New genetic discovery could change how Friedreich’s ataxia is diagnosed
A University of Oklahoma researcher is the first to discover that the sequence of the genetic defect in…
Scientists discover how two distinct genes guide regeneration of sensory cells in zebrafish
While humans can regularly replace certain cells, like those in our blood and gut, we cannot naturally regrow…
Cognitive bias in clinical large language models
Biases affecting clinical LLM systems can arise at multiple stages, including data-related biases from collection and representation, model-related…
Why your infant is crying
How much an infant cries is largely steered by their genetics and there is probably not much that…
Discovery of a genetic dimmer switch controlling embryonic development
A team of scientists at the MRC Laboratory of Medical Sciences (LMS) has uncovered a previously unknown mechanism…
OMRF scientist receives $1 million to study genetic link to lupus
Listen to this article With a new $1 million grant from the U.S. Department of Defense, Oklahoma Medical…
Few shot learning for phenotype-driven diagnosis of patients with rare genetic diseases
Overview of the undiagnosed diseases network patient cohort We assemble a cohort of 465 patients in the Undiagnosed…
Treatment that is tailored just for you – Life News
A new study, published in The New England Journal of Medicine in May this year, brought to light…
A lightweight scalable hybrid authentication framework for Internet of Medical Things (IoMT) using blockchain hyperledger consortium network with edge computing
Although managing resources at the edge, particularly in the context of highly dynamic IoMT environments, remains a significant…
Cyberchondria, somatic symptoms, and internet-based self-diagnosis among the Saudi population
Study design and settings This cross-sectional observational study was conducted between January and March 2024 using an anonymous…