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Lunetta, Kathryn L
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2021
Zhang X
,
Farrell JJ
,
Tong T
,
Hu J
,
Zhu C
,
San Wang L-
,
Mayeux R
,
Haines JL
,
Pericak-Vance MA
,
Schellenberg GD
et al.
. 2021.
Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease.
.
Alzheimers Dement.
PubMed
Patel D
,
Zhang X
,
Farrell JJ
,
Chung J
,
Stein TD
,
Lunetta KL
,
Farrer LA
. 2021.
Cell-type-specific expression quantitative trait loci associated with Alzheimer disease in blood and brain tissue.
.
Transl Psychiatry. 11(1):250.
PubMed
Panitch R
,
Hu J
,
Chung J
,
Zhu C
,
Meng G
,
Xia W
,
Bennett DA
,
Lunetta KL
,
Ikezu T
,
Au R
et al.
. 2021.
Integrative brain transcriptome analysis links complement component 4 and HSPA2 to the APOE ε2 protective effect in Alzheimer disease.
.
Mol Psychiatry. 26(10):6054-6064.
PubMed
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.
PubMed
Patel D
,
Zhang X
,
Farrell JJ
,
Lunetta KL
,
Farrer LA
. 2021.
Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants.
.
Genes (Basel). 12(3)
PubMed
2020
Reiman EM
,
Arboleda-Velasquez JF
,
Quiroz YT
,
Huentelman MJ
,
Beach TG
,
Caselli RJ
,
Chen Y
,
Su Y
,
Myers AJ
,
Hardy J
et al.
. 2020.
Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study.
.
Nat Commun. 11(1):667.
PubMed
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.
PubMed
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.
PubMed
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.
PubMed
Kunkle BW
,
Grenier-Boley B
,
Sims R
,
Bis JC
,
Damotte V
,
Naj AC
,
Boland A
,
Vronskaya M
,
van der Lee SJ
,
Amlie-Wolf A
et al.
. 2019.
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
.
Nat Genet. 51(3):414-430.
PubMed
Choi KYeong
,
Lee JJae
,
Gunasekaran TIniyan
,
Kang S
,
Lee W
,
Jeong J
,
Lim HJae
,
Zhang X
,
Zhu C
,
Won S-Y
et al.
. 2019.
Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of ε4 on Alzheimer's Disease Risk in a Multiracial Sample.
.
J Clin Med. 8(8)
PubMed
Zhang X
,
Zhu C
,
Beecham G
,
Vardarajan BN
,
Ma Y
,
Lancour D
,
Farrell JJ
,
Chung J
,
Mayeux R
,
Haines JL
et al.
. 2019.
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease.
.
Alzheimers Dement. 15(3):441-452.
PubMed
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.
PubMed
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.
PubMed
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