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ADGC Publications
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2020
Sherva R
,
Gross A
,
Mukherjee S
,
Koesterer R
,
Amouyel P
,
Bellenguez C
,
Dufouil C
,
Bennett DA
,
Chibnik L
,
Cruchaga C
et al.
. 2020.
Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways.
.
Alzheimers Dement. 16(8):1134-1145.
2017
Deming Y
,
Li Z
,
Kapoor M
,
Harari O
,
Del-Aguila JL
,
Black K
,
Carrell D
,
Cai Y
,
Fernandez MVictoria
,
Budde J
et al.
. 2017.
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.
.
Acta Neuropathol. 133(5):839-856.
Tan CHong
,
Hyman BT
,
Tan JJX
,
Hess CP
,
Dillon WP
,
Schellenberg GD
,
Besser LM
,
Kukull WA
,
Kauppi K
,
McEvoy LK
et al.
. 2017.
Polygenic hazard scores in preclinical Alzheimer disease.
.
Ann Neurol. 82(3):484-488.
2016
Hohman TJ
,
Bush WS
,
Jiang L
,
Brown-Gentry KD
,
Torstenson ES
,
Dudek SM
,
Mukherjee S
,
Naj A
,
Kunkle BW
,
Ritchie MD
et al.
. 2016.
Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium.
.
Neurobiol Aging. 38:141-150.
2015
Wheeler JM
,
McMillan PJ
,
Hawk M
,
Iba M
,
Robinson L
,
Xu GJ
,
Dombroski BA
,
Jeong D
,
Dichter MA
,
Juul H
et al.
. 2015.
High copy wildtype human 1N4R tau expression promotes early pathological tauopathy accompanied by cognitive deficits without progressive neurofibrillary degeneration.
.
Acta Neuropathol Commun. 3:33.
Nho K
,
Kim S
,
Risacher SL
,
Shen L
,
Corneveaux JJ
,
Swaminathan S
,
Lin H
,
Ramanan VK
,
Liu Y
,
Foroud TM
et al.
. 2015.
Protective variant for hippocampal atrophy identified by whole exome sequencing.
.
Ann Neurol. 77(3):547-52.
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.
Carney RM
,
Kohli MA
,
Kunkle BW
,
Naj AC
,
Gilbert JR
,
Züchner S
,
Pericak-Vance MA
. 2014.
Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.
.
Alzheimers Dement. 10(3):360-5.