Latest Genetic association Stories
The power of genome-wide association studies (GWAS) to detect genetic influences on human disease can be substantially increased using a statistical testing framework.
Researchers have identified a new genome-wide significant locus (the place a gene occupies on a chromosome) for infantile hypertrophic pyloric stenosis (IHPS), a serious gastrointestinal condition associated with gastrointestinal obstruction.
A large collaborative study has added to the growing list of genetic variants that determine how tall a person will be.
International collaboration maps height 'hotspots' in the genome BOSTON, Sept.
23andMe, Inc., a leading personal genetics company, announced today that it has published the first data to come out of its novel participant-driven research program.
By investigating the association between genetic loci related to Alzheimer's disease and neuroimaging measures related to disease risk, researchers may have uncovered additional evidence that several previously studied genetic variants are associated with the development and progression of Alzheimer's disease and also may have identified new genetic risk factors for further study.
Creation of a genetic risk score comprised of multiple genetic markers associated with cardiovascular disease (CVD) was not associated with significant improvement in CVD risk prediction in a study that included more than 19,000 women.
Genome-wide meta-analysis identifies 22 regions associated with blood cell traits.
The single-nucleotide polymorphism (SNP) known as 2q35-rs13387042 is associated with increased risk of estrogen receptor (ER) -positive and -negative breast cancer, according to a study published online July 1 in the Journal of the National Cancer Institute.
- The parings of haberdine; also, any kind of fragments.