-
1
-
-
84868502906
-
Imputation of exome sequence variants into populationbased samples and blood-cell-trait-associated loci in African Americans: NHLBI GO exome sequencing project
-
Auer, P.L. et al. (2012) Imputation of exome sequence variants into populationbased samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project. Am. J. Hum. Genet., 91, 794-808.
-
(2012)
Am. J. Hum. Genet.
, vol.91
, pp. 794-808
-
-
Auer, P.L.1
-
2
-
-
84872410521
-
Detecting rare variant effects using extreme phenotype sampling in sequencing association studies
-
Barnett, I.J. et al. (2013) Detecting rare variant effects using extreme phenotype sampling in sequencing association studies. Genet. Epidemiol., 37, 142-151.
-
(2013)
Genet. Epidemiol.
, vol.37
, pp. 142-151
-
-
Barnett, I.J.1
-
3
-
-
0036840537
-
Multi-Ethnic Study of Atherosclerosis: Objectives and design
-
DOI 10.1093/aje/kwf113
-
Bild, D.E. et al. (2002) Multi-ethnic study of atherosclerosis: objectives and design. Am. J. Epidemiol., 156, 871-881. (Pubitemid 35215769)
-
(2002)
American Journal of Epidemiology
, vol.156
, Issue.9
, pp. 871-881
-
-
Bild, D.E.1
Bluemke, D.A.2
Burke, G.L.3
Detrano, R.4
Diez Roux, A.V.5
Folsom, A.R.6
Greenland, P.7
Jacobs Jr., D.R.8
Kronmal, R.9
Liu, K.10
Nelson, J.C.11
O'Leary, D.12
Saad, M.F.13
Shea, S.14
Szklo, M.15
Tracy, R.P.16
-
4
-
-
71149112981
-
Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies
-
Browning, B.L. and Yu, Z. (2009) Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am. J. Hum. Genet., 85, 847-861.
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 847-861
-
-
Browning, B.L.1
Yu, Z.2
-
5
-
-
84860014014
-
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: The PAGE study
-
Buyske, S. et al. (2012) Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. PLoS One, 7, e35651.
-
(2012)
PLoS One
, vol.7
-
-
Buyske, S.1
-
6
-
-
84655162045
-
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
-
Cho, Y.S. et al. (2012) Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat. Genet., 44, 67-72.
-
(2012)
Nat. Genet.
, vol.44
, pp. 67-72
-
-
Cho, Y.S.1
-
7
-
-
84859238629
-
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: A multi-ethnic meta-analysis of 45, 891 individuals
-
Dastani, Z. et al. (2012) Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45, 891 individuals. PLoS Genet., 8, e1002607.
-
(2012)
PLoS Genet.
, vol.8
-
-
Dastani, Z.1
-
8
-
-
58149345887
-
Practical aspects of imputation-driven meta-analysis of genome-wide association studies
-
De Bakker, P.I.W. et al. (2008) Practical aspects of imputation-driven meta-analysis of genome-wide association studies. Hum. Mol. Genet., 17, R122-R128.
-
(2008)
Hum. Mol. Genet.
, vol.17
-
-
De Bakker, P.I.W.1
-
9
-
-
77956197018
-
Utilizing genotype imputation for the augmentation of sequence data
-
Fridley, B.L. et al. (2010) Utilizing genotype imputation for the augmentation of sequence data. PLoS One, 5, e11018.
-
(2010)
PLoS One
, vol.5
-
-
Fridley, B.L.1
-
10
-
-
0024270614
-
CARDIA: Study design, recruitment, and some characteristics of the examined subjects
-
DOI 10.1016/0895-4356(88)90080-7
-
Friedman, G.D. et al. (1988) Cardia: study design, recruitment, and some characteristics of the examined subjects. J. Clin. Epidemiol., 41, 1105-1116. (Pubitemid 19039041)
-
(1988)
Journal of Clinical Epidemiology
, vol.41
, Issue.11
, pp. 1105-1116
-
-
Friedman, G.D.1
Cutter, G.R.2
Donahue, R.P.3
Hughes, G.H.4
Hulley, S.B.5
Jacobs Jr., D.R.6
Liu, K.7
Savage, P.J.8
-
11
-
-
84872143942
-
Analysis of 6, 515 exomes reveals the recent origin of most human protein-coding variants
-
Fu, W. et al. (2012) Analysis of 6, 515 exomes reveals the recent origin of most human protein-coding variants. Nature, 493, 216-220.
-
(2012)
Nature
, vol.493
, pp. 216-220
-
-
Fu, W.1
-
12
-
-
84886071792
-
The value of population-specific reference panels for genotype imputation in the age of whole-genome sequencing
-
In: San Francisco, CA
-
Fuchsberger, C. et al. (2012) The value of population-specific reference panels for genotype imputation in the age of whole-genome sequencing. In: Presented at the 62nd Annual Meeting of The American Society of Human Genetics. San Francisco, CA.
-
(2012)
Presented at the 62nd Annual Meeting of the American Society of Human Genetics
-
-
Fuchsberger, C.1
-
13
-
-
84870257531
-
Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia
-
Futema, M. et al. (2012) Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia. J. Med. Genet., 49, 644-649.
-
(2012)
J. Med. Genet.
, vol.49
, pp. 644-649
-
-
Futema, M.1
-
14
-
-
79959557454
-
Power in the phenotypic extremes: A simulation study of power in discovery and replication of rare variants
-
Guey, L.T. et al. (2011) Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. Genet. Epidemiol., 35, 236-246.
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 236-246
-
-
Guey, L.T.1
-
15
-
-
79953212557
-
A rare variant in MYH6 is associated with high risk of sick sinus syndrome
-
Holm, H. et al. (2011) A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nat. Genet., 43, 316-320.
-
(2011)
Nat. Genet.
, vol.43
, pp. 316-320
-
-
Holm, H.1
-
16
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie, B. et al. (2012) Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat. Genet., 44, 955-959.
-
(2012)
Nat. Genet.
, vol.44
, pp. 955-959
-
-
Howie, B.1
-
17
-
-
84863724842
-
1000 Genomes-based imputation identifies novel and refined associations for the wellcome trust case control consortium phase 1 Data
-
Huang, J. et al. (2012) 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Eur. J. Hum. Genet., 20, 801-805.
-
(2012)
Eur. J. Hum. Genet.
, vol.20
, pp. 801-805
-
-
Huang, J.1
-
18
-
-
84875181490
-
AbCD: Arbitrary coverage design for sequencing-based genetic studies
-
Kang, J. et al. (2013) AbCD: arbitrary coverage design for sequencing-based genetic studies. Bioinformatics, 29, 799-801.
-
(2013)
Bioinformatics
, vol.29
, pp. 799-801
-
-
Kang, J.1
-
19
-
-
62649084535
-
Power of deep, all-exon resequencing for discovery of human trait genes
-
Kryukov, G.V. et al. (2009) Power of deep, all-exon resequencing for discovery of human trait genes. Proc. Natl Acad. Sci. USA, 106, 3871-3876.
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 3871-3876
-
-
Kryukov, G.V.1
-
20
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li, H. and Durbin, R. (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25, 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
22
-
-
78649508578
-
MaCH: Using sequence and genotype data to estimate haplotypes and unobserved genotypes
-
Li, Y. et al. (2010) MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet. Epidemiol., 34, 816-834.
-
(2010)
Genet. Epidemiol.
, vol.34
, pp. 816-834
-
-
Li, Y.1
-
23
-
-
79957951017
-
Low-coverage sequencing: Implications for design of complex trait association studies
-
Li, Y. et al. (2011) Low-coverage sequencing: implications for design of complex trait association studies. Genome Res., 21, 940-951.
-
(2011)
Genome Res.
, vol.21
, pp. 940-951
-
-
Li, Y.1
-
24
-
-
84859120701
-
Genotype imputation of metabochip SNPs using a studyspecific reference panel of -4, 000 haplotypes in African Americans from the Women's Health Initiative
-
Liu, E.Y. et al. (2012) Genotype imputation of metabochip SNPs using a studyspecific reference panel of -4, 000 haplotypes in African Americans from the Women's Health Initiative. Genet. Epidemiol., 36, 107-117.
-
(2012)
Genet. Epidemiol.
, vol.36
, pp. 107-117
-
-
Liu, E.Y.1
-
25
-
-
84871083616
-
MaCH-Admix: Genotype imputation for admixed populations
-
Liu, E.Y. et al. (2013) MaCH-Admix: genotype imputation for admixed populations. Genet. Epidemiol., 37, 25-37.
-
(2013)
Genet. Epidemiol.
, vol.37
, pp. 25-37
-
-
Liu, E.Y.1
-
26
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini, J. and 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
-
27
-
-
0031951803
-
Work organization and atherosclerosis: Findings from the ARIC study
-
DOI 10.1016/S0749-3797(97)00018-4, PII S0749379797000184
-
Muntaner, C. et al. (1998) Work organization and atherosclerosis: findings from the ARIC study. Am. J. Prev. Med., 14, 9-18. (Pubitemid 28099232)
-
(1998)
American Journal of Preventive Medicine
, vol.14
, Issue.1
, pp. 9-18
-
-
Muntaner, C.1
Javier Nieto, F.2
Cooper, L.3
Meyer, J.4
Szklo, M.5
Tyroler, H.A.6
-
28
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
DOI 10.1038/ng1847, PII NG1847
-
Price, A.L. et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet., 38, 904-909. (Pubitemid 44141658)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
29
-
-
0034977045
-
Linkage disequilibrium in humans: Models and data
-
DOI 10.1086/321275
-
Pritchard, J.K. and Przeworski, M. (2001) Linkage disequilibrium in humans: models and data. Am. J. Hum. Genet., 69, 1-14. (Pubitemid 32614013)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.1
, pp. 1-14
-
-
Pritchard, J.K.1
Przeworski, M.2
-
30
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
DOI 10.1086/519795
-
Purcell, S. et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet., 81, 559-75. (Pubitemid 47330214)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.W.9
Daly, M.J.10
Sham, P.C.11
-
31
-
-
79959812503
-
Genome-wide association study of white blood cell count in 16, 388 African Americans: The continental origins and genetic epidemiology network (COGENT)
-
Reiner, A.P. et al. (2011) Genome-wide association study of white blood cell count in 16, 388 African Americans: the continental origins and genetic epidemiology network (COGENT). PLoS Genet., 7, e1002108.
-
(2011)
PLoS Genet.
, vol.7
-
-
Reiner, A.P.1
-
32
-
-
84886024054
-
Using low-pass whole genome sequencing to create a reference population for genome imputation in an isolated population: Examples from the SardiNIA study
-
In: San Francisco, CA
-
Sanna, S. (2012) Using low-pass whole genome sequencing to create a reference population for genome imputation in an isolated population: examples from the SardiNIA study. In: Presented at the 62nd Annual Meeting of The American Society of Human Genetics. San Francisco, CA.
-
(2012)
Presented at the 62nd Annual Meeting of the American Society of Human Genetics
-
-
Sanna, S.1
-
33
-
-
29244477198
-
Toward resolution of cardiovascular health disparities in African Americans: Design and methods of the Jackson heart study
-
Taylor, H.A. et al. (2005) Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study. Ethn. Dis., 15, S6-4-17.
-
(2005)
Ethn. Dis.
, vol.15
-
-
Taylor, H.A.1
-
34
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
Tennessen, J.A. et al. (2012) Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science, 337, 64-69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
-
35
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich, T.M. 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
-
36
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
The 1000 Genomes Project Consortium
-
The 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
-
-
-
37
-
-
84975795680
-
An integrated map of genetic variation from 1, 092 human genomes
-
The 1000 Genomes Project Consortium
-
The 1000 Genomes Project Consortium. (2012) An integrated map of genetic variation from 1, 092 human genomes. Nature, 491, 56-65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
38
-
-
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. Control. Clin. Trials, 19, 61-109.
-
(1998)
Control. Clin. Trials
, vol.19
, pp. 61-109
-
-
-
39
-
-
84865693681
-
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits
-
Voight, B.F. et al. (2012) The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. PLoS Genet., 8, e1002793.
-
(2012)
PLoS Genet.
, vol.8
-
-
Voight, B.F.1
|