Athina Ververi
Thessaloniki, ESYE12, Greece
Last Updated: 09/26/2026
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Found 45 publications
Abstracts of the 36th World Congress on Ultrasound in Obstetrics and Gynecology, 4-7 September 2026, London, UK.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: July 06, 2026
Obtaining a Diagnostic Yield via Scan findings prior to the introduction of SEquencing retrospectivelY (ODYSSEY): a cohort study.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: March 18, 2026
Pediatric hematuria as a gateway to family genetic investigation in type IV collagen nephropathies: experience from a regional cohort.
Journal: Journal of nephrology
Published: January 27, 2026
Introducing whole genome sequencing in newborn screening in Greece: ethical, clinical, and policy considerations in the European context.
Journal: European journal of human genetics : EJHG
Published: December 03, 2025
When Genes Reveal the Truth: Alport Syndrome Mimicking Steroid-Resistant Nephrotic Syndrome.
Journal: Pediatric reports
Published: November 18, 2025
Gillespie Syndrome: Greek Patient with Novel Mutation and Atypical Presentation - Expansion of the Phenotype and Literature Review.
Journal: Molecular syndromology
Published: October 06, 2025
Human Breast Milk miRNAs: Investigation of Association Between Breastfeeding Children and Maternal Obesity in Obesity Development in Offspring.
Journal: Genes
Published: September 15, 2025
Broadening the inherited ASXL3 spectrum and unveiling molecular mechanisms through detailed genotypic-phenotypic analyses.
Journal: Genetics in medicine open
Published: July 29, 2025
Three-generation familial transmission of a GNAS variant: from gestational phenotype in the mother to evolving prenatal/neonatal phenotype in the offspring.
Journal: Hormones (Athens, Greece)
Published: June 19, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations.
Journal: American journal of medical genetics. Part A
Published: April 28, 2025
Partial loss of FITM2 function causes hereditary spastic paraplegia.
Journal: medRxiv : the preprint server for health sciences
Published: February 20, 2025
Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta-analysis.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: October 24, 2024
Last Updated: 09/26/2026