معرفی
Ieva Grīnfelde is an Acting Assistant in the Department of Biology and Microbiology at Riga Stradins University, actively contributing to genetic research with a focus on prenatal diagnosis, genetic disorders, and molecular biology. Her work spans clinical genetics, inherited metabolic diseases, and fetal anomaly research.
Her research interests center on genetic screening methodologies, prenatal diagnosis of chromosomal abnormalities, molecular genetics of inherited disorders, and exome sequencing applications. She has made significant contributions to understanding genetic variants causing structural fetal malformations, Danon disease, and various metabolic disorders through deep phenotyping and genotyping approaches.
Analysis of her publication trends shows a strong focus on applying advanced genetic testing methods to clinical problems, particularly in prenatal and pediatric settings. Her work spans from basic genetic analysis to direct clinical applications, with increasing emphasis on next-generation sequencing technologies and their implementation in Latvian healthcare.
- Characterisation of genetic variance induced fetal structural anomalies using deep-phenotyping and deep-genotyping (2020-2021)
- Characteristics of Genetic Variations Causing Structural Foetal Malformations (2019-2020)
Her research has practical applications in improving prenatal diagnosis and genetic counseling in Latvia, with media appearances discussing how assisted reproduction methods can prevent transmission of genetic diseases to children.
