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Found 19 results
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2023
Bouzid H
,
Belk JA
,
Jan M
,
Qi Y
,
Sarnowski C
,
Wirth S
,
Ma L
,
Chrostek MR
,
Ahmad H
,
Nachun D
et al.
. 2023.
Clonal hematopoiesis is associated with protection from Alzheimer's disease.
.
Nat Med. 29(7):1662-1670.
2022
Vardarajan BN
,
Reyes-Dumeyer D
,
Piriz AL
,
Lantigua RA
,
Medrano M
,
Rivera D
,
Jimenez-Velazquez IZ
,
Martin E
,
Pericak-Vance MA
,
Bush W
et al.
. 2022.
Progranulin mutations in clinical and neuropathological Alzheimer's disease.
.
Alzheimers Dement. 18(12):2458-2467.
2019
Patel D
,
Mez J
,
Vardarajan BN
,
Staley L
,
Chung J
,
Zhang X
,
Farrell JJ
,
Rynkiewicz MJ
,
Cannon-Albright LA
,
Teerlink CC
et al.
. 2019.
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
.
JAMA Netw Open. 2(3):e191350.
2018
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
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
Tosto G
,
Reitz C
. 2016.
Genomics of Alzheimer's disease: Value of high-throughput genomic technologies to dissect its etiology.
.
Mol Cell Probes. 30(6):397-403.
Jakobsdottir J
,
van der Lee SJ
,
Bis JC
,
Chouraki V
,
Li-Kroeger D
,
Yamamoto S
,
Grove ML
,
Naj A
,
Vronskaya M
,
Salazar JL
et al.
. 2016.
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
.
PLoS Genet. 12(10):e1006327.
2014
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.
Warmus BA
,
Sekar DR
,
McCutchen E
,
Schellenberg GD
,
Roberts RC
,
McMahon LL
,
Roberson ED
. 2014.
Tau-mediated NMDA receptor impairment underlies dysfunction of a selectively vulnerable network in a mouse model of frontotemporal dementia.
.
J Neurosci. 34(49):16482-95.
2013
Kalimo H
,
Lalowski M
,
Bogdanovic N
,
Philipson O
,
Bird TD
,
Nochlin D
,
Schellenberg GD
,
Brundin R
,
Olofsson T
,
Soliymani R
et al.
. 2013.
The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ.
.
Acta Neuropathol Commun. 1:60.
Reitz C
,
Mayeux R
. 2013.
TREM2 and neurodegenerative disease.
.
N Engl J Med. 369(16):1564-5.
Schafer CM
,
Campbell NG
,
Cai G
,
Yu F
,
Makarov V
,
Yoon S
,
Daly MJ
,
Gibbs RA
,
Schellenberg GD
,
Devlin B
et al.
. 2013.
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.
.
Genomics. 102(4):270-7.
2012
Whitcomb DC
,
LaRusch J
,
Krasinskas AM
,
Klei L
,
Smith JP
,
Brand RE
,
Neoptolemos JP
,
Lerch MM
,
Tector M
,
Sandhu BS
et al.
. 2012.
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
.
Nat Genet. 44(12):1349-54.
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.
Schellenberg GD
,
Montine TJ
. 2012.
The genetics and neuropathology of Alzheimer's disease.
.
Acta Neuropathol. 124(3):305-23.
Liu N
,
Landreh M
,
Cao K
,
Abe M
,
Hendriks G-J
,
Kennerdell JR
,
Zhu Y
,
Wang L-S
,
Bonini NM
. 2012.
The microRNA miR-34 modulates ageing and neurodegeneration in Drosophila.
.
Nature. 482(7386):519-23.
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.
2010
Kraemer BC
,
Schuck T
,
Wheeler JM
,
Robinson LC
,
Trojanowski JQ
,
M Y Lee V
,
Schellenberg GD
. 2010.
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.
.
Acta Neuropathol. 119(4):409-19.