Hyderabad (Telangana) [India], November 22: MapmyGenome, a leader in genetic testing and personalized health solutions, proudly announces the publication of its latest research in NPJ Aging (Nature.com). The study, titled 'Genetic Variants Associated with Longevity in Long-Living Indians,' e
Researchers have identified thousands of genetic variants in a gene that could raise an individual's risk of ovarian and breast cancer, opening the door to more accurate risk assessment and individualised treatment.
A study co-led by Professor Kelly Metcalfe of the Lawrence Bloomberg Faculty of Nursing and researchers from the Familial Breast Cancer Research Unit at Women's College Hospital discovered that risk-reducing mastectomies (RRM) in women with a BRCA1 or BRCA2 genetic variant significantly redu
A preclinical study conducted by Weill Cornell Medicine researchers reveals that a certain human genetic variant of a receptor that increases insulin release may help individuals be more resistant to obesity. The researchers revealed that this version operates differently in the cell, which
A recent study published in the Journal of Clinical Immunology has provided light on the particular alterations causing a rare and fatal ailment called 'RAD50 deficiency/Nijmegen breakage syndrome-like disorder'.
Scientists investigating Alzheimer's disease (AD) have discovered millions of genetic variations in the genome that contribute to the progression of this progressive neurological illness.
The genetic basis and polygenic nature of hair whorl orientation are both shown by the first gene mapping study on human scalp hair whorls. An article in the Elsevier-distributed Journal of Investigative Dermatology reports the discovery of four linked genetic variants that are likely to hav
It's tough to tell the difference between the dozens of varieties of limb girdle muscular dystrophy, an uncommon, genetic muscle disease characterised by weakness in the hips and shoulders that makes walking and lifting the arms difficult. Until date, defining the subtype was not crucial in
Cedars-Sinai researchers discovered a genetic variant that increases the risk of developing perianal Crohn's disease, the most debilitating form of Crohn's disease.
A genetic variant of autism and schizophrenia that causes social deficits and seizures in mice and people has been linked to a cause, according to researchers from Northwestern Medicine.
Determining an individual's blood group based on genetic tests instead of merely traditional blood tests can provide a better picture of the risk of cardiovascular diseases. If a patient has two genetic variants of A, B or AB, the risk is twice as high compared with if one is O. This is the
A new analysis has uncovered a potential link between higher prostate cancer risk and genetic variants associated with higher bloodstream levels of the cholesterol-transporting molecule lipoprotein A. Anna Ioannidou of Imperial College London, U.K., and colleagues present these findings in t