-
1
-
-
0032510639
-
Prediction of coronary heart disease using risk factor categories
-
COI: 1:STN:280:DyaK1c3msVOjsA%3D%3D
-
Wilson PW, D’Agostino RB, Levy D, Belanger AM, Silbershatz H, Kannel WB. Prediction of coronary heart disease using risk factor categories. Circulation. 1998;97:1837–47.
-
(1998)
Circulation
, vol.97
, pp. 1837-1847
-
-
Wilson, P.W.1
D’Agostino, R.B.2
Levy, D.3
Belanger, A.M.4
Silbershatz, H.5
Kannel, W.B.6
-
2
-
-
47149088261
-
Predicting cardiovascular risk in England and Wales: prospective derivation and validation of QRISK2
-
Hippisley-Cox J, Coupland C, Vinogradova Y, Robson J, Minhas R, Sheikh A, et al. Predicting cardiovascular risk in England and Wales: prospective derivation and validation of QRISK2. BMJ. 2008;336:1475–82.
-
(2008)
BMJ
, vol.336
, pp. 1475-1482
-
-
Hippisley-Cox, J.1
Coupland, C.2
Vinogradova, Y.3
Robson, J.4
Minhas, R.5
Sheikh, A.6
-
3
-
-
84896829244
-
Should patients with acute coronary disease be stratified for management according to their risk? Derivation, external validation and outcomes using the updated GRACE risk score
-
Fox KAA, Fitzgerald G, Puymirat E, Huang W, Carruthers K, Simon T, et al. Should patients with acute coronary disease be stratified for management according to their risk? Derivation, external validation and outcomes using the updated GRACE risk score. BMJ Open. 2014;4:e004425.
-
(2014)
BMJ Open
, vol.4
, pp. 004425
-
-
Fox, K.A.A.1
Fitzgerald, G.2
Puymirat, E.3
Huang, W.4
Carruthers, K.5
Simon, T.6
-
5
-
-
70450081001
-
Major lipids, apolipoproteins, and risk of vascular disease
-
Di Angelantonio E, Sarwar N, Perry P, Kaptoge S, Ray KK, Thompson A, et al. Major lipids, apolipoproteins, and risk of vascular disease. JAMA. 2009;302:1993–2000.
-
(2009)
JAMA
, vol.302
, pp. 1993-2000
-
-
Di Angelantonio, E.1
Sarwar, N.2
Perry, P.3
Kaptoge, S.4
Ray, K.K.5
Thompson, A.6
-
6
-
-
84901808693
-
Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1·25 million people
-
Rapsomaniki E, Timmis A, George J, Pujades-Rodriguez M, Shah AD, Denaxas S, et al. Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1·25 million people. Lancet. 2014;383:1899–911.
-
(2014)
Lancet
, vol.383
, pp. 1899-1911
-
-
Rapsomaniki, E.1
Timmis, A.2
George, J.3
Pujades-Rodriguez, M.4
Shah, A.D.5
Denaxas, S.6
-
7
-
-
73449130797
-
C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysis
-
Kaptoge S, Di Angelantonio E, Lowe G, Pepys MB, Thompson SG, Collins R, et al. C-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysis. Lancet. 2010;375:132–40.
-
(2010)
Lancet
, vol.375
, pp. 132-140
-
-
Kaptoge, S.1
Di Angelantonio, E.2
Lowe, G.3
Pepys, M.B.4
Thompson, S.G.5
Collins, R.6
-
8
-
-
43249118045
-
Long-term interleukin-6 levels and subsequent risk of coronary heart disease: two new prospective studies and a systematic review
-
Danesh J, Kaptoge S, Mann AG, Sarwar N, Wood A, Angleman SB, et al. Long-term interleukin-6 levels and subsequent risk of coronary heart disease: two new prospective studies and a systematic review. PLoS Med. 2008;5:e78.
-
(2008)
PLoS Med
, vol.5
, pp. 78
-
-
Danesh, J.1
Kaptoge, S.2
Mann, A.G.3
Sarwar, N.4
Wood, A.5
Angleman, S.B.6
-
9
-
-
79952260576
-
Diabetes mellitus, fasting glucose, and risk of cause-specific death
-
Seshasai SRK, Kaptoge S, Thompson A, Di Angelantonio E, Gao P, et al. Diabetes mellitus, fasting glucose, and risk of cause-specific death. N Engl J Med. 2011;364:829–41.
-
(2011)
N Engl J Med
, vol.364
, pp. 829-841
-
-
Seshasai, S.R.K.1
Kaptoge, S.2
Thompson, A.3
Di Angelantonio, E.4
Gao, P.5
-
10
-
-
84892772956
-
Residual macrovascular risk in 2013: what have we learned?
-
Fruchart J-C, Davignon J, Hermans MP, Al-Rubeaan K, Amarenco P, Assmann G, et al. Residual macrovascular risk in 2013: what have we learned? Cardiovasc Diabetol. 2014;13:26.
-
(2014)
Cardiovasc Diabetol
, vol.13
, pp. 26
-
-
Fruchart, J.-C.1
Davignon, J.2
Hermans, M.P.3
Al-Rubeaan, K.4
Amarenco, P.5
Assmann, G.6
-
11
-
-
84890461947
-
Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society
-
COI: 1:CAS:528:DC%2BC3sXhvVOqu7vI, Recent European guidance on the clinical management of familial hypercholesterolaemia
-
Nordestgaard BG, Chapman MJ, Humphries SE, Ginsberg HN, Masana L, Descamps OS, et al. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society. Eur Heart J. 2013;34:3478–90a. Recent European guidance on the clinical management of familial hypercholesterolaemia.
-
(2013)
Eur Heart J
, vol.34
, pp. 3478-3490
-
-
Nordestgaard, B.G.1
Chapman, M.J.2
Humphries, S.E.3
Ginsberg, H.N.4
Masana, L.5
Descamps, O.S.6
-
12
-
-
84905437783
-
Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations
-
COI: 1:CAS:528:DC%2BC2cXhslaksrzK
-
Futema M, Plagnol V, Li K, Whittall RA, Neil HAW, Seed M, et al. Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations. J Med Genet. 2014;51:537–44.
-
(2014)
J Med Genet
, vol.51
, pp. 537-544
-
-
Futema, M.1
Plagnol, V.2
Li, K.3
Whittall, R.A.4
Neil, H.A.W.5
Seed, M.6
-
13
-
-
84907140876
-
Mutations in STAP1 are associated with autosomal dominant hypercholesterolemia
-
COI: 1:CAS:528:DC%2BC2cXhsVeqtrzP, Report of a novel locus responsible for causing familial hypercholesterolaemia
-
Fouchier SW, Dallinga-Thie GM, Meijers JCM, Zelcer N, Kastelein JJP, Defesche JC, et al. Mutations in STAP1 are associated with autosomal dominant hypercholesterolemia. Circ Res. 2014;115:552–5. Report of a novel locus responsible for causing familial hypercholesterolaemia.
-
(2014)
Circ Res
, vol.115
, pp. 552-555
-
-
Fouchier, S.W.1
Dallinga-Thie, G.M.2
Meijers, J.C.M.3
Zelcer, N.4
Kastelein, J.J.P.5
Defesche, J.C.6
-
14
-
-
84893720400
-
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
-
COI: 1:CAS:528:DC%2BC2cXitVyqu78%3D, Demonstration of the use of whole-exome sequencing for investigating genetic determinants of atherosclerosis and coronary heart disease
-
Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang Z-Z, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am J Hum Genet. 2014;94:233–45. Demonstration of the use of whole-exome sequencing for investigating genetic determinants of atherosclerosis and coronary heart disease.
-
(2014)
Am J Hum Genet
, vol.94
, pp. 233-245
-
-
Lange, L.A.1
Hu, Y.2
Zhang, H.3
Xue, C.4
Schmidt, E.M.5
Tang, Z.-Z.6
-
15
-
-
42349112088
-
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
-
COI: 1:CAS:528:DC%2BD1cXkvVOhs7Y%3D, A guide to the development, application and utility of genome-wide association studies
-
McCarthy MI, Abecasis GR, Cardon LR, Goldstein DB, Little J, Ioannidis JPA, et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet. 2008;9:356–69. A guide to the development, application and utility of genome-wide association studies.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.A.6
-
16
-
-
84928309638
-
Jun 30]
-
Hindorff LA, Junkins HA, Hall P, Mehta JP, Manolio TA. A catalog of published genome-wide association studies [Internet]. Cat Publ Genome-Wide Assoc Stud. [cited 2011 Jun 30]. Available from: www.genome.gov/gwastudies.
-
(2011)
Available from:
-
-
-
17
-
-
84871969762
-
Large-scale association analysis identifies new risk loci for coronary artery disease
-
The largest meta-analysis of genome-wide association studies of coronary heart disease published to date
-
Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet. 2012;45:25–33. The largest meta-analysis of genome-wide association studies of coronary heart disease published to date.
-
(2012)
Nat Genet
, vol.45
, pp. 25-33
-
-
Deloukas, P.1
Kanoni, S.2
Willenborg, C.3
Farrall, M.4
Assimes, T.L.5
Thompson, J.R.6
-
18
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
COI: 1:CAS:528:DC%2BD1cXhtl2rsro%3D
-
Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, et al. Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet. 2008;40:161–9.
-
(2008)
Nat Genet
, vol.40
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
Scuteri, A.4
Bonnycastle, L.L.5
Clarke, R.6
-
19
-
-
84903123480
-
Lipoprotein(a) levels, genotype, and incident aortic valve stenosis: a prospective Mendelian randomization study and replication in a case-control cohort
-
COI: 1:CAS:528:DC%2BC2cXht1Smtb7O
-
Arsenault BJ, Boekholdt SM, Dubé M-P, Rhéaume E, Wareham NJ, Khaw K-T, et al. Lipoprotein(a) levels, genotype, and incident aortic valve stenosis: a prospective Mendelian randomization study and replication in a case-control cohort. Circ Cardiovasc Genet. 2014;7:304–10.
-
(2014)
Circ Cardiovasc Genet
, vol.7
, pp. 304-310
-
-
Arsenault, B.J.1
Boekholdt, S.M.2
Dubé, M.-P.3
Rhéaume, E.4
Wareham, N.J.5
Khaw, K.-T.6
-
20
-
-
67049167090
-
Genetically elevated lipoprotein(a) and increased risk of myocardial infarction
-
COI: 1:CAS:528:DC%2BD1MXntFCms7w%3D
-
Kamstrup PR, Tybjaerg-Hansen A, Steffensen R, Nordestgaard BG. Genetically elevated lipoprotein(a) and increased risk of myocardial infarction. JAMA. 2009;301:2331–9.
-
(2009)
JAMA
, vol.301
, pp. 2331-2339
-
-
Kamstrup, P.R.1
Tybjaerg-Hansen, A.2
Steffensen, R.3
Nordestgaard, B.G.4
-
21
-
-
68549124902
-
COL4A1 is associated with arterial stiffness by genome-wide association scan
-
COI: 1:CAS:528:DC%2BD1MXmvVyhtr8%3D
-
Tarasov KV, Sanna S, Scuteri A, Strait JB, Orrù M, Parsa A, et al. COL4A1 is associated with arterial stiffness by genome-wide association scan. Circ Cardiovasc Genet. 2009;2:151–8.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 151-158
-
-
Tarasov, K.V.1
Sanna, S.2
Scuteri, A.3
Strait, J.B.4
Orrù, M.5
Parsa, A.6
-
22
-
-
84928328386
-
-
Swerdlow DI, Holmes MV, Kuchenbaecker KB, Engmann J, Shah T, Sofat R, et al. The interleukin-6 receptor as a potential target for coronary heart disease prevention: evaluation using Mendelian randomisation. Lancet. 2012;2012. A Mendelian randomisation study of the interleukin-6 receptor as a potential therapeutic target in coronary disease, providing evidence that this pathway has a causal role and may hold benefit for disease prevention. Findings were corroborated in a similar study by Sarwar et al., below
-
Swerdlow DI, Holmes MV, Kuchenbaecker KB, Engmann J, Shah T, Sofat R, et al. The interleukin-6 receptor as a potential target for coronary heart disease prevention: evaluation using Mendelian randomisation. Lancet. 2012;2012. A Mendelian randomisation study of the interleukin-6 receptor as a potential therapeutic target in coronary disease, providing evidence that this pathway has a causal role and may hold benefit for disease prevention. Findings were corroborated in a similar study by Sarwar et al., below.
-
-
-
-
23
-
-
84859210770
-
Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies
-
A Mendelian randomisation study of the interleukin-6 receptor as a potential therapeutic target in coronary disease, providing evidence that this pathway has a causal role and may hold benefit for disease prevention. Findings were corroborated in a similar study by Swerdlow et al
-
Sarwar N, Butterworth AS, Freitag DF, Gregson J, Willeit P, Gorman DN, et al. Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies. Lancet. 2012;379:1205–13. A Mendelian randomisation study of the interleukin-6 receptor as a potential therapeutic target in coronary disease, providing evidence that this pathway has a causal role and may hold benefit for disease prevention. Findings were corroborated in a similar study by Swerdlow et al.
-
(2012)
Lancet
, vol.379
, pp. 1205-1213
-
-
Sarwar, N.1
Butterworth, A.S.2
Freitag, D.F.3
Gregson, J.4
Willeit, P.5
Gorman, D.N.6
-
24
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
COI: 1:CAS:528:DC%2BC3sXhsFOitb7O
-
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, et al. Discovery and refinement of loci associated with lipid levels. Nat Genet. 2013;45:1274–83.
-
(2013)
Nat Genet
, vol.45
, pp. 1274-1283
-
-
Willer, C.J.1
Schmidt, E.M.2
Sengupta, S.3
Peloso, G.M.4
Gustafsson, S.5
Kanoni, S.6
-
25
-
-
79953204259
-
-
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. [Internet]. 2011 [cited 2011 Mar 13]
-
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. [Internet]. 2011 [cited 2011 Mar 13]; Available from: http://www.ncbi.nlm.nih.gov/pubmed/21378990.
-
-
-
-
26
-
-
79953221100
-
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
-
COI: 1:CAS:528:DC%2BC3MXivVSms7s%3D
-
Peden JF, Hopewell JC, Saleheen D, Chambers JC, Hager J, Soranzo N, et al. A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet. 2011;43:339–44.
-
(2011)
Nat Genet
, vol.43
, pp. 339-344
-
-
Peden, J.F.1
Hopewell, J.C.2
Saleheen, D.3
Chambers, J.C.4
Hager, J.5
Soranzo, N.6
-
27
-
-
84874115034
-
Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study
-
Johnson AD, Hwang S-J, Voorman A, Morrison A, Peloso GM, Hsu Y-H, 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
Morrison, A.4
Peloso, G.M.5
Hsu, Y.-H.6
-
28
-
-
84856068773
-
9p21 and the genetic revolution for coronary artery disease
-
COI: 1:CAS:528:DC%2BC38XnvFektw%3D%3D
-
Roberts R, Stewart AFR. 9p21 and the genetic revolution for coronary artery disease. Clin Chem. 2012;58:104–12.
-
(2012)
Clin Chem
, vol.58
, pp. 104-112
-
-
Roberts, R.1
Stewart, A.F.R.2
-
29
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
A large genome-wide association study reporting common genetic determinants of blood pressure
-
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011;478:103–9. A large genome-wide association study reporting common genetic determinants of blood pressure.
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
Munroe, P.B.2
Rice, K.M.3
Bochud, M.4
Johnson, A.D.5
-
30
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
COI: 1:CAS:528:DC%2BC3cXht1KmsL%2FN, A very large genome-wide association study reporting novel genetic determinants of obesity-related traits
-
Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010;42:937–48. A very large genome-wide association study reporting novel genetic determinants of obesity-related traits.
-
(2010)
Nat Genet
, vol.42
, pp. 937-948
-
-
Speliotes, E.K.1
Willer, C.J.2
Berndt, S.I.3
Monda, K.L.4
Thorleifsson, G.5
Jackson, A.U.6
-
31
-
-
77951751034
-
Meta-analysis and imputation refines the association of 15q25 with smoking quantity
-
COI: 1:CAS:528:DC%2BC3cXltFKlsro%3D
-
Liu JZ, Tozzi F, Waterworth DM, Pillai SG, Muglia P, Middleton L, et al. Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet. 2010;42:436–40.
-
(2010)
Nat Genet
, vol.42
, pp. 436-440
-
-
Liu, J.Z.1
Tozzi, F.2
Waterworth, D.M.3
Pillai, S.G.4
Muglia, P.5
Middleton, L.6
-
32
-
-
84861636519
-
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
-
COI: 1:CAS:528:DC%2BC38Xmt1GrsLw%3D
-
Ellinor PT, Lunetta KL, Albert CM, Glazer NL, Ritchie MD, Smith AV, et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet. 2012;44:670–5.
-
(2012)
Nat Genet
, vol.44
, pp. 670-675
-
-
Ellinor, P.T.1
Lunetta, K.L.2
Albert, C.M.3
Glazer, N.L.4
Ritchie, M.D.5
Smith, A.V.6
-
33
-
-
77649191092
-
Common variants in KCNN3 are associated with lone atrial fibrillation
-
COI: 1:CAS:528:DC%2BC3cXit1SmtLk%3D
-
Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet. 2010;42:240–4.
-
(2010)
Nat Genet
, vol.42
, pp. 240-244
-
-
Ellinor, P.T.1
Lunetta, K.L.2
Glazer, N.L.3
Pfeufer, A.4
Alonso, A.5
Chung, M.K.6
-
34
-
-
84873918452
-
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts
-
COI: 1:CAS:528:DC%2BC3sXisVKqur0%3D
-
Butler AM, Yin X, Evans DS, Nalls MA, Smith EN, Tanaka T, et al. Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circ Cardiovasc Genet. 2012;5:639–46.
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 639-646
-
-
Butler, A.M.1
Yin, X.2
Evans, D.S.3
Nalls, M.A.4
Smith, E.N.5
Tanaka, T.6
-
35
-
-
84947899543
-
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
-
COI: 1:CAS:528:DC%2BC3cXhsVWmurnM
-
Sotoodehnia N, Isaacs A, de Bakker PIW, Dörr M, Newton-Cheh C, Nolte IM, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat Genet. 2010;42:1068–76.
-
(2010)
Nat Genet
, vol.42
, pp. 1068-1076
-
-
Sotoodehnia, N.1
Isaacs, A.2
de Bakker, P.I.W.3
Dörr, M.4
Newton-Cheh, C.5
Nolte, I.M.6
-
36
-
-
84875931887
-
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
-
COI: 1:CAS:528:DC%2BC3sXltFCgt74%3D
-
Ritchie MD, Denny JC, Zuvich RL, Crawford DC, Schildcrout JS, Bastarache L, et al. Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Circulation. 2013;127:1377–85.
-
(2013)
Circulation
, vol.127
, pp. 1377-1385
-
-
Ritchie, M.D.1
Denny, J.C.2
Zuvich, R.L.3
Crawford, D.C.4
Schildcrout, J.S.5
Bastarache, L.6
-
37
-
-
75749097235
-
Genome-wide association study of PR interval
-
COI: 1:CAS:528:DC%2BC3cXjsVehsA%3D%3D
-
Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, et al. Genome-wide association study of PR interval. Nat Genet. 2010;42:153–9.
-
(2010)
Nat Genet
, vol.42
, pp. 153-159
-
-
Pfeufer, A.1
van Noord, C.2
Marciante, K.D.3
Arking, D.E.4
Larson, M.G.5
Smith, A.V.6
-
38
-
-
75749102498
-
Genetic variation in SCN10A influences cardiac conduction
-
COI: 1:CAS:528:DC%2BC3cXjsVegtg%3D%3D
-
Chambers JC, Zhao J, Terracciano CMN, Bezzina CR, Zhang W, Kaba R, et al. Genetic variation in SCN10A influences cardiac conduction. Nat Genet. 2010;42:149–52.
-
(2010)
Nat Genet
, vol.42
, pp. 149-152
-
-
Chambers, J.C.1
Zhao, J.2
Terracciano, C.M.N.3
Bezzina, C.R.4
Zhang, W.5
Kaba, R.6
-
39
-
-
75749122164
-
Several common variants modulate heart rate, PR interval and QRS duration
-
COI: 1:CAS:528:DC%2BC3cXjsVemtQ%3D%3D
-
Holm H, Gudbjartsson DF, Arnar DO, Thorleifsson G, Thorgeirsson G, Stefansdottir H, et al. Several common variants modulate heart rate, PR interval and QRS duration. Nat Genet. 2010;42:117–22.
-
(2010)
Nat Genet
, vol.42
, pp. 117-122
-
-
Holm, H.1
Gudbjartsson, D.F.2
Arnar, D.O.3
Thorleifsson, G.4
Thorgeirsson, G.5
Stefansdottir, H.6
-
40
-
-
84873884896
-
Impact of ancestry and common genetic variants on QT interval in African Americans
-
Smith JG, Avery CL, Evans DS, Nalls MA, Meng YA, Smith EN, et al. Impact of ancestry and common genetic variants on QT interval in African Americans. Circ Cardiovasc Genet. 2012;5:647–55.
-
(2012)
Circ Cardiovasc Genet
, vol.5
, pp. 647-655
-
-
Smith, J.G.1
Avery, C.L.2
Evans, D.S.3
Nalls, M.A.4
Meng, Y.A.5
Smith, E.N.6
-
41
-
-
41949127122
-
CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart
-
COI: 1:CAS:528:DC%2BD1cXkt1eiu70%3D
-
Chang K-C, Barth AS, Sasano T, Kizana E, Kashiwakura Y, Zhang Y, et al. CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart. Proc Natl Acad Sci. 2008;105:4477–82.
-
(2008)
Proc Natl Acad Sci
, vol.105
, pp. 4477-4482
-
-
Chang, K.-C.1
Barth, A.S.2
Sasano, T.3
Kizana, E.4
Kashiwakura, Y.5
Zhang, Y.6
-
42
-
-
77955868822
-
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
-
COI: 1:CAS:528:DC%2BC3cXpt1aqs78%3D
-
Smith NL, Felix JF, Morrison AC, Demissie S, Glazer NL, Loehr LR, et al. Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Circ Cardiovasc Genet. 2010;3:256–66.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 256-266
-
-
Smith, N.L.1
Felix, J.F.2
Morrison, A.C.3
Demissie, S.4
Glazer, N.L.5
Loehr, L.R.6
-
43
-
-
80052186988
-
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
-
COI: 1:CAS:528:DC%2BC3MXlvVOqtbo%3D
-
Villard E, Perret C, Gary F, Proust C, Dilanian G, Hengstenberg C, et al. A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. Eur Heart J. 2011;32:1065–76.
-
(2011)
Eur Heart J
, vol.32
, pp. 1065-1076
-
-
Villard, E.1
Perret, C.2
Gary, F.3
Proust, C.4
Dilanian, G.5
Hengstenberg, C.6
-
44
-
-
66649106445
-
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study
-
Arnett DK, Li N, Tang W, Rao DC, Devereux RB, Claas SA, et al. Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. BMC Med Genet. 2009;10:43.
-
(2009)
BMC Med Genet
, vol.10
, pp. 43
-
-
Arnett, D.K.1
Li, N.2
Tang, W.3
Rao, D.C.4
Devereux, R.B.5
Claas, S.A.6
-
45
-
-
79953104103
-
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster
-
Del Greco MF, Pattaro C, Luchner A, Pichler I, Winkler T, Hicks AA, et al. Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Hum Mol Genet. 2011;20:1660–71.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 1660-1671
-
-
Del Greco, M.F.1
Pattaro, C.2
Luchner, A.3
Pichler, I.4
Winkler, T.5
Hicks, A.A.6
-
46
-
-
84873513160
-
Genetic associations with valvular calcification and aortic stenosis
-
COI: 1:CAS:528:DC%2BC3sXitFeltrY%3D
-
Thanassoulis G, Campbell CY, Owens DS, Smith JG, Smith AV, Peloso GM, et al. Genetic associations with valvular calcification and aortic stenosis. N Engl J Med. 2013;368:503–12.
-
(2013)
N Engl J Med
, vol.368
, pp. 503-512
-
-
Thanassoulis, G.1
Campbell, C.Y.2
Owens, D.S.3
Smith, J.G.4
Smith, A.V.5
Peloso, G.M.6
-
47
-
-
84893333521
-
Elevated lipoprotein(a) and risk of aortic valve stenosis in the general population
-
COI: 1:CAS:528:DC%2BC2cXhvFGlsLg%3D
-
Kamstrup PR, Tybjærg-Hansen A, Nordestgaard BG. Elevated lipoprotein(a) and risk of aortic valve stenosis in the general population. J Am Coll Cardiol. 2014;63:470–7.
-
(2014)
J Am Coll Cardiol
, vol.63
, pp. 470-477
-
-
Kamstrup, P.R.1
Tybjærg-Hansen, A.2
Nordestgaard, B.G.3
-
48
-
-
61349137526
-
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease
-
Trégouët D-A, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet. 2009;41:283–5.
-
(2009)
Nat Genet
, vol.41
, pp. 283-285
-
-
Trégouët, D.-A.1
König, I.R.2
Erdmann, J.3
Munteanu, A.4
Braund, P.S.5
Hall, A.S.6
-
49
-
-
84893659261
-
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
-
COI: 1:CAS:528:DC%2BC2cXitFymtLs%3D, A valuable comparison between the common genetic determinants of stroke and coronary heart disease highlighting shared aetiological pathways
-
Dichgans M, Malik R, König IR, Rosand J, Clarke R, Gretarsdottir S, et al. Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Stroke J Cereb Circ. 2014;45:24–36. A valuable comparison between the common genetic determinants of stroke and coronary heart disease highlighting shared aetiological pathways.
-
(2014)
Stroke J Cereb Circ
, vol.45
, pp. 24-36
-
-
Dichgans, M.1
Malik, R.2
König, I.R.3
Rosand, J.4
Clarke, R.5
Gretarsdottir, S.6
-
50
-
-
84867645825
-
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
-
Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng Y-C, et al. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. Lancet Neurol. 2012;11:951–62.
-
(2012)
Lancet Neurol
, vol.11
, pp. 951-962
-
-
Traylor, M.1
Farrall, M.2
Holliday, E.G.3
Sudlow, C.4
Hopewell, J.C.5
Cheng, Y.-C.6
-
51
-
-
0037121247
-
The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial
-
COI: 1:STN:280:DC%2BD38not12lsg%3D%3D
-
Ashton HA, Buxton MJ, Day NE, Kim LG, Marteau TM, Scott RAP, et al. The Multicentre Aneurysm Screening Study (MASS) into the effect of abdominal aortic aneurysm screening on mortality in men: a randomised controlled trial. Lancet. 2002;360:1531–9.
-
(2002)
Lancet
, vol.360
, pp. 1531-1539
-
-
Ashton, H.A.1
Buxton, M.J.2
Day, N.E.3
Kim, L.G.4
Marteau, T.M.5
Scott, R.A.P.6
-
52
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
COI: 1:CAS:528:DC%2BD2sXmtFSjtro%3D
-
Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491–3.
-
(2007)
Science
, vol.316
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
-
53
-
-
38649091662
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
-
COI: 1:CAS:528:DC%2BD1cXhsVSjsLY%3D
-
Helgadottir A, Thorleifsson G, Magnusson KP, Grétarsdottir S, Steinthorsdottir V, Manolescu A, et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008;40:217–24.
-
(2008)
Nat Genet
, vol.40
, pp. 217-224
-
-
Helgadottir, A.1
Thorleifsson, G.2
Magnusson, K.P.3
Grétarsdottir, S.4
Steinthorsdottir, V.5
Manolescu, A.6
-
54
-
-
84858272182
-
Genomic research to identify novel pathways in the development of abdominal aortic aneurysm
-
Harrison SC, Kalea AZ, Holmes MV, Agu O, Humphries SE. Genomic research to identify novel pathways in the development of abdominal aortic aneurysm. Cardiol Res Pract. 2012;2012:852829.
-
(2012)
Cardiol. Res. Pract
, vol.2012
, pp. 852829
-
-
Harrison, S.C.1
Kalea, A.Z.2
Holmes, M.V.3
Agu, O.4
Humphries, S.E.5
-
55
-
-
84947899513
-
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
-
COI: 1:CAS:528:DC%2BC3cXos1aitbo%3D
-
Gretarsdottir S, Baas AF, Thorleifsson G, Holm H, den Heijer M, de Vries J-PPM, et al. Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Nat Genet. 2010;42:692–7.
-
(2010)
Nat Genet
, vol.42
, pp. 692-697
-
-
Gretarsdottir, S.1
Baas, A.F.2
Thorleifsson, G.3
Holm, H.4
den Heijer, M.5
de Vries, J.-P.P.M.6
-
56
-
-
84945173643
-
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1
-
COI: 1:CAS:528:DC%2BC3MXhsVKhurfE
-
Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, et al. Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. Am J Hum Genet. 2011;89:619–27.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 619-627
-
-
Bown, M.J.1
Jones, G.T.2
Harrison, S.C.3
Wright, B.J.4
Bumpstead, S.5
Baas, A.F.6
-
57
-
-
84892385162
-
A variant in LDLR is associated with abdominal aortic aneurysm
-
COI: 1:CAS:528:DC%2BC3sXhs1Cis7fL
-
Bradley DT, Hughes AE, Badger SA, Jones GT, Harrison SC, Wright BJ, et al. A variant in LDLR is associated with abdominal aortic aneurysm. Circ Cardiovasc Genet. 2013;6:498–504.
-
(2013)
Circ Cardiovasc Genet
, vol.6
, pp. 498-504
-
-
Bradley, D.T.1
Hughes, A.E.2
Badger, S.A.3
Jones, G.T.4
Harrison, S.C.5
Wright, B.J.6
-
58
-
-
84891514939
-
Interleukin-6 receptor pathways in abdominal aortic aneurysm
-
Harrison SC, Smith AJP, Jones GT, Swerdlow DI, Rampuri R, Bown MJ, et al. Interleukin-6 receptor pathways in abdominal aortic aneurysm. Eur Heart J. 2012;34:3707–16.
-
(2012)
Eur Heart J
, vol.34
, pp. 3707-3716
-
-
Harrison, S.C.1
Smith, A.J.P.2
Jones, G.T.3
Swerdlow, D.I.4
Rampuri, R.5
Bown, M.J.6
-
59
-
-
84897908258
-
Technology: the $1,000 genome
-
Hayden EC. Technology: the $1,000 genome. Nature. 2014;507:294–5.
-
(2014)
Nature
, vol.507
, pp. 294-295
-
-
Hayden, E.C.1
-
60
-
-
79953197851
-
Utility of genetic determinants of lipids and cardiovascular events in assessing risk
-
COI: 1:CAS:528:DC%2BC3MXjvVKns74%3D, A comprehensive review of the underlying research and clinical utility of using genetics for predicting cardiovascular disease risk
-
Holmes MV, Harrison S, Talmud PJ, Hingorani AD, Humphries SE. Utility of genetic determinants of lipids and cardiovascular events in assessing risk. Nat Rev Cardiol. 2011;8:207–21. A comprehensive review of the underlying research and clinical utility of using genetics for predicting cardiovascular disease risk.
-
(2011)
Nat Rev Cardiol
, vol.8
, pp. 207-221
-
-
Holmes, M.V.1
Harrison, S.2
Talmud, P.J.3
Hingorani, A.D.4
Humphries, S.E.5
-
61
-
-
77951589703
-
Clinical assessment incorporating a personal genome
-
COI: 1:CAS:528:DC%2BC3cXlsVOnt74%3D
-
Ashley EA, Butte AJ, Wheeler MT, Chen R, Klein TE, Dewey FE, et al. Clinical assessment incorporating a personal genome. Lancet. 2010;375:1525–35.
-
(2010)
Lancet
, vol.375
, pp. 1525-1535
-
-
Ashley, E.A.1
Butte, A.J.2
Wheeler, M.T.3
Chen, R.4
Klein, T.E.5
Dewey, F.E.6
-
62
-
-
84883286898
-
Multilocus genetic risk scores for coronary heart disease prediction
-
COI: 1:CAS:528:DC%2BC3sXht1Oqtr7M
-
Ganna A, Magnusson PKE, Pedersen NL, de Faire U, Reilly M, Arnlöv J, et al. Multilocus genetic risk scores for coronary heart disease prediction. Arterioscler Thromb Vasc Biol. 2013;33:2267–72.
-
(2013)
Arterioscler Thromb Vasc Biol
, vol.33
, pp. 2267-2272
-
-
Ganna, A.1
Magnusson, P.K.E.2
Pedersen, N.L.3
de Faire, U.4
Reilly, M.5
Arnlöv, J.6
-
63
-
-
84883302693
-
Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease
-
COI: 1:CAS:528:DC%2BC3sXht1OqsbfF
-
Tikkanen E, Havulinna AS, Palotie A, Salomaa V, Ripatti S. Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease. Arterioscler Thromb Vasc Biol. 2013;33:2261–6.
-
(2013)
Arterioscler Thromb Vasc Biol
, vol.33
, pp. 2261-2266
-
-
Tikkanen, E.1
Havulinna, A.S.2
Palotie, A.3
Salomaa, V.4
Ripatti, S.5
-
64
-
-
84864335233
-
Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts
-
COI: 1:CAS:528:DC%2BC38XhtFamsr3F
-
Hughes MF, Saarela O, Stritzke J, Kee F, Silander K, Klopp N, et al. Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts. PLoS One. 2012;7:e40922.
-
(2012)
PLoS One
, vol.7
, pp. 40922
-
-
Hughes, M.F.1
Saarela, O.2
Stritzke, J.3
Kee, F.4
Silander, K.5
Klopp, N.6
-
65
-
-
84864762687
-
A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies
-
COI: 1:CAS:528:DC%2BC38XhtVWgtb3M
-
Brautbar A, Pompeii LA, Dehghan A, Ngwa JS, Nambi V, Virani SS, et al. A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies. Atherosclerosis. 2012;223:421–6.
-
(2012)
Atherosclerosis
, vol.223
, pp. 421-426
-
-
Brautbar, A.1
Pompeii, L.A.2
Dehghan, A.3
Ngwa, J.S.4
Nambi, V.5
Virani, S.S.6
-
66
-
-
84856292621
-
Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey—a meta-analysis of three independent studies
-
COI: 1:CAS:528:DC%2BC38Xit1Cis78%3D
-
Hernesniemi JA, Seppälä I, Lyytikäinen L-P, Mononen N, Oksala N, Hutri-Kähönen N, et al. Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey—a meta-analysis of three independent studies. PLoS One. 2012;7:e28931.
-
(2012)
PLoS One
, vol.7
, pp. 28931
-
-
Hernesniemi, J.A.1
Seppälä, I.2
Lyytikäinen, L.-P.3
Mononen, N.4
Oksala, N.5
Hutri-Kähönen, N.6
-
67
-
-
78049314943
-
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
-
A clinically focused report of a study investigating the incorporation of genetic information into coronary heart disease risk prediction
-
Ripatti S, Tikkanen E, Orho-Melander M, Havulinna AS, Silander K, Sharma A, et al. A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses. Lancet. 2010;376:1393–400. A clinically focused report of a study investigating the incorporation of genetic information into coronary heart disease risk prediction.
-
(2010)
Lancet
, vol.376
, pp. 1393-1400
-
-
Ripatti, S.1
Tikkanen, E.2
Orho-Melander, M.3
Havulinna, A.S.4
Silander, K.5
Sharma, A.6
-
68
-
-
77952981215
-
Coronary heart disease risk prediction in the era of genome-wide association studies: current status and what the future holds
-
Humphries SE, Drenos F, Ken-Dror G, Talmud PJ. Coronary heart disease risk prediction in the era of genome-wide association studies: current status and what the future holds. Circulation. 2010;121:2235–48.
-
(2010)
Circulation
, vol.121
, pp. 2235-2248
-
-
Humphries, S.E.1
Drenos, F.2
Ken-Dror, G.3
Talmud, P.J.4
-
69
-
-
84896788068
-
23andMe and the FDA
-
COI: 1:CAS:528:DC%2BC2cXkvVyqtL8%3D
-
Annas GJ, Elias S. 23andMe and the FDA. N Engl J Med. 2014;370:985–8.
-
(2014)
N Engl J Med
, vol.370
, pp. 985-988
-
-
Annas, G.J.1
Elias, S.2
-
70
-
-
0037322022
-
Mendelian randomization”: can genetic epidemiology contribute to understanding environmental determinants of disease?
-
A guide to the theoretical and practical basis of Mendelian randomisation
-
Davey Smith G, Ebrahim S. “Mendelian randomization”: can genetic epidemiology contribute to understanding environmental determinants of disease? Int J Epidemiol. 2003;32:1–22. A guide to the theoretical and practical basis of Mendelian randomisation.
-
(2003)
Int J Epidemiol
, vol.32
, pp. 1-22
-
-
Davey Smith, G.1
Ebrahim, S.2
-
71
-
-
38949127024
-
Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?
-
A review of the role of Mendelian randomisation in overcoming some of the limitations of traditional epidemiology
-
Ebrahim S, Davey Smith G. Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology? Hum Genet. 2008;123:15–33. A review of the role of Mendelian randomisation in overcoming some of the limitations of traditional epidemiology.
-
(2008)
Hum Genet
, vol.123
, pp. 15-33
-
-
Ebrahim, S.1
Davey Smith, G.2
-
72
-
-
78449281377
-
Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials
-
COI: 1:STN:280:DC%2BC3cbmvVGmsQ%3D%3D
-
Baigent C, Blackwell L, Emberson J, Holland LE, Reith C, Bhala N, et al. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet. 2010;376:1670–81.
-
(2010)
Lancet
, vol.376
, pp. 1670-1681
-
-
Baigent, C.1
Blackwell, L.2
Emberson, J.3
Holland, L.E.4
Reith, C.5
Bhala, N.6
-
73
-
-
84886914661
-
Blood pressure lowering and major cardiovascular events in people with and without chronic kidney disease: meta-analysis of randomised controlled trials
-
Ninomiya T, Perkovic V, Turnbull F, Neal B, Barzi F, et al. Blood pressure lowering and major cardiovascular events in people with and without chronic kidney disease: meta-analysis of randomised controlled trials. BMJ. 2013;347:f5680.
-
(2013)
BMJ
, vol.347
, pp. 5680
-
-
Ninomiya, T.1
Perkovic, V.2
Turnbull, F.3
Neal, B.4
Barzi, F.5
-
74
-
-
84873344743
-
Efficacy of vitamin and antioxidant supplements in prevention of cardiovascular disease: systematic review and meta-analysis of randomised controlled trials
-
Myung S-K, Ju W, Cho B, Oh S-W, Park SM, Koo B-K, et al. Efficacy of vitamin and antioxidant supplements in prevention of cardiovascular disease: systematic review and meta-analysis of randomised controlled trials. BMJ. 2013;346:f10.
-
(2013)
BMJ
, vol.346
, pp. 10
-
-
Myung, S.-K.1
Ju, W.2
Cho, B.3
Oh, S.-W.4
Park, S.M.5
Koo, B.-K.6
-
75
-
-
28244453652
-
Nature’s randomised trials
-
A concise introduction to the similarities between Mendelian randomisation and the traditional randomised controlled trial
-
Hingorani A, Humphries S. Nature’s randomised trials. Lancet. 2005;366:1906–8. A concise introduction to the similarities between Mendelian randomisation and the traditional randomised controlled trial.
-
(2005)
Lancet
, vol.366
, pp. 1906-1908
-
-
Hingorani, A.1
Humphries, S.2
-
76
-
-
84928349473
-
Gregor Mendel’s seminal work on the inheritance of pea plant characteristics. The seminal description of the laws of what has become known as ‘Mendelian’ inheritance
-
Mendel G. Experiments in plant-hybridisation. Brunn Nat Hist Soc. 1865. Gregor Mendel’s seminal work on the inheritance of pea plant characteristics. The seminal description of the laws of what has become known as ‘Mendelian’ inheritance. These underly the Mendelian randomisation principle.
-
(1865)
These underly the Mendelian randomisation principle
-
-
-
77
-
-
52349083201
-
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease—a Mendelian Randomisation study
-
Linsel-Nitschke P, Götz A, Erdmann J, Braenne I, Braund P, Hengstenberg C, et al. Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease—a Mendelian Randomisation study. PLoS One. 2008;3:e2986.
-
(2008)
PLoS One
, vol.3
, pp. 2986
-
-
Linsel-Nitschke, P.1
Götz, A.2
Erdmann, J.3
Braenne, I.4
Braund, P.5
Hengstenberg, C.6
-
78
-
-
84902285272
-
Clinical effect of naturally random allocation to lower systolic blood pressure beginning before the development of hypertension
-
COI: 1:CAS:528:DC%2BC2cXpt1Kruro%3D
-
Ference BA, Julius S, Mahajan N, Levy PD, Williams KA, Flack JM. Clinical effect of naturally random allocation to lower systolic blood pressure beginning before the development of hypertension. Hypertension. 2014;63:1182–8.
-
(2014)
Hypertension
, vol.63
, pp. 1182-1188
-
-
Ference, B.A.1
Julius, S.2
Mahajan, N.3
Levy, P.D.4
Williams, K.A.5
Flack, J.M.6
-
79
-
-
34548171994
-
A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease
-
COI: 1:CAS:528:DC%2BD2sXpt1Cju7Y%3D
-
Luke MM, Kane JP, Liu DM, Rowland CM, Shiffman D, Cassano J, et al. A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arterioscler Thromb Vasc Biol. 2007;27:2030–6.
-
(2007)
Arterioscler Thromb Vasc Biol
, vol.27
, pp. 2030-2036
-
-
Luke, M.M.1
Kane, J.P.2
Liu, D.M.3
Rowland, C.M.4
Shiffman, D.5
Cassano, J.6
-
80
-
-
77951875017
-
Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies
-
COI: 1:CAS:528:DC%2BC3cXlslylu74%3D, A large-scale Mendelian randomisation study implicating triglyceride-mediated aetiological pathways in the development of coronary heart disease
-
Sarwar N, Sandhu MS, Ricketts SL, Butterworth AS, Di Angelantonio E, Boekholdt SM, et al. Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies. Lancet. 2010;375:1634–9. A large-scale Mendelian randomisation study implicating triglyceride-mediated aetiological pathways in the development of coronary heart disease.
-
(2010)
Lancet
, vol.375
, pp. 1634-1639
-
-
Sarwar, N.1
Sandhu, M.S.2
Ricketts, S.L.3
Butterworth, A.S.4
Di Angelantonio, E.5
Boekholdt, S.M.6
-
81
-
-
84907810393
-
-
Eur Heart J, Report of a study using Mendelian randomisation techniques to investigate the causal contributions of major blood lipid fractions in coronary heart disease:
-
Holmes MV, Asselbergs FW, Palmer TM, Drenos F, Lanktree MB, Nelson CP, et al. Mendelian randomization of blood lipids for coronary heart disease. Eur Heart J. 2014. Report of a study using Mendelian randomisation techniques to investigate the causal contributions of major blood lipid fractions in coronary heart disease.
-
(2014)
Mendelian randomization of blood lipids for coronary heart disease
-
-
Holmes, M.V.1
Asselbergs, F.W.2
Palmer, T.M.3
Drenos, F.4
Lanktree, M.B.5
Nelson, C.P.6
-
82
-
-
84887058576
-
Common variants associated with plasma triglycerides and risk for coronary artery disease
-
COI: 1:CAS:528:DC%2BC3sXhsFOiur%2FN, An innovative Mendelian randomisation study using novel techniques to investigate further the causal contributions of plasma triglycerides in coronary disease
-
Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013;45:1345–52. An innovative Mendelian randomisation study using novel techniques to investigate further the causal contributions of plasma triglycerides in coronary disease.
-
(2013)
Nat Genet
, vol.45
, pp. 1345-1352
-
-
Do, R.1
Willer, C.J.2
Schmidt, E.M.3
Sengupta, S.4
Gao, C.5
Peloso, G.M.6
-
83
-
-
84879373355
-
HDL, atherosclerosis, and emerging therapies
-
A review discussing the controversial role of HDL cholesterol in coronary heart disease and the potential utility of pharmacological modulation of HDL-C
-
Hafiane A, Genest J. HDL, atherosclerosis, and emerging therapies. Cholesterol. 2013;2013:891403. A review discussing the controversial role of HDL cholesterol in coronary heart disease and the potential utility of pharmacological modulation of HDL-C.
-
(2013)
Cholesterol
, vol.2013
, pp. 891403
-
-
Hafiane, A.1
Genest, J.2
-
84
-
-
44649140474
-
Association of loss-of-function mutations in the ABCA1 gene with high-density lipoprotein cholesterol levels and risk of ischemic heart disease
-
COI: 1:CAS:528:DC%2BD1cXmvVyitL8%3D
-
Frikke-Schmidt R, Nordestgaard BG, Stene MCA, Sethi AA, Remaley AT, Schnohr P, et al. Association of loss-of-function mutations in the ABCA1 gene with high-density lipoprotein cholesterol levels and risk of ischemic heart disease. JAMA. 2008;299:2524–32.
-
(2008)
JAMA
, vol.299
, pp. 2524-2532
-
-
Frikke-Schmidt, R.1
Nordestgaard, B.G.2
Stene, M.C.A.3
Sethi, A.A.4
Remaley, A.T.5
Schnohr, P.6
-
85
-
-
84856786437
-
LCAT, HDL cholesterol and ischemic cardiovascular disease: a Mendelian randomization study of HDL cholesterol in 54,500 individuals
-
COI: 1:CAS:528:DC%2BC38XisFOns70%3D
-
Haase CL, Tybjærg-Hansen A, Qayyum AA, Schou J, Nordestgaard BG, Frikke-Schmidt R. LCAT, HDL cholesterol and ischemic cardiovascular disease: a Mendelian randomization study of HDL cholesterol in 54,500 individuals. J Clin Endocrinol Metab. 2012;97:E248–56.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. 248-256
-
-
Haase, C.L.1
Tybjærg-Hansen, A.2
Qayyum, A.A.3
Schou, J.4
Nordestgaard, B.G.5
Frikke-Schmidt, R.6
-
86
-
-
84864845456
-
-
Voight BF, Peloso GM, Orho-Melander M, Frikke-Schmidt R, Barbalic M, Jensen MK, et al. Plasma HDL cholesterol and risk of myocardial infarction: a Mendelian randomisation study. Lancet [Internet]. 2012 [cited 2012 Jun 2]; Available from:. An important Mendelian randomisation study providing evidence that one aspect of HDL cholesterol metabolism appears not to have a causal role in the development of coronary heart disease
-
Voight BF, Peloso GM, Orho-Melander M, Frikke-Schmidt R, Barbalic M, Jensen MK, et al. Plasma HDL cholesterol and risk of myocardial infarction: a Mendelian randomisation study. Lancet [Internet]. 2012 [cited 2012 Jun 2]; Available from: http://www.ncbi.nlm.nih.gov/pubmed/22607825. An important Mendelian randomisation study providing evidence that one aspect of HDL cholesterol metabolism appears not to have a causal role in the development of coronary heart disease.
-
-
-
-
87
-
-
57849117801
-
Atherosclerosis—an immune disease: the Anitschkov Lecture 2007
-
COI: 1:CAS:528:DC%2BD1cXhsFajsb%2FP
-
Hansson GK. Atherosclerosis—an immune disease: the Anitschkov Lecture 2007. Atherosclerosis. 2009;202:2–10.
-
(2009)
Atherosclerosis
, vol.202
, pp. 2-10
-
-
Hansson, G.K.1
-
88
-
-
84880230242
-
Association between C reactive protein and coronary heart disease: Mendelian randomisation analysis based on individual participant data
-
A large collaborative Mendelian randomisation study providing strong evidence against a causal role for C-reactive protein in coronary heart disease
-
Wensley F, Gao P, Burgess S, Kaptoge S, Di Angelantonio E, Shah T, et al. Association between C reactive protein and coronary heart disease: Mendelian randomisation analysis based on individual participant data. BMJ. 2011;342:d548. A large collaborative Mendelian randomisation study providing strong evidence against a causal role for C-reactive protein in coronary heart disease.
-
(2011)
BMJ
, vol.342
, pp. 548
-
-
Wensley, F.1
Gao, P.2
Burgess, S.3
Kaptoge, S.4
Di Angelantonio, E.5
Shah, T.6
-
89
-
-
77955503774
-
-
Singh JA, Beg S, Lopez-Olivo MA. Tocilizumab for rheumatoid arthritis. Cochrane Database Syst. Rev. Online. 2010;CD008331
-
Singh JA, Beg S, Lopez-Olivo MA. Tocilizumab for rheumatoid arthritis. Cochrane Database Syst. Rev. Online. 2010;CD008331
-
-
-
-
90
-
-
84893735878
-
Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis
-
COI: 1:CAS:528:DC%2BC2cXht1KhtL8%3D, An allele score-based Mendelian randomisation study investigating the causal contribution of body mass index—a complex phenotype—in other areas of cardiometabolic disease
-
Holmes MV, Lange LA, Palmer T, Lanktree MB, North KE, Almoguera B, et al. Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis. Am J Hum Genet. 2014;94:198–208. An allele score-based Mendelian randomisation study investigating the causal contribution of body mass index—a complex phenotype—in other areas of cardiometabolic disease.
-
(2014)
Am J Hum Genet
, vol.94
, pp. 198-208
-
-
Holmes, M.V.1
Lange, L.A.2
Palmer, T.3
Lanktree, M.B.4
North, K.E.5
Almoguera, B.6
-
91
-
-
84861537866
-
The effect of elevated body mass index on ischemic heart disease risk: causal estimates from a Mendelian randomisation approach
-
Nordestgaard BG, Palmer TM, Benn M, Zacho J, Tybjærg-Hansen A, Davey Smith G, et al. The effect of elevated body mass index on ischemic heart disease risk: causal estimates from a Mendelian randomisation approach. PLoS Med. 2012;9:e1001212.
-
(2012)
PLoS Med
, vol.9
, pp. 1001212
-
-
Nordestgaard, B.G.1
Palmer, T.M.2
Benn, M.3
Zacho, J.4
Tybjærg-Hansen, A.5
Davey Smith, G.6
-
92
-
-
79952058740
-
Association of alcohol consumption with selected cardiovascular disease outcomes: a systematic review and meta-analysis
-
Ronksley PE, Brien SE, Turner BJ, Mukamal KJ, Ghali WA. Association of alcohol consumption with selected cardiovascular disease outcomes: a systematic review and meta-analysis. BMJ. 2011;342:d671.
-
(2011)
BMJ
, vol.342
, pp. 671
-
-
Ronksley, P.E.1
Brien, S.E.2
Turner, B.J.3
Mukamal, K.J.4
Ghali, W.A.5
-
93
-
-
84904064886
-
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
-
A landmark genetic investigation of the much-debated causal role of alcohol consumption in a range of cardiometabolic disease phenotypes
-
Holmes MV, Dale CE, Zuccolo L, Silverwood RJ, Guo Y, Ye Z, et al. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data. BMJ. 2014;349:g4164. A landmark genetic investigation of the much-debated causal role of alcohol consumption in a range of cardiometabolic disease phenotypes.
-
(2014)
BMJ
, vol.349
, pp. 4164
-
-
Holmes, M.V.1
Dale, C.E.2
Zuccolo, L.3
Silverwood, R.J.4
Guo, Y.5
Ye, Z.6
-
94
-
-
38649120829
-
Drugs and their molecular targets: an updated overview
-
COI: 1:CAS:528:DC%2BD1cXis12ktr0%3D
-
Landry Y, Gies J-P. Drugs and their molecular targets: an updated overview. Fundam Clin Pharmacol. 2008;22:1–18.
-
(2008)
Fundam Clin Pharmacol
, vol.22
, pp. 1-18
-
-
Landry, Y.1
Gies, J.-P.2
-
95
-
-
84857792744
-
Inhibition of secretory phospholipase A(2) in patients with acute coronary syndromes: rationale and design of the vascular inflammation suppression to treat acute coronary syndrome for 16 weeks (VISTA-16) trial
-
COI: 1:CAS:528:DC%2BC38XivFOrsr4%3D
-
Nicholls SJ, Cavender MA, Kastelein JJP, Schwartz G, Waters DD, Rosenson RS, et al. Inhibition of secretory phospholipase A(2) in patients with acute coronary syndromes: rationale and design of the vascular inflammation suppression to treat acute coronary syndrome for 16 weeks (VISTA-16) trial. Cardiovasc Drugs Ther. 2012;26:71–5.
-
(2012)
Cardiovasc Drugs Ther
, vol.26
, pp. 71-75
-
-
Nicholls, S.J.1
Cavender, M.A.2
Kastelein, J.J.P.3
Schwartz, G.4
Waters, D.D.5
Rosenson, R.S.6
-
96
-
-
84888256840
-
Secretory phospholipase A2-IIA and cardiovascular disease: a Mendelian randomization study
-
COI: 1:CAS:528:DC%2BC3sXhslKqsLbO
-
Holmes MV, Simon T, Exeter HJ, Folkersen L, Asselbergs FW, Guardiola M, et al. Secretory phospholipase A2-IIA and cardiovascular disease: a Mendelian randomization study. J Am Coll Cardiol. 2013;62(21):1966–76.
-
(2013)
J Am Coll Cardiol
, vol.62
, Issue.21
, pp. 1966-1976
-
-
Holmes, M.V.1
Simon, T.2
Exeter, H.J.3
Folkersen, L.4
Asselbergs, F.W.5
Guardiola, M.6
-
97
-
-
84891142213
-
Varespladib and cardiovascular events in patients with an acute coronary syndrome: the VISTA-16 randomized clinical trial
-
COI: 1:CAS:528:DC%2BC2cXisVGisrY%3D
-
Nicholls SJ, Kastelein JJP, Schwartz GG, Bash D, Rosenson RS, Cavender MA, et al. Varespladib and cardiovascular events in patients with an acute coronary syndrome: the VISTA-16 randomized clinical trial. JAMA. 2014;311:252–62.
-
(2014)
JAMA
, vol.311
, pp. 252-262
-
-
Nicholls, S.J.1
Kastelein, J.J.P.2
Schwartz, G.G.3
Bash, D.4
Rosenson, R.S.5
Cavender, M.A.6
-
98
-
-
1842815777
-
Effects of an inhibitor of cholesteryl ester transfer protein on HDL cholesterol
-
COI: 1:CAS:528:DC%2BD2cXjtVeqt7Y%3D
-
Brousseau ME, Schaefer EJ, Wolfe ML, Bloedon LT, Digenio AG, Clark RW, et al. Effects of an inhibitor of cholesteryl ester transfer protein on HDL cholesterol. N Engl J Med. 2004;350:1505–15.
-
(2004)
N Engl J Med
, vol.350
, pp. 1505-1515
-
-
Brousseau, M.E.1
Schaefer, E.J.2
Wolfe, M.L.3
Bloedon, L.T.4
Digenio, A.G.5
Clark, R.W.6
-
99
-
-
36348975228
-
Effects of torcetrapib in patients at high risk for coronary events
-
COI: 1:CAS:528:DC%2BD2sXhtlGns7bL
-
Barter PJ, Caulfield M, Eriksson M, Grundy SM, Kastelein JJP, Komajda M, et al. Effects of torcetrapib in patients at high risk for coronary events. N Engl J Med. 2007;357:2109–22.
-
(2007)
N Engl J Med
, vol.357
, pp. 2109-2122
-
-
Barter, P.J.1
Caulfield, M.2
Eriksson, M.3
Grundy, S.M.4
Kastelein, J.J.P.5
Komajda, M.6
-
100
-
-
74549185752
-
Separating the mechanism-based and off-target actions of cholesteryl ester transfer protein inhibitors with CETP gene polymorphisms
-
COI: 1:CAS:528:DC%2BD1MXhs1WjtrnO, A novel application of Mendelian randomisation for investigating adverse drug effects, providing evidence that the hypertensive effect of torcetrapib therapy was an off-target action of the drug
-
Sofat R, Hingorani AD, Smeeth L, Humphries SE, Talmud PJ, Cooper J, et al. Separating the mechanism-based and off-target actions of cholesteryl ester transfer protein inhibitors with CETP gene polymorphisms. Circulation. 2010;121:52–62. A novel application of Mendelian randomisation for investigating adverse drug effects, providing evidence that the hypertensive effect of torcetrapib therapy was an off-target action of the drug.
-
(2010)
Circulation
, vol.121
, pp. 52-62
-
-
Sofat, R.1
Hingorani, A.D.2
Smeeth, L.3
Humphries, S.E.4
Talmud, P.J.5
Cooper, J.6
-
101
-
-
77549087054
-
Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials
-
COI: 1:CAS:528:DC%2BC3cXisFart74%3D, A large meta-analysis of randomised trials demonstrating the increased risk of new-onset type 2 diabetes with statin treatment
-
Sattar N, Preiss D, Murray HM, Welsh P, Buckley BM, de Craen AJ, et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials. Lancet. 2010;375:735–42. A large meta-analysis of randomised trials demonstrating the increased risk of new-onset type 2 diabetes with statin treatment.
-
(2010)
Lancet
, vol.375
, pp. 735-742
-
-
Sattar, N.1
Preiss, D.2
Murray, H.M.3
Welsh, P.4
Buckley, B.M.5
de Craen, A.J.6
-
102
-
-
79959428660
-
Risk of incident diabetes with intensive-dose compared with moderate-dose statin therapy: a meta-analysis
-
COI: 1:CAS:528:DC%2BC3MXotVantLs%3D, Corroboration of the increased diabetes risk with statin therapy, showing that high-intensity statin therapy led to the greatest risk of diabetes
-
Preiss D, Seshasai SRK, Welsh P, Murphy SA, Ho JE, Waters DD, et al. Risk of incident diabetes with intensive-dose compared with moderate-dose statin therapy: a meta-analysis. JAMA. 2011;305:2556–64. Corroboration of the increased diabetes risk with statin therapy, showing that high-intensity statin therapy led to the greatest risk of diabetes.
-
(2011)
JAMA
, vol.305
, pp. 2556-2564
-
-
Preiss, D.1
Seshasai, S.R.K.2
Welsh, P.3
Murphy, S.A.4
Ho, J.E.5
Waters, D.D.6
-
103
-
-
84928330888
-
-
Swerdlow DI, Preiss D, Kuchenbaecker KB, Holmes MV, Engmann JEL, Shah T, et al. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. The Lancet [Internet]. 2014 [cited 2014 Sep 24]; Available from:. A study using data from randomised trials and Mendelian randomisation to investigate the aetiology of the increased risk of diabetes with statin therapy
-
Swerdlow DI, Preiss D, Kuchenbaecker KB, Holmes MV, Engmann JEL, Shah T, et al. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials. The Lancet [Internet]. 2014 [cited 2014 Sep 24]; Available from: http://linkinghub.elsevier.com/retrieve/pii/S0140673614611831. A study using data from randomised trials and Mendelian randomisation to investigate the aetiology of the increased risk of diabetes with statin therapy.
-
-
-
|