Genetic dissection of Alzheimer disease, a heterogeneous disorder.

Por Schellenberg, G D
Publicado em 1995

Influence of apolipoprotein E genotype on the transmission of Alzheimer disease in a community-based sample.

Por Jarvik, G., Larson, E. B., Goddard, K., Schellenberg, G. D., Wijsman, E. M.
Publicado em 1996

Evidence that the apolipoprotein E-genotype effects on lipid levels can change with age in males: a longitudinal analysis.

Por Jarvik, G P, Goode, E L, Austin, M A, Auwerx, J, Deeb, S, Schellenberg, G D, Reed, T
Publicado em 1997

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.

Por Goddard, K. A., Yu, C. E., Oshima, J., Miki, T., Nakura, J., Piussan, C., Martin, G. M., Schellenberg, G. D., Wijsman, E. M.
Publicado em 1996

ABCB1 Genotype and CSF β-Amyloid in Alzheimer Disease

Por Kohen, R., Shofer, J. B., Korvatska, O., Petrie, E. C., Wang, L. Y., Schellenberg, G. D., Peskind, E. R., Wilkinson, C. W.
Publicado em 2011

Mutations in the TSGA14 gene in families with autism spectrum disorders

Por Korvatska, O, Estes, A, Munson, J, Dawson, G, Bekris, L M, Kohen, R, Yu, C-E, Schellenberg, G D, Raskind, W H
Publicado em 2011

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Por Yu, C E, Oshima, J, Wijsman, E M, Nakura, J, Miki, T, Piussan, C, Matthews, S, Fu, Y H, Mulligan, J, Martin, G M, Schellenberg, G D
Publicado em 1997

Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.

Por Payami, H., Zareparsi, S., Montee, K. R., Sexton, G. J., Kaye, J. A., Bird, T. D., Yu, C. E., Wijsman, E. M., Heston, L. L., Litt, M., Schellenberg, G. D.
Publicado em 1996

Intranasal Insulin Administration Dose-Dependently Modulates Verbal Memory and Plasma β-Amyloid in Memory-Impaired Older Adults

Por Reger, M.A., Watson, G.S., Green, P.S., Baker, L.D., Cholerton, B., Fishel, M.A., Plymate, S.R., Cherrier, M.M., Schellenberg, G.D., Frey, W.H., Craft, S.
Publicado em 2008

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

Por Reitz, C, Tosto, G, Vardarajan, B, Rogaeva, E, Ghani, M, Rogers, R S, Conrad, C, Haines, J L, Pericak-Vance, M A, Fallin, M D, Foroud, T, Farrer, L A, Schellenberg, G D, George-Hyslop, P S, Mayeux, R
Publicado em 2013

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

Por Kay, D.M., Stevens, C.F., Hamza, T.H., Montimurro, J.S., Zabetian, C.P., Factor, S.A., Samii, A., Griffith, A., Roberts, J.W., Molho, E.S., Higgins, D.S., Gancher, S., Moses, L., Zareparsi, S., Poorkaj, P., Bird, T., Nutt, J., Schellenberg, G.D., Payami, H.
Publicado em 2010

APP Processing Genes and Cerebrospinal Fluid APP Cleavage Product Levels in Alzheimer’s Disease

Por Bekris, L.M., Galloway, N.M., Millard, S., Lockhart, D., Li, G., Galasko, D.R., Farlow, M.R., Clark, C.M., Quinn, J.F., Kaye, J.A., Schellenberg, G.D., Leverenz, J.B., Seubert, P., Tsuang, D.W., Peskind, E.R., Yu, C.E.
Publicado em 2010

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

Por Maestrini, E, Pagnamenta, A T, Lamb, J A, Bacchelli, E, Sykes, N H, Sousa, I, Toma, C, Barnby, G, Butler, H, Winchester, L, Scerri, T S, Minopoli, F, Reichert, J, Cai, G, Buxbaum, J D, Korvatska, O, Schellenberg, G D, Dawson, G, Bildt, A de, Minderaa, R B, Mulder, E J, Morris, A P, Bailey, A J, Monaco, A P
Publicado em 2010

Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice

Por Melrose, H. L., Dächsel, J. C., Behrouz, B., Lincoln, S. J., Yue, M., Hinkle, K. M., Kent, C., Korvatska, E., Taylor, J. P., Witten, L., Liang, Y-Q, Beevers, J. E., Boules, M., Serna, V., Gaukhman, A., Yu, X., Castanedes-Casey, M., Braithwaite, A. T., Ogholikhan, S., Yu, N., Bass, D., Tyndall, G., Schellenberg, G. D., Dickson, D. W., Janus, C., Farrer, M. J.
Publicado em 2010

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

Por Ruiz, A, Heilmann, S, Becker, T, Hernández, I, Wagner, H, Thelen, M, Mauleón, A, Rosende-Roca, M, Bellenguez, C, Bis, J C, Harold, D, Gerrish, A, Sims, R, Sotolongo-Grau, O, Espinosa, A, Alegret, M, Arrieta, J L, Lacour, A, Leber, M, Becker, J, Lafuente, A, Ruiz, S, Vargas, L, Rodríguez, O, Ortega, G, Dominguez, M-A, Mayeux, R, Haines, J L, Pericak-Vance, M A, Farrer, L A, Schellenberg, G D, Chouraki, V, Launer, L J, van Duijn, C, Seshadri, S, Antúnez, C, Breteler, M M, Serrano-Ríos, M, Jessen, F, Tárraga, L, Nöthen, M M, Maier, W, Boada, M, Ramírez, A
Publicado em 2014