Genetic variations linked to COVID-19 severity

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Genetic variations linked to COVID-19 severity   A new report by researchers from Thailand's Mahidol University and published on the preprint server medRxiv in May 2020 reports that the clinical severity of COVID-19 may be linked to the genetic makeup of the patient in addition to external factors.

Research project launched to find new treatments for rare genetic diseases   The University Carlos III Madrid, Almirall, S.A. and the MEDINA Foundation have launched a project to find new treatments for recessive dystrophic epidermolysis bullosa and other genetic diseases caused by nonsense mutations.         ADHD-associated genetic variants have reduced progressively in human lineage   According to a study published in the Scientific Reports journal, the frequency of genetic variants linked to attention-deficit/hyperactivity disorder (ADHD) has reduced progressively in the evolutionary human lineage from the Palaeolithic to the present day.

Genome rewiring could help explain evolution of multi-cellular organisms   InsideOutBio expert Dr Alan Herbert has explained a pioneering research in a paper recently published online by the Royal Society Open Science journal.       Gene expression may be a decisive factor for controlling possible comorbidities   A study concludes that the specific characteristics of each patient, such as gene expression, may be a decisive factor in the development of clinical strategies aimed at addressing and controlling possible comorbidities.       Researchers identify genetic codes of COVID-19 and SARS viruses that may promote their lifecycles   Researchers have identified specific portions of the genetic codes of the COVID-19 and SARS viruses that may promote the viruses' lifecycles. The new technique is researchers' first tool for determining what genetic sequences stored as RNA are more stable.       Genetic studies analyze genome-wide set of genetic variants in different individuals   Genome-wide association studies (GWAS) analyze a genome-wide set of genetic variants in different individuals to see if any are associated with a trait or disease.

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