المؤلفون: Guerreiro, R, Wojtas, A, Bras, J, Carrasquillo, M, Rogaeva, E, Majounie, E, Cruchaga, C, Sassi, C, Kauwe, Js, Lupton, Mk, Ryten, M, Brown, K, Lowe, J, Ridge, Pg, Hammer, Mb, Wakutani, Y, Hazrati, L, Proitsi, P, Newhouse, S, Lohmann, E, Erginel Unaltuna, N, Medway, C, Hanagasi, H, Troakes, C, Gurvit, H, Bilgic, B, Al Sarraj, S, Benitez, B, Cooper, B, Carrell, D, Emre, M, Zou, F, Ma, L, Murray, M, Dickson, D, Younkin, S, Petersen, Rc, Corcoran, Cd, Cai, Y, Oliveira, C, Ribeiro, Mh, Santana, I, Tschanz, Jt, Gibbs, J, Norton, Mc, Kloszewska, I, Mecocci, Patrizia, Soininen, H, Tsolaki, M, Vellas, B, Munger, Rg, Mann, Dm, Pickering Brown, S, Lovestone, S, Beck, J, Mead, S, Collinge, J, Parsons, L, Pocock, J, Morris, Jc, Revesz, T, Lashley, T, Fox, Nc, Rossor, Mn, Grenier Boley, B, Bellenguez, C, Moskvina, V, Sims, R, Harold, D, Williams, J, Lambert, Jc, Amouyel, P, Graff Radford, N, Goate, A, Rademakers, R, Morgan, K, Powell, J, St George Hyslop, P, Singleton, A, Hardy, J, Gerrish, A, Chapman, J, Abraham, R, Hollingworth, P, Hamshere, M, Pahwa, Js, Dowzell, K, Williams, A, Jones, N, Thomas, C, Stretton, A, Morgan, A, Williams, K, Thomas, S, Brayne, C, Rubinsztein, Dc, Gill, M, Lawlor, B, Lynch, A, Passmore, P, Craig, D, Mcguinness, B, Johnston, Ja, Todd, S, Holmes, C, Smith, A, Love, S, Kehoe, Pg, Maier, W, Jessen, F, Heun, R, Kölsch, H, Schürmann, B, Ramirez, A, van den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Frölich, L, Hampel, H, Hüll, M, Rujescu, D, Nowotny, P, Mayo, K, Livingston, G, Bass, Nj, Gurling, H, Mcquillin, A, Gwilliam, R, Deloukas, P, Nöthen, Mm, Holmans, P, O'Donovan, M, Owen, Mj, Zelenika, D, Epelbaum, J, Dartigues, Jf, Tzourio, C, Berr, C, Boland, A, Campion, D, Alpérovitch, A, Lathrop, M, Smith, C, Trabzuni, D, Walker, R, Weale, M.

المساهمون: Wiltfang, J. (Beitragende*r), EADI Consortium, GERAD Consortium, UKBE Consortium, Alzheimer Genetic Anal Grp

المصدر: The New England journal of medicine

مصطلحات موضوعية: Genetics, TREM2, SORL1, Medizin, Genome-wide association study, General Medicine, Biology, medicine.disease, PSEN2, medicine, Dementia, Human medicine, Alzheimer's disease, Exome, Common disease-common variant

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6c8092ff8f294daa5201834bda07deTest
https://www.ncbi.nlm.nih.gov/pubmed/23150934Test

المؤلفون: Gurvit H., Emre M., Tinaz S., Bilgic B., Hanagasi H., Sahin H., Harmanci H.

المساهمون: Ondokuz Mayıs Üniversitesi

مصطلحات موضوعية: Alzheimer's disease, Dementia, Epidemiology, Prevalence

العلاقة: American Journal of Alzheimer's Disease and other Dementias; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://doi.org/10.1177/1533317507310570Test; https://hdl.handle.net/20.500.12712/3876Test; 23; 67; 76

الإتاحة: https://doi.org/20.500.12712/3876Test
https://doi.org/10.1177/1533317507310570Test
https://hdl.handle.net/20.500.12712/3876Test

المؤلفون: Gurvit, H.¹, Bilgic, B.¹, Hanagasi, H.¹, Guven, G.², Guerreiro, R.³, Hardy, J.³

المصدر: Journal of the Neurological Sciences. Oct2015 Supplement 1, Vol. 357, pe127-e127. 1p.

مصطلحات موضوعية: *GENETIC mutation, *CEREBRAL cortex diseases, *CEREBRAL atrophy, *ALZHEIMER'S disease, *NEUROLOGICAL disorders