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Found 30 results
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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
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.
Tan CHong
,
Bonham LW
,
Fan CChieh
,
Mormino EC
,
Sugrue LP
,
Broce IJ
,
Hess CP
,
Yokoyama JS
,
Rabinovici GD
,
Miller BL
et al.
. 2019.
Polygenic hazard score, amyloid deposition and Alzheimer's neurodegeneration.
.
Brain. 142(2):460-470.
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.
Chen P
,
Guarino PD
,
Dysken MW
,
Pallaki M
,
Asthana S
,
Llorente MD
,
Love S
,
Vertrees JE
,
Schellenberg GD
,
Sano M
. 2018.
Neuropsychiatric Symptoms and Caregiver Burden in Individuals With Alzheimer's Disease: The TEAM-AD VA Cooperative Study.
.
J Geriatr Psychiatry Neurol. 31(4):177-185.
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
Dysken MW
,
Sano M
,
Asthana S
,
Vertrees JE
,
Pallaki M
,
Llorente M
,
Love S
,
Schellenberg GD
,
J McCarten R
,
Malphurs J
et al.
. 2014.
Effect of vitamin E and memantine on functional decline in Alzheimer disease: the TEAM-AD VA cooperative randomized trial.
.
JAMA. 311(1):33-44.
Samocha KE
,
Robinson EB
,
Sanders SJ
,
Stevens C
,
Sabo A
,
McGrath LM
,
Kosmicki JA
,
Rehnström K
,
Mallick S
,
Kirby A
et al.
. 2014.
A framework for the interpretation of de novo mutation in human disease.
.
Nat Genet. 46(9):944-50.
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.
Borenstein AR
,
Wu Y
,
Bowen JD
,
McCormick WC
,
Uomoto J
,
McCurry SM
,
Schellenberg GD
,
Larson EB
. 2014.
Incidence rates of dementia, Alzheimer disease, and vascular dementia in the Japanese American population in Seattle, WA: the Kame Project.
.
Alzheimer Dis Assoc Disord. 28(1):23-9.
Dysken MW
,
Guarino PD
,
Vertrees JE
,
Asthana S
,
Sano M
,
Llorente M
,
Pallaki M
,
Love S
,
Schellenberg GD
,
J McCarten R
et al.
. 2014.
Vitamin E and memantine in Alzheimer's disease: clinical trial methods and baseline data.
.
Alzheimers Dement. 10(1):36-44.
2013
Tsuang D
,
Leverenz JB
,
Lopez OL
,
Hamilton RL
,
Bennett DA
,
Schneider JA
,
Buchman AS
,
Larson EB
,
Crane PK
,
Kaye JA
et al.
. 2013.
APOE ε4 increases risk for dementia in pure synucleinopathies.
.
JAMA Neurol. 70(2):223-8.
Dombroski BA
,
Galasko DR
,
Mata IF
,
Zabetian CP
,
Craig U-K
,
Garruto RM
,
Oyanagi K
,
Schellenberg GD
. 2013.
C9orf72 hexanucleotide repeat expansion and Guam amyotrophic lateral sclerosis-Parkinsonism-dementia complex.
.
JAMA Neurol. 70(6):742-5.
Zhao W
,
Marchani EE
,
Cheung CYK
,
Steinbart EJ
,
Schellenberg GD
,
Bird TD
,
Wijsman EM
. 2013.
Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset.
.
Am J Med Genet B Neuropsychiatr Genet. 162B(2):201-12.
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.
2012
Majounie E
,
Renton AE
,
Mok K
,
Dopper EGP
,
Waite A
,
Rollinson S
,
Chiò A
,
Restagno G
,
Nicolaou N
,
Simon-Sanchez J
et al.
. 2012.
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
.
Lancet Neurol. 11(4):323-30.
Tsuang D
,
Leverenz JB
,
Lopez OL
,
Hamilton RL
,
Bennett DA
,
Schneider JA
,
Buchman AS
,
Larson EB
,
Crane PK
,
Kaye JA
et al.
. 2012.
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
.
Neurology. 79(19):1944-50.
2011
Chen-Plotkin AS
,
Martinez-Lage M
,
Sleiman PMA
,
Hu W
,
Greene R
,
Wood EMcCarty
,
Bing S
,
Grossman M
,
Schellenberg GD
,
Hatanpaa KJ
et al.
. 2011.
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
.
Arch Neurol. 68(4):488-97.
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