Leung YY - Search Results

1

VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project.

Leung YY, Valladares O, Chou YF, Lin HJ, Kuzma AB, Cantwell L, Qu L, Gangadharan P, Salerno WJ, Schellenberg GD, Wang LS. Leung YY, et al. Bioinformatics. 2019 Jun 1;35(11):1985. doi: 10.1093/bioinformatics/btz216. Bioinformatics. 2019. PMID: 31004159 Free PMC article. No abstract available.

2

DASHR: database of small human noncoding RNAs.

Leung YY, Kuksa PP, Amlie-Wolf A, Valladares O, Ungar LH, Kannan S, Gregory BD, Wang LS. Leung YY, et al. Nucleic Acids Res. 2016 Jan 4;44(D1):D216-22. doi: 10.1093/nar/gkv1188. Epub 2015 Nov 8. Nucleic Acids Res. 2016. PMID: 26553799 Free PMC article.

3

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.

Butkiewicz M, Blue EE, Leung YY, Jian X, Marcora E, Renton AE, Kuzma A, Wang LS, Koboldt DC, Haines JL, Bush WS. Butkiewicz M, et al. Among authors: leung yy. Bioinformatics. 2018 Aug 15;34(16):2724-2731. doi: 10.1093/bioinformatics/bty177. Bioinformatics. 2018. PMID: 29590295 Free PMC article.

4

SPAR: small RNA-seq portal for analysis of sequencing experiments.

Kuksa PP, Amlie-Wolf A, Katanic Ž, Valladares O, Wang LS, Leung YY. Kuksa PP, et al. Among authors: leung yy. Nucleic Acids Res. 2018 Jul 2;46(W1):W36-W42. doi: 10.1093/nar/gky330. Nucleic Acids Res. 2018. PMID: 29733404 Free PMC article.

5

VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project.

Leung YY, Valladares O, Chou YF, Lin HJ, Kuzma AB, Cantwell L, Qu L, Gangadharan P, Salerno WJ, Schellenberg GD, Wang LS. Leung YY, et al. Bioinformatics. 2019 May 15;35(10):1768-1770. doi: 10.1093/bioinformatics/bty894. Bioinformatics. 2019. PMID: 30351394 Free PMC article.

6

A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease.

Zhang X, Zhu C, Beecham G, Vardarajan BN, Ma Y, Lancour D, Farrell JJ, Chung J; Alzheimer's Disease Sequencing Project; Mayeux R, Haines JL, Schellenberg GD, Pericak-Vance MA, Lunetta KL, Farrer LA. Zhang X, et al. Alzheimers Dement. 2019 Mar;15(3):441-452. doi: 10.1016/j.jalz.2018.10.005. Epub 2019 Jan 3. Alzheimers Dement. 2019. PMID: 30503768 Free PMC article.

7

DASHR 2.0: integrated database of human small non-coding RNA genes and mature products.

Kuksa PP, Amlie-Wolf A, Katanić Ž, Valladares O, Wang LS, Leung YY. Kuksa PP, et al. Among authors: leung yy. Bioinformatics. 2019 Mar 15;35(6):1033-1039. doi: 10.1093/bioinformatics/bty709. Bioinformatics. 2019. PMID: 30668832 Free PMC article.

8

Inferring the Molecular Mechanisms of Noncoding Alzheimer's Disease-Associated Genetic Variants.

Amlie-Wolf A, Tang M, Way J, Dombroski B, Jiang M, Vrettos N, Chou YF, Zhao Y, Kuzma A, Mlynarski EE, Leung YY, Brown CD, Wang LS, Schellenberg GD. Amlie-Wolf A, et al. Among authors: leung yy. J Alzheimers Dis. 2019;72(1):301-318. doi: 10.3233/JAD-190568. J Alzheimers Dis. 2019. PMID: 31561366 Free PMC article.

9

SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants.

Kuksa PP, Lee CY, Amlie-Wolf A, Gangadharan P, Mlynarski EE, Chou YF, Lin HJ, Issen H, Greenfest-Allen E, Valladares O, Leung YY, Wang LS. Kuksa PP, et al. Among authors: leung yy. Bioinformatics. 2020 Jun 1;36(12):3879-3881. doi: 10.1093/bioinformatics/btaa246. Bioinformatics. 2020. PMID: 32330239 Free PMC article.

10

Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project.

Lee WP, Tucci AA, Conery M, Leung YY, Kuzma AB, Valladares O, Chou YF, Lu W, Wang LS, Schellenberg GD, Tzeng JY. Lee WP, et al. Among authors: leung yy. Front Genet. 2021 Nov 4;12:752390. doi: 10.3389/fgene.2021.752390. eCollection 2021. Front Genet. 2021. PMID: 34804120 Free PMC article.

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