-
1
-
-
84891790401
-
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
-
Welter, D. et al. The NHGRI GWAS Catalog, a curated resource of SNP-trait associations. Nucleic Acids Res. 42, D1001-D1006 (2014).
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D1001-D1006
-
-
Welter, D.1
-
2
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff, L. A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. USA 106, 9362-9367 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
-
3
-
-
84867744660
-
Genetic variation in metabolic phenotypes: Study designs and applications
-
Suhre, K. & Gieger, C. Genetic variation in metabolic phenotypes: study designs and applications. Nat. Rev. Genet. 13, 759-769 (2012).
-
(2012)
Nat. Rev. Genet.
, vol.13
, pp. 759-769
-
-
Suhre, K.1
Gieger, C.2
-
4
-
-
84857648463
-
Genome-wide association study identifies multiple loci influencing human serum metabolite levels
-
Kettunen, J. et al. Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nature Genet. 44, 269-276 (2012).
-
(2012)
Nature Genet.
, vol.44
, pp. 269-276
-
-
Kettunen, J.1
-
5
-
-
84901686870
-
An atlas of genetic influences on human blood metabolites
-
Shin, S. Y. et al. An atlas of genetic influences on human blood metabolites. Nature Genet. 46, 543-550 (2014).
-
(2014)
Nature Genet.
, vol.46
, pp. 543-550
-
-
Shin, S.Y.1
-
6
-
-
80052398214
-
Human metabolic individuality in biomedical and pharmaceutical research
-
Suhre, K. et al. Human metabolic individuality in biomedical and pharmaceutical research. Nature 477, 54-60 (2011).
-
(2011)
Nature
, vol.477
, pp. 54-60
-
-
Suhre, K.1
-
7
-
-
33646375453
-
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
-
Service, S. et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nature Genet. 38, 556-560 (2006).
-
(2006)
Nature Genet.
, vol.38
, pp. 556-560
-
-
Service, S.1
-
8
-
-
84930090376
-
The impact of low-frequency and rare variants on lipid levels
-
Surakka, I. et al. The impact of low-frequency and rare variants on lipid levels. Nature Genet. 47, 589-597 (2015).
-
(2015)
Nature Genet.
, vol.47
, pp. 589-597
-
-
Surakka, I.1
-
9
-
-
84929001104
-
Human genomics. the Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
-
Consortium, G. T. Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 348, 648-660 (2015).
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
Consortium, G.T.1
-
10
-
-
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
-
11
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
Tregouet, D. A. et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nature Genet. 41, 283-285 (2009).
-
(2009)
Nature Genet.
, vol.41
, pp. 283-285
-
-
Tregouet, D.A.1
-
12
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert, H. et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nature Genet. 43, 333-338 (2011).
-
(2011)
Nature Genet.
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
-
13
-
-
67049167090
-
Genetically elevated lipoprotein(a) and increased risk of myocardial infarction
-
Kamstrup, P. R., Tybjaerg-Hansen, A., Steffensen, R. & Nordestgaard, B. G. Genetically elevated lipoprotein(a) and increased risk of myocardial infarction. JAMA 301, 2331-2339 (2009).
-
(2009)
JAMA
, vol.301
, pp. 2331-2339
-
-
Kamstrup, P.R.1
Tybjaerg-Hansen, A.2
Steffensen, R.3
Nordestgaard, B.G.4
-
14
-
-
84860271201
-
Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: Importance of Lp(a)
-
Deshmukh, H. A. et al. Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a). J. Lipid Res. 53, 1000-1011 (2012).
-
(2012)
J. Lipid Res.
, vol.53
, pp. 1000-1011
-
-
Deshmukh, H.A.1
-
15
-
-
84860798384
-
Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: The Justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin (JUPITER) trial
-
Chasman, D. I. et al. Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. Circ. Cardiovasc. Genet. 5, 257-264 (2012).
-
(2012)
Circ. Cardiovasc. Genet.
, vol.5
, pp. 257-264
-
-
Chasman, D.I.1
-
16
-
-
84906838227
-
Mendelian randomization: Genetic anchors for causal inference in epidemiological studies
-
Davey Smith, G. & Hemani, G. Mendelian randomization: genetic anchors for causal inference in epidemiological studies. Hum. Mol. Genet. 23, R89-R98 (2014).
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. R89-R98
-
-
Davey Smith, G.1
Hemani, G.2
-
17
-
-
0032816711
-
Lipoprotein(a): Intrigues and insights
-
Hobbs, H. H. & White, A. L. Lipoprotein(a): intrigues and insights. Curr. Opin. Lipidol. 10, 225-236 (1999).
-
(1999)
Curr. Opin. Lipidol.
, vol.10
, pp. 225-236
-
-
Hobbs, H.H.1
White, A.L.2
-
18
-
-
84858792393
-
Lipoprotein(a): More interesting than ever after 50 years
-
Dube, J. B., Boffa, M. B., Hegele, R. A. & Koschinsky, M. L. Lipoprotein(a): more interesting than ever after 50 years. Curr. Opin. Lipidol. 23, 133-140 (2012).
-
(2012)
Curr. Opin. Lipidol.
, vol.23
, pp. 133-140
-
-
Dube, J.B.1
Boffa, M.B.2
Hegele, R.A.3
Koschinsky, M.L.4
-
19
-
-
0030724884
-
Modulation of lipoprotein(a) atherogenicity by high density lipoprotein cholesterol levels in middle-aged men with symptomatic coronary artery disease and normal to moderately elevated serum cholesterol. Regression Growth Evaluation Statin Study (REGRESS) Study Group
-
Cobbaert, C. et al. Modulation of lipoprotein(a) atherogenicity by high density lipoprotein cholesterol levels in middle-aged men with symptomatic coronary artery disease and normal to moderately elevated serum cholesterol. Regression Growth Evaluation Statin Study (REGRESS) Study Group. J. Am. Coll. Cardiol. 30, 1491-1499 (1997).
-
(1997)
J. Am. Coll. Cardiol.
, vol.30
, pp. 1491-1499
-
-
Cobbaert, C.1
-
20
-
-
84893853699
-
Lipoprotein(a) concentrations, rosuvastatin therapy, and residual vascular risk: An analysis from the JUPITER Trial (Justification for the Use of Statins in Prevention: An Intervention Trial Evaluating Rosuvastatin)
-
Khera, A. V. et al. Lipoprotein(a) concentrations, rosuvastatin therapy, and residual vascular risk: an analysis from the JUPITER Trial (Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin). Circulation 129, 635-642 (2014).
-
(2014)
Circulation
, vol.129
, pp. 635-642
-
-
Khera, A.V.1
-
21
-
-
84944152398
-
Antisense therapy targeting apolipoprotein(a): A randomised, double-blind, placebo-controlled phase 1 study
-
Tsimikas, S. et al. Antisense therapy targeting apolipoprotein(a): a randomised, double-blind, placebo-controlled phase 1 study. Lancet 386, 1472-1483 (2015).
-
(2015)
Lancet
, vol.386
, pp. 1472-1483
-
-
Tsimikas, S.1
-
22
-
-
84905460411
-
Distribution and medical impact of loss-of-function variants in the Finnish founder population
-
Lim, E. T. et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet. 10, e1004494 (2014).
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004494
-
-
Lim, E.T.1
-
23
-
-
84866259021
-
Quality of the Finnish Hospital Discharge Register: A systematic review
-
Sund, R. Quality of the Finnish Hospital Discharge Register: a systematic review. Scand. J. Public Health 40, 505-515 (2012).
-
(2012)
Scand. J. Public Health
, vol.40
, pp. 505-515
-
-
Sund, R.1
-
24
-
-
70349324702
-
High-throughput serum NMR metabonomics for cost-effective holistic studies on systemic metabolism
-
Soininen, P. et al. High-throughput serum NMR metabonomics for cost-effective holistic studies on systemic metabolism. Analyst 134, 1781-1785 (2009).
-
(2009)
Analyst
, vol.134
, pp. 1781-1785
-
-
Soininen, P.1
-
25
-
-
84924533418
-
Quantitative serum nuclear magnetic resonance metabolomics in cardiovascular epidemiology and genetics
-
Soininen, P., Kangas, A. J., Wurtz, P., Suna, T. & Ala-Korpela, M. Quantitative serum nuclear magnetic resonance metabolomics in cardiovascular epidemiology and genetics. Circ. Cardiovasc Genet. 8, 192-206 (2015).
-
(2015)
Circ. Cardiovasc Genet.
, vol.8
, pp. 192-206
-
-
Soininen, P.1
Kangas, A.J.2
Wurtz, P.3
Suna, T.4
Ala-Korpela, M.5
-
26
-
-
84924402386
-
Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses
-
Demirkan, A. et al. Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses. PLoS Genet. 11, e1004835 (2015).
-
(2015)
PLoS Genet.
, vol.11
, pp. e1004835
-
-
Demirkan, A.1
-
27
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Genomes Project, C. et al. A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073 (2010).
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Genomes Project, C.1
-
28
-
-
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.P.2
-
29
-
-
84862832570
-
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
-
Yang, J. et al. Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genet. 44(S1-S3): 369-375 (2012).
-
(2012)
Nature Genet.
, vol.44
, Issue.S1-S3
, pp. 369-375
-
-
Yang, J.1
-
30
-
-
84878682420
-
The Genotype-Tissue Expression (GTEx) project
-
Consortium, G.T. The Genotype-Tissue Expression (GTEx) project. Nature Genet. 45, 580-585 (2013).
-
(2013)
Nature Genet.
, vol.45
, pp. 580-585
-
-
Consortium, G.T.1
-
31
-
-
84861153094
-
Matrix eQTL: Ultra fast eQTL analysis via large matrix operations
-
Shabalin, A. A. Matrix eQTL: ultra fast eQTL analysis via large matrix operations. Bioinformatics 28, 1353-1358 (2012).
-
(2012)
Bioinformatics
, vol.28
, pp. 1353-1358
-
-
Shabalin, A.A.1
|