Author

Teddi Gray

Washington University in St. LouisORCID 0009-0009-0233-9538Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Aaron M. WengeriD· 1 shared Ari Grudo· 1 shared Christina A. GurnettiD· 1 shared Elvisa MehinoviciD· 1 shared Jane GrimwoodiD· 1 shared Jenny M. EkholmiD· 1 shared John Nicholas ConstantinoiD· 1 shared Jonas KorlachiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aaron M. WengerORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineAmerican Journal of Medical Genetics Part APeer-reviewedApr 2, 2022

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy

Elvisa Mehinovic, Teddi Gray, Meghan C. Campbell…·Tychele N. Turner

The paper identifies a de novo missense variant in KCNC2 in two affected siblings with autism and epilepsy using long-read sequencing, showing its potential clinical relevance.

14 citations

humanlong-read sequencing

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