Author

Kameryn M. Butler

Greenwood Genetic CenterORCID 0000-0001-6770-0026Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:zebrafish· 1

Frequent Co-Authors

Abiola Harrison· 1 shared Aleš MaveriD· 1 shared Alexandre ReymondiD· 1 shared Alfredo BruscoiD· 1 shared Anabelle Tuttle· 1 shared Annabelle TuttleiD· 1 shared Binnaz YalciniD· 1 shared Boris KereniD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abiola Harrison

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintFeb 10, 2025

Variants in BSN, encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

Stacy G. Guzman, Sarah McKeown Ruggiero, Shiva Ganesan…·Ingo Helbig

The paper identifies BSN variants as a cause of a new neurodevelopmental disorder with a broad phenotypic range, using clinical data and computational phenotyping.

DOI 10.1101/2025.02.10.25321755

humanstatistical model

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Genetic & Genomic MedicinemedRxivPreprintJan 14, 2024

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles

Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini…·Alexandre Reymond

The paper identifies variant-specific effects of AFF3 on transcriptome profiles through analysis of patient cohorts and zebrafish models, showing distinct pathophysiological mechanisms for different types of AFF3 variants.

1 citation

humanzebrafish

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