-
1
-
-
0026567697
-
Epidemiology of stroke
-
Bonita R. Epidemiology of stroke. Lancet. 1992;339:342-344.
-
(1992)
Lancet
, vol.339
, pp. 342-344
-
-
Bonita, R.1
-
2
-
-
33646799069
-
Global and regional burden of disease and risk factors 2001: Systematic analysis of population health data
-
Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet. 2006;367:1747-1757.
-
(2006)
Lancet
, vol.367
, pp. 1747-1757
-
-
Lopez, A.D.1
Mathers, C.D.2
Ezzati, M.3
Jamison, D.T.4
Murray, C.J.5
-
3
-
-
33846185489
-
Genetics of ischaemic stroke
-
Dichgans M. Genetics of ischaemic stroke. Lancet Neurol. 2007;6:149-161.
-
(2007)
Lancet Neurol
, vol.6
, pp. 149-161
-
-
Dichgans, M.1
-
4
-
-
84870931409
-
Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations
-
Bevan S, Traylor M, Adib-Samii P, Malik R, Paul NL, Jackson C, et al. Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations. Stroke. 2012;43:3161-3167.
-
(2012)
Stroke
, vol.43
, pp. 3161-3167
-
-
Bevan, S.1
Traylor, M.2
Adib-Samii, P.3
Malik, R.4
Paul, N.L.5
Jackson, C.6
-
5
-
-
84893659261
-
Shared genetic susceptibility to ischemic stroke and coronary artery disease: A genome-wide analysis of common variants
-
November 21, 2013. doi: 10.1161/STROKEAHA.113.00270. Accessed December 21, 2013
-
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 November 21, 2013. doi: 10.1161/STROKEAHA.113.00270. http://stroke.ahajournals. org/content/early/2013/11/21/STROKEAHA.113.002707.long. Accessed December 21, 2013.
-
Stroke
-
-
Dichgans, M.1
Malik, R.2
König, I.R.3
Rosand, J.4
Clarke, R.5
Gretarsdottir, S.6
-
6
-
-
84863393715
-
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
-
Bellenguez C, Bevan S, Gschwendtner A, Spencer CC, Burgess AI, Pirinen M, et al. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nat Genet. 2012;44:328-333.
-
(2012)
Nat Genet
, vol.44
, pp. 328-333
-
-
Bellenguez, C.1
Bevan, S.2
Gschwendtner, A.3
Spencer, C.C.4
Burgess, A.I.5
Pirinen, M.6
-
7
-
-
84866930896
-
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke
-
Australian Stroke Genetics Collaborative; International Stroke Genetics Consortium; Wellcome Trust Case Control Consortium
-
Holliday EG, Maguire JM, Evans TJ, Koblar SA, Jannes J, Sturm JW, et al; Australian Stroke Genetics Collaborative; International Stroke Genetics Consortium; Wellcome Trust Case Control Consortium. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nat Genet. 2012;44:1147-1151.
-
(2012)
Nat Genet
, vol.44
, pp. 1147-1151
-
-
Holliday, E.G.1
Maguire, J.M.2
Evans, T.J.3
Koblar, S.A.4
Jannes, J.5
Sturm, J.W.6
-
8
-
-
84861636519
-
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
-
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;44:670-675.
-
(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
-
9
-
-
79953204259
-
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
-
Cardiogenics; CARDIoGRAM Consortium
-
Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al; Cardiogenics; CARDIoGRAM Consortium. 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
König, I.R.2
Kathiresan, S.3
Reilly, M.P.4
Assimes, T.L.5
Holm, H.6
-
10
-
-
84871969762
-
Large-scale association analysis identifies new risk loci for coronary artery disease
-
CARDIoGRAMplusC4D Consortium
-
CARDIoGRAMplusC4D Consortium, Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, et al. 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
-
-
Deloukas, P.1
Kanoni, S.2
Willenborg, C.3
Farrall, M.4
Assimes, T.L.5
-
11
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011;478:103-109.
-
(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
Chasman, D.I.6
-
12
-
-
67349208839
-
Genome-wide association study of blood pressure and hypertension
-
Levy D, Ehret GB, Rice K, Verwoert GC, Launer LJ, Dehghan A, et al. Genome-wide association study of blood pressure and hypertension. Nat Genet. 2009;41:677-687.
-
(2009)
Nat Genet
, vol.41
, pp. 677-687
-
-
Levy, D.1
Ehret, G.B.2
Rice, K.3
Verwoert, G.C.4
Launer, L.J.5
Dehghan, A.6
-
13
-
-
67249112107
-
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke
-
International Stroke Genetics Consortium
-
Gschwendtner A, Bevan S, Cole JW, Plourde A, Matarin M, Ross-Adams H, et al; International Stroke Genetics Consortium. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann Neurol. 2009;65:531-539.
-
(2009)
Ann Neurol
, vol.65
, pp. 531-539
-
-
Gschwendtner, A.1
Bevan, S.2
Cole, J.W.3
Plourde, A.4
Matarin, M.5
Ross-Adams, H.6
-
14
-
-
84875299446
-
Ischemic stroke is associated with the ABO locus: The EuroCLOT study
-
EuroCLOT Investigators; Wellcome Trust Case Control Consortium 2; MOnica Risk, Genetics, Archiving and Monograph; MetaStroke; International Stroke Genetics Consortium
-
Williams FM, Carter AM, Hysi PG, Surdulescu G, Hodgkiss D, Soranzo N, et al; EuroCLOT Investigators; Wellcome Trust Case Control Consortium 2; MOnica Risk, Genetics, Archiving and Monograph; MetaStroke; International Stroke Genetics Consortium. Ischemic stroke is associated with the ABO locus: the EuroCLOT study. Ann Neurol. 2013;73:16-31.
-
(2013)
Ann Neurol
, vol.73
, pp. 16-31
-
-
Williams, F.M.1
Carter, A.M.2
Hysi, P.G.3
Surdulescu, G.4
Hodgkiss, D.5
Soranzo, N.6
-
15
-
-
84867645825
-
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): A meta-analysis of genome-wide association studies
-
Australian Stroke Genetics Collaborative Wellcome Trust Case Control Consortium 2 (WTCCC2); International Stroke Genetics Consortium
-
Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng YC, et al; Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2); International Stroke Genetics Consortium. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. Lancet Neurol. 2012;11:951-962.
-
(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
-
16
-
-
55849100349
-
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
-
Gretarsdottir S, Thorleifsson G, Manolescu A, Styrkarsdottir U, Helgadottir A, Gschwendtner A, et al. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann Neurol. 2008;64:402-409.
-
(2008)
Ann Neurol
, vol.64
, pp. 402-409
-
-
Gretarsdottir, S.1
Thorleifsson, G.2
Manolescu, A.3
Styrkarsdottir, U.4
Helgadottir, A.5
Gschwendtner, A.6
-
17
-
-
68149137739
-
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
-
Gudbjartsson DF, Holm H, Gretarsdottir S, Thorleifsson G, Walters GB, Thorgeirsson G, et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet. 2009;41:876-878.
-
(2009)
Nat Genet
, vol.41
, pp. 876-878
-
-
Gudbjartsson, D.F.1
Holm, H.2
Gretarsdottir, S.3
Thorleifsson, G.4
Walters, G.B.5
Thorgeirsson, G.6
-
18
-
-
0027958469
-
Stroke risk profile: Adjustment for antihypertensive medication. The Framingham Study
-
D'Agostino RB, Wolf PA, Belanger AJ, Kannel WB. Stroke risk profile: adjustment for antihypertensive medication. The Framingham Study. Stroke. 1994;25:40-43.
-
(1994)
Stroke
, vol.25
, pp. 40-43
-
-
D'Agostino, R.B.1
Wolf, P.A.2
Belanger, A.J.3
Kannel, W.B.4
-
19
-
-
84866382284
-
Routinely available biomarkers improve prediction of long-term mortality in stable coronary artery disease: The Vienna and Ludwigshafen Coronary Artery Disease (VILCAD) risk score
-
Goliasch G, Kleber ME, Richter B, Plischke M, Hoke M, Haschemi A, et al. Routinely available biomarkers improve prediction of long-term mortality in stable coronary artery disease: the Vienna and Ludwigshafen Coronary Artery Disease (VILCAD) risk score. Eur Heart J. 2012;33:2282-2289.
-
(2012)
Eur Heart J
, vol.33
, pp. 2282-2289
-
-
Goliasch, G.1
Kleber, M.E.2
Richter, B.3
Plischke, M.4
Hoke, M.5
Haschemi, A.6
-
20
-
-
84860797764
-
Multiple biomarkers for risk prediction in chronic heart failure
-
Ky B, French B, Levy WC, Sweitzer NK, Fang JC, Wu AH, et al. Multiple biomarkers for risk prediction in chronic heart failure. Circ Heart Fail. 2012;5:183-190.
-
(2012)
Circ Heart Fail
, vol.5
, pp. 183-190
-
-
Ky, B.1
French, B.2
Levy, W.C.3
Sweitzer, N.K.4
Fang, J.C.5
Wu, A.H.6
-
21
-
-
83655201232
-
Vascular biomarkers in the prediction of clinical cardiovascular disease: The Strong Heart Study
-
Roman MJ, Kizer JR, Best LG, Lee ET, Howard BV, Shara NM, et al. Vascular biomarkers in the prediction of clinical cardiovascular disease: the Strong Heart Study. Hypertension. 2012;59:29-35.
-
(2012)
Hypertension
, vol.59
, pp. 29-35
-
-
Roman, M.J.1
Kizer, J.R.2
Best, L.G.3
Lee, E.T.4
Howard, B.V.5
Shara, N.M.6
-
22
-
-
84864335233
-
Genetic markers enhance coronary risk prediction in men: The MORGAM prospective cohorts
-
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
-
-
Hughes, M.F.1
Saarela, O.2
Stritzke, J.3
Kee, F.4
Silander, K.5
Klopp, N.6
-
23
-
-
78049314943
-
A multilocus genetic risk score for coronary heart disease: Case-control and prospective cohort analyses
-
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;376:1393-1400.
-
(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
-
24
-
-
40949149395
-
Polymorphisms associated with cholesterol and risk of cardiovascular events
-
Kathiresan S, Melander O, Anevski D, Guiducci C, Burtt NP, Roos C, et al. Polymorphisms associated with cholesterol and risk of cardiovascular events. N Engl J Med. 2008;358:1240-1249.
-
(2008)
N Engl J Med
, vol.358
, pp. 1240-1249
-
-
Kathiresan, S.1
Melander, O.2
Anevski, D.3
Guiducci, C.4
Burtt, N.P.5
Roos, C.6
-
25
-
-
78649379906
-
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies
-
Davies RW, Dandona S, Stewart AF, Chen L, Ellis SG, Tang WH, et al. Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies. Circ Cardiovasc Genet. 2010;3:468-474.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 468-474
-
-
Davies, R.W.1
Dandona, S.2
Stewart, A.F.3
Chen, L.4
Ellis, S.G.5
Tang, W.H.6
-
26
-
-
84893729545
-
-
23 and Me. Accessed August 2, 2013
-
Stroke Genetic Risk. 23 and Me. Https://www.23andme.Com/health/ stroke/. Accessed August 2, 2013.
-
Stroke Genetic Risk
-
-
-
27
-
-
63449100039
-
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts
-
CHARGE Consortium
-
Psaty BM, O'Donnell CJ, Gudnason V, Lunetta KL, Folsom AR, Rotter JI, et al; CHARGE Consortium. Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circ Cardiovasc Genet. 2009;2:73-80.
-
(2009)
Circ Cardiovasc Genet
, vol.2
, pp. 73-80
-
-
Psaty, B.M.1
O'Donnell, C.J.2
Gudnason, V.3
Lunetta, K.L.4
Folsom, A.R.5
Rotter, J.I.6
-
28
-
-
79251601596
-
Guidelines for the primary prevention of stroke: A guideline for healthcare professionals from the American Heart Association/American Stroke Association
-
American Heart Association Stroke Council; Council on Cardiovascular Nursing; Council on Epidemiology and Prevention; Council for High Blood Pressure Research Council on Peripheral Vascular Disease, and Interdisciplinary Council on Quality of Care and Outcomes Research
-
Goldstein LB, Bushnell CD, Adams RJ, Appel LJ, Braun LT, Chaturvedi S, et al; American Heart Association Stroke Council; Council on Cardiovascular Nursing; Council on Epidemiology and Prevention; Council for High Blood Pressure Research, Council on Peripheral Vascular Disease, and Interdisciplinary Council on Quality of Care and Outcomes Research. Guidelines for the primary prevention of stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2011;42:517-584.
-
(2011)
Stroke
, vol.42
, pp. 517-584
-
-
Goldstein, L.B.1
Bushnell, C.D.2
Adams, R.J.3
Appel, L.J.4
Braun, L.T.5
Chaturvedi, S.6
-
29
-
-
77951487868
-
Cardiovascular risk prediction: Basic concepts, current status, and future directions
-
Lloyd-Jones DM. Cardiovascular risk prediction: basic concepts, current status, and future directions. Circulation. 2010;121:1768-1777.
-
(2010)
Circulation
, vol.121
, pp. 1768-1777
-
-
Lloyd-Jones, D.M.1
-
30
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, 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
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
-
31
-
-
73449129712
-
From disease association to risk assessment: An optimistic view from genome-wide association studies on type 1 diabetes
-
Wei Z, Wang K, Qu HQ, Zhang H, Bradfield J, Kim C, et al. From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes. PLoS Genet. 2009;5:e1000678.
-
(2009)
PLoS Genet
, vol.5
-
-
Wei, Z.1
Wang, K.2
Qu, H.Q.3
Zhang, H.4
Bradfield, J.5
Kim, C.6
-
32
-
-
84875700256
-
Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies
-
405e1
-
Chatterjee N, Wheeler B, Sampson J, Hartge P, Chanock SJ, Park JH. Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies. Nat Genet. 2013;45:400-405, 405e1.
-
(2013)
Nat Genet
, vol.45
, pp. 400-405
-
-
Chatterjee, N.1
Wheeler, B.2
Sampson, J.3
Hartge, P.4
Chanock, S.J.5
Park, J.H.6
-
33
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population- based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. PLINK: a tool set for whole-genome association and population- based linkage analyses. Am J Hum Genet. 2007;81:559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
-
34
-
-
0020524559
-
A method of comparing the areas under receiver operating characteristic curves derived from the same cases
-
Hanley JA, McNeil BJ. A method of comparing the areas under receiver operating characteristic curves derived from the same cases. Radiology. 1983;148:839-843.
-
(1983)
Radiology
, vol.148
, pp. 839-843
-
-
Hanley, J.A.1
McNeil, B.J.2
-
35
-
-
78649477601
-
Extensions of net reclassification improvement calculations to measure usefulness of new biomarkers
-
Pencina MJ, D'Agostino RB Sr, Steyerberg EW. Extensions of net reclassification improvement calculations to measure usefulness of new biomarkers. Stat Med. 2011;30:11-21.
-
(2011)
Stat Med
, vol.30
, pp. 11-21
-
-
Pencina, M.J.1
D'Agostino Sr., R.B.2
Steyerberg, E.W.3
-
36
-
-
0036144041
-
A stroke prediction score in the elderly: Validation and Web-based application
-
Lumley T, Kronmal RA, Cushman M, Manolio TA, Goldstein S. A stroke prediction score in the elderly: validation and Web-based application. J Clin Epidemiol. 2002;55:129-136.
-
(2002)
J Clin Epidemiol
, vol.55
, pp. 129-136
-
-
Lumley, T.1
Kronmal, R.A.2
Cushman, M.3
Manolio, T.A.4
Goldstein, S.5
-
37
-
-
77949578084
-
Performance of common genetic variants in breast- cancer risk models
-
Wacholder S, Hartge P, Prentice R, Garcia-Closas M, Feigelson HS, Diver WR, et al. Performance of common genetic variants in breast- cancer risk models. N Engl J Med. 2010;362:986-993.
-
(2010)
N Engl J Med
, vol.362
, pp. 986-993
-
-
Wacholder, S.1
Hartge, P.2
Prentice, R.3
Garcia-Closas, M.4
Feigelson, H.S.5
Diver, W.R.6
-
38
-
-
55649105963
-
Clinical risk factors, DNA variants, and the development of type 2 diabetes
-
Lyssenko V, Jonsson A, Almgren P, Pulizzi N, Isomaa B, Tuomi T, et al. Clinical risk factors, DNA variants, and the development of type 2 diabetes. N Engl J Med. 2008;359:2220-2232.
-
(2008)
N Engl J Med
, vol.359
, pp. 2220-2232
-
-
Lyssenko, V.1
Jonsson, A.2
Almgren, P.3
Pulizzi, N.4
Isomaa, B.5
Tuomi, T.6
-
39
-
-
56749101779
-
Genotype score in addition to common risk factors for prediction of type 2 diabetes
-
Meigs JB, Shrader P, Sullivan LM, McAteer JB, Fox CS, Dupuis J, et al. Genotype score in addition to common risk factors for prediction of type 2 diabetes. N Engl J Med. 2008;359:2208-2219.
-
(2008)
N Engl J Med
, vol.359
, pp. 2208-2219
-
-
Meigs, J.B.1
Shrader, P.2
Sullivan, L.M.3
McAteer, J.B.4
Fox, C.S.5
Dupuis, J.6
-
40
-
-
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
-
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;223:421-426.
-
(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
-
41
-
-
71849098862
-
Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: A weighted genetic risk score
-
Steering committee of the BENEFIT study; Steering committee of the BEYOND study; Steering committee of the LTF study; Steering committee of the CCR1 study
-
De Jager PL, Chibnik LB, Cui J, Reischl J, Lehr S, Simon KC, et al; Steering committee of the BENEFIT study; Steering committee of the BEYOND study; Steering committee of the LTF study; Steering committee of the CCR1 study. Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: a weighted genetic risk score. Lancet Neurol. 2009;8:1111-1119.
-
(2009)
Lancet Neurol
, vol.8
, pp. 1111-1119
-
-
De Jager, P.L.1
Chibnik, L.B.2
Cui, J.3
Reischl, J.4
Lehr, S.5
Simon, K.C.6
-
42
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. Finding the missing heritability of complex diseases. Nature. 2009;461:747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
-
43
-
-
65949099120
-
Genetic risk prediction-are we there yet?
-
Kraft P, Hunter DJ. Genetic risk prediction-are we there yet? N Engl J Med. 2009;360:1701-1703.
-
(2009)
N Engl J Med
, vol.360
, pp. 1701-1703
-
-
Kraft, P.1
Hunter, D.J.2
-
44
-
-
1842576536
-
Heritability of ischemic stroke in relation to age, vascular risk factors, and subtypes of incident stroke in population-based studies
-
Schulz UG, Flossmann E, Rothwell PM. Heritability of ischemic stroke in relation to age, vascular risk factors, and subtypes of incident stroke in population-based studies. Stroke. 2004;35:819-824.
-
(2004)
Stroke
, vol.35
, pp. 819-824
-
-
Schulz, U.G.1
Flossmann, E.2
Rothwell, P.M.3
-
45
-
-
0043124261
-
Differences in vascular risk factors between etiological subtypes of ischemic stroke: Importance of population-based studies
-
Schulz UG, Rothwell PM. Differences in vascular risk factors between etiological subtypes of ischemic stroke: importance of population-based studies. Stroke. 2003;34:2050-2059.
-
(2003)
Stroke
, vol.34
, pp. 2050-2059
-
-
Schulz, U.G.1
Rothwell, P.M.2
-
46
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS, et al. Genomewide association studies of stroke. N Engl J Med. 2009;360:1718-1728.
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
Fornage, M.4
Destefano, A.L.5
Aulchenko, Y.S.6
-
47
-
-
56049123219
-
Decoding cryptogenic cardioembolism
-
Meschia JF. Decoding cryptogenic cardioembolism. Ann Neurol. 2008;64:364-366.
-
(2008)
Ann Neurol
, vol.64
, pp. 364-366
-
-
Meschia, J.F.1
|