Author

Anabelle Tuttle

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Abiola Harrison· 1 shared Boris KereniD· 1 shared Chaya Nautiyal MuraliiD· 1 shared CHOP Birth Defects Biorepository· 1 shared Colin A. EllisiD· 1 shared Courtney Jensen· 1 shared Deborah J. WatsoniD· 1 shared Hakon H. HakonarsoniD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abiola Harrison

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1 paper

Recent·Most cited

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, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan, Zornitza Stark, Natasha J. Brown, Sajel Lala Kana, Anabelle Tuttle, Jair Antonio Tenorio, Pablo Daniel Lapunzina, Julián B. Nevado, Marie McDonald, Courtney Jensen, , 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.

medRxiv · Feb 10, 2025 · PreprintGenetic & Genomic Medicine