Elisavet Fotiou
Publications by Year
Research Areas
Congenital heart defects research, Congenital Heart Disease Studies, Genomics and Rare Diseases, Blood properties and coagulation, Erythrocyte Function and Pathophysiology
Most-Cited Works
- → Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis(2015)316 cited
- → Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot(2019)193 cited
- → EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis(2016)103 cited
- → Using zebrafish larval models to study brain injury, locomotor and neuroinflammatory outcomes following intracerebral haemorrhage(2018)29 cited
- → Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease(2019)29 cited
- → Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability(2022)11 cited
- → Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis(2019)5 cited
- → Predicting congenital renal tract malformation genes using machine learning(2023)5 cited
- → 139 Identification of the major genetic contributors to tetralogy of fallot(2019)3 cited