Sampson Lab for Kidney Genomics

Our summer interns are finishing up at the end of July, and it's been great having them around the lab. From helping with current projects to fostering new collaborations, they've been a big part of the team these past few months. We'll miss having them around!

What lies beyond GWAS? 🧬 Last Wednesday Sidhant Puntambekar, computational biologist in the Sampson Lab gave a presentation breaking down the complexity of mapping mechanisms that go beyondunderlie pediatric steroid-sensitive nephrotic syndrome GWAS associations.#kidneyomics

Meet Anthea, one of our amazing summer interns at the Sampson Lab! This summer, she is helping support our research on nephrotic syndrome, bringing fresh perspective, curiosity, and a whole lot of energy to the team. 🧬✨ #InternSpotlight #SampsonLab #SummerInternship

Every child who joins the BIGKiDs Study brings us closer to a future with better treatments and hope for a cure. By donating a sample, you're helping researchers uncover the genetic causes of this rare kidney disease. 📩 Sign up or learn more at buff.ly/GCEmnrm

Last week, Dr. Dongwon Lee represented the lab at the 2025 Gordon Research Conference on Human Genetics and Genomics in Portland, Maine. This year’s theme focused on bridging gaps between statistical, molecular, and clinical genetics, something at the heart of our work.

Every trial, every study, every sample matters. Because behind the data, there are real people, real families, and real futures at stake. #research #raredisease #sampsonlab #genomics #MedicalResearch #ScienceToSolutions #BIGKiDsStudy #nephroticsyndrome #NephrologyResearch

Your kidneys are working hard for you every day, every hour. Return the favor with these small habits that lead to lifelong health. 💬 Which of these do you already do? Which one could you start this week? #KidneyFacts #HealthyKidneys #NephrologyTips #BIGKiDsStudy #sampsonlab

Nephrotic syndrome is considered rare, but for the children who face it, the challenges are far from rare. That’s why research like the BIGKiDs Study is so important, because every child deserves a future where treatment doesn’t just work, it lasts. #NephroticSyndrome #SampsonLab

We’re proud to team up with The Nephrotic Syndrome Foundation, a nonprofit supporting families impacted by nephrotic syndrome 💛 It’s a pleasure to stand alongside a mission so deeply rooted in empathy, advocacy, and action. Get involved at nephroticsyndromefoundation.org

Last week, we dove into Motif Enrichment Analysis with Dr. Arif Rather, a post-doc in @dongwon_lee lab. This identifies short, recurring DNA patterns that may influence gene activity. From setup to interpretation, Arif led an insightful @celldiscovnet workshop! #WorkshopRecap

We learned a lot & had fun all the while at the Podocyte Conference in Hamburg last month. Thank you so much to the organizers for putting together a terrific set of scientific sessions and social activities @PodocyteIPC @ISGDtweets @Tobias_B_Huber @SannaCherchiLab #kidneyomics

Happy 4th of July from all of us at Sampson Lab! While you’re out enjoying the fireworks, BBQs, and sunshine, don’t forget to stay hydrated, especially important for kidney health! 💧🧬

Most kids with nephrotic syndrome are diagnosed with minimal change disease, meaning their kidneys look almost normal under a microscope, but symptoms tell a different story. #nephrology #genomics #kidneyomics #pediatrics #pediatricnephrology #nephroticsyndrome #raredisease

By participating in the BIGKiDs Study, families help us uncover the genetic causes of nephrotic syndrome in children. Your involvement helps improve diagnosis, treatment, and long-term care for kids worldwide. Let’s build a healthier future together.

Nephrotic syndrome can be difficult to detect early, but here are two common signs to watch for. These symptoms can be subtle at first. Raising awareness helps families and clinicians catch it early and take action. #NephroticSyndrome #SampsonLab #Genomics #RareDisease

🏳️‍🌈 Happy Pride Month from the Sampson Lab! We honor and support the LGBTQ+ community this month and every month. Inclusion, representation, and respect are at the heart of everything we do—because science moves forward when everyone belongs. 💙

Why does your DNA matter?🧬 Because it holds clues that can unlock answers, not just for your child’s care, but for families everywhere facing nephrotic syndrome. 💙 Swipe to see how your sample can spark change. #thesampsonlab #nephroticsyndrome #DNA #raredisease

She eventually agreed 🤝 @kidneyomicsamps