Over the past 15 years, researchers have identified hundreds of regions in the human genome associated with heart attack risk. However, researchers lack efficient ways to explore how these genetic variants are molecularly ...
Feb 7, 2024
0
24
While it is well established that chromosomal abnormalities are a major cause of miscarriages the biology behind pregnancy losses with or without chromosomal errors is not well understood. Over 114 thousand women from Iceland, ...
Jan 29, 2024
0
53
Just by looking at a short portion of a man's genome it is possible to estimate the probability that he will die from prostate cancer—even before he has the cancer—thanks to a massive genetic study by RIKEN researchers. ...
Jan 25, 2024
0
53
A large team of medical researchers affiliated with multiple entities in the U.S. and China has found that the risk of developing type 2 diabetes is reduced for people with a certain gene variant.
Glaucoma is the leading cause of irreversible blindness around the globe, affecting up to 44 million people. Although people of African ancestry are most frequently and severely affected by this hereditary disease, its genetic ...
Jan 18, 2024
0
38
More than 200 genes linked to depression have been newly identified in a worldwide study led by UCL researchers.
Jan 10, 2024
0
146
Anxiety disorders (ADs) affect more than 280 million people worldwide, making them one of the most common mental health conditions. ADs have a genetic basis, as seen from inheritance in families, and people with one subtype ...
Dec 19, 2023
0
44
Genome-wide association studies (GWAS) on patient blood samples are useful for identifying the genetic basis of blood cell traits and their links to common diseases. While previous experiments have focused on characterizing ...
Dec 15, 2023
0
22
A comprehensive study that integrates multiple analytic approaches has linked a regulatory gene network and functional defects in insulin-producing pancreatic beta cells to type 2 diabetes. The study, published Nov. 8 in ...
Nov 8, 2023
0
39
While any two human genomes are about 99.9% identical, genetic variation in the remaining 0.1% plays an important role in shaping human diversity, including a person's risk for developing certain diseases.
Oct 26, 2023
0
31
