So excited to announce my next patient-inspired adventure as Chief Scientific Officer Christopher & Dana Reeve Foundation!! prnewswire.com/news-releases/… It’s time to retire the wheelchair. I can’t wait to help translate basic science into new treatments and ultimately a cure for spinal cord injury!

Thank you to @forbes for recognizing insitro on the list of 50 most promising AI companies! forbes.com/sites/jilliand… #insitro #ML4Medicines

Our Friend Onno Faber has been a patient collaborator, and research participant with SVAI and now he is speaking at @TEDxSFbay on October 3rd! Use "SVAITEDx2019" for a 20% discount! valid thru the end of September. Register: eventbrite.com/e/tedxsanfranc… Thanks Sam De Brouwer :)

TODAY at noon. Come by to hear about our patient classifier & genotype-phenotype analysis of neurocognitive phenotypes. Noon-1pm, Red Room, Donnelly Centre (160 College ST).

Problems don’t solve themselves, people do! I'm speaking next week at TEDx San Francisco about my journey and rare diseases. If you are in town, join me there! tedxsanfrancisco.com/speakers/Onno-… #tedx #raredisease #nf #nf2

Great inaugural meet yesterday for PRiME - Precision Medicine Initiative at UofT! Trans-disciplinary program for #precisionmedicine. Representing Gary Bader lab as PRIME trainee. Great science talks Jim Wells, Milica Radisic, Leah Cowen + industry panel + entrepreneur advice. Look forward to more crosstalk!

I just penned my first post for the Christopher & Dana Reeve Foundation blog, introducing myself in my own words. I will generate research-focused content for the blog on a regular basis moving forward. And I’d like to invite members of the SCI researcher community to guest blog from time to time.

Software to annotate VCF SNPs with tissue- and disease-specific prior knowledge. Article: tinyurl.com/y2runctq Created with Michael Apostolides Matthew Moss, PhD 🧬 Andrew Jung during SVAI Undiagnosed-1 hackathon. In F1000Research. Please use & improve!

Nothing like a naturally occurring forward genetics screen to reveal an ultra-rare Alzheimer’s suppressor mutation in APOE! nytimes.com/2019/11/04/hea…

New Partner, New Data: Anthem.ai’s First Hackathon -Downtown Palo Alto, Nov 16-17. This is a unique opportunity to work with medical data at the scale of millions of records! Join at: svai.co/anthem-hackath… - there ARE spaces available DM us.

My TEDx talk is online!

Congratulations Jane Metcalfe and NEO.LIFE on your 100th issue! Extraordinary reporting on the neobiological revolution. neo.life/2019/11/the-da…

Thanks Pete and SVAI. We got a lot more stories where this one came from... and we're just getting started. #neobio

Last checks for this weekend anthem.ai 's hackathon to solve healthcare’s big problems. Can't wait to meet all students participating from UC Berkeley Stanford University San José State University & more... #AI for #healthcare #AI for the #People Elevance Health doc.ai SVAI NVIDIA

Dr. Dave Prakash from Elevance Health ai talking about diabetes and why this can be a data problem. Young minds tackling hard problems with AI and healthcare - my optimism for the future continues to rise 😀. With doc.ai #ai #health

.Onno Faber loves to sing. He’s also deaf in his left ear because of tumors caused by the #RareDisease neurofibromatosis type 2. A breast cancer therapy stabilized tumor growth, but he’s still one of the many patients who’s leading his own research #RareAsOne

Our patient research cases have moved to Research to the People | Stanford Medicine! researchtothepeople.org

Wow, Thank you @acolavin! It is amazing to have you involved :)

Updated. We are hosting Leila's event at Stanford Center for Genomics and Personalized Medicine! January 10th -12th. All clinical data, sequencing data, and medical reports are now available. Read full case: research2people.org/leila #ResearchForLeila

All: Our Research cases have moved to Research to the People | Stanford Medicine and our next case is #ResearchforLeila, happening January 10th - 12th at Stanford Center for Genomics and Personalized Medicine! #Genomics #Bioinformatics #CancerResearch #CompBio #MachineLearning