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Items: 1 to 20 of 115

1.

Probability of detecting disease-associated single nucleotide polymorphisms in case-control genome-wide association studies.

Gail MH, Pfeiffer RM, Wheeler W, Pee D.

Biostatistics. 2008 Apr;9(2):201-15. Epub 2007 Sep 14.

PMID:
17873152
3.

Probability that a two-stage genome-wide association study will detect a disease-associated snp and implications for multistage designs.

Gail MH, Pfeiffer RM, Wheeler W, Pee D.

Ann Hum Genet. 2008 Nov;72(Pt 6):812-20. doi: 10.1111/j.1469-1809.2008.00467.x. Epub 2008 Jul 24.

4.

Comparing the efficacy of SNP filtering methods for identifying a single causal SNP in a known association region.

Spencer AV, Cox A, Walters K.

Ann Hum Genet. 2014 Jan;78(1):50-61. doi: 10.1111/ahg.12043. Epub 2013 Nov 11.

5.

[How about the uncertainty in the haplotypes in the population-based KORA studies?].

Heid IM, Lamina C, Bongardt F, Fischer G, Klopp N, Huth C, Küchenhoff H, Kronenberg F, Wichmann HE, Illig T.

Gesundheitswesen. 2005 Aug;67 Suppl 1:S132-6. German.

PMID:
16032531
6.

Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan.

Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF.

Br J Dermatol. 2004 Jun;150(6):1104-11.

PMID:
15214895
7.

MAX-rank: a simple and robust genome-wide scan for case-control association studies.

Li Q, Yu K, Li Z, Zheng G.

Hum Genet. 2008 Jul;123(6):617-23. doi: 10.1007/s00439-008-0514-8. Epub 2008 May 20.

PMID:
18491142
8.

Ranking of genome-wide association scan signals by different measures.

Strömberg U, Björk J, Vineis P, Broberg K, Zeggini E.

Int J Epidemiol. 2009 Oct;38(5):1364-73. doi: 10.1093/ije/dyp285. Epub 2009 Sep 4.

9.

[Variations within OLF1/EBF-associated zinc finger protein gene confer susceptibility to lupus nephritis in Chinese population].

Liang D, Huang XQ, Shen N, Mao HQ, Feng XB, Huang XF, Tang JP, Chen XX, Chen SL, Gu YY, Bao CD, Wang Y, Qian J.

Zhonghua Yi Xue Za Zhi. 2005 Apr 13;85(14):949-54. Chinese.

PMID:
16061000
10.

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
12.

Association of HHIP polymorphisms with COPD and COPD-related phenotypes in a Chinese Han population.

Wang B, Zhou H, Yang J, Xiao J, Liang B, Li D, Zhou H, Zeng Q, Fang C, Rao Z, Yu H, Ou X, Feng Y.

Gene. 2013 Nov 15;531(1):101-5. doi: 10.1016/j.gene.2013.08.069. Epub 2013 Aug 30.

PMID:
23994291
13.

Strategies for developing prediction models from genome-wide association studies.

Wu J, Pfeiffer RM, Gail MH.

Genet Epidemiol. 2013 Dec;37(8):768-77. doi: 10.1002/gepi.21762. Epub 2013 Oct 25.

PMID:
24166696
14.
15.

Poor replication of candidate genes for major depressive disorder using genome-wide association data.

Bosker FJ, Hartman CA, Nolte IM, Prins BP, Terpstra P, Posthuma D, van Veen T, Willemsen G, DeRijk RH, de Geus EJ, Hoogendijk WJ, Sullivan PF, Penninx BW, Boomsma DI, Snieder H, Nolen WA.

Mol Psychiatry. 2011 May;16(5):516-32. doi: 10.1038/mp.2010.38. Epub 2010 Mar 30.

PMID:
20351714
16.

Genetic variants at 5p12 and risk of breast cancer in Han Chinese.

Liu X, Qin Z, Shen H, Xue J, Jiang Y, Hu Z, Shen H, Wang S.

J Hum Genet. 2012 Oct;57(10):638-41. doi: 10.1038/jhg.2012.83. Epub 2012 Jul 26.

PMID:
22832384
17.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

18.

A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.

Heit JA, Armasu SM, Asmann YW, Cunningham JM, Matsumoto ME, Petterson TM, De Andrade M.

J Thromb Haemost. 2012 Aug;10(8):1521-31. doi: 10.1111/j.1538-7836.2012.04810.x.

19.

The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.

Liu W, Zhao W, Chase GA.

Hum Hered. 2006;61(1):31-44. Epub 2006 Mar 23.

PMID:
16557026
20.

SNP-based pathway enrichment analysis for genome-wide association studies.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.

BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99.

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