-
2
-
-
0024604248
-
Infarcts of undetermined cause: The NINCDS Stroke Data Bank
-
DOI 10.1002/ana.410250410
-
Sacco, R.L. et al. Infarcts of undetermined cause: the NINCDS Stroke Data Bank. Ann. Neurol. 25, 382-390 (1989). (Pubitemid 19104170)
-
(1989)
Annals of Neurology
, vol.25
, Issue.4
, pp. 382-390
-
-
Sacco, R.L.1
Ellenberg, J.H.2
Mohr, J.P.3
Tatemichi, T.K.4
Hier, D.B.5
Price, T.R.6
Wolf, P.A.7
-
3
-
-
33846185489
-
Genetics of ischaemic stroke
-
DOI 10.1016/S1474-4422(07)70028-5, PII S1474442207700285
-
Dichgans, M. Genetics of ischaemic stroke. Lancet Neurol. 6, 149-161 (2007). (Pubitemid 46097541)
-
(2007)
Lancet Neurology
, vol.6
, Issue.2
, pp. 149-161
-
-
Dichgans, M.1
-
4
-
-
0037534908
-
Evaluating the genetic component of ischemic stroke subtypes: A family history study
-
DOI 10.1161/01.STR.0000069723.17984.FD
-
Jerrard-Dunne, P., Cloud, G., Hassan, A. & Markus, H.S. Evaluating the genetic component of ischemic stroke subtypes: a family history study. Stroke 34, 1364-1369 (2003). (Pubitemid 36693499)
-
(2003)
Stroke
, vol.34
, Issue.6
, pp. 1364-1369
-
-
Jerrard-Dunne, P.1
Cloud, G.2
Hassan, A.3
Markus, H.S.4
-
5
-
-
55849100349
-
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
-
Gretarsdottir, S. et al. Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann. Neurol. 64, 402-409 (2008).
-
(2008)
Ann. Neurol.
, vol.64
, pp. 402-409
-
-
Gretarsdottir, S.1
-
6
-
-
77956419347
-
The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology
-
Lemmens, R. et al. The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology. Stroke 41, 1850-1857 (2010).
-
(2010)
Stroke
, vol.41
, pp. 1850-1857
-
-
Lemmens, R.1
-
7
-
-
67249112107
-
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke
-
Gschwendtner, A. et al. Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann. Neurol. 65, 531-539 (2009).
-
(2009)
Ann. Neurol.
, vol.65
, pp. 531-539
-
-
Gschwendtner, A.1
-
8
-
-
78649461096
-
Genetics studies in ischaemic stroke
-
Markus, H.S. Genetics studies in ischaemic stroke. Transl. Stroke Res. 1, 238-245 (2010).
-
(2010)
Transl. Stroke Res.
, vol.1
, pp. 238-245
-
-
Markus, H.S.1
-
9
-
-
0027514354
-
Classification of subtype of acute ischemic stroke: Definitions for use in a multicenter clinical trial
-
Adams, H.P. Jr. et al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment. Stroke 24, 35-41 (1993). (Pubitemid 23014379)
-
(1993)
Stroke
, vol.24
, Issue.1
, pp. 35-41
-
-
Adams Jr., H.P.1
Bendixen, B.H.2
Kappelle, L.J.3
Biller, J.4
Love, B.B.5
Gordon, D.L.6
Marsh III, E.E.7
-
10
-
-
68149137739
-
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
-
Gudbjartsson, D.F. et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat. Genet. 41, 876-878 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 876-878
-
-
Gudbjartsson, D.F.1
-
11
-
-
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. 22, 1547-1550 (2010).
-
(2010)
N. Engl. J. Med.
, vol.22
, pp. 1547-1550
-
-
-
12
-
-
79451468882
-
Genetic variant on chromosome 12p13 does mot show association to ischemic stroke in 3 Swedish case-control studies
-
Olsson, S. et al. Genetic variant on chromosome 12p13 does mot show association to ischemic stroke in 3 Swedish case-control studies. Stroke 42, 214-216 (2011).
-
(2011)
Stroke
, vol.42
, pp. 214-216
-
-
Olsson, S.1
-
13
-
-
65949090748
-
Genomewide association studies of stroke
-
Ikram, M.A. et al. Genomewide association studies of stroke. N. Engl. J. Med. 360, 1718-1728 (2009).
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1718-1728
-
-
Ikram, M.A.1
-
14
-
-
80053191623
-
Strong association between the NINJ2 gene polymorphism and the susceptibility of stroke in Chinese Han population in Fangshan district
-
Chen, K. et al. Strong association between the NINJ2 gene polymorphism and the susceptibility of stroke in Chinese Han population in Fangshan district. Beijing Da Xue Xue Bao 42, 498-502 (2010).
-
(2010)
Beijing da Xue Xue Bao
, vol.42
, pp. 498-502
-
-
Chen, K.1
-
15
-
-
67349085063
-
Genome-wide association study identifies eight loci associated with blood pressure
-
Newton-Cheh, C. et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat. Genet. 41, 666-676 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 666-676
-
-
Newton-Cheh, C.1
-
16
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich, T.M. et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature 468, 707-713 (2010).
-
(2010)
Nature
, vol.468
, pp. 707-713
-
-
Teslovich, T.M.1
-
17
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight, B.F. et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet. 42, 579-589 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 579-589
-
-
Voight, B.F.1
-
18
-
-
57749170458
-
The many roles of histone deacetylases in development and physiology: Implications for disease and therapy
-
Haberland, M., Montgomery, R.L. & Olson, E.N. The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat. Rev. Genet. 10, 32-42 (2009).
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 32-42
-
-
Haberland, M.1
Montgomery, R.L.2
Olson, E.N.3
-
19
-
-
4544358659
-
Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development
-
DOI 10.1128/MCB.24.19.8467-8476.2004
-
Chang, S. et al. Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development. Mol. Cell Biol 24, 8467-8476 (2004). (Pubitemid 39245069)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.19
, pp. 8467-8476
-
-
Chang, S.1
McKinsey, T.A.2
Zhang, C.L.3
Richardson, J.A.4
Hill, J.A.5
Olson, E.N.6
-
20
-
-
0034654011
-
Acetylation: A regulatory modification to rival phosphorylation
-
Kouzarides, T. Acetylation: a regulatory modification to rival phosphorylation? EMBO J. 19, 1176-1179 (2000). (Pubitemid 30151013)
-
(2000)
EMBO Journal
, vol.19
, Issue.6
, pp. 1176-1179
-
-
Kouzarides, T.1
-
21
-
-
0042905956
-
Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: Defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines
-
Glaser, K.B. et al. Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma cell lines. Mol. Cancer Ther. 2, 151-163 (2003).
-
(2003)
Mol. Cancer Ther.
, vol.2
, pp. 151-163
-
-
Glaser, K.B.1
-
22
-
-
68749117698
-
Targeting histone deacetylases as a multifaceted approach to treat the diverse outcomes of stroke
-
Langley, B., Brochier, C. & Rivieccio, M.A. Targeting histone deacetylases as a multifaceted approach to treat the diverse outcomes of stroke. Stroke 40, 2899-2905 (2009).
-
(2009)
Stroke
, vol.40
, pp. 2899-2905
-
-
Langley, B.1
Brochier, C.2
Rivieccio, M.A.3
-
23
-
-
33846587067
-
A nonsynonymous SNP in PRKCH (protein kinase C η) increases the risk of cerebral infarction
-
DOI 10.1038/ng1945, PII NG1945
-
Kubo, M. et al. A nonsynonymous SNP in PRKCH (protein kinase C ?) increases the risk of cerebral infarction. Nat. Genet. 39, 212-217 (2007). (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
-
24
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad, D.F. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704-712 (2010).
-
(2010)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
-
25
-
-
35748941336
-
A genotype calling algorithm for the Illumina BeadArray platform
-
DOI 10.1093/bioinformatics/btm443
-
Teo, Y.Y. et al. A genotype calling algorithm for the Illumina BeadArray platform. Bioinformatics 23, 2741-2746 (2007). (Pubitemid 350048339)
-
(2007)
Bioinformatics
, vol.23
, Issue.20
, pp. 2741-2746
-
-
Teo, Y.Y.1
Inouye, M.2
Small, K.S.3
Gwilliam, R.4
Deloukas, P.5
Kwiatkowski, D.P.6
Clark, T.G.7
-
26
-
-
78049347495
-
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
-
Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2
-
Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2. A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Nat. Genet. 42, 985-990 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 985-990
-
-
-
27
-
-
78650550275
-
Dissection of the genetics of Parkinson's disease identifies an additional association 5? of SNCA and multiple associated haplotypes at 17q21
-
The UK Parkinson's Disease Consortium & The Wellcome Trust Case Control Consortium 2
-
The UK Parkinson's Disease Consortium & The Wellcome Trust Case Control Consortium 2. Dissection of the genetics of Parkinson's disease identifies an additional association 5? of SNCA and multiple associated haplotypes at 17q21. Hum. Mol. Genet. 20, 345-353 (2011).
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 345-353
-
-
-
28
-
-
84855177237
-
A robust clustering algorithm for identifying problematic samples in genome-wide association studies
-
Bellenguez, C. et al. A robust clustering algorithm for identifying problematic samples in genome-wide association studies. Bioinformatics 28, 134-135 (2012).
-
(2012)
Bioinformatics
, vol.28
, pp. 134-135
-
-
Bellenguez, C.1
-
29
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
Browning, B.L. & Browning, S. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am. J. Hum. Genet. 84, 210-223 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.2
-
30
-
-
77953810149
-
A Bayesian method for detecting and characterizing allelic heterogeneity and boosting signals in genome-wide association studies
-
Su, Z., Cardin, N., Donnelly, P. & Marchini, J. A Bayesian method for detecting and characterizing allelic heterogeneity and boosting signals in genome-wide association studies. Stat. Sci. 24, 430-450 (2009).
-
(2009)
Stat. Sci.
, vol.24
, pp. 430-450
-
-
Su, Z.1
Cardin, N.2
Donnelly, P.3
Marchini, J.4
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