taubman J, Lorincz I, Evans C, Lipsky RH, Enoch MA, Max MB, Goldman D.

J Hum Genet. 2005;50(1):12-20. Epub 2004 Dec 8.

PMID:
15592690
18.

Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C.

Nair RP, Stuart P, Henseler T, Jenisch S, Chia NV, Westphal E, Schork NJ, Kim J, Lim HW, Christophers E, Voorhees JJ, Elder JT.

Am J Hum Genet. 2000 Jun;66(6):1833-44. Epub 2000 May 5. Erratum in: Am J Hum Genet 2002 Apr;70(4):1074.

19.

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia.

Hennah W, Varilo T, Paunio T, Peltonen L.

Ann Med. 2004;36(5):322-31. Review.

PMID:
15478307
20.

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

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