Jump to Content
ADGC
Alzheimer's Disease
Genetics Consortium
Home
ADGC Core Projects
Contact
About
Program Overview
Members
Committees
Links
Alzheimer's Disease
Acknowledgements
Collaborative Data Access (SAGs)
SAG Proposal Instructions
SAG Overview
Current ADGC Special Analysis Group Projects (SAGs)
Publications
ADGC Publications
Publications Supported by the ADGC
Publications Using ADGC and IGAP Summary Statistics
For Members
Login
You are here
Home
» ADGC Publications
ADGC Publications
Found 15 results
Filters:
Keyword
is
Polymorphism, Single Nucleotide
and
Author
is
Schellenberg, Gerard D
[Clear All Filters]
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.
Shade LMp
,
Katsumata Y
,
Hohman TJ
,
Nho K
,
Saykin AJ
,
Mukherjee S
,
Boehme KL
,
Kauwe JSk
,
Farrer LA
,
Schellenberg GD
et al.
. 2022.
Genome-wide association study of brain arteriolosclerosis.
.
J Cereb Blood Flow Metab. 42(8):1437-1450.
2019
Baker E
,
Sims R
,
Leonenko G
,
Frizzati A
,
Harwood JC
,
Grozeva D
,
Morgan K
,
Passmore P
,
Holmes C
,
Powell J
et al.
. 2019.
Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease.
.
PLoS One. 14(7):e0218111.
2018
Bonham LW
,
Karch CM
,
Fan CC
,
Tan C
,
Geier EG
,
Wang Y
,
Wen N
,
Broce IJ
,
Li Y
,
Barkovich MJ
et al.
. 2018.
CXCR4 involvement in neurodegenerative diseases.
.
Transl Psychiatry. 8(1):73.
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.
2017
Huang K-L
,
Marcora E
,
Pimenova AA
,
Di Narzo AF
,
Kapoor M
,
Jin SChih
,
Harari O
,
Bertelsen S
,
Fairfax BP
,
Czajkowski J
et al.
. 2017.
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.
.
Nat Neurosci. 20(8):1052-1061.
2016
Allen M
,
Burgess JD
,
Ballard T
,
Serie D
,
Wang X
,
Younkin CS
,
Sun Z
,
Kouri N
,
Baheti S
,
Wang C
et al.
. 2016.
Gene expression, methylation and neuropathology correlations at progressive supranuclear palsy risk loci.
.
Acta Neuropathol. 132(2):197-211.
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.
2014
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
McDavid A
,
Crane PK
,
Newton KM
,
Crosslin DR
,
McCormick W
,
Weston N
,
Ehrlich K
,
Hart E
,
Harrison R
,
Kukull WA
et al.
. 2013.
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records.
.
PLoS One. 8(6):e63481.
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
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.