Biblio
Found 24 results
Author Keyword Title [ Type
Filters: Author is Wang, Li-San [Clear All Filters]
Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.. Curr Protoc Hum Genet. 79:Unit1.27..
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2013. Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals.. JAMA Neurol. 72(11):1313-23.
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2015. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.. Nat Genet. 43(5):436-41.
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2011. CoRAL: predicting non-coding RNAs from small RNA-sequencing data.. Nucleic Acids Res. 41(14):e137.
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2013. DASHR: database of small human noncoding RNAs.. Nucleic Acids Res. 44(D1):D216-22.
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2016. DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experiments.. Bioinformatics. 29(19):2498-500.
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2013. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.. JAMA Neurol. 71(11):1394-404.
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2014. Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.. Bioinformatics. 34(16):2724-2731.
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2018. 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.
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2019. 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.
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2018. HAMR: high-throughput annotation of modified ribonucleotides.. RNA. 19(12):1684-92.
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2013. High-throughput identification of long-range regulatory elements and their target promoters in the human genome.. Nucleic Acids Res. 41(9):4835-46.
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2013. HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements.. Bioinformatics. 31(8):1290-2.
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2015. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.. Nat Genet. 43(7):699-705.
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2011. PASTA: Ultra-Large Multiple Sequence Alignment for Nucleotide and Amino-Acid Sequences.. J Comput Biol. 22(5):377-86.
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2015. .
2018. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.. Nat Genet. 49(9):1373-1384.
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2017. Rarity of the Alzheimer disease-protective APP A673T variant in the United States.. JAMA Neurol. 72(2):209-16.
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2015. Transcriptomic Changes Due to Cytoplasmic TDP-43 Expression Reveal Dysregulation of Histone Transcripts and Nuclear Chromatin.. PLoS One. 10(10):e0141836.
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2015. Transethnic genome-wide scan identifies novel Alzheimer's disease loci.. Alzheimers Dement. 13(7):727-738.
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2017. Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs.. Methods. 67(1):28-35.
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2014. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.. JAMA. 309(14):1483-92.
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2013. Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.. Ann Clin Transl Neurol. 5(4):406-417.
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2018. Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.. Ann Clin Transl Neurol. 5(4):406-417.
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