Author details

Full Name

Li-San Wang

Affiliation

ORCID

Career Start Year

2000

Papers

131

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37578203	DNA from multiple viral species is associated with Alzheimer's disease risk.	Alzheimers Dement	2024
37162864	hipFG: High-throughput harmonization and integration pipeline for functional genomics data.		2023
37947320	hipFG: high-throughput harmonization and integration pipeline for functional genomics data.		2023
37577355	The prediction of Alzheimer's disease through multi-trait genetic modeling.		2023
37693521	Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.	medRxiv	2023
37459083	Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults.	JAMA Neurol	2023
37390458	The Early-Onset Alzheimer's Disease Whole-Genome Sequencing Project: Study design and methodology.	Alzheimers Dement	2023
37260021	Novel loci for Alzheimer's disease identified by a genome-wide association study in Ashkenazi Jews.	Alzheimers Dement	2023
37536975	Using community-based geographical information system (GIS) to recruit older Asian Americans in an Alzheimer's disease study.	BMJ Open	2023
37349795	A genome-wide search for pleiotropy in more than 100,000 harmonized longitudinal cognitive domain scores.	Mol Neurodegener	2023
35068457	Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease.	Journal of Alzheimer's Disease	2022
35379992	New insights into the genetic etiology of Alzheimer's disease and related dementias.	Nat Genet	2022
35943817	Scalable approaches for functional analyses of whole-genome sequencing non-coding variants.	Human Molecular Genetics	2022
35938255	The Advisory Group on Risk Evidence Education for Dementia: Multidisciplinary and Open to All.	J Alzheimers Dis	2022
35552371	Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease.	Brain	2022
35980155	Omnibus and robust deconvolution scheme for bulk RNA sequencing data integrating multiple single-cell reference sets and prior biological knowledge.		2022
36411364	Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.	Nat Genet	2022
36846102	The role of structural variations in Alzheimer's disease and other neurodegenerative diseases.		2022
34152079	Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease.	Alzheimers Dement	2022
35047815	FILER: a framework for harmonizing and querying large-scale functional genomics knowledge.	NAR Genomics and Bioinformatics	2022
35258170	Progranulin mutations in clinical and neuropathological Alzheimer's disease.	Alzheimers Dement	2022
35210353	An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns.	Genome Res	2022
35142023	Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE É¿2 for Alzheimer's disease.	Alzheimers Dement	2022
34795690	SEAGLE: A Scalable Exact Algorithm for Large-Scale Set-Based Gene-Environment Interaction Tests in Biobank Data.	Frontiers in Genetics	2021
33863950	Reconcile the debate over protective effects of BCG vaccine against COVID-19.	Scientific Reports	2021
33326071	Using INFERNO to Infer the Molecular Mechanisms Underlying Noncoding Genetic Associations.	Methods in Molecular Biology	2021
34804120	Copy Number Variation Identification on 3,800 Alzheimer's Disease Whole Genome Sequencing Data from the Alzheimer's Disease Sequencing Project.	Frontiers in Genetics	2021
32715599	Circulating ethanolamine plasmalogen indices in Alzheimer's disease: Relation to diagnosis, cognition, and CSF tau.	Alzheimers Dement	2020
32330239	SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants.		2020
32270138	HIPPIE2: a method for fine-scale identification of physically interacting chromatin regions.	NAR Genomics and Bioinformatics	2020
32989324	An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer's disease.	Nat Genet	2020
33033384	Author Correction: An integrated multi-omics approach identifies epigenetic alterations associated with Alzheimer's disease.	Nat Genet	2020
32527607	LRP10 variants in progressive supranuclear palsy.	Neurobiol Aging	2020
32637050	HiPR: High-throughput probabilistic RNA structure inference.	Computational and Structural Biotechnology Journal	2020
32844198	Genetic variants and functional pathways associated with resilience to Alzheimer's disease.	Brain	2020
32716361	A Coordinated Approach by Public Domain Bioinformatics Resources to Aid the Fight Against Alzheimer's Disease Through Expert Curation of Key Protein Targets.	J Alzheimers Dis	2020
30668832	DASHR 2.0: integrated database of human small non-coding RNA genes and mature products.		2019
31852801	Activity of the poly(A) binding protein MSUT2 determines susceptibility to pathological tau in the mammalian brain.	Sci Transl Med	2019
31561366	Inferring the Molecular Mechanisms of Noncoding Alzheimer's Disease-Associated Genetic Variants.	Journal of Alzheimer's Disease	2019
30478448	Targeting EIF4E signaling with ribavirin in infant acute lymphoblastic leukemia.	Oncogene	2019
29857119	Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.	Genomics	2019
30820047	Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates AÎ², tau, immunity and lipid processing.	Nat Genet	2019
29733404	SPAR: small RNA-seq portal for analysis of sequencing experiments.	Nucleic Acids Research	2018
30113658	INFERNO: inferring the molecular mechanisms of noncoding genetic variants.	Nucleic Acids Research	2018
29986742	Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci.	Mol Neurodegener	2018
29486463	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	2018
29556027	Publisher Correction: Dysregulation of the epigenetic landscape of normal aging in Alzheimer's disease.	Nat Neurosci	2018
29507413	Dysregulation of the epigenetic landscape of normal aging in Alzheimer's disease.	Nat Neurosci	2018
29688227	Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.	Ann Clin Transl Neurol	2018
28183528	Transethnic genome-wide scan identifies novel Alzheimer's disease loci.	Alzheimers Dement	2017