معرفی
Zane Dobele is a researcher at Riga Stradins University, Latvia, actively contributing to medical genetics through publications and collaborative projects. His work focuses on identifying genetic variations linked to diseases across oncology, endocrinology, and cardiology.
His research spans Medical Genetics, Molecular Genetics, Genomics, Oncology, Endocrinology, and Reproductive Medicine. Key emphases include genetic polymorphisms in chronic lymphocytic leukemia, polycystic ovary syndrome, and cardiac disorders like arrhythmogenic right ventricular cardiomyopathy, utilizing techniques such as exome sequencing and somatic variant detection.
Analysis of his 2016-2021 publications reveals consistent focus on characterizing single-nucleotide polymorphisms, indels, and structural variants in patient populations. His work bridges genetic discovery with clinical applications for improved diagnosis and prognosis, particularly in cancer genomics and reproductive medicine.
Dobele participated in the RSU-funded project "Characteristics of Genetic Variations Causing Structural Foetal Malformations, Using Deep Phenotyping and Genotyping" (2019-2020), employing exome sequencing to investigate prenatal genetic conditions. He also engaged in collaborative activities like the 2020 conference on genetic variation classification in next-generation sequencing.
