-
1
-
-
79953187895
-
Lipid parameters for measuring risk of cardiovascular disease
-
Arsenault, B. J., Boekholdt, S. M. & Kastelein, J. J. Lipid parameters for measuring risk of cardiovascular disease. Nat. Rev. Cardiol. 8, 197-206 (2011
-
(2011)
Nat. Rev. Cardiol.
, vol.8
, pp. 197-206
-
-
Arsenault, B.J.1
Boekholdt, S.M.2
Kastelein, J.J.3
-
2
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
Global Lipids Genetics, C. et al.
-
Global Lipids Genetics, C. et al. Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013
-
(2013)
Nat. Genet.
, vol.45
, pp. 1274-1283
-
-
-
3
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
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
-
4
-
-
31744449136
-
The sex-specific genetic architecture of quantitative traits in humans
-
Weiss, L. A., Pan, L., Abney, M. & Ober, C. The sex-specific genetic architecture of quantitative traits in humans. Nat. Genet. 38, 218-222 (2006
-
(2006)
Nat. Genet.
, vol.38
, pp. 218-222
-
-
Weiss, L.A.1
Pan, L.2
Abney, M.3
Ober, C.4
-
5
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk, O., Hechter, E., Sunyaev, S. R. & Lander, E. S. The mystery of missing heritability: Genetic interactions create phantom heritability. Proc. Natl Acad. Sci. 109, 1193-1198 (2012
-
(2012)
Proc. Natl Acad. Sci.
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
-
6
-
-
77955070766
-
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
-
Johansen, C. T. et al. Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. Nat. Genet. 42, 684-687 (2010
-
(2010)
Nat. Genet.
, vol.42
, pp. 684-687
-
-
Johansen, C.T.1
-
7
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of hdl cholesterol
-
Cohen, J. et al. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science (New York, NY) 305, 869-872 (2004
-
(2004)
Science (New York, NY)
, vol.305
, pp. 869-872
-
-
Cohen, J.1
-
8
-
-
84888201938
-
Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia
-
Stitziel, N. O. et al. Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia. Arterioscler. Thromb. Vasc. Biol. 33, 2909-2914 (2013
-
(2013)
Arterioscler. Thromb. Vasc. Biol.
, vol.33
, pp. 2909-2914
-
-
Stitziel, N.O.1
-
9
-
-
84893720400
-
Whole-exome sequencing identifies rare and low-frequency coding variants associated with ldl cholesterol
-
Lange, L. A. et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014
-
(2014)
Am. J. Hum. Genet.
, vol.94
, pp. 233-245
-
-
Lange, L.A.1
-
10
-
-
84893756641
-
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks
-
Peloso, Gina 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 Gina, M.1
-
11
-
-
84898058547
-
Systematic evaluation of coding variation identifies a candidate causal variant in tm6sf2 influencing total cholesterol and myocardial infarction risk
-
Holmen, O. L. et al. Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nat. Genet. 46, 345-351 (2014
-
(2014)
Nat. Genet.
, vol.46
, pp. 345-351
-
-
Holmen, O.L.1
-
12
-
-
84879411643
-
Sequencing studies in human genetics: Design and interpretation
-
Goldstein, D. B. et al. Sequencing studies in human genetics: design and interpretation. Nat. Rev. Genet. 14, 460-470 (2013
-
(2013)
Nat. Rev. Genet.
, vol.14
, pp. 460-470
-
-
Goldstein, D.B.1
-
13
-
-
33344464808
-
A spectrum of pcsk9 alleles contributes to plasma levels of low-density lipoprotein cholesterol
-
Kotowski, I. K. et al. A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol. Am. J. Hum. Genet. 78, 410-422 (2006
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 410-422
-
-
Kotowski, I.K.1
-
14
-
-
84875631900
-
Cohort profile: Twinsuk and healthy ageing twin study
-
Moayyeri, A., Hammond, C. J., Valdes, A. M. & Spector, T. D. Cohort Profile: TwinsUK and healthy ageing twin study. Int. J. Epidemiol. 42, 76-85 (2013
-
(2013)
Int. J. Epidemiol.
, vol.42
, pp. 76-85
-
-
Moayyeri, A.1
Hammond, C.J.2
Valdes, A.M.3
Spector, T.4
-
15
-
-
84875577737
-
Cohort profile: The 'children of the 90s'-the index offspring of the avon longitudinal study of parents and children
-
Boyd, A. et al. Cohort Profile: the 'children of the 90s'-the index offspring of the Avon Longitudinal Study of Parents and Children. Int. J. Epidemiol. 42, 111-127 (2013
-
(2013)
Int. J. Epidemiol.
, vol.42
, pp. 111-127
-
-
Boyd, A.1
-
16
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu, M. C. et al. Rare-variant association testing for sequencing data with the sequence kernel association test. Am. J. Hum. Genet. 89, 82-93 (2011
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
-
17
-
-
34248594090
-
A common variant in the fto gene is associated with body mass index and predisposes to childhood and adult obesity
-
Frayling, T. M. et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science 316, 889-894 (2007
-
(2007)
Science
, vol.316
, pp. 889-894
-
-
Frayling, T.M.1
-
18
-
-
0008393474
-
Apolipoprotein multigene family: Tandem organization of human apolipoprotein ai ciii, and aiv genes
-
Karathanasis, S. K. Apolipoprotein multigene family: tandem organization of human apolipoprotein AI, CIII, and AIV genes. Proc. Natl Acad. Sci. USA 82, 6374-6378 (1985
-
(1985)
Proc. Natl Acad. Sci. USA
, vol.82
, pp. 6374-6378
-
-
Karathanasis, S.K.1
-
19
-
-
0023919128
-
Human apolipoprotein ciii gene expression is regulated by positive and negative cis-Acting elements and tissue-specific protein factors
-
Reue, K., Leff, T. & Breslow, J. L. Human apolipoprotein CIII gene expression is regulated by positive and negative cis-Acting elements and tissue-specific protein factors. J. Biol. Chem. 263, 6857-6864 (1988
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 6857-6864
-
-
Reue, K.1
Leff, T.2
Breslow, J.L.3
-
20
-
-
0025309751
-
Promoter elements and factors required for hepatic and intestinal transcription of the human apociii gene
-
Ogami, K., Hadzopoulou-Cladaras, M., Cladaras, C. & Zannis, V. I. Promoter elements and factors required for hepatic and intestinal transcription of the human ApoCIII gene. J. Biol. Chem. 265, 9808-9815 (1990
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 9808-9815
-
-
Ogami, K.1
Hadzopoulou-Cladaras, M.2
Cladaras, C.3
Zannis, V.I.4
-
21
-
-
0031577661
-
The apolipoprotein a-i/c-iii/a-iv gene cluster: Apoc-iii and apoa-iv expression is regulated by two common enhancers
-
Vergnes, L., Taniguchi, T., Omori, K., Zakin, M. M. & Ochoa, A. The apolipoprotein A-I/C-III/A-IV gene cluster: ApoC-III and ApoA-IV expression is regulated by two common enhancers. Biochim. Biophys. Acta. 1348, 299-310 (1997
-
(1997)
Biochim. Biophys. Acta.
, vol.1348
, pp. 299-310
-
-
Vergnes, L.1
Taniguchi, T.2
Omori, K.3
Zakin, M.M.4
Ochoa, A.5
-
22
-
-
0017235537
-
Changing relative proportions of apolipoproteins cii and ciii of very low density lipoproteins in hypertriglyceridaemia
-
Carlson, L. A. & Ballantyne, D. Changing relative proportions of apolipoproteins CII and CIII of very low density lipoproteins in hypertriglyceridaemia. Atherosclerosis 23, 563-568 (1976
-
(1976)
Atherosclerosis
, vol.23
, pp. 563-568
-
-
Carlson, L.A.1
Ballantyne, D.2
-
23
-
-
0024474642
-
Apolipoproteins c-ii and c-iii metabolism in hypertriglyceridemic patients effect of a drastic triglyceride reduction by combined diet restriction and fenofibrate administration
-
Malmendier, C. L. et al. Apolipoproteins C-II and C-III metabolism in hypertriglyceridemic patients. Effect of a drastic triglyceride reduction by combined diet restriction and fenofibrate administration. Atherosclerosis 77, 139-149 (1989
-
(1989)
Atherosclerosis
, vol.77
, pp. 139-149
-
-
Malmendier, C.L.1
-
24
-
-
0029791717
-
Further characterization of the metabolic properties of triglyceride-rich lipoproteins from human and mouse apoc-iii transgenic mice
-
Aalto-Setala, K. et al. Further characterization of the metabolic properties of triglyceride-rich lipoproteins from human and mouse apoC-III transgenic mice. J. Lipid Res. 37, 1802-1811 (1996
-
(1996)
J. Lipid Res.
, vol.37
, pp. 1802-1811
-
-
Aalto-Setala, K.1
-
25
-
-
0030911585
-
Chylomicronemia due to apolipoprotein ciii overexpression in apolipoprotein e-null mice. Apolipoprotein ciii-induced hypertriglyceridemia is not mediated by effects on apolipoprotein e
-
Ebara, T., Ramakrishnan, R., Steiner, G. & Shachter, N. S. Chylomicronemia due to apolipoprotein CIII overexpression in apolipoprotein E-null mice. Apolipoprotein CIII-induced hypertriglyceridemia is not mediated by effects on apolipoprotein E. J. Clin. Invest. 99, 2672-2681 (1997
-
(1997)
J. Clin. Invest.
, vol.99
, pp. 2672-2681
-
-
Ebara, T.1
Ramakrishnan, R.2
Steiner, G.3
Shachter, N.S.4
-
26
-
-
0030937346
-
Complex genetic contribution of the apo ai-ciiiaiv gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes
-
Dallinga-Thie, G. M. et al. Complex genetic contribution of the Apo AI-CIIIAIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes. J. Clin. Invest. 99, 953-961 (1997
-
(1997)
J. Clin. Invest.
, vol.99
, pp. 953-961
-
-
Dallinga-Thie, G.M.1
-
27
-
-
0030069735
-
Apolipoprotein a-i/c-iii/a-iv gene cluster in familial combined hyperlipidemia: Effects on ldl-cholesterol and apolipoproteins b and c-iii
-
Dallinga-Thie, G. M. et al. Apolipoprotein A-I/C-III/A-IV gene cluster in familial combined hyperlipidemia: effects on LDL-cholesterol and apolipoproteins B and C-III. J. Lipid Res. 37, 136-147 (1996
-
(1996)
J. Lipid Res.
, vol.37
, pp. 136-147
-
-
Dallinga-Thie, G.M.1
-
28
-
-
0030978794
-
A variation in the apolipoprotein c-iii gene is associated with an increased number of circulating vldl and idl particles in familial combined hyperlipidemia
-
Ribalta, J. et al. A variation in the apolipoprotein C-III gene is associated with an increased number of circulating VLDL and IDL particles in familial combined hyperlipidemia. J. Lipid Res. 38, 1061-1069 (1997
-
(1997)
J. Lipid Res.
, vol.38
, pp. 1061-1069
-
-
Ribalta, J.1
-
29
-
-
84890690821
-
A rare functional cardioprotective apoc3 variant has risen in frequency in distinct population isolates
-
Tachmazidou, I. et al. A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates. Nat. Commun. 4, 2872 (2013
-
(2013)
Nat. Commun.
, vol.4
, pp. 2872
-
-
Tachmazidou, I.1
-
30
-
-
58149262866
-
A null mutation in human apoc3 confers a favorable plasma lipid profile and apparent cardioprotection
-
Pollin, T. I. et al. A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science 322, 1702-1705 (2008
-
(2008)
Science
, vol.322
, pp. 1702-1705
-
-
Pollin, T.I.1
-
31
-
-
2442441507
-
Maximum entropy modeling of short sequence motifs with applications to rna splicing signals
-
Yeo, G. & Burge, C. B. Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals. J. Comput. Biol. 11, 377-394 (2004
-
(2004)
J. Comput. Biol.
, vol.11
, pp. 377-394
-
-
Yeo, G.1
Burge, C.B.2
-
32
-
-
84878682420
-
The genotype-tissue expression (gtex) project
-
Consortium, G. The Genotype-Tissue Expression (GTEx) project. Nat. Genet. 45, 580-585 (2013
-
(2013)
Nat. Genet.
, vol.45
, pp. 580-585
-
-
Consortium, G.1
-
33
-
-
23744458086
-
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes
-
Siepel, A. et al. Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. Genome Res. 15, 1034-1050 (2005
-
(2005)
Genome Res.
, vol.15
, pp. 1034-1050
-
-
Siepel, A.1
-
34
-
-
84892366435
-
Remnant cholesterol as a cause of ischemic heart disease: Evidence, definition, measurement, atherogenicity, high risk patients, and present and future treatment
-
Varbo, A., Benn, M. & Nordestgaard, B. G. Remnant cholesterol as a cause of ischemic heart disease: Evidence, definition, measurement, atherogenicity, high risk patients, and present and future treatment. Pharmacol. Ther. 141, 358-367 (2014
-
(2014)
Pharmacol. Ther.
, vol.141
, pp. 358-367
-
-
Varbo, A.1
Benn, M.2
Nordestgaard, B.G.3
-
35
-
-
0029838433
-
Plasma triglyceride level is a risk factor for cardiovascular disease independent of high-density lipoprotein cholesterol level: A meta-Analysis of population-based prospective studies
-
Hokanson, J. E. & Austin, M. A. Plasma triglyceride level is a risk factor for cardiovascular disease independent of high-density lipoprotein cholesterol level: a meta-Analysis of population-based prospective studies. J. Cardiovasc. Risk 3, 213-219 (1996
-
(1996)
J. Cardiovasc. Risk
, vol.3
, pp. 213-219
-
-
Hokanson, J.E.1
Austin, M.A.2
-
36
-
-
0035572890
-
Do total and high density lipoprotein cholesterol and triglycerides act independently in the prediction of ischemic heart disease? Ten-year follow-up of caerphilly and speedwell cohorts
-
Yarnell, J. W. et al. Do total and high density lipoprotein cholesterol and triglycerides act independently in the prediction of ischemic heart disease? Ten-year follow-up of Caerphilly and Speedwell Cohorts. Arterioscler. Thromb. Vasc. Biol. 21, 1340-1345 (2001
-
(2001)
Arterioscler. Thromb. Vasc. Biol.
, vol.21
, pp. 1340-1345
-
-
Yarnell, J.W.1
-
37
-
-
84884284181
-
Elevated remnant cholesterol causes both low-grade inflammation and ischemic heart disease, whereas elevated low-density lipoprotein cholesterol causes ischemic heart disease without inflammation
-
Varbo, A., Benn, M., Tybjaerg-Hansen, A. & Nordestgaard, B. G. Elevated remnant cholesterol causes both low-grade inflammation and ischemic heart disease, whereas elevated low-density lipoprotein cholesterol causes ischemic heart disease without inflammation. Circulation 128, 1298-1309 (2013
-
(2013)
Circulation
, vol.128
, pp. 1298-1309
-
-
Varbo, A.1
Benn, M.2
Tybjaerg-Hansen, A.3
Nordestgaard, B.G.4
-
38
-
-
84887058576
-
Common variants associated with plasma triglycerides and risk for coronary artery disease
-
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
-
39
-
-
70450081001
-
Major lipids, apolipoproteins, and risk of vascular disease
-
The Emerging Risk Factors, C
-
The Emerging Risk Factors, C. MAjor lipids, apolipoproteins, and risk of vascular disease. JAMA 302, 1993-2000 (2009
-
(2009)
JAMA
, vol.302
, pp. 1993-2000
-
-
-
40
-
-
84863582389
-
Antisense oligonucleotides for the treatment of dyslipidaemia
-
Visser, M. E., Witztum, J. L., Stroes, E. S. & Kastelein, J. J. Antisense oligonucleotides for the treatment of dyslipidaemia. Eur. Heart. J. 33, 1451-1458 (2012
-
(2012)
Eur. Heart. J.
, vol.33
, pp. 1451-1458
-
-
Visser, M.E.1
Witztum, J.L.2
Stroes, E.S.3
Kastelein, J.J.4
-
41
-
-
1942436221
-
Mendelian randomization: Prospects, potentials, and limitations
-
Davey Smith, G. & Ebrahim, S. Mendelian randomization: prospects, potentials, and limitations. Int. J. Epidemiol. 33, 30-42 (2004
-
(2004)
Int. J. Epidemiol.
, vol.33
, pp. 30-42
-
-
Davey Smith, G.1
Ebrahim, S.2
-
42
-
-
84888025756
-
Associations of maternal 25-hydroxyvitamin d in pregnancy with offspring cardiovascular risk factors in childhood and adolescence: Findings from the avon longitudinal study of parents and children
-
Williams, D. M. et al. Associations of maternal 25-hydroxyvitamin D in pregnancy with offspring cardiovascular risk factors in childhood and adolescence: findings from the Avon Longitudinal Study of Parents and Children. Heart. 99, 1849-1856 (2013
-
(2013)
Heart.
, vol.99
, pp. 1849-1856
-
-
Williams, D.M.1
-
43
-
-
0015348189
-
Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge
-
Friedewald, W. T., Levy, R. I. & Fredrickson, D. S. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin. Chem. 18, 499-502 (1972
-
(1972)
Clin. Chem.
, vol.18
, pp. 499-502
-
-
Friedewald, W.T.1
Levy, R.I.2
Fredrickson, D.S.3
-
44
-
-
77949587649
-
Fast and accurate long-read alignment with burrows-wheeler transform
-
Li, H. & Durbin, R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26, 589-595 (2010
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
45
-
-
80054915847
-
A statistical framework for snp calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
-
Li, H. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data. Bioinformatics 27, 2987-2993 (2011
-
(2011)
Bioinformatics
, vol.27
, pp. 2987-2993
-
-
Li, H.1
-
46
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation dna sequencing data
-
DePristo, M. A. et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43, 491-498 (2011
-
(2011)
Nat. Genet.
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
-
47
-
-
35348817330
-
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering
-
Browning, S. R. & Browning, B. L. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am. J. Hum. Genet. 81, 1084-1097 (2007
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 1084-1097
-
-
Browning, S.R.1
Browning, B.2
-
48
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
International HapMap, C. et al. Integrating common and rare genetic variation in diverse human populations. Nature 467, 52-58 (2010
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
International HapMap, C.1
-
49
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
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
-
50
-
-
84901370399
-
A general approach for haplotype phasing across the full spectrum of relatedness
-
O'Connell, J. et al. A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet. 10, e1004234 (2014
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004234
-
-
O'Connell, J.1
-
51
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie, B. N., Donnelly, P. & Marchini, J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet. 5, e1000529 (2009
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
52
-
-
74949138753
-
Human genome sequencing using unchained base reads on self-Assembling dna nanoarrays
-
Drmanac, R. et al. Human genome sequencing using unchained base reads on self-Assembling DNA nanoarrays. Science 327, 78-81 (2010
-
(2010)
Science
, vol.327
, pp. 78-81
-
-
Drmanac, R.1
-
53
-
-
84872021031
-
Genes contributing to pain sensitivity in the normal population: An exome sequencing study
-
Williams, F. M. et al. Genes contributing to pain sensitivity in the normal population: an exome sequencing study. PLoS Genet. 8, e1003095 (2012
-
(2012)
PLoS Genet.
, vol.8
, pp. e1003095
-
-
Williams, F.M.1
-
54
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
Marchini, J. & Howie, B. Genotype imputation for genome-wide association studies. Nat. Rev. Genet. 11, 499-511 (2010
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
55
-
-
84863003734
-
Genome-wide efficient mixed-model analysis for association studies
-
Zhou, X. & Stephens, M. Genome-wide efficient mixed-model analysis for association studies. Nat. Genet. 44, 821-824 (2012
-
(2012)
Nat. Genet.
, vol.44
, pp. 821-824
-
-
Zhou, X.1
Stephens, M.2
-
56
-
-
77952714079
-
Gwama: Software for genome-wide association meta-Analysis
-
Magi, R. & Morris, A. P. GWAMA: software for genome-wide association meta-Analysis. BMC Bioinformatics 11, 288 (2010
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 288
-
-
Magi, R.1
Morris, A.2
-
57
-
-
34548292504
-
Plink: A tool for whole-genome association and populationbased linkage analyses
-
Purcell, S. et al. PLINK: A tool for whole-genome association and populationbased linkage analyses. Am. J. Hum. Genet. 81, 559-575 (2007
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
-
58
-
-
78650856517
-
Gcta: A tool for genome-wide complex trait analysis
-
Yang, J., Lee, S. H., Goddard, M. E. & Visscher, P. M. GCTA: a tool for genome-wide complex trait analysis. Am. J. Hum. Genet. 88, 76-82 (2011
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.4
-
59
-
-
84864845456
-
Plasma hdl cholesterol and risk of myocardial infarction: A mendelian randomisation study
-
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
-
60
-
-
0021737190
-
Isolation and sequence analysis of the human apolipoprotein ciii gene and the intergenic region between the apo ai and apo ciii genes
-
Protter, A. A. et al. Isolation and sequence analysis of the human apolipoprotein CIII gene and the intergenic region between the apo AI and apo CIII genes. DNA 3, 449-456 (1984).
-
(1984)
DNA
, vol.3
, pp. 449-456
-
-
Protter, A.A.1
|