-
2
-
-
58149161560
-
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
-
Aulchenko Y.S., et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat. Genet. 2009, 41(1):47-55.
-
(2009)
Nat. Genet.
, vol.41
, Issue.1
, pp. 47-55
-
-
Aulchenko, Y.S.1
-
3
-
-
64749093590
-
Validating an alternate version of the chewing function questionnaire in partially dentate patients
-
Baba K., et al. Validating an alternate version of the chewing function questionnaire in partially dentate patients. BMC Oral Health 2009, 9:9.
-
(2009)
BMC Oral Health
, vol.9
, pp. 9
-
-
Baba, K.1
-
4
-
-
70949106022
-
Haploview: visualization and analysis of SNP genotype data
-
(p. pdb ip71)
-
Barrett J.C. Haploview: visualization and analysis of SNP genotype data. Cold Spring Harb Protoc 2009, 2009(10). (p. pdb ip71).
-
(2009)
Cold Spring Harb Protoc
, vol.2009
, Issue.10
-
-
Barrett, J.C.1
-
5
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett J.C., et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005, 21(2):263-265.
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
-
6
-
-
0004059262
-
-
Harcourt/Academic Press, San Diego.
-
Bhagavan N.V. Medical Biochemistry 2002, Harcourt/Academic Press, San Diego, (1016 pp.). 4th ed.
-
(2002)
Medical Biochemistry
, pp. 1016
-
-
Bhagavan, N.V.1
-
7
-
-
84862101328
-
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides
-
Braun, T.R. et al., A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PLoS One. 7(5), e37056.
-
PLoS One.
, vol.7
, Issue.5
, pp. e37056
-
-
Braun, T.R.1
-
8
-
-
55449105227
-
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13
-
Burkhardt R., et al. Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arterioscler. Thromb. Vasc. Biol. 2008, 28(11):2078-2084.
-
(2008)
Arterioscler. Thromb. Vasc. Biol.
, vol.28
, Issue.11
, pp. 2078-2084
-
-
Burkhardt, R.1
-
9
-
-
0024468864
-
Structure of the human hepatic triglyceride lipase gene
-
Cai S.J., et al. Structure of the human hepatic triglyceride lipase gene. Biochemistry 1989, 28(23):8966-8971.
-
(1989)
Biochemistry
, vol.28
, Issue.23
, pp. 8966-8971
-
-
Cai, S.J.1
-
10
-
-
0035869117
-
WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, is a new member of the Mlx transcription factor network
-
Cairo S., et al. WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, is a new member of the Mlx transcription factor network. Hum. Mol. Genet. 2001, 10(6):617-627.
-
(2001)
Hum. Mol. Genet.
, vol.10
, Issue.6
, pp. 617-627
-
-
Cairo, S.1
-
11
-
-
0037053389
-
ANGPTL3 stimulates endothelial cell adhesion and migration via integrin alpha vbeta 3 and induces blood vessel formation in vivo
-
Camenisch G., et al. ANGPTL3 stimulates endothelial cell adhesion and migration via integrin alpha vbeta 3 and induces blood vessel formation in vivo. J. Biol. Chem. 2002, 277(19):17281-17290.
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.19
, pp. 17281-17290
-
-
Camenisch, G.1
-
12
-
-
58149214774
-
Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and apolipoprotein B among 6382 white women in genome-wide analysis with replication
-
Chasman D.I., et al. Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and apolipoprotein B among 6382 white women in genome-wide analysis with replication. Circ. Cardiovasc. Genet. 2008, 1(1):21-30.
-
(2008)
Circ. Cardiovasc. Genet.
, vol.1
, Issue.1
, pp. 21-30
-
-
Chasman, D.I.1
-
13
-
-
79952217437
-
Practical and theoretical considerations in study design for detecting gene-gene interactions using MDR and GMDR approaches
-
Chen, G.B. et al., Practical and theoretical considerations in study design for detecting gene-gene interactions using MDR and GMDR approaches. PLoS One. 6(2), e16981.
-
PLoS One.
, vol.6
, Issue.2
, pp. e16981
-
-
Chen, G.B.1
-
14
-
-
0033951707
-
New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulation
-
Dachet C., et al. New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulation. Arterioscler. Thromb. Vasc. Biol. 2000, 20(2):507-515.
-
(2000)
Arterioscler. Thromb. Vasc. Biol.
, vol.20
, Issue.2
, pp. 507-515
-
-
Dachet, C.1
-
15
-
-
0042329251
-
Dyslipidaemia
-
Durrington P. Dyslipidaemia. Lancet 2003, 362(9385):717-731.
-
(2003)
Lancet
, vol.362
, Issue.9385
, pp. 717-731
-
-
Durrington, P.1
-
16
-
-
79959694832
-
Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol
-
Edmondson, A.C. et al., Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circ. Cardiovasc. Genet. 4(2), 145-155.
-
Circ. Cardiovasc. Genet.
, vol.4
, Issue.2
, pp. 145-155
-
-
Edmondson, A.C.1
-
17
-
-
0026758170
-
The candidate oncoprotein Bcl-3 is an antagonist of p50/NF-kappa B-mediated inhibition
-
Franzoso G., et al. The candidate oncoprotein Bcl-3 is an antagonist of p50/NF-kappa B-mediated inhibition. Nature 1992, 359(6393):339-342.
-
(1992)
Nature
, vol.359
, Issue.6393
, pp. 339-342
-
-
Franzoso, G.1
-
19
-
-
84916200705
-
-
(September 2013 [cited 2014 31.01.2014]; Available from:)
-
Goldberg A.C.Dyslipidemia (September 2013 [cited 2014 31.01.2014]; Available from:). http://www.merckmanuals.com/professional/endocrine_and_metabolic_disorders/lipid_disorders/dyslipidemia.html.
-
-
-
Goldberg, A.C.D.1
-
20
-
-
57149114180
-
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions
-
Heid I.M., et al. Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. Circ. Cardiovasc. Genet. 2008, 1(1):10-20.
-
(2008)
Circ. Cardiovasc. Genet.
, vol.1
, Issue.1
, pp. 10-20
-
-
Heid, I.M.1
-
21
-
-
84859921736
-
A novel ChREBP isoform in adipose tissue regulates systemic glucose metabolism
-
Herman, M.A. et al., A novel ChREBP isoform in adipose tissue regulates systemic glucose metabolism. Nature. 484(7394), 333-338.
-
Nature
, vol.484
, Issue.7394
, pp. 333-338
-
-
Herman, M.A.1
-
22
-
-
67649875301
-
Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study
-
Hiura Y., et al. Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. Circ. J. 2009, 73(6):1119-1126.
-
(2009)
Circ. J.
, vol.73
, Issue.6
, pp. 1119-1126
-
-
Hiura, Y.1
-
23
-
-
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. 2009, 5(6):e1000529.
-
(2009)
PLoS Genet.
, vol.5
, Issue.6
, pp. e1000529
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
24
-
-
76749113896
-
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels
-
Igl, W., et al., Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. PLoS Genet. 6(1), e1000798.
-
PLoS Genet.
, vol.6
, Issue.1
, pp. e1000798
-
-
Igl, W.1
-
25
-
-
84455160630
-
Single nucleotide polymorphisms of the purinergic 1 receptor are not associated with myocardial infarction in a Latvian population
-
Ignatovica V., et al. Single nucleotide polymorphisms of the purinergic 1 receptor are not associated with myocardial infarction in a Latvian population. Mol. Biol. Rep. 2011, 39(2):1917-1925.
-
(2011)
Mol. Biol. Rep.
, vol.39
, Issue.2
, pp. 1917-1925
-
-
Ignatovica, V.1
-
26
-
-
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(8), 684-687.
-
Nat. Genet.
, vol.42
, Issue.8
, pp. 684-687
-
-
Johansen, C.T.1
-
27
-
-
38649132270
-
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
-
Kathiresan S., et al. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat. Genet. 2008, 40(2):189-197.
-
(2008)
Nat. Genet.
, vol.40
, Issue.2
, pp. 189-197
-
-
Kathiresan, S.1
-
28
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S., et al. Common variants at 30 loci contribute to polygenic dyslipidemia. Nat. Genet. 2009, 41(1):56-65.
-
(2009)
Nat. Genet.
, vol.41
, Issue.1
, pp. 56-65
-
-
Kathiresan, S.1
-
29
-
-
0035923516
-
Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein
-
Kawaguchi T., et al. Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein. Proc. Natl. Acad. Sci. U. S. A. 2001, 98(24):13710-13715.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, Issue.24
, pp. 13710-13715
-
-
Kawaguchi, T.1
-
30
-
-
84891491840
-
Resequencing CETP, LIPC and LIPG Genes in Thai Subjects With Hyperalphalipoproteinemia
-
Khovidhunkit, W., et al., Resequencing CETP, LIPC and LIPG Genes in Thai Subjects With Hyperalphalipoproteinemia. Am. J. Cardiol.
-
Am. J. Cardiol.
-
-
Khovidhunkit, W.1
-
31
-
-
38649084407
-
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides
-
Kooner J.S., et al. Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Nat. Genet. 2008, 40(2):149-151.
-
(2008)
Nat. Genet.
, vol.40
, Issue.2
, pp. 149-151
-
-
Kooner, J.S.1
-
32
-
-
67650566615
-
Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample
-
Lanktree M.B., et al. Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample. J. Lipid Res. 2009, 50(7):1487-1496.
-
(2009)
J. Lipid Res.
, vol.50
, Issue.7
, pp. 1487-1496
-
-
Lanktree, M.B.1
-
33
-
-
34250821108
-
A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence
-
Lou X.Y., et al. A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence. Am. J. Hum. Genet. 2007, 80(6):1125-1137.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, Issue.6
, pp. 1125-1137
-
-
Lou, X.Y.1
-
34
-
-
77950535601
-
Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data
-
Ma, L., et al., Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data. BMC Med. Genet. 11, 55.
-
BMC Med. Genet.
, vol.11
, pp. 55
-
-
Ma, L.1
-
35
-
-
26444617632
-
Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment
-
Marcais C., et al. Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment. J. Clin. Invest. 2005, 115(10):2862-2869.
-
(2005)
J. Clin. Invest.
, vol.115
, Issue.10
, pp. 2862-2869
-
-
Marcais, C.1
-
36
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J., et al. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet. 2007, 39(7):906-913.
-
(2007)
Nat. Genet.
, vol.39
, Issue.7
, pp. 906-913
-
-
Marchini, J.1
-
37
-
-
78649755576
-
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia
-
Musunuru, K., et al., Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia. N. Engl. J. Med. 363(23), 2220-2227.
-
N. Engl. J. Med.
, vol.363
, Issue.23
, pp. 2220-2227
-
-
Musunuru, K.1
-
38
-
-
65549126774
-
Genetic structure of Europeans: a view from the North-East
-
Nelis M., et al. Genetic structure of Europeans: a view from the North-East. PLoS One 2009, 4(5):e5472.
-
(2009)
PLoS One
, vol.4
, Issue.5
, pp. e5472
-
-
Nelis, M.1
-
39
-
-
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 2008, 322(5908):1702-1705.
-
(2008)
Science
, vol.322
, Issue.5908
, pp. 1702-1705
-
-
Pollin, T.I.1
-
40
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S., et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 2007, 81(3):559-575.
-
(2007)
Am. J. Hum. Genet.
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
-
41
-
-
84877642474
-
The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population
-
Radovica I., et al. The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population. PLoS One 2013, 8(5):e64191.
-
(2013)
PLoS One
, vol.8
, Issue.5
, pp. e64191
-
-
Radovica, I.1
-
42
-
-
67649367650
-
Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study
-
Ridker P.M., et al. Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study. Circ. Cardiovasc. Genet. 2009, 2(1):26-33.
-
(2009)
Circ. Cardiovasc. Genet.
, vol.2
, Issue.1
, pp. 26-33
-
-
Ridker, P.M.1
-
43
-
-
58149159573
-
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
-
Sabatti C., et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat. Genet. 2009, 41(1):35-46.
-
(2009)
Nat. Genet.
, vol.41
, Issue.1
, pp. 35-46
-
-
Sabatti, C.1
-
44
-
-
38849166666
-
LDL-cholesterol concentrations: a genome-wide association study
-
Sandhu M.S., et al. LDL-cholesterol concentrations: a genome-wide association study. Lancet 2008, 371(9611):483-491.
-
(2008)
Lancet
, vol.371
, Issue.9611
, pp. 483-491
-
-
Sandhu, M.S.1
-
45
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
Saxena R., et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 2007, 316(5829):1331-1336.
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1331-1336
-
-
Saxena, R.1
-
46
-
-
78149383007
-
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish
-
Shen, H., et al., Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. Arch. Intern. Med. 170(20), 1850-1855.
-
Arch. Intern. Med.
, vol.170
, Issue.20
, pp. 1850-1855
-
-
Shen, H.1
-
47
-
-
0024558892
-
Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100
-
Soria L.F., et al. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100. Proc. Natl. Acad. Sci. U. S. A. 1989, 86(2):587-591.
-
(1989)
Proc. Natl. Acad. Sci. U. S. A.
, vol.86
, Issue.2
, pp. 587-591
-
-
Soria, L.F.1
-
48
-
-
77952343394
-
Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study
-
Suchindran, S., et al., Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. PLoS Genet. 6(4), e1000928.
-
PLoS Genet.
, vol.6
, Issue.4
, pp. e1000928
-
-
Suchindran, S.1
-
49
-
-
4544381909
-
Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol
-
Thompson J.F., et al. Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol. Clin. Genet. 2004, 66(3):223-228.
-
(2004)
Clin. Genet.
, vol.66
, Issue.3
, pp. 223-228
-
-
Thompson, J.F.1
-
50
-
-
20444426225
-
CETP polymorphisms associated with HDL cholesterol may differ from those associated with cardiovascular disease
-
Thompson J.F., et al. CETP polymorphisms associated with HDL cholesterol may differ from those associated with cardiovascular disease. Atherosclerosis 2005, 181(1):45-53.
-
(2005)
Atherosclerosis
, vol.181
, Issue.1
, pp. 45-53
-
-
Thompson, J.F.1
-
51
-
-
33846893443
-
High-density genotyping and functional SNP localization in the CETP gene
-
Thompson J.F., et al. High-density genotyping and functional SNP localization in the CETP gene. J. Lipid Res. 2007, 48(2):434-443.
-
(2007)
J. Lipid Res.
, vol.48
, Issue.2
, pp. 434-443
-
-
Thompson, J.F.1
-
52
-
-
0018341195
-
Polymorphism of apolipoprotein E II. Genetics of hyperlipoproteinemia type III
-
Utermann G., et al. Polymorphism of apolipoprotein E II. Genetics of hyperlipoproteinemia type III. Clin. Genet. 1979, 15(1):37-62.
-
(1979)
Clin. Genet.
, vol.15
, Issue.1
, pp. 37-62
-
-
Utermann, G.1
-
53
-
-
85013842944
-
-
Elsevier, Amsterdam, Boston.
-
Vance D.E., Vance J.E. Biochemistry of Lipids, Lipoproteins and Membranes 2008, Elsevier, Amsterdam, Boston, (631 pp.). 5th ed.
-
(2008)
Biochemistry of Lipids, Lipoproteins and Membranes
, pp. 631
-
-
Vance, D.E.1
Vance, J.E.2
-
54
-
-
38749149611
-
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia
-
Wallace C., et al. Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Am. J. Hum. Genet. 2008, 82(1):139-149.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, Issue.1
, pp. 139-149
-
-
Wallace, C.1
-
55
-
-
78149245489
-
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
-
Waterworth, D.M. et al., Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Arterioscler. Thromb. Vasc. Biol. 30(11), 2264-2276.
-
Arterioscler. Thromb. Vasc. Biol.
, vol.30
, Issue.11
, pp. 2264-2276
-
-
Waterworth, D.M.1
-
56
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer C.J., et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat. Genet. 2008, 40(2):161-169.
-
(2008)
Nat. Genet.
, vol.40
, Issue.2
, pp. 161-169
-
-
Willer, C.J.1
-
58
-
-
0026783677
-
Candidate proto-oncogene bcl-3 encodes a subunit-specific inhibitor of transcription factor NF-kappa B
-
Wulczyn F.G., Naumann M., Scheidereit C. Candidate proto-oncogene bcl-3 encodes a subunit-specific inhibitor of transcription factor NF-kappa B. Nature 1992, 358(6387):597-599.
-
(1992)
Nature
, vol.358
, Issue.6387
, pp. 597-599
-
-
Wulczyn, F.G.1
Naumann, M.2
Scheidereit, C.3
|