Gareth S Baynam

21PUBLICATIONS
205CO-AUTHORS
Artificial life and complex adaptive systemsPsychosocial aspects of childbirth and perinatal mental healthDisease surveillanceInfant and child healthMedical molecular engineering of nucleic acids and proteins
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Publications (21)

|Feb 26, 2026
Reimagining care of people living with rare diseases with artificial intelligence.

Tudor Groza, Gareth Baynam, Saumya Shekhar Jamuar

|Jan 15, 2026
Functional skills in MECP2 duplication syndrome: developmental dynamics and regression.

Daniel Ta, Jenny Downs, Gareth Baynam

|Nov 01, 2025
Digital health technology use in clinical trials of rare diseases: a systematic review.

Xiangyun Mao, Dian Zeng, Xiaocong Wang

|Jan 24, 2025
Congenital Titinopathy: Comprehensive Characterization of the Most Severe End of the Disease Spectrum.

Sandra Coppens, Nicolas Deconinck, Patricia Sullivan

|Nov 04, 2024
The state-of-the-art of N-of-1 therapies and the IRDiRC N-of-1 development roadmap.

Anneliene H Jonker, Elena-Alexandra Tataru, Holm Graessner

|Oct 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

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