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Found 11 results
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Author
is
Boerwinkle, Eric
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2023
Zhang Y
,
Liu X
,
Wiggins KL
,
Kurniansyah N
,
Guo X
,
Rodrigue AL
,
Zhao W
,
Yanek LR
,
Ratliff SM
,
Pitsillides A
et al.
. 2023.
Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.
.
Neurology. 100(18):e1930-e1943.
2019
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.
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.
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.
Beecham GW
,
Vardarajan B
,
Blue E
,
Bush W
,
Jaworski J
,
Barral S
,
DeStefano A
,
Hamilton-Nelson K
,
Kunkle B
,
Martin ER
et al.
. 2018.
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease.
.
Neurol Genet. 4(6):e286.
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.
Vardarajan BN
,
Barral S
,
Jaworski J
,
Beecham GW
,
Blue E
,
Tosto G
,
Reyes-Dumeyer D
,
Medrano M
,
Lantigua R
,
Naj A
et al.
. 2018.
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.
.
Ann Clin Transl Neurol. 5(4):406-417.
2016
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.
2015
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.
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.
Escott-Price V
,
Bellenguez C
,
Wang L-S
,
Choi S-H
,
Harold D
,
Jones L
,
Holmans P
,
Gerrish A
,
Vedernikov A
,
Richards A
et al.
. 2014.
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
.
PLoS One. 9(6):e94661.