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Found 26 results
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Genome-Wide Association Study
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Mayeux, Richard
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2022
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.
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.
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.
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
Blue EE
,
Bis JC
,
Dorschner MO
,
Tsuang DW
,
Barral SM
,
Beecham G
,
Below JE
,
Bush WS
,
Butkiewicz M
,
Cruchaga C
et al.
. 2018.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
.
Dement Geriatr Cogn Disord. 45(1-2):1-17.
Lancour D
,
Naj A
,
Mayeux R
,
Haines JL
,
Pericak-Vance MA
,
Schellenberg GD
,
Crovella M
,
Farrer LA
,
Kasif S
. 2018.
One for all and all for One: Improving replication of genetic studies through network diffusion.
.
PLoS Genet. 14(4):e1007306.
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.
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.
Jun GR
,
Chung J
,
Mez J
,
Barber R
,
Beecham GW
,
Bennett DA
,
Buxbaum JD
,
Byrd GS
,
Carrasquillo MM
,
Crane PK
et al.
. 2017.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
.
Alzheimers Dement. 13(7):727-738.
Mez J
,
Chung J
,
Jun G
,
Kriegel J
,
Bourlas AP
,
Sherva R
,
Logue MW
,
Barnes LL
,
Bennett DA
,
Buxbaum JD
et al.
. 2017.
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.
.
Alzheimers Dement. 13(2):119-129.
2016
Ridge PG
,
Hoyt KB
,
Boehme K
,
Mukherjee S
,
Crane PK
,
Haines JL
,
Mayeux R
,
Farrer LA
,
Pericak-Vance MA
,
Schellenberg GD
et al.
. 2016.
Assessment of the genetic variance of late-onset Alzheimer's disease.
.
Neurobiol Aging. 41:200.e13-200.e20.
2015
Ghani M
,
Reitz C
,
Cheng R
,
Vardarajan BNarayan
,
Jun G
,
Sato C
,
Naj A
,
Rajbhandary R
,
Wang L-S
,
Valladares O
et al.
. 2015.
Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.
.
JAMA Neurol. 72(11):1313-23.
Barral S
,
Cheng R
,
Reitz C
,
Vardarajan B
,
Lee J
,
Kunkle B
,
Beecham G
,
Cantwell LS
,
Pericak-Vance MA
,
Farrer LA
et al.
. 2015.
Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease.
.
Alzheimers Dement. 11(12):1397-1406.
Desikan RS
,
Schork AJ
,
Wang Y
,
Thompson WK
,
Dehghan A
,
Ridker PM
,
Chasman DI
,
McEvoy LK
,
Holland D
,
Chen C-H
et al.
. 2015.
Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease.
.
Circulation. 131(23):2061-2069.
2014
Barral S
,
Cosentino S
,
Christensen K
,
Newman AB
,
Perls TT
,
Province MA
,
Mayeux R
. 2014.
Common genetic variants on 6q24 associated with exceptional episodic memory performance in the elderly.
.
JAMA Neurol. 71(12):1514-9.
Jun G
,
Asai H
,
Zeldich E
,
Drapeau E
,
Chen CD
,
Chung J
,
Park J-H
,
Kim S
,
Haroutunian V
,
Foroud T
et al.
. 2014.
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation.
.
Ann Neurol. 76(3):379-92.
2013
Cruchaga C
,
Kauwe JSK
,
Harari O
,
Jin SChih
,
Cai Y
,
Karch CM
,
Benitez BA
,
Jeng AT
,
Skorupa T
,
Carrell D
et al.
. 2013.
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
.
Neuron. 78(2):256-68.
Holton P
,
Ryten M
,
Nalls M
,
Trabzuni D
,
Weale ME
,
Hernandez D
,
Crehan H
,
J Gibbs R
,
Mayeux R
,
Haines JL
et al.
. 2013.
Initial assessment of the pathogenic mechanisms of the recently identified Alzheimer risk Loci.
.
Ann Hum Genet. 77(2):85-105.
Reitz C
,
Jun G
,
Naj A
,
Rajbhandary R
,
Vardarajan BNarayan
,
Wang L-S
,
Valladares O
,
Lin C-F
,
Larson EB
,
Graff-Radford NR
et al.
. 2013.
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.
.
JAMA. 309(14):1483-92.
2012
Zou F
,
Chai HSeng
,
Younkin CS
,
Allen M
,
Crook J
,
V Pankratz S
,
Carrasquillo MM
,
Rowley CN
,
Nair AA
,
Middha S
et al.
. 2012.
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.
.
PLoS Genet. 8(6):e1002707.
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.
2011
Naj AC
,
Jun G
,
Beecham GW
,
Wang L-S
,
Vardarajan BNarayan
,
Buros J
,
Gallins PJ
,
Buxbaum JD
,
Jarvik GP
,
Crane PK
et al.
. 2011.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
.
Nat Genet. 43(5):436-41.
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.
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