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Author Details
Full Name
Peter J Park
Affiliation
Harvard Medical School
ORCID
Career Start Year
2001
Papers
251
H Index
89
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36711756
Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brain.
bioRxiv
2023
37986891
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
bioRxiv
2023
37985666
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.
Sci Data
2023
37773632
Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.
Clin Cancer Res
2023
36711756
Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brain.
bioRxiv
2023
37438524
A framework for individualized splice-switching oligonucleotide therapy.
Nature
2023
37419111
Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project.
Mol Cell
2023
37986891
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
bioRxiv
2023
37985666
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.
Sci Data
2023
37773632
Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.
Clin Cancer Res
2023
37419111
Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project.
Mol Cell
2023
37438524
A framework for individualized splice-switching oligonucleotide therapy.
Nature
2023
35228538
Single-cell gene fusion detection by scFusion.
Nat Commun
2022
36048535
Mutational Signature 3 Detected from Clinical Panel Sequencing is Associated with Responses to Olaparib in Breast and Ovarian Cancers.
Clin Cancer Res
2022
36163278
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Nat Genet
2022
35501320
The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
36323678
Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
36481818
Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer.
Nat Commun
2022
35320348
Reverse Transcriptase Inhibition Disrupts Repeat Element Life Cycle in Colorectal Cancer.
Cancer Discov
2022
35228538
Single-cell gene fusion detection by scFusion.
Nat Commun
2022
34880424
Computational analysis of cancer genome sequencing data.
Nat Rev Genet
2022
35501320
The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
36481818
Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer.
Nat Commun
2022
36163278
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Nat Genet
2022
36323678
Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.
Nat Commun
2022
36048535
Mutational Signature 3 Detected from Clinical Panel Sequencing is Associated with Responses to Olaparib in Breast and Ovarian Cancers.
Clin Cancer Res
2022
35320348
Reverse Transcriptase Inhibition Disrupts Repeat Element Life Cycle in Colorectal Cancer.
Cancer Discov
2022
34880424
Computational analysis of cancer genome sequencing data.
Nat Rev Genet
2022
33416869
BamSnap: a lightweight viewer for sequencing reads in BAM files.
Bioinformatics
2021
33753749
The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.
Nat Commun
2021
33737485
Landmarks of human embryonic development inscribed in somatic mutations.
Science
2021
33735618
Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation.
Dev Cell
2021
34158502
Comprehensive identification of transposable element insertions using multiple sequencing technologies.
Nat Commun
2021
33514515
Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in <i>TP53-</i> and <i>BRCA1</i>-Deficient Cells.
Cancer Res
2021
33459505
Deletions in CWH43 cause idiopathic normal pressure hydrocephalus.
EMBO Mol Med
2021
33450522
Resources and challenges for integrative analysis of nuclear architecture data.
Curr Opin Genet Dev
2021
33929509
Cis-regulatory dissection of cone development reveals a broad role for Otx2 and Oc transcription factors.
Development
2021
34316001
Somatic mutation accumulation seen through a single-molecule lens.
Cell Res
2021
33136153
HiTea: a computational pipeline to identify non-reference transposable element insertions in Hi-C data.
Bioinformatics
2021
33416869
BamSnap: a lightweight viewer for sequencing reads in BAM files.
Bioinformatics
2021
33432194
Large mosaic copy number variations confer autism risk.
Nat Neurosci
2021
34862503
Micro-Meta App: an interactive tool for collecting microscopy metadata based on community specifications.
Nat Methods
2021
34838103
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.
Mob DNA
2021
33514515
Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in <i>TP53-</i> and <i>BRCA1</i>-Deficient Cells.
Cancer Res
2021
33737485
Landmarks of human embryonic development inscribed in somatic mutations.
Science
2021
33735618
Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation.
Dev Cell
2021
33753749
The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.
Nat Commun
2021
33929509
Cis-regulatory dissection of cone development reveals a broad role for Otx2 and Oc transcription factors.
Development
2021
34862503
Micro-Meta App: an interactive tool for collecting microscopy metadata based on community specifications.
Nat Methods
2021
34838103
Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.
Mob DNA
2021
1 - 50 of 502
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