NATO is a Cold War relic that needs to be relegated to a talking kiosk at the Smithsonian.

RT @elonmusk: The reality of war

Check out our new article on #SLC6A1 variant pathogenicity, molecular function, and phenotype📢 All data can be interactively explored in the SLC6A1 Portal (slc6a1-portal.broadinstitute…)‼️ #Epilepsy🧠 #Genetics🧬 @LalDennis @EdoPerezP @arthurste 💪👏 academic.oup.com/brain/advan…

P hi le

With Yuri Zarate, we developed the satb2-portal.broadinstitute.… sharing the largest curated #SATB2 disorder dataset. Hopefully the analytics & documentation will empower families and enhance clinical use of genomics 🧬. Check it out. Great work by @BruengerTobias, @arthurste

#humbled 🙏 This months three editorials/commentaries where published on 3 new papers from our team around @gramm_marie, @BruengerTobias, @Sumaiyalqbal, @EdoPerezP and larger team.Great to see that our work is read & critically discussed.Thank you. #variantinterpretation #ACMG

Pretty proud 💪that the NINDS director @NINDSdirector featured a polygenic risk study that builds on our previous work with @CostinLeu. He also featured our recent oligogenic paper with @arthurste. Cool to see that people read our work 🤩. Go genetics 🧬 ! @CCLRI

Cleveland Clinic launched the largest clinical study ever for brain disease. The goal is to prevent neurological diseases like Alzheimer's, Parkinson's disease, multiple sclerosis, stroke & epilepsy. #NationalAlzheimersAwarenessMonth Learn more: clevelandclinic.org/brainstu…

Brünger et al. identify biological properties associated with ion-channel malfunction and show that they are correlated with in vitro functional read-outs and clinical phenotypes in patients with neurodevelopmental disorders. bit.ly/3Rs24yY

Joining the kick-off of the #CACNA1A 2022 conference @cacna1a with @LeahEDSCN2A and team @arthurste , @EdoPerezP , @AlinaIvaniuk #ionchannels #RareDisease #epilepsy #ataxia #migraine . A lot of community building & science ahead

Please tell others that take these. We expect to add more than 1k more meds over the next 12 months, if not sooner.

Looking through some older presentation slides from a couple years ago (that I never used) in preparation for a talk. I wonder when this type of analysis will finally enter the rare disease space. Still haven’t seen an example. Important considering that no patient is drug-naive.

#Rarediseas are not rare on a global scale. If the worlds starts sharing data even for rare disorders e.g. monogenic #epilepsies #SCN1A #Dravet outcome prediction models are possible. An international team effort of many by @a_brunklaus & @EdoPerezP lerner.ccf.org/news/details/…

Dr. Robert Malone is a valuable expert contributor to much-needed discourse on a range of COVID policy issues. It's unconscionable that Twitter has seen fit to 'protect' me & other twitter users from his comments. #ReinstateRWMaloneMD #WeAreNotChildren

Proud to present our SLC6A1 disorder info Video in collaboration with @SLC6A1_Mom and many contributors in @GroupLal & @Katrine92658231 @FiladelfiaGene1 youtu.be/No9SDig4WQQ

🚨🚨🚨Tomorrow we will have an amazing talk with my Twitter buddy @AMoosaMD 🚨🚨🚨 don't miss out! @yesILAE @IlaeWeb