Author

Christie M. Buchovecky

Baylor College of MedicineORCID 0000-0002-2617-9518Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Adebola EnikanolaiyeiD· 1 shared Amanda M. KoireiD· 1 shared Christine Taylor· 1 shared Elif Fidan AcariD· 1 shared Jay ShendureiD· 1 shared Julie Ruston· 1 shared Marijke Schrock· 1 shared Monica J. JusticeiD· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Adebola EnikanolaiyeORCID

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2 papers

Recent·Most cited

GeneticsGenome ResearchPeer-reviewedApr 1, 2020

Suppressor mutations in Mecp2-null mice reveal that the DNA damage response is key to Rett syndrome pathology

Adebola Enikanolaiye, Julie Ruston, Rong Zeng…·Monica J. Justice

The paper identifies suppressor mutations in Mecp2-null mice that alleviate Rett syndrome symptoms by modulating DNA damage response pathways.

24 citations

mousestatistical model

𝕏 PostBluesky

GenomicsbioRxivPreprintJun 30, 2017

Evolutionary Action of de novo missense variants across pathways prioritizes genes linked to autism and predicts patient phenotypic severity

Amanda M. Koire, Christie M. Buchovecky, Panagiotis Katsonis…·Olivier Lichtarge

The paper assesses de novo missense variants in autism spectrum disorder using Evolutionary Action to identify pathway biases and links variant impact to phenotypic severity.

DOI 10.1101/158329

humanstatistical model

𝕏 PostBluesky