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Found 23 results
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Genome-Wide Association Study
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Schellenberg, Gerard D
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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.
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.
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.
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.
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.
Eissman JM
,
Dumitrescu L
,
Mahoney ER
,
Smith AN
,
Mukherjee S
,
Lee ML
,
Scollard P
,
Choi SEun
,
Bush WS
,
Engelman CD
et al.
. 2022.
Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease.
.
Brain. 145(7):2541-2554.
2021
Kunkle BW
,
Schmidt M
,
Klein H-U
,
Naj AC
,
Hamilton-Nelson KL
,
Larson EB
,
Evans DA
,
De Jager PL
,
Crane PK
,
Buxbaum JD
et al.
. 2021.
Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
.
JAMA Neurol. 78(1):102-113.
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
Rajabli F
,
Feliciano BE
,
Celis K
,
Hamilton-Nelson KL
,
Whitehead PL
,
Adams LD
,
Bussies PL
,
Manrique CP
,
Rodriguez A
,
Rodriguez V
et al.
. 2018.
Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations.
.
PLoS Genet. 14(12):e1007791.
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.
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
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.
Gerstenecker A
,
Roberson ED
,
Schellenberg GD
,
Standaert DG
,
Shprecher DR
,
Kluger BM
,
Litvan I
. 2017.
Genetic influences on cognition in progressive supranuclear palsy.
.
Mov Disord. 32(12):1764-1771.
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.
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.