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Top News In Genetic Algorithm Today - Breaking & Trending Today

BGI Genomics report uncovers knowledge gaps and barriers to thalassemia screening

According to Thailand's Ministry of Public Health, approximately 18-24 million or 30-40 percent of the Thai population carries the thalassemia gene, with moderately severe thalassemia patients requiring regular treatment, including blood transfusion and chelation therapy to remove excess iron from the blood. ....

Saudi Arabia , Zhiyu Peng , Androulla Eleftheriou , Thailand Ministry Of Public Health , Thalassaemia International Federation , Public Health , Thalassemia Awareness , Thalassemia Awareness Report , Blood Transfusion , Chelation Therapy , Public Health ,

New report highlights urgent need to improve thalassemia awareness among Azerbaijan women

5.2% of the global population carry hemoglobin abnormalities, resulting in 300,000 to 400,000 children born with severe hemoglobinopathies annually. ....

Saudi Arabia , Androulla Eleftheriou , Zhiyu Peng , Thalassaemia International Federation , Middle East , Southeast Asia , Thalassemia Awareness , Thalassemia Awareness Report ,

"Christchurch mutation" can block detrimental effects of Alzheimer's risk factor

Researchers at Gladstone Institutes have discovered that a rare genetic variant known as the "Christchurch mutation" can block detrimental effects of apolipoprotein E4, the best-established risk factor for the most common form of Alzheimer's disease. ....

New Zealand , Maxine Nelson , Robert Mahley , Yadong Huang , Gladstone Institutes , Gladstone Investigator Yadong Huang , Translational Advancement , Gladstone Investigator Robert Mahley , Lzheimer 39s Disease , Tau Protein ,

5 things Canadians should know about inherited retinal diseases

Protecting our eye health is an important part of overall health. Whether you re going for a comprehensive eye exam, limiting your phone or compute. ....

Joel Staveley Getty , Edward Jenner , Retinal Disease , Inherited Retinal , Joel Staveley ,

Australian study shows combined genomic screening for major hereditary diseases is cost-effective and health-saving

In an Australian study published in EClinicalMedicine, researchers evaluated the impact of a combined genomic screening program for hereditary breast and ovarian cancer, Lynch syndrome, and familial hypercholesterolemia in young adults. The program proved to be cost-effective, reducing healthcare costs and averting numerous health events, while emphasizing the need for further optimization and equitable access within public healthcare systems. ....

Monte Carlo , Proprotein Convertase Subtilisin Kexin , Marina Litvinova Shutterstock , Save Share Reprints Request Combined , Figures Save Share Reprints Request Combined , Breast Cancer , Mutl Homolog , Muts Homolog , Low Density Lipoprotein Receptor , Proprotein Convertase , Kexin Type , Familial Hypercholesterolemia , Heart Disease , Lynch Syndrome , Ovarian Cancer , Public Health ,