Author

Michael Wright

Centre for LifeORCID 0000-0001-7483-5404Unclaimed ORCID profile · follow to get notified of new preprints

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Michael Wright1 paper · National Marrow Donor Program

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Gabriela Sánchez-AndradeiD· 2 shared Matthew E. HurlesiD· 2 shared Pradeep C. VasudevaniD· 2 shared Sebastian S. GeretyiD· 2 shared Adam Hunter· 1 shared Alexandra S. NeaversoniD· 1 shared Alice Hulbert· 1 shared Andrew Day· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetics

Gabriela Sánchez-AndradeORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 15, 2022

Mouse and cellular models of KPTN-related disorder implicate mTOR signalling in cognitive and progressive overgrowth phenotypes

Maria O. Levitin, Lettie E. Rawlins, Gabriela Sánchez-Andrade…·Sebastian S. Gerety

The paper investigates KPTN-related disorder using mouse and human stem cell models, identifying mTOR pathway dysregulation as a key mechanism underlying cognitive and overgrowth phenotypes.

1 citation

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GeneticsSciencePeer-reviewedNov 8, 2018

Quantifying the contribution of recessive coding variation to developmental disorders

Hilary C. Martin, Wendy D. Jones, Rebecca E. McIntyre…·on behalf of the Deciphering Developmental Disorders Study

The paper estimates the contribution of recessive coding variants to developmental disorders using exome data from 7,448 families, finding low prevalence in European ancestry but higher in Pakistani ancestry.

200 citationstop 1%

humanwhole-exome sequencing

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