메뉴 건너뛰기




Volumn 542, Issue 2, 2014, Pages 141-145

Progranulin polymorphism rs5848 is associated with increased risk of Alzheimer's disease

Author keywords

Alzheimer's disease; Meta analysis; Polymorphism; Progranulin

Indexed keywords

ALZHEIMER'S DISEASE; META-ANALYSIS; POLYMORPHISM; PROGRANULIN;

EID: 84898832482     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2014.03.041     Document Type: Article
Times cited : (49)

References (25)
  • 1
    • 33746919083 scopus 로고    scopus 로고
    • Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    • Baker M., Mackenzie I.R., Pickering-Brown S.M., Gass J., Rademakers R., et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 2006, 442:916-919.
    • (2006) Nature , vol.442 , pp. 916-919
    • Baker, M.1    Mackenzie, I.R.2    Pickering-Brown, S.M.3    Gass, J.4    Rademakers, R.5
  • 2
    • 0028659004 scopus 로고
    • Operating characteristics of a rank correlation test for publication bias
    • Begg C.B., Mazumdar M. Operating characteristics of a rank correlation test for publication bias. Biometrics 1994, 50:1088-1101.
    • (1994) Biometrics , vol.50 , pp. 1088-1101
    • Begg, C.B.1    Mazumdar, M.2
  • 3
    • 52449110477 scopus 로고    scopus 로고
    • Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
    • Brouwers N., Sleegers K., Engelborghs S., Maurer-Stroh S., Gijselinck I., et al. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. Neurology 2008, 71:656-664.
    • (2008) Neurology , vol.71 , pp. 656-664
    • Brouwers, N.1    Sleegers, K.2    Engelborghs, S.3    Maurer-Stroh, S.4    Gijselinck, I.5
  • 4
    • 84872463000 scopus 로고    scopus 로고
    • Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population
    • Chang K.H., Chen C.M., Chen Y.C., Hsiao Y.C., Huang C.C., et al. Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population. PLoS One 2013, 8:e54448.
    • (2013) PLoS One , vol.8
    • Chang, K.H.1    Chen, C.M.2    Chen, Y.C.3    Hsiao, Y.C.4    Huang, C.C.5
  • 6
    • 33746910649 scopus 로고    scopus 로고
    • Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    • Cruts M., Gijselinck I., van der Zee J., Engelborghs S., Wils H., et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 2006, 442:920-924.
    • (2006) Nature , vol.442 , pp. 920-924
    • Cruts, M.1    Gijselinck, I.2    van der Zee, J.3    Engelborghs, S.4    Wils, H.5
  • 7
    • 77449111778 scopus 로고    scopus 로고
    • Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly
    • Dickson D.W., Baker M., Rademakers R. Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. Neuro-Degenerative Diseases 2010, 7:170-174.
    • (2010) Neuro-Degenerative Diseases , vol.7 , pp. 170-174
    • Dickson, D.W.1    Baker, M.2    Rademakers, R.3
  • 8
    • 84873861410 scopus 로고    scopus 로고
    • The genetics of corticobasal syndrome
    • Doi H., Tanaka F. The genetics of corticobasal syndrome. Brain and Nerve 2013, 65:19-30.
    • (2013) Brain and Nerve , vol.65 , pp. 19-30
    • Doi, H.1    Tanaka, F.2
  • 9
    • 75149192605 scopus 로고    scopus 로고
    • Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease
    • Fenoglio C., Galimberti D., Cortini F., Kauwe J.S., Cruchaga C., et al. Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease. Journal of Alzheimer's Disease 2009, 18:603-612.
    • (2009) Journal of Alzheimer's Disease , vol.18 , pp. 603-612
    • Fenoglio, C.1    Galimberti, D.2    Cortini, F.3    Kauwe, J.S.4    Cruchaga, C.5
  • 10
    • 28344452460 scopus 로고    scopus 로고
    • Systematic evaluation and comparison of statistical tests for publication bias
    • Hayashino Y., Noguchi Y., Fukui T. Systematic evaluation and comparison of statistical tests for publication bias. Journal of Epidemiology 2005, 15:235-243.
    • (2005) Journal of Epidemiology , vol.15 , pp. 235-243
    • Hayashino, Y.1    Noguchi, Y.2    Fukui, T.3
  • 13
    • 79955830791 scopus 로고    scopus 로고
    • Rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population
    • Lee M.J., Chen T.F., Cheng T.W., Chiu M.J. rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population. Neuro-Degenerative Diseases 2011, 8:216-220.
    • (2011) Neuro-Degenerative Diseases , vol.8 , pp. 216-220
    • Lee, M.J.1    Chen, T.F.2    Cheng, T.W.3    Chiu, M.J.4
  • 15
    • 79952195593 scopus 로고    scopus 로고
    • Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation
    • Moreno F., Alzualde A., Camblor P.M., Barandiaran M., Van Deerlin V.M., et al. Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation. Alzheimer Disease and Associated Disorders 2011, 25:93-95.
    • (2011) Alzheimer Disease and Associated Disorders , vol.25 , pp. 93-95
    • Moreno, F.1    Alzualde, A.2    Camblor, P.M.3    Barandiaran, M.4    Van Deerlin, V.M.5
  • 16
    • 55249086715 scopus 로고    scopus 로고
    • Progranulin variability has no major role in Parkinson disease genetic etiology
    • Nuytemans K., Pals P., Sleegers K., Engelborghs S., Corsmit E., et al. Progranulin variability has no major role in Parkinson disease genetic etiology. Neurology 2008, 71:1147-1151.
    • (2008) Neurology , vol.71 , pp. 1147-1151
    • Nuytemans, K.1    Pals, P.2    Sleegers, K.3    Engelborghs, S.4    Corsmit, E.5
  • 17
    • 81855175349 scopus 로고    scopus 로고
    • Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically
    • Pao W.C., Dickson D.W., Crook J.E., Finch N.A., Rademakers R., et al. Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically. Alzheimer Disease and Associated Disorders 2011, 25:364-368.
    • (2011) Alzheimer Disease and Associated Disorders , vol.25 , pp. 364-368
    • Pao, W.C.1    Dickson, D.W.2    Crook, J.E.3    Finch, N.A.4    Rademakers, R.5
  • 18
    • 70349091081 scopus 로고    scopus 로고
    • Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
    • Pereson S., Wils H., Kleinberger G., McGowan E., Vandewoestyne M., et al. Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models. The Journal of Pathology 2009, 219:173-181.
    • (2009) The Journal of Pathology , vol.219 , pp. 173-181
    • Pereson, S.1    Wils, H.2    Kleinberger, G.3    McGowan, E.4    Vandewoestyne, M.5
  • 20
    • 84872109456 scopus 로고    scopus 로고
    • The global prevalence of dementia: a systematic review and metaanalysis
    • Prince M., Bryce R., Albanese E., Wimo A., Ribeiro W., et al. The global prevalence of dementia: a systematic review and metaanalysis. Alzheimers Dement 2013, 9(63-75):e2.
    • (2013) Alzheimers Dement , vol.9 , Issue.63-75
    • Prince, M.1    Bryce, R.2    Albanese, E.3    Wimo, A.4    Ribeiro, W.5
  • 21
    • 34548633862 scopus 로고    scopus 로고
    • Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C->T (Arg493X) mutation: an international initiative
    • Rademakers R., Baker M., Gass J., Adamson J., Huey E.D., et al. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C->T (Arg493X) mutation: an international initiative. Lancet Neurology 2007, 6:857-868.
    • (2007) Lancet Neurology , vol.6 , pp. 857-868
    • Rademakers, R.1    Baker, M.2    Gass, J.3    Adamson, J.4    Huey, E.D.5
  • 22
    • 56049083010 scopus 로고    scopus 로고
    • Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
    • Rademakers R., Eriksen J.L., Baker M., Robinson T., Ahmed Z., et al. Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. Human Molecular Genetics 2008, 17:3631-3642.
    • (2008) Human Molecular Genetics , vol.17 , pp. 3631-3642
    • Rademakers, R.1    Eriksen, J.L.2    Baker, M.3    Robinson, T.4    Ahmed, Z.5
  • 23
    • 0031839545 scopus 로고    scopus 로고
    • Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam study
    • Slooter A.J., Cruts M., Kalmijn S., Hofman A., Breteler M.M., et al. Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam study. Archives of Neurology 1998, 55:964-968.
    • (1998) Archives of Neurology , vol.55 , pp. 964-968
    • Slooter, A.J.1    Cruts, M.2    Kalmijn, S.3    Hofman, A.4    Breteler, M.M.5
  • 24
    • 79953276507 scopus 로고    scopus 로고
    • BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
    • Venturelli E., Villa C., Fenoglio C., Clerici F., Marcone A., et al. BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease. Journal of Alzheimer's Disease 2011, 23:701-707.
    • (2011) Journal of Alzheimer's Disease , vol.23 , pp. 701-707
    • Venturelli, E.1    Villa, C.2    Fenoglio, C.3    Clerici, F.4    Marcone, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.