Author

Abiola Harrison

Children's Hospital of Philadelphia

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

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Ingo HelbigiD· 2 shared Sarah McKeown RuggieroiD· 2 shared Shiva GanesaniD· 2 shared Alisa MoiD· 1 shared Anabelle Tuttle· 1 shared Andreas van BaaleniD· 1 shared Ange‐Line BrueliD· 1 shared Annapurna PoduriiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ingo HelbigORCID

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2 papers

Recent·Most cited

DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneity

Abiola Harrison, Shiva Ganesan, Hongbo Michael Xie, Shridhar Parthasarathy, Jillian L. McKee, Jan H. Magielski, Kim Marie Thalwitzer, Rohit Lobo, Manuela Pendziwiat, Andreas van Baalen, Hiltrud Muhle, Annapurna Poduri, Alisa Mo, Gert Wiegand, Katrin Õunap, , Ingo Helbig

The paper analyzes a large DNM1 cohort to identify mutational hotspots and genotype-phenotype correlations in DNM1-related disorder.

medRxiv · Apr 6, 2026 · PreprintGenetic & Genomic Medicine

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