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Author
Title
Type
[
Year
]
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.
PubMed
2016
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.
PubMed
2017
Crane PK
,
Foroud T
,
Montine TJ
,
Larson EB
. 2017.
Alzheimer's Disease Sequencing Project discovery and replication criteria for cases and controls: Data from a community-based prospective cohort study with autopsy follow-up.
.
Alzheimers Dement. 13(12):1410-1413.
PubMed
Beecham GW
,
Bis JC
,
Martin ER
,
Choi S-H
,
DeStefano AL
,
van Duijn CM
,
Fornage M
,
Gabriel SB
,
Koboldt DC
,
Larson DE
et al.
. 2017.
The Alzheimer's Disease Sequencing Project: Study design and sample selection.
.
Neurol Genet. 3(5):e194.
PubMed
Fernández MVictoria
,
Kim JHun
,
Budde JP
,
Black K
,
Medvedeva A
,
Saef B
,
Deming Y
,
Del-Aguila J
,
Ibañez L
,
Dube U
et al.
. 2017.
Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer Disease.
.
PLoS Genet. 13(11):e1007045.
PubMed
Butkiewicz M
,
Haines JL
,
Bush WS
. 2017.
Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants.
.
Bioinformatics. 33(10):1561-1562.
PubMed
Adams SL
,
Benayoun L
,
Tilton K
,
Chavez OR
,
Himali JJ
,
Blusztajn JKrzysztof
,
Seshadri S
,
Delalle I
. 2017.
Methionine Sulfoxide Reductase-B3 (MsrB3) Protein Associates with Synaptic Vesicles and its Expression Changes in the Hippocampi of Alzheimer's Disease Patients.
.
J Alzheimers Dis. 60(1):43-56.
PubMed
Lin H
,
Satizabal C
,
Xie Z
,
Yang Q
,
Huan T
,
Joehanes R
,
Wen C
,
Munson PJ
,
Beiser A
,
Levy D
et al.
. 2017.
Whole blood gene expression and white matter Hyperintensities.
.
Mol Neurodegener. 12(1):67.
PubMed
2018
Nafikov RA
,
Nato AQ
,
Sohi H
,
Wang B
,
Brown L
,
Horimoto AR
,
Vardarajan BN
,
Barral SM
,
Tosto G
,
Mayeux RP
et al.
. 2018.
Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.
.
Genet Epidemiol. 42(6):500-515.
PubMed
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.
PubMed
Kulminski AM
,
Barochia AV
,
Loika Y
,
Raghavachari N
,
Arbeev KG
,
Wojczynski MK
,
Thyagarajan B
,
Vardarajan BN
,
Christensen K
,
Yashin AI
et al.
. 2018.
The APOE ε4 allele is associated with a reduction in FEV1/FVC in women: A cross-sectional analysis of the Long Life Family Study.
.
PLoS One. 13(11):e0206873.
PubMed
Tynkkynen J
,
Chouraki V
,
van der Lee SJ
,
Hernesniemi J
,
Yang Q
,
Li S
,
Beiser A
,
Larson MG
,
Sääksjärvi K
,
Shipley MJ
et al.
. 2018.
Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts.
.
Alzheimers Dement. 14(6):723-733.
PubMed
Raman MR
,
Himali JJ
,
Conner SC
,
DeCarli C
,
Vasan RS
,
Beiser AS
,
Seshadri S
,
Maillard P
,
Satizabal CL
. 2018.
Circulating Vascular Growth Factors and Magnetic Resonance Imaging Markers of Small Vessel Disease and Atrophy in Middle-Aged Adults.
.
Stroke. 49(9):2227-2229.
PubMed
Fernández MV
,
Budde J
,
Del-Aguila JL
,
Ibañez L
,
Deming Y
,
Harari O
,
Norton J
,
Morris JC
,
Goate AM
,
Cruchaga C
. 2018.
Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease.
.
Front Neurosci. 12:209.
PubMed
Jian X
,
Satizabal CL
,
Smith AV
,
Wittfeld K
,
Bis JC
,
Smith JA
,
Hsu F-C
,
Nho K
,
Hofer E
,
Hagenaars SP
et al.
. 2018.
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
.
Stroke. 49(8):1812-1819.
PubMed
Butkiewicz M
,
Blue EE
,
Leung YYee
,
Jian X
,
Marcora E
,
Renton AE
,
Kuzma A
,
San Wang L-
,
Koboldt DC
,
Haines JL
et al.
. 2018.
Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.
.
Bioinformatics. 34(16):2724-2731.
PubMed
Peloso GM
,
Beiser AS
,
DeStefano AL
,
Seshadri S
. 2018.
Genetic Interaction with Plasma Lipids on Alzheimer's Disease in the Framingham Heart Study.
.
J Alzheimers Dis. 66(3):1275-1282.
PubMed
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
Kunji K
,
Ullah E
,
Nato AQ
,
Wijsman EM
,
Saad M
. 2018.
GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data.
.
Bioinformatics. 34(9):1591-1593.
PubMed
Marioni RE
,
Harris SE
,
Zhang Q
,
McRae AF
,
Hagenaars SP
,
W Hill D
,
Davies G
,
Ritchie CW
,
Gale CR
,
Starr JM
et al.
. 2018.
GWAS on family history of Alzheimer's disease.
.
Transl Psychiatry. 8(1):99.
PubMed
Amlie-Wolf A
,
Tang M
,
Mlynarski EE
,
Kuksa PP
,
Valladares O
,
Katanić Ž
,
Tsuang D
,
Brown CD
,
Schellenberg GD
,
San Wang L-
. 2018.
INFERNO: inferring the molecular mechanisms of noncoding genetic variants.
.
Nucleic Acids Res. 46(17):8740-8753.
PubMed
Zhou Z
,
Wang W
,
San Wang L-
,
Zhang NRuonan
. 2018.
Integrative DNA copy number detection and genotyping from sequencing and array-based platforms.
.
Bioinformatics. 34(14):2349-2355.
PubMed
Jiang S
,
Wen N
,
Li Z
,
Dube U
,
Del Aguila J
,
Budde J
,
Martinez R
,
Hsu S
,
Fernández MV
,
Cairns NJ
et al.
. 2018.
Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP.
.
Transl Psychiatry. 8(1):265.
PubMed
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.
PubMed
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.
PubMed
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