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Found 9 results
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Genotype
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Van Deerlin, Vivianna M
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2018
Deming Y
,
Dumitrescu L
,
Barnes LL
,
Thambisetty M
,
Kunkle B
,
Gifford KA
,
Bush WS
,
Chibnik LB
,
Mukherjee S
,
De Jager PL
et al.
. 2018.
Sex-specific genetic predictors of Alzheimer's disease biomarkers.
.
Acta Neuropathol. 136(6):857-872.
2017
Deming Y
,
Li Z
,
Kapoor M
,
Harari O
,
Del-Aguila JL
,
Black K
,
Carrell D
,
Cai Y
,
Fernandez MVictoria
,
Budde J
et al.
. 2017.
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.
.
Acta Neuropathol. 133(5):839-856.
2015
Wang L-S
,
Naj AC
,
Graham RR
,
Crane PK
,
Kunkle BW
,
Cruchaga C
,
Murcia JDGonzalez
,
Cannon-Albright L
,
Baldwin CT
,
Zetterberg H
et al.
. 2015.
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
.
JAMA Neurol. 72(2):209-16.
2014
Naj AC
,
Jun G
,
Reitz C
,
Kunkle BW
,
Perry W
,
Park YSon
,
Beecham GW
,
Rajbhandary RA
,
Hamilton-Nelson KL
,
Wang L-S
et al.
. 2014.
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
.
JAMA Neurol. 71(11):1394-404.
Toledo JB
,
Van Deerlin VM
,
Lee EB
,
Suh ER
,
Baek Y
,
Robinson JL
,
Xie SX
,
McBride J
,
Wood EM
,
Schuck T
et al.
. 2014.
A platform for discovery: The University of Pennsylvania Integrated Neurodegenerative Disease Biobank.
.
Alzheimers Dement. 10(4):477-484.e1.
2013
Cruchaga C
,
Kauwe JSK
,
Harari O
,
Jin SChih
,
Cai Y
,
Karch CM
,
Benitez BA
,
Jeng AT
,
Skorupa T
,
Carrell D
et al.
. 2013.
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
.
Neuron. 78(2):256-68.
2012
Coppola G
,
Chinnathambi S
,
Lee JJiYong
,
Dombroski BA
,
Baker MC
,
Soto-Ortolaza AI
,
Lee SE
,
Klein E
,
Huang AY
,
Sears R
et al.
. 2012.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
.
Hum Mol Genet. 21(15):3500-12.
Majounie E
,
Renton AE
,
Mok K
,
Dopper EGP
,
Waite A
,
Rollinson S
,
ChiĆ² A
,
Restagno G
,
Nicolaou N
,
Simon-Sanchez J
et al.
. 2012.
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
.
Lancet Neurol. 11(4):323-30.
2010
Van Deerlin VM
,
Sleiman PMA
,
Martinez-Lage M
,
Chen-Plotkin A
,
San Wang L-
,
Graff-Radford NR
,
Dickson DW
,
Rademakers R
,
Boeve BF
,
Grossman M
et al.
. 2010.
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
.
Nat Genet. 42(3):234-9.