Advertisement · 728 × 90

Posts by Teddy Drivas 🏳️‍🌈 (he/him)

Leon’s Backroom Bar:
maps.app.goo.gl/6eDavR4xQWP7...

1 month ago 0 0 0 0

The Owl Bar (at the Belvedere Hotel): maps.app.goo.gl/oN6DEgSTG5Rv...

1 month ago 0 0 1 0

Queer folks at @theacmg.bsky.social — let’s get together! 🌈🧬 #ACMGMtg26

A chance for community, mentorship, and fun during the meeting:

Tonight (Thu) 7:30 PM: The Owl Bar

Tomorrow (Fri) 7:30 PM: Leon’s Backroom Bar
2-for-1 drinks + Drag Race viewing

Hope to see you there!

1 month ago 0 0 1 0

On tap: discussion of exome/genome coverage in adults, cancer MRI screening, adult mito workup, PRSs, ideas for future SIG events, and great conversation and connection making! 🧬

#MedicalGenetics #AdultGenetics #ClinicalGenetics @theacmg.bsky.social

1 month ago 0 0 0 0

👋 Adult genetics folks at #ACMGMtg26 — don't miss the Adult Genetics SIG meeting TODAY!

📅 Tuesday, March 10 | 5:15–6:15 PM
📍 BCC, Room 337-338

Whether you care for adult patients, want to connect with providers who do, or are a trainee curious about a career in adult genetics — come join us!

1 month ago 0 0 1 0
Preview
Racial and socioeconomic disparities in genetic evaluation and testing in the adult patient population This study of over 14,000 adults in two major health systems reveals striking racial and socioeconomic disparities in access to genetics evaluation and testing. Black individuals and those from disadv...

📣New from @tdrivas.bsky.social & co!
📄Racial and socioeconomic disparities in genetic evaluation and testing in the adult patient population

4 months ago 3 1 0 0
Post image

The perils of being a #geneticist — when I look at my adorable nephew’s bath towel, all I see is a vaso-occlusive crisis waiting to happen…

4 months ago 3 0 0 0
Preview
Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization in Over 7,000 Patients Precision medicine increasingly relies on genetic testing for individualized care, yet the practice patterns of genetic evaluation in adults remain under-characterized and few guidelines exist to info...

We built the first practice-level map of adult genomic medicine, showing high yield (>30% for exome!), rising demand & a clear need for updated guidelines to ensure testing is accessible, reimbursable, and routine.
Preprint 👉 bit.ly/3L9euh9

6 months ago 1 0 0 0
Post image

🏥Wed (Poster 3010W) - I’ll present our clinical work on how #AdultGenetics care is organized and delivered in over 8,000 adult patient visits over 8 years. We chart referral patterns, testing use & outcomes across indications, revealing how #PrecisionMedicine is practiced today.

6 months ago 1 0 1 0
Post image

📊Fri (Poster 4909F) - Yunjun Kang applied #GraphTheory & #MachineLearning to find hidden gene-gene links in big human data, identifying 2 novel cilium genes that validated in the wet lab; his approach could change how we uncover mechanism & therapeutic targets in human datasets

6 months ago 1 0 1 0
Advertisement
Post image

🧪Thurs (Poster 5047T) - Ekta Singh shows how different nutritional states reshape primary #cilia, altering how cells sense and respond to external cues. Her thesis work will have important implications both for rare #ciliopathy patients and for common complex disease!

6 months ago 1 0 1 0

🧬 Thrilled to be at #ASHG2025 with my students Ekta Singh & Yunjun Kang who are sharing incredible science out of our lab on #cilia, #metabolism, #genetics & #MachineLearning - and to present my own new clinical data on #AdultGenetics. Come say hi!

#ASHG #genetics #genomics

6 months ago 5 0 1 0

Yesterday at lab meeting we went around the table with introductions for a new student. Of the 7 people in attendance, I was the only one born in the USA. Diversity and immigration are what make America, and Science, great, and my heart breaks watching these pillars of our greatness crumble.

8 months ago 6 0 1 0
Post image

New research out in @ajhgnews.bsky.social suggests that the implementation of genetic testing in critically ill adults has the potential to improve patient care & combat healthcare delivery disparities ft Colleen Kripke & @tdrivas.bsky.social‬ (@pennmedicine.bsky.social) www.cell.com/ajhg/fulltex...

8 months ago 1 2 0 0

🔗 Check out the full paper:
www.cell.com/ajhg/fulltex...

📢 Read the Science coverage:
www.science.org/content/arti...

💙 Excited to keep pushing this conversation forward!

9 months ago 2 0 2 0

Huge thanks to our amazing team, patients, and families who made this possible. We hope these data inform broader conversations about when and for whom genetic testing should be routine — not just for children, but for adults too.

9 months ago 1 0 1 0
Preview
Genetic testing of critically ill adults can yield surprises—and reveal disparities in treatment of Black patients Adults in the ICU often don’t know about the genetic diagnoses related to their symptoms, DNA sequencing study shows

We’re super grateful to see our work amplified by @sciencenews.bsky.social , which covered our study’s implications for ICU practice, surprise diagnoses, and what must change for genetic testing to help more adults.

📰 Read the feature:
www.science.org/content/arti...

9 months ago 4 1 2 1
Advertisement

Our study also uncovered concerning disparities: Black patients were significantly less likely than White patients to be aware of their genetic diagnosis, and this was linked to higher mortality rate, potentially contributing to worse ICU outcomes for Black patients.

9 months ago 1 0 1 0

Key finding: Nearly 1 in 4 critically ill young adults age 18-40 had a genetic diagnosis directly related to their illness; half of these diagnoses were unknown to the patients or their doctors. This is a wake-up call for how we think about genetic disease in adult medicine.

9 months ago 0 0 1 1
Preview
Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing In ICU-admitted adults 18–40 years old, exome sequencing, a broad genetic test examining all protein-coding genes, reveals a diagnosis in 24.4% of patients and significant race-based disparities. This...

#genetic testing can reveal life-altering diagnoses — but it’s rarely offered to adults in the #ICU. We asked: How often do genetic conditions underlie critical illness? What do these findings mean for patient care, #disparities, and health outcomes?

📄 AJHG: www.cell.com/ajhg/fulltex...

9 months ago 0 0 1 0

Thrilled to share that our latest study on genetic testing in critically ill adults at @pennmedicine.bsky.social is now published in The American Journal of Human Genetics (@ajhgnews.bsky.social) -- and was featured in
@sciencenews.bsky.social!

9 months ago 4 1 1 0

That’s awesome! Let’s us know if you have any thoughts or feedback after the discussion!

1 year ago 2 0 0 0

I learned a lot working on this project: (1) rare genetic variants can be surprisingly common and affect risk for common diseases like breast cancer (2) mosaicism is important and we need to be paying more attention to it as a research community (3) collaborations introduce you to fantastic people!

1 year ago 1 0 0 0

We believe much of this can be explained by somatic mosaicism in the PV-Only group — our data suggests that many of these patients only have their NF1 variant in some of their cells. This might explain why they lack Neurofibromatosis features, but still carry an increased cancer risk.

1 year ago 1 0 1 0

Importantly, only about half of these patients have features of Neurofibromatosis on exam. However, even in the absence of Neurofibromatosis features, patients with NF1 pathogenic variants (the PV-Only group) were found to have a 50% increased odds of having a cancer diagnosis.

1 year ago 0 0 1 0

This was a mega-collaboration using data from the PennMedicine Biobank @pennmedicine.bsky.social, @ukbiobank.bsky.social, @natera.bsky.social, Ambry Genetics, and the All of Us Research Program to assemble a cohort of over 1 million patients, finding nearly 1 in 1,000 have a pathogenic NF1 variant.

1 year ago 0 0 1 0
Advertisement
Preview
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations - Nature Communications Our current understanding of neurofibromatosis type 1 (NF1) is based on patients ascertained through phenotype-first approaches, which estimate a low prevalence at 1 in 3,000. Here, the authors levera...

Patience, collaboration, and perseverance pay off! Our investigation of the population prevalence of NF1 pathogenic variants is out today in @naturecomms.bsky.social! We find these variants are much more common than anticipated and confer increased risk for cancer.

www.nature.com/articles/s41...

1 year ago 5 1 6 0
Post image

www.nytimes.com/2025/03/10/o...

1 year ago 1229 366 17 15

It was heartening to see so many people standing up for #science today at #Philadelphia City Hall. At a time when it’s easy to feel powerless against a wannabe-fascist government, this was such an excellent reminder of where the real power lies — in the hands of the people. #standupfightback

1 year ago 5 0 1 0