JUPITER, FL, June 11, 2010 – In a pair of related studies, scientists from the Florida campus of The Scripps Research Institute have identified several proteins that help regulate cells’ response to light—and the development of night blindness, a rare disease that abolishes the ability to see in dim light.

A large survey of human genetic variation, published today in the online version of the journal Science, shows that rare genetic variants are not so rare after all and offers insights into human diseases.

Researchers at Johns Hopkins have identified a gene that modifies the risk of newborns with cystic fibrosis (CF) developing neonatal intestinal obstruction, a potentially lethal complication of CF. Their findings, which appeared online March 15 in PLoS Genetics, along with the findings of their Toronto-based colleagues, published April 1 in Nature Genetics, may lead to a better understanding of how the intestines work and pave the way for identifying genes involved in secondary complications of other disorders.

TAMPA, Fla. (March 6, 2012) - Researchers at Moffitt Cancer Center and colleagues from 11 other institutions in the United States and the United Kingdom have used two genome-wide association studies (GWAS) - one from the U.S. and one from the U.K. - to detect a novel set of genes found to be associated with epithelial ovarian cancer patient survival. The discovery could open the door to new therapies for treating epithelial ovarian cancer (EOC), the most lethal kind of gynecologic malignancy.

Inner Mongolia and Shenzhen, China – Inner Mongolia Agricultural University (IMAU), Inner Mongolia University for the Nationalities (IMUN) and BGI, the world's largest genomics organization, jointly announced the first complete sequencing of Mongolian genome. This genomic study will help researchers to better understand the evolutionary process and migration of Mongolians and their ancestors from Africa to Asia, which also lays an important genomic foundation for further development of human genetic diseases research.

A University of Cambridge study, which set out to investigate DNA methylation in the human heart and the 'missing link' between our lifestyle and our health, has now mapped the link in detail across the entire human genome.

The new data collected greatly benefits a field that is still in its scientific infancy and is a significant leap ahead of where the researchers were, even 18 months ago.

JUPITER, FL, November 23, 2011 – Against the backdrop of the growing epidemic of obesity in the United States, scientists from the Florida campus of The Scripps Research Institute have made an important new discovery regarding a specific gene that plays an important role in keeping a steady balance between our food intake and energy expenditure. The study may help scientists better understand the keys to fighting obesity and related disorders such as diabetes.

NEW YORK (GenomeWeb News) – Auburn University has broken ground on a $28.8 million research center that will house a range of scientific disciplines including genomics, bioinformatics, water, and ecological research, as well as architecture and forestry studies.

Results Presented at AHA 2011

A blood-based gene expression test was found to be more effective for ruling out obstructive coronary artery disease in stable symptomatic patients than myocardial perfusion imaging (MPI), a common test that uses a radioactive agent to evaluate the blood flow and function of the heart.

Cofactor Genomics today said it has completed a collaboration with a network of researchers in Kentucky to design experiments and generate and analyze next-generation sequencing data for the state.