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Volumn 14, Issue 8, 2015, Pages 783-785

Expanding the genomic roadmap of Alzheimer's disease

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; AMYLOID BETA PROTEIN; AMYLOID PRECURSOR PROTEIN; APOLIPOPROTEIN E4; ATP BINDING CASSETTE TRANSPORTER PROTEIN 7; PRESENILIN 1; PRESENILIN 2; UNCLASSIFIED DRUG;

EID: 84937521532     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(15)00146-5     Document Type: Note
Times cited : (12)

References (11)
  • 1
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    • Sherva R, Farrer LA Power and pitfalls of the genome wide association study approach to identify genes for Alzheimer disease. Curr Psych Rep 2011, 13:138-146.
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    • Sherva, R.1    Farrer, L.A.2
  • 2
    • 84888317489 scopus 로고    scopus 로고
    • Extended meta-analysis of 74,538 individuals identifies 11 new susceptibility loci for Alzheimer's disease
    • Lambert J-C, Ibrahim-Verbaas CA, Harold D, et al. Extended meta-analysis of 74,538 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nat Genet 2013, 45:1452-1458.
    • (2013) Nat Genet , vol.45 , pp. 1452-1458
    • Lambert, J.-C.1    Ibrahim-Verbaas, C.A.2    Harold, D.3
  • 3
    • 84872088087 scopus 로고    scopus 로고
    • Variant of TREM2 associated with the risk of Alzheimer's disease
    • Jonsson T, Stefansson H, Steinberg S, et al. Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med 2013, 368:107-116.
    • (2013) N Engl J Med , vol.368 , pp. 107-116
    • Jonsson, T.1    Stefansson, H.2    Steinberg, S.3
  • 4
    • 84872057940 scopus 로고    scopus 로고
    • TREM2 variants in Alzheimer's disease
    • Guerreiro R, Wojtas A, Bras J, et al. TREM2 variants in Alzheimer's disease. N Engl J Med 2013, 368:117-127.
    • (2013) N Engl J Med , vol.368 , pp. 117-127
    • Guerreiro, R.1    Wojtas, A.2    Bras, J.3
  • 5
    • 84937526426 scopus 로고    scopus 로고
    • A rare mutation in UNC5C predisposes to Alzheimer's disease and increases neuronal cell death
    • Wetzel-Smith MK, Hunkapiller J, Bhangale TR, et al. A rare mutation in UNC5C predisposes to Alzheimer's disease and increases neuronal cell death. Nature Med 2014, 20:1452-1457.
    • (2014) Nature Med , vol.20 , pp. 1452-1457
    • Wetzel-Smith, M.K.1    Hunkapiller, J.2    Bhangale, T.R.3
  • 6
    • 84927158295 scopus 로고    scopus 로고
    • Two rare AKAP9 missense variants are associated with Alzheimer disease in African Americans
    • Logue MW, Schu M, Vardarajan BN, et al. Two rare AKAP9 missense variants are associated with Alzheimer disease in African Americans. Alzheimers Dement 2014, 10:609-618.
    • (2014) Alzheimers Dement , vol.10 , pp. 609-618
    • Logue, M.W.1    Schu, M.2    Vardarajan, B.N.3
  • 7
    • 84937526438 scopus 로고    scopus 로고
    • Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study
    • published online July 1.
    • Cuyvers E, De Roeck A, Van den Bossche T, et al. Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study. Lancet Neurol 2015, published online July 1. http://dx.doi.org/10.1016/S1474-4422(15)00133-7.
    • (2015) Lancet Neurol
    • Cuyvers, E.1    De Roeck, A.2    Van den Bossche, T.3
  • 8
    • 79955484414 scopus 로고    scopus 로고
    • Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
    • Hollingworth P, Harold D, Sims R, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet 2011, 43:429-435.
    • (2011) Nat Genet , vol.43 , pp. 429-435
    • Hollingworth, P.1    Harold, D.2    Sims, R.3
  • 9
    • 79955464911 scopus 로고    scopus 로고
    • Genome-wide association study of late-onset Alzheimer disease identifies disease associated variants in MS4A4/MS4A6E, CD2AP, CD33, and EPHA1
    • Naj AC, Jun G, Beecham GW, et al. Genome-wide association study of late-onset Alzheimer disease identifies disease associated variants in MS4A4/MS4A6E, CD2AP, CD33, and EPHA1. Nat Genet 2011, 43:436-441.
    • (2011) Nat Genet , vol.43 , pp. 436-441
    • Naj, A.C.1    Jun, G.2    Beecham, G.W.3
  • 10
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    • Deletion of Abca7 increases cerebral amyloid-β accumulation in the J20 mouse model of Alzheimer's disease
    • Kim WS, Li H, Ruberu K, et al. Deletion of Abca7 increases cerebral amyloid-β accumulation in the J20 mouse model of Alzheimer's disease. J Neurosci 2013, 33:4387-4394.
    • (2013) J Neurosci , vol.33 , pp. 4387-4394
    • Kim, W.S.1    Li, H.2    Ruberu, K.3
  • 11
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    • Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
    • Steinberg S, Stefansson H, Jonsson T, et al. Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease. Nat Genet 2015, 47:445-447.
    • (2015) Nat Genet , vol.47 , pp. 445-447
    • Steinberg, S.1    Stefansson, H.2    Jonsson, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.