हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।
ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं
Bob Bezlik
Type 2 diabetes is a widespread metabolic disorder influenced by a combination of genetic and environmental factors. Recent genetic research has led to significant discoveries regarding the genetic basis of type 2 diabetes and its risk assessment in diverse populations. Genome-wide association studies (GWAS) have identified specific genetic variants associated with increased or decreased risk of developing the disease. These variants are located in genes involved in various biological processes, such as insulin production and glucose metabolism. Ethnic diversity plays a crucial role in the genetic predisposition to type 2 diabetes, as certain variants exhibit variable frequencies and effects across populations. Rare genetic variants are also important, particularly in monogenic forms of the disease. Polygenic risk scores (PRS) have been developed to assess an individual’s overall genetic risk, incorporating information from multiple genetic variants associated with the disease. PRS can be utilized for personalized risk assessments and early identification of individuals at high risk. The genetic discoveries and risk assessment tools have implications for prevention, treatment, and personalized management of type 2 diabetes. Understanding the genetic basis of the disease aids in identifying therapeutic targets and guiding intervention strategies. Continued research, especially with diverse populations, will contribute to a comprehensive understanding of type 2 diabetes genetics and improve its management globally.