-
1
-
-
33846185489
-
Genetics of ischaemic stroke
-
DOI 10.1016/S1474-4422(07)70028-5, PII S1474442207700285
-
M Dichgans 2007 Genetics of ischaemic stroke Lancet Neurol 6 149 161 1:CAS:528:DC%2BD2sXitVehtL8%3D 10.1016/S1474-4422(07)70028-5 17239802 (Pubitemid 46097541)
-
(2007)
Lancet Neurology
, vol.6
, Issue.2
, pp. 149-161
-
-
Dichgans, M.1
-
2
-
-
77949816268
-
Parental occurrence of stroke and risk of stroke in their children: The Framingham study
-
10.1161/CIRCULATIONAHA.109.854240 20212282
-
S Seshadri A Beiser A Pikula, et al. 2010 Parental occurrence of stroke and risk of stroke in their children: the Framingham study Circulation 121 1304 1312 10.1161/CIRCULATIONAHA.109.854240 20212282
-
(2010)
Circulation
, vol.121
, pp. 1304-1312
-
-
Seshadri, S.1
Beiser, A.2
Pikula, A.3
-
3
-
-
0141819194
-
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke
-
DOI 10.1038/ng1245
-
S Gretarsdottir G Thorleifsson ST Reynisdottir, et al. 2003 The gene encoding phosphodiesterase 4D confers risk of ischemic stroke Nat Genet 35 131 138 1:CAS:528:DC%2BD3sXns1WgtLs%3D 10.1038/ng1245 14517540 (Pubitemid 37187631)
-
(2003)
Nature Genetics
, vol.35
, Issue.2
, pp. 131-138
-
-
Gretarsdottir, S.1
Thorleifsson, G.2
Reynisdottir, S.Th.3
Manolescu, A.4
Jonsdottir, S.5
Jonsdottir, T.6
Gudmundsdottir, T.7
Bjarnadottir, S.M.8
Einarsson, O.B.9
Gudjonsdottir, H.M.10
Hawkins, M.11
Gudmundsson, G.12
Gudmundsdottir, H.13
Andrason, H.14
Gudmundsdottir, A.S.15
Sigurdardottir, M.16
Chou, T.T.17
Nahmias, J.18
Goss, S.19
Sveinbjornsdottir, S.20
Valdimarsson, E.M.21
Jakobsson, F.22
Agnarsson, U.23
Gudnason, V.24
Thorgeirsson, G.25
Fingerle, J.26
Gurney, M.27
Gudbjartsson, D.28
Frigge, M.L.29
Kong, A.30
Stefansson, K.31
Gulcher, J.R.32
more..
-
4
-
-
47649111461
-
Variation in the PDE4D gene and ischemic stroke risk: A systematic review and meta-analysis on 5200 cases and 6600 controls
-
1:CAS:528:DC%2BD1cXnt1emt7c%3D 10.1161/STROKEAHA.107.509992 18420948
-
S Bevan M Dichgans A Gschwendtner, et al. 2008 Variation in the PDE4D gene and ischemic stroke risk: a systematic review and meta-analysis on 5200 cases and 6600 controls Stroke 39 1966 1971 1:CAS:528:DC%2BD1cXnt1emt7c%3D 10.1161/STROKEAHA.107.509992 18420948
-
(2008)
Stroke
, vol.39
, pp. 1966-1971
-
-
Bevan, S.1
Dichgans, M.2
Gschwendtner, A.3
-
5
-
-
65149106113
-
Multilocus Bayesian meta-analysis of gene-disease associations
-
1:CAS:528:DC%2BD1MXmvFCmtbc%3D 10.1016/j.ajhg.2009.04.001 19409523
-
PJ Newcombe C Verzilli JP Casas, et al. 2009 Multilocus Bayesian meta-analysis of gene-disease associations Am J Hum Genet 84 567 580 1:CAS:528:DC%2BD1MXmvFCmtbc%3D 10.1016/j.ajhg.2009.04.001 19409523
-
(2009)
Am J Hum Genet
, vol.84
, pp. 567-580
-
-
Newcombe, P.J.1
Verzilli, C.2
Casas, J.P.3
-
6
-
-
70350539764
-
Candidate gene polymorphisms for ischemic stroke
-
1:CAS:528:DC%2BD1MXhtlWgu7nK 10.1161/STROKEAHA.109.558015 19729601
-
M Matarin WM Brown H Dena, et al. 2009 Candidate gene polymorphisms for ischemic stroke Stroke 40 3436 3442 1:CAS:528:DC%2BD1MXhtlWgu7nK 10.1161/STROKEAHA.109.558015 19729601
-
(2009)
Stroke
, vol.40
, pp. 3436-3442
-
-
Matarin, M.1
Brown, W.M.2
Dena, H.3
-
7
-
-
60549095802
-
Gene variants associated with ischemic stroke: The cardiovascular health study
-
1:CAS:528:DC%2BD1MXmvVejtA%3D%3D 10.1161/STROKEAHA.108.521328 19023099
-
MM Luke ES O'Meara CM Rowland, et al. 2009 Gene variants associated with ischemic stroke: the cardiovascular health study Stroke 40 363 368 1:CAS:528:DC%2BD1MXmvVejtA%3D%3D 10.1161/STROKEAHA.108.521328 19023099
-
(2009)
Stroke
, vol.40
, pp. 363-368
-
-
Luke, M.M.1
O'Meara, E.S.2
Rowland, C.M.3
-
8
-
-
34249996115
-
A common allele on chromosome 9 associated with coronary heart disease
-
DOI 10.1126/science.1142447
-
R McPherson A Pertsemlidis N Kavaslar, et al. 2007 A common allele on chromosome 9 associated with coronary heart disease Science 316 1488 1491 1:CAS:528:DC%2BD2sXmtFSjtr0%3D 10.1126/science.1142447 17478681 (Pubitemid 46906617)
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1488-1491
-
-
McPherson, R.1
Pertsemlidis, A.2
Kavaslar, N.3
Stewart, A.4
Roberts, R.5
Cox, D.R.6
Hinds, D.A.7
Pennacchio, L.A.8
Tybjaerg-Hansen, A.9
Folsom, A.R.10
Boerwinkle, E.11
Hobbs, H.H.12
Cohen, J.C.13
-
9
-
-
34250010480
-
A common variant on chromosome 9p21 affects the risk of myocardial infarction
-
DOI 10.1126/science.1142842
-
A Helgadottir G Thorleifsson A Manolescu, et al. 2007 A common variant on chromosome 9p21 affects the risk of myocardial infarction Science 316 1491 1493 1:CAS:528:DC%2BD2sXmtFSjtro%3D 10.1126/science.1142842 17478679 (Pubitemid 46906618)
-
(2007)
Science
, vol.316
, Issue.5830
, pp. 1491-1493
-
-
Helgadottir, A.1
Thorleifsson, G.2
Manolescu, A.3
Gretarsdottir, S.4
Blondal, T.5
Jonasdottir, A.6
Jonasdottir, A.7
Sigurdsson, A.8
Baker, A.9
Palsson, A.10
Masson, G.11
Gudbjartsson, D.F.12
Magnusson, K.P.13
Andersen, K.14
Levey, A.I.15
Backman, V.M.16
Matthiasdottir, S.17
Jonsdottir, T.18
Palsson, S.19
Einarsdottir, H.20
Gunnarsdottir, S.21
Gylfason, A.22
Vaccarino, V.23
Hooper, W.C.24
Reilly, M.P.25
Granger, C.B.26
Austin, H.27
Rader, D.J.28
Shah, S.H.29
Quyyumi, A.A.30
Gulcher, J.R.31
Thorgeirsson, G.32
Thorsteinsdottir, U.33
Kong, A.34
Stefansson, K.35
more..
-
10
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
DOI 10.1038/nature05911, PII NATURE05911
-
Wellcome Trust Case Control Consortium 2007 Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls Nature 447 661 678 10.1038/nature05911 (Pubitemid 46889737)
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.P.7
McCarthy, M.I.8
Ouwehand, W.H.9
Samani, N.J.10
Todd, J.A.11
Donnelly, P.12
Barrett, J.C.13
Davison, D.14
Easton, D.15
Evans, D.16
Leung, H.-T.17
Marchini, J.L.18
Morris, A.P.19
Spencer, C.C.A.20
Tobin, M.D.21
more..
-
11
-
-
34547623750
-
Genomewide association analysis of coronary artery disease
-
DOI 10.1056/NEJMoa072366
-
NJ Samani J Erdmann AS Hall, et al. 2007 Genomewide association analysis of coronary artery disease N Engl J Med 357 443 453 1:CAS:528: DC%2BD2sXos1emsrk%3D 10.1056/NEJMoa072366 17634449 (Pubitemid 47204873)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.5
, pp. 443-453
-
-
Samani, N.J.1
Erdmann, J.2
Hall, A.S.3
Hengstenberg, C.4
Mangino, M.5
Mayer, B.6
Dixon, R.J.7
Meitinger, T.8
Braund, P.9
Wichmann, H.-E.10
Barrett, J.H.11
Konig, I.R.12
Stevens, S.E.13
Szymczak, S.14
Tregouet, D.-A.15
Iles, M.M.16
Pahlke, F.17
Pollard, H.18
Lieb, W.19
Cambien, F.20
Fischer, M.21
Ouwehand, W.22
Blankenberg, S.23
Balmforth, A.J.24
Baessler, A.25
Ball, S.G.26
Strom, T.M.27
Braenne, I.28
Gieger, C.29
Deloukas, P.30
Tobin, M.D.31
Ziegler, A.32
Thompson, J.R.33
Schunkert, H.34
more..
-
12
-
-
67249112107
-
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke
-
1:CAS:528:DC%2BD1MXnvFahsLg%3D 10.1002/ana.21590 19475673 The 9p21.3 locus, previously shown to be a risk factor for coronary artery disease, is an independent risk factor for large artery atherosclerosis-type ischemic stroke
-
A Gschwendtner S Bevan JW Cole, et al. 2009 Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke Ann Neurol 65 531 539 1:CAS:528:DC%2BD1MXnvFahsLg%3D 10.1002/ana.21590 19475673 The 9p21.3 locus, previously shown to be a risk factor for coronary artery disease, is an independent risk factor for large artery atherosclerosis-type ischemic stroke
-
(2009)
Ann Neurol
, vol.65
, pp. 531-539
-
-
Gschwendtner, A.1
Bevan, S.2
Cole, J.W.3
-
13
-
-
55849100349
-
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
-
10.1002/ana.21480 18991354
-
S Gretarsdottir G Thorleifsson A Manolescu, et al. 2008 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke Ann Neurol 64 402 409 10.1002/ana.21480 18991354
-
(2008)
Ann Neurol
, vol.64
, pp. 402-409
-
-
Gretarsdottir, S.1
Thorleifsson, G.2
Manolescu, A.3
-
14
-
-
77956419347
-
The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology
-
10.1161/STROKEAHA.110.587980 20671249
-
R Lemmens I Buysschaert V Geelen, et al. 2010 The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology Stroke 41 1850 1857 10.1161/STROKEAHA.110.587980 20671249
-
(2010)
Stroke
, vol.41
, pp. 1850-1857
-
-
Lemmens, R.1
Buysschaert, I.2
Geelen, V.3
-
15
-
-
68149137739
-
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
-
1:CAS:528:DC%2BD1MXosFWhtro%3D 10.1038/ng.417 19597491
-
DF Gudbjartsson H Holm S Gretarsdottir, et al. 2009 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke Nat Genet 41 876 878 1:CAS:528:DC%2BD1MXosFWhtro%3D 10.1038/ng.417 19597491
-
(2009)
Nat Genet
, vol.41
, pp. 876-878
-
-
Gudbjartsson, D.F.1
Holm, H.2
Gretarsdottir, S.3
-
16
-
-
34047274599
-
A genome-wide genotyping study in patients with ischaemic stroke: Initial analysis and data release
-
DOI 10.1016/S1474-4422(07)70081-9, PII S1474442207700819
-
M Matarin WM Brown S Scholz, et al. 2007 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Lancet Neurol 6 414 420 1:CAS:528:DC%2BD2sXmtVyrsb8%3D 10.1016/S1474-4422(07)70081-9 17434096 (Pubitemid 46551853)
-
(2007)
Lancet Neurology
, vol.6
, Issue.5
, pp. 414-420
-
-
Matarin, M.1
Brown, W.M.2
Scholz, S.3
Simon-Sanchez, J.4
Fung, H.-C.5
Hernandez, D.6
Gibbs, J.R.7
De Vrieze, F.W.8
Crews, C.9
Britton, A.10
Langefeld, C.D.11
Brott, T.G.12
Brown Jr., R.D.13
Worrall, B.B.14
Frankel, M.15
Silliman, S.16
Case, L.D.17
Singleton, A.18
Hardy, J.A.19
Rich, S.S.20
Meschia, J.F.21
more..
-
17
-
-
74049143132
-
Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke
-
10.1161/STROKEAHA.109.567099 19910543
-
H Ding Y Xu X Bao, et al. 2010 Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke Stroke 41 177 180 10.1161/STROKEAHA.109.567099 19910543
-
(2010)
Stroke
, vol.41
, pp. 177-180
-
-
Ding, H.1
Xu, Y.2
Bao, X.3
-
18
-
-
33846587067
-
A nonsynonymous SNP in PRKCH (protein kinase C) increases the risk of cerebral infarction
-
DOI 10.1038/ng1945, PII NG1945
-
M Kubo J Hata T Ninomiya, et al. 2007 A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction Nat Genet 39 212 217 1:CAS:528:DC%2BD2sXpvFersw%3D%3D 10.1038/ng1945 17206144 (Pubitemid 46184352)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 212-217
-
-
Kubo, M.1
Hata, J.2
Ninomiya, T.3
Matsuda, K.4
Yonemoto, K.5
Nakano, T.6
Matsushita, T.7
Yamazaki, K.8
Ohnishi, Y.9
Saito, S.10
Kitazono, T.11
Ibayashi, S.12
Sueishi, K.13
Iida, M.14
Nakamura, Y.15
Kiyohara, Y.16
-
19
-
-
70349234481
-
The 1425 G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population
-
1:CAS:528:DC%2BD1MXhtVSisL3M 10.1161/STROKEAHA.109.551747 19520989
-
L Wu Y Shen X Liu, et al. 2009 The 1425 G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population Stroke 40 2973 2976 1:CAS:528:DC%2BD1MXhtVSisL3M 10.1161/STROKEAHA.109.551747 19520989
-
(2009)
Stroke
, vol.40
, pp. 2973-2976
-
-
Wu, L.1
Shen, Y.2
Liu, X.3
-
20
-
-
34247116957
-
Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction
-
DOI 10.1093/hmg/ddm005
-
J Hata K Matsuda T Ninomiya, et al. 2007 Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction Hum Mol Genet 16 630 639 1:CAS:528:DC%2BD2sXktlWjsr8%3D 10.1093/hmg/ddm005 17309882 (Pubitemid 46585664)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.6
, pp. 630-639
-
-
Hata, J.1
Matsuda, K.2
Ninomiya, T.3
Yonemoto, K.4
Matsushita, T.5
Ohnishi, Y.6
Saito, S.7
Kitazono, T.8
Ibayashi, S.9
Iida, M.10
Kiyohara, Y.11
Nakamura, Y.12
Kubo, M.13
-
21
-
-
65949090748
-
Genomewide association studies of stroke
-
1:CAS:528:DC%2BD1MXkvVOrsbs%3D 10.1056/NEJMoa0900094 19369658
-
MA Ikram S Seshadri JC Bis, et al. 2009 Genomewide association studies of stroke N Engl J Med 360 1718 1728 1:CAS:528:DC%2BD1MXkvVOrsbs%3D 10.1056/NEJMoa0900094 19369658
-
(2009)
N Engl J Med
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
Seshadri, S.2
Bis, J.C.3
-
22
-
-
77951427974
-
-
International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2: Failure to validate association between 12p13 variants and ischemic stroke
-
International Stroke Genetics Consortium; Wellcome Trust Case-Control Consortium 2: Failure to validate association between 12p13 variants and ischemic stroke. N Engl J Med 2010, 362:1547-1550.
-
(2010)
N Engl J Med
, vol.362
, pp. 1547-1550
-
-
-
23
-
-
70350574629
-
Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
-
1:CAS:528:DC%2BD1MXhtlyrtbbP 10.1016/j.atherosclerosis.2009.03.038 19403135
-
Y Yamada N Fuku M Tanaka, et al. 2009 Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study Atherosclerosis 207 144 149 1:CAS:528:DC%2BD1MXhtlyrtbbP 10.1016/j.atherosclerosis.2009.03.038 19403135
-
(2009)
Atherosclerosis
, vol.207
, pp. 144-149
-
-
Yamada, Y.1
Fuku, N.2
Tanaka, M.3
-
24
-
-
77950221224
-
Advances in genomic analysis of stroke: What have we learned and where are we headed?
-
1:CAS:528:DC%2BC3cXjvFCgs7g%3D 10.1161/STROKEAHA.109.570523 20167918
-
MB Lanktree M Dichgans RA Hegele 2010 Advances in genomic analysis of stroke: what have we learned and where are we headed? Stroke 41 825 832 1:CAS:528:DC%2BC3cXjvFCgs7g%3D 10.1161/STROKEAHA.109.570523 20167918
-
(2010)
Stroke
, vol.41
, pp. 825-832
-
-
Lanktree, M.B.1
Dichgans, M.2
Hegele, R.A.3
-
25
-
-
33644876583
-
Genome-wide scan for white matter hyperintensity: The framingham heart study
-
DOI 10.1161/01.STR.0000196987.68770.b3, PII 0000767020060100000020
-
AL DeStefano LD Atwood JM Massaro, et al. 2006 Genome-wide scan for white matter hyperintensity: the Framingham Heart Study Stroke 37 77 81 10.1161/01.STR.0000196987.68770.b3 16322484 (Pubitemid 43732051)
-
(2006)
Stroke
, vol.37
, Issue.1
, pp. 77-81
-
-
DeStefano, A.L.1
Atwood, L.D.2
Massaro, J.M.3
Heard-Costa, N.4
Beiser, A.5
Au, R.6
Wolf, P.A.7
Decarli, C.8
-
26
-
-
15744392128
-
Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study
-
DOI 10.1161/01.HYP.0000154685.54766.2d
-
ST Turner M Fornage CR Jack, et al. 2005 Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study Hypertension 45 793 798 1:CAS:528:DC%2BD2MXisV2jurw%3D 10.1161/01.HYP.0000154685.54766.2d 15699467 (Pubitemid 40418383)
-
(2005)
Hypertension
, vol.45
, Issue.4 SUPPL.
, pp. 793-798
-
-
Turner, S.T.1
Fornage, M.2
Jack Jr., C.R.3
Mosley, T.H.4
Kardia, S.L.R.5
Boerwinkle, E.6
De Andrade, M.7
-
27
-
-
66849141259
-
Genetic determinants of white matter hyperintensities on brain scans: A systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19, 000 subjects
-
10.1161/STROKEAHA.108.542050 19407234
-
L Paternoster W Chen CL Sudlow 2009 Genetic determinants of white matter hyperintensities on brain scans: a systematic assessment of 19 candidate gene polymorphisms in 46 studies in 19, 000 subjects Stroke 40 2020 2026 10.1161/STROKEAHA.108.542050 19407234
-
(2009)
Stroke
, vol.40
, pp. 2020-2026
-
-
Paternoster, L.1
Chen, W.2
Sudlow, C.L.3
-
28
-
-
74049102343
-
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients
-
1:STN:280:DC%2BD1Mfksl2gtQ%3D%3D 10.1212/WNL.0b013e3181c7da7c 20038773
-
L Pantoni F Pescini S Nannucci, et al. 2010 Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients Neurology 74 57 63 1:STN:280:DC%2BD1Mfksl2gtQ%3D%3D 10.1212/WNL.0b013e3181c7da7c 20038773
-
(2010)
Neurology
, vol.74
, pp. 57-63
-
-
Pantoni, L.1
Pescini, F.2
Nannucci, S.3
-
29
-
-
65249114174
-
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients
-
19174371
-
S Tikka K Mykkanen MM Ruchoux, et al. 2009 Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients Brain 132 Pt 4 933 939 19174371
-
(2009)
Brain
, vol.132
, Issue.PART 4
, pp. 933-939
-
-
Tikka, S.1
Mykkanen, K.2
Ruchoux, M.M.3
-
30
-
-
67649413524
-
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain
-
10.1093/brain/awp049 19293235
-
M Monet-Lepretre B Bardot B Lemaire, et al. 2009 Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain Brain 132 Pt 6 1601 1612 10.1093/brain/awp049 19293235
-
(2009)
Brain
, vol.132
, Issue.PART 6
, pp. 1601-1612
-
-
Monet-Lepretre, M.1
Bardot, B.2
Lemaire, B.3
-
31
-
-
60549106489
-
MRI correlates of cognitive decline in CADASIL: A 7-year follow-up study
-
1:STN:280:DC%2BD1M%2Fms12ltA%3D%3D 10.1212/01.wnl.0000339038.65508.96 19139365
-
MK Liem SA Lesnik Oberstein J Haan, et al. 2009 MRI correlates of cognitive decline in CADASIL: a 7-year follow-up study Neurology 72 143 148 1:STN:280:DC%2BD1M%2Fms12ltA%3D%3D 10.1212/01.wnl.0000339038.65508.96 19139365
-
(2009)
Neurology
, vol.72
, pp. 143-148
-
-
Liem, M.K.1
Lesnik Oberstein, S.A.2
Haan, J.3
-
32
-
-
64049098726
-
Apathy: A major symptom in CADASIL
-
1:STN:280:DC%2BD1M7psleqtQ%3D%3D 10.1212/01.wnl.0000344166.03470.f8 19273824
-
S Reyes A Viswanathan O Godin, et al. 2009 Apathy: a major symptom in CADASIL Neurology 72 905 910 1:STN:280:DC%2BD1M7psleqtQ%3D%3D 10.1212/01.wnl.0000344166.03470.f8 19273824
-
(2009)
Neurology
, vol.72
, pp. 905-910
-
-
Reyes, S.1
Viswanathan, A.2
Godin, O.3
-
33
-
-
66849099874
-
Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutation
-
10.1161/STROKEAHA.108.528661 19372454
-
K Mykkanen M Junna K Amberla, et al. 2009 Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutation Stroke 40 2215 2218 10.1161/STROKEAHA.108.528661 19372454
-
(2009)
Stroke
, vol.40
, pp. 2215-2218
-
-
Mykkanen, K.1
Junna, M.2
Amberla, K.3
-
34
-
-
65949097072
-
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease
-
1:CAS:528:DC%2BD1MXkvVOrtb4%3D 10.1056/NEJMoa0801560 19387015 Variants in the HtrA serine protease 1 gene cause CARASIL
-
K Hara A Shiga T Fukutake, et al. 2009 Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease N Engl J Med 360 1729 1739 1:CAS:528:DC%2BD1MXkvVOrtb4%3D 10.1056/NEJMoa0801560 19387015 Variants in the HtrA serine protease 1 gene cause CARASIL
-
(2009)
N Engl J Med
, vol.360
, pp. 1729-1739
-
-
Hara, K.1
Shiga, A.2
Fukutake, T.3
-
35
-
-
66849141261
-
Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms
-
10.1161/STROKEAHA.108.542571 19228834 A positive family history of IAs may dramatically increase the risk of rupture of small (≤ 6 mm) IAs
-
JP Broderick RD Brown Jr L Sauerbeck, et al. 2009 Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms Stroke 40 1952 1957 10.1161/STROKEAHA.108.542571 19228834 A positive family history of IAs may dramatically increase the risk of rupture of small (≤ 6 mm) IAs
-
(2009)
Stroke
, vol.40
, pp. 1952-1957
-
-
Broderick, J.P.1
Brown Jr., R.D.2
Sauerbeck, L.3
-
36
-
-
63849102909
-
Smoking and family history and risk of aneurysmal subarachnoid hemorrhage
-
1:STN:280:DC%2BD1M%2FltFegtQ%3D%3D 10.1212/01.wnl.0000338567.90260.46 19122033
-
D Woo J Khoury MM Haverbusch, et al. 2009 Smoking and family history and risk of aneurysmal subarachnoid hemorrhage Neurology 72 69 72 1:STN:280:DC%2BD1M%2FltFegtQ%3D%3D 10.1212/01.wnl.0000338567.90260.46 19122033
-
(2009)
Neurology
, vol.72
, pp. 69-72
-
-
Woo, D.1
Khoury, J.2
Haverbusch, M.M.3
-
37
-
-
62349103774
-
Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study
-
1:STN:280:DC%2BD1M7ms1eisQ%3D%3D 10.1212/01.wnl.0000342999.99907.fd 19237697
-
D Woo R Hornung L Sauerbeck, et al. 2009 Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study Neurology 72 695 698 1:STN:280:DC%2BD1M7ms1eisQ%3D%3D 10.1212/01.wnl.0000342999.99907.fd 19237697
-
(2009)
Neurology
, vol.72
, pp. 695-698
-
-
Woo, D.1
Hornung, R.2
Sauerbeck, L.3
-
38
-
-
77952120521
-
Optimal screening strategy for familial intracranial aneurysms: A cost-effectiveness analysis
-
10.1212/WNL.0b013e3181e04297 20498435 Screening for unruptured IAs every 7 years in patients 20 to 80 years old appears to be cost effective if they have two or more first-degree relatives with subarachnoid hemorrhage
-
AS Bor H Koffijberg MJ Wermer, et al. 2010 Optimal screening strategy for familial intracranial aneurysms: a cost-effectiveness analysis Neurology 74 1671 1679 10.1212/WNL.0b013e3181e04297 20498435 Screening for unruptured IAs every 7 years in patients 20 to 80 years old appears to be cost effective if they have two or more first-degree relatives with subarachnoid hemorrhage
-
(2010)
Neurology
, vol.74
, pp. 1671-1679
-
-
Bor, A.S.1
Koffijberg, H.2
Wermer, M.J.3
-
39
-
-
77951768060
-
Genome-wide association study of intracranial aneurysm identifies three new risk loci
-
1:CAS:528:DC%2BC3cXkt1aqtb4%3D 10.1038/ng.563 20364137 This is a large European and Japanese collaborative genome-wide association that confirmed two loci (8q11.23-q12.1 and 9p21.3) and discovered three new loci for IAs
-
K Yasuno K Bilguvar P Bijlenga, et al. 2010 Genome-wide association study of intracranial aneurysm identifies three new risk loci Nat Genet 42 420 425 1:CAS:528:DC%2BC3cXkt1aqtb4%3D 10.1038/ng.563 20364137 This is a large European and Japanese collaborative genome-wide association that confirmed two loci (8q11.23-q12.1 and 9p21.3) and discovered three new loci for IAs
-
(2010)
Nat Genet
, vol.42
, pp. 420-425
-
-
Yasuno, K.1
Bilguvar, K.2
Bijlenga, P.3
-
40
-
-
73349084959
-
Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome
-
1:STN:280:DC%2BD1Mjpt1CitA%3D%3D 10.1212/WNL.0b013e3181c3fd12 19949034
-
S Alamowitch E Plaisier P Favrole, et al. 2009 Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome Neurology 73 1873 1882 1:STN:280:DC%2BD1Mjpt1CitA%3D%3D 10.1212/WNL.0b013e3181c3fd12 19949034
-
(2009)
Neurology
, vol.73
, pp. 1873-1882
-
-
Alamowitch, S.1
Plaisier, E.2
Favrole, P.3
-
41
-
-
65149088429
-
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease
-
1:CAS:528:DC%2BD1MXmvFCmur0%3D 10.1016/j.ajhg.2009.04.007 19409525
-
DC Guo CL Papke V Tran-Fadulu, et al. 2009 Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease Am J Hum Genet 84 617 627 1:CAS:528:DC%2BD1MXmvFCmur0%3D 10.1016/j.ajhg.2009.04.007 19409525
-
(2009)
Am J Hum Genet
, vol.84
, pp. 617-627
-
-
Guo, D.C.1
Papke, C.L.2
Tran-Fadulu, V.3
-
42
-
-
33747012109
-
CNS manifestations of Fabry's disease
-
DOI 10.1016/S1474-4422(06)70548-8, PII S1474442206705488
-
A Fellgiebel MJ Muller L Ginsberg 2006 CNS manifestations of Fabry's disease Lancet Neurol 5 791 795 10.1016/S1474-4422(06)70548-8 16914407 (Pubitemid 44205515)
-
(2006)
Lancet Neurology
, vol.5
, Issue.9
, pp. 791-795
-
-
Fellgiebel, A.1
Muller, M.J.2
Ginsberg, L.3
-
43
-
-
71649111830
-
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: An analysis of registry data
-
1:CAS:528:DC%2BD1MXhsFGgtLrN 10.1016/S0140-6736(09)61493-8 19959221
-
A Mehta M Beck P Elliott, et al. 2009 Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data Lancet 374 1986 1996 1:CAS:528:DC%2BD1MXhsFGgtLrN 10.1016/S0140-6736(09)61493-8 19959221
-
(2009)
Lancet
, vol.374
, pp. 1986-1996
-
-
Mehta, A.1
Beck, M.2
Elliott, P.3
-
44
-
-
27844440793
-
Prevalence of Fabry disease in patients with cryptogenic stroke: A prospective study
-
DOI 10.1016/S0140-6736(05)67635-0, PII S0140673605676350
-
A Rolfs T Bottcher M Zschiesche, et al. 2005 Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study Lancet 366 1794 1796 10.1016/S0140-6736(05)67635-0 16298216 (Pubitemid 41642643)
-
(2005)
Lancet
, vol.366
, Issue.9499
, pp. 1794-1796
-
-
Rolfs, A.1
Bottcher, T.2
Zschiesche, M.3
Morris, P.4
Winchester, B.5
Bauer, P.6
Walter, U.7
Mix, E.8
Lohr, M.9
Harzer, K.10
Strauss, U.11
Pahnke, J.12
Grossmann, A.13
Benecke, R.14
-
45
-
-
74049117508
-
Frequency of unrecognized Fabry disease among young European-American and African-American men with first ischemic stroke
-
10.1161/STROKEAHA.109.558320 20007919
-
MA Wozniak SJ Kittner S Tuhrim, et al. 2010 Frequency of unrecognized Fabry disease among young European-American and African-American men with first ischemic stroke Stroke 41 78 81 10.1161/STROKEAHA.109.558320 20007919
-
(2010)
Stroke
, vol.41
, pp. 78-81
-
-
Wozniak, M.A.1
Kittner, S.J.2
Tuhrim, S.3
-
46
-
-
77955144625
-
Prasugrel
-
10.1161/CIRCULATIONAHA.109.921502 20660815
-
SD Wiviott EM Antman E Braunwald 2010 Prasugrel Circulation 122 394 403 10.1161/CIRCULATIONAHA.109.921502 20660815
-
(2010)
Circulation
, vol.122
, pp. 394-403
-
-
Wiviott, S.D.1
Antman, E.M.2
Braunwald, E.3
-
47
-
-
77958567291
-
Prasugrel versus clopidogrel for Cytochrome P450 2 C19 genotyped subgroups: Integration of the TRITON-TIMI 38 trial data
-
May 21 [Epub ahead of print]
-
Sorich MJ, Vitry A, Ward MB, et al.: Prasugrel versus clopidogrel for Cytochrome P450 2 C19 genotyped subgroups: integration of the TRITON-TIMI 38 trial data. J Thromb Haemost 2010 May 21 [Epub ahead of print].
-
(2010)
J Thromb Haemost
-
-
Sorich, M.J.1
Vitry, A.2
Ward, M.B.3
-
48
-
-
35648976555
-
A computerized algorithm for etiologic classification of ischemic stroke: The causative classification of stroke system
-
DOI 10.1161/STROKEAHA.107.490896, PII 0000767020071100000019
-
H Ay T Benner EM Arsava, et al. 2007 A computerized algorithm for etiologic classification of ischemic stroke: the Causative Classification of Stroke System Stroke 38 2979 2984 10.1161/STROKEAHA.107.490896 17901381 (Pubitemid 350035693)
-
(2007)
Stroke
, vol.38
, Issue.11
, pp. 2979-2984
-
-
Ay, H.1
Benner, T.2
Arsava, E.M.3
Furie, K.L.4
Singhal, A.B.5
Jensen, M.B.6
Ayata, C.7
Towfighi, A.8
Smith, E.E.9
Chong, J.Y.10
Koroshetz, W.J.11
Sorensen, A.G.12
|