Sunanjay Bajaj (@sunanjayb) 's Twitter Profile
Sunanjay Bajaj

@sunanjayb

Neurology PGY-2 @UTHealth_Neuro | Chair-Elect CNRF @AANMember | MD @UniHeidelberg | 🧠 Dev @IMBA_Vienna @Knoblich_Lab | Onco-Immunology @NCT_HD

ID: 1316850313035472897

calendar_today15-10-2020 21:16:06

108 Tweet

229 Followers

823 Following

Dennis Lal (@laldennis) 's Twitter Profile Photo

New paper: Bioinformatic variant classification tools gaining importance in clinical genetic guidelines, but performance varies across disorders. We carefully❗️ selected patient variants & functional data to identify the most effective tools for epilepsy doi.org/10.1111/epi.18…

New paper: Bioinformatic variant classification tools gaining importance in clinical genetic guidelines, but performance varies across disorders. We carefully❗️ selected patient variants & functional data to identify the most effective tools for epilepsy doi.org/10.1111/epi.18…
Sunanjay Bajaj (@sunanjayb) 's Twitter Profile Photo

Fantastic news! Launch of our second genetic epilepsy clinic, with the focus on GATOR1. Excited to work on this under the leadership of Dennis Lal !

Chaitanya Ganne (@ganne_chaitanya) 's Twitter Profile Photo

Incredible journey! Worked with him for 10 years to date. His defining qualities: Hardworking, determined, simplicity, kindness, unconditional support, selfless, hustler ....the list goes on. You are a genius, Dr. Pati! Best of luck for your next big gig! 😎Epilepsy Lab

Dennis Lal (@laldennis) 's Twitter Profile Photo

1/2 The largest study of its kind in #epilepsy: We characterized ~1400 epileptic human brain tissues for somatic variants & identified novel epilepsy associated genes & show that show that such genes are strong candidates for cancer drug repurposing #precisonmedicine ...

1/2 The largest study of its kind in #epilepsy: We characterized ~1400 epileptic human brain tissues for somatic variants & identified novel epilepsy associated  genes & show that show that such genes are strong candidates for cancer drug repurposing #precisonmedicine ...
Sunanjay Bajaj (@sunanjayb) 's Twitter Profile Photo

Great to be here at #AES2024 and #SCN8A conference and working with many patients, siblings and parents. Thankful to Dennis Lal for the opportunity to work on rare genetic epilepsy patients. American Epilepsy Society International SCN8A Alliance Rare Epilepsy Network

Dennis Lal (@laldennis) 's Twitter Profile Photo

Day 2: After a long day of meetings, clinical assessments and critical discussions at and around #AES2024. Our team is enjoying the #SCN8A The Cute Syndrome conference.

Day 2: After a long day of meetings, clinical assessments and critical discussions at and around #AES2024. Our team is enjoying the #SCN8A <a href="/TheCuteSyndrome/">The Cute Syndrome</a> conference.
Dennis Lal (@laldennis) 's Twitter Profile Photo

Please retweet 📢: Are you skilled in coding & eager to make a meaningful impact in clinical research? Join our large, friendly, & diverse team! I’m seeking motivated postdocs with strong coding expertise in R and/or Python. Details attached! UTHealth Houston

Please retweet 📢: Are you skilled in coding &amp; eager to make a meaningful impact in clinical research? Join our large, friendly, &amp; diverse team! I’m seeking motivated postdocs with strong coding expertise in R and/or Python. Details attached! <a href="/UTHealthHouston/">UTHealth Houston</a>
Rosa Ritunnano (@rritunnano) 's Twitter Profile Photo

Instead of listing my publications, as the year draws to an end, I want to put pressure on the commonplace assumption that productivity must always increase. Good research is disruptive and thinking time is central to high quality scholarship and necessary for disruptive research

Instead of listing my publications, as the year draws to an end, I want to put pressure on the commonplace assumption that productivity must always increase. Good research is disruptive and thinking time is central to high quality scholarship and necessary for disruptive research
Sunanjay Bajaj (@sunanjayb) 's Twitter Profile Photo

Great to have the preprint out showcasing our work on long-term VNS efficacy in SCN1A patients, particularly when considering anti-seizure medications as confounders. Looking forward to further studies such as this in defined genetic populations!

Dennis Lal (@laldennis) 's Twitter Profile Photo

Please share this job add for a PA that provides advanced medical care to patients in a multidisciplinary clinic specializing in rare genetic neurological disorders and epilepsy, often with comorbidities. careers.uth.tmc.edu/us/en/job/2500…

Please share this job add for a PA that provides advanced medical care to patients in a multidisciplinary clinic specializing in rare genetic neurological disorders and epilepsy, often with comorbidities. 

careers.uth.tmc.edu/us/en/job/2500…
Dennis Lal (@laldennis) 's Twitter Profile Photo

Save the date! The first Avanced Workshop for Clinical Genetics in Epilepsies & Neurodevelopmental Disorders December 2025, All details: med.uth.edu/neurology/adva…

Save the date! 

The first Avanced Workshop for Clinical Genetics in Epilepsies &amp; Neurodevelopmental Disorders

December 2025, All details: 

med.uth.edu/neurology/adva…
Sunanjay Bajaj (@sunanjayb) 's Twitter Profile Photo

Save the date! Our team is organizing the first advanced workshop for genetic in epilepsy and NDD. Looking forward to seeing you in December!

Sunanjay Bajaj (@sunanjayb) 's Twitter Profile Photo

Join our fun, interactive session discussion showcasing learning theories and their application to education in neurology!

Dennis Lal (@laldennis) 's Twitter Profile Photo

New paper on advanced missense variant classification from our team: Our para-SAME/DIFF extension pulls in paralogue evidence, expanding interpretable residues five-fold across all genetic disease. Great work by [email protected] & team. Link to paper: link.springer.com/article/10.118…

New paper on advanced missense variant classification from our team: Our para-SAME/DIFF extension pulls in paralogue evidence, expanding interpretable residues five-fold across all genetic disease. Great work by <a href="/BruengerTobias/">tobias.bruenger@netcologne.de</a> &amp; team. 

Link to paper: 
link.springer.com/article/10.118…