Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 107

1.

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries.

Park JH, Wacholder S, Gail MH, Peters U, Jacobs KB, Chanock SJ, Chatterjee N.

Nat Genet. 2010 Jul;42(7):570-5. doi: 10.1038/ng.610. Epub 2010 Jun 20.

2.

Hints of hidden heritability in GWAS.

Gibson G.

Nat Genet. 2010 Jul;42(7):558-60. doi: 10.1038/ng0710-558.

PMID:
20581876
3.

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
4.

Estimating the total number of susceptibility variants underlying complex diseases from genome-wide association studies.

So HC, Yip BH, Sham PC.

PLoS One. 2010 Nov 17;5(11):e13898. doi: 10.1371/journal.pone.0013898.

5.

Common SNPs explain a large proportion of the heritability for human height.

Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, Madden PA, Heath AC, Martin NG, Montgomery GW, Goddard ME, Visscher PM.

Nat Genet. 2010 Jul;42(7):565-9. doi: 10.1038/ng.608. Epub 2010 Jun 20.

6.

An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies.

Thompson WK, Wang Y, Schork AJ, Witoelar A, Zuber V, Xu S, Werge T, Holland D; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Andreassen OA, Dale AM.

PLoS Genet. 2015 Dec 29;11(12):e1005717. doi: 10.1371/journal.pgen.1005717. eCollection 2015 Dec.

7.

Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults.

Chen F, He J, Zhang J, Chen GK, Thomas V, Ambrosone CB, Bandera EV, Berndt SI, Bernstein L, Blot WJ, Cai Q, Carpten J, Casey G, Chanock SJ, Cheng I, Chu L, Deming SL, Driver WR, Goodman P, Hayes RB, Hennis AJ, Hsing AW, Hu JJ, Ingles SA, John EM, Kittles RA, Kolb S, Leske MC, Millikan RC, Monroe KR, Murphy A, Nemesure B, Neslund-Dudas C, Nyante S, Ostrander EA, Press MF, Rodriguez-Gil JL, Rybicki BA, Schumacher F, Stanford JL, Signorello LB, Strom SS, Stevens V, Van Den Berg D, Wang Z, Witte JS, Wu SY, Yamamura Y, Zheng W, Ziegler RG, Stram AH, Kolonel LN, Le Marchand L, Henderson BE, Haiman CA, Stram DO.

PLoS One. 2015 Jun 30;10(6):e0131106. doi: 10.1371/journal.pone.0131106. eCollection 2015.

8.

Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.

Whiffin N, Dobbins SE, Hosking FJ, Palles C, Tenesa A, Wang Y, Farrington SM, Jones AM, Broderick P, Campbell H, Newcomb PA, Casey G, Conti DV, Schumacher F, Gallinger S, Lindor NM, Hopper J, Jenkins M, Dunlop MG, Tomlinson IP, Houlston RS.

Hum Mol Genet. 2013 Dec 15;22(24):5075-82. doi: 10.1093/hmg/ddt357. Epub 2013 Jul 30.

9.

Genome-wide association studies in cancer.

Easton DF, Eeles RA.

Hum Mol Genet. 2008 Oct 15;17(R2):R109-15. doi: 10.1093/hmg/ddn287.

PMID:
18852198
10.

A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.

Yamazaki K, Umeno J, Takahashi A, Hirano A, Johnson TA, Kumasaka N, Morizono T, Hosono N, Kawaguchi T, Takazoe M, Yamada T, Suzuki Y, Tanaka H, Motoya S, Hosokawa M, Arimura Y, Shinomura Y, Matsui T, Matsumoto T, Iida M, Tsunoda T, Nakamura Y, Kamatani N, Kubo M.

Gastroenterology. 2013 Apr;144(4):781-8. doi: 10.1053/j.gastro.2012.12.021. Epub 2012 Dec 22.

PMID:
23266558
11.

Genome-wide association studies in common cancers--what have we learnt?

Varghese JS, Easton DF.

Curr Opin Genet Dev. 2010 Jun;20(3):201-9. doi: 10.1016/j.gde.2010.03.012. Epub 2010 Apr 24. Review.

PMID:
20418093
12.

Germline DNA variations in breast cancer predisposition and prognosis: a systematic review of the literature.

Sapkota Y.

Cytogenet Genome Res. 2014;144(2):77-91. doi: 10.1159/000369045. Epub 2014 Nov 15. Review.

PMID:
25401968
13.

Estimation of heritability for nine common cancers using data from genome-wide association studies in Chinese population.

Dai J, Shen W, Wen W, Chang J, Wang T, Chen H, Jin G, Ma H, Wu C, Li L, Song F, Zeng Y, Jiang Y, Chen J, Wang C, Zhu M, Zhou W, Du J, Xiang Y, Shu XO, Hu Z, Zhou W, Chen K, Xu J, Jia W, Lin D, Zheng W, Shen H.

Int J Cancer. 2017 Jan 15;140(2):329-336. doi: 10.1002/ijc.30447. Epub 2016 Oct 11.

PMID:
27668986
14.

FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.

Huang J, Wang K, Wei P, Liu X, Liu X, Tan K, Boerwinkle E, Potash JB, Han S.

Genetics. 2016 Mar;202(3):919-29. doi: 10.1534/genetics.115.185009. Epub 2016 Jan 15.

15.

A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.

Ioannidis JP, Castaldi P, Evangelou E.

J Natl Cancer Inst. 2010 Jun 16;102(12):846-58. doi: 10.1093/jnci/djq173. Epub 2010 May 26. Review.

16.

Quantifying the underestimation of relative risks from genome-wide association studies.

Spencer C, Hechter E, Vukcevic D, Donnelly P.

PLoS Genet. 2011 Mar;7(3):e1001337. doi: 10.1371/journal.pgen.1001337. Epub 2011 Mar 17.

17.

Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study.

So HC, Li M, Sham PC.

Genet Epidemiol. 2011 Sep;35(6):447-56. doi: 10.1002/gepi.20593. Epub 2011 May 26.

PMID:
21618601
18.

On beyond GWAS.

[No authors listed]

Nat Genet. 2010 Jul;42(7):551. doi: 10.1038/ng0710-551.

PMID:
20581872
19.

Low penetrance breast cancer predisposition SNPs are site specific.

Mcinerney N, Colleran G, Rowan A, Walther A, Barclay E, Spain S, Jones AM, Tuohy S, Curran C, Miller N, Kerin M, Tomlinson I, Sawyer E.

Breast Cancer Res Treat. 2009 Sep;117(1):151-9. doi: 10.1007/s10549-008-0235-7. Epub 2008 Nov 13.

PMID:
19005751
20.

Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population.

Gaj P, Maryan N, Hennig EE, Ledwon JK, Paziewska A, Majewska A, Karczmarski J, Nesteruk M, Wolski J, Antoniewicz AA, Przytulski K, Rutkowski A, Teumer A, Homuth G, StarzyƄska T, Regula J, Ostrowski J.

PLoS One. 2012;7(4):e35307. doi: 10.1371/journal.pone.0035307. Epub 2012 Apr 19.

Supplemental Content

Support Center