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The TEDDY Study Turns 20: A New Era for T1D Insights
Explore the groundbreaking TEDDY Study’s 20 years of research into type 1 diabetes (T1D). Discover how genetics and the environment interact to shape T1D risk and prevention strategies.
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Solving the Unsolved Cases of Rare Diseases
Dr. Cláudia Carvalho and her team at PNRI are on a mission to diagnose rare diseases that have long baffled the medical community. With a focus on genetic structural variants, often undetected in standard tests, their work is pushing the boundaries of what’s possible in genetics.
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Changing the Tide of Cancer With Clams
Explore Dr. Michael Metzger’s groundbreaking research on contagious cancer in clams, uncovering insights that could revolutionize cancer treatment in humans.
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Two-Decade Dedication
Explore how two decades of diabetes research by Dr. Bill Hagopian and Michael Killian at PNRI have paved the way for groundbreaking discoveries in type 1 diabetes prevention.
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Introducing “PNRI Science: Mystery and Discovery” – A New PNRI Podcast
PNRI Science: Mystery & Discovery goes beyond the jargon to explore the passion and people at the forefront of genetic research. Our host, Jack Faris, PNRI CEO, interviews PNRI’s brilliant scientists to share what excites them about genetic research, what inspired them to become scientists, and those myths about science they would love to bust.…
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The Dark Side of the Genome
Join us for an engaging Q&A with PNRI’s Dr. Rick McLaughlin as he explores the mysteries of our DNA, focusing on the 98% once considered “junk.” Discover how his groundbreaking research on transposable elements is transforming our understanding of genetics and its impact on diseases like lupus and cancer. Learn about his journey, the exciting…
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Pacific Northwest Research Institute Uncovers Hidden DNA Mechanisms of Rare Genetic Diseases
Researchers in PNRI’s Carvalho Lab, in collaboration with other institutions, have uncovered how specific DNA rearrangements called inverted triplications contribute to the development of various genetic diseases. This discovery opens new avenues for understanding and treating rare genetic disorders.
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PNRI’s Inaugural Rare Disease Hackathon: Uniting Experts to Solve Genetic Mysteries
For three dynamic days, participants immersed themselves in solving genetic mysteries in PNRI’s first-ever Rare Disease Hackathon. Read on to learn about their mission to uncover disease-causing genetic variants in unresolved rare disease families.
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Study Reveals Role of Newly Inherited DNA Variants in Recessive Diseases
A team of researchers from Baylor College of Medicine, including PNRI’s own Dr. Cláudia Carvalho, conducted a decade-long exploration into Turkish genetics, uncovering a vital piece of the puzzle behind why some rare diseases emerge.
