Genetic study reveals why some children respond better to myopia lenses

Myopia, or nearsightedness, has reached epidemic levels worldwide, particularly in East and Southeast Asia. Orthokeratology, which involves wearing specially designed contact lenses overnight to reshape the cornea, has proven effective in slowing axial eye growth—a key factor in myopia progression. Yet not all children benefit equally. Traditional predictors like age or initial degree of myopia … Read more

Funding Gaps Threaten Genomic Advances in Latin America

In Latin America, efforts to implement preventive strategies, diagnostic tools, and personalized treatment for patients with rheumatic diseases often face significant barriers. However, there have been promising developments, many of which have been driven by the growing field of genomic medicine. One such initiative is the Ibero-American Research Consortium on the Genetics of Rheumatic Diseases … Read more

Early brain wiring holds clues to infant emotional development

In a comprehensive Genomic Press research article, scientists have uncovered remarkable insights into how the earliest brain connections shape infant emotional development, potentially offering new ways to identify children at risk for future behavioral and emotional challenges. The groundbreaking study, led by Dr. Yicheng Zhang and Dr. Mary L. Phillips at the University of Pittsburgh … Read more

Genome doubling identified as common event in metastatic cancer evolution

When cancer spreads from a primary tumor to new sites throughout the body, it undergoes changes that increase its genetic complexity. A new study from researchers at Weill Cornell Medicine and Memorial Sloan Kettering Cancer Center (MSK) provides fresh insights about how cancers evolve when they metastasize – insights that could aid in developing strategies … Read more

Genetic Tests in AF Patients May Flag Heart Failure Risk

Genetic testing in patients with atrial fibrillation (AF) may identify those at higher risk of developing incident cardiomyopathy or heart failure, new research from the Netherlands suggested. In a study that included two longitudinal cohorts (the All of Us Research program and the UK Biobank), the prevalence of inherited rare gene variants associated with cardiomyopathy … Read more

Dementia Risk: Gene Variant Affects Men Differently

BREAKING: Gene Variant Doubles Dementia Risk in Men BREAKING: Gene variant Doubles Dementia Risk in Men By Anya Sharma | SYDNEY – 2025/05/30 22:16:57 A new study reveals… The post Dementia Risk: Gene Variant Affects Men Differently appeared first on NewsyList. Source link

Depression, Bipolar, or Hormones?

Archyde: Latest World News, Economy, Entertainment, Health, Technology & Sports Updates Hormone Imbalance Linked to Mental Health Issues in Women: New insights Table of Contents 1. Hormone Imbalance Linked to Mental Health Issues in Women: New insights 2. The Estrogen Connection:… You can read the full story here: Depression, Bipolar, or Hormones?. Source link

Insomnia & Mental Health: Genetics, Sleep Aids & Inflammation

Confront the crucial interplay between sleep and mental health. Discover how insomnia can significantly worsen conditions like anxiety and depression, ‍creating a vicious⁤ cycle that demands attention. ⁢This piece unravels the complex relationship,exploring how inflammation,triggered by sleep‍ deprivation,fuels psychiatric disorders. Learn about the specific connection between disordered eating, mental health issues, and poor sleep quality. … Read more

Donor with cancer gene fathers 67 kids; 10 later develop cancer

At the annual conference of the European Society of Human Genetics in Milan, biologist Dr. Edwige Kasper from the University Hospital of Rouen presented a case involving a sperm donor who unknowingly carried a rare mutation of the TP53 gene associated with Li-Fraumeni syndrome, a severe hereditary cancer predisposition. Between 2008 and 2015, this … Read more

New blood test speeds up diagnosis of rare childhood diseases

A new, rapid testing method will greatly help the diagnosis of rare diseases in babies and children, according to research to be presented to the annual conference of the European Society of Human Genetics today (Monday). While rare genetic diseases are uncommon, as their name suggests, there are more than 7,000 types of disease caused … Read more