From renal biopsy to genetic diagnosis: EYA1 mutation in branchio-oto-renal syndrome with renal insufficiency | BMC Nephrology
Zou D, Silvius D, Rodrigo-Blomqvist S, Enerbäck S, Xu PX. Eya1 regulates the growth of otic epithelium and…
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…
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…
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…
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…
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…
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…
Knowing patient’s genetic make-up may change the way medicines are prescribed
SINGAPORE – Not all medicines work the same way on every patient, and part of the answer lies…
Pacbio’s Puretarget simplifies carrier screening
Up to 71% of people carry at least one pathogenic variant that could contribute to development of a…
Is your heart at risk? The answers lie in your lifestyle and your genes, ETHealthworld
Heart attacks, for a long time, have been associated with older age groups, coupled with other underlying issues,…