Long-read sequencing offers new hope for diagnosing rare genetic conditions.
― 4 min read
Cutting edge science explained simply
Long-read sequencing offers new hope for diagnosing rare genetic conditions.
― 4 min read
Study reveals key gene interactions affecting blood traits and autoimmune disease risks.
― 5 min read
ExonViz simplifies gene diagram creation for researchers and clinicians.
― 5 min read
Study explores genetic links in various types of epilepsy, revealing new risk factors.
― 6 min read
Examining how fat placement in the body affects health risks.
― 4 min read
Study confirms gene signatures for tailored treatment in head and neck cancer patients.
― 7 min read
Study examines genetic factors linked to Alzheimer's and Parkinson's across diverse populations.
― 6 min read
New findings link specific genes to knee pain, offering potential treatment avenues.
― 7 min read
AI is changing how we study and treat brain diseases.
― 6 min read
A new method improves genetic variant discovery in GWAS, especially for rare diseases.
― 5 min read
SLC6A1 mutations affect brain function, leading to epilepsy and developmental challenges.
― 6 min read
New guidelines and treatments offer hope for rare disease patients.
― 6 min read
CASK variants affect development, leading to various challenges in children.
― 5 min read
A study reveals important genetic links across various ancestry groups.
― 6 min read
This study assesses participant diversity in the All of Us program.
― 6 min read
Understanding the role of genetic testing in ALS and its implications.
― 8 min read
Exploring the connection between SLC19A1 gene changes and congenital heart issues.
― 9 min read
MDA5 balances defense against infections and autoimmune diseases, revealing complex health implications.
― 5 min read
FGWAS provides clearer insights into genetic influences on health and traits.
― 7 min read
Pompe disease is a rare genetic disorder affecting muscle and nerve function.
― 5 min read
Study investigates how MUTYH gene mutations affect cancer risk and mutation rates.
― 7 min read
New research examines health risks linked to Fragile X premutation carriers.
― 5 min read
New insights into genetic testing reveal challenges in predicting disease risk for healthy individuals.
― 8 min read
Study compares EHR models and genetic scores for predicting disease risks.
― 5 min read
A look at how heart structure and genetics influence health.
― 7 min read
Research reveals how snRNA mutations affect neurodevelopmental disorders.
― 6 min read
A new database enhances AI tools for recognizing facial traits across ancestries.
― 6 min read
New ARTIC-Amp method enhances virus detection in low viral load samples.
― 4 min read
Study reveals genetic links between RASopathies and unexpected health challenges.
― 5 min read
Study reveals genetic links and protein factors in delirium risk among older adults.
― 6 min read
Study reveals important genetic factors influencing breast cancer rates in Brunei patients.
― 5 min read
Research reveals genetic impacts on survival in idiopathic pulmonary fibrosis.
― 6 min read
Research reveals how genes and lifestyle choices influence obesity risks.
― 6 min read
A study on CKD progression and early detection methods.
― 6 min read
A look at the physical and immune challenges linked to Down syndrome.
― 4 min read
A closer look at genetic causes of neurodevelopmental disorders.
― 6 min read
A new method combines genetics and lifestyle data to evaluate cancer risk more accurately.
― 6 min read
A look at how DNA sequencing is changing genetics and healthcare.
― 4 min read
Introducing tailored screening methods to enhance early breast cancer detection.
― 6 min read
XPRS clarifies how genes influence polygenic risk scores for improved healthcare insights.
― 5 min read