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Frontiers in Pediatrics|December 31, 2024
Variants in RHOBTB2 associated with cancer and rare developmental and epileptic encephalopathyElaina Solano, Aleksandra Foksinska, Camerron M CrowderClinical Case Reports|June 12, 2026
Understanding the Role of Genetic Testing in Diagnosing a Complex Pediatric CaseGiavanna Verdi, Aleksandra Foksinska, Elizabeth L Nichols, et al.Epilepsy Research|April 9, 2026
Microtubule-stabilizing drugs suppress convulsions in a C. elegans model of CAMSAP disordersAva Schaak, Madison Walker, Braiden Worden, et al.Frontiers in Artificial Intelligence|October 17, 2022
The precision medicine process for treating rare disease using the artificial intelligence tool mediKanrenAleksandra Foksinska, Camerron M Crowder, Andrew B Crouse, et al.Clinical and Translational Science|July 10, 2025
Announcing the Biomedical Data Translator: Initial Public ReleaseKaramarie Fecho, Gwênlyn Glusman, Sergio E Baranzini, et al.Journal of Clinical and Translational Science|October 30, 2023
An approach for collaborative development of a federated biomedical knowledge graph-based question-answering system: Question-of-the-Month challengesKaramarie Fecho, Chris Bizon, Tursynay Issabekova, et al.Pageof 1