Advances in Clinical Genomics Profiling
After Prenatal Screening Study Picks up Cancer Risk Variants, Researchers Want Clearer Guidelines
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Researchers seek more guidance on handling cancer risk variants detected in prenatal screening after nearly 5 percent of specimens in a study had such variants.
Bipolar Funding Consortium Aims to Unravel Disorder's Genetics, Reduce Healthcare Disparities
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The ambitious set of projects funded by BD² aims to improve our understanding of bipolar disorder and inform care across the entire spectrum of research and clinical practice.
Exome sequencing of more than 17,000 men with prostate cancer identified known and novel gene variants linked to risk of aggressive disease.
Breast Cancer Risk Genes Unearthed in Exome Sequence Meta-Analysis
Researchers tracked down a handful of previously unappreciated susceptibility genes using exome sequences for more than 244,000 European women with or without breast cancer.
In a report, healthcare experts underscored the clinical and economic benefits of NGS testing for lung cancer patients and recommended much-needed policy changes.