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Volumn 30, Issue 6, 2016, Pages 386-396

Corrigendum to “Genetics of Parkinson's disease” [Mol. Cell. Probes (2016) 386–396](S0890850816301037)(10.1016/j.mcp.2016.11.001);Genetics of Parkinson's disease

Author keywords

Environment; Epidemiology; Genetic association; Genetic risk score; Genome wide association study; GWAS; Interaction; Parkinson's disease; Prediction

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; DNAJC6 GENE; EPIGENETICS; EXOME; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC RISK; GENETIC VARIABILITY; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE ENVIRONMENT INTERACTION; HEREDITY; HUMAN; LRRK2 GENE; NONHUMAN; PARKIN GENE; PARKINSON DISEASE; PENETRANCE; PINK1 GENE; PRIORITY JOURNAL; REVIEW; SNCA GENE; VPS35 GENE; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; PROCEDURES; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84997497966     PISSN: 08908508     EISSN: 10961194     Source Type: Journal    
DOI: 10.1016/j.mcp.2020.101537     Document Type: Erratum
Times cited : (275)

References (144)
  • 1
    • 33745919520 scopus 로고    scopus 로고
    • Epidemiology of Parkinson's disease
    • Jun
    • [1] de Lau, L.M.L., Breteler, M.M.B., Epidemiology of Parkinson's disease. Lancet Neurol. 5:6 (2006 Jun), 525–535.
    • (2006) Lancet Neurol. , vol.5 , Issue.6 , pp. 525-535
    • de Lau, L.M.L.1    Breteler, M.M.B.2
  • 2
    • 33846572874 scopus 로고    scopus 로고
    • Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030
    • Jan 30
    • [2] Dorsey, E.R., Constantinescu, R., Thompson, J.P., Biglan, K.M., Holloway, R.G., Kieburtz, K., et al. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology 68:5 (2007 Jan 30), 384–386.
    • (2007) Neurology , vol.68 , Issue.5 , pp. 384-386
    • Dorsey, E.R.1    Constantinescu, R.2    Thompson, J.P.3    Biglan, K.M.4    Holloway, R.G.5    Kieburtz, K.6
  • 3
    • 0001509014 scopus 로고
    • Paralysis agitans: pathologische Anatomie
    • M. Lewandowski Springer Berlin
    • [3] Lewy, F.H., Paralysis agitans: pathologische Anatomie. Lewandowski, M., (eds.) Handbuch der Neurologie, 1912, Springer, Berlin, 920–933.
    • (1912) Handbuch der Neurologie , pp. 920-933
    • Lewy, F.H.1
  • 6
    • 84865864065 scopus 로고    scopus 로고
    • The genetics and neuropathology of Parkinson's disease
    • Sep
    • [6] Houlden, H., Singleton, A.B., The genetics and neuropathology of Parkinson's disease. Acta Neuropathol. 124:3 (2012 Sep), 325–338.
    • (2012) Acta Neuropathol. , vol.124 , Issue.3 , pp. 325-338
    • Houlden, H.1    Singleton, A.B.2
  • 7
    • 0026514953 scopus 로고
    • Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
    • Mar
    • [7] Hughes, A.J., Daniel, S.E., Kilford, L., Lees, A.J., Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J. Neurol. Neurosurg. Psychiatr. 55:3 (1992 Mar), 181–184.
    • (1992) J. Neurol. Neurosurg. Psychiatr. , vol.55 , Issue.3 , pp. 181-184
    • Hughes, A.J.1    Daniel, S.E.2    Kilford, L.3    Lees, A.J.4
  • 8
    • 0032937059 scopus 로고    scopus 로고
    • Diagnostic criteria for Parkinson disease
    • Jan
    • [8] Gelb, D.J., Oliver, E., Gilman, S., Diagnostic criteria for Parkinson disease. Arch. Neurol. 56:1 (1999 Jan), 33–39.
    • (1999) Arch. Neurol. , vol.56 , Issue.1 , pp. 33-39
    • Gelb, D.J.1    Oliver, E.2    Gilman, S.3
  • 9
    • 45749155306 scopus 로고    scopus 로고
    • A critical reappraisal of current staging of Lewy-related pathology in human brain
    • Jul
    • [9] Jellinger, K.A., A critical reappraisal of current staging of Lewy-related pathology in human brain. Acta Neuropathol. 116:1 (2008 Jul), 1–16.
    • (2008) Acta Neuropathol. , vol.116 , Issue.1 , pp. 1-16
    • Jellinger, K.A.1
  • 10
    • 67349279396 scopus 로고    scopus 로고
    • Unified staging system for Lewy body disorders: correlation with nigrostriatal degeneration, cognitive impairment and motor dysfunction
    • Jun
    • [10] Beach, T.G., Adler, C.H., Lue, L., Sue, L.I., Bachalakuri, J., Henry-Watson, J., et al. Unified staging system for Lewy body disorders: correlation with nigrostriatal degeneration, cognitive impairment and motor dysfunction. Acta Neuropathol. 117:6 (2009 Jun), 613–634.
    • (2009) Acta Neuropathol. , vol.117 , Issue.6 , pp. 613-634
    • Beach, T.G.1    Adler, C.H.2    Lue, L.3    Sue, L.I.4    Bachalakuri, J.5    Henry-Watson, J.6
  • 11
    • 84918571393 scopus 로고    scopus 로고
    • Prediagnostic presentations of Parkinson's disease in primary care: a case-control study
    • Jan
    • [11] Schrag, A., Horsfall, L., Walters, K., Noyce, A., Petersen, I., Prediagnostic presentations of Parkinson's disease in primary care: a case-control study. Lancet Neurol. 14:1 (2015 Jan), 57–64.
    • (2015) Lancet Neurol. , vol.14 , Issue.1 , pp. 57-64
    • Schrag, A.1    Horsfall, L.2    Walters, K.3    Noyce, A.4    Petersen, I.5
  • 12
    • 33750569361 scopus 로고    scopus 로고
    • The impact of 29 chronic conditions on health-related quality of life: a general population survey in Finland using 15D and EQ-5D
    • Oct
    • [12] Saarni, S.I., Härkänen, T., Sintonen, H., Suvisaari, J., Koskinen, S., Aromaa, A., et al. The impact of 29 chronic conditions on health-related quality of life: a general population survey in Finland using 15D and EQ-5D. Qual. Life Res. 15:8 (2006 Oct), 1403–1414.
    • (2006) Qual. Life Res. , vol.15 , Issue.8 , pp. 1403-1414
    • Saarni, S.I.1    Härkänen, T.2    Sintonen, H.3    Suvisaari, J.4    Koskinen, S.5    Aromaa, A.6
  • 13
    • 84920829708 scopus 로고    scopus 로고
    • Initial management of Parkinson's disease
    • [13] Goetz, C.G., Pal, G., Initial management of Parkinson's disease. BMJ, 349, 2014, g6258.
    • (2014) BMJ , vol.349 , pp. g6258
    • Goetz, C.G.1    Pal, G.2
  • 14
    • 77952926102 scopus 로고    scopus 로고
    • Clinical progression in Parkinson disease and the neurobiology of axons
    • Jun
    • [14] Cheng, H.-C., Ulane, C.M., Burke, R.E., Clinical progression in Parkinson disease and the neurobiology of axons. Ann. Neurol. 67:6 (2010 Jun), 715–725.
    • (2010) Ann. Neurol. , vol.67 , Issue.6 , pp. 715-725
    • Cheng, H.-C.1    Ulane, C.M.2    Burke, R.E.3
  • 15
    • 84893071526 scopus 로고    scopus 로고
    • Pathogenesis-targeted, disease-modifying therapies in Parkinson disease
    • Jan
    • [15] AlDakheel, A., Kalia, L.V., Lang, A.E., Pathogenesis-targeted, disease-modifying therapies in Parkinson disease. Neurotherapeutics 11:1 (2014 Jan), 6–23.
    • (2014) Neurotherapeutics , vol.11 , Issue.1 , pp. 6-23
    • AlDakheel, A.1    Kalia, L.V.2    Lang, A.E.3
  • 16
    • 0000334724 scopus 로고
    • A pedigree of paralysis agitans
    • [16] Bell, J., Clark, A.J., A pedigree of paralysis agitans. Ann. Eugen. 1 (1926), 455–462.
    • (1926) Ann. Eugen. , vol.1 , pp. 455-462
    • Bell, J.1    Clark, A.J.2
  • 17
    • 0000328701 scopus 로고
    • Inheritance of shaking pals
    • [17] Allan, W., Inheritance of shaking pals. Arch. Intern Med. 60 (1937), 424–436.
    • (1937) Arch. Intern Med. , vol.60 , pp. 424-436
    • Allan, W.1
  • 18
    • 0028331444 scopus 로고
    • A clinical genetic study of Parkinson's disease: evidence for dominant transmission
    • Mar
    • [18] Lazzarini, A.M., Myers, R.H., Zimmerman, T.R., Mark, M.H., Golbe, L.I., Sage, J.I., et al. A clinical genetic study of Parkinson's disease: evidence for dominant transmission. Neurology 44:3 Pt 1 (1994 Mar), 499–506.
    • (1994) Neurology , vol.44 , Issue.3 , pp. 499-506
    • Lazzarini, A.M.1    Myers, R.H.2    Zimmerman, T.R.3    Mark, M.H.4    Golbe, L.I.5    Sage, J.I.6
  • 20
    • 84965025445 scopus 로고    scopus 로고
    • Launching the movement disorders society genetic mutation database (MDSGene)
    • May
    • [20] Lill, C.M., Mashychev, A., Hartmann, C., Lohmann, K., Marras, C., Lang, A.E., et al. Launching the movement disorders society genetic mutation database (MDSGene). Mov. Disord. 31:5 (2016 May), 607–609.
    • (2016) Mov. Disord. , vol.31 , Issue.5 , pp. 607-609
    • Lill, C.M.1    Mashychev, A.2    Hartmann, C.3    Lohmann, K.4    Marras, C.5    Lang, A.E.6
  • 21
    • 84939599004 scopus 로고    scopus 로고
    • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
    • Sep
    • [21] Nalls, M.A., Pankratz, N., Lill, C.M., Do, C.B., Hernandez, D.G., Saad, M., et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat. Genet. 46:9 (2014 Sep), 989–993.
    • (2014) Nat. Genet. , vol.46 , Issue.9 , pp. 989-993
    • Nalls, M.A.1    Pankratz, N.2    Lill, C.M.3    Do, C.B.4    Hernandez, D.G.5    Saad, M.6
  • 22
    • 84859339977 scopus 로고    scopus 로고
    • Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database
    • [22] Lill, C.M., Roehr, J.T., McQueen, M.B., Kavvoura, F.K., Bagade, S., Schjeide, B.-M.M., et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database. PLoS Genet., 8(3), 2012, e1002548.
    • (2012) PLoS Genet. , vol.8 , Issue.3 , pp. e1002548
    • Lill, C.M.1    Roehr, J.T.2    McQueen, M.B.3    Kavvoura, F.K.4    Bagade, S.5    Schjeide, B.-M.M.6
  • 23
    • 0030744876 scopus 로고    scopus 로고
    • Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
    • Jun 27
    • [23] Polymeropoulos, M.H., Lavedan, C., Leroy, E., Ide, S.E., Dehejia, A., Dutra, A., et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 276:5321 (1997 Jun 27), 2045–2047.
    • (1997) Science , vol.276 , Issue.5321 , pp. 2045-2047
    • Polymeropoulos, M.H.1    Lavedan, C.2    Leroy, E.3    Ide, S.E.4    Dehejia, A.5    Dutra, A.6
  • 24
    • 0031990490 scopus 로고    scopus 로고
    • Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
    • Feb
    • [24] Krüger, R., Kuhn, W., Müller, T., Woitalla, D., Graeber, M., Kösel, S., et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nat. Genet. 18:2 (1998 Feb), 106–108.
    • (1998) Nat. Genet. , vol.18 , Issue.2 , pp. 106-108
    • Krüger, R.1    Kuhn, W.2    Müller, T.3    Woitalla, D.4    Graeber, M.5    Kösel, S.6
  • 25
    • 10744230149 scopus 로고    scopus 로고
    • The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia
    • Feb
    • [25] Zarranz, J.J., Alegre, J., Gómez-Esteban, J.C., Lezcano, E., Ros, R., Ampuero, I., et al. The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. Ann. Neurol. 55:2 (2004 Feb), 164–173.
    • (2004) Ann. Neurol. , vol.55 , Issue.2 , pp. 164-173
    • Zarranz, J.J.1    Alegre, J.2    Gómez-Esteban, J.C.3    Lezcano, E.4    Ros, R.5    Ampuero, I.6
  • 26
    • 84878405578 scopus 로고    scopus 로고
    • G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome
    • Apr
    • [26] Lesage, S., Anheim, M., Letournel, F., Bousset, L., Honoré, A., Rozas, N., et al. G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome. Ann. Neurol. 73:4 (2013 Apr), 459–471.
    • (2013) Ann. Neurol. , vol.73 , Issue.4 , pp. 459-471
    • Lesage, S.1    Anheim, M.2    Letournel, F.3    Bousset, L.4    Honoré, A.5    Rozas, N.6
  • 27
    • 84885461450 scopus 로고    scopus 로고
    • α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
    • May
    • [27] Kiely, A.P., Asi, Y.T., Kara, E., Limousin, P., Ling, H., Lewis, P., et al. α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?. Acta Neuropathol. 125:5 (2013 May), 753–769.
    • (2013) Acta Neuropathol. , vol.125 , Issue.5 , pp. 753-769
    • Kiely, A.P.1    Asi, Y.T.2    Kara, E.3    Limousin, P.4    Ling, H.5    Lewis, P.6
  • 28
    • 84879605541 scopus 로고    scopus 로고
    • Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease
    • Jun
    • [28] Appel-Cresswell, S., Vilarino-Guell, C., Encarnacion, M., Sherman, H., Yu, I., Shah, B., et al. Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. Mov. Disord. 28:6 (2013 Jun), 811–813.
    • (2013) Mov. Disord. , vol.28 , Issue.6 , pp. 811-813
    • Appel-Cresswell, S.1    Vilarino-Guell, C.2    Encarnacion, M.3    Sherman, H.4    Yu, I.5    Shah, B.6
  • 29
    • 84876226920 scopus 로고    scopus 로고
    • A novel α-synuclein missense mutation in Parkinson disease
    • Mar 12
    • [29] Proukakis, C., Dudzik, C.G., Brier, T., MacKay, D.S., Cooper, J.M., Millhauser, G.L., et al. A novel α-synuclein missense mutation in Parkinson disease. Neurology 80:11 (2013 Mar 12), 1062–1064.
    • (2013) Neurology , vol.80 , Issue.11 , pp. 1062-1064
    • Proukakis, C.1    Dudzik, C.G.2    Brier, T.3    MacKay, D.S.4    Cooper, J.M.5    Millhauser, G.L.6
  • 30
    • 4644290985 scopus 로고    scopus 로고
    • Alpha-synuclein locus duplication as a cause of familial Parkinson's disease
    • Oct 25
    • [30] Chartier-Harlin, M.-C., Kachergus, J., Roumier, C., Mouroux, V., Douay, X., Lincoln, S., et al. Alpha-synuclein locus duplication as a cause of familial Parkinson's disease. Lancet 364:9440 (2004 Oct 25), 1167–1169.
    • (2004) Lancet , vol.364 , Issue.9440 , pp. 1167-1169
    • Chartier-Harlin, M.-C.1    Kachergus, J.2    Roumier, C.3    Mouroux, V.4    Douay, X.5    Lincoln, S.6
  • 31
    • 4644236043 scopus 로고    scopus 로고
    • Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
    • Oct 25
    • [31] Ibáñez, P., Bonnet, A.-M., Débarges, B., Lohmann, E., Tison, F., Pollak, P., et al. Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease. Lancet 364:9440 (2004 Oct 25), 1169–1171.
    • (2004) Lancet , vol.364 , Issue.9440 , pp. 1169-1171
    • Ibáñez, P.1    Bonnet, A.-M.2    Débarges, B.3    Lohmann, E.4    Tison, F.5    Pollak, P.6
  • 32
    • 0242300619 scopus 로고    scopus 로고
    • alpha-Synuclein locus triplication causes Parkinson's disease
    • Oct 31
    • [32] Singleton, A.B., Farrer, M., Johnson, J., Singleton, A., Hague, S., Kachergus, J., et al. alpha-Synuclein locus triplication causes Parkinson's disease. Science, 302(5646), 2003 Oct 31, 841.
    • (2003) Science , vol.302 , Issue.5646 , pp. 841
    • Singleton, A.B.1    Farrer, M.2    Johnson, J.3    Singleton, A.4    Hague, S.5    Kachergus, J.6
  • 33
    • 84884250340 scopus 로고    scopus 로고
    • The function of α-synuclein
    • Sep 18
    • [33] Bendor, J.T., Logan, T.P., Edwards, R.H., The function of α-synuclein. Neuron 79:6 (2013 Sep 18), 1044–1066.
    • (2013) Neuron , vol.79 , Issue.6 , pp. 1044-1066
    • Bendor, J.T.1    Logan, T.P.2    Edwards, R.H.3
  • 34
    • 84856200093 scopus 로고    scopus 로고
    • Towards unveiling the genetics of neurodegenerative diseases
    • Nov
    • [34] Lill, C.M., Bertram, L., Towards unveiling the genetics of neurodegenerative diseases. Semin. Neurol. 31:5 (2011 Nov), 531–541.
    • (2011) Semin. Neurol. , vol.31 , Issue.5 , pp. 531-541
    • Lill, C.M.1    Bertram, L.2
  • 35
    • 84926513913 scopus 로고    scopus 로고
    • Spreading of pathology in neurodegenerative diseases: a focus on human studies
    • Feb
    • [35] Brettschneider, J., Del Tredici, K., Lee, V.M.-Y., Trojanowski, J.Q., Spreading of pathology in neurodegenerative diseases: a focus on human studies. Nat. Rev. Neurosci. 16:2 (2015 Feb), 109–120.
    • (2015) Nat. Rev. Neurosci. , vol.16 , Issue.2 , pp. 109-120
    • Brettschneider, J.1    Del Tredici, K.2    Lee, V.M.-Y.3    Trojanowski, J.Q.4
  • 36
    • 84962081972 scopus 로고    scopus 로고
    • A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration
    • Mar 18
    • [36] Walsh, D.M., Selkoe, D.J., A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration. Nat. Rev. Neurosci. 17:4 (2016 Mar 18), 251–260.
    • (2016) Nat. Rev. Neurosci. , vol.17 , Issue.4 , pp. 251-260
    • Walsh, D.M.1    Selkoe, D.J.2
  • 37
    • 8844233579 scopus 로고    scopus 로고
    • Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
    • Nov 18
    • [37] Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44:4 (2004 Nov 18), 601–607.
    • (2004) Neuron , vol.44 , Issue.4 , pp. 601-607
    • Zimprich, A.1    Biskup, S.2    Leitner, P.3    Lichtner, P.4    Farrer, M.5    Lincoln, S.6
  • 38
    • 8844266996 scopus 로고    scopus 로고
    • Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
    • Nov 18
    • [38] Paisán-Ruíz, C., Jain, S., Evans, E.W., Gilks, W.P., Simón, J., van der Brug, M., et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 44:4 (2004 Nov 18), 595–600.
    • (2004) Neuron , vol.44 , Issue.4 , pp. 595-600
    • Paisán-Ruíz, C.1    Jain, S.2    Evans, E.W.3    Gilks, W.P.4    Simón, J.5    van der Brug, M.6
  • 39
    • 50049104725 scopus 로고    scopus 로고
    • Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
    • Jul
    • [39] Healy, D.G., Falchi, M., O'Sullivan, S.S., Bonifati, V., Durr, A., Bressman, S., et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol. 7:7 (2008 Jul), 583–590.
    • (2008) Lancet Neurol. , vol.7 , Issue.7 , pp. 583-590
    • Healy, D.G.1    Falchi, M.2    O'Sullivan, S.S.3    Bonifati, V.4    Durr, A.5    Bressman, S.6
  • 40
    • 80052967403 scopus 로고    scopus 로고
    • Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
    • Oct
    • [40] Ross, O.A., Soto-Ortolaza, A.I., Heckman, M.G., Aasly, J.O., Abahuni, N., Annesi, G., et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet Neurol. 10:10 (2011 Oct), 898–908.
    • (2011) Lancet Neurol. , vol.10 , Issue.10 , pp. 898-908
    • Ross, O.A.1    Soto-Ortolaza, A.I.2    Heckman, M.G.3    Aasly, J.O.4    Abahuni, N.5    Annesi, G.6
  • 42
    • 70350450693 scopus 로고    scopus 로고
    • LRRK2 in Parkinson's disease: function in cells and neurodegeneration
    • Nov
    • [42] Webber, P.J., West, A.B., LRRK2 in Parkinson's disease: function in cells and neurodegeneration. FEBS J. 276:22 (2009 Nov), 6436–6444.
    • (2009) FEBS J. , vol.276 , Issue.22 , pp. 6436-6444
    • Webber, P.J.1    West, A.B.2
  • 43
    • 84958567797 scopus 로고    scopus 로고
    • Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases
    • [43] Steger, M., Tonelli, F., Ito, G., Davies, P., Trost, M., Vetter, M., et al. Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases. Elife, 2016, 5.
    • (2016) Elife , pp. 5
    • Steger, M.1    Tonelli, F.2    Ito, G.3    Davies, P.4    Trost, M.5    Vetter, M.6
  • 44
    • 80051534540 scopus 로고    scopus 로고
    • A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease
    • Jul 15
    • [44] Zimprich, A., Benet-Pagès, A., Struhal, W., Graf, E., Eck, S.H., Offman, M.N., et al. A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease. Am. J. Hum. Genet. 89:1 (2011 Jul 15), 168–175.
    • (2011) Am. J. Hum. Genet. , vol.89 , Issue.1 , pp. 168-175
    • Zimprich, A.1    Benet-Pagès, A.2    Struhal, W.3    Graf, E.4    Eck, S.H.5    Offman, M.N.6
  • 46
    • 84870287920 scopus 로고    scopus 로고
    • A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
    • Nov
    • [46] Sharma, M., Ioannidis, J.P.A., Aasly, J.O., Annesi, G., Brice, A., Bertram, L., et al. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. J. Med. Genet. 49:11 (2012 Nov), 721–726.
    • (2012) J. Med. Genet. , vol.49 , Issue.11 , pp. 721-726
    • Sharma, M.1    Ioannidis, J.P.A.2    Aasly, J.O.3    Annesi, G.4    Brice, A.5    Bertram, L.6
  • 47
    • 84881376726 scopus 로고    scopus 로고
    • Advances in the genetics of Parkinson disease
    • Aug
    • [47] Trinh, J., Farrer, M., Advances in the genetics of Parkinson disease. Nat. Rev. Neurol. 9:8 (2013 Aug), 445–454.
    • (2013) Nat. Rev. Neurol. , vol.9 , Issue.8 , pp. 445-454
    • Trinh, J.1    Farrer, M.2
  • 48
    • 0032499264 scopus 로고    scopus 로고
    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Apr 9
    • [48] Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 392:6676 (1998 Apr 9), 605–608.
    • (1998) Nature , vol.392 , Issue.6676 , pp. 605-608
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3    Matsumine, H.4    Yamamura, Y.5    Minoshima, S.6
  • 49
    • 2442668926 scopus 로고    scopus 로고
    • Hereditary early-onset Parkinson's disease caused by mutations in PINK1
    • May 21
    • [49] Valente, E.M., Abou-Sleiman, P.M., Caputo, V., Muqit, M.M.K., Harvey, K., Gispert, S., et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304:5674 (2004 May 21), 1158–1160.
    • (2004) Science , vol.304 , Issue.5674 , pp. 1158-1160
    • Valente, E.M.1    Abou-Sleiman, P.M.2    Caputo, V.3    Muqit, M.M.K.4    Harvey, K.5    Gispert, S.6
  • 50
    • 0037428241 scopus 로고    scopus 로고
    • Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
    • Jan 10
    • [50] Bonifati, V., Rizzu, P., van Baren, M.J., Schaap, O., Breedveld, G.J., Krieger, E., et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 299:5604 (2003 Jan 10), 256–259.
    • (2003) Science , vol.299 , Issue.5604 , pp. 256-259
    • Bonifati, V.1    Rizzu, P.2    van Baren, M.J.3    Schaap, O.4    Breedveld, G.J.5    Krieger, E.6
  • 51
    • 84867746758 scopus 로고    scopus 로고
    • Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease
    • Oct
    • [51] Kilarski, L.L., Pearson, J.P., Newsway, V., Majounie, E., Knipe, M.D.W., Misbahuddin, A., et al. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease. Mov. Disord. 27:12 (2012 Oct), 1522–1529.
    • (2012) Mov. Disord. , vol.27 , Issue.12 , pp. 1522-1529
    • Kilarski, L.L.1    Pearson, J.P.2    Newsway, V.3    Majounie, E.4    Knipe, M.D.W.5    Misbahuddin, A.6
  • 52
    • 0345490853 scopus 로고    scopus 로고
    • A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
    • Apr
    • [52] Abbas, N., Lücking, C.B., Ricard, S., Dürr, A., Bonifati, V., De Michele, G., et al. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. Hum. Mol. Genet. 8:4 (1999 Apr), 567–574.
    • (1999) Hum. Mol. Genet. , vol.8 , Issue.4 , pp. 567-574
    • Abbas, N.1    Lücking, C.B.2    Ricard, S.3    Dürr, A.4    Bonifati, V.5    De Michele, G.6
  • 53
    • 7244261867 scopus 로고    scopus 로고
    • Distribution, type, and origin of Parkin mutations: review and case studies
    • Oct
    • [53] Hedrich, K., Eskelson, C., Wilmot, B., Marder, K., Harris, J., Garrels, J., et al. Distribution, type, and origin of Parkin mutations: review and case studies. Mov. Disord. 19:10 (2004 Oct), 1146–1157.
    • (2004) Mov. Disord. , vol.19 , Issue.10 , pp. 1146-1157
    • Hedrich, K.1    Eskelson, C.2    Wilmot, B.3    Marder, K.4    Harris, J.5    Garrels, J.6
  • 54
    • 55949128232 scopus 로고    scopus 로고
    • Emerging pathways in genetic Parkinson's disease: autosomal-recessive genes in Parkinson's disease–a common pathway?
    • Dec
    • [54] Fitzgerald, J.C., Plun-Favreau, H., Emerging pathways in genetic Parkinson's disease: autosomal-recessive genes in Parkinson's disease–a common pathway?. FEBS J. 275:23 (2008 Dec), 5758–5766.
    • (2008) FEBS J. , vol.275 , Issue.23 , pp. 5758-5766
    • Fitzgerald, J.C.1    Plun-Favreau, H.2
  • 55
    • 84868575932 scopus 로고    scopus 로고
    • Mitochondrial quality control mediated by PINK1 and Parkin: links to parkinsonism
    • Nov
    • [55] Narendra, D., Walker, J.E., Youle, R., Mitochondrial quality control mediated by PINK1 and Parkin: links to parkinsonism. Cold Spring Harb. Perspect. Biol., 4(11), 2012 Nov.
    • (2012) Cold Spring Harb. Perspect. Biol. , vol.4 , Issue.11
    • Narendra, D.1    Walker, J.E.2    Youle, R.3
  • 56
    • 20144389422 scopus 로고    scopus 로고
    • Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress
    • Apr 5
    • [56] Kim, R.H., Smith, P.D., Aleyasin, H., Hayley, S., Mount, M.P., Pownall, S., et al. Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrindine (MPTP) and oxidative stress. Proc. Natl. Acad. Sci. U. S. A. 102:14 (2005 Apr 5), 5215–5220.
    • (2005) Proc. Natl. Acad. Sci. U. S. A. , vol.102 , Issue.14 , pp. 5215-5220
    • Kim, R.H.1    Smith, P.D.2    Aleyasin, H.3    Hayley, S.4    Mount, M.P.5    Pownall, S.6
  • 57
    • 84860487766 scopus 로고    scopus 로고
    • A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism
    • [57] Edvardson, S., Cinnamon, Y., Ta-Shma, A., Shaag, A., Yim, Y.-I., Zenvirt, S., et al. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. PLoS One, 7(5), 2012, e36458.
    • (2012) PLoS One , vol.7 , Issue.5 , pp. e36458
    • Edvardson, S.1    Cinnamon, Y.2    Ta-Shma, A.3    Shaag, A.4    Yim, Y.-I.5    Zenvirt, S.6
  • 58
    • 84874271513 scopus 로고    scopus 로고
    • DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability
    • Mar
    • [58] Köroğlu, Ç., Baysal, L., Cetinkaya, M., Karasoy, H., Tolun, A., DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability. Park. Relat. Disord. 19:3 (2013 Mar), 320–324.
    • (2013) Park. Relat. Disord. , vol.19 , Issue.3 , pp. 320-324
    • Köroğlu, Ç.1    Baysal, L.2    Cetinkaya, M.3    Karasoy, H.4    Tolun, A.5
  • 59
    • 84958106531 scopus 로고    scopus 로고
    • DNAJC6 mutations associated with early-onset Parkinson's disease
    • Feb
    • [59] Olgiati, S., Quadri, M., Fang, M., Rood, J.P.M.A., Saute, J.A., Chien, H.F., et al. DNAJC6 mutations associated with early-onset Parkinson's disease. Ann. Neurol. 79:2 (2016 Feb), 244–256.
    • (2016) Ann. Neurol. , vol.79 , Issue.2 , pp. 244-256
    • Olgiati, S.1    Quadri, M.2    Fang, M.3    Rood, J.P.M.A.4    Saute, J.A.5    Chien, H.F.6
  • 60
    • 84958122839 scopus 로고    scopus 로고
    • A novel nonsense mutation in DNAJC6 expands the phenotype of autosomal-recessive juvenile-onset Parkinson's disease
    • Feb
    • [60] Elsayed, L.E.O., Drouet, V., Usenko, T., Mohammed, I.N., Hamed, A.A.A., Elseed, M.A., et al. A novel nonsense mutation in DNAJC6 expands the phenotype of autosomal-recessive juvenile-onset Parkinson's disease. Ann. Neurol. 79:2 (2016 Feb), 335–337.
    • (2016) Ann. Neurol. , vol.79 , Issue.2 , pp. 335-337
    • Elsayed, L.E.O.1    Drouet, V.2    Usenko, T.3    Mohammed, I.N.4    Hamed, A.A.A.5    Elseed, M.A.6
  • 61
    • 34249058118 scopus 로고    scopus 로고
    • Multiple roles of auxilin and hsc70 in clathrin-mediated endocytosis
    • Jun
    • [61] Eisenberg, E., Greene, L.E., Multiple roles of auxilin and hsc70 in clathrin-mediated endocytosis. Traffic 8:6 (2007 Jun), 640–646.
    • (2007) Traffic , vol.8 , Issue.6 , pp. 640-646
    • Eisenberg, E.1    Greene, L.E.2
  • 62
    • 33749133430 scopus 로고    scopus 로고
    • Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
    • Oct
    • [62] Ramirez, A., Heimbach, A., Gründemann, J., Stiller, B., Hampshire, D., Cid, L.P., et al. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nat. Genet. 38:10 (2006 Oct), 1184–1191.
    • (2006) Nat. Genet. , vol.38 , Issue.10 , pp. 1184-1191
    • Ramirez, A.1    Heimbach, A.2    Gründemann, J.3    Stiller, B.4    Hampshire, D.5    Cid, L.P.6
  • 63
    • 84929654352 scopus 로고    scopus 로고
    • The role of ATP13A2 in Parkinson's disease: clinical phenotypes and molecular mechanisms
    • May
    • [63] Park, J.-S., Blair, N.F., Sue, C.M., The role of ATP13A2 in Parkinson's disease: clinical phenotypes and molecular mechanisms. Mov. Disord. 30:6 (2015 May), 770–779.
    • (2015) Mov. Disord. , vol.30 , Issue.6 , pp. 770-779
    • Park, J.-S.1    Blair, N.F.2    Sue, C.M.3
  • 64
    • 44449112128 scopus 로고    scopus 로고
    • Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays
    • Jun
    • [64] Shojaee, S., Sina, F., Banihosseini, S.S., Kazemi, M.H., Kalhor, R., Shahidi, G.-A., et al. Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays. Am. J. Hum. Genet. 82:6 (2008 Jun), 1375–1384.
    • (2008) Am. J. Hum. Genet. , vol.82 , Issue.6 , pp. 1375-1384
    • Shojaee, S.1    Sina, F.2    Banihosseini, S.S.3    Kazemi, M.H.4    Kalhor, R.5    Shahidi, G.-A.6
  • 65
    • 60849121924 scopus 로고    scopus 로고
    • Characterization of PLA2G6 as a locus for dystonia-parkinsonism
    • Jan
    • [65] Paisan-Ruiz, C., Bhatia, K.P., Li, A., Hernandez, D., Davis, M., Wood, N.W., et al. Characterization of PLA2G6 as a locus for dystonia-parkinsonism. Ann. Neurol. 65:1 (2009 Jan), 19–23.
    • (2009) Ann. Neurol. , vol.65 , Issue.1 , pp. 19-23
    • Paisan-Ruiz, C.1    Bhatia, K.P.2    Li, A.3    Hernandez, D.4    Davis, M.5    Wood, N.W.6
  • 66
    • 84881610810 scopus 로고    scopus 로고
    • The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures
    • Sep
    • [66] Krebs, C.E., Karkheiran, S., Powell, J.C., Cao, M., Makarov, V., Darvish, H., et al. The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures. Hum. Mutat. 34:9 (2013 Sep), 1200–1207.
    • (2013) Hum. Mutat. , vol.34 , Issue.9 , pp. 1200-1207
    • Krebs, C.E.1    Karkheiran, S.2    Powell, J.C.3    Cao, M.4    Makarov, V.5    Darvish, H.6
  • 67
    • 84881612311 scopus 로고    scopus 로고
    • Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism
    • Sep
    • [67] Quadri, M., Fang, M., Picillo, M., Olgiati, S., Breedveld, G.J., Graafland, J., et al. Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. Hum. Mutat. 34:9 (2013 Sep), 1208–1215.
    • (2013) Hum. Mutat. , vol.34 , Issue.9 , pp. 1208-1215
    • Quadri, M.1    Fang, M.2    Picillo, M.3    Olgiati, S.4    Breedveld, G.J.5    Graafland, J.6
  • 68
    • 84929773699 scopus 로고    scopus 로고
    • A new F-box protein 7 gene mutation causing typical Parkinson's disease
    • Jul
    • [68] Lohmann, E., Coquel, A.-S., Honoré, A., Gurvit, H., Hanagasi, H., Emre, M., et al. A new F-box protein 7 gene mutation causing typical Parkinson's disease. Mov. Disord. 30:8 (2015 Jul), 1130–1133.
    • (2015) Mov. Disord. , vol.30 , Issue.8 , pp. 1130-1133
    • Lohmann, E.1    Coquel, A.-S.2    Honoré, A.3    Gurvit, H.4    Hanagasi, H.5    Emre, M.6
  • 69
    • 84963550642 scopus 로고    scopus 로고
    • Nomenclature of genetic movement disorders: recommendations of the international parkinson and movement disorder society task force
    • Apr
    • [69] Marras, C., Lang, A., van de Warrenburg, B.P., Sue, C., Tabrizi, S.J., Bertram, L., et al. Nomenclature of genetic movement disorders: recommendations of the international parkinson and movement disorder society task force. Mov. Disord. 31:4 (2016 Apr), 436–457.
    • (2016) Mov. Disord. , vol.31 , Issue.4 , pp. 436-457
    • Marras, C.1    Lang, A.2    van de Warrenburg, B.P.3    Sue, C.4    Tabrizi, S.J.5    Bertram, L.6
  • 71
    • 84923226964 scopus 로고    scopus 로고
    • CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
    • Mar
    • [71] Funayama, M., Ohe, K., Amo, T., Furuya, N., Yamaguchi, J., Saiki, S., et al. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Lancet Neurol. 14:3 (2015 Mar), 274–282.
    • (2015) Lancet Neurol. , vol.14 , Issue.3 , pp. 274-282
    • Funayama, M.1    Ohe, K.2    Amo, T.3    Furuya, N.4    Yamaguchi, J.5    Saiki, S.6
  • 72
    • 84976285813 scopus 로고    scopus 로고
    • Identification of TMEM230 mutations in familial Parkinson's disease
    • Jul
    • [72] Deng, H.-X., Shi, Y., Yang, Y., Ahmeti, K.B., Miller, N., Huang, C., et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nat. Genet. 48:7 (2016 Jul), 733–739.
    • (2016) Nat. Genet. , vol.48 , Issue.7 , pp. 733-739
    • Deng, H.-X.1    Shi, Y.2    Yang, Y.3    Ahmeti, K.B.4    Miller, N.5    Huang, C.6
  • 73
    • 84959881559 scopus 로고    scopus 로고
    • Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-Dependent Mitophagy
    • Mar 3
    • [73] Lesage, S., Drouet, V., Majounie, E., Deramecourt, V., Jacoupy, M., Nicolas, A., et al. Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-Dependent Mitophagy. Am. J. Hum. Genet. 98:3 (2016 Mar 3), 500–513.
    • (2016) Am. J. Hum. Genet. , vol.98 , Issue.3 , pp. 500-513
    • Lesage, S.1    Drouet, V.2    Majounie, E.3    Deramecourt, V.4    Jacoupy, M.5    Nicolas, A.6
  • 74
    • 84919650942 scopus 로고    scopus 로고
    • Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology
    • Dec 4
    • [74] Wilson, G.R., Sim, J.C.H., McLean, C., Giannandrea, M., Galea, C.A., Riseley, J.R., et al. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. Am. J. Hum. Genet. 95:6 (2014 Dec 4), 729–735.
    • (2014) Am. J. Hum. Genet. , vol.95 , Issue.6 , pp. 729-735
    • Wilson, G.R.1    Sim, J.C.H.2    McLean, C.3    Giannandrea, M.4    Galea, C.A.5    Riseley, J.R.6
  • 76
    • 85058205841 scopus 로고    scopus 로고
    • DNAJ mutations are rare in Chinese Parkinson's disease patients and controls
    • e1–2 Apr
    • [76] Foo, J.N., Liany, H., Tan, L.C., Au, W.-L., Prakash, K.-M., Liu, J., et al. DNAJ mutations are rare in Chinese Parkinson's disease patients and controls. Neurobiol. Aging, 35(4), 2014 Apr, 935 e1–2.
    • (2014) Neurobiol. Aging , vol.35 , Issue.4 , pp. 935
    • Foo, J.N.1    Liany, H.2    Tan, L.C.3    Au, W.-L.4    Prakash, K.-M.5    Liu, J.6
  • 77
    • 84939427402 scopus 로고    scopus 로고
    • DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients
    • Sep
    • [77] Lorenzo-Betancor, O., Ogaki, K., Soto-Ortolaza, A.I., Labbe, C., Walton, R.L., Strongosky, A.J., et al. DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients. Eur. J. Neurol. 22:9 (2015 Sep), 1323–1325.
    • (2015) Eur. J. Neurol. , vol.22 , Issue.9 , pp. 1323-1325
    • Lorenzo-Betancor, O.1    Ogaki, K.2    Soto-Ortolaza, A.I.3    Labbe, C.4    Walton, R.L.5    Strongosky, A.J.6
  • 78
    • 84969627695 scopus 로고    scopus 로고
    • Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease
    • e13–7 Sep
    • [78] Ross, J.P., Dupre, N., Dauvilliers, Y., Strong, S., Ambalavanan, A., Spiegelman, D., et al. Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiol. Aging, 45, 2016 Sep, 212 e13–7.
    • (2016) Neurobiol. Aging , vol.45 , pp. 212
    • Ross, J.P.1    Dupre, N.2    Dauvilliers, Y.3    Strong, S.4    Ambalavanan, A.5    Spiegelman, D.6
  • 79
    • 84947031214 scopus 로고    scopus 로고
    • Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease
    • e7–8 Nov
    • [79] Liu, Z., Guo, J., Li, K., Qin, L., Kang, J., Shu, L., et al. Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease. Neurobiol. Aging, 36(11), 2015 Nov, 3117 e7–8.
    • (2015) Neurobiol. Aging , vol.36 , Issue.11 , pp. 3117
    • Liu, Z.1    Guo, J.2    Li, K.3    Qin, L.4    Kang, J.5    Shu, L.6
  • 80
    • 85017075140 scopus 로고    scopus 로고
    • Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease
    • e7–8 Feb
    • [80] Zhang, M., Xi, Z., Fang, S., Ghani, M., Sato, C., Moreno, D., et al. Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease. Neurobiol. Aging, 38, 2016 Feb, 217 e7–8.
    • (2016) Neurobiol. Aging , vol.38 , pp. 217
    • Zhang, M.1    Xi, Z.2    Fang, S.3    Ghani, M.4    Sato, C.5    Moreno, D.6
  • 81
    • 84951051504 scopus 로고    scopus 로고
    • Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population
    • e1–2 Feb
    • [81] Fan, T.-S., Lin, H.-I., Lin, C.-H., Wu, R.-M., Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population. Neurobiol. Aging, 38, 2016 Feb, 218 e1–2.
    • (2016) Neurobiol. Aging , vol.38 , pp. 218
    • Fan, T.-S.1    Lin, H.-I.2    Lin, C.-H.3    Wu, R.-M.4
  • 84
    • 84940959375 scopus 로고    scopus 로고
    • Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease
    • e11–2 Oct
    • [84] Yuan, L., Deng, X., Song, Z., Yang, Z., Ni, B., Chen, Y., et al. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease. Neurobiol. Aging, 36(10), 2015 Oct, 2907 e11–2.
    • (2015) Neurobiol. Aging , vol.36 , Issue.10 , pp. 2907
    • Yuan, L.1    Deng, X.2    Song, Z.3    Yang, Z.4    Ni, B.5    Chen, Y.6
  • 85
    • 84976423807 scopus 로고    scopus 로고
    • RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies
    • Sep
    • [85] Hodges, K., Brewer, S.S., Labbé, C., Soto-Ortolaza, A.I., Walton, R.L., Strongosky, A.J., et al. RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodies. Neurobiol. Aging 45 (2016 Sep), 107–108.
    • (2016) Neurobiol. Aging , vol.45 , pp. 107-108
    • Hodges, K.1    Brewer, S.S.2    Labbé, C.3    Soto-Ortolaza, A.I.4    Walton, R.L.5    Strongosky, A.J.6
  • 87
    • 84964203331 scopus 로고    scopus 로고
    • EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts
    • Jan
    • [87] Huttenlocher, J., Krüger, R., Capetian, P., Lohmann, K., Brockmann, K., Csoti, I., et al. EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts. J. Med. Genet. 52:1 (2015 Jan), 37–41.
    • (2015) J. Med. Genet. , vol.52 , Issue.1 , pp. 37-41
    • Huttenlocher, J.1    Krüger, R.2    Capetian, P.3    Lohmann, K.4    Brockmann, K.5    Csoti, I.6
  • 89
    • 84906663944 scopus 로고    scopus 로고
    • Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
    • Sep
    • [89] Mencacci, N.E., Isaias, I.U., Reich, M.M., Ganos, C., Plagnol, V., Polke, J.M., et al. Parkinson's disease in GTP cyclohydrolase 1 mutation carriers. Brain 137:Pt 9 (2014 Sep), 2480–2492.
    • (2014) Brain , vol.137 , pp. 2480-2492
    • Mencacci, N.E.1    Isaias, I.U.2    Reich, M.M.3    Ganos, C.4    Plagnol, V.5    Polke, J.M.6
  • 90
    • 84871256724 scopus 로고    scopus 로고
    • Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs
    • Dec
    • [90] Tadic, V., Kasten, M., Brüggemann, N., Stiller, S., Hagenah, J., Klein, C., Dopa-responsive dystonia revisited: diagnostic delay, residual signs, and nonmotor signs. Arch. Neurol. 69:12 (2012 Dec), 1558–1562.
    • (2012) Arch. Neurol. , vol.69 , Issue.12 , pp. 1558-1562
    • Tadic, V.1    Kasten, M.2    Brüggemann, N.3    Stiller, S.4    Hagenah, J.5    Klein, C.6
  • 91
    • 84906663946 scopus 로고    scopus 로고
    • Hereditary dystonia and parkinsonism: two sides of the same coin?
    • Sep
    • [91] Weissbach, A., Klein, C., Hereditary dystonia and parkinsonism: two sides of the same coin?. Brain 137:Pt 9 (2014 Sep), 2402–2404.
    • (2014) Brain , vol.137 , pp. 2402-2404
    • Weissbach, A.1    Klein, C.2
  • 92
    • 84997102150 scopus 로고    scopus 로고
    • Chapt. 1: the neurogenetics of Parkinson's disease and putative links to other neurodegenerative disorders
    • Patrik Verstreken Elsevier, Inc in press
    • [92] Lill, C.M., Klein, C., Chapt. 1: the neurogenetics of Parkinson's disease and putative links to other neurodegenerative disorders. Verstreken, Patrik, (eds.) Parkinson's Disease, 2016, Elsevier, Inc in press.
    • (2016) Parkinson's Disease
    • Lill, C.M.1    Klein, C.2
  • 93
    • 0342950666 scopus 로고    scopus 로고
    • Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
    • May
    • [93] Krüger, R., Vieira-Saecker, A.M., Kuhn, W., Berg, D., Müller, T., Kühnl, N., et al. Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype. Ann. Neurol. 45:5 (1999 May), 611–617.
    • (1999) Ann. Neurol. , vol.45 , Issue.5 , pp. 611-617
    • Krüger, R.1    Vieira-Saecker, A.M.2    Kuhn, W.3    Berg, D.4    Müller, T.5    Kühnl, N.6
  • 94
    • 28744453588 scopus 로고    scopus 로고
    • Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease
    • Dec 1
    • [94] Skipper, L., Li, Y., Bonnard, C., Pavanni, R., Yih, Y., Chua, E., et al. Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Hum. Mol. Genet. 14:23 (2005 Dec 1), 3549–3556.
    • (2005) Hum. Mol. Genet. , vol.14 , Issue.23 , pp. 3549-3556
    • Skipper, L.1    Li, Y.2    Bonnard, C.3    Pavanni, R.4    Yih, Y.5    Chua, E.6
  • 95
    • 24644431901 scopus 로고    scopus 로고
    • LRRK2 gene in Parkinson disease: mutation analysis and case control association study
    • Sep 13
    • [95] Paisán-Ruíz, C., Lang, A.E., Kawarai, T., Sato, C., Salehi-Rad, S., Fisman, G.K., et al. LRRK2 gene in Parkinson disease: mutation analysis and case control association study. Neurology 65:5 (2005 Sep 13), 696–700.
    • (2005) Neurology , vol.65 , Issue.5 , pp. 696-700
    • Paisán-Ruíz, C.1    Lang, A.E.2    Kawarai, T.3    Sato, C.4    Salehi-Rad, S.5    Fisman, G.K.6
  • 96
    • 28544447258 scopus 로고    scopus 로고
    • Common variants of LRRK2 are not associated with sporadic Parkinson's disease
    • Dec
    • [96] Biskup, S., Mueller, J.C., Sharma, M., Lichtner, P., Zimprich, A., Berg, D., et al. Common variants of LRRK2 are not associated with sporadic Parkinson's disease. Ann. Neurol. 58:6 (2005 Dec), 905–908.
    • (2005) Ann. Neurol. , vol.58 , Issue.6 , pp. 905-908
    • Biskup, S.1    Mueller, J.C.2    Sharma, M.3    Lichtner, P.4    Zimprich, A.5    Berg, D.6
  • 97
    • 33746869343 scopus 로고    scopus 로고
    • Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease
    • Aug 9
    • [97] Maraganore, D.M., de Andrade, M., Elbaz, A., Farrer, M.J., Ioannidis, J.P., Krüger, R., et al. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA 296:6 (2006 Aug 9), 661–670.
    • (2006) JAMA , vol.296 , Issue.6 , pp. 661-670
    • Maraganore, D.M.1    de Andrade, M.2    Elbaz, A.3    Farrer, M.J.4    Ioannidis, J.P.5    Krüger, R.6
  • 98
    • 84997147946 scopus 로고    scopus 로고
    • Allelic heterogeneity and risk stratification at the SNCA locus in Parkinson's disease. in preparation;
    • [98] Pihlstrøm L, Lill CM, Hansen J, Bjørnarå KA, Dizdar N, Fardell C, et al. Allelic heterogeneity and risk stratification at the SNCA locus in Parkinson's disease. in preparation;.
    • Pihlstrøm, L.1    Lill, C.M.2    Hansen, J.3    Bjørnarå, K.A.4    Dizdar, N.5    Fardell, C.6
  • 99
    • 33746079596 scopus 로고    scopus 로고
    • A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
    • Jul
    • [99] Di Fonzo, A., Wu-Chou, Y.-H., Lu, C.-S., van Doeselaar, M., Simons, E.J., Rohé, C.F., et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 7:3 (2006 Jul), 133–138.
    • (2006) Neurogenetics , vol.7 , Issue.3 , pp. 133-138
    • Di Fonzo, A.1    Wu-Chou, Y.-H.2    Lu, C.-S.3    van Doeselaar, M.4    Simons, E.J.5    Rohé, C.F.6
  • 100
    • 0032892668 scopus 로고    scopus 로고
    • The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases
    • May
    • [100] Morris, H.R., Janssen, J.C., Bandmann, O., Daniel, S.E., Rossor, M.N., Lees, A.J., et al. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. J. Neurol. Neurosurg. Psychiatr. 66:5 (1999 May), 665–667.
    • (1999) J. Neurol. Neurosurg. Psychiatr. , vol.66 , Issue.5 , pp. 665-667
    • Morris, H.R.1    Janssen, J.C.2    Bandmann, O.3    Daniel, S.E.4    Rossor, M.N.5    Lees, A.J.6
  • 103
    • 0035861048 scopus 로고    scopus 로고
    • Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease
    • Nov 14
    • [103] Martin, E.R., Scott, W.K., Nance, M.A., Watts, R.L., Hubble, J.P., Koller, W.C., et al. Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. JAMA 286:18 (2001 Nov 14), 2245–2250.
    • (2001) JAMA , vol.286 , Issue.18 , pp. 2245-2250
    • Martin, E.R.1    Scott, W.K.2    Nance, M.A.3    Watts, R.L.4    Hubble, J.P.5    Koller, W.C.6
  • 105
    • 70549084415 scopus 로고    scopus 로고
    • Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
    • Dec
    • [105] Satake, W., Nakabayashi, Y., Mizuta, I., Hirota, Y., Ito, C., Kubo, M., et al. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat. Genet. 41:12 (2009 Dec), 1303–1307.
    • (2009) Nat. Genet. , vol.41 , Issue.12 , pp. 1303-1307
    • Satake, W.1    Nakabayashi, Y.2    Mizuta, I.3    Hirota, Y.4    Ito, C.5    Kubo, M.6
  • 106
    • 79959689333 scopus 로고    scopus 로고
    • Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
    • Jul
    • [106] Höglinger, G.U., Melhem, N.M., Dickson, D.W., Sleiman, P.M.A., Wang, L.-S., Klei, L., et al. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nat. Genet. 43:7 (2011 Jul), 699–705.
    • (2011) Nat. Genet. , vol.43 , Issue.7 , pp. 699-705
    • Höglinger, G.U.1    Melhem, N.M.2    Dickson, D.W.3    Sleiman, P.M.A.4    Wang, L.-S.5    Klei, L.6
  • 107
    • 84935832302 scopus 로고    scopus 로고
    • Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy
    • [107] Kouri, N., Ross, O.A., Dombroski, B., Younkin, C.S., Serie, D.J., Soto-Ortolaza, A., et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Nat. Commun., 6, 2015, 7247.
    • (2015) Nat. Commun. , vol.6 , pp. 7247
    • Kouri, N.1    Ross, O.A.2    Dombroski, B.3    Younkin, C.S.4    Serie, D.J.5    Soto-Ortolaza, A.6
  • 108
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
    • Jun 18
    • [108] Hutton, M., Lendon, C.L., Rizzu, P., Baker, M., Froelich, S., Houlden, H., et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 393:6686 (1998 Jun 18), 702–705.
    • (1998) Nature , vol.393 , Issue.6686 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3    Baker, M.4    Froelich, S.5    Houlden, H.6
  • 109
    • 0029773625 scopus 로고    scopus 로고
    • Occurrence of Parkinson's syndrome in type I Gaucher disease
    • Sep
    • [109] Neudorfer, O., Giladi, N., Elstein, D., Abrahamov, A., Turezkite, T., Aghai, E., et al. Occurrence of Parkinson's syndrome in type I Gaucher disease. QJM 89:9 (1996 Sep), 691–694.
    • (1996) QJM , vol.89 , Issue.9 , pp. 691-694
    • Neudorfer, O.1    Giladi, N.2    Elstein, D.3    Abrahamov, A.4    Turezkite, T.5    Aghai, E.6
  • 110
    • 10744226352 scopus 로고    scopus 로고
    • Gaucher's disease with Parkinson's disease: clinical and pathological aspects
    • Jul 8
    • [110] Bembi, B., Zambito Marsala, S., Sidransky, E., Ciana, G., Carrozzi, M., Zorzon, M., et al. Gaucher's disease with Parkinson's disease: clinical and pathological aspects. Neurology 61:1 (2003 Jul 8), 99–101.
    • (2003) Neurology , vol.61 , Issue.1 , pp. 99-101
    • Bembi, B.1    Zambito Marsala, S.2    Sidransky, E.3    Ciana, G.4    Carrozzi, M.5    Zorzon, M.6
  • 111
    • 70350319531 scopus 로고    scopus 로고
    • Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
    • Oct 22
    • [111] Sidransky, E., Nalls, M.A., Aasly, J.O., Aharon-Peretz, J., Annesi, G., Barbosa, E.R., et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N. Engl. J. Med. 361:17 (2009 Oct 22), 1651–1661.
    • (2009) N. Engl. J. Med. , vol.361 , Issue.17 , pp. 1651-1661
    • Sidransky, E.1    Nalls, M.A.2    Aasly, J.O.3    Aharon-Peretz, J.4    Annesi, G.5    Barbosa, E.R.6
  • 113
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • Feb 15
    • [113] Lander, E.S., Linton, L.M., Birren, B., Nusbaum, C., Zody, M.C., Baldwin, J., et al. Initial sequencing and analysis of the human genome. Nature 409:6822 (2001 Feb 15), 860–921.
    • (2001) Nature , vol.409 , Issue.6822 , pp. 860-921
    • Lander, E.S.1    Linton, L.M.2    Birren, B.3    Nusbaum, C.4    Zody, M.C.5    Baldwin, J.6
  • 114
    • 79959524146 scopus 로고    scopus 로고
    • A haplotype map of the human genome
    • Oct 27
    • [114] International HapMap Consortium. A haplotype map of the human genome. Nature 437:7063 (2005 Oct 27), 1299–1320.
    • (2005) Nature , vol.437 , Issue.7063 , pp. 1299-1320
  • 115
    • 77956331627 scopus 로고    scopus 로고
    • Integrating common and rare genetic variation in diverse human populations
    • Sep 2
    • [115] International HapMap 3 Consortium, Altshuler, D.M., Gibbs, R.A., Peltonen, L., Altshuler, D.M., Gibbs, R.A., et al. Integrating common and rare genetic variation in diverse human populations. Nature 467:7311 (2010 Sep 2), 52–58.
    • (2010) Nature , vol.467 , Issue.7311 , pp. 52-58
    • Altshuler, D.M.1    Gibbs, R.A.2    Peltonen, L.3    Altshuler, D.M.4    Gibbs, R.A.5
  • 116
    • 84975742565 scopus 로고    scopus 로고
    • A map of human genome variation from population-scale sequencing
    • Oct 28
    • [116] 1000 Genomes Project Consortium. A map of human genome variation from population-scale sequencing. Nature 467:7319 (2010 Oct 28), 1061–1073.
    • (2010) Nature , vol.467 , Issue.7319 , pp. 1061-1073
  • 117
    • 77953806824 scopus 로고    scopus 로고
    • Bayes factors in complex genetics
    • Jul
    • [117] Sawcer, S., Bayes factors in complex genetics. Eur. J. Hum. Genet. 18:7 (2010 Jul), 746–750.
    • (2010) Eur. J. Hum. Genet. , vol.18 , Issue.7 , pp. 746-750
    • Sawcer, S.1
  • 118
    • 33749667345 scopus 로고    scopus 로고
    • Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
    • Nov
    • [118] Fung, H.-C., Scholz, S., Matarin, M., Simón-Sánchez, J., Hernandez, D., Britton, A., et al. Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Lancet Neurol. 5:11 (2006 Nov), 911–916.
    • (2006) Lancet Neurol. , vol.5 , Issue.11 , pp. 911-916
    • Fung, H.-C.1    Scholz, S.2    Matarin, M.3    Simón-Sánchez, J.4    Hernandez, D.5    Britton, A.6
  • 120
    • 70549088602 scopus 로고    scopus 로고
    • Genome-wide association study reveals genetic risk underlying Parkinson's disease
    • Dec
    • [120] Simón-Sánchez, J., Schulte, C., Bras, J.M., Sharma, M., Gibbs, J.R., Berg, D., et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 41:12 (2009 Dec), 1308–1312.
    • (2009) Nat. Genet. , vol.41 , Issue.12 , pp. 1308-1312
    • Simón-Sánchez, J.1    Schulte, C.2    Bras, J.M.3    Sharma, M.4    Gibbs, J.R.5    Berg, D.6
  • 121
    • 58149100151 scopus 로고    scopus 로고
    • Genomewide association study for susceptibility genes contributing to familial Parkinson disease
    • Jan
    • [121] Pankratz, N., Wilk, J.B., Latourelle, J.C., DeStefano, A.L., Halter, C., Pugh, E.W., et al. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum. Genet. 124:6 (2009 Jan), 593–605.
    • (2009) Hum. Genet. , vol.124 , Issue.6 , pp. 593-605
    • Pankratz, N.1    Wilk, J.B.2    Latourelle, J.C.3    DeStefano, A.L.4    Halter, C.5    Pugh, E.W.6
  • 123
    • 78650550275 scopus 로고    scopus 로고
    • Dissection of the genetics of Parkinson's disease identifies an additional association 5’ of SNCA and multiple associated haplotypes at 17q21
    • Jan 15
    • [123] Spencer, C.C.A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., et al. Dissection of the genetics of Parkinson's disease identifies an additional association 5’ of SNCA and multiple associated haplotypes at 17q21. Hum. Mol. Genet. 20:2 (2011 Jan 15), 345–353.
    • (2011) Hum. Mol. Genet. , vol.20 , Issue.2 , pp. 345-353
    • Spencer, C.C.A.1    Plagnol, V.2    Strange, A.3    Gardner, M.4    Paisan-Ruiz, C.5    Band, G.6
  • 124
    • 79951811351 scopus 로고    scopus 로고
    • Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
    • Feb 19
    • [124] Nalls, M.A., Plagnol, V., Hernandez, D.G., Sharma, M., Sheerin, U.-M., Saad, M., et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet 377:9766 (2011 Feb 19), 641–649.
    • (2011) Lancet , vol.377 , Issue.9766 , pp. 641-649
    • Nalls, M.A.1    Plagnol, V.2    Hernandez, D.G.3    Sharma, M.4    Sheerin, U.-M.5    Saad, M.6
  • 125
    • 84859199353 scopus 로고    scopus 로고
    • Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
    • Mar
    • [125] Pankratz, N., Beecham, G.W., DeStefano, A.L., Dawson, T.M., Doheny, K.F., Factor, S.A., et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Ann. Neurol. 71:3 (2012 Mar), 370–384.
    • (2012) Ann. Neurol. , vol.71 , Issue.3 , pp. 370-384
    • Pankratz, N.1    Beecham, G.W.2    DeStefano, A.L.3    Dawson, T.M.4    Doheny, K.F.5    Factor, S.A.6
  • 126
    • 77956646167 scopus 로고    scopus 로고
    • Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
    • Sep
    • [126] Hamza, T.H., Zabetian, C.P., Tenesa, A., Laederach, A., Montimurro, J., Yearout, D., et al. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nat. Genet. 42:9 (2010 Sep), 781–785.
    • (2010) Nat. Genet. , vol.42 , Issue.9 , pp. 781-785
    • Hamza, T.H.1    Zabetian, C.P.2    Tenesa, A.3    Laederach, A.4    Montimurro, J.5    Yearout, D.6
  • 127
    • 84887083013 scopus 로고    scopus 로고
    • The role of inflammation in sporadic and familial Parkinson's disease
    • Nov
    • [127] Deleidi, M., Gasser, T., The role of inflammation in sporadic and familial Parkinson's disease. Cell Mol. Life Sci. 70:22 (2013 Nov), 4259–4273.
    • (2013) Cell Mol. Life Sci. , vol.70 , Issue.22 , pp. 4259-4273
    • Deleidi, M.1    Gasser, T.2
  • 128
    • 84942981489 scopus 로고    scopus 로고
    • Class II HLA interactions modulate genetic risk for multiple sclerosis
    • Oct
    • [128] Moutsianas, L., Jostins, L., Beecham, A.H., Dilthey, A.T., Xifara, D.K., Ban, M., et al. Class II HLA interactions modulate genetic risk for multiple sclerosis. Nat. Genet. 47:10 (2015 Oct), 1107–1113.
    • (2015) Nat. Genet. , vol.47 , Issue.10 , pp. 1107-1113
    • Moutsianas, L.1    Jostins, L.2    Beecham, A.H.3    Dilthey, A.T.4    Xifara, D.K.5    Ban, M.6
  • 129
    • 84940590102 scopus 로고    scopus 로고
    • Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases
    • Sep
    • [129] Lenz, T.L., Deutsch, A.J., Han, B., Hu, X., Okada, Y., Eyre, S., et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nat. Genet. 47:9 (2015 Sep), 1085–1090.
    • (2015) Nat. Genet. , vol.47 , Issue.9 , pp. 1085-1090
    • Lenz, T.L.1    Deutsch, A.J.2    Han, B.3    Hu, X.4    Okada, Y.5    Eyre, S.6
  • 130
    • 84904386052 scopus 로고    scopus 로고
    • Recent advances and future challenges in the genetics of multiple sclerosis
    • [130] Lill, C.M., Recent advances and future challenges in the genetics of multiple sclerosis. Front. Neurol., 5, 2014, 130.
    • (2014) Front. Neurol. , vol.5 , pp. 130
    • Lill, C.M.1
  • 131
    • 84888317489 scopus 로고    scopus 로고
    • Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
    • Dec
    • [131] Lambert, J.C., Ibrahim-Verbaas, C.A., Harold, D., Naj, A.C., Sims, R., Bellenguez, C., et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat. Genet. 45:12 (2013 Dec), 1452–1458.
    • (2013) Nat. Genet. , vol.45 , Issue.12 , pp. 1452-1458
    • Lambert, J.C.1    Ibrahim-Verbaas, C.A.2    Harold, D.3    Naj, A.C.4    Sims, R.5    Bellenguez, C.6
  • 132
    • 68449096727 scopus 로고    scopus 로고
    • Common variants on chromosome 6p22.1 are associated with schizophrenia
    • Aug 6
    • [132] Shi, J., Levinson, D.F., Duan, J., Sanders, A.R., Zheng, Y., Pe'er, I., et al. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460:7256 (2009 Aug 6), 753–757.
    • (2009) Nature , vol.460 , Issue.7256 , pp. 753-757
    • Shi, J.1    Levinson, D.F.2    Duan, J.3    Sanders, A.R.4    Zheng, Y.5    Pe'er, I.6
  • 133
  • 134
    • 84944512337 scopus 로고    scopus 로고
    • Cumulative genetic risk and age at onset in Parkinson's disease
    • Aug 3
    • [134] Pihlstrøm, L., Toft, M., Cumulative genetic risk and age at onset in Parkinson's disease. Mov. Disord., 2015 Aug 3.
    • (2015) Mov. Disord.
    • Pihlstrøm, L.1    Toft, M.2
  • 135
    • 84883557700 scopus 로고    scopus 로고
    • SNCA: major genetic modifier of age at onset of Parkinson's disease
    • Aug
    • [135] Brockmann, K., Schulte, C., Hauser, A.-K., Lichtner, P., Huber, H., Maetzler, W., et al. SNCA: major genetic modifier of age at onset of Parkinson's disease. Mov. Disord. 28:9 (2013 Aug), 1217–1221.
    • (2013) Mov. Disord. , vol.28 , Issue.9 , pp. 1217-1221
    • Brockmann, K.1    Schulte, C.2    Hauser, A.-K.3    Lichtner, P.4    Huber, H.5    Maetzler, W.6
  • 136
    • 84929654195 scopus 로고    scopus 로고
    • Impact of Parkinson's disease risk loci on age at onset
    • May
    • [136] Lill, C.M., Hansen, J., Olsen, J.H., Binder, H., Ritz, B., Bertram, L., Impact of Parkinson's disease risk loci on age at onset. Mov. Disord 30:6 (2015 May), 847–850.
    • (2015) Mov. Disord , vol.30 , Issue.6 , pp. 847-850
    • Lill, C.M.1    Hansen, J.2    Olsen, J.H.3    Binder, H.4    Ritz, B.5    Bertram, L.6
  • 138
  • 139
    • 80052328932 scopus 로고    scopus 로고
    • Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
    • Aug
    • [139] Hamza, T.H., Chen, H., Hill-Burns, E.M., Rhodes, S.L., Montimurro, J., Kay, D.M., et al. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. PLoS Genet., 7(8), 2011 Aug, e1002237.
    • (2011) PLoS Genet. , vol.7 , Issue.8 , pp. e1002237
    • Hamza, T.H.1    Chen, H.2    Hill-Burns, E.M.3    Rhodes, S.L.4    Montimurro, J.5    Kay, D.M.6
  • 140
    • 84912099083 scopus 로고    scopus 로고
    • Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease
    • Nov
    • [140] Ahmed, I., Lee, P.-C., Lill, C.M., Searles Nielsen, S., Artaud, F., Gallagher, L.G., et al. Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease. PLoS Genet., 10(11), 2014 Nov, e1004788.
    • (2014) PLoS Genet. , vol.10 , Issue.11 , pp. e1004788
    • Ahmed, I.1    Lee, P.-C.2    Lill, C.M.3    Searles Nielsen, S.4    Artaud, F.5    Gallagher, L.G.6
  • 141
    • 84888138764 scopus 로고    scopus 로고
    • A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease
    • Dec
    • [141] Hill-Burns, E.M., Singh, N., Ganguly, P., Hamza, T.H., Montimurro, J., Kay, D.M., et al. A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease. Pharmacogenomics J. 13:6 (2013 Dec), 530–537.
    • (2013) Pharmacogenomics J. , vol.13 , Issue.6 , pp. 530-537
    • Hill-Burns, E.M.1    Singh, N.2    Ganguly, P.3    Hamza, T.H.4    Montimurro, J.5    Kay, D.M.6
  • 142
    • 84906716826 scopus 로고    scopus 로고
    • Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease
    • Sep
    • [142] Lunnon, K., Smith, R., Hannon, E., De Jager, P.L., Srivastava, G., Volta, M., et al. Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease. Nat. Neurosci. 17:9 (2014 Sep), 1164–1170.
    • (2014) Nat. Neurosci. , vol.17 , Issue.9 , pp. 1164-1170
    • Lunnon, K.1    Smith, R.2    Hannon, E.3    De Jager, P.L.4    Srivastava, G.5    Volta, M.6
  • 143
    • 84919784465 scopus 로고    scopus 로고
    • Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci
    • Sep
    • [143] De Jager, P.L., Srivastava, G., Lunnon, K., Burgess, J., Schalkwyk, L.C., Yu, L., et al. Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci. Nat. Neurosci. 17:9 (2014 Sep), 1156–1163.
    • (2014) Nat. Neurosci. , vol.17 , Issue.9 , pp. 1156-1163
    • De Jager, P.L.1    Srivastava, G.2    Lunnon, K.3    Burgess, J.4    Schalkwyk, L.C.5    Yu, L.6
  • 144
    • 84964199875 scopus 로고    scopus 로고
    • Probing the epigenome by EWAS: a new era in brain disease research
    • Feb
    • [144] Lill, C.M., Bertram, L., Probing the epigenome by EWAS: a new era in brain disease research. Mov. Disord., 30(2), 2015 Feb, 197.
    • (2015) Mov. Disord. , vol.30 , Issue.2 , pp. 197
    • Lill, C.M.1    Bertram, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.