Segui
Margaret Pericak-Vance
Margaret Pericak-Vance
Professor of Human Genetics, university of Miami
Email verificata su med.miami.edu
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Citata da
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Anno
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
EH Corder, AM Saunders, WJ Strittmatter, DE Schmechel, PC Gaskell, ...
Science 261 (5123), 921-923, 1993
117351993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
DR Rosen, T Siddique, D Patterson, DA Figlewicz, P Sapp, A Hentati, ...
Nature 362 (6415), 59-62, 1993
88881993
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
A Goate, MC Chartier-Harlin, M Mullan, J Brown, F Crawford, L Fidani, ...
Nature 349 (6311), 704-706, 1991
64051991
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.
WJ Strittmatter, AM Saunders, D Schmechel, M Pericak-Vance, J Enghild, ...
Proceedings of the National Academy of Sciences 90 (5), 1977-1981, 1993
57031993
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R Sherrington, EI Rogaev, Y Liang, EA Rogaeva, G Levesque, M Ikeda, ...
Nature 375 (6534), 754-760, 1995
56101995
Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease: a meta-analysis
LA Farrer, LA Cupples, JL Haines, B Hyman, WA Kukull, R Mayeux, ...
Jama 278 (16), 1349-1356, 1997
55901997
Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease
AM Saunders, WJ Strittmatter, D Schmechel, PH St. George-Hyslop, ...
Neurology 43 (8), 1467-1467, 1993
49801993
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
45842013
Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
TJ Kwiatkowski Jr, DA Bosco, AL Leclerc, E Tamrazian, CR Vanderburg, ...
Science 323 (5918), 1205-1208, 2009
31452009
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
30622011
Complement factor H variant increases the risk of age-related macular degeneration
JL Haines, MA Hauser, S Schmidt, WK Scott, LM Olson, P Gallins, ...
Science 308 (5720), 419-421, 2005
30582005
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
EH Corder, AM Saunders, NJ Risch, WJ Strittmatter, DE Schmechel, ...
Nature genetics 7 (2), 180-184, 1994
25231994
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
24692019
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
24032013
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
23612010
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436-441, 2011
22132011
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
19442020
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer disease.
DE Schmechel, AM Saunders, WJ Strittmatter, BJ Crain, CM Hulette, ...
Proceedings of the National Academy of Sciences 90 (20), 9649-9653, 1993
19411993
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ...
Nature genetics 36 (5), 449-451, 2004
19022004
Amyotrophic lateral Ssclerosis and structural defects in cu, Zn superoxide dismutase
HX Deng, A Hentati, JA Tainer, Z Iqbal, A Cayabyab, WY Hung, ...
Science 261 (5124), 1047-1051, 1993
18961993
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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