Deletions in a gene (πππππππ) that encodes a long noncoding RNA cause severe developmental delay and an increase in expression of a neighboring gene, πππ2. Read the Brief Report: https://t.co/CGJBEJsLWz
Excited to report our study in @NEJM on the discovery of deletions in a long noncoding RNA gene 𧬠(πππππππ) as the cause of a newly defined human neurodevelopmental disorder π§ . π§΅1/10 https://t.co/a0V99Xqjaw
Currently Iβm ~$400 short from reaching my fundraising goal of $1750. If youβd consider donating, itβd mean a lot to me and go a long way in helping families be together during hard times π
https://t.co/yyHQHTSnOn
For the past 4 mos Iβve been training for the Chicago Marathon, which has been a dream/challenge of mine since Iβve started my training @NUMSTP. Iβll be running for Ronald McDonald House Chicago, a group that provides housing/meals for families when their child is hospitalized.
As an MD/PhD student studying rare pediatric diseases, Iβve been deeply impacted by the stories of the challenges families face while seeking care for their children and want to do more to help relieve their financial/emotional burden.
Thank you to the organizers for an amazing inaugural @curechd2 conference. Such a special time getting to know the families and learning about all the cool ongoing scientific work! Iβm back in lab more motivated than ever to help find a cure for CHD2!
Many people had already left when these pictures were taken, but wow. Incredibly blown away by the number of people who came, the deep connections we all made and the sheer sense of pride we all felt at the end. #curechd2
Happy to share our recently-published literature review authored by myself, NUMSTP colleagues, and @ArdehaliHossein on the impact URM and marginalized identity status has on MD-PhD student experiences and academic outcomes.
https://t.co/5XP3Lpmu92