Lauren Testa
laurenctesta.bsky.social
Lauren Testa
@laurenctesta.bsky.social
470 followers 150 following 220 posts
PhD candidate and #raredisease patient-scientist in Gene Therapy and Vaccines at Penn. Interested in genetic therapies, aortas, and climbing. #BillsMafia
Posts Media Videos Starter Packs
Pinned
🚨Exciting news! Dr. T. incoming! 🚨

I will be defending my #PhD, "Therapeutic genome editing for hereditary connective tissue disorders", on January 23, 2026!

My defense will be at 11AM on Penn's campus and Zoom. Message me for the link if you'd like to attend.
Reposted by Lauren Testa
He orders extrajudicial killings. He sent troops into our cities. He terrorizes citizens with ICE raids. He raised taxes without congressional approval. He has ruined American farmers and ranchers. He plans to starve the vulnerable. He demolished our house.

Remove him from office.
@ anyone who’s gotten a #phd how do you figure out what to do next #science #gradschool #sciencesky
Reposted by Lauren Testa
“My name is Dr. Sara Teichholtz.
And I’m here because in 2023, NIH saved my life.”

From the NIH #NoKings rally this weekend.

Powerful and honest and brave from Sara. 🧪
Reposted by Lauren Testa
Heart is so full after #ASHG25. I learned a lot not just about biomedical science but also newborn screening, health insurance, forensic science, genetic counseling, and so much more. It feels like my career path is on the right track 🥲
Thanks to all who came to my talk, asked questions, and shared your stories with me afterward! I love meeting other #RareDiseaae advocates and so many have come to this meeting and reached out to me! #ASHG25
Huge congratulations to my former rotation PI Dr. Elizabeth Bhoj, and my former NHGRI Institute Director Dr. Eric Green for their awards at #ASHG25 !! Two fantastic mentors who have shaped my career!!
I won’t be talking about #marfan tomorrow but I’ll be talking about my work on another cardiovascular connective tissue disorder called PXE (Thurs at 1:30, room 206). Should be fun !!
Here’s to people with #marfansyndrome living longer healthier lives 🥺 #ASHG25
🎖️Congratulations to the ASHG 2025 Lifetime Achievement Awardee Harry (Hal) Dietz, MD, and Mentorship Awardee Carole Ober, PhD! Learn more about the award and their work here: www.ashg.org/membership/a... #ASHG25
Everybody in this room now knows what #MarfanSyndrome is. That knowledge alone will save lives. #ASHG25 #Marfan
Also the fact that ASHG voted to award this honor to a scientist studying connective tissue disorders reminds me that people do care about patients with connective tissue disorders and making our lives better. I am so lucky. So lucky. #ASHG25
Incredibly surreal moment watching Dr. Hal Dietz win the #ASHG25 Lifetime Achievement Award. The discovery that FBN1 is the causal gene of #MarfanSyndrome has saved my life and my family’s lives. I hope to continue contributing to this field to help patients like me.
Listened to some great talks today on Mendelian disease gene discovery, then saw some fascinating posters about my favorite topic, aortopathy genetics! #ASHG25
Time to learn about authentic community engagement outside the lab! super relevant topic for me as both a #raredisease patient and scientist! I want to learn how to use this unique perspective to advance science that matters to the community :) #ASHG25
Of course I’m here in my science role, but being surrounded by other geneticists at #ASHG25 has made me think a lot about my identity as someone with a genetic disorder. There are 6000 people in this room who care about developing therapies for people like me. It is so cool 🥲
Looking forward to connecting with all of you at #ASHG25 (once our flight is able to take off! 😅)!

Excited to meet others in the #raredisease field! my talk is Thursday at 1:30 - the last talk of my #PhD before I’m doctor and I couldnt ask for a better venue for it!
More exciting news: want a sneak peek of what I've been up to the last four years? I'll be presenting my work in a Platform Talk at #ASHG25 in Boston on Thursday, October 16 in the "Gene Editing and Gene Replacement for Rare Disease" session at 1:30PM!
really well said, as someone with a life-limiting genetic disorder it was both beautiful and really challenging to witness the baby KJ story unfold every day before my eyes in real time. obviously I am so so so happy for him and his family!
Reposted by Lauren Testa
Today my @nytimes.com colleagues and I are launching a new series called Lost Science. We interview US scientists who can no longer discover something new about our world, thanks to this year‘s cuts. Here is my first interview with a scientist who studied bees and fires. Gift link: nyti.ms/3IWXbiE
nyti.ms
Wanted to share my talk details for those attending #ASHG25 !
My talk "Therapeutic genome editing for the hereditary connective tissue disorder pseudoxanthoma elasticum" will be Thursday in the Gene Editing and Gene Replacement for Rare Disease session!
Excited to connect with all of you!
More exciting news: want a sneak peek of what I've been up to the last four years? I'll be presenting my work in a Platform Talk at #ASHG25 in Boston on Thursday, October 16 in the "Gene Editing and Gene Replacement for Rare Disease" session at 1:30PM!
and no I do not have them anymore otherwise I would not be STRESSED right now, I’d be comatose
story time, my resting HR has always been ~58 but I used to be on beta blockade which wrecked me and brought my midday HR to 40s. I took them every night before bed (to not pass out during the day), except Sundays in fall, when I took them before bills games to sedate myself before kickoff 😭
It’s that time of the bills game where I start contemplating the antihypertensives a liiiittle bit earlier than scheduled 😬😬😬😬😬😬😬😬😬😬
Every day of writing my dissertation I alternate between “I am a subject matter expert” and “I’ve learned nothing in five years” and there is no in between