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Author Details

Yun Li
University of British Columbia
2007
170
58
PMIDPaper TitleJournal TitlePublished Year
37461300Truncated TDP-43 proteoforms diagnostic of frontotemporal dementia with TDP-43 pathology.Alzheimers Dement2024
37461300Truncated TDP-43 proteoforms diagnostic of frontotemporal dementia with TDP-43 pathology.Alzheimers Dement2024
36380236Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.Mol Psychiatry2023
36380236Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia.Mol Psychiatry2023
36824788DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network.Res Sq2023
37262162Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images.Science2023
36921087Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.Am J Respir Crit Care Med2023
37262162Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images.Science2023
36921087Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients.Am J Respir Crit Care Med2023
36824788DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network.Res Sq2023
34779012A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.Genet Epidemiol2022
35753702A comprehensive comparison on cell-type composition inference for spatial transcriptomics data.Brief Bioinform2022
33839759Single-cell dual-omics reveals the transcriptomic and epigenomic diversity of cardiac non-myocytes.Cardiovasc Res2022
34987162Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.Nat Commun2022
35266368GMEPS: a fast and efficient likelihood approach for genome-wide mediation analysis under extreme phenotype sequencing.Stat Appl Genet Mol Biol2022
34779012A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.Genet Epidemiol2022
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
34376796Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.J Hum Genet2022
35240980Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm.J Neurodev Disord2022
35138379Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.Hum Mol Genet2022
35121757Placental genomics mediates genetic associations with complex health traits and disease.Nat Commun2022
35753702A comprehensive comparison on cell-type composition inference for spatial transcriptomics data.Brief Bioinform2022
33839759Single-cell dual-omics reveals the transcriptomic and epigenomic diversity of cardiac non-myocytes.Cardiovasc Res2022
35121757Placental genomics mediates genetic associations with complex health traits and disease.Nat Commun2022
35240980Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm.J Neurodev Disord2022
35266368GMEPS: a fast and efficient likelihood approach for genome-wide mediation analysis under extreme phenotype sequencing.Stat Appl Genet Mol Biol2022
35138379Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.Hum Mol Genet2022
34987162Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia.Nat Commun2022
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
34376796Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.J Hum Genet2022
32591778SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection.Brief Bioinform2021
31666681Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (nâ¿¿=â¿¿17,706).Mol Psychiatry2021
34296751Corrigendum to: Heritability of regional brain volumes in large-scale neuroimaging and genetic studies.Cereb Cortex2021
34284719Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing.BMC Bioinformatics2021
33684137MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies.PLoS Genet2021
33895111Epigenetically mediated electrocardiographic manifestations of sub-chronic exposures to ambient particulate matter air pollution in the Women's Health Initiative and Atherosclerosis Risk in Communities Study.Environ Res2021
34001886Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits.Nat Commun2021
34140357Common genetic variation influencing human white matter microstructure.Science2021
33872308MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity.PLoS Genet2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
32989764TWO-SIGMA: A novel two-component single cell model-based association method for single-cell RNA-seq data.Genet Epidemiol2021
32591778SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection.Brief Bioinform2021
33418499Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.EBioMedicine2021
35047852From GWAS variant to function: A study of ⿼148,000 variants for blood cell traits.HGG Adv2021
34517814Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.BMC Genomics2021
34563051HPRep: Quantifying Reproducibility in HiChIP and PLAC-Seq Datasets.Curr Issues Mol Biol2021
34446921SnapHiC: a computational pipeline to identify chromatin loops from single-cell Hi-C data.Nat Methods2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
34524848Parallel characterization of cis-regulatory elements for multiple genes using CRISPRpath.Sci Adv2021
33684137MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies.PLoS Genet2021
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Collaborators

Alexander P Reiner
Co-authored papers 42
Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
Co-authored papers 31
Qing Duan
Co-authored papers 31
Leslie A Lange
Co-authored papers 27
Kari E North
Co-authored papers 27
Karen L Mohlke
Co-authored papers 23
Ruth J F Loos
Co-authored papers 20
Jerome I Rotter
Co-authored papers 20
James G Wilson
Beth Israel Deaconess Medical Center
Co-authored papers 19
Charles Kooperberg
Co-authored papers 19
Bruce M Psaty
Co-authored papers 19
Lifang Hou
Co-authored papers 16
Ethan M Lange
Co-authored papers 16
Luigi Ferrucci
National Institute on Aging, National Institutes of Health
Co-authored papers 15
Michael Boehnke
Co-authored papers 15
Laura M Raffield
Co-authored papers 15
Andrea A Baccarelli
Mailman School of Public Health, Columbia University
Co-authored papers 15
Myriam Fornage
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Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 14
Eric Boerwinkle
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Co-authored papers 14
Paul L Auer
Co-authored papers 13
Steve Horvath
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Co-authored papers 13
Jennifer A Brody
Co-authored papers 12
Themistocles L Assimes
Co-authored papers 12
Cristen J Willer
Co-authored papers 12
Yii-Der Ida Chen
Co-authored papers 12
Kent D Taylor
Co-authored papers 11
Paul Elliott
Co-authored papers 11
Kirk C Wilhelmsen
West Virginia University
Co-authored papers 11
Andrew B Singleton
National Institute on Aging
Co-authored papers 11
Release 1.2