메뉴 건너뛰기




Volumn 3, Issue , 2015, Pages 96-106

Genetics of ischaemic stroke in young adults

Author keywords

Genetics; GWAS; Stroke

Indexed keywords

ALPHA GALACTOSIDASE; ARGININE; ARYLDIALKYLPHOSPHATASE; CARNITINE; COLLAGEN TYPE 3; CORTICOSTEROID; CREATINE; FIBRILLIN 1; FIBRINOGEN RECEPTOR; IDEBENONE; LACTIC ACID; LINEZOLID; LIPOPROTEIN LIPASE; MATRIX METALLOPROTEINASE; METFORMIN; MITOCHONDRIAL DNA; PYRIDOXINE; UBIDECARENONE; VALPROIC ACID; VERY LATE ACTIVATION ANTIGEN 2;

EID: 84920973857     PISSN: 22146474     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbacli.2014.12.004     Document Type: Review
Times cited : (28)

References (141)
  • 1
    • 0030996001 scopus 로고    scopus 로고
    • Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study
    • Murray C.J., Lopez A.D. Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet 1997, 349:1436-1442.
    • (1997) Lancet , vol.349 , pp. 1436-1442
    • Murray, C.J.1    Lopez, A.D.2
  • 4
    • 0023578615 scopus 로고
    • Alzheimer's disease and other demeting illnesses in a defined United States population: incidence rates and clinical features
    • Dec
    • Schoenberg B.S., Kokmen E., Okazaki H. Alzheimer's disease and other demeting illnesses in a defined United States population: incidence rates and clinical features. Ann. Neurol. Dec 1987, 22(6):724-729.
    • (1987) Ann. Neurol. , vol.22 , Issue.6 , pp. 724-729
    • Schoenberg, B.S.1    Kokmen, E.2    Okazaki, H.3
  • 6
    • 10744224198 scopus 로고    scopus 로고
    • A prospective community-based study of stroke in Southern Italy: the Vibo Valentia incidence of stroke study (VISS). Methodology, incidence and case fatality at 28days, 3 and 12months
    • Di Carlo A., Inzitari D., Galati F., Baldereschi M., Giunta V., Grillo G., Furchì A., Manno V., Naso F., Vecchio A., Consoli D. A prospective community-based study of stroke in Southern Italy: the Vibo Valentia incidence of stroke study (VISS). Methodology, incidence and case fatality at 28days, 3 and 12months. Cerebrovasc. Dis. 2003, 16(4):410-417.
    • (2003) Cerebrovasc. Dis. , vol.16 , Issue.4 , pp. 410-417
    • Di Carlo, A.1    Inzitari, D.2    Galati, F.3    Baldereschi, M.4    Giunta, V.5    Grillo, G.6    Furchì, A.7    Manno, V.8    Naso, F.9    Vecchio, A.10    Consoli, D.11
  • 7
    • 0345830736 scopus 로고    scopus 로고
    • Burden of first-ever ischemic stroke in the oldest old: evidence from a population-based study
    • Jan 13
    • Marini C., Baldassarre M., Russo T., De Santis F., Sacco S., Ciancarelli I., Carolei A. Burden of first-ever ischemic stroke in the oldest old: evidence from a population-based study. Neurology Jan 13 2004, 62(1):77-81.
    • (2004) Neurology , vol.62 , Issue.1 , pp. 77-81
    • Marini, C.1    Baldassarre, M.2    Russo, T.3    De Santis, F.4    Sacco, S.5    Ciancarelli, I.6    Carolei, A.7
  • 8
    • 4344675745 scopus 로고    scopus 로고
    • Prospective community-based study of stroke in Northern Portugal: Incidence and case fatality in rural and urban populations
    • Sep (Epub 2004 Jul 15)
    • Correia M., Silva M.R., Matos I., Magalhães R., Lopes J.C., Ferro J.M., Silva M.C. Prospective community-based study of stroke in Northern Portugal: Incidence and case fatality in rural and urban populations. Stroke Sep 2004, 35(9):2048-2053. (Epub 2004 Jul 15).
    • (2004) Stroke , vol.35 , Issue.9 , pp. 2048-2053
    • Correia, M.1    Silva, M.R.2    Matos, I.3    Magalhães, R.4    Lopes, J.C.5    Ferro, J.M.6    Silva, M.C.7
  • 9
    • 65249138157 scopus 로고    scopus 로고
    • Analysis of 1008 consecutive patients aged 15 to 49 with first-ever ischemic stroke: the Helsinki young stroke registry
    • Putaala J., Metso A.J., Metso T.M., et al. Analysis of 1008 consecutive patients aged 15 to 49 with first-ever ischemic stroke: the Helsinki young stroke registry. Stroke 2009, 40:1195-1203.
    • (2009) Stroke , vol.40 , pp. 1195-1203
    • Putaala, J.1    Metso, A.J.2    Metso, T.M.3
  • 11
    • 77955972020 scopus 로고    scopus 로고
    • Management of cryptogenic stroke
    • Finsterer J. Management of cryptogenic stroke. Acta Neurol. Belg. Jun 2010, 110(2):135-147.
    • (2010) Acta Neurol. Belg. , vol.110 , Issue.2 Mar , pp. 135-147
    • Finsterer, J.1
  • 12
    • 33846185489 scopus 로고    scopus 로고
    • Genetics of ischaemic stroke
    • Dichgans M. Genetics of ischaemic stroke. Lancet Neurol. 2007, 6(2):149-161.
    • (2007) Lancet Neurol. , vol.6 , Issue.2 , pp. 149-161
    • Dichgans, M.1
  • 13
    • 44849105645 scopus 로고    scopus 로고
    • Genetic polymorphisms for the study of multifactorial stroke
    • Jun
    • Bersano A., Ballabio E., Bresolin N., Candelise L. Genetic polymorphisms for the study of multifactorial stroke. Hum. Mutat. Jun 2008, 29(6):776-795.
    • (2008) Hum. Mutat. , vol.29 , Issue.6 , pp. 776-795
    • Bersano, A.1    Ballabio, E.2    Bresolin, N.3    Candelise, L.4
  • 14
    • 84920945508 scopus 로고    scopus 로고
    • Stroke genetics: a review and update
    • Sep (Epub 2014 Sep 30)
    • Lindgren A. Stroke genetics: a review and update. J. Stroke Sep 2014, 16(3):114-123. (Epub 2014 Sep 30).
    • (2014) J. Stroke , vol.16 , Issue.3 , pp. 114-123
    • Lindgren, A.1
  • 15
    • 65949104586 scopus 로고    scopus 로고
    • Genomewide association studies and human disease
    • Hardy J., Singleton A. Genomewide association studies and human disease. N. Engl. J. Med. 2009, 360(17):1759-1768.
    • (2009) N. Engl. J. Med. , vol.360 , Issue.17 , pp. 1759-1768
    • Hardy, J.1    Singleton, A.2
  • 16
    • 0037534908 scopus 로고    scopus 로고
    • Evaluating the genetic component of ischemic stroke subtypes: A family history study
    • Jun (Epub 2003 Apr 24)
    • Jerrard-Dunne P., Cloud G., Hassan A., Markus H.S. Evaluating the genetic component of ischemic stroke subtypes: A family history study. Stroke Jun 2003, 34(6):1364-1369. (Epub 2003 Apr 24).
    • (2003) Stroke , vol.34 , Issue.6 , pp. 1364-1369
    • Jerrard-Dunne, P.1    Cloud, G.2    Hassan, A.3    Markus, H.S.4
  • 18
    • 84870931409 scopus 로고    scopus 로고
    • Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations
    • Dec (Epub 2012 Oct 4)
    • Bevan S., Traylor M., Adib-Samii P., Malik R., Paul N.L., Jackson C., Farrall M., Rothwell P.M., Sudlow C., Dichgans M., Markus H.S. Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations. Stroke Dec 2012, 43(12):3161-3167. (Epub 2012 Oct 4). 10.1161/STROKEAHA.112.665760.
    • (2012) Stroke , vol.43 , Issue.12 , pp. 3161-3167
    • Bevan, S.1    Traylor, M.2    Adib-Samii, P.3    Malik, R.4    Paul, N.L.5    Jackson, C.6    Farrall, M.7    Rothwell, P.M.8    Sudlow, C.9    Dichgans, M.10    Markus, H.S.11
  • 19
    • 84896068950 scopus 로고    scopus 로고
    • Current concepts and clinical applications of stroke genetics
    • Apr
    • Falcone G.J., Malik R., Dichgans M., Rosand J. Current concepts and clinical applications of stroke genetics. Lancet Neurol. Apr 2014, 13(4):405-418.
    • (2014) Lancet Neurol , vol.13 , Issue.4 , pp. 405-418
    • Falcone, G.J.1    Malik, R.2    Dichgans, M.3    Rosand, J.4
  • 20
    • 77957965123 scopus 로고    scopus 로고
    • Aetiological diagnosis of ischaemic stroke in young adults
    • Ferro J.M., Massaro A.R., Mas J.-L. Aetiological diagnosis of ischaemic stroke in young adults. Lancet Neurol. 2010, 9:1085-1096.
    • (2010) Lancet Neurol. , vol.9 , pp. 1085-1096
    • Ferro, J.M.1    Massaro, A.R.2    Mas, J.-L.3
  • 21
    • 0026708671 scopus 로고
    • Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation
    • Goto Y., Horai S., Matsuoka T., Koga Y., Nihei K., Kobayashi M., Nonaka I. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation. Neurology 1992, 42:545-550.
    • (1992) Neurology , vol.42 , pp. 545-550
    • Goto, Y.1    Horai, S.2    Matsuoka, T.3    Koga, Y.4    Nihei, K.5    Kobayashi, M.6    Nonaka, I.7
  • 25
    • 73249119723 scopus 로고    scopus 로고
    • Diagnostic approach to mitochondrial disorders: the need for a reliable biomarker
    • Dec
    • Mancuso M., Orsucci D., Coppedè F., Nesti C., Choub A., Siciliano G. Diagnostic approach to mitochondrial disorders: the need for a reliable biomarker. Curr. Mol. Med. Dec 2009, 9(9):1095-1107.
    • (2009) Curr. Mol. Med. , vol.9 , Issue.9 , pp. 1095-1107
    • Mancuso, M.1    Orsucci, D.2    Coppedè, F.3    Nesti, C.4    Choub, A.5    Siciliano, G.6
  • 26
    • 34248586627 scopus 로고    scopus 로고
    • MELAS associated with mutations in the POLG1 gene
    • Deschauer M., Tennant S., Rokicka A., et al. MELAS associated with mutations in the POLG1 gene. Neurology 2007, 68(20):1741-1742.
    • (2007) Neurology , vol.68 , Issue.20 , pp. 1741-1742
    • Deschauer, M.1    Tennant, S.2    Rokicka, A.3
  • 27
    • 67649409167 scopus 로고    scopus 로고
    • Recessive twinkle mutations cause severe epileptic encephalopathy
    • Lonnqvist T., Paetau A., Valanne L., Pihko H. Recessive twinkle mutations cause severe epileptic encephalopathy. Brain 2009, 132(Pt 6):1553-1562.
    • (2009) Brain , vol.132 , Issue.Pt 6 , pp. 1553-1562
    • Lonnqvist, T.1    Paetau, A.2    Valanne, L.3    Pihko, H.4
  • 28
    • 0032763818 scopus 로고    scopus 로고
    • Vasogenic edema on MELAS: A serial study with diffusion-weighted MR imaging
    • Dec 10
    • Yoneda M., Maeda M., Kimura H., Fujii A., Katayama K., Kuriyama M. Vasogenic edema on MELAS: A serial study with diffusion-weighted MR imaging. Neurology Dec 10 1999, 53(9):2182-2184.
    • (1999) Neurology , vol.53 , Issue.9 , pp. 2182-2184
    • Yoneda, M.1    Maeda, M.2    Kimura, H.3    Fujii, A.4    Katayama, K.5    Kuriyama, M.6
  • 30
    • 74949124717 scopus 로고    scopus 로고
    • Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
    • Jan
    • Testai F.D., Gorelick P.B. Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Arch. Neurol. Jan 2010, 67(1):19-24. 10.1001/archneurol.2009.309.
    • (2010) Arch. Neurol. , vol.67 , Issue.1 , pp. 19-24
    • Testai, F.D.1    Gorelick, P.B.2
  • 33
    • 70350135504 scopus 로고    scopus 로고
    • Management of mitochondrial stroke-like-episodes
    • Finsterer J. Management of mitochondrial stroke-like-episodes. Eur. J. Neurol. 2009, 16(11):1178-1184.
    • (2009) Eur. J. Neurol. , vol.16 , Issue.11 , pp. 1178-1184
    • Finsterer, J.1
  • 34
    • 78149309407 scopus 로고    scopus 로고
    • Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
    • Santa K.M. Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. Pharmacotherapy 2010, 30:1179-1196.
    • (2010) Pharmacotherapy , vol.30 , pp. 1179-1196
    • Santa, K.M.1
  • 36
    • 84857298896 scopus 로고    scopus 로고
    • Drugs and mitochondrial diseases: 40 queries and answers
    • Mar (Epub 2012 Jan 31)
    • Mancuso M., Orsucci D., Filosto M., Simoncini C., Siciliano G. Drugs and mitochondrial diseases: 40 queries and answers. Expert. Opin. Pharmacother. Mar 2012, 13(4):527-543. (Epub 2012 Jan 31). 10.1517/14656566.2012.657177.
    • (2012) Expert. Opin. Pharmacother. , vol.13 , Issue.4 , pp. 527-543
    • Mancuso, M.1    Orsucci, D.2    Filosto, M.3    Simoncini, C.4    Siciliano, G.5
  • 37
    • 0036742661 scopus 로고    scopus 로고
    • Corticosteroid treatment of mitochondrial encephalomyopathies
    • Rossi F.H., Okun M., Yachnis A., Quisling R., Triggs W.J. Corticosteroid treatment of mitochondrial encephalomyopathies. Neurologist 2002, 8(5):313-315.
    • (2002) Neurologist , vol.8 , Issue.5 , pp. 313-315
    • Rossi, F.H.1    Okun, M.2    Yachnis, A.3    Quisling, R.4    Triggs, W.J.5
  • 39
    • 33745547032 scopus 로고    scopus 로고
    • Single gene disorders causing ischaemic stroke
    • Razvi S., Bone I. Single gene disorders causing ischaemic stroke. J. Neurol. 2006, 253(6):685-700.
    • (2006) J. Neurol. , vol.253 , Issue.6 , pp. 685-700
    • Razvi, S.1    Bone, I.2
  • 40
    • 84867573107 scopus 로고    scopus 로고
    • Hereditary cerebral small vessel diseases: A review
    • Federico A., Di Donato I., Bianchi S., et al. Hereditary cerebral small vessel diseases: A review. J. Neurol. Sci. 2012, 322(1-2):25-30.
    • (2012) J. Neurol. Sci. , vol.322 , Issue.1-2 , pp. 25-30
    • Federico, A.1    Di Donato, I.2    Bianchi, S.3
  • 42
    • 53549094678 scopus 로고    scopus 로고
    • Psychiatric disturbances in CADASIL: A brief review
    • Nor (Epub 2008 Mar 26)
    • Valenti R., Poggesi A., Pescini F., Inzitari D., Pantoni L. Psychiatric disturbances in CADASIL: A brief review. Acta Neurol. Scand. Nov 2008, 118(5):291-295. (Epub 2008 Mar 26). 10.1111/j.1600-0404.2008.01015.x.
    • (2008) Acta Neurol. Scand. , vol.118 , Issue.5 , pp. 291-295
    • Valenti, R.1    Poggesi, A.2    Pescini, F.3    Inzitari, D.4    Pantoni, L.5
  • 44
    • 77958006065 scopus 로고    scopus 로고
    • CADASIL: Experimental insights from animal models
    • Ayata C. CADASIL: Experimental insights from animal models. Stroke 2010, 41:S129-S134.
    • (2010) Stroke , vol.41 , pp. S129-S134
    • Ayata, C.1
  • 45
    • 0037229286 scopus 로고    scopus 로고
    • Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis
    • Jan
    • Dong Y., Hassan A., Zhang Z., Huber D., Dalageorgou C., Markus H.S. Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis. Stroke Jan 2003, 34(1):203-205.
    • (2003) Stroke , vol.34 , Issue.1 , pp. 203-205
    • Dong, Y.1    Hassan, A.2    Zhang, Z.3    Huber, D.4    Dalageorgou, C.5    Markus, H.S.6
  • 47
  • 49
    • 79951865527 scopus 로고    scopus 로고
    • Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): From discovery to gene identification
    • Fukutake T. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): From discovery to gene identification. J. Stroke Cerebrovasc. Dis. 2011, 20:85-93.
    • (2011) J. Stroke Cerebrovasc. Dis. , vol.20 , pp. 85-93
    • Fukutake, T.1
  • 50
    • 0346847505 scopus 로고    scopus 로고
    • Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome)
    • Arima K., Yanagawa S., Ito N., Ikeda S. Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome). Neuropathology 2003, 23:327-334.
    • (2003) Neuropathology , vol.23 , pp. 327-334
    • Arima, K.1    Yanagawa, S.2    Ito, N.3    Ikeda, S.4
  • 52
    • 53749104902 scopus 로고    scopus 로고
    • Fabry's disease
    • Zarate Y.A., Hopkin R.J. Fabry's disease. Lancet 2008, 372(9647):1427-1435.
    • (2008) Lancet , vol.372 , Issue.9647 , pp. 1427-1435
    • Zarate, Y.A.1    Hopkin, R.J.2
  • 55
    • 77955896908 scopus 로고    scopus 로고
    • Nervous system and Fabry disease, from symptoms to diagnosis: Damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy
    • Salviati A., Burlina A.P., Borsini W. Nervous system and Fabry disease, from symptoms to diagnosis: Damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. Neurol. Sci. 2010, 31(3):299-306.
    • (2010) Neurol. Sci. , vol.31 , Issue.3 , pp. 299-306
    • Salviati, A.1    Burlina, A.P.2    Borsini, W.3
  • 59
    • 77951546978 scopus 로고    scopus 로고
    • Screening for Fabry disease in high-risk populations: A systematic review
    • Apr (Epub 2009 Sep 24)
    • Linthorst G.E., Bouwman M.G., Wijburg F.A., Aerts J.M., Poorthuis B.J., Hollak C.E. Screening for Fabry disease in high-risk populations: A systematic review. J. Med. Genet. Apr 2010, 47(4):217-222. (Epub 2009 Sep 24). 10.1136/jmg.2009.072116.
    • (2010) J. Med. Genet. , vol.47 , Issue.4 , pp. 217-222
    • Linthorst, G.E.1    Bouwman, M.G.2    Wijburg, F.A.3    Aerts, J.M.4    Poorthuis, B.J.5    Hollak, C.E.6
  • 60
    • 79451474588 scopus 로고    scopus 로고
    • Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: A guideline for healthcare professionals for the American heart association/American stroke association
    • American Heart Association Stroke Council, Council on Cardiovascular Nursing, Council on Cardiovascular Nursing, Council on Clinical Cardiology, Council on Clinical Cardiology, Interdisciplinary Council on Quality of Care and Outcomes Research Interdisciplinary Council on Quality of Care and Outcomes Research
    • Furie K.L., Kasner S.E., Adams R.J., Albers G.W., Bush R.L., Fagan S.C., Halperin J.L., Johnston S.C., Katzan I., Kernan W.N., Mitchell P.H., Ovbiagele B., Palesch Y.Y., Sacco R.L., Schwamm L.H., Wassertheil-Smoller S., Turan T.N., Wentworth D. Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: A guideline for healthcare professionals for the American heart association/American stroke association. Stroke 2011, 42:227-276. American Heart Association Stroke Council, Council on Cardiovascular NursingCouncil on Cardiovascular Nursing, Council on Clinical CardiologyCouncil on Clinical Cardiology, Interdisciplinary Council on Quality of Care and Outcomes ResearchInterdisciplinary Council on Quality of Care and Outcomes Research.
    • (2011) Stroke , vol.42 , pp. 227-276
    • Furie, K.L.1    Kasner, S.E.2    Adams, R.J.3    Albers, G.W.4    Bush, R.L.5    Fagan, S.C.6    Halperin, J.L.7    Johnston, S.C.8    Katzan, I.9    Kernan, W.N.10    Mitchell, P.H.11    Ovbiagele, B.12    Palesch, Y.Y.13    Sacco, R.L.14    Schwamm, L.H.15    Wassertheil-Smoller, S.16    Turan, T.N.17    Wentworth, D.18
  • 61
    • 34250214447 scopus 로고    scopus 로고
    • Fabry disease: the need to stratify patient populations to better understand the outcome of enzyme replacement therapy
    • Germain D.P. Fabry disease: the need to stratify patient populations to better understand the outcome of enzyme replacement therapy. Clin. Ther. 2007, 29(Suppl. A):S17-S18.
    • (2007) Clin. Ther. , vol.29 , pp. S17-S18
    • Germain, D.P.1
  • 62
    • 77955173802 scopus 로고    scopus 로고
    • COL4A1 mutations as a monogenic cause of cerebral small vessel disease: A systematic review
    • Lanfranconi S., Markus H.S. COL4A1 mutations as a monogenic cause of cerebral small vessel disease: A systematic review. Stroke 2010, 41(8):e513-e518.
    • (2010) Stroke , vol.41 , Issue.8 , pp. e513-e518
    • Lanfranconi, S.1    Markus, H.S.2
  • 64
    • 79952126081 scopus 로고    scopus 로고
    • Hereditary connective tissue diseases in young adult stroke: A comprehensive synthesis
    • Vanakker O.M., Hemelsoet D., De Paepe A. Hereditary connective tissue diseases in young adult stroke: A comprehensive synthesis. Stroke Res. Treat. 2011, 2011:712903.
    • (2011) Stroke Res. Treat. , vol.2011 , pp. 712903
    • Vanakker, O.M.1    Hemelsoet, D.2    De Paepe, A.3
  • 66
    • 79959529113 scopus 로고    scopus 로고
    • Pseudoxanthoma elasticum: progress in diagnostics and research towards treatment: Summary of the 2010 PXE International Research Meeting
    • Jul
    • Uitto J., Bercovitch L., Terry S.F., Terry P.F. Pseudoxanthoma elasticum: progress in diagnostics and research towards treatment: Summary of the 2010 PXE International Research Meeting. Am. J. Med. Genet. A Jul 2011, 155A(7):1517-1526.
    • (2011) Am. J. Med. Genet. A , vol.155 A , Issue.7 , pp. 1517-1526
    • Uitto, J.1    Bercovitch, L.2    Terry, S.F.3    Terry, P.F.4
  • 67
    • 0034957036 scopus 로고    scopus 로고
    • Homocysteine levels in patients with stroke: Clinical relevance and therapeutic implications
    • Hankey G.J., Eikelboom J.W. Homocysteine levels in patients with stroke: Clinical relevance and therapeutic implications. CNS Drugs 2001, 15(6):437-443.
    • (2001) CNS Drugs , vol.15 , Issue.6 , pp. 437-443
    • Hankey, G.J.1    Eikelboom, J.W.2
  • 68
    • 0037172570 scopus 로고    scopus 로고
    • Apolipoproteins and prediction of fatal myocardial infarction
    • May 25
    • Wald N.J., Law M., Haddow J.E., Craig W.Y. Apolipoproteins and prediction of fatal myocardial infarction. Lancet May 25 2002, 359(9320):1864.
    • (2002) Lancet , vol.359 , Issue.9320 , pp. 1864
    • Wald, N.J.1    Law, M.2    Haddow, J.E.3    Craig, W.Y.4
  • 69
    • 12344309062 scopus 로고    scopus 로고
    • Homocysteine and stroke: Evidence on a causal link from mendelian randomization
    • Casas J.P., Bautista L.E., Smeeth L., Sharma P., Hingorani A.D. Homocysteine and stroke: Evidence on a causal link from mendelian randomization. Lancet 2005, 365:224-232.
    • (2005) Lancet , vol.365 , pp. 224-232
    • Casas, J.P.1    Bautista, L.E.2    Smeeth, L.3    Sharma, P.4    Hingorani, A.D.5
  • 72
    • 0032171257 scopus 로고    scopus 로고
    • Association between angiotensin I-converting enzyme genotypes, extracranial artery stenosis and stroke
    • Sep
    • Pfohl M., Fetter M., Koch M., Barth C.M., Rudiger W., Haring H.U. Association between angiotensin I-converting enzyme genotypes, extracranial artery stenosis and stroke. Atherosclerosis Sep 1998, 140(1):161-166.
    • (1998) Atherosclerosis , vol.140 , Issue.1 , pp. 161-166
    • Pfohl, M.1    Fetter, M.2    Koch, M.3    Barth, C.M.4    Rudiger, W.5    Haring, H.U.6
  • 73
    • 0025165779 scopus 로고
    • An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
    • Oct
    • Rigat B., Hubert C., Alhenc-Gelas F., Cambien F., Corvol P., Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J. Clin. Invest. Oct 1990, 86(4):1343-1346.
    • (1990) J. Clin. Invest. , vol.86 , Issue.4 , pp. 1343-1346
    • Rigat, B.1    Hubert, C.2    Alhenc-Gelas, F.3    Cambien, F.4    Corvol, P.5    Soubrier, F.6
  • 74
    • 0026675062 scopus 로고
    • Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction
    • Oct 15
    • Cambien F., Poirier O., Lecerf L., Evans A., Cambou J.P., Arveiler D., Luc G., Bard J.M., Bara L., Ricard S., et al. Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature Oct 15 1992, 359(6396):641-644.
    • (1992) Nature , vol.359 , Issue.6396 , pp. 641-644
    • Cambien, F.1    Poirier, O.2    Lecerf, L.3    Evans, A.4    Cambou, J.P.5    Arveiler, D.6    Luc, G.7    Bard, J.M.8    Bara, L.9    Ricard, S.10
  • 75
    • 33644540513 scopus 로고    scopus 로고
    • Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischemic stroke
    • Tuncer N., Tuglular S., Kiliç G., Sazci A., Us O., Kara I. Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischemic stroke. J. Clin. Neurosci. 2006, 13:224-227.
    • (2006) J. Clin. Neurosci. , vol.13 , pp. 224-227
    • Tuncer, N.1    Tuglular, S.2    Kiliç, G.3    Sazci, A.4    Us, O.5    Kara, I.6
  • 76
    • 0032452421 scopus 로고    scopus 로고
    • The renin-angiotensin system: physiology, pathophysiology, and pharmacology
    • Reid I.A. The renin-angiotensin system: physiology, pathophysiology, and pharmacology. Adv. Physiol. Educ. 1998, 275:236-245.
    • (1998) Adv. Physiol. Educ. , vol.275 , pp. 236-245
    • Reid, I.A.1
  • 79
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Nov 15
    • Poort S.R., Rosendaal F.R., Reitsma P.H., Bertina R.M. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood Nov 15 1996, 88(10):3698-3703.
    • (1996) Blood , vol.88 , Issue.10 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 80
    • 0033669567 scopus 로고    scopus 로고
    • Trombophilia, polymorphisms, and vascular disease
    • Dec
    • Sykes T.C., Fegan C., Mosquera D. Trombophilia, polymorphisms, and vascular disease. Mol. Pathol. Dec 2000, 53(6):300-306.
    • (2000) Mol. Pathol. , vol.53 , Issue.6 , pp. 300-306
    • Sykes, T.C.1    Fegan, C.2    Mosquera, D.3
  • 81
    • 0037375566 scopus 로고    scopus 로고
    • Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis
    • Apr (Review)
    • Endler G., Mannhalter C. Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis. Clin. Chim. Acta Apr 2003, 330(1-2):31-55. (Review).
    • (2003) Clin. Chim. Acta , vol.330 , Issue.1-2 , pp. 31-55
    • Endler, G.1    Mannhalter, C.2
  • 82
    • 0033501907 scopus 로고    scopus 로고
    • Prothrombin and the prothrombin 20210G to A polymorphism: their relationship with hypercoagulability and thrombosis
    • Dec (Review)
    • Girolami A., Simioni P., Scarano L., Carraro G. Prothrombin and the prothrombin 20210G to A polymorphism: their relationship with hypercoagulability and thrombosis. Blood Rev. Dec 1999, 13(4):205-210. (Review).
    • (1999) Blood Rev. , vol.13 , Issue.4 , pp. 205-210
    • Girolami, A.1    Simioni, P.2    Scarano, L.3    Carraro, G.4
  • 83
    • 7744222619 scopus 로고    scopus 로고
    • Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls
    • Nov
    • Casas J.P., Hingorani A.D., Bautista L.E., Sharma P. Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch. Neurol. Nov 2004, 61(11):1652-1661.
    • (2004) Arch. Neurol. , vol.61 , Issue.11 , pp. 1652-1661
    • Casas, J.P.1    Hingorani, A.D.2    Bautista, L.E.3    Sharma, P.4
  • 85
    • 0028110027 scopus 로고
    • The mechanism of inactivation of human factor V and human factor Va by activated protein C
    • Dec 16
    • Kalafatis M., Rand M.D., Mann K.G. The mechanism of inactivation of human factor V and human factor Va by activated protein C. J. Biol. Chem. Dec 16 1994, 269(50):31869-31880.
    • (1994) J. Biol. Chem , vol.269 , Issue.50 , pp. 31869-31880
    • Kalafatis, M.1    Rand, M.D.2    Mann, K.G.3
  • 87
    • 33947166241 scopus 로고    scopus 로고
    • The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies
    • Berger K., Stogbauer F., Stoll M., Wellmann J., Huge A., Cheng S., Kessler C., John U., Assmann G., Ringelstein E.B., Funke H. The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies. Hum. Genet. 2007, 121:169-178.
    • (2007) Hum. Genet. , vol.121 , pp. 169-178
    • Berger, K.1    Stogbauer, F.2    Stoll, M.3    Wellmann, J.4    Huge, A.5    Cheng, S.6    Kessler, C.7    John, U.8    Assmann, G.9    Ringelstein, E.B.10    Funke, H.11
  • 88
    • 4544378312 scopus 로고    scopus 로고
    • Prognosis of young ischemic stroke in Taiwan: Impact of prothrombotic genetic polymorphism
    • Yeh P.S., Lin H.J., Li Y.H., Lin K.C., Cheng T.J., Chang C.Y., Ke D.S. Prognosis of young ischemic stroke in Taiwan: Impact of prothrombotic genetic polymorphism. Thromb. Haemost. 2004, 92:583-589.
    • (2004) Thromb. Haemost. , vol.92 , pp. 583-589
    • Yeh, P.S.1    Lin, H.J.2    Li, Y.H.3    Lin, K.C.4    Cheng, T.J.5    Chang, C.Y.6    Ke, D.S.7
  • 89
    • 0032521229 scopus 로고    scopus 로고
    • A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level
    • Mar 15
    • Kanaji T., Okamura T., Osaki K., Kuroiwa M., Shimoda K., Hamasaki N., Niho Y. A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood Mar 15 1998, 91(6):2010-2014.
    • (1998) Blood , vol.91 , Issue.6 , pp. 2010-2014
    • Kanaji, T.1    Okamura, T.2    Osaki, K.3    Kuroiwa, M.4    Shimoda, K.5    Hamasaki, N.6    Niho, Y.7
  • 90
    • 2442465593 scopus 로고    scopus 로고
    • Association after linkage analysis indicates that homozygosity for the 46C->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis
    • May
    • Tirado I., Soria J.M., Mateo J., Oliver A., Souto J.C., Santamaria A., Felices R., Borrell M., Fontcuberta J. Association after linkage analysis indicates that homozygosity for the 46C->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis. Thromb. Haemost. May 2004, 91(5):899-904.
    • (2004) Thromb. Haemost. , vol.91 , Issue.5 , pp. 899-904
    • Tirado, I.1    Soria, J.M.2    Mateo, J.3    Oliver, A.4    Souto, J.C.5    Santamaria, A.6    Felices, R.7    Borrell, M.8    Fontcuberta, J.9
  • 91
    • 0032825571 scopus 로고    scopus 로고
    • Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency - a study on 73 subjects from 14 Swiss families
    • Oct
    • Zeerleder S., Schloesser M., Redondo M., Wuillelmin W.A., Engel W., Furlan M., Lammle B. Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency - a study on 73 subjects from 14 Swiss families. Thromb. Haemost. Oct 1999, 82(4):1240-1246.
    • (1999) Thromb. Haemost. , vol.82 , Issue.4 , pp. 1240-1246
    • Zeerleder, S.1    Schloesser, M.2    Redondo, M.3    Wuillelmin, W.A.4    Engel, W.5    Furlan, M.6    Lammle, B.7
  • 92
    • 0036840704 scopus 로고    scopus 로고
    • WOSCOPS Study Group West of Scotland Coronary Prevention Study
    • Nov
    • Zito F., Lowe G.D., Rumley A., McMahon A.D., Humphries S.E. WOSCOPS Study Group West of Scotland Coronary Prevention Study. Atherosclerosis Nov 2002, 165(1):153-158.
    • (2002) Atherosclerosis , vol.165 , Issue.1 , pp. 153-158
    • Zito, F.1    Lowe, G.D.2    Rumley, A.3    McMahon, A.D.4    Humphries, S.E.5
  • 93
    • 0035894635 scopus 로고    scopus 로고
    • The SmaI polymorphism in the von Willebrand Factor gene associated with acute ischemic stroke
    • Dai K., Gao W., Ruan C. The SmaI polymorphism in the von Willebrand Factor gene associated with acute ischemic stroke. Thromb. Res. 2001, 104:389-395.
    • (2001) Thromb. Res. , vol.104 , pp. 389-395
    • Dai, K.1    Gao, W.2    Ruan, C.3
  • 95
    • 0032564442 scopus 로고    scopus 로고
    • High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women: Evidence for the fibrinolytic system as an independent primary risk factor
    • Nov 24
    • Thögersen A.M., Jansson J.H., Boman K., Nilsson T.K., Weinehall L., Huhtasaari F., Hallmans G. High plasminogen activator inhibitor and tissue plasminogen activator levels in plasma precede a first acute myocardial infarction in both men and women: Evidence for the fibrinolytic system as an independent primary risk factor. Circulation Nov 24 1998, 98(21):2241-2247.
    • (1998) Circulation , vol.98 , Issue.21 , pp. 2241-2247
    • Thögersen, A.M.1    Jansson, J.H.2    Boman, K.3    Nilsson, T.K.4    Weinehall, L.5    Huhtasaari, F.6    Hallmans, G.7
  • 96
    • 0034161456 scopus 로고    scopus 로고
    • Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
    • (Review), Mar 1
    • Lane D.A., Grant P.J. Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease. Blood Mar 1 2000, 95(5):1517-1532. (Review).
    • (2000) Blood , vol.95 , Issue.5 , pp. 1517-1532
    • Lane, D.A.1    Grant, P.J.2
  • 97
    • 33845304321 scopus 로고    scopus 로고
    • Plasminogen activator inhibitor type 1 gene polymorphisms and haplotypes are associated with plasma plasminogen activator inhibitor type 1 levels but not with myocardial infarction or stroke
    • Dec
    • Ding J., Nicklas B.J., Fallin M.D., de Rekeneire N., Kritchevsky S.B., Pahor M., Rodondi N., Li R., Zmuda J.M., Harris T.B. Plasminogen activator inhibitor type 1 gene polymorphisms and haplotypes are associated with plasma plasminogen activator inhibitor type 1 levels but not with myocardial infarction or stroke. Am. Heart J. Dec 2006, 152(6):1109-1115.
    • (2006) Am. Heart J. , vol.152 , Issue.6 , pp. 1109-1115
    • Ding, J.1    Nicklas, B.J.2    Fallin, M.D.3    de Rekeneire, N.4    Kritchevsky, S.B.5    Pahor, M.6    Rodondi, N.7    Li, R.8    Zmuda, J.M.9    Harris, T.B.10
  • 98
    • 0035467596 scopus 로고    scopus 로고
    • Platelet glycoprotein gene polymorphisms and risk of thrombosis: Facts and fancies
    • Sep
    • Reiner A.P., Siscovick D.S., Rosentaal F.R. Platelet glycoprotein gene polymorphisms and risk of thrombosis: Facts and fancies. Rev. Clin. Exp. Hematol. Sep 2001, 5(3):262-287.
    • (2001) Rev. Clin. Exp. Hematol. , vol.5 , Issue.3 , pp. 262-287
    • Reiner, A.P.1    Siscovick, D.S.2    Rosentaal, F.R.3
  • 99
    • 33846897782 scopus 로고    scopus 로고
    • Platelet glycoprotein polymorphisms: Risk, in vivo expression and severity of atherothrombotic stroke in Chinese
    • Zhang Y., Wang Y., Cui C., Hiang P., Li X., Liu S., Lendon C., Guo N. Platelet glycoprotein polymorphisms: Risk, in vivo expression and severity of atherothrombotic stroke in Chinese. Clin. Chim. Acta 2007, 378:99-104.
    • (2007) Clin. Chim. Acta , vol.378 , pp. 99-104
    • Zhang, Y.1    Wang, Y.2    Cui, C.3    Hiang, P.4    Li, X.5    Liu, S.6    Lendon, C.7    Guo, N.8
  • 100
    • 0032752066 scopus 로고    scopus 로고
    • Association of the platelet glycoprotein IIb HPA-3 polymorphism with survival after acute ischemic stroke
    • Dec
    • Carter A.M., Catto A.J., Bamford J.M., Grant P.J. Association of the platelet glycoprotein IIb HPA-3 polymorphism with survival after acute ischemic stroke. Stroke Dec 1999, 30(12):2606-2611.
    • (1999) Stroke , vol.30 , Issue.12 , pp. 2606-2611
    • Carter, A.M.1    Catto, A.J.2    Bamford, J.M.3    Grant, P.J.4
  • 102
    • 0033137302 scopus 로고    scopus 로고
    • The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2beta1 might be a genetic risk factor for the development of stroke in younger patients
    • Jun 1
    • Carlsson L.E., Santoso S., Spitzer C., Kessler C., Greinacher A. The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2beta1 might be a genetic risk factor for the development of stroke in younger patients. Blood Jun 1 1999, 93(11):3583-3586.
    • (1999) Blood , vol.93 , Issue.11 , pp. 3583-3586
    • Carlsson, L.E.1    Santoso, S.2    Spitzer, C.3    Kessler, C.4    Greinacher, A.5
  • 104
    • 0026610362 scopus 로고
    • NH2-terminal globular domain of human platelet glycoprotein Ib alpha has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens
    • Feb
    • Kuijpers R.W., Faber N.M., Cuypers H.T., Ouwehand W.H., Von Dem Borne A.E. NH2-terminal globular domain of human platelet glycoprotein Ib alpha has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens. J. Clin. Invest. Feb 1992, 89(2):381-384.
    • (1992) J. Clin. Invest. , vol.89 , Issue.2 , pp. 381-384
    • Kuijpers, R.W.1    Faber, N.M.2    Cuypers, H.T.3    Ouwehand, W.H.4    Von Dem Borne, A.E.5
  • 107
    • 84903625438 scopus 로고    scopus 로고
    • Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype
    • Jul 2
    • Hsieh M.M., Fitzhugh C.D., Weitzel R.P., Link M.E., Coles W.A., Zhao X., Rodgers G.P., Powell J.D., Tisdale J.F. Nonmyeloablative HLA-matched sibling allogeneic hematopoietic stem cell transplantation for severe sickle cell phenotype. JAMA Jul 2 2014, 312(1):48-56.
    • (2014) JAMA , vol.312 , Issue.1 , pp. 48-56
    • Hsieh, M.M.1    Fitzhugh, C.D.2    Weitzel, R.P.3    Link, M.E.4    Coles, W.A.5    Zhao, X.6    Rodgers, G.P.7    Powell, J.D.8    Tisdale, J.F.9
  • 108
    • 46049104177 scopus 로고    scopus 로고
    • Association of apolipoprotein E genotype and cerebrovascular disease risk factors in a Turkish population
    • Tasdemir N., Tamam Y., Toprak R., Tamam B., Tasdemir M.S. Association of apolipoprotein E genotype and cerebrovascular disease risk factors in a Turkish population. Int. J. Neurosci. 2008, 118:1109-1129.
    • (2008) Int. J. Neurosci. , vol.118 , pp. 1109-1129
    • Tasdemir, N.1    Tamam, Y.2    Toprak, R.3    Tamam, B.4    Tasdemir, M.S.5
  • 109
    • 36049044523 scopus 로고    scopus 로고
    • Association of apolipoprotein E polymorphism with ischemic stroke subtypes in Taiwan
    • Oct
    • Lai C.L., Liu C.K., Lin R.T., Tai C.T. Association of apolipoprotein E polymorphism with ischemic stroke subtypes in Taiwan. Kaohsiung J. Med. Sci. Oct 2007, 23(10):491-497.
    • (2007) Kaohsiung J. Med. Sci. , vol.23 , Issue.10 , pp. 491-497
    • Lai, C.L.1    Liu, C.K.2    Lin, R.T.3    Tai, C.T.4
  • 111
    • 34247882890 scopus 로고    scopus 로고
    • Association of apolipoprotein E epsilon2 with white matter disease but not with microbleeds
    • Lemmens R., Görner A., Schrooten M., Thijs V. Association of apolipoprotein E epsilon2 with white matter disease but not with microbleeds. Stroke 2007, 38:1185-1188.
    • (2007) Stroke , vol.38 , pp. 1185-1188
    • Lemmens, R.1    Görner, A.2    Schrooten, M.3    Thijs, V.4
  • 112
    • 0025940314 scopus 로고
    • Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein
    • Oct 1
    • Beisiegel U., Weber W., Bengtsson-Olivecrona G. Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein. Proc. Natl. Acad. Sci. U. S. A. Oct 1 1991, 88(19):8342-8346.
    • (1991) Proc. Natl. Acad. Sci. U. S. A. , vol.88 , Issue.19 , pp. 8342-8346
    • Beisiegel, U.1    Weber, W.2    Bengtsson-Olivecrona, G.3
  • 113
    • 0024500560 scopus 로고
    • Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases
    • (Review), Apr 20
    • Eckel R.H. Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases. N. Engl. J. Med. Apr 20 1989, 320(16):1060-1068. (Review).
    • (1989) N. Engl. J. Med. , vol.320 , Issue.16 , pp. 1060-1068
    • Eckel, R.H.1
  • 115
    • 33845650701 scopus 로고    scopus 로고
    • Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury
    • Fornage M., Mosley T.H., Jack C.R., de Andrade M., Kardia S.L., Boerwinkle E., Turner S.T. Family-based association study of matrix metalloproteinase-3 and -9 haplotypes with susceptibility to ischemic white matter injury. Hum. Genet. 2007, 120:671-680.
    • (2007) Hum. Genet. , vol.120 , pp. 671-680
    • Fornage, M.1    Mosley, T.H.2    Jack, C.R.3    de Andrade, M.4    Kardia, S.L.5    Boerwinkle, E.6    Turner, S.T.7
  • 116
    • 1642399003 scopus 로고    scopus 로고
    • Genetic risk factors for stroke and carotid atherosclerosis: Insights into pathophysiology from candidate gene approaches
    • Humphries S.E., Morgan L. Genetic risk factors for stroke and carotid atherosclerosis: Insights into pathophysiology from candidate gene approaches. Lancet Neurol. 2004, 3:227-236.
    • (2004) Lancet Neurol. , vol.3 , pp. 227-236
    • Humphries, S.E.1    Morgan, L.2
  • 117
    • 53849138794 scopus 로고    scopus 로고
    • Matrix metalloproteinase-3 (MMP3) and MMP9 genes and risk of myocardial infarction, ischemic stroke, and hemorrhagic stroke
    • Kaplan R.C., Smith N.L., Zucker S., Heckbert S.R., Rice K., Psaty B.M. Matrix metalloproteinase-3 (MMP3) and MMP9 genes and risk of myocardial infarction, ischemic stroke, and hemorrhagic stroke. Atherosclerosis 2008, 201:130-137.
    • (2008) Atherosclerosis , vol.201 , pp. 130-137
    • Kaplan, R.C.1    Smith, N.L.2    Zucker, S.3    Heckbert, S.R.4    Rice, K.5    Psaty, B.M.6
  • 118
    • 84880259302 scopus 로고    scopus 로고
    • Wellcome Trust Genome-Wide Association Study of Ischemic Stroke
    • Markus H.S. Wellcome Trust Genome-Wide Association Study of Ischemic Stroke. Stroke 2013, 44:S20-S22.
    • (2013) Stroke , vol.44 , pp. S20-S22
    • Markus, H.S.1
  • 119
    • 80053534400 scopus 로고    scopus 로고
    • Genetics of common polygenic ischaemic stroke: Current understanding and future challenges
    • Bevan S., Markus H.S. Genetics of common polygenic ischaemic stroke: Current understanding and future challenges. Stroke Res. Treat. 2011, 179061.
    • (2011) Stroke Res. Treat. , pp. 179061
    • Bevan, S.1    Markus, H.S.2
  • 122
    • 84908698727 scopus 로고    scopus 로고
    • The single nucleotide polymorphism rs2208454 confers an increased risk for ischemic stroke: A case-control study
    • Oct
    • Luo M., Li J.X., Sun X.S., Lai R., Wang Y.F., Xu X.W., Sheng W.L. The single nucleotide polymorphism rs2208454 confers an increased risk for ischemic stroke: A case-control study. CNS Neurosci. Ther. Oct 2014, 20(10):893-897.
    • (2014) CNS Neurosci. Ther. , vol.20 , Issue.10 , pp. 893-897
    • Luo, M.1    Li, J.X.2    Sun, X.S.3    Lai, R.4    Wang, Y.F.5    Xu, X.W.6    Sheng, W.L.7
  • 128
    • 84908156575 scopus 로고    scopus 로고
    • Association between 12p13 SNP rs11833579 and ischemic stroke in Asian population: An updated meta-analysis
    • Oct 15
    • Wang L., Zhao C., Xia Q.X., Qiao S.J. Association between 12p13 SNP rs11833579 and ischemic stroke in Asian population: An updated meta-analysis. J. Neurol. Sci. Oct 15 2014, 345(1-2):198-201.
    • (2014) J. Neurol. Sci. , vol.345 , Issue.1-2 , pp. 198-201
    • Wang, L.1    Zhao, C.2    Xia, Q.X.3    Qiao, S.J.4
  • 134
    • 84871491077 scopus 로고    scopus 로고
    • A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke
    • Dec 20
    • Arning A., Hiersche M., Witten A., Kurlemann G., Kurnik K., Manner D., Stoll M., Nowak-Göttl U. A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke. Blood Dec 20 2012, 120(26):5231-5236.
    • (2012) Blood , vol.120 , Issue.26 , pp. 5231-5236
    • Arning, A.1    Hiersche, M.2    Witten, A.3    Kurlemann, G.4    Kurnik, K.5    Manner, D.6    Stoll, M.7    Nowak-Göttl, U.8
  • 138
    • 78650417130 scopus 로고    scopus 로고
    • Personalized approaches to clopidogrel therapy: Are we there yet?
    • Anderson C.D., Biffi A., Greensberg S.M., Rosand J. Personalized approaches to clopidogrel therapy: Are we there yet?. Stroke 2010, 41:2997-3002.
    • (2010) Stroke , vol.41 , pp. 2997-3002
    • Anderson, C.D.1    Biffi, A.2    Greensberg, S.M.3    Rosand, J.4
  • 141
    • 79951715410 scopus 로고    scopus 로고
    • Paediatric stroke: Genetic insights into disease mechanisms and treatment targets
    • Mar, (Review)
    • Munot P., Crow Y.J., Ganesan V. Paediatric stroke: Genetic insights into disease mechanisms and treatment targets. Lancet Neurol. Mar 2011, 10(3):264-274. (Review). 10.1016/S1474-4422(10)70327-6.
    • (2011) Lancet Neurol. , vol.10 , Issue.3 , pp. 264-274
    • Munot, P.1    Crow, Y.J.2    Ganesan, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.