Cellular atlases and omics studies, such as genomics, transcriptomics and proteomics, have become key tools for identifying the diversity of all the elements that make up the cardiovascular system.

Rare genetic diseases are challenging for patients and their families—made all the more overwhelming because symptoms tend to ...

The Byers Award recognizes outstanding research by faculty members in the middle of their careers. Martin Kampman’s honorary 2025 lecture is titled “A CRISPR approach to neurodegenerative diseases.” ...

In a nutshell Scientists identified four distinct disease pathways that lead to Alzheimer’s: mental health ...

When it comes to cutting-edge health technology, Jecizer Biosciences is quickly becoming the name you’ve probably haven’t ...

Up to half of patients with Crohn's disease, an inflammatory bowel disease, develop a complication called fibrosis, where the ...

The research findings clearly show that CRNKL1 is crucial for healthy brain development, said lead author Dr. Sankalita Ray Das, a Postdoctoral researcher in the Rare Disorder Genetics Laboratory.

Cancer epidemiologist Christopher Wild first proposed “an ‘exposome’ to match the ‘genome’” in a 2005 paper. Similar to a person’s unique genetic makeup, the exposome would describe, Wild continued, ...

A baby in the US is among the first people with a rare genetic disorder to be treated with CRISPR, a customised gene-editing therapy that allows scientists to edit DNA. The baby, known as KJ, was ...

Kiran Musunuru, MD, PhD, the Barry J. Gertz Professor for Translational Research in Penn’s Perelman School of Medicine (left), and Rebecca Ahrens-Nicklas, MD, PhD, director of the Gene Therapy for ...

Rare Disease Genetic Testing Market- The global rare disease genetic testing market size was estimated at USD 887.80 million in 2022 and is expected to surpass around USD 3,381.87 million by 2032 and ...