Medical University of South Carolina (MUSC) researchers discovered a biomarker in blood samples that with predictive analytics can determine which patients will develop COVID-19 symptoms.
It remains...
By examining specific regions of the human genome, Baylor College of Medicine researchers developed a machine learning algorithm called SPLS-DA to look for epigenetic markers for schizophrenia.
The...
Georgetown Lombardi Comprehensive Cancer Center researchers are studying DNA tags in blood-based tests to better assess and treat cancer and other diseases using precision medicine.
During cell death,...
Researchers at St. Jude Children’s Research Hospital have discovered that comprehensive genomic sequencing of all pediatric cancer patients is achievable and essential in the development of...
A study led by researchers at The Ohio State University Wexner Medical Center and The Ohio State University College of Medicine shows that a new method of gene therapy is providing...
Scientists at UCL National Amyloidosis Centre at the Royal Free Hospital, London are hoping their gene editing therapy using CRISPR will be a breakthrough for patients suffering from hereditary...
Many cardiomyopathies in children are the result of genetic mutations, making a strong case for routine genetic testing to improve patient outcomes, according to a study published in the Journal of the...
A study of genomic data in patients with advanced small-cell lung cancer provided new insights into the patterns of treatment resistance, potentially paving the way for precision medicine...
The University of Alabama at Birmingham School of Medicine and UAB Hospital laboratories have launched the Genomic Diagnostics Lab (GDL), an effort to increase genetic testing and advance precision...
For organizations that want to deepen their knowledge of disease risk and health outcomes, genomic data has emerged as a comprehensive resource that can provide clinicians with new insights.
While the...
Genomic data can provide more targeted insights into chronic disease management than those generated from traditional ethnic or racial labels like Hispanic or Black, a study published in Cell...
In a study of end-stage heart failure patients, researchers at the University of Alabama at Birmingham (UAB) found that race and socioeconomic factors may contribute to differences heart failure...
Brigham Young University’s (BYU) Center for Family History and Genealogy and the University of Washington have partnered to prevent hereditary cancer using genetic data.
The Connect My Variant...
Genetic testing can help providers identify the appropriate anti-platelet drugs for patients, leading to enhanced efficacy and fewer side effects, according to a study published in JACC: Cardiovascular...
As disease treatments continue to advance and become more personalized, researchers are increasingly relying on genomic data to accelerate the development of precision medicine for a range of...
UCLA has received a $29 million gift to establish a precision medicine center where scientists can leverage big data and genomic technologies to improve genetic disease treatment and diagnosis.
The...
Intermountain Primary Children’s Hospital has launched the HerediGene: Children’s Study, an effort to speed the development of precision medicine therapies for children with genetic...
Machine learning tools identified patterns of maternal autoantibodies indicating the likelihood and severity of autism in children, according to a study published in Molecular Psychiatry.
The team...
To improve breast cancer risk assessment, providers should perform genetic testing in women who aren’t at high risk of developing the disease, according to a study published in The New England...
A gene variant found in approximately one in 300 people is a significant genetic risk factor for stroke in older adults, according to a study conducted by researchers at Geisinger.
Cerebral small...
