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Results: 1 to 20 of 94

1.

Genome partitioning of genetic variation for complex traits using common SNPs.

Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, Feingold E, Hayes MG, Hill WG, Landi MT, Alonso A, Lettre G, Lin P, Ling H, Lowe W, Mathias RA, Melbye M, Pugh E, Cornelis MC, Weir BS, Goddard ME, Visscher PM.

Nat Genet. 2011 Jun;43(6):519-25. doi: 10.1038/ng.823. Epub 2011 May 8.

PMID:
21552263
[PubMed - indexed for MEDLINE]
2.

Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans.

Yang J, Lee T, Kim J, Cho MC, Han BG, Lee JY, Lee HJ, Cho S, Kim H.

PLoS Genet. 2013;9(3):e1003355. doi: 10.1371/journal.pgen.1003355. Epub 2013 Mar 7.

PMID:
23505390
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A commentary on 'common SNPs explain a large proportion of the heritability for human height' by Yang et al. (2010).

Visscher PM, Yang J, Goddard ME.

Twin Res Hum Genet. 2010 Dec;13(6):517-24. doi: 10.1375/twin.13.6.517.

PMID:
21142928
[PubMed - indexed for MEDLINE]
4.

Genome partitioning of genetic variation for height from 11,214 sibling pairs.

Visscher PM, Macgregor S, Benyamin B, Zhu G, Gordon S, Medland S, Hill WG, Hottenga JJ, Willemsen G, Boomsma DI, Liu YZ, Deng HW, Montgomery GW, Martin NG.

Am J Hum Genet. 2007 Nov;81(5):1104-10. Epub 2007 Oct 1.

PMID:
17924350
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability.

Kutalik Z, Whittaker J, Waterworth D; GIANT consortium, Beckmann JS, Bergmann S.

Genet Epidemiol. 2011 Jul;35(5):341-9. doi: 10.1002/gepi.20582. Epub 2011 Apr 4.

PMID:
21465548
[PubMed - indexed for MEDLINE]
6.

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.

PMID:
20562875
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Recent progress in the study of the genetics of height.

Lettre G.

Hum Genet. 2011 May;129(5):465-72. doi: 10.1007/s00439-011-0969-x. Epub 2011 Feb 22. Review.

PMID:
21340692
[PubMed - indexed for MEDLINE]
8.

Estimation and partition of heritability in human populations using whole-genome analysis methods.

Vinkhuyzen AA, Wray NR, Yang J, Goddard ME, Visscher PM.

Annu Rev Genet. 2013;47:75-95. doi: 10.1146/annurev-genet-111212-133258. Epub 2013 Aug 22. Review.

PMID:
23988118
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings.

Visscher PM, Medland SE, Ferreira MA, Morley KI, Zhu G, Cornes BK, Montgomery GW, Martin NG.

PLoS Genet. 2006 Mar;2(3):e41. Epub 2006 Mar 24.

PMID:
16565746
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

GCTA: a tool for genome-wide complex trait analysis.

Yang J, Lee SH, Goddard ME, Visscher PM.

Am J Hum Genet. 2011 Jan 7;88(1):76-82. doi: 10.1016/j.ajhg.2010.11.011. Epub 2010 Dec 17.

PMID:
21167468
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.

Lee SH, Harold D, Nyholt DR; ANZGene Consortium; International Endogene Consortium; Genetic and Environmental Risk for Alzheimer's disease Consortium, Goddard ME, Zondervan KT, Williams J, Montgomery GW, Wray NR, Visscher PM.

Hum Mol Genet. 2013 Feb 15;22(4):832-41. doi: 10.1093/hmg/dds491. Epub 2012 Nov 28.

PMID:
23193196
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Finding the missing heritability in pediatric obesity: the contribution of genome-wide complex trait analysis.

Llewellyn CH, Trzaskowski M, Plomin R, Wardle J.

Int J Obes (Lond). 2013 Nov;37(11):1506-9. doi: 10.1038/ijo.2013.30. Epub 2013 Mar 26.

PMID:
23528754
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

FTO genotype is associated with phenotypic variability of body mass index.

Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, Steinthorsdottir V, Mägi R, Waite L, Smith AV, Yerges-Armstrong LM, Monda KL, Hadley D, Mahajan A, Li G, Kapur K, Vitart V, Huffman JE, Wang SR, Palmer C, Esko T, Fischer K, Zhao JH, Demirkan A, Isaacs A, Feitosa MF, Luan J, Heard-Costa NL, White C, Jackson AU, Preuss M, Ziegler A, Eriksson J, Kutalik Z, Frau F, Nolte IM, Van Vliet-Ostaptchouk JV, Hottenga JJ, Jacobs KB, Verweij N, Goel A, Medina-Gomez C, Estrada K, Bragg-Gresham JL, Sanna S, Sidore C, Tyrer J, Teumer A, Prokopenko I, Mangino M, Lindgren CM, Assimes TL, Shuldiner AR, Hui J, Beilby JP, McArdle WL, Hall P, Haritunians T, Zgaga L, Kolcic I, Polasek O, Zemunik T, Oostra BA, Junttila MJ, Grönberg H, Schreiber S, Peters A, Hicks AA, Stephens J, Foad NS, Laitinen J, Pouta A, Kaakinen M, Willemsen G, Vink JM, Wild SH, Navis G, Asselbergs FW, Homuth G, John U, Iribarren C, Harris T, Launer L, Gudnason V, O'Connell JR, Boerwinkle E, Cadby G, Palmer LJ, James AL, Musk AW, Ingelsson E, Psaty BM, Beckmann JS, Waeber G, Vollenweider P, Hayward C, Wright AF, Rudan I, Groop LC, Metspalu A, Khaw KT, van Duijn CM, Borecki IB, Province MA, Wareham NJ, Tardif JC, Huikuri HV, Cupples LA, Atwood LD, Fox CS, Boehnke M, Collins FS, Mohlke KL, Erdmann J, Schunkert H, Hengstenberg C, Stark K, Lorentzon M, Ohlsson C, Cusi D, Staessen JA, Van der Klauw MM, Pramstaller PP, Kathiresan S, Jolley JD, Ripatti S, Jarvelin MR, de Geus EJ, Boomsma DI, Penninx B, Wilson JF, Campbell H, Chanock SJ, van der Harst P, Hamsten A, Watkins H, Hofman A, Witteman JC, Zillikens MC, Uitterlinden AG, Rivadeneira F, Zillikens MC, Kiemeney LA, Vermeulen SH, Abecasis GR, Schlessinger D, Schipf S, Stumvoll M, Tönjes A, Spector TD, North KE, Lettre G, McCarthy MI, Berndt SI, Heath AC, Madden PA, Nyholt DR, Montgomery GW, Martin NG, McKnight B, Strachan DP, Hill WG, Snieder H, Ridker PM, Thorsteinsdottir U, Stefansson K, Frayling TM, Hirschhorn JN, Goddard ME, Visscher PM.

Nature. 2012 Oct 11;490(7419):267-72. doi: 10.1038/nature11401. Epub 2012 Sep 16.

PMID:
22982992
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia.

Zhang G, Karns R, Sun G, Indugula SR, Cheng H, Havas-Augustin D, Novokmet N, Rudan D, Durakovic Z, Missoni S, Chakraborty R, Rudan P, Deka R.

PLoS One. 2011;6(12):e29475. doi: 10.1371/journal.pone.0029475. Epub 2011 Dec 27.

PMID:
22216288
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.

Post W, Shen H, Damcott C, Arking DE, Kao WH, Sack PA, Ryan KA, Chakravarti A, Mitchell BD, Shuldiner AR.

Hum Hered. 2007;64(4):214-9. Epub 2007 Jun 12.

PMID:
17565224
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.

Lee SH, DeCandia TR, Ripke S, Yang J; Schizophrenia Psychiatric Genome-Wide Association Study Consortium (PGC-SCZ); International Schizophrenia Consortium (ISC); Molecular Genetics of Schizophrenia Collaboration (MGS), Sullivan PF, Goddard ME, Keller MC, Visscher PM, Wray NR.

Nat Genet. 2012 Feb 19;44(3):247-50. doi: 10.1038/ng.1108.

PMID:
22344220
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Genome-wide association study of height and body mass index in Australian twin families.

Liu JZ, Medland SE, Wright MJ, Henders AK, Heath AC, Madden PA, Duncan A, Montgomery GW, Martin NG, McRae AF.

Twin Res Hum Genet. 2010 Apr;13(2):179-93. doi: 10.1375/twin.13.2.179.

PMID:
20397748
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic regulation of adult stature.

Lettre G.

Curr Opin Pediatr. 2009 Aug;21(4):515-22. doi: 10.1097/MOP.0b013e32832c6dce. Review.

PMID:
19455035
[PubMed - indexed for MEDLINE]
19.

Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs.

Hemani G, Yang J, Vinkhuyzen A, Powell JE, Willemsen G, Hottenga JJ, Abdellaoui A, Mangino M, Valdes AM, Medland SE, Madden PA, Heath AC, Henders AK, Nyholt DR, de Geus EJ, Magnusson PK, Ingelsson E, Montgomery GW, Spector TD, Boomsma DI, Pedersen NL, Martin NG, Visscher PM.

Am J Hum Genet. 2013 Nov 7;93(5):865-75. doi: 10.1016/j.ajhg.2013.10.005. Epub 2013 Oct 31.

PMID:
24183453
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Comprehensive survey of common genetic variation at the plasminogen activator inhibitor-1 locus and relations to circulating plasminogen activator inhibitor-1 levels.

Kathiresan S, Gabriel SB, Yang Q, Lochner AL, Larson MG, Levy D, Tofler GH, Hirschhorn JN, O'Donnell CJ.

Circulation. 2005 Sep 20;112(12):1728-35.

PMID:
16172282
[PubMed - indexed for MEDLINE]
Free Article

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