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Author Details
Full Name
Michael D Wilson
Affiliation
SickKids Research Institute
ORCID
Career Start Year
2000
Papers
91
H Index
34
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36909614
Transcriptional buffering and 3'UTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load.
bioRxiv
2023
37481629
Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodeling.
Commun Biol
2023
37350250
Transcriptomic effects of the foraging gene shed light on pathways of pleiotropy and plasticity.
Ann N Y Acad Sci
2023
37019888
Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models.
Nat Commun
2023
36990084
Trio RNA sequencing in a cohort of medically complex children.
Am J Hum Genet
2023
36694664
Differential Expression Enrichment Tool (DEET): an interactive atlas of human differential gene expression.
NAR Genom Bioinform
2023
36810851
Postnatal oogenesis leads to an exceptionally large ovarian reserve in naked mole-rats.
Nat Commun
2023
34865988
Cardiac specification during gastrulation - The Yellow Brick Road leading to Tinman.
Semin Cell Dev Biol
2022
35603789
Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.
JCI Insight
2022
35719359
Homology 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 Microbiol
2022
36108220
Loss of Epigenetic Regulation Disrupts Lineage Integrity, Induces Aberrant Alveogenesis, and Promotes Breast Cancer.
Cancer Discov
2022
36322662
Untangling the roles of TOP2A and TOP2B in transcription and cancer.
Sci Adv
2022
36221127
Postnatal developmental trajectory of sex-biased gene expression in the mouse pituitary gland.
Biol Sex Differ
2022
36083289
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Genet Med
2022
33212270
Maternal obesity persistently alters cardiac progenitor gene expression and programs adult-onset heart disease susceptibility.
Mol Metab
2021
33883273
Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents.
Sci Transl Med
2021
33655208
Single-cell mapper (scMappR): using scRNA-seq to infer the cell-type specificities of differentially expressed genes.
NAR Genom Bioinform
2021
33777110
Heart Enhancers: Development and Disease Control at a Distance.
Front Genet
2021
33495464
Conserved regulatory logic at accessible and inaccessible chromatin during the acute inflammatory response in mammals.
Nat Commun
2021
34919436
Alternative polyadenylation is a determinant of oncogenic Ras function.
Sci Adv
2021
34410578
Identification of TIA1 mRNA targets during human neuronal development.
Mol Biol Rep
2021
32761872
Thrombin generation abnormalities in Quebec platelet disorder.
Int J Lab Hematol
2020
31910361
Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup Medulloblastoma.
Dev Cell
2020
31954095
Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks.
Mol Cell
2020
33082323
Selective neuronal degeneration in MATR3 S85C knock-in mouse model of early-stage ALS.
Nat Commun
2020
32663239
Enhancer-gene rewiring in the pathogenesis of Quebec platelet disorder.
Blood
2020
32881472
Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization.
Invest Ophthalmol Vis Sci
2020
30554943
Interactome Rewiring Following Pharmacological Targeting of BET Bromodomains.
Mol Cell
2019
31410901
Phosphoproteomic analysis reveals plant DNA damage signalling pathways with a functional role for histone H2AX phosphorylation in plant growth under genotoxic stress.
Plant J
2019
31350345
Regulation of <i>CCL2</i> expression in human vascular endothelial cells by a neighboring divergently transcribed long noncoding RNA.
Proc Natl Acad Sci U S A
2019
31348877
Break Check: Transcription-Driven Topoisomerase II Collisions near Chromatin Loop Anchors Are Hotspots for DNA Damage and Translocations.
Mol Cell
2019
31604927
Sufu- and Spop-mediated downregulation of Hedgehog signaling promotes beta cell differentiation through organ-specific niche signals.
Nat Commun
2019
30554998
Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup Medulloblastoma.
Dev Cell
2019
29610276
The transcriptional regulator CCCTC-binding factor limits oxidative stress in endothelial cells.
J Biol Chem
2018
30348985
Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations.
Nat Commun
2018
30478328
Heart enhancers with deeply conserved regulatory activity are established early in zebrafish development.
Nat Commun
2018
30355727
Hey2 regulates the size of the cardiac progenitor pool during vertebrate heart development.
Development
2018
28714989
Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism.
Nat Med
2017
28257691
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.
Am J Hum Genet
2017
28455378
G9a controls placental vascular maturation by activating the Notch Pathway.
Development
2017
28301587
The duplication mutation of Quebec platelet disorder dysregulates PLAU, but not C10orf55, selectively increasing production of normal PLAU transcripts by megakaryocytes but not granulocytes.
PLoS One
2017
28291707
Epigenetics of Atherosclerosis: Emerging Mechanisms and Methods.
Trends Mol Med
2017
28421636
Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels.
Genet Epidemiol
2017
28371330
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.
Am J Med Genet A
2017
29066515
Cross-Cancer Analysis Reveals Novel Pleiotropic Associations-Response.
Cancer Res
2017
28536097
Dynamic regulation of VEGF-inducible genes by an ERK/ERG/p300 transcriptional network.
Development
2017
28911201
Gene expression profiling of puberty-associated genes reveals abundant tissue and sex-specific changes across postnatal development.
Hum Mol Genet
2017
28552956
Sex-specific effect of CPB2 Ala147Thr but not Thr325Ile variants on the risk of venous thrombosis: A comprehensive meta-analysis.
PLoS One
2017
28894120
Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.
Sci Rep
2017
26882985
Decreased Transcription Factor Binding Levels Nearby Primate Pseudogenes Suggest Regulatory Degeneration.
Mol Biol Evol
2016
1 - 50 of 91
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Sean M Grimmond
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Richard M Myers
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Wyeth W Wasserman
BC Children's Hospital Research Institute, University of British Columbia
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Kelly A Frazer
University of California, USA Institute for Genomic Medicine
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Cancer Research UK Cambridge Institute, University of Cambridge
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Liis Uusk??la-Reimand
SickKids Research Institute
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11
Minggao Liang
University of Toronto
Co-authored papers
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Stephen Watt
Wellcome Sanger Institute
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Paul Flicek
European Bioinformatics Institute
Co-authored papers
7
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers
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Anna Goldenberg
SickKids Research Institute
Co-authored papers
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Azad Alizada
Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers
4
Simon Tavar??
Irving Institute for Cancer Dynamics, Columbia University
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3
Lap-Chee Tsui
The University of Hong Kong
Co-authored papers
3
Stephane Angers
Department of Pharmaceutical Sciences, University of Toronto
Co-authored papers
2
Helen He Zhu
Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine
Co-authored papers
2
Lauren Erdman
Center for Computational Medicine, Hospital for Sick Children Research Institute
Co-authored papers
2
Mathieu Lemire
The Hospital for Sick Children
Co-authored papers
2
John C Marioni
Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers
2
Andrew D Paterson
The Hospital for Sick Children
Co-authored papers
2
Qun Pan
University of Toronto
Co-authored papers
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Benjamin J Blencowe
University of Toronto
Co-authored papers
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Diana Wang
University of Victoria
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Hernan Gonorazky
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