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Found 8 results
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Polymorphism, Single Nucleotide
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Author
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Trojanowski, John Q
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2015
Kouri N
,
Ross OA
,
Dombroski B
,
Younkin CS
,
Serie DJ
,
Soto-Ortolaza A
,
Baker M
,
Finch NCole A
,
Yoon H
,
Kim J
et al.
. 2015.
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
.
Nat Commun. 6:7247.
Beecham GW
,
Dickson DW
,
Scott WK
,
Martin ER
,
Schellenberg GD
,
Nuytemans K
,
Larson EB
,
Buxbaum JD
,
Trojanowski JQ
,
Van Deerlin VM
et al.
. 2015.
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.
.
Neurology. 84(10):972-80.
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.
McMillan CT
,
Toledo JB
,
Avants BB
,
Cook PA
,
Wood EM
,
Suh ER
,
Irwin DJ
,
Powers J
,
Olm C
,
Elman L
et al.
. 2014.
Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration.
.
Neurobiol Aging. 35(6):1473-82.
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.
Stutzbach LD
,
Xie SX
,
Naj AC
,
Albin R
,
Gilman S
,
M Y Lee V
,
Trojanowski JQ
,
Devlin B
,
Schellenberg GD
. 2013.
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
.
Acta Neuropathol Commun. 1:31.
2011
Naj AC
,
Jun G
,
Beecham GW
,
Wang L-S
,
Vardarajan BNarayan
,
Buros J
,
Gallins PJ
,
Buxbaum JD
,
Jarvik GP
,
Crane PK
et al.
. 2011.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
.
Nat Genet. 43(5):436-41.
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.