Madeleine Oudin
madeleineoudin.bsky.social
Madeleine Oudin
@madeleineoudin.bsky.social
Tiampo Family Associate Professor at Tufts University, cancer and epilepsy researcher, fierce advocate for diversity and inclusion, mom of a daughter with the SCN8A epilepsy
Coming up next week our 3rd BME UNITE seminar series featuring talented BME postdocs on the market - Monday Sept 15th at 1PM EST with @bmeunite.bsky.social

Register here: ucla.zoom.us/meeting/regi...
September 9, 2025 at 3:45 PM
Coming up next week Monday Aug 25th at 1PM EST our second BME UNITE seminar : with Taj Yeruva, @matteaallert.bsky.social and @saidaral.bsky.social . Register here: ucla.zoom.us/meeting/regi... @bmeunite.bsky.social
August 19, 2025 at 7:29 PM
Come meet outstanding BME postdocs on the faculty job market: our first set of speakers next Monday Aug 11th at 1PM EST with Julia Brisbane, @sindhujatg.bsky.social and @prnano9.bsky.social . Register here: ucla.zoom.us/meeting/regi...
August 4, 2025 at 2:53 PM
Excited to share our new cohort of 2025 @bmeunite.bsky.social Future Faculty Fellows! These outstanding scientists are all on the job market this year. Register here for upcoming seminars to learn about their amazing work! ucla.zoom.us/meeting/regi...
August 4, 2025 at 2:48 PM
BME UNITE @bmeunite.bsky.social is launching Year 5 of our Future Faculty Program! BME Faculty candidates from marginalized groups on the job market - apply here by July 11th to present your work and receive mentorship to successfully navigate the academic job market: forms.gle/sVto2GRQauNA...
June 24, 2025 at 12:40 PM
Proud to advocate for NIH funding today at the @standupforscience.bsky.social event in Boston - from basic science to disease focused and translational research.
March 7, 2025 at 8:40 PM
Rare Disease Day 2025: it’s hard to celebrate this with the NIH budget cuts, threats to Medicaid funding and lawsuit to end Section 504 Disability rights - all of which will severely impact individuals with rare diseases like my daughter Margot. We wear our stripes, we advocate and we fight!
February 28, 2025 at 4:56 PM
Proud to share our daughter’s story for Infantile Spasms Awareness Week - a catastrophic form of epilepsy caused by her SCN8A genetic mutation which led us to start new research to develop novel treatments for pediatric epilepsies. Listen here: podcasts.apple.com/us/podcast/s...
December 5, 2024 at 1:23 PM