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Found 9 results
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Genome-Wide Association Study
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Author
is
Wang, Li-San
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2023
Kang M
,
Ang TFang Alvin
,
Devine SA
,
Sherva R
,
Mukherjee S
,
Trittschuh EH
,
Gibbons LE
,
Scollard P
,
Lee M
,
Choi S-E
et al.
. 2023.
A genome-wide search for pleiotropy in more than 100,000 harmonized longitudinal cognitive domain scores.
.
Mol Neurodegener. 18(1):40.
2022
Kuksa PP
,
Liu C-L
,
Fu W
,
Qu L
,
Zhao Y
,
Katanic Z
,
Clark K
,
Kuzma AB
,
Ho P-C
,
Tzeng K-T
et al.
. 2022.
Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease.
.
J Alzheimers Dis. 86(1):461-477.
Holstege H
,
Hulsman M
,
Charbonnier C
,
Grenier-Boley B
,
Quenez O
,
Grozeva D
,
van Rooij JGJ
,
Sims R
,
Ahmad S
,
Amin N
et al.
. 2022.
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
.
Nat Genet. 54(12):1786-1794.
Jun GR
,
You Y
,
Zhu C
,
Meng G
,
Chung J
,
Panitch R
,
Hu J
,
Xia W
,
Bennett DA
,
Foroud TM
et al.
. 2022.
Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ɛ2 for Alzheimer's disease.
.
Alzheimers Dement. 18(11):2042-2054.
2018
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.
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.
2011
Höglinger GU
,
Melhem NM
,
Dickson DW
,
Sleiman PMA
,
San Wang L-
,
Klei L
,
Rademakers R
,
de Silva R
,
Litvan I
,
Riley DE
et al.
. 2011.
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
.
Nat Genet. 43(7):699-705.
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.
Han M-R
,
Schellenberg GD
,
San Wang L-
. 2010.
Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.
.
BMC Neurol. 10:90.