Landmark Discovery Reveals How Chromosomes Are Passed From One Generation to the Next
When a woman becomes pregnant, the outcome of that pregnancy depends on many things — including a crucial…
Harmony Biosciences’ Genetic Disorder Drug Disappoints In Phase 3 Study
Harmony Biosciences Holdings, Inc. (NASDAQ:HRMY) released topline results from its Phase 3 registrational clinical trial (the RECONNECT Study)…
2025 Art In Science Competition Winners Announced
In celebration of University Research Week (October 20-24), the UNC School of Medicine is proud to announce the…
Huntington’s disease treated successfully for the first time in UK gene therapy trial, researchers report breakthrough
Huntington’s disease, one of the most devastating inherited brain disorders, has been treated successfully for the first time.…
Sask. conservation group educates on the “genetic legacy” of bison
Folks across the province can tune into an educational session next week that will dive into the genetic…
Global Experts Call for Action on Elevated Lipoprotein(a)
Cardiovascular disease (CVD) claims nearly 18 million lives worldwide each year, with India accounting for roughly one-fifth of…
Genetic testing pilot aims to catch a silent killer
FH Education Message
A potentially life-saving pilot program is launching in Bloomington, Illinois to…
Acadia Pharmaceuticals drug for rare genetic condition fails late-stage study
Adam Feuerstein is a senior writer and biotech columnist, reporting on the crossroads of drug development, business, Wall…
The Hidden Genetic Threat Putting 1 in 5 at Cardiovascular Disease Risk: Global Experts Call for Action on Elevated Lipoprotein(a)
• Cardiovascular disease (CVD) kills nearly 18 million people each year, more than all cancers combined1,2 • Elevated…
Advances in haplotype phasing and genotype imputation
Voight, B. F., Kudaravalli, S., Wen, X. & Pritchard, J. K. A map of recent positive selection in…
One in four Indians faces silent genetic threat to heart health, shows study
In the Asia Pacific and Middle East region, two in three individuals (66%) skip routine heart tests, while…
Identification of novel mutations in EYA3 and EFTUD2 in a family with craniofacial microsomia: evidence of digenic inheritance
Researchers from Peking Union Medical College and Chinese Academy of Medical Sciences have conducted a study entitled “Identification of novel mutations…