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Found 16 results
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Author
is
Kunkle, Brian W
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2019
Ma Y
,
Jun GR
,
Zhang X
,
Chung J
,
Naj AC
,
Chen Y
,
Bellenguez C
,
Hamilton-Nelson K
,
Martin ER
,
Kunkle BW
et al.
. 2019.
Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.
.
JAMA Neurol. 76:(9):1099-1108.
Bis JC
,
Jian X
,
Kunkle BW
,
Chen Y
,
Hamilton-Nelson KL
,
Bush WS
,
Salerno WJ
,
Lancour D
,
Ma Y
,
Renton AE
et al.
. 2019.
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
.
Mol Psychiatry.
Ma Y
,
Jun GR
,
Chung J
,
Zhang X
,
Kunkle BW
,
Naj AC
,
White CC
,
Bennett DA
,
De Jager PL
,
Mayeux R
et al.
. 2019.
CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease.
.
Aging Cell. 18(4):e12964.
Hu Y
,
Li M
,
Lu Q
,
Weng H
,
Wang J
,
Zekavat SM
,
Yu Z
,
Li B
,
Gu J
,
Muchnik S
et al.
. 2019.
A Statistical Framework for Cross-tissue Transcriptome-wide Association Analysis.
.
Nat Genet. 51(3):568-576.
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.
Naj AC
,
Lin H
,
Vardarajan BN
,
White S
,
Lancour D
,
Ma Y
,
Schmidt M
,
Sun F
,
Butkiewicz M
,
Bush WS
et al.
. 2018.
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
.
Genomics.
Bis JC
,
Jian X
,
Kunkle BW
,
Chen Y
,
Hamilton-Nelson KL
,
Bush WS
,
Salerno WJ
,
Lancour D
,
Ma Y
,
Renton AE
et al.
. 2018.
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
.
Mol Psychiatry.
2017
Kunkle BW
,
Vardarajan BN
,
Naj AC
,
Whitehead PL
,
Rolati S
,
Slifer S
,
Carney RM
,
Cuccaro ML
,
Vance JM
,
Gilbert JR
et al.
. 2017.
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
.
JAMA Neurol. 74(9):1113-1122.
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.
2016
Cukier HN
,
Kunkle BW
,
Vardarajan BN
,
Rolati S
,
Hamilton-Nelson KL
,
Kohli MA
,
Whitehead PL
,
Dombroski BA
,
Van Booven D
,
Lang R
et al.
. 2016.
ABCA7 frameshift deletion associated with Alzheimer disease in African Americans.
.
Neurol Genet. 2(3):e79.
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.
Kunkle BW
,
Jaworski J
,
Barral S
,
Vardarajan B
,
Beecham GW
,
Martin ER
,
Cantwell LS
,
Partch A
,
Bird TD
,
Raskind WH
et al.
. 2016.
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.
.
Alzheimers Dement. 12(1):2-10.
Kohli MA
,
Cukier HN
,
Hamilton-Nelson KL
,
Rolati S
,
Kunkle BW
,
Whitehead PL
,
Züchner SL
,
Farrer LA
,
Martin ER
,
Beecham GW
et al.
. 2016.
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease.
.
Neurol Genet. 2(1):e41.
2015
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
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.
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.