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Author Details

Thomas E Wilson
University of Michigan ann arbor
1955
93
41
PMIDPaper TitleJournal TitlePublished Year
37181851svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing.NAR Genom Bioinform2023
37181851svCapture: efficient and specific detection of very low frequency structural variant junctions by error-minimized capture sequencing.NAR Genom Bioinform2023
35166010Bur1 functions with TORC1 for vacuole-mediated cell cycle progression.EMBO Rep2022
36179663Reverse transcriptase meets DNA, again: Possible roles for transposable elements in host DNA repair.Cell2022
35166010Bur1 functions with TORC1 for vacuole-mediated cell cycle progression.EMBO Rep2022
36179663Reverse transcriptase meets DNA, again: Possible roles for transposable elements in host DNA repair.Cell2022
33975916Co-transcriptional splicing efficiencies differ within genes and between cell types.RNA2021
34181717Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay.Nucleic Acids Res2021
34263309Mapping yeast mitotic 5' resection at base resolution reveals the sequence and positional dependence of nucleases in vivo.Nucleic Acids Res2021
33975916Co-transcriptional splicing efficiencies differ within genes and between cell types.RNA2021
34181717Locus-specific transcription silencing at the FHIT gene suppresses replication stress-induced copy number variant formation and associated replication delay.Nucleic Acids Res2021
34263309Mapping yeast mitotic 5' resection at base resolution reveals the sequence and positional dependence of nucleases in vivo.Nucleic Acids Res2021
31321486Double-strand breaks in motion: implications for chromosomal rearrangement.Curr Genet2020
31709421Characterization of novel primary miRNA transcription units in human cells using Bru-seq nascent RNA sequencing.NAR Genom Bioinform2020
32665662Twin peaks: finding fragile sites with MiDAS-seq.Cell Res2020
31321486Double-strand breaks in motion: implications for chromosomal rearrangement.Curr Genet2020
31709421Characterization of novel primary miRNA transcription units in human cells using Bru-seq nascent RNA sequencing.NAR Genom Bioinform2020
32665662Twin peaks: finding fragile sites with MiDAS-seq.Cell Res2020
30679249Identification of Suppressor of Clathrin Deficiency-1 (<i>SCD1</i>) and Its Connection to Clathrin-Mediated Endocytosis in <i>Saccharomyces cerevisiae</i>.G3 (Bethesda)2019
31019070Frequency of DNA end joining <i>in trans</i> is not determined by the predamage spatial proximity of double-strand breaks in yeast.Proc Natl Acad Sci U S A2019
30955886Genome-wide de novo L1 Retrotransposition Connects Endonuclease Activity with Replication.Cell2019
30679249Identification of Suppressor of Clathrin Deficiency-1 (<i>SCD1</i>) and Its Connection to Clathrin-Mediated Endocytosis in <i>Saccharomyces cerevisiae</i>.G3 (Bethesda)2019
31019070Frequency of DNA end joining <i>in trans</i> is not determined by the predamage spatial proximity of double-strand breaks in yeast.Proc Natl Acad Sci U S A2019
30955886Genome-wide de novo L1 Retrotransposition Connects Endonuclease Activity with Replication.Cell2019
30218578Effects of hydroxyurea on CNV induction in the mouse germline.Environ Mol Mutagen2018
30218578Effects of hydroxyurea on CNV induction in the mouse germline.Environ Mol Mutagen2018
28740117Fragile sites in cancer: more than meets the eye.Nat Rev Cancer2017
28333944Mechanisms of glycosylase induced genomic instability.PLoS One2017
28740117Fragile sites in cancer: more than meets the eye.Nat Rev Cancer2017
28256581Transcriptional and post-transcriptional regulation of the ionizing radiation response by ATM and p53.Sci Rep2017
28256581Transcriptional and post-transcriptional regulation of the ionizing radiation response by ATM and p53.Sci Rep2017
28333944Mechanisms of glycosylase induced genomic instability.PLoS One2017
27007850Molecular biology: Breaks in the brain.Nature2016
27007850Molecular biology: Breaks in the brain.Nature2016
26905816An efficient method and device for transfer of semisolid materials into solid-state NMR spectroscopy rotors.J Magn Reson2016
26773053Overhang polarity of chromosomal double-strand breaks impacts kinetics and fidelity of yeast non-homologous end joining.Nucleic Acids Res2016
26773053Overhang polarity of chromosomal double-strand breaks impacts kinetics and fidelity of yeast non-homologous end joining.Nucleic Acids Res2016
26905816An efficient method and device for transfer of semisolid materials into solid-state NMR spectroscopy rotors.J Magn Reson2016
25373142Large transcription units unify copy number variants and common fragile sites arising under replication stress.Genome Res2015
25373142Large transcription units unify copy number variants and common fragile sites arising under replication stress.Genome Res2015
26656874Identifying transcription start sites and active enhancer elements using BruUV-seq.Sci Rep2015
26656874Identifying transcription start sites and active enhancer elements using BruUV-seq.Sci Rep2015
23973811Use of Bru-Seq and BruChase-Seq for genome-wide assessment of the synthesis and stability of RNA.Methods2014
25457772Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding.DNA Repair (Amst)2014
23973811Use of Bru-Seq and BruChase-Seq for genome-wide assessment of the synthesis and stability of RNA.Methods2014
24327335Copy number variants are produced in response to low-dose ionizing radiation in cultured cells.Environ Mol Mutagen2014
24636257Release from myosin V via regulated recruitment of an E3 ubiquitin ligase controls organelle localization.Dev Cell2014
24714810Rate of elongation by RNA polymerase II is associated with specific gene features and epigenetic modifications.Genome Res2014
25144783Pooled segregant sequencing reveals genetic determinants of yeast pseudohyphal growth.PLoS Genet2014
25457772Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding.DNA Repair (Amst)2014
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Collaborators

University of Michigan ann arbor
Co-authored papers 14
Co-authored papers 12
Co-authored papers 9
Co-authored papers 7
University of Colorado School of Medicine
Co-authored papers 3
Baylor College of Medicine
Co-authored papers 3
Michigan Center for Translational Pathology, University of Michigan ann arbor
Co-authored papers 2
Hussman Institute for Human Genomics, University of Miami
Co-authored papers 2
National Institute of Environmental Health Sciences/National Institutes of Health
Co-authored papers 2
Center for Environmental Measurement and Modeling
Co-authored papers 2
New York University School of Medicine
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
University of Ottawa
Co-authored papers 2
University of California Los Angeles
Co-authored papers 1
McGill University and Genome Quebec Innovation Centre
Co-authored papers 1
McGill University and Research Institute of the McGill University Health Centre
Co-authored papers 1
Center for Sickle Cell Disease, Howard University College of Medicine
Co-authored papers 1
University of Leicester
Co-authored papers 1
University of Michigan ann arbor
Co-authored papers 1
Ontario Institute for Cancer Research
Co-authored papers 1
Co-authored papers 1
National Institute of Environmental Health Sciences, National Institutes of Health
Co-authored papers 1
Washington University School of Medicine
Co-authored papers 1
McGill University
Co-authored papers 1
University of Oklahoma
Co-authored papers 1
Harvard Medical School, Beth Israel Hospital
Co-authored papers 1
University of Pittsburgh
Co-authored papers 1
National Institute of Environmental Health Sciences
Co-authored papers 1
Center for Devices and Radiological Health
Co-authored papers 1
Children's Hospital
Co-authored papers 1