GenomeIndia project publishes preliminary findings from sequencing 10,000 Indian genomes, highlighting unique genetic ...

A research team has decoded the genome of historic potato cultivars and used this resource to develop an efficient method for analysis of hundreds of additional potato genomes.

Hemophilia, a rare inherited bleeding disorder, is primarily caused by mutations in specific genes that impair the body’s ...

Genetic factors are thought to play a major role in the development of autism – but for decades what they are has proven elusive. Now scientists are starting to uncover clues.

The GenomeIndia study found 180 million genetic variants from the whole genome sequencing of 9,772 individuals.

With Non-Invasive Prenatal Testing (NIPT), molecular genetics enables the correlation between changes in the structure and ...

After more than 60 years of genetic guessing, scientists have finally cracked the code behind what makes orange cats so… ...

A seminal study has uncovered a new genetic cause of neurodevelopmental disorders (NDDs). The discovery offers both closure and hope to potentially thousands of families worldwide who have long been ...

When even one tiny section of a person’s genetic code becomes mutated or modified, cells can begin to act out of ...

In a bid to advance healthcare access for patients with rare and genetic diseases, Burjeel Holdings, a leading super-specialty healthcare provider in the MENA region, has launched the Genetics and ...

A new multicenter study by researchers at the Icahn School of Medicine at Mount Sinai, in collaboration with the National Cancer Institute-funded Clinical Proteomic Tumor Analysis Consortium (CPTAC) ...

Researchers have discovered an experimental medication that significantly reduces a cholesterol-like particle that can ...