-
1
-
-
0033843087
-
Genetics and ischaemic stroke
-
Hassan A, Markus HS (2000) Genetics and ischaemic stroke. Brain 123(Pt 9):1784-1812 (Pubitemid 30664283)
-
(2000)
Brain
, vol.123
, Issue.9
, pp. 1784-1812
-
-
Hassan, A.1
Markus, H.S.2
-
2
-
-
0036193062
-
Genetic liability in stroke: A long-term follow-up study of Danish twins
-
DOI 10.1161/hs0302.103619
-
Bak S, Gaist D, Sindrup SH, Skytthe A, Christensen K (2002) Genetic liability in stroke: a long-term follow-up study of Danish twins. Stroke 33:769-774 (Pubitemid 34204005)
-
(2002)
Stroke
, vol.33
, Issue.3
, pp. 769-774
-
-
Bak, S.1
Gaist, D.2
Sindrup, S.H.3
Skytthe, A.4
Christensen, K.5
-
3
-
-
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 HS (2003) Evaluating the genetic component of ischemic stroke subtypes: a family history study. Stroke 34:1364-1369 (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
-
4
-
-
0030839917
-
Parental history of cardiovascular disease and risk of stroke: A prospective follow-up of 14 371 middle-aged men and women in Finland
-
Jousilahti P, Rastenyte D, Tuomilehto J, Sarti C, Vartiainen E (1997) Parental history of cardiovascular disease and risk of stroke: a prospective follow-up of 14371 middle-aged men and women in Finland. Stroke 8:1361-1366 (Pubitemid 27300671)
-
(1997)
Stroke
, vol.28
, Issue.7
, pp. 1361-1366
-
-
Jousilahti, P.1
Rastenyte, D.2
Tuomilehto, J.3
Sarti, C.4
Vartiainen, E.5
-
5
-
-
33846185489
-
Genetics of ischemic stroke
-
Dichgans M (2007) Genetics of ischemic stroke. Lancet Neurol 6:149-161
-
(2007)
Lancet Neurol
, vol.6
, pp. 149-161
-
-
Dichgans, M.1
-
6
-
-
34247480919
-
Genetics of ischemic stroke among persons of non- European descent: A meta-analysis of eight genes involving approximately 32,500 individuals
-
Ariyaratnam R, Casas JP, Whittaker J, Smeeth L, Hingorani AD, Sharma P (2007) Genetics of ischemic stroke among persons of non- European descent: a meta-analysis of eight genes involving approximately 32,500 individuals. PLoS Med 4:e131
-
(2007)
PLoS Med
, vol.4
-
-
Ariyaratnam, R.1
Casas, J.P.2
Whittaker, J.3
Smeeth, L.4
Hingorani, A.D.5
Sharma, P.6
-
7
-
-
7744222619
-
Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18 000 cases and 58 000 controls
-
DOI 10.1001/archneur.61.11.1652
-
Casas JP, Hingorani AD, Bautista LE, Sharma P (2004) Metaanalysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol 61:1652-1661 (Pubitemid 39463422)
-
(2004)
Archives of Neurology
, vol.61
, Issue.11
, pp. 1652-1661
-
-
Casas, J.P.1
Hingorani, A.D.2
Bautista, L.E.3
Sharma, P.4
-
8
-
-
56749157973
-
Susceptibility loci for intracranial aneurysm in European and Japanese populations
-
Bilguvar K, Yasuno K, Niemela M, Ruigrok YM, von Und Zu Fraunberg M, van Duijn CM et al (2008) Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet 40:1472-1477
-
(2008)
Nat Genet
, vol.40
, pp. 1472-1477
-
-
Bilguvar, K.1
Yasuno, K.2
Niemela, M.3
Ruigrok, Y.M.4
Von Und Zu Fraunberg, M.5
Van Duijn, C.M.6
-
9
-
-
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 (2008) Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Ann Neurol 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
-
10
-
-
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 (2009) A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet 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
-
11
-
-
34247116957
-
Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction
-
DOI 10.1093/hmg/ddm005
-
Hata J,Matsuda K, Ninomiya T, Yonemoto K,Matsushita T, Ohnishi Y 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 (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
-
12
-
-
65949090748
-
Genome-wide association studies of stroke
-
Ikram MA, Seshadri S, Bis JC, Fornage M, DeStefano AL, Aulchenko YS et al (2009) Genome-wide association studies of stroke. N Engl J Med 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
-
13
-
-
33846587067
-
A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction
-
DOI 10.1038/ng1945, PII NG1945
-
Kubo M, Hata J, Ninomiya T, Matsuda K, Yonemoto K, Nakano T et al (2007) A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. Nat Genet 39:212-217 (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
-
14
-
-
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
-
Matarin M, Brown WM, Scholz S, Simon-Sanchez J, Fung HC, Hernandez D et al (2007) A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Lancet Neurol 6:414-420 (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..
-
15
-
-
70350574629
-
Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
-
Yamada Y, Fuku N, Tanaka M, Aoyagi Y, Sawabe M, Metoki N 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
-
(2009)
Atherosclerosis
, vol.207
, pp. 144-149
-
-
Yamada, Y.1
Fuku, N.2
Tanaka, M.3
Aoyagi, Y.4
Sawabe, M.5
Metoki, N.6
-
16
-
-
84862782085
-
Association between 12p13 SNPs rs11833579/rs12425791 near NINJ2 gene and ischemic stroke in East Asian population: Evidence from a meta-analysis
-
Li BH, Zhang LL, Yin YW, Pi Y, Guo L, Yang QW, Gao CY, Fang CQ, Wang JZ, Li JC (2012) Association between 12p13 SNPs rs11833579/rs12425791 near NINJ2 gene and ischemic stroke in East Asian population: evidence from a meta-analysis. J Neurol Sci 316(1-2):116-121
-
(2012)
J Neurol Sci
, vol.316
, Issue.1-2
, pp. 116-121
-
-
Li, B.H.1
Zhang, L.L.2
Yin, Y.W.3
Pi, Y.4
Guo, L.5
Yang, Q.W.6
Gao, C.Y.7
Fang, C.Q.8
Wang, J.Z.9
Li, J.C.10
-
17
-
-
0016109198
-
The genetics of human populations
-
Cavalli-Sforza LL (1974) The genetics of human populations. Sci Am 231(3):80-89
-
(1974)
Sci Am
, vol.231
, Issue.3
, pp. 80-89
-
-
Cavalli-Sforza, L.L.1
-
18
-
-
82455199464
-
Capability of common SNPs to tag rare variants
-
Sun X, Namkung J, Zhu X, Elston RC (2011) Capability of common SNPs to tag rare variants. BMC Proc 5(Suppl 9):S88
-
(2011)
BMC Proc
, vol.5
, Issue.SUPPL. 9
-
-
Sun, X.1
Namkung, J.2
Zhu, X.3
Elston, R.C.4
-
19
-
-
82455194213
-
Do rare variant genotypes predict common variant genotypes?
-
Kent JW Jr, Farook V, Göring HHH, Dyer TD, Almasy L, Duggirala R, Blangero J (2011) Do rare variant genotypes predict common variant genotypes? BMC Proc 5(Suppl 9):S87
-
(2011)
BMC Proc
, vol.5
, Issue.SUPPL. 9
-
-
Kent Jr., J.W.1
Farook, V.2
Göring, H.H.H.3
Dyer, T.D.4
Almasy, L.5
Duggirala, R.6
Blangero, J.7
-
20
-
-
77951427974
-
Failure to validate association between 12p13 variants and ischemic stroke
-
Nalls MA, Biffi A, Matarin M, Anderson CD, Chasman DI, Bevan S, Spencer CC, Gschwendtner A, Sale MM, Wu L et al (2010) Failure to validate association between 12p13 variants and ischemic stroke. N Engl J Med 362(16):1547-1550
-
(2010)
N Engl J Med
, vol.362
, Issue.16
, pp. 1547-1550
-
-
Nalls, M.A.1
Biffi, A.2
Matarin, M.3
Anderson, C.D.4
Chasman, D.I.5
Bevan, S.6
Spencer, C.C.7
Gschwendtner, A.8
Sale, M.M.9
Wu, L.10
-
21
-
-
80052913078
-
Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: Evidence for additional functions of EYS
-
Isackson PJ, Ochs-Balcom HM, Ma C, Harley JB, Peltier W, Tarnopolsky M et al (2011) Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYS. Muscle Nerve 44:531-538
-
(2011)
Muscle Nerve
, vol.44
, pp. 531-538
-
-
Isackson, P.J.1
Ochs-Balcom, H.M.2
Ma, C.3
Harley, J.B.4
Peltier, W.5
Tarnopolsky, M.6
-
22
-
-
33745033287
-
Influence of polymorphisms in the NOD1/CARD4 and NOD2/CARD15 genes on the clinical outcome of Helicobacter pylori infection
-
DOI 10.1111/j.1462-5822.2006.00701.x
-
Rosenstiel P, Hellmig S, Hampe J, Ott S, Till A, Fischbach Wet al (2006) Influence of polymorphisms in the NOD1/CARD4 and NOD2/CARD15 genes on the clinical outcome of Helicobacter pylori infection. Cell Microbiol 8:1188-1198 (Pubitemid 43871652)
-
(2006)
Cellular Microbiology
, vol.8
, Issue.7
, pp. 1188-1198
-
-
Rosenstiel, P.1
Hellmig, S.2
Hampe, J.3
Ott, S.4
Till, A.5
Fischbach, W.6
Sahly, H.7
Lucius, R.8
Folsch, U.R.9
Philpott, D.10
Schreiber, S.11
-
23
-
-
70749146442
-
Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer
-
Mockelmann N, von Schönfels W, Buch S, von Kampen O, Sipos B, Egberts JH et al (2009) Investigation of innate immunity genes CARD4, CARD8 and CARD15 as germline susceptibility factors for colorectal cancer. BMC Gastroenterol 9:79
-
(2009)
BMC Gastroenterol
, vol.9
, pp. 79
-
-
Mockelmann, N.1
Von Schönfels, W.2
Buch, S.3
Von Kampen, O.4
Sipos, B.5
Egberts, J.H.6
-
24
-
-
77954680620
-
Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk
-
Ashton KA, Proietto A, Otton G, Symonds I, McEvoy M, Attia J et al (2010) Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk. BMC Cancer 10:382
-
(2010)
BMC Cancer
, vol.10
, pp. 382
-
-
Ashton, K.A.1
Proietto, A.2
Otton, G.3
Symonds, I.4
McEvoy, M.5
Attia, J.6
-
25
-
-
12244297741
-
A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans
-
DOI 10.1016/S0895-7061(02)03246-6, PII S0895706102032466
-
Thiel BA, Chakravarti A, Cooper RS, Luke A, Lewis S, Lynn A et al (2003) A genome-wide linkage analysis investigating the determinants of blood pressure in Whites and African Americans. Am J Hypertens 16:151-153 (Pubitemid 36143436)
-
(2003)
American Journal of Hypertension
, vol.16
, Issue.2
, pp. 151-153
-
-
Thiel, B.A.1
Chakravarti, A.2
Cooper, R.S.3
Luke, A.4
Lewis, S.5
Lynn, A.6
Tiwari, H.7
Schork, N.J.8
Weder, A.B.9
-
26
-
-
70450227480
-
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study
-
Ehret GB, O'Connor AA, Weder A, Cooper RS, Chakravarti A (2009) Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study. Eur J Hum Genet 17:1650-1657
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1650-1657
-
-
Ehret, G.B.1
O'Connor, A.A.2
Weder, A.3
Cooper, R.S.4
Chakravarti, A.5
-
27
-
-
0031689304
-
Genomic structure of a novel human gene (XYLB) on chromosome 3p22→p21.3 encoding a xylulokinase-like protein
-
Tamari M, Daigo Y, Ishikawa S, Nakamura Y (1998)Genomic structure of a novel human gene (XYLB) on chromosome 3p22→p21.3 encoding a xylulokinase-like protein. Cytogenet CellGenet 82:101-104 (Pubitemid 28472789)
-
(1998)
Cytogenetics and Cell Genetics
, vol.82
, Issue.1-2
, pp. 101-104
-
-
Tamari, M.1
Daigo, Y.2
Ishikawa, S.3
Nakamura, Y.4
-
28
-
-
0346258291
-
13C NMR spectroscopy
-
Sonnewald U, Kondziella D (2003) Neuronal glial interaction in different neurological diseases studied by ex vivo 13C NMR spectroscopy. NMR Biomed 16:424-429 (Pubitemid 38008367)
-
(2003)
NMR in Biomedicine
, vol.16
, Issue.6-7
, pp. 424-429
-
-
Sonnewald, U.1
Kondziella, D.2
-
29
-
-
0038304345
-
Hyperbaric oxygen reduces neuronal death and improves neurological outcome after canine cardiac arrest
-
Rosenthal RE, Silbergleit R, Hof PR, Haywood Y, Fiskum G (2010) Hyperbaric oxygen reduces neuronal death and improves neurological outcome after canine cardiac arrest. Stroke 34:1311-1316
-
(2010)
Stroke
, vol.34
, pp. 1311-1316
-
-
Rosenthal, R.E.1
Silbergleit, R.2
Hof, P.R.3
Haywood, Y.4
Fiskum, G.5
|