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K
Kuksa PP
,
Amlie-Wolf A
,
Katanić Ž
,
Valladares O
,
San Wang L-
,
Leung YYee
. 2019.
DASHR 2.0: integrated database of human small non-coding RNA genes and mature products.
.
Bioinformatics. 35(6):1033-1039.
PubMed
Kuksa PP
,
Li F
,
Kannan S
,
Gregory BD
,
Leung YYee
,
San Wang L-
. 2020.
HiPR: High-throughput probabilistic RNA structure inference.
.
Comput Struct Biotechnol J. 18:1539-1547.
PubMed
Kuksa PP
,
Lee C-Y
,
Amlie-Wolf A
,
Gangadharan P
,
Mlynarski EE
,
Chou Y-F
,
Lin H-J
,
Issen H
,
Greenfest-Allen E
,
Valladares O
et al.
. 2020.
SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants.
.
Bioinformatics. 36(12):3879-3881.
PubMed
Kuksa PP
,
Amlie-Wolf A
,
Hwang Y-C
,
Valladares O
,
Gregory BD
,
San Wang L-
. 2020.
HIPPIE2: a method for fine-scale identification of physically interacting chromatin regions.
.
NAR Genom Bioinform. 2(2):lqaa022.
PubMed
Kowalski MH
,
Qian H
,
Hou Z
,
Rosen JD
,
Tapia AL
,
Shan Y
,
Jain D
,
Argos M
,
Arnett DK
,
Avery C
et al.
. 2019.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
.
PLoS Genet. 15(12):e1008500.
PubMed
Knopman D
,
Lemere CA
,
Lamb BT
,
Craft S
,
Gitlin LN
,
Golde TE
,
Pericak-Vance M
,
Sano M
,
Schellenberg G
,
Schneider JA
et al.
. 2020.
Scientific Advising and Reviewing: On strengthening the bond between the Alzheimer's Association and the scientific community.
.
Alzheimers Dement. 16(7):1095-1098.
PubMed
Kling MA
,
Goodenowe DB
,
Senanayake V
,
MahmoudianDehkordi S
,
Arnold M
,
Massaro TJ
,
Baillie R
,
Han X
,
Leung Y-Y
,
Saykin AJ
et al.
. 2020.
Circulating ethanolamine plasmalogen indices in Alzheimer's disease: Relation to diagnosis, cognition, and CSF tau.
.
Alzheimers Dement. 16(9):1234-1247.
PubMed
Kirola L
,
Budde JP
,
Wang F
,
Norton J
,
Morris JC
,
Cruchaga C
,
Fernández MVictoria
. 2021.
Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population.
.
Acta Neuropathol. 141(4):623-624.
PubMed
Kim M
,
Bao J
,
Liu K
,
Park B-Y
,
Park H
,
Baik JYoung
,
Shen L
. 2021.
A structural enriched functional network: An application to predict brain cognitive performance.
.
Med Image Anal. 71:102026.
PubMed
Kim JPyo
,
Kim B-H
,
Bice PJ
,
Seo SWon
,
Bennett DA
,
Saykin AJ
,
Nho K
. 2021.
BMI1 is associated with CS8F amyloid-β and rates of cognitive decline in Alzheimer's disease.
.
Alzheimers Res Ther. 13(1):164.
PubMed
Keys KL
,
C Y Mak A
,
White MJ
,
Eckalbar WL
,
Dahl AW
,
Mefford J
,
Mikhaylova AV
,
Contreras MG
,
Elhawary JR
,
Eng C
et al.
. 2020.
On the cross-population generalizability of gene expression prediction models.
.
PLoS Genet. 16(8):e1008927.
PubMed
Kenny RAnne
. 2020.
New Insights and Knowledge on Cognition and Dementia from Population-Based Cohort of Older Adults in India.
.
J Am Geriatr Soc. 68 Suppl 3:S1-S2.
PubMed
Katsumata Y
,
Nelson PT
,
Estus S
,
Fardo DW
. 2019.
Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs.
.
Neurobiol Aging. 74:135-146.
PubMed
J
Jo T
,
Nho K
,
Risacher SL
,
Saykin AJ
. 2020.
Deep learning detection of informative features in tau PET for Alzheimer's disease classification.
.
BMC Bioinformatics. 21(Suppl 21):496.
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
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
Ji Z
,
Liao Y
,
Zheng L
,
Wu L
,
Yu M
,
Feng Y
. 2019.
An Assembled Detector Based on Geometrical Constraint for Power Component Recognition.
.
Sensors (Basel). 19(16)
PubMed
I
Ibañez L
,
Bahena JA
,
Yang C
,
Dube U
,
Farias FHG
,
Budde JP
,
Bergmann K
,
Brenner-Webster C
,
Morris JC
,
Perrin RJ
et al.
. 2020.
Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease.
.
Acta Neuropathol Commun. 8(1):196.
PubMed
H
Huan T
,
Joehanes R
,
Song C
,
Peng F
,
Guo Y
,
Mendelson M
,
Yao C
,
Liu C
,
Ma J
,
Richard M
et al.
. 2019.
Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
.
Nat Commun. 10(1):4267.
PubMed
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.
PubMed
Hsu S
,
Pimenova AA
,
Hayes K
,
Villa JA
,
Rosene MJ
,
Jere M
,
Goate AM
,
Karch CM
. 2020.
Systematic validation of variants of unknown significance in APP, PSEN1 and PSEN2.
.
Neurobiol Dis. 139:104817.
PubMed
Horimoto ARVR
,
Xue D
,
Thornton TA
,
Blue EE
. 2021.
Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics.
.
Alzheimers Res Ther. 13(1):122.
PubMed
Hofer E
,
Roshchupkin GV
,
Adams HHH
,
Knol MJ
,
Lin H
,
Li S
,
Zare H
,
Ahmad S
,
Armstrong NJ
,
Satizabal CL
et al.
. 2020.
Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
.
Nat Commun. 11(1):4796.
PubMed
He Z
,
McBride JD
,
Xu H
,
Changolkar L
,
Kim S-J
,
Zhang B
,
Narasimhan S
,
Gibbons GS
,
Guo JL
,
Kozak M
et al.
. 2020.
Transmission of tauopathy strains is independent of their isoform composition.
.
Nat Commun. 11(1):7.
PubMed
He Z
,
Liu L
,
Wang C
,
Le Guen Y
,
Lee J
,
Gogarten S
,
Lu F
,
Montgomery S
,
Tang H
,
Silverman EK
et al.
. 2021.
Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
.
Nat Commun. 12(1):3152.
PubMed
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