-
1
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
Helgadottir A, Thorleifsson G, Manolescu A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007; 316:1491-1493
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
-
2
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
McPherson R, Pertsemlidis A, Kavaslar N, et al. A common allele on chromosome 9 associated with coronary heart disease. Science 2007; 316:1488-1491
-
(2007)
Science
, vol.316
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
-
3
-
-
34547623750
-
Genome-wide association analysis of coronary artery disease
-
Samani NJ, Erdmann J, Hall AS, et al. Genome-wide association analysis of coronary artery disease. N Engl J Med 2007; 357:443-453
-
(2007)
N Engl J Med
, vol.357
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
-
4
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
WTCCC
-
WTCCC. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447:661-678
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
5
-
-
61349137526
-
2-LPA gene cluster as a risk locus for coronary artery disease
-
2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 2009; 41:283-285
-
(2009)
Nat Genet
, vol.41
, pp. 283-285
-
-
Tregouet, D.A.1
Konig, I.R.2
Erdmann, J.3
-
6
-
-
61349177857
-
New susceptibility locus for coronary artery disease on chromosome 3q22.3
-
Erdmann J, Grosshennig A, Braund PS, et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009; 41:280-282
-
(2009)
Nat Genet
, vol.41
, pp. 280-282
-
-
Erdmann, J.1
Grosshennig, A.2
Braund, P.S.3
-
8
-
-
79251619566
-
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies
-
Reilly MP, Li M, He J, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: Two genome-wide association studies. Lancet 2011; 377:383-392
-
(2011)
Lancet
, vol.377
, pp. 383-392
-
-
Reilly, M.P.1
Li, M.2
He, J.3
-
9
-
-
79953221100
-
A genome-wide association study in europeans and south asians identifies five new loci for coronary artery disease
-
Coronary Artery Disease (C4D). Genetics Consortium
-
Coronary Artery Disease (C4D) Genetics Consortium. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet 2011; 43:339-344
-
(2011)
Nat Genet
, vol.43
, pp. 339-344
-
-
-
10
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Schunkert H, Konig IR, Kathiresan S, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011; 43:333-338
-
(2011)
Nat Genet
, vol.43
, pp. 333-338
-
-
Schunkert, H.1
Konig, I.R.2
Kathiresan, S.3
-
11
-
-
80052733701
-
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease
-
Wild PS, Zeller T, Schillert A, et al. A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ Cardiovasc Genet 2011; 4:403-412
-
(2011)
Circ Cardiovasc Genet
, vol.4
, pp. 403-412
-
-
Wild, P.S.1
Zeller, T.2
Schillert, A.3
-
12
-
-
82555194123
-
Two-marker association tests yield new disease associations for coronary artery disease and hypertension
-
Slavin TP, Feng T, Schnell A, et al. Two-marker association tests yield new disease associations for coronary artery disease and hypertension. Hum Genet 2011; 130:725-733
-
(2011)
Hum Genet
, vol.130
, pp. 725-733
-
-
Slavin, T.P.1
Feng, T.2
Schnell, A.3
-
13
-
-
84857192818
-
Genome-wide association study of coronary artery disease in the Japanese
-
Takeuchi F, Yokota M, Yamamoto K, et al. Genome-wide association study of coronary artery disease in the Japanese. Eur J Hum Genet 2012; 20:333-340
-
(2012)
Eur J Hum Genet
, vol.20
, pp. 333-340
-
-
Takeuchi, F.1
Yokota, M.2
Yamamoto, K.3
-
14
-
-
84860790053
-
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex
-
Davies RW, Wells GA, Stewart AF, et al. A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Circ Cardiovasc Genet 2012; 5:217-225
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 217-225
-
-
Davies, R.W.1
Wells, G.A.2
Stewart, A.F.3
-
15
-
-
84862682331
-
Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis
-
Hager J, Kamatani Y, Cazier JB, et al. Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis. PLoS One 2012; 7:e38663
-
(2012)
PLoS One
, vol.7
-
-
Hager, J.1
Kamatani, Y.2
Cazier, J.B.3
-
16
-
-
84864407698
-
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
-
Lu X, Wang L, Chen S, et al. Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat Genet 2012; 44:890-894
-
(2012)
Nat Genet
, vol.44
, pp. 890-894
-
-
Lu, X.1
Wang, L.2
Chen, S.3
-
17
-
-
84875467239
-
A genome-wide association study of a coronary artery disease risk variant
-
Lee JY, Lee BS, Shin DJ, et al. A genome-wide association study of a coronary artery disease risk variant. J Hum Genet 2013; 58:120-126
-
(2013)
J Hum Genet
, vol.58
, pp. 120-126
-
-
Lee, J.Y.1
Lee, B.S.2
Shin, D.J.3
-
18
-
-
84871969762
-
Large-scale association analysis identifies new risk loci for coronary artery disease
-
CARDIoGRAMplusC4D Consortium
-
CARDIoGRAMplusC4D Consortium. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet 2013; 45:25-33
-
(2013)
Nat Genet
, vol.45
, pp. 25-33
-
-
-
19
-
-
70749096913
-
Genome-wide association of earlyonset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan S, Voight BF, Purcell S, et al. Genome-wide association of earlyonset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009; 41:334-341
-
(2009)
Nat Genet
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
-
20
-
-
79251608213
-
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
-
Aoki A, Ozaki K, Sato H, et al. SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population. J Hum Genet 2011; 56:47-51
-
(2011)
J Hum Genet
, vol.56
, pp. 47-51
-
-
Aoki, A.1
Ozaki, K.2
Sato, H.3
-
21
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci U S A 2009; 106:9362-9367
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
-
22
-
-
77950221224
-
Advances in genomic analysis of stroke: What have we learned and where are we headed
-
Lanktree MB, Dichgans M, Hegele RA. Advances in genomic analysis of stroke: What have we learned and where are we headed? Stroke 2010; 41:825-832
-
(2010)
Stroke
, vol.41
, pp. 825-832
-
-
Lanktree, M.B.1
Dichgans, M.2
Hegele, R.A.3
-
23
-
-
84860862315
-
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-Analysis of 21 genome-wide association studies
-
Murabito JM, White CC, Kavousi M, et al. Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-Analysis of 21 genome-wide association studies. Circ Cardiovasc Genet 2012; 5:100-112
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 100-112
-
-
Murabito, J.M.1
White, C.C.2
Kavousi, M.3
-
24
-
-
77956327982
-
Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export
-
Kjolby M, Andersen OM, Breiderhoff T, et al. Sort1, encoded by the cardiovascular risk locus 1p13.3, is a regulator of hepatic lipoprotein export. Cell Metab 2010; 12:213-223
-
(2010)
Cell Metab
, vol.12
, pp. 213-223
-
-
Kjolby, M.1
Andersen, O.M.2
Breiderhoff, T.3
-
25
-
-
73649141739
-
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease
-
Linsel-Nitschke P, Heeren J, Aherrahrou Z, et al. Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 2010; 208:183-189
-
(2010)
Atherosclerosis
, vol.208
, pp. 183-189
-
-
Linsel-Nitschke, P.1
Heeren, J.2
Aherrahrou, Z.3
-
26
-
-
77955499945
-
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
-
Musunuru K, Strong A, Frank-Kamenetsky M, et al. From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature 2010; 466:714-719
-
(2010)
Nature
, vol.466
, pp. 714-719
-
-
Musunuru, K.1
Strong, A.2
Frank-Kamenetsky, M.3
-
27
-
-
84864759987
-
Hepatic sortilin regulates both apolipoprotein B secretion and LDL catabolism
-
Strong A, Ding Q, Edmondson AC, et al. Hepatic sortilin regulates both apolipoprotein B secretion and LDL catabolism. J Clin Invest 2012; 122:2807-2816
-
(2012)
J Clin Invest
, vol.122
, pp. 2807-2816
-
-
Strong, A.1
Ding, Q.2
Edmondson, A.C.3
-
28
-
-
78649246183
-
Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease
-
Folkersen L, van't Hooft F, Chernogubova E, et al. Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease. Circ Cardiovasc Genet 2010; 3:365-373
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 365-373
-
-
Folkersen, L.1
Van't Hooft, F.2
Chernogubova, E.3
-
29
-
-
77956637896
-
Genetics and beyond-The transcriptome of human monocytes and disease susceptibility
-
Zeller T, Wild P, Szymczak S, et al. Genetics and beyond-The transcriptome of human monocytes and disease susceptibility. PLoS One 2010; 5:e10693
-
(2010)
PLoS One
, vol.5
-
-
Zeller, T.1
Wild, P.2
Szymczak, S.3
-
30
-
-
84856136800
-
Recent studies of the human chromosome 9p21 locus, which is associated with atherosclerosis in human populations
-
Holdt LM, Teupser D. Recent studies of the human chromosome 9p21 locus, which is associated with atherosclerosis in human populations. Arterioscler Thromb Vasc Biol 2012; 32:196-206
-
(2012)
Arterioscler Thromb Vasc Biol
, vol.32
, pp. 196-206
-
-
Holdt, L.M.1
Teupser, D.2
-
31
-
-
84856068773
-
9p21 and the genetic revolution for coronary artery disease
-
Roberts R, Stewart AF. 9p21 and the genetic revolution for coronary artery disease. Clin Chem 2012; 58:104-112
-
(2012)
Clin Chem
, vol.58
, pp. 104-112
-
-
Roberts, R.1
Stewart, A.F.2
-
32
-
-
83055161438
-
New gene functions in megakaryopoiesis and platelet formation
-
Gieger C, Radhakrishnan A, Cvejic A, et al. New gene functions in megakaryopoiesis and platelet formation. Nature 2011; 480:201-208
-
(2011)
Nature
, vol.480
, pp. 201-208
-
-
Gieger, C.1
Radhakrishnan, A.2
Cvejic, A.3
-
33
-
-
77954164213
-
A genome-wide association study of optic disc parameters
-
Ramdas WD, van Koolwijk LM, Ikram MK, et al. A genome-wide association study of optic disc parameters. PLoS Genet 2010; 6:e1000978
-
(2010)
PLoS Genet
, vol.6
-
-
Ramdas, W.D.1
Van Koolwijk, L.M.2
Ikram, M.K.3
-
34
-
-
79959793196
-
Chromosome 7p11.2 (EGFR) variation influences glioma risk
-
Sanson M, Hosking FJ, Shete S, et al. Chromosome 7p11.2 (EGFR) variation influences glioma risk. Hum Mol Genet 2011; 20:2897-2904
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2897-2904
-
-
Sanson, M.1
Hosking, F.J.2
Shete, S.3
-
35
-
-
84860556002
-
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
-
Wiggs JL, Yaspan BL, Hauser MA, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet 2012; 8:e1002654
-
(2012)
PLoS Genet
, vol.8
-
-
Wiggs, J.L.1
Yaspan, B.L.2
Hauser, M.A.3
-
36
-
-
77954143076
-
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci
-
Bei JX, Li Y, Jia WH, et al. A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. Nat Genet 2010; 42:599-603
-
(2010)
Nat Genet
, vol.42
, pp. 599-603
-
-
Bei, J.X.1
Li, Y.2
Jia, W.H.3
-
37
-
-
77952887426
-
Genome-wide association study identifies five new breast cancer susceptibility loci
-
Turnbull C, Ahmed S, Morrison J, et al. Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet 2010; 42:504-507
-
(2010)
Nat Genet
, vol.42
, pp. 504-507
-
-
Turnbull, C.1
Ahmed, S.2
Morrison, J.3
-
38
-
-
77951768060
-
Genome-wide association study of intracranial aneurysm identifies three new risk loci
-
Yasuno K, Bilguvar K, Bijlenga P, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010; 42:420-425
-
(2010)
Nat Genet
, vol.42
, pp. 420-425
-
-
Yasuno, K.1
Bilguvar, K.2
Bijlenga, P.3
-
39
-
-
77955087088
-
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese
-
Uno S, Zembutsu H, Hirasawa A, et al. A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. Nat Genet 2010; 42:707-710
-
(2010)
Nat Genet
, vol.42
, pp. 707-710
-
-
Uno, S.1
Zembutsu, H.2
Hirasawa, A.3
-
40
-
-
84155163079
-
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction
-
O'Donnell CJ, Kavousi M, Smith AV, et al. Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 2011; 124:2855-2864
-
(2011)
Circulation
, vol.124
, pp. 2855-2864
-
-
O'Donnell, C.J.1
Kavousi, M.2
Smith, A.V.3
-
41
-
-
42349106044
-
Meta-Analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
-
Zeggini E, Scott LJ, Saxena R, et al. Meta-Analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008; 40:638-645
-
(2008)
Nat Genet
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
-
42
-
-
84862976129
-
Genome-wide association analysis identifies susceptibility loci for migraine without aura
-
Freilinger T, Anttila V, de Vries B, et al. Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat Genet 2012; 44:777-782
-
(2012)
Nat Genet
, vol.44
, pp. 777-782
-
-
Freilinger, T.1
Anttila, V.2
De Vries, B.3
-
43
-
-
35748963239
-
Genome-wide association with bone mass and geometry in the framingham heart study
-
Kiel DP, Demissie S, Dupuis J, et al. Genome-wide association with bone mass and geometry in the Framingham Heart Study. BMC Med Genet 2007; 8 (Suppl 1):S1
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Kiel, D.P.1
Demissie, S.2
Dupuis, J.3
-
44
-
-
84868592524
-
Genome-wide linkage and association scans for pulse pressure in Chinese twins
-
Zhang D, Pang Z, Li S, et al. Genome-wide linkage and association scans for pulse pressure in Chinese twins. Hypertens Res 2012; 35:1051-1057
-
(2012)
Hypertens Res
, vol.35
, pp. 1051-1057
-
-
Zhang, D.1
Pang, Z.2
Li, S.3
-
45
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature 2010; 466:707-713
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
-
46
-
-
77951766263
-
New loci associated with kidney function and chronic kidney disease
-
Kottgen A, Pattaro C, Boger CA, et al. New loci associated with kidney function and chronic kidney disease. Nat Genet 2010; 42:376-384
-
(2010)
Nat Genet
, vol.42
, pp. 376-384
-
-
Kottgen, A.1
Pattaro, C.2
Boger, C.A.3
-
47
-
-
79151477241
-
Genome-wide association study of recurrent early-onset major depressive disorder
-
Shi J, Potash JB, Knowles JA, et al. Genome-wide association study of recurrent early-onset major depressive disorder. Mol Psychiatry 2011; 16:193-201
-
(2011)
Mol Psychiatry
, vol.16
, pp. 193-201
-
-
Shi, J.1
Potash, J.B.2
Knowles, J.A.3
-
48
-
-
33750030758
-
The regulation of INK4/ARF in cancer and aging
-
Kim WY, Sharpless NE. The regulation of INK4/ARF in cancer and aging. Cell 2006; 127:265-275
-
(2006)
Cell
, vol.127
, pp. 265-275
-
-
Kim, W.Y.1
Sharpless, N.E.2
-
49
-
-
79151486394
-
Expression of Chr9p21 genes CDKN2B (p15(INK4b)), CDKN2A (p16(INK4a), p14(ARF)) and MTAP in human atherosclerotic plaque
-
Holdt LM, Sass K, Gabel G, et al. Expression of Chr9p21 genes CDKN2B (p15(INK4b)), CDKN2A (p16(INK4a), p14(ARF)) and MTAP in human atherosclerotic plaque. Atherosclerosis 2011; 214:264-270
-
(2011)
Atherosclerosis
, vol.214
, pp. 264-270
-
-
Holdt, L.M.1
Sass, K.2
Gabel, G.3
-
50
-
-
84867276514
-
Effect of 9p21.3 coronary artery disease locus neighboring genes on atherosclerosis in mice
-
Kim JB, Deluna A, Mungrue IN, et al. Effect of 9p21.3 coronary artery disease locus neighboring genes on atherosclerosis in mice. Circulation 2012; 126:1896-1906
-
(2012)
Circulation
, vol.126
, pp. 1896-1906
-
-
Kim, J.B.1
Deluna, A.2
Mungrue, I.N.3
-
51
-
-
84871727742
-
Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation
-
Leeper NJ, Raiesdana A, Kojima Y, et al. Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation. Arterioscler Thromb Vasc Biol 2013; 33:e1-e10
-
(2013)
Arterioscler Thromb Vasc Biol
, vol.33
-
-
Leeper, N.J.1
Raiesdana, A.2
Kojima, Y.3
-
52
-
-
84857031381
-
Increased gene dosage of the Ink4/Arf locus does not attenuate atherosclerosis development in hypercholesterolaemic mice
-
Fuster JJ, Molina-Sanchez P, Jovani D, et al. Increased gene dosage of the Ink4/Arf locus does not attenuate atherosclerosis development in hypercholesterolaemic mice. Atherosclerosis 2012; 221:98-105
-
(2012)
Atherosclerosis
, vol.221
, pp. 98-105
-
-
Fuster, J.J.1
Molina-Sanchez, P.2
Jovani, D.3
-
53
-
-
80054951104
-
Cdkn2a is an atherosclerosis modifier locus that regulates monocyte/macrophage proliferation
-
Kuo CL, Murphy AJ, Sayers S, et al. Cdkn2a is an atherosclerosis modifier locus that regulates monocyte/macrophage proliferation. Arterioscler Thromb Vasc Biol 2011; 31:2483-2492
-
(2011)
Arterioscler Thromb Vasc Biol
, vol.31
, pp. 2483-2492
-
-
Kuo, C.L.1
Murphy, A.J.2
Sayers, S.3
-
54
-
-
84857696511
-
Bone marrow p16INK4a-deficiency does not modulate obesity, glucose homeostasis or atherosclerosis development
-
Wouters K, Cudejko C, Gijbels MJ, et al. Bone marrow p16INK4a-deficiency does not modulate obesity, glucose homeostasis or atherosclerosis development. PLoS One 2012; 7:e32440
-
(2012)
PLoS One
, vol.7
-
-
Wouters, K.1
Cudejko, C.2
Gijbels, M.J.3
-
55
-
-
78650696753
-
Expression of linear and novel circular forms of an INK4/ARF-Associated noncoding RNA correlates with atherosclerosis risk
-
Burd CE, Jeck WR, Liu Y, et al. Expression of linear and novel circular forms of an INK4/ARF-Associated noncoding RNA correlates with atherosclerosis risk. PLoS Genet 2010; 6:e1001233
-
(2010)
PLoS Genet
, vol.6
-
-
Burd, C.E.1
Jeck, W.R.2
Liu, Y.3
-
56
-
-
77952363272
-
Chromosome 9p21 SNPs associated with multiple disease phenotypes correlate with ANRIL expression
-
Cunnington MS, Santibanez Koref M, Mayosi BM, et al. Chromosome 9p21 SNPs associated with multiple disease phenotypes correlate with ANRIL expression. PLoS Genet 2010; 6:e1000899
-
(2010)
PLoS Genet
, vol.6
-
-
Cunnington, M.S.1
Santibanez Koref, M.2
Mayosi, B.M.3
-
57
-
-
70449555143
-
Relationship between cad risk genotype in the chromosome 9p21 locus and gene expression identification of eight new anril splice variants
-
Folkersen L, Kyriakou T, Goel A, et al. Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants. PLoS One 2009; 4:e7677
-
(2009)
PLoS One
, vol.4
-
-
Folkersen, L.1
Kyriakou, T.2
Goel, A.3
-
58
-
-
77649166974
-
ANRIL expression is associated with atherosclerosis risk at chromosome 9p21
-
Holdt LM, Beutner F, Scholz M, et al. ANRIL expression is associated with atherosclerosis risk at chromosome 9p21. Arterioscler Thromb Vasc Biol 2010; 30:620-627
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 620-627
-
-
Holdt, L.M.1
Beutner, F.2
Scholz, M.3
-
59
-
-
84880799429
-
Alu elements in ANRIL non-coding RNA at chromosome 9p21 modulate atherogenic cell functions through transregulation of gene networks
-
Holdt LM, Hoffmann S, Sass K, et al. Alu elements in ANRIL non-coding RNA at chromosome 9p21 modulate atherogenic cell functions through transregulation of gene networks. PLoS Genet 2013; 9:e1003588
-
(2013)
PLoS Genet
, vol.9
-
-
Holdt, L.M.1
Hoffmann, S.2
Sass, K.3
-
60
-
-
70349569056
-
Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus
-
Jarinova O, Stewart AF, Roberts R, et al. Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus. Arterioscler Thromb Vasc Biol 2009; 29:1671-1677
-
(2009)
Arterioscler Thromb Vasc Biol
, vol.29
, pp. 1671-1677
-
-
Jarinova, O.1
Stewart, A.F.2
Roberts, R.3
-
61
-
-
84874115034
-
Resequencing and clinical associations of the 9p21.3 region: A comprehensive investigation in the Framingham heart study
-
Johnson AD, Hwang SJ, Voorman A, et al. Resequencing and clinical associations of the 9p21.3 region: A comprehensive investigation in the Framingham heart study. Circulation 2013; 127:799-810
-
(2013)
Circulation
, vol.127
, pp. 799-810
-
-
Johnson, A.D.1
Hwang, S.J.2
Voorman, A.3
-
62
-
-
64549083268
-
INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis
-
Liu Y, Sanoff HK, Cho H, et al. INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis. PLoS One 2009; 4:e5027
-
(2009)
PLoS One
, vol.4
-
-
Liu, Y.1
Sanoff, H.K.2
Cho, H.3
-
63
-
-
79951473520
-
9p21 DNA variants associated with coronary artery disease impair interferon-gamma signalling response
-
Harismendy O, Notani D, Song X, et al. 9p21 DNA variants associated with coronary artery disease impair interferon-gamma signalling response. Nature 2011; 470:264-268
-
(2011)
Nature
, vol.470
, pp. 264-268
-
-
Harismendy, O.1
Notani, D.2
Song, X.3
-
64
-
-
84863421652
-
CVD-Associated noncoding RNA, ANRIL, modulates expression of atherogenic pathways in VSMC
-
Congrains A, Kamide K, Katsuya T, et al. CVD-Associated noncoding RNA, ANRIL, modulates expression of atherogenic pathways in VSMC. Biochem Biophys Res Commun 2012; 419:612-616
-
(2012)
Biochem Biophys Res Commun
, vol.419
, pp. 612-616
-
-
Congrains, A.1
Kamide, K.2
Katsuya, T.3
-
65
-
-
84855976300
-
Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B
-
Congrains A, Kamide K, Oguro R, et al. Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B. Atherosclerosis 2012; 220:449-455
-
(2012)
Atherosclerosis
, vol.220
, pp. 449-455
-
-
Congrains, A.1
Kamide, K.2
Oguro, R.3
-
66
-
-
79955468280
-
Long noncoding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene
-
Kotake Y, Nakagawa T, Kitagawa K, et al. Long noncoding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene. Oncogene 2011; 30:1956-1962
-
(2011)
Oncogene
, vol.30
, pp. 1956-1962
-
-
Kotake, Y.1
Nakagawa, T.2
Kitagawa, K.3
-
67
-
-
77953096072
-
Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a
-
Yap KL, Li S, Munoz-Cabello AM, et al. Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a. Mol Cell 2010; 38:662-674
-
(2010)
Mol Cell
, vol.38
, pp. 662-674
-
-
Yap, K.L.1
Li, S.2
Munoz-Cabello, A.M.3
-
68
-
-
78649339069
-
Long noncoding RNA in genome regulation: Prospects and mechanisms
-
Hung T, Chang HY. Long noncoding RNA in genome regulation: Prospects and mechanisms. RNA Biol 2010; 7:582-585
-
(2010)
RNA Biol
, vol.7
, pp. 582-585
-
-
Hung, T.1
Chang, H.Y.2
-
69
-
-
84871069553
-
Epigenetic regulation by long noncoding RNAs
-
Lee JT. Epigenetic regulation by long noncoding RNAs. Science 2012; 338:1435-1439
-
(2012)
Science
, vol.338
, pp. 1435-1439
-
-
Lee, J.T.1
-
70
-
-
80053118688
-
Long noncoding RNAs and human disease
-
21, pg 354, 2011
-
Wapinski O, Chang HY. Long noncoding RNAs and human disease (vol 21, pg 354, 2011). Trends in Cell Biology 2011; 21:561-1561
-
(2011)
Trends in Cell Biology
, vol.21
, pp. 561-1561
-
-
Wapinski, O.1
Chang, H.Y.2
-
71
-
-
67649982750
-
High levels of dRYBP induce apoptosis in Drosophila imaginal cells through the activation of reaper and the requirement of trithorax, dredd and dFADD
-
Gonzalez I, Busturia A. High levels of dRYBP induce apoptosis in Drosophila imaginal cells through the activation of reaper and the requirement of trithorax, dredd and dFADD. Cell Res 2009; 19:747-757
-
(2009)
Cell Res
, vol.19
, pp. 747-757
-
-
Gonzalez, I.1
Busturia, A.2
-
72
-
-
84875212339
-
Essential and unexpected role of YY1 to promote mesodermal cardiac differentiation
-
Gregoire S, Karra R, Passer D, et al. Essential and unexpected role of YY1 to promote mesodermal cardiac differentiation. Circ Res 2013; 112:900-910
-
(2013)
Circ Res
, vol.112
, pp. 900-910
-
-
Gregoire, S.1
Karra, R.2
Passer, D.3
-
73
-
-
77956315255
-
ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1
-
Sato K, Nakagawa H, Tajima A, et al. ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1. Oncol Rep 2010; 24:701-707
-
(2010)
Oncol Rep
, vol.24
, pp. 701-707
-
-
Sato, K.1
Nakagawa, H.2
Tajima, A.3
-
74
-
-
0019868389
-
Base sequence studies of 300 nucleotide renatured repeated human DNA clones
-
Deininger PL, Jolly DJ, Rubin CM, et al. Base sequence studies of 300 nucleotide renatured repeated human DNA clones. J Mol Biol 1981; 151:17-33
-
(1981)
J Mol Biol
, vol.151
, pp. 17-33
-
-
Deininger, P.L.1
Jolly, D.J.2
Rubin, C.M.3
-
75
-
-
84862004740
-
Visualising individual sequencespecific protein-DNA interactions in situ
-
Weibrecht I, Gavrilovic M, Lindbom L, et al. Visualising individual sequencespecific protein-DNA interactions in situ. N Biotechnol 2012; 29:589-598
-
(2012)
N Biotechnol
, vol.29
, pp. 589-598
-
-
Weibrecht, I.1
Gavrilovic, M.2
Lindbom, L.3
-
76
-
-
84872531655
-
Circular RNAs are abundant, conserved, and associated with ALU repeats
-
Jeck WR, Sorrentino JA, Wang K, et al. Circular RNAs are abundant, conserved, and associated with ALU repeats. RNA 2013; 19:141-157
-
(2013)
RNA
, vol.19
, pp. 141-157
-
-
Jeck, W.R.1
Sorrentino, J.A.2
Wang, K.3
-
77
-
-
0034739882
-
Prediction of the coding sequences of unidentified human genes XIX The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro
-
Nagase T, Kikuno R, Hattori A, et al. Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. DNA Res 2000; 7:347-355
-
(2000)
DNA Res
, vol.7
, pp. 347-355
-
-
Nagase, T.1
Kikuno, R.2
Hattori, A.3
-
78
-
-
2342617354
-
Phactrs 1-4: A family of protein phosphatase 1 and actin regulatory proteins
-
Allen PB, Greenfield AT, Svenningsson P, et al. Phactrs 1-4: A family of protein phosphatase 1 and actin regulatory proteins. Proc Natl Acad Sci U S A 2004; 101:7187-7192
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 7187-7192
-
-
Allen, P.B.1
Greenfield, A.T.2
Svenningsson, P.3
-
79
-
-
84872773091
-
Structural basis for protein phosphatase 1 regulation and specificity
-
Peti W, Nairn AC, Page R. Structural basis for protein phosphatase 1 regulation and specificity. FEBS J 2013; 280:596-611
-
(2013)
FEBS J
, vol.280
, pp. 596-611
-
-
Peti, W.1
Nairn, A.C.2
Page, R.3
-
80
-
-
84876890415
-
MicroRNA-584 and the protein phosphatase and actin regulator 1 (PHACTR1), a new signaling route through which transforming growth factor-beta mediates the migration and actin dynamics of breast cancer cells
-
Fils-Aime N, Dai M, Guo J, et al. MicroRNA-584 and the protein phosphatase and actin regulator 1 (PHACTR1), a new signaling route through which transforming growth factor-beta mediates the migration and actin dynamics of breast cancer cells. J Biol Chem 2013; 288:11807-11823
-
(2013)
J Biol Chem
, vol.288
, pp. 11807-11823
-
-
Fils-Aime, N.1
Dai, M.2
Guo, J.3
-
81
-
-
84868584901
-
G-Actin regulates the shuttling and PP1 binding of the RPEL protein Phactr1 to control actomyosin assembly
-
Wiezlak M, Diring J, Abella J, et al. G-Actin regulates the shuttling and PP1 binding of the RPEL protein Phactr1 to control actomyosin assembly. J Cell Sci 2012; 125:5860-5872
-
(2012)
J Cell Sci
, vol.125
, pp. 5860-5872
-
-
Wiezlak, M.1
Diring, J.2
Abella, J.3
-
82
-
-
80755132107
-
Neuropilin-1 regulates a new VEGFinduced gene, Phactr-1, which controls tubulogenesis and modulates lamellipodial dynamics in human endothelial cells
-
Allain B, Jarray R, Borriello L, et al. Neuropilin-1 regulates a new VEGFinduced gene, Phactr-1, which controls tubulogenesis and modulates lamellipodial dynamics in human endothelial cells. Cell Signal 2012; 24:214-223
-
(2012)
Cell Signal
, vol.24
, pp. 214-223
-
-
Allain, B.1
Jarray, R.2
Borriello, L.3
-
83
-
-
80052081312
-
Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis
-
Jarray R, Allain B, Borriello L, et al. Depletion of the novel protein PHACTR-1 from human endothelial cells abolishes tube formation and induces cell death receptor apoptosis. Biochimie 2011; 93:1668-1675
-
(2011)
Biochimie
, vol.93
, pp. 1668-1675
-
-
Jarray, R.1
Allain, B.2
Borriello, L.3
-
84
-
-
38649132270
-
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
-
Kathiresan S, Melander O, Guiducci C, et al. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet 2008; 40:189-197
-
(2008)
Nat Genet
, vol.40
, pp. 189-197
-
-
Kathiresan, S.1
Melander, O.2
Guiducci, C.3
-
85
-
-
38849166666
-
LDL-cholesterol concentrations: A genome-wide association study
-
Sandhu MS, Waterworth DM, Debenham SL, et al. LDL-cholesterol concentrations: A genome-wide association study. Lancet 2008; 371:483-491
-
(2008)
Lancet
, vol.371
, pp. 483-491
-
-
Sandhu, M.S.1
Waterworth, D.M.2
Debenham, S.L.3
-
86
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer CJ, Sanna S, Jackson AU, et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 2008; 40:161-169
-
(2008)
Nat Genet
, vol.40
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
-
87
-
-
45149108420
-
Mapping the genetic architecture of gene expression in human liver
-
Schadt EE, Molony C, Chudin E, et al. Mapping the genetic architecture of gene expression in human liver. PLoS Biol 2008; 6:e107
-
(2008)
PLoS Biol
, vol.6
-
-
Schadt, E.E.1
Molony, C.2
Chudin, E.3
-
89
-
-
56549111118
-
VPS10P-domain receptors-regulators of neuronal viability and function
-
Willnow TE, Petersen CM, Nykjaer A. VPS10P-domain receptors-regulators of neuronal viability and function. Nat Rev Neurosci 2008; 9:899-909
-
(2008)
Nat Rev Neurosci
, vol.9
, pp. 899-909
-
-
Willnow, T.E.1
Petersen, C.M.2
Nykjaer, A.3
-
90
-
-
84869497619
-
Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia
-
Tveten K, Strom TB, Cameron J, et al. Mutations in the SORT1 gene are unlikely to cause autosomal dominant hypercholesterolemia. Atherosclerosis 2012; 225:370-375
-
(2012)
Atherosclerosis
, vol.225
, pp. 370-375
-
-
Tveten, K.1
Strom, T.B.2
Cameron, J.3
|