메뉴 건너뛰기




Volumn 38, Issue , 2016, Pages 141-150

Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium

(17)  Hohman, Timothy J a   Bush, William S b   Jiang, Lan a   Brown Gentry, Kristin D a   Torstenson, Eric S a   Dudek, Scott M a   Mukherjee, Shubhabrata c   Naj, Adam d   Kunkle, Brian W e   Ritchie, Marylyn D f   Martin, Eden R e   Schellenberg, Gerard D g   Mayeux, Richard h   Farrer, Lindsay A i,j   Pericak Vance, Margaret A e   Haines, Jonathan L b   Thornton Wells, Tricia A k  


Author keywords

Alzheimer disease; Biofilter; Epistasis; Gene gene interactions

Indexed keywords

ALPHA 1A ADRENERGIC RECEPTOR; MULTIDRUG RESISTANCE PROTEIN 1; N METHYL DEXTRO ASPARTIC ACID RECEPTOR 2B; RYANODINE RECEPTOR 3; SIRTUIN 1; ABCB1 PROTEIN, HUMAN; ADRA1A PROTEIN, HUMAN; ALPHA 1 ADRENERGIC RECEPTOR; CACNA1C PROTEIN, HUMAN; CADHERIN; CALCIUM CHANNEL L TYPE; CDH23 PROTEIN, HUMAN; MULTIDRUG RESISTANCE PROTEIN; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NR2B NMDA RECEPTOR; PE-BINDING PROTEIN 4, HUMAN; PHOSPHATIDYLETHANOLAMINE BINDING PROTEIN; PSAP PROTEIN, HUMAN; RYANODINE RECEPTOR; SIRT1 PROTEIN, HUMAN; SPHINGOLIPID ACTIVATOR PROTEIN;

EID: 84962285532     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2015.10.031     Document Type: Article
Times cited : (41)

References (42)
  • 1
    • 84901306605 scopus 로고    scopus 로고
    • Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease
    • Andreoli V., De Marco E.V., Trecroci F., Cittadella R., Di Palma G., Gambardella A. Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease. J. Neural Transm. 2014, 121:533-542.
    • (2014) J. Neural Transm. , vol.121 , pp. 533-542
    • Andreoli, V.1    De Marco, E.V.2    Trecroci, F.3    Cittadella, R.4    Di Palma, G.5    Gambardella, A.6
  • 5
    • 61949417042 scopus 로고    scopus 로고
    • Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies
    • Bush W.S., Dudek S.M., Ritchie M.D. Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies. Pac. Symp. Biocomput. 2009, 368-379.
    • (2009) Pac. Symp. Biocomput. , pp. 368-379
    • Bush, W.S.1    Dudek, S.M.2    Ritchie, M.D.3
  • 9
    • 77955046461 scopus 로고    scopus 로고
    • SIRT1 suppresses beta-amyloid production by activating the alpha-secretase gene ADAM10
    • Donmez G., Wang D., Cohen D.E., Guarente L. SIRT1 suppresses beta-amyloid production by activating the alpha-secretase gene ADAM10. Cell 2010, 142:320-332.
    • (2010) Cell , vol.142 , pp. 320-332
    • Donmez, G.1    Wang, D.2    Cohen, D.E.3    Guarente, L.4
  • 10
    • 84879495507 scopus 로고    scopus 로고
    • The role of ABCB1 and ABCA1 in beta-amyloid clearance at the neurovascular unit in Alzheimer's disease
    • Elali A., Rivest S. The role of ABCB1 and ABCA1 in beta-amyloid clearance at the neurovascular unit in Alzheimer's disease. Front. Physiol. 2013, 4:45.
    • (2013) Front. Physiol. , vol.4 , pp. 45
    • Elali, A.1    Rivest, S.2
  • 11
    • 32244435907 scopus 로고    scopus 로고
    • Role of genes and environments for explaining Alzheimer disease
    • Gatz M., Reynolds C.A., Fratiglioni L. Role of genes and environments for explaining Alzheimer disease. Arch. Gen. Psychiatry 2006, 63:168-174.
    • (2006) Arch. Gen. Psychiatry , vol.63 , pp. 168-174
    • Gatz, M.1    Reynolds, C.A.2    Fratiglioni, L.3
  • 12
  • 14
    • 84894094478 scopus 로고    scopus 로고
    • Epistatic effects among Alzheimer's candidate genes
    • Hohman T.J., Koran M.I., Thornton-Wells T.A. Epistatic effects among Alzheimer's candidate genes. PLoS One 2013, 8:e80839.
    • (2013) PLoS One , vol.8 , pp. e80839
    • Hohman, T.J.1    Koran, M.I.2    Thornton-Wells, T.A.3
  • 19
    • 84887221030 scopus 로고    scopus 로고
    • Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size
    • Koran M.I., Hohman T.J., Meda S.A., Thornton-Wells T. Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size. J. Alzheimer's Dis. 2014, 38:145-154.
    • (2014) J. Alzheimer's Dis. , vol.38 , pp. 145-154
    • Koran, M.I.1    Hohman, T.J.2    Meda, S.A.3    Thornton-Wells, T.4
  • 20
    • 84891869466 scopus 로고    scopus 로고
    • Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography
    • Koran M.I., Hohman T.J., Thornton-Wells T.A. Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography. Hum. Genet. 2014, 133:85-93.
    • (2014) Hum. Genet. , vol.133 , pp. 85-93
    • Koran, M.I.1    Hohman, T.J.2    Thornton-Wells, T.A.3
  • 25
    • 84906703212 scopus 로고    scopus 로고
    • The epigenetic landscape of Alzheimer's disease
    • Lord J., Cruchaga C. The epigenetic landscape of Alzheimer's disease. Nat. Neurosci. 2014, 17:1138-1140.
    • (2014) Nat. Neurosci. , vol.17 , pp. 1138-1140
    • Lord, J.1    Cruchaga, C.2
  • 28
    • 0021271971 scopus 로고
    • Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease
    • McKhann G., Drachman D., Folstein M., Katzman R., Price D., Stadlan E.M. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology 1984, 34:939-944.
    • (1984) Neurology , vol.34 , pp. 939-944
    • McKhann, G.1    Drachman, D.2    Folstein, M.3    Katzman, R.4    Price, D.5    Stadlan, E.M.6
  • 29
    • 84865031797 scopus 로고    scopus 로고
    • Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study
    • Miyagawa M., Nishio S.Y., Usami S. Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study. PLoS One 2012, 7:e40366.
    • (2012) PLoS One , vol.7 , pp. e40366
    • Miyagawa, M.1    Nishio, S.Y.2    Usami, S.3
  • 37
    • 84892407135 scopus 로고    scopus 로고
    • Alzheimer's disease: analyzing the missing heritability
    • Ridge P.G., Mukherjee S., Crane P.K., Kauwe J.S.K. Alzheimer's disease: analyzing the missing heritability. PLoS One 2013, 8:e79771.
    • (2013) PLoS One , vol.8 , pp. e79771
    • Ridge, P.G.1    Mukherjee, S.2    Crane, P.K.3    Kauwe, J.S.K.4
  • 38
    • 0029981722 scopus 로고    scopus 로고
    • Effects of combined block of α 1-adrenoceptors and NMDA receptors on spatial and passive avoidance behavior in rats
    • Riekkinen M., Stefanski R., Kuitunen J., Riekkinen P. Effects of combined block of α 1-adrenoceptors and NMDA receptors on spatial and passive avoidance behavior in rats. Eur. J. Pharmacol. 1996, 300:9-16.
    • (1996) Eur. J. Pharmacol. , vol.300 , pp. 9-16
    • Riekkinen, M.1    Stefanski, R.2    Kuitunen, J.3    Riekkinen, P.4
  • 39
    • 1942469548 scopus 로고    scopus 로고
    • Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease
    • Robson K.J., Lehmann D.J., Wimhurst V.L., Livesey K.J., Combrinck M., Merryweather-Clarke A.T., Warden D.R., Smith A.D. Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease. J. Med. Genet. 2004, 41:261-265.
    • (2004) J. Med. Genet. , vol.41 , pp. 261-265
    • Robson, K.J.1    Lehmann, D.J.2    Wimhurst, V.L.3    Livesey, K.J.4    Combrinck, M.5    Merryweather-Clarke, A.T.6    Warden, D.R.7    Smith, A.D.8
  • 40
    • 79955841697 scopus 로고    scopus 로고
    • Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases
    • So H.-C., Gui A.H., Cherny S.S., Sham P.C. Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases. Genet. Epidemiol. 2011, 35:310-317.
    • (2011) Genet. Epidemiol. , vol.35 , pp. 310-317
    • So, H.-C.1    Gui, A.H.2    Cherny, S.S.3    Sham, P.C.4
  • 41
    • 84880236916 scopus 로고    scopus 로고
    • Emerging roles of SIRT1 in Cancer drug Resistance
    • Wang Z., Chen W. Emerging roles of SIRT1 in Cancer drug Resistance. Genes Cancer 2013, 4:82-90.
    • (2013) Genes Cancer , vol.4 , pp. 82-90
    • Wang, Z.1    Chen, W.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.