Skip to Main Content

Author Details

Michael D Wilson
SickKids Research Institute
2000
91
34
PMIDPaper TitleJournal TitlePublished Year
36909614Transcriptional buffering and 3'UTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load.bioRxiv2023
37481629Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodeling.Commun Biol2023
37350250Transcriptomic effects of the foraging gene shed light on pathways of pleiotropy and plasticity.Ann N Y Acad Sci2023
37019888Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models.Nat Commun2023
36990084Trio RNA sequencing in a cohort of medically complex children.Am J Hum Genet2023
36694664Differential Expression Enrichment Tool (DEET): an interactive atlas of human differential gene expression.NAR Genom Bioinform2023
36810851Postnatal oogenesis leads to an exceptionally large ovarian reserve in naked mole-rats.Nat Commun2023
34865988Cardiac specification during gastrulation - The Yellow Brick Road leading to Tinman.Semin Cell Dev Biol2022
35603789Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.JCI Insight2022
35719359Homology Modeling, <i>de Novo</i> Design of Ligands, and Molecular Docking Identify Potential Inhibitors of <i>Leishmania donovani</i> 24-Sterol Methyltransferase.Front Cell Infect Microbiol2022
36108220Loss of Epigenetic Regulation Disrupts Lineage Integrity, Induces Aberrant Alveogenesis, and Promotes Breast Cancer.Cancer Discov2022
36322662Untangling the roles of TOP2A and TOP2B in transcription and cancer.Sci Adv2022
36221127Postnatal developmental trajectory of sex-biased gene expression in the mouse pituitary gland.Biol Sex Differ2022
36083289Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.Genet Med2022
33212270Maternal obesity persistently alters cardiac progenitor gene expression and programs adult-onset heart disease susceptibility.Mol Metab2021
33883273Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents.Sci Transl Med2021
33655208Single-cell mapper (scMappR): using scRNA-seq to infer the cell-type specificities of differentially expressed genes.NAR Genom Bioinform2021
33777110Heart Enhancers: Development and Disease Control at a Distance.Front Genet2021
33495464Conserved regulatory logic at accessible and inaccessible chromatin during the acute inflammatory response in mammals.Nat Commun2021
34919436Alternative polyadenylation is a determinant of oncogenic Ras function.Sci Adv2021
34410578Identification of TIA1 mRNA targets during human neuronal development.Mol Biol Rep2021
32761872Thrombin generation abnormalities in Quebec platelet disorder.Int J Lab Hematol2020
31910361Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup Medulloblastoma.Dev Cell2020
31954095Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks.Mol Cell2020
33082323Selective neuronal degeneration in MATR3 S85C knock-in mouse model of early-stage ALS.Nat Commun2020
32663239Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorder.Blood2020
32881472Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization.Invest Ophthalmol Vis Sci2020
30554943Interactome Rewiring Following Pharmacological Targeting of BET Bromodomains.Mol Cell2019
31410901Phosphoproteomic analysis reveals plant DNA damage signalling pathways with a functional role for histone H2AX phosphorylation in plant growth under genotoxic stress.Plant J2019
31350345Regulation of <i>CCL2</i> expression in human vascular endothelial cells by a neighboring divergently transcribed long noncoding RNA.Proc Natl Acad Sci U S A2019
31348877Break Check: Transcription-Driven Topoisomerase II Collisions near Chromatin Loop Anchors Are Hotspots for DNA Damage and Translocations.Mol Cell2019
31604927Sufu- and Spop-mediated downregulation of Hedgehog signaling promotes beta cell differentiation through organ-specific niche signals.Nat Commun2019
30554998Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup Medulloblastoma.Dev Cell2019
29610276The transcriptional regulator CCCTC-binding factor limits oxidative stress in endothelial cells.J Biol Chem2018
30348985Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations.Nat Commun2018
30478328Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development.Nat Commun2018
30355727Hey2 regulates the size of the cardiac progenitor pool during vertebrate heart development.Development2018
28714989Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism.Nat Med2017
28257691CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.Am J Hum Genet2017
28455378G9a controls placental vascular maturation by activating the Notch Pathway.Development2017
28301587The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes.PLoS One2017
28291707Epigenetics of Atherosclerosis: Emerging Mechanisms and Methods.Trends Mol Med2017
28421636Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels.Genet Epidemiol2017
28371330A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.Am J Med Genet A2017
29066515Cross-Cancer Analysis Reveals Novel Pleiotropic Associations-Response.Cancer Res2017
28536097Dynamic regulation of VEGF-inducible genes by an ERK/ERG/p300 transcriptional network.Development2017
28911201Gene expression profiling of puberty-associated genes reveals abundant tissue and sex-specific changes across postnatal development.Hum Mol Genet2017
28552956Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis.PLoS One2017
28894120Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.Sci Rep2017
26882985Decreased Transcription Factor Binding Levels Nearby Primate Pseudogenes Suggest Regulatory Degeneration.Mol Biol Evol2016
  • 1 - 50 of 91

Recommended Authors

UT Southwestern Medical Center
Career Start Year 2008
Number of shared co-authors 2
The University of Texas MD Anderson Cancer Center
Career Start Year 2006
Number of shared co-authors 1
The University of North Carolina at Chapel Hill
Career Start Year 2005
Number of shared co-authors 0
Altius Institute for Biomedical Sciences
Career Start Year 2005
Number of shared co-authors 3
National Institute of Environmental Health Sciences, National Institutes of Health
Career Start Year 2005
Number of shared co-authors 1
Genome Institute of Singapore (GIS)
Career Start Year 2004
Number of shared co-authors 0
Michigan State University College of Human Medicine
Career Start Year 2004
Number of shared co-authors 1
Center for Genomic and Computational Biology, Duke University Medical Center
Career Start Year 2003
Number of shared co-authors 0
Folkhalsan Research Center
Career Start Year 2003
Number of shared co-authors 2
Harvard University, USA Broad Institute, USA Harvard Stem Cell Institute
Career Start Year 2001
Number of shared co-authors 1
University of North Carolina at Chapel Hill
Career Start Year 2000
Number of shared co-authors 9
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 2000
Number of shared co-authors 9
Center for Omics Sciences, IRCCS San Raffaele Scientific Institute
Career Start Year 2000
Number of shared co-authors 4
Center for Genomic & Computational Biology, Duke University
Career Start Year 1999
Number of shared co-authors 5
University of British Columbia
Career Start Year 1998
Number of shared co-authors 11
University of California san francisco
Career Start Year 1998
Number of shared co-authors 4
Institute of Genetics and Cancer, University of Edinburgh
Career Start Year 1997
Number of shared co-authors 4
University of Pennsylvania Perelman School of Medicine
Career Start Year 1997
Number of shared co-authors 0
National Human Genome Research Institute
Career Start Year 1997
Number of shared co-authors 7
MRC London Institute of Medical Sciences
Career Start Year 1996
Number of shared co-authors 4
Case Western Reserve University School of Medicine
Career Start Year 1995
Number of shared co-authors 13
Lawrence Berkeley National Laboratory
Career Start Year 1995
Number of shared co-authors 6
Center for Epigenomics, University of California San Diego
Career Start Year 1995
Number of shared co-authors 8
RIKEN Center for Integrative Medical Sciences
Career Start Year 1994
Number of shared co-authors 3
Center for Personal Dynamic Regulomes, Stanford University
Career Start Year 1992
Number of shared co-authors 2
Max Planck Institute for Molecular Genetics
Career Start Year 1992
Number of shared co-authors 8
The University of Melbourne
Career Start Year 1990
Number of shared co-authors 8
HudsonAlpha Institute for Biotechnology
Career Start Year 1980
Number of shared co-authors 13
BC Children's Hospital Research Institute, University of British Columbia
Career Start Year 1974
Number of shared co-authors 4
University of California, USA Institute for Genomic Medicine
Career Start Year 1967
Number of shared co-authors 7

Collaborators

Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers 18
SickKids Research Institute
Co-authored papers 11
University of Toronto
Co-authored papers 11
Wellcome Sanger Institute
Co-authored papers 7
European Bioinformatics Institute
Co-authored papers 7
The Hospital for Sick Children
Co-authored papers 6
SickKids Research Institute
Co-authored papers 4
Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers 4
Irving Institute for Cancer Dynamics, Columbia University
Co-authored papers 3
The University of Hong Kong
Co-authored papers 3
Department of Pharmaceutical Sciences, University of Toronto
Co-authored papers 2
Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine
Co-authored papers 2
Center for Computational Medicine, Hospital for Sick Children Research Institute
Co-authored papers 2
The Hospital for Sick Children
Co-authored papers 2
Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers 2
The Hospital for Sick Children
Co-authored papers 2
University of Toronto
Co-authored papers 2
University of Toronto
Co-authored papers 2
University of Victoria
Co-authored papers 2
The Hospital for Sick Children, University of Toronto
Co-authored papers 2
University of Toronto
Co-authored papers 2
Co-authored papers 2
Cumming School of Medicine, University of Calgary
Co-authored papers 2
Co-authored papers 2
BioBox Analytics Inc.
Co-authored papers 2
Lunenfeld-Tanenbaum Research Institute
Co-authored papers 2
University of Cincinnati College of Medicine
Co-authored papers 2
Wisconsin Institute for Discovery, University of Wisconsin-Madison
Co-authored papers 2
The Hospital for Sick Children, University of Toronto
Co-authored papers 2
The Wright Center for Graduate Medical Education
Co-authored papers 2