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Found 16 results
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Graff-Radford, Neill R
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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.
2017
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
Hohman TJ
,
Cooke-Bailey JN
,
Reitz C
,
Jun G
,
Naj A
,
Beecham GW
,
Liu Z
,
Carney RM
,
Vance JM
,
Cuccaro ML
et al.
. 2016.
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk.
.
Alzheimers Dement. 12(3):233-43.
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.
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.
Wang L-S
,
Naj AC
,
Graham RR
,
Crane PK
,
Kunkle BW
,
Cruchaga C
,
Murcia JDGonzalez
,
Cannon-Albright L
,
Baldwin CT
,
Zetterberg H
et al.
. 2015.
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
.
JAMA Neurol. 72(2):209-16.
2014
Allen M
,
Kachadoorian M
,
Quicksall Z
,
Zou F
,
Chai HSeng
,
Younkin C
,
Crook JE
,
V Pankratz S
,
Carrasquillo MM
,
Krishnan S
et al.
. 2014.
Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.
.
Alzheimers Res Ther. 6(4):39.
Naj AC
,
Jun G
,
Reitz C
,
Kunkle BW
,
Perry W
,
Park YSon
,
Beecham GW
,
Rajbhandary RA
,
Hamilton-Nelson KL
,
Wang L-S
et al.
. 2014.
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
.
JAMA Neurol. 71(11):1394-404.
Logue MW
,
Schu M
,
Vardarajan BN
,
Farrell J
,
Bennett DA
,
Buxbaum JD
,
Byrd GS
,
Ertekin-Taner N
,
Evans D
,
Foroud T
et al.
. 2014.
Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans.
.
Alzheimers Dement. 10(6):609-618.e11.
2013
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.
Allen M
,
Zou F
,
Chai HSeng
,
Younkin CS
,
Crook J
,
V Pankratz S
,
Carrasquillo MM
,
Rowley CN
,
Nair AA
,
Middha S
et al.
. 2012.
Novel late-onset Alzheimer disease loci variants associate with brain gene expression.
.
Neurology. 79(3):221-8.
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.
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
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.