-
1
-
-
84859215798
-
What makes UK Biobank special?
-
Collins, R. What makes UK Biobank special? Lancet 379, 1173–1174 (2012)
-
(2012)
Lancet
, vol.379
, pp. 1173-1174
-
-
Collins, R.1
-
2
-
-
84957436835
-
Million Veteran Program: a mega-biobank to study genetic influences on health and disease
-
Gaziano, J. M. et al. Million Veteran Program: a mega-biobank to study genetic influences on health and disease. J. Clin. Epidemiol. 70, 214–223 (2016)
-
(2016)
J. Clin. Epidemiol.
, vol.70
, pp. 214-223
-
-
Gaziano, J.M.1
-
3
-
-
70450081001
-
Major lipids, apolipoproteins, and risk of vascular disease
-
The Emerging Risk Factors Collaboration. Major lipids, apolipoproteins, and risk of vascular disease. J. Am. Med. Assoc. 302, 1993–2000 (2009)
-
(2009)
J. Am. Med. Assoc.
, vol.302
, pp. 1993-2000
-
-
-
4
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
COI: 1:CAS:528:DC%2BC3cXhtVSmurfI
-
Teslovich, T. M. et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707–713 (2010)
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
-
5
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
Global Lipids Genetics Consortium. Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274–1283 (2013)
-
(2013)
Nat. Genet.
, vol.45
, pp. 1274-1283
-
-
-
6
-
-
73649103089
-
Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis
-
Chasman, D. I. et al. Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. PLoS Genet. 5, e1000730 (2009)
-
(2009)
PLoS Genet.
, vol.5
-
-
Chasman, D.I.1
-
7
-
-
84876276050
-
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
-
COI: 1:CAS:528:DC%2BC3sXlt1GksQ%3D%3D
-
Albrechtsen, A. et al. Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. Diabetologia 56, 298–310 (2013)
-
(2013)
Diabetologia
, vol.56
, pp. 298-310
-
-
Albrechtsen, A.1
-
8
-
-
84893756641
-
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
-
COI: 1:CAS:528:DC%2BC2cXitVyksbs%3D
-
Peloso, G. M. et al. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. Am. J. Hum. Genet. 94, 223–232 (2014)
-
(2014)
Am. J. Hum. Genet.
, vol.94
, pp. 223-232
-
-
Peloso, G.M.1
-
9
-
-
84868470681
-
Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci
-
COI: 1:CAS:528:DC%2BC38XhsV2qu73F
-
Asselbergs, F. W. et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am. J. Hum. Genet. 91, 823–838 (2012)
-
(2012)
Am. J. Hum. Genet.
, vol.91
, pp. 823-838
-
-
Asselbergs, F.W.1
-
10
-
-
84955263526
-
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
-
COI: 1:CAS:528:DC%2BC28Xht1elsLY%3D
-
Below, J. E. et al. Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Sci. Rep. 6, 19429 (2016)
-
(2016)
Sci. Rep.
, vol.6
-
-
Below, J.E.1
-
11
-
-
85035766416
-
Exome-wide association study of plasma lipids in >300,000 individuals
-
COI: 1:CAS:528:DC%2BC2sXhslehtrjL
-
Liu, D. J. et al. Exome-wide association study of plasma lipids in >300,000 individuals. Nat. Genet. 49, 1758–1766 (2017)
-
(2017)
Nat. Genet.
, vol.49
, pp. 1758-1766
-
-
Liu, D.J.1
-
12
-
-
85035814059
-
Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease
-
COI: 1:CAS:528:DC%2BC2sXhslehtrjP
-
Lu, X. et al. Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease. Nat. Genet. 49, 1722–1730 (2017)
-
(2017)
Nat. Genet.
, vol.49
, pp. 1722-1730
-
-
Lu, X.1
-
13
-
-
85017341929
-
Evolocumab and clinical outcomes in patients with cardiovascular disease
-
COI: 1:CAS:528:DC%2BC2sXhtlOns7nM
-
Sabatine, M. S. et al. Evolocumab and clinical outcomes in patients with cardiovascular disease. N. Engl. J. Med. 376, 1713–1722 (2017)
-
(2017)
N. Engl. J. Med.
, vol.376
, pp. 1713-1722
-
-
Sabatine, M.S.1
-
14
-
-
84962230620
-
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
-
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators. Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease. N. Engl. J. Med. 374, 1134–1144 (2016)
-
(2016)
N. Engl. J. Med.
, vol.374
, pp. 1134-1144
-
-
-
15
-
-
84961948174
-
Inactivating variants in ANGPTL4 and risk of coronary artery disease
-
COI: 1:CAS:528:DC%2BC28Xht1Cqu7jK
-
Dewey, F. E. et al. Inactivating variants in ANGPTL4 and risk of coronary artery disease. N. Engl. J. Med. 374, 1123–1133 (2016)
-
(2016)
N. Engl. J. Med.
, vol.374
, pp. 1123-1133
-
-
Dewey, F.E.1
-
16
-
-
36348975228
-
Effects of torcetrapib in patients at high risk for coronary events
-
COI: 1:CAS:528:DC%2BD2sXhtlGns7bL
-
Barter, P. J. et al. Effects of torcetrapib in patients at high risk for coronary events. N. Engl. J. Med. 357, 2109–2122 (2007)
-
(2007)
N. Engl. J. Med.
, vol.357
, pp. 2109-2122
-
-
Barter, P.J.1
-
17
-
-
84890107642
-
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
-
COI: 1:CAS:528:DC%2BC3sXhvVaiu7jE
-
Denny, J. C. et al. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nat. Biotechnol. 31, 1102–1111 (2013)
-
(2013)
Nat. Biotechnol.
, vol.31
, pp. 1102-1111
-
-
Denny, J.C.1
-
18
-
-
84903727023
-
Loss-of-function mutations in APOC3, triglycerides, and coronary disease
-
The TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute. Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N. Engl. J. Med. 371, 22–31 (2014)
-
(2014)
N. Engl. J. Med.
, vol.371
, pp. 22-31
-
-
-
19
-
-
33645103550
-
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
-
COI: 1:CAS:528:DC%2BD28Xislequr8%3D
-
Cohen, J. C., Boerwinkle, E., Mosley, T. H. Jr. & Hobbs, H. H. Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N. Engl. J. Med. 354, 1264–1272 (2006)
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 1264-1272
-
-
Cohen, J.C.1
Boerwinkle, E.2
Mosley, T.H.3
Hobbs, H.H.4
-
20
-
-
85007138010
-
Genetic identification of familial hypercholesterolemia within a single U.S. health care system
-
Abul-Husn, N. S. et al. Genetic identification of familial hypercholesterolemia within a single U.S. health care system. Science 354, aaf7000 (2016)
-
(2016)
Science
, vol.354
, pp. aaf7000
-
-
Abul-Husn, N.S.1
-
21
-
-
84943171338
-
A global reference for human genetic variation
-
The 1000 Genomes Project Consortium. A global reference for human genetic variation. Nature 526, 68–74 (2015)
-
(2015)
Nature
, vol.526
, pp. 68-74
-
-
-
22
-
-
66249116333
-
The genetic structure and history of Africans and African Americans
-
COI: 1:CAS:528:DC%2BD1MXmtVKlsbs%3D
-
Tishkoff, S. A. et al. The genetic structure and history of Africans and African Americans. Science 324, 1035–1044 (2009)
-
(2009)
Science
, vol.324
, pp. 1035-1044
-
-
Tishkoff, S.A.1
-
23
-
-
84959547986
-
Integrative approaches for large-scale transcriptome-wide association studies
-
COI: 1:CAS:528:DC%2BC28Xit1ajtbc%3D
-
Gusev, A. et al. Integrative approaches for large-scale transcriptome-wide association studies. Nat. Genet. 48, 245–252 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 245-252
-
-
Gusev, A.1
-
24
-
-
84899642574
-
Heritability and genomics of gene expression in peripheral blood
-
COI: 1:CAS:528:DC%2BC2cXmtlWrtb8%3D
-
Wright, F. A. et al. Heritability and genomics of gene expression in peripheral blood. Nat. Genet. 46, 430–437 (2014)
-
(2014)
Nat. Genet.
, vol.46
, pp. 430-437
-
-
Wright, F.A.1
-
25
-
-
85031313737
-
Genetic effects on gene expression across human tissues
-
GTEx Consortium. Genetic effects on gene expression across human tissues. Nature 550, 204–213 (2017)
-
(2017)
Nature
, vol.550
, pp. 204-213
-
-
-
26
-
-
85013638666
-
Integrating gene expression with summary association statistics to identify genes associated with 30 complex traits
-
COI: 1:CAS:528:DC%2BC2sXjtlGrtbw%3D
-
Mancuso, N. et al. Integrating gene expression with summary association statistics to identify genes associated with 30 complex traits. Am. J. Hum. Genet. 100, 473–487 (2017)
-
(2017)
Am. J. Hum. Genet.
, vol.100
, pp. 473-487
-
-
Mancuso, N.1
-
27
-
-
84982253941
-
Analysis of protein-coding genetic variation in 60,706 humans
-
COI: 1:CAS:528:DC%2BC28XhtlOnsbbP
-
Lek, M. et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature 536, 285–291 (2016)
-
(2016)
Nature
, vol.536
, pp. 285-291
-
-
Lek, M.1
-
28
-
-
85012918562
-
Rare and low-frequency coding variants alter human adult height
-
COI: 1:CAS:528:DC%2BC2sXhvV2ht78%3D
-
Marouli, E. et al. Rare and low-frequency coding variants alter human adult height. Nature 542, 186–190 (2017)
-
(2017)
Nature
, vol.542
, pp. 186-190
-
-
Marouli, E.1
-
29
-
-
77955405475
-
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
-
COI: 1:CAS:528:DC%2BC3cXpvFSlsLc%3D
-
McLaren, W. et al. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 26, 2069–2070 (2010)
-
(2010)
Bioinformatics
, vol.26
, pp. 2069-2070
-
-
McLaren, W.1
-
30
-
-
85015922086
-
Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease
-
COI: 1:CAS:528:DC%2BC2sXhtlyktLbI
-
Khera, A. V. et al. Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease. J. Am. Med. Assoc. 317, 937–946 (2017)
-
(2017)
J. Am. Med. Assoc.
, vol.317
, pp. 937-946
-
-
Khera, A.V.1
-
31
-
-
85007028930
-
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
-
Dewey, F. E. et al. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study. Science 354, aaf6814 (2016)
-
(2016)
Science
, vol.354
, pp. aaf6814
-
-
Dewey, F.E.1
-
32
-
-
84945370533
-
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
-
COI: 1:CAS:528:DC%2BC2MXhsV2lt7zM
-
Sidore, C. et al. Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers. Nat. Genet. 47, 1272–1281 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 1272-1281
-
-
Sidore, C.1
-
33
-
-
84893904007
-
A polygenic burden of rare disruptive mutations in schizophrenia
-
COI: 1:CAS:528:DC%2BC2cXisVamurc%3D
-
Purcell, S. M. et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506, 185–190 (2014)
-
(2014)
Nature
, vol.506
, pp. 185-190
-
-
Purcell, S.M.1
-
35
-
-
85042368356
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
-
COI: 1:CAS:528:DC%2BC1cXnsVGrsbc%3D
-
Mahajan, A. et al. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat. Genet. 50, 559–571 (2018)
-
(2018)
Nat. Genet.
, vol.50
, pp. 559-571
-
-
Mahajan, A.1
-
36
-
-
84936755918
-
Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression
-
Bowden, J., Davey Smith, G. & Burgess, S. Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression. Int. J. Epidemiol. 44, 512–525 (2015)
-
(2015)
Int. J. Epidemiol.
, vol.44
, pp. 512-525
-
-
Bowden, J.1
Davey Smith, G.2
Burgess, S.3
-
37
-
-
85028691716
-
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease
-
COI: 1:CAS:528:DC%2BC2sXhtFOru7vK
-
Klarin, D. et al. Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. Nat. Genet. 49, 1392–1397 (2017)
-
(2017)
Nature Genetics
, vol.49
, Issue.9
, pp. 1392-1397
-
-
Klarin, D.1
Zhu, Q.M.2
Emdin, C.A.3
Chaffin, M.4
Horner, S.5
McMillan, B.J.6
Leed, A.7
Weale, M.E.8
Spencer, C.C.A.9
Aguet, F.10
Segrè, A.V.11
Ardlie, K.G.12
Khera, A.V.13
Kaushik, V.K.14
Natarajan, P.15
Kathiresan, S.16
-
38
-
-
85028693072
-
Association analyses based on false discovery rate implicate new loci for coronary artery disease
-
COI: 1:CAS:528:DC%2BC2sXhtFOru7vE
-
Nelson, C. P. et al. Association analyses based on false discovery rate implicate new loci for coronary artery disease. Nat. Genet. 49, 1385–1391 (2017)
-
(2017)
Nat. Genet.
, vol.49
, pp. 1385-1391
-
-
Nelson, C.P.1
-
39
-
-
79952000272
-
Perilipin deficiency and autosomal dominant partial lipodystrophy
-
COI: 1:CAS:528:DC%2BC3MXis1ymsbo%3D
-
Gandotra, S. et al. Perilipin deficiency and autosomal dominant partial lipodystrophy. N. Engl. J. Med. 364, 740–748 (2011)
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 740-748
-
-
Gandotra, S.1
-
40
-
-
85026557006
-
T2DiACoD: a gene atlas of type 2 diabetes mellitus associated complex disorders
-
Rani, J. et al. T2DiACoD: a gene atlas of type 2 diabetes mellitus associated complex disorders. Sci. Rep. 7, 6892 (2017)
-
(2017)
Sci. Rep.
, vol.7
-
-
Rani, J.1
-
41
-
-
78649755576
-
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia
-
COI: 1:CAS:528:DC%2BC3cXhsFaju7zM
-
Musunuru, K. et al. Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia. N. Engl. J. Med. 363, 2220–2227 (2010)
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 2220-2227
-
-
Musunuru, K.1
-
42
-
-
85025630463
-
Cardiovascular and metabolic effects of ANGPTL3 antisense oligonucleotides
-
COI: 1:CAS:528:DC%2BC2sXhtlyksrnJ
-
Graham, M. J. et al. Cardiovascular and metabolic effects of ANGPTL3 antisense oligonucleotides. N. Engl. J. Med. 377, 222–232 (2017)
-
(2017)
N. Engl. J. Med.
, vol.377
, pp. 222-232
-
-
Graham, M.J.1
-
43
-
-
34548829636
-
Thrombin regulates intracellular cyclic AMP concentration in human platelets through phosphorylation/activation of phosphodiesterase 3A
-
COI: 1:CAS:528:DC%2BD2sXhtVSgsbzI
-
Zhang, W. & Colman, R. W. Thrombin regulates intracellular cyclic AMP concentration in human platelets through phosphorylation/activation of phosphodiesterase 3A. Blood 110, 1475–1482 (2007)
-
(2007)
Blood
, vol.110
, pp. 1475-1482
-
-
Zhang, W.1
Colman, R.W.2
-
44
-
-
84930065286
-
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
-
COI: 1:CAS:528:DC%2BC2MXht1Wltb7F
-
Maass, P. G. et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nat. Genet. 47, 647–653 (2015)
-
(2015)
Nat. Genet.
, vol.47
, pp. 647-653
-
-
Maass, P.G.1
-
45
-
-
84889660239
-
Selective regulation of cyclic nucleotide phosphodiesterase PDE3A isoforms
-
COI: 1:CAS:528:DC%2BC3sXhvFKms7zJ
-
Vandeput, F. et al. Selective regulation of cyclic nucleotide phosphodiesterase PDE3A isoforms. Proc. Natl Acad. Sci. USA 110, 19778–19783 (2013)
-
(2013)
Proc. Natl Acad. Sci. USA
, vol.110
, pp. 19778-19783
-
-
Vandeput, F.1
-
46
-
-
84965187422
-
Cilostazol for intermittent claudication
-
Bedenis, R. et al. Cilostazol for intermittent claudication. Cochrane Database Syst. Rev. 10, CD003748 (2014)
-
(2014)
Cochrane Database Syst. Rev.
, vol.10
, pp. CD003748
-
-
Bedenis, R.1
-
47
-
-
0033529402
-
Impact of cilostazol on restenosis after percutaneous coronary balloon angioplasty
-
COI: 1:CAS:528:DyaK1MXksFyltbY%3D
-
Tsuchikane, E. et al. Impact of cilostazol on restenosis after percutaneous coronary balloon angioplasty. Circulation 100, 21–26 (1999)
-
(1999)
Circulation
, vol.100
, pp. 21-26
-
-
Tsuchikane, E.1
-
48
-
-
77956884231
-
Cilostazol for prevention of secondary stroke (CSPS 2): an aspirin-controlled, double-blind, randomised non-inferiority trial
-
COI: 1:CAS:528:DC%2BC3cXhtFOntbvK
-
Shinohara, Y. et al. Cilostazol for prevention of secondary stroke (CSPS 2): an aspirin-controlled, double-blind, randomised non-inferiority trial. Lancet Neurol. 9, 959–968 (2010)
-
(2010)
Lancet Neurol.
, vol.9
, pp. 959-968
-
-
Shinohara, Y.1
-
49
-
-
84975492597
-
Phosphodiesterase 3B (PDE3B) regulates NLRP3 inflammasome in adipose tissue
-
COI: 1:CAS:528:DC%2BC28XhtVahu7nI
-
Ahmad, F. et al. Phosphodiesterase 3B (PDE3B) regulates NLRP3 inflammasome in adipose tissue. Sci. Rep. 6, 28056 (2016)
-
(2016)
Sci. Rep.
, vol.6
-
-
Ahmad, F.1
-
50
-
-
84928558139
-
Targeted disruption of PDE3B, but not PDE3A, protects murine heart from ischemia/reperfusion injury
-
COI: 1:CAS:528:DC%2BC2MXmsFSmsrw%3D
-
Chung, Y. W. et al. Targeted disruption of PDE3B, but not PDE3A, protects murine heart from ischemia/reperfusion injury. Proc. Natl Acad. Sci. USA 112, E2253–E2262 (2015)
-
(2015)
Proc. Natl Acad. Sci. USA
, vol.112
, pp. E2253-E2262
-
-
Chung, Y.W.1
-
51
-
-
85041475144
-
Genetic association of lipids and lipid drug targets with abdominal aortic aneurysm: a meta-analysis
-
Harrison, S. C. et al. Genetic association of lipids and lipid drug targets with abdominal aortic aneurysm: a meta-analysis. JAMA Cardiol. 3, 26–33 (2018)
-
(2018)
JAMA Cardiol.
, vol.3
, pp. 26-33
-
-
Harrison, S.C.1
-
52
-
-
84983780951
-
Hypercholesterolemia induced by a PCSK9 gain-of-function mutation augments angiotensin II-induced abdominal aortic aneurysms in C57BL/6 mice—brief report
-
COI: 1:CAS:528:DC%2BC28Xhtl2msLvP
-
Lu, H. et al. Hypercholesterolemia induced by a PCSK9 gain-of-function mutation augments angiotensin II-induced abdominal aortic aneurysms in C57BL/6 mice—brief report. Arterioscler. Thromb. Vasc. Biol. 36, 1753–1757 (2016)
-
(2016)
Arterioscler. Thromb. Vasc. Biol.
, vol.36
, pp. 1753-1757
-
-
Lu, H.1
-
53
-
-
84864845456
-
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
-
COI: 1:CAS:528:DC%2BC38Xnt1Cmsrc%3D
-
Voight, B. F. et al. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet 380, 572–580 (2012)
-
(2012)
Lancet
, vol.380
, pp. 572-580
-
-
Voight, B.F.1
-
54
-
-
84887058576
-
Common variants associated with plasma triglycerides and risk for coronary artery disease
-
COI: 1:CAS:528:DC%2BC3sXhsFOiur%2FN
-
Do, R. et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345–1352 (2013)
-
(2013)
Nat. Genet.
, vol.45
, pp. 1345-1352
-
-
Do, R.1
-
55
-
-
84976331409
-
Fast and accurate long-range phasing in a UK Biobank cohort
-
COI: 1:CAS:528:DC%2BC28XpsVCrsrs%3D
-
Loh, P. R., Palamara, P. F. & Price, A. L. Fast and accurate long-range phasing in a UK Biobank cohort. Nat. Genet. 48, 811–816 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 811-816
-
-
Loh, P.R.1
Palamara, P.F.2
Price, A.L.3
-
56
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
COI: 1:CAS:528:DC%2BC38XhtVKnt7jI
-
Howie, B., Fuchsberger, C., Stephens, M., Marchini, J. & Abecasis, G. R. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat. Genet. 44, 955–959 (2012)
-
(2012)
Nat. Genet.
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
57
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
COI: 1:CAS:528:DC%2BD28XnsVCgsrg%3D
-
Price, A. L. et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet. 38, 904–909 (2006)
-
(2006)
Nat. Genet.
, vol.38
, pp. 904-909
-
-
Price, A.L.1
-
58
-
-
84899540947
-
Quality control and conduct of genome-wide association meta-analyses
-
Winkler, T. W. et al. Quality control and conduct of genome-wide association meta-analyses. Nat. Protoc. 9, 1192–1212 (2014)
-
(2014)
Nat. Protoc.
, vol.9
, pp. 1192-1212
-
-
Winkler, T.W.1
-
59
-
-
84980347551
-
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent
-
COI: 1:CAS:528:DC%2BC28Xht1KlsrrJ
-
Hyde, C. L. et al. Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. Nat. Genet. 48, 1031–1036 (2016)
-
(2016)
Nat. Genet.
, vol.48
, pp. 1031-1036
-
-
Hyde, C.L.1
-
60
-
-
84874783818
-
Polygenic modeling with Bayesian sparse linear mixed models
-
COI: 1:CAS:528:DC%2BC3sXktlSksLw%3D
-
Zhou, X., Carbonetto, P. & Stephens, M. Polygenic modeling with Bayesian sparse linear mixed models. PLoS Genet. 9, e1003264 (2013)
-
(2013)
PLoS Genet.
, vol.9
-
-
Zhou, X.1
Carbonetto, P.2
Stephens, M.3
|