4 sisters with mysterious symptoms diagnosed with the same rare brain condition |
A West Virginia family’s youngest daughter, Austyn, was diagnosed with Chiari malformation, a rare brain condition. This led…
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function
Institute of Medical Genetics, University of Zurich, Zurich, Switzerland Reza Asadollahi, Paranchai Boonsawat, Dennis Kraemer & Anita Rauch Faculty of Engineering and…
From diagnosis to recovery: How genetic profiling is helping to detect silent diseases in India
Genetic profiling is reshaping preventive healthcare by identifying hidden health risks long before symptoms appear. Through a simple…
Genetic disease testing – what you should know before looking for bad genes | Ukrainian News
Genetic testing is becoming increasingly popular – it seems to be able to tell you everything: from the…
Building A Future Without Missed Diagnoses
Despite advances, whole genome sequencing—and with it the promise of early, life-altering therapies—still isn’t a routine part of…
Baylor Genetics Presents New Data on Clinical and
HOUSTON, Oct. 15, 2025 (GLOBE NEWSWIRE) — Baylor Genetics, a clinical diagnostic laboratory at the forefront of genetic…
Baylor Genetics Presents New Data on Clinical and Diagnostic Utility of RNA Sequencing for Rare Disease at the American Society of Human Genetics 2025 Annual Meeting
Baylor Genetics Research underscores clinical utility of RNA sequencing in providing critical insights to drive diagnoses and medical…
Genetic testing of common and rare variants in dementia patients from a memory clinic | Alzheimer’s Research & Therapy
2023 Alzheimer’s disease facts and figures. Alzheimers Dement 19, 1598–1695 (2023). Campion D, et al. Early-onset autosomal dominant…
Las Cruces medical center introduces genetic testing to boost cancer prevention efforts
LAS CRUCES, N.M. (KFOX14/CBS4) — Memorial Medical Center in Las Cruces is introducing a new genetic testing tool…
The LMSz method – an automatable scalable approach to constructing gene-specific growth charts in rare disorders
We have developed a method for producing gene-specific z-score centile charts and growth charts based on small datasets…
Bio-Techne and Oxford Nanopore Technologies Expand Agreement to Accelerate Development of Genetics Portfolio Through 2032
Grants Bio-Techne expanded commercial rights to develop a portfolio of genetics products beyond the recently launched AmplideX® Nanopore…
Baylor Genetics to Showcase Clinical and Diagnostic Utility of Genome Sequencing and Multi-omics Across Rare Disease at the American Society of Human Genetics 2025 Annual Meeting
Baylor Genetics Company to share eight poster presentations highlighting advanced diagnostic tools to gain critical insights and shorten…