-
1
-
-
58049217860
-
A Catalog of Published Genome-Wide Association Studies
-
Available:. Accessed 2011 July 1
-
Hindorff LA, MacArthur J, Wise A, Junkins HA, Hall PN, et al. (2011) A Catalog of Published Genome-Wide Association Studies. Available: http://www.genome.gov/gwastudies. Accessed 2011 July 1.
-
(2011)
-
-
Hindorff, L.A.1
MacArthur, J.2
Wise, A.3
Junkins, H.A.4
Hall, P.N.5
-
2
-
-
77951133654
-
Genome-wide association studies in diverse populations
-
Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, et al. (2010) Genome-wide association studies in diverse populations. Nat Rev Genet 11: 356-366.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 356-366
-
-
Rosenberg, N.A.1
Huang, L.2
Jewett, E.M.3
Szpiech, Z.A.4
Jankovic, I.5
-
3
-
-
75649149885
-
Methodological challenges of genome-wide association analysis in Africa
-
Teo YY, Small KS, Kwiatkowski DP, (2010) Methodological challenges of genome-wide association analysis in Africa. Nat Rev Genet 11: 149-160.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 149-160
-
-
Teo, Y.Y.1
Small, K.S.2
Kwiatkowski, D.P.3
-
4
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium
-
1000 Genomes Project Consortium (2010) A map of human genome variation from population-scale sequencing. Nature 467: 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
5
-
-
79960943621
-
Fine mapping of five Loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
-
Sanna S, Li B, Mulas A, Sidore C, Kang HM, et al. (2011) Fine mapping of five Loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability. PLoS Genet 7: e1002198.
-
(2011)
PLoS Genet
, vol.7
-
-
Sanna, S.1
Li, B.2
Mulas, A.3
Sidore, C.4
Kang, H.M.5
-
6
-
-
79960279940
-
Promise and pitfalls of the Immunochip
-
Cortes A, Brown MA, (2011) Promise and pitfalls of the Immunochip. Arthritis Res Ther 13: 101.
-
(2011)
Arthritis Res Ther
, vol.13
, pp. 101
-
-
Cortes, A.1
Brown, M.A.2
-
7
-
-
82255192188
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
-
Trynka G, Hunt KA, Bockett NA, Romanos J, Mistry V, et al. (2011) Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat Genet 43: 1193-1201.
-
(2011)
Nat Genet
, vol.43
, pp. 1193-1201
-
-
Trynka, G.1
Hunt, K.A.2
Bockett, N.A.3
Romanos, J.4
Mistry, V.5
-
8
-
-
80053206058
-
The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study
-
Matise TC, Ambite JL, Buyske S, Carlson CS, Cole SA, et al. (2011) The Next PAGE in Understanding Complex Traits: Design for the Analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study. Am J Epidemiol.
-
(2011)
Am J Epidemiol
-
-
Matise, T.C.1
Ambite, J.L.2
Buyske, S.3
Carlson, C.S.4
Cole, S.A.5
-
9
-
-
0024591825
-
The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives
-
The ARIC Investigators
-
The ARIC Investigators (1989) The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. American Journal of Epidemiology 129: 687-702.
-
(1989)
American Journal of Epidemiology
, vol.129
, pp. 687-702
-
-
-
10
-
-
18844474648
-
A multiethnic cohort in Hawaii and Los Angeles: baseline characteristics
-
Kolonel LN, Henderson BE, Hankin JH, Nomura AM, Wilkens LR, et al. (2000) A multiethnic cohort in Hawaii and Los Angeles: baseline characteristics. American Journal of Epidemiology 151: 346-357.
-
(2000)
American Journal of Epidemiology
, vol.151
, pp. 346-357
-
-
Kolonel, L.N.1
Henderson, B.E.2
Hankin, J.H.3
Nomura, A.M.4
Wilkens, L.R.5
-
11
-
-
6844255857
-
Design of the Women's Health Initiative clinical trial and observational study
-
The Women's Health Initiative Study Group
-
The Women's Health Initiative Study Group (1998) Design of the Women's Health Initiative clinical trial and observational study. Controlled Clinical Trials 19: 61-109.
-
(1998)
Controlled Clinical Trials
, vol.19
, pp. 61-109
-
-
-
12
-
-
52949089727
-
GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population
-
Giannoulatou E, Yau C, Colella S, Ragoussis J, Holmes CC, (2008) GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population. Bioinformatics 24: 2209-2214.
-
(2008)
Bioinformatics
, vol.24
, pp. 2209-2214
-
-
Giannoulatou, E.1
Yau, C.2
Colella, S.3
Ragoussis, J.4
Holmes, C.C.5
-
13
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, et al. (2010) Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466: 707-713.
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
Edmondson, A.C.4
Stylianou, I.M.5
-
14
-
-
0041876133
-
Measuring inconsistency in meta-analyses
-
Higgins JP, Thompson SG, Deeks JJ, Altman DG, (2003) Measuring inconsistency in meta-analyses. BMJ 327: 557-560.
-
(2003)
BMJ
, vol.327
, pp. 557-560
-
-
Higgins, J.P.1
Thompson, S.G.2
Deeks, J.J.3
Altman, D.G.4
-
15
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, et al. (2009) Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 41: 56-65.
-
(2009)
Nat Genet
, vol.41
, pp. 56-65
-
-
Kathiresan, S.1
Willer, C.J.2
Peloso, G.M.3
Demissie, S.4
Musunuru, K.5
-
16
-
-
79952262430
-
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project
-
Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, et al. (2011) Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. PLoS Genet 7: e1001300.
-
(2011)
PLoS Genet
, vol.7
-
-
Lettre, G.1
Palmer, C.D.2
Young, T.3
Ejebe, K.G.4
Allayee, H.5
-
17
-
-
4544381909
-
Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol
-
Thompson JF, Lloyd DB, Lira ME, Milos PM, (2004) Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol. Clin Genet 66: 223-228.
-
(2004)
Clin Genet
, vol.66
, pp. 223-228
-
-
Thompson, J.F.1
Lloyd, D.B.2
Lira, M.E.3
Milos, P.M.4
-
18
-
-
80053149973
-
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
-
Wood AR, Hernandez DG, Nalls MA, Yaghootkar H, Gibbs JR, et al. (2011) Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. Hum Mol Genet 20: 4082-4092.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 4082-4092
-
-
Wood, A.R.1
Hernandez, D.G.2
Nalls, M.A.3
Yaghootkar, H.4
Gibbs, J.R.5
-
19
-
-
79959851441
-
Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
-
Tomlinson IP, Carvajal-Carmona LG, Dobbins SE, Tenesa A, Jones AM, et al. (2011) Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer. PLoS Genet 7: e1002105.
-
(2011)
PLoS Genet
, vol.7
-
-
Tomlinson, I.P.1
Carvajal-Carmona, L.G.2
Dobbins, S.E.3
Tenesa, A.4
Jones, A.M.5
-
20
-
-
77955499945
-
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
-
Musunuru K, Strong A, Frank-Kamenetsky M, Lee NE, Ahfeldt T, et al. (2010) From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature 466: 714-719.
-
(2010)
Nature
, vol.466
, pp. 714-719
-
-
Musunuru, K.1
Strong, A.2
Frank-Kamenetsky, M.3
Lee, N.E.4
Ahfeldt, T.5
-
21
-
-
33748645500
-
GENCODE: producing a reference annotation for ENCODE
-
Harrow J, Denoeud F, Frankish A, Reymond A, Chen CK, et al. (2006) GENCODE: producing a reference annotation for ENCODE. Genome Biol 7 (Suppl 1): S4 1-9.
-
(2006)
Genome Biol
, vol.7
, Issue.SUPPL. 1
, pp. 1-9
-
-
Harrow, J.1
Denoeud, F.2
Frankish, A.3
Reymond, A.4
Chen, C.K.5
-
22
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, et al. (2010) A method and server for predicting damaging missense mutations. Nat Methods 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
23
-
-
57249114505
-
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
-
Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, et al. (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24: 2938-2939.
-
(2008)
Bioinformatics
, vol.24
, pp. 2938-2939
-
-
Johnson, A.D.1
Handsaker, R.E.2
Pulit, S.L.3
Nizzari, M.M.4
O'Donnell, C.J.5
-
24
-
-
84855174922
-
Performance of Genotype Imputations Using Data from the 1000 Genomes Project
-
Sung YJ, Wang L, Rankinen T, Bouchard C, Rao DC, (2011) Performance of Genotype Imputations Using Data from the 1000 Genomes Project. Hum Hered 73: 18-25.
-
(2011)
Hum Hered
, vol.73
, pp. 18-25
-
-
Sung, Y.J.1
Wang, L.2
Rankinen, T.3
Bouchard, C.4
Rao, D.C.5
-
25
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini J, Howie B, (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11: 499-511.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
26
-
-
84859120701
-
Genotype Imputation of MetabochipSNPs Using a Study-Specific Reference Panel of ~4,000 Haplotypes in African Americans From the Women's Health Initiative
-
Liu EY, Buyske S, Aragaki AK, Peters U, Boerwinkle E, et al. (2012) Genotype Imputation of MetabochipSNPs Using a Study-Specific Reference Panel of ~4,000 Haplotypes in African Americans From the Women's Health Initiative. Genetic Epidemiology 36: 107-117.
-
(2012)
Genetic Epidemiology
, vol.36
, pp. 107-117
-
-
Liu, E.Y.1
Buyske, S.2
Aragaki, A.K.3
Peters, U.4
Boerwinkle, E.5
-
27
-
-
79952330384
-
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips
-
Ritchie ME, Liu R, Carvalho BS, Irizarry RA, (2011) Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips. BMC Bioinformatics 12: 68.
-
(2011)
BMC Bioinformatics
, vol.12
, pp. 68
-
-
Ritchie, M.E.1
Liu, R.2
Carvalho, B.S.3
Irizarry, R.A.4
-
28
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. American Journal of Human Genetics 81: 559-575.
-
(2007)
American Journal of Human Genetics
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
-
29
-
-
77952574876
-
Quality control for genome-wide association studies
-
Weale ME, (2010) Quality control for genome-wide association studies. Methods Mol Biol 628: 341-372.
-
(2010)
Methods Mol Biol
, vol.628
, pp. 341-372
-
-
Weale, M.E.1
-
31
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nature Genetics 38: 904-909.
-
(2006)
Nature Genetics
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
-
32
-
-
0027343586
-
The Malmo Diet and Cancer Study. Design and feasibility
-
Berglund G, Elmstahl S, Janzon L, Larsson SA, (1993) The Malmo Diet and Cancer Study. Design and feasibility. Journal of internal medicine 233: 45-51.
-
(1993)
Journal of Internal Medicine
, vol.233
, pp. 45-51
-
-
Berglund, G.1
Elmstahl, S.2
Janzon, L.3
Larsson, S.A.4
-
33
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Altshuler DM, Gibbs RA, Peltonen L, Dermitzakis E, Schaffner SF, et al. (2010) Integrating common and rare genetic variation in diverse human populations. Nature 467: 52-58.
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
Altshuler, D.M.1
Gibbs, R.A.2
Peltonen, L.3
Dermitzakis, E.4
Schaffner, S.F.5
-
34
-
-
0015348189
-
Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge
-
Friedewald WT, Levy RI, Fredrickson DS, (1972) Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem 18: 499-502.
-
(1972)
Clin Chem
, vol.18
, pp. 499-502
-
-
Friedewald, W.T.1
Levy, R.I.2
Fredrickson, D.S.3
-
35
-
-
79959835081
-
Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study
-
Dumitrescu L, Carty CL, Taylor K, Schumacher FR, Hindorff LA, et al. (2011) Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study. PLoS Genet 7: e1002138.
-
(2011)
PLoS Genet
, vol.7
-
-
Dumitrescu, L.1
Carty, C.L.2
Taylor, K.3
Schumacher, F.R.4
Hindorff, L.A.5
-
36
-
-
77955894071
-
METAL: fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR, (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26: 2190-2191.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
37
-
-
77956586071
-
LocusZoom: regional visualization of genome-wide association scan results
-
Pruim RJ, Welch RP, Sanna S, Teslovich TM, Chines PS, et al. (2010) LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26: 2336-2337.
-
(2010)
Bioinformatics
, vol.26
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
-
38
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
The International HapMap Consortium
-
The International HapMap Consortium (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
|