Two projects in which healthy individuals have had their genomes sequenced have revealed that searching for unanticipated genetic results in newborns and adults can unearth far more variants associated with diseases than ...
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In the largest genetic sequencing study of autism spectrum disorder (ASD) to date, researchers have identified 102 genes associated with ASD, and report significant progress toward teasing apart the genes associated with ...
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As anyone who has played "Where's Waldo" knows, searching for a single item in a landscape filled with a mélange of characters and objects can be a challenge. Chrissy O'Keefe, a Ph.D. student in the Department of Biomedical ...
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A study in Biological Psychiatry has established a new analytical method for investigating the complex genetic origins of mental illnesses using brain cells that are grown in a dish from human embryonic stem cells. Researchers ...
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When a young athlete suddenly dies of a heart attack, chances are high that they suffer from familial hypertrophic cardiomyopathy (HCM). Itis the most common genetic heart disease in the US and affects an estimated 1 in 500 ...
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The Deciphering Developmental Disorders (DDD) project aims to provide diagnoses for the families of around 13,600 children with severe undiagnosed developmental disorders. Launched eight years ago this month at the Wellcome ...
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In a study published in iScience, Professor Akiyoshi Fukamizu of the University of Tsukuba has reported the discovery of the important role of PRMT1 in dilated cardiomyopathy (DCM).
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Working with researchers from Stanford University and St. Anna Children's Cancer Research, researchers from Jürgen Pollheimer's laboratory at the Medical University of Vienna's Department of Obstetrics and Gynecology have ...
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A team from I.M. Sechenov First Moscow State Medical University, together with foreign colleagues, analyzed the genomes of several families that have members with ADHD. The results have shown that all patients had specific ...
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A genome bank for the Japanese population can better identify rare genetic variants and disease susceptibilities by adding samples from distant areas of the country.
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