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Found 8 results
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Ross, Owen A
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2022
Hopfner F
,
Tietz AK
,
Ruf VC
,
Ross OA
,
Koga S
,
Dickson D
,
Aguzzi A
,
Attems J
,
Beach T
,
Beller A
et al.
. 2022.
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
.
Mov Disord. 37(10):2110-2121.
2018
Broce I
,
Karch CM
,
Wen N
,
Fan CC
,
Wang Y
,
Tan CHong
,
Kouri N
,
Ross OA
,
Höglinger GU
,
Müller U
et al.
. 2018.
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.
.
PLoS Med. 15(1):e1002487.
Sanchez-Contreras MY
,
Kouri N
,
Cook CN
,
Serie DJ
,
Heckman MG
,
Finch NCA
,
Caselli RJ
,
Uitti RJ
,
Wszolek ZK
,
Graff-Radford N
et al.
. 2018.
Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci.
.
Mol Neurodegener. 13(1):37.
Karch CM
,
Wen N
,
Fan CC
,
Yokoyama JS
,
Kouri N
,
Ross OA
,
Höglinger G
,
Müller U
,
Ferrari R
,
Hardy J
et al.
. 2018.
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.
.
JAMA Neurol. 75(7):860-875.
2017
Yokoyama JS
,
Karch CM
,
Fan CC
,
Bonham LW
,
Kouri N
,
Ross OA
,
Rademakers R
,
Kim J
,
Wang Y
,
Höglinger GU
et al.
. 2017.
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.
.
Acta Neuropathol. 133(5):825-837.
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.
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.