Michael D. Wilson

Michael D. Wilson

University of Toronto

H-index: 41

North America-Canada

About Michael D. Wilson

Michael D. Wilson, With an exceptional h-index of 41 and a recent h-index of 31 (since 2020), a distinguished researcher at University of Toronto, specializes in the field of comparative genomics, developmental biology, genome biology, bioinformatics, human genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodeling

An ectopic enhancer restores CFTR expression through de novo chromatin looping

Trio RNA sequencing in a cohort of medically complex children

Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models

Transcriptional buffering and 3ʹUTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load

Differential Expression Enrichment Tool (DEET): an interactive atlas of human differential gene expression

Postnatal oogenesis leads to an exceptionally large ovarian reserve in naked mole-rats

Epigenetic control of cellular crosstalk defines gastrointestinal organ fate and function

Michael D. Wilson Information

University

Position

and SickKids Research Institute

Citations(all)

9290

Citations(since 2020)

4685

Cited By

6501

hIndex(all)

41

hIndex(since 2020)

31

i10Index(all)

69

i10Index(since 2020)

55

Email

University Profile Page

Google Scholar

Michael D. Wilson Skills & Research Interests

comparative genomics

developmental biology

genome biology

bioinformatics

human genetics

Top articles of Michael D. Wilson

Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodeling

Communications Biology

2023/7/22

An ectopic enhancer restores CFTR expression through de novo chromatin looping

Gene therapy

2023/6

Trio RNA sequencing in a cohort of medically complex children

The American Journal of Human Genetics

2023/5/4

Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models

Nature Communications

2023/4/5

Transcriptional buffering and 3ʹUTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load

bioRxiv

2023/3/1

Differential Expression Enrichment Tool (DEET): an interactive atlas of human differential gene expression

NAR Genomics and Bioinformatics

2023/3/1

Postnatal oogenesis leads to an exceptionally large ovarian reserve in naked mole-rats

Nature Communications

2023/2/21

Epigenetic control of cellular crosstalk defines gastrointestinal organ fate and function

Nature Communications

2023/1/30

Age, sex, and cell type-resolved hypothalamic gene expression across the pubertal transition in mice

bioRxiv

2023

A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methods

medRxiv

2023

Transcriptomic effects of the foraging gene shed light on pathways of pleiotropy and plasticity

Annals of the New York Academy of Sciences

2023/8

Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome

Genetics in Medicine

2022/11/1

Multi-species analysis of inflammatory response elements reveals ancient and lineage-specific contributions of transposable elements to NF-κB binding

bioRxiv

2022/10/26

Postnatal developmental trajectory of sex-biased gene expression in the mouse pituitary gland

Biology of sex Differences

2022/10/11

A noncoding single-nucleotide polymorphism at 8q24 drives IDH1-mutant glioma formation

Science

2022/10/6

X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition

Acta neuropathologica

2022/9

A chromosomal duplication encompassing interleukin-33 causes a novel hyper IgE phenotype characterized by eosinophilic esophagitis and generalized autoimmunity

Gastroenterology

2022/8/1

Cardiac specification during gastrulation–The Yellow Brick Road leading to Tinman

2022/7/1

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome

JCI insight

2022/5/5

GATA4/5/6 family transcription factors are conserved determinants of cardiac versus pharyngeal mesoderm fate

Science advances

2022/3/11

See List of Professors in Michael D. Wilson University(University of Toronto)

Co-Authors

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