Author

Teresa Easterbrooks

Boston Children's HospitalORCID 0000-0002-6360-8713Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:zebrafish· 2 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adriano MagliiD· 1 shared Angelina White· 1 shared Anne O’Donnell‐LuriaiD· 1 shared Brandon M. PrattiD· 1 shared Brenda J. BarryiD· 1 shared Caroline D. RobsoniD· 1 shared Cristina Rivera QuilesiD· 1 shared Daniel K. TanakaiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperNeuroscience

Adriano MagliORCID

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2 papers

Recent·Most cited

Myosin light chain proteins cooperatively promote sarcomere growth in fast-twitch muscle

Tayo E Adekeye, Troy Hupper, Teresa Easterbrooks, Emily M. Teets, Emily A. Tomak, Sadie Waterman, Kailee Sprague, Angelina White, Maddison Coffin, Daniel K. Tanaka, Sabrina Varga, Mason Soares, Sarah J. Shepherd, Jared D Austin, Dmitrii Krivorotko, , Jared Coffin Talbot

This study shows that Mylpf proteins are essential for sarcomere growth in fast-twitch muscle, with their dosage affecting sarcomere formation and myofilament localization.

Nature Communications · Jun 4, 2026Peer-reviewedDevelopmental Biology

Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

Julie A. Jurgens, Paola M. Matos Ruiz, Jessica King, Emma E. Foster, Lindsay Berube, Wai Man Chan, Brenda J. Barry, Raehoon Jeong, Elisabeth Rothman, Mary C. Whitman, Sarah E. MacKinnon, Cristina Rivera Quiles, Brandon M. Pratt, Teresa Easterbrooks, Fiona M. Mensching, , Elizabeth C. Engle

The paper identifies three novel candidate genes for ocular congenital cranial dysinnervation disorders using zebrafish CRISPR screening and protein binding microarrays to assess variant functionality.

bioRxiv · Sep 12, 2024 · PreprintNeuroscience