Ashwin Seetharaman

research scientist investigating the genetic underpinnings of human disease

[John D Hamilton @HamiltonJohnD]

@theJagmeetSingh DYK
"1 in 12 Canadians have a rare disease. To date, however, no official definition for “rare disease” has been adopted by the gov of Canada"
How can "we" change the conversation?
#cdnpoli
@IStedman @wolfeofscience @scienceoframen

https://t.co/gH4WbTT227 via @ConversationCA

[Ashwin Seetharaman @scienceoframen]

@Michael_Aregger @DonnellyCentre @spaiglass @UofT Great job Michael!

[Ashwin Seetharaman @scienceoframen]

It was a real honor to present at the CORD meeting today!

[rareDIG @McGill_rareDIG]

@rareDIG_TO founders @wolfeofscience and @scienceoframen present "using CRISPR to unravel gene networks in rare disorders" #RareDialogue2019 @raredisorders

[Ashwin Seetharaman @scienceoframen]

Let’s think about this ..

[Ashwin Seetharaman @scienceoframen]

Excited to take part in this initiative!

[The Conversation Canada @ConversationCA]

#Budget2019: A Canadian Drug Agency and rare disease funding are not enough, says @joel_lexchin of @UofTFamilyMed
#cdnpoli #cdnhealth
https://t.co/WSLrZk5ITq

[Ashwin Seetharaman @scienceoframen]

An absolute previlage hosting Emily and her Family at the lab this week!

[Grace Science @gracescience]

Happy #RareDiseaseDay to all rare disease patients, families, clinicians & scientists! Can't think of a more meaningful tribute than Emily & family visiting the GSF team at the U of Toronto. Our global team connects families, scientists, & families w/ scientists. #NGLY1

[Ashwin Seetharaman @scienceoframen]

It's time to rethink what the medical profession considers a 'rare disease' https://t.co/p2rBLEeGzi

[Ashwin Seetharaman @scienceoframen]

It's time to rethink what the medical profession considers a 'rare disease' https://t.co/S5YlOOZxdw