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Author Details
Full Name
Wing Hung Wong
Affiliation
Stanford University
ORCID
Career Start Year
1991
Papers
206
H Index
67
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37502861
EpiGePT: a Pretrained Transformer model for epigenomics.
bioRxiv
2024
37502861
EpiGePT: a Pretrained Transformer model for epigenomics.
bioRxiv
2024
36215037
HiChIPdb: a comprehensive database of HiChIP regulatory interactions.
Nucleic Acids Res
2023
35503836
Revealing Free Energy Landscape From MD Data via Conditional Angle Partition Tree.
IEEE/ACM Trans Comput Biol Bioinform
2023
36215037
HiChIPdb: a comprehensive database of HiChIP regulatory interactions.
Nucleic Acids Res
2023
37584462
Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.
Hum Mol Genet
2023
37399400
Comprehensive tissue deconvolution of cell-free DNA by deep learning for disease diagnosis and monitoring.
Proc Natl Acad Sci U S A
2023
37023129
NeuronMotif: Deciphering cis-regulatory codes by layer-wise demixing of deep neural networks.
Proc Natl Acad Sci U S A
2023
36494035
CNEReg Interprets Ruminant-specific Conserved Non-coding Elements by Developmental Gene Regulatory Network.
Genomics Proteomics Bioinformatics
2023
37258665
Deterministic evolution and stringent selection during preneoplasia.
Nature
2023
37053313
The origins and functional effects of postzygotic mutations throughout the human life span.
Science
2023
37292801
scTIE: data integration and inference of gene regulation using single-cell temporal multimodal data.
bioRxiv
2023
37584462
Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.
Hum Mol Genet
2023
35503836
Revealing Free Energy Landscape From MD Data via Conditional Angle Partition Tree.
IEEE/ACM Trans Comput Biol Bioinform
2023
37292801
scTIE: data integration and inference of gene regulation using single-cell temporal multimodal data.
bioRxiv
2023
37258665
Deterministic evolution and stringent selection during preneoplasia.
Nature
2023
37023129
NeuronMotif: Deciphering cis-regulatory codes by layer-wise demixing of deep neural networks.
Proc Natl Acad Sci U S A
2023
37053313
The origins and functional effects of postzygotic mutations throughout the human life span.
Science
2023
37399400
Comprehensive tissue deconvolution of cell-free DNA by deep learning for disease diagnosis and monitoring.
Proc Natl Acad Sci U S A
2023
36494035
CNEReg Interprets Ruminant-specific Conserved Non-coding Elements by Developmental Gene Regulatory Network.
Genomics Proteomics Bioinformatics
2023
34304711
Loss of KMT2C reprograms the epigenomic landscape in hPSCs resulting in NODAL overexpression and a failure of hemogenic endothelium specification.
Epigenetics
2022
36175411
Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.
Nat Commun
2022
35901781
"Fateful" encounter: Lineage tracing meets phylogeny to unravel mysteries of cancer progression.
Dev Cell
2022
36229829
Author Correction: Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.
Genome Biol
2022
35578363
Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.
Genome Biol
2022
35951677
Nested epistasis enhancer networks for robust genome regulation.
Science
2022
35992073
Unfolding the genotype-to-phenotype black box of cardiovascular diseases through cross-scale modeling.
iScience
2022
36525361
Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification.
Elife
2022
34304711
Loss of KMT2C reprograms the epigenomic landscape in hPSCs resulting in NODAL overexpression and a failure of hemogenic endothelium specification.
Epigenetics
2022
35293310
DeepCAGE: Incorporating Transcription Factors in Genome-wide Prediction of Chromatin Accessibility.
Genomics Proteomics Bioinformatics
2022
34978563
On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.
Bioinformatics
2022
35058621
scJoint integrates atlas-scale single-cell RNA-seq and ATAC-seq data with transfer learning.
Nat Biotechnol
2022
34930827
Leveraging cell-type-specific regulatory networks to interpret genetic variants in abdominal aortic aneurysm.
Proc Natl Acad Sci U S A
2022
35578363
Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.
Genome Biol
2022
36525361
Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification.
Elife
2022
36175411
Cost-effective methylome sequencing of cell-free DNA for accurately detecting and locating cancer.
Nat Commun
2022
35901781
"Fateful" encounter: Lineage tracing meets phylogeny to unravel mysteries of cancer progression.
Dev Cell
2022
35992073
Unfolding the genotype-to-phenotype black box of cardiovascular diseases through cross-scale modeling.
iScience
2022
36229829
Author Correction: Regulatory analysis of single cell multiome gene expression and chromatin accessibility data with scREG.
Genome Biol
2022
35951677
Nested epistasis enhancer networks for robust genome regulation.
Science
2022
34978563
On the identifiability of the isoform deconvolution problem: application to select the proper fragment length in an RNA-seq library.
Bioinformatics
2022
35058621
scJoint integrates atlas-scale single-cell RNA-seq and ATAC-seq data with transfer learning.
Nat Biotechnol
2022
34930827
Leveraging cell-type-specific regulatory networks to interpret genetic variants in abdominal aortic aneurysm.
Proc Natl Acad Sci U S A
2022
35293310
DeepCAGE: Incorporating Transcription Factors in Genome-wide Prediction of Chromatin Accessibility.
Genomics Proteomics Bioinformatics
2022
32919612
Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons.
Biol Psychiatry
2021
34180954
MIMIC: an optimization method to identify cell type-specific marker panel for cell sorting.
Brief Bioinform
2021
34179690
Simultaneous deep generative modeling and clustering of single cell genomic data.
Nat Mach Intell
2021
34234141
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis.
Nat Commun
2021
34285077
Dynamic chromatin regulatory landscape of human CAR T cell exhaustion.
Proc Natl Acad Sci U S A
2021
33990562
Modeling regulatory network topology improves genome-wide analyses of complex human traits.
Nat Commun
2021
1 - 50 of 412
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Co-authored papers
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Icahn School of Medicine at Mount Sinai
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David Geffen School of Medicine, University of California at Los Angeles
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4
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Co-authored papers
4
Cameron Brennan
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4
Wenyuan Li
Harvard Medical School
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4
Howard Y Chang
Center for Personal Dynamic Regulomes, Stanford University
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Alexej Abyzov
Co-authored papers
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Junhee Seok
Korea University
Co-authored papers
3
Lei S Qi
Stanford University
Co-authored papers
3
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