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Author Details

Peter J Park
Harvard Medical School
2001
251
89
PMIDPaper TitleJournal TitlePublished Year
36711756Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brain.bioRxiv2023
37986891Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.bioRxiv2023
37985666Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.Sci Data2023
37773632Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.Clin Cancer Res2023
36711756Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brain.bioRxiv2023
37438524A framework for individualized splice-switching oligonucleotide therapy.Nature2023
37419111Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project.Mol Cell2023
37986891Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.bioRxiv2023
37985666Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.Sci Data2023
37773632Hyper-Dependence on NHEJ Enables Synergy between DNA-PK Inhibitors and Low-Dose Doxorubicin in Leiomyosarcoma.Clin Cancer Res2023
37419111Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project.Mol Cell2023
37438524A framework for individualized splice-switching oligonucleotide therapy.Nature2023
35228538Single-cell gene fusion detection by scFusion.Nat Commun2022
36048535Mutational Signature 3 Detected from Clinical Panel Sequencing is Associated with Responses to Olaparib in Breast and Ovarian Cancers.Clin Cancer Res2022
36163278Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.Nat Genet2022
35501320The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
36323678Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
36481818Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer.Nat Commun2022
35320348Reverse Transcriptase Inhibition Disrupts Repeat Element Life Cycle in Colorectal Cancer.Cancer Discov2022
35228538Single-cell gene fusion detection by scFusion.Nat Commun2022
34880424Computational analysis of cancer genome sequencing data.Nat Rev Genet2022
35501320The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
36481818Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer.Nat Commun2022
36163278Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.Nat Genet2022
36323678Author Correction: The 4D Nucleome Data Portal as a resource for searching and visualizing curated nucleomics data.Nat Commun2022
36048535Mutational Signature 3 Detected from Clinical Panel Sequencing is Associated with Responses to Olaparib in Breast and Ovarian Cancers.Clin Cancer Res2022
35320348Reverse Transcriptase Inhibition Disrupts Repeat Element Life Cycle in Colorectal Cancer.Cancer Discov2022
34880424Computational analysis of cancer genome sequencing data.Nat Rev Genet2022
33416869BamSnap: a lightweight viewer for sequencing reads in BAM files.Bioinformatics2021
33753749The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.Nat Commun2021
33737485Landmarks of human embryonic development inscribed in somatic mutations.Science2021
33735618Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation.Dev Cell2021
34158502Comprehensive identification of transposable element insertions using multiple sequencing technologies.Nat Commun2021
33514515Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in <i>TP53-</i> and <i>BRCA1</i>-Deficient Cells.Cancer Res2021
33459505Deletions in CWH43 cause idiopathic normal pressure hydrocephalus.EMBO Mol Med2021
33450522Resources and challenges for integrative analysis of nuclear architecture data.Curr Opin Genet Dev2021
33929509Cis-regulatory dissection of cone development reveals a broad role for Otx2 and Oc transcription factors.Development2021
34316001Somatic mutation accumulation seen through a single-molecule lens.Cell Res2021
33136153HiTea: a computational pipeline to identify non-reference transposable element insertions in Hi-C data.Bioinformatics2021
33416869BamSnap: a lightweight viewer for sequencing reads in BAM files.Bioinformatics2021
33432194Large mosaic copy number variations confer autism risk.Nat Neurosci2021
34862503Micro-Meta App: an interactive tool for collecting microscopy metadata based on community specifications.Nat Methods2021
34838103Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.Mob DNA2021
33514515Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in <i>TP53-</i> and <i>BRCA1</i>-Deficient Cells.Cancer Res2021
33737485Landmarks of human embryonic development inscribed in somatic mutations.Science2021
33735618Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation.Dev Cell2021
33753749The origins and genetic interactions of KRAS mutations are allele- and tissue-specific.Nat Commun2021
33929509Cis-regulatory dissection of cone development reveals a broad role for Otx2 and Oc transcription factors.Development2021
34862503Micro-Meta App: an interactive tool for collecting microscopy metadata based on community specifications.Nat Methods2021
34838103Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder.Mob DNA2021
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University of Chicago, USA University of Chicago Comprehensive Cancer Center
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University of Massachusetts Chan Medical School
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Harvard Medical School
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Samsung Genome Institute, Samsung Medical Center
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Tulane University School of Medicine
Co-authored papers 10
Joslin Diabetes Center, Harvard Medical School
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The University of Hong Kong
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University of California Berkeley
Co-authored papers 9
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The University of Texas MD Anderson Cancer Center
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