Joanne Synodinos-Traeger

Athens, ESYE31, Greece

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 78 publications

Cardiomyopathy in an Adolescent with McLeod Syndrome: Searching Beyond the Routine Assessment.

Cardiomyopathy in an Adolescent with McLeod Syndrome: Searching Beyond the Routine Assessment.

Journal: Advances in experimental medicine and biology

Published: January 01, 2026

Mapping diagnostic practices in hemoglobinopathies: a cross-country HELIOS COST Action study.

Mapping diagnostic practices in hemoglobinopathies: a cross-country HELIOS COST Action study.

Journal: Blood advances

Published: November 13, 2025

Assessing concordance of genetic parameters between trophectoderm and inner cell mass in morphologically scored day-5 embryos via NGS.

Assessing concordance of genetic parameters between trophectoderm and inner cell mass in morphologically scored day-5 embryos via NGS.

Journal: Reproduction & fertility

Published: October 03, 2025

ASSESSING CONCORDANCE OF GENETIC PARAMETERS BETWEEN TROPHECTODERM AND INNER CELL MASS IN MORPHOLOGICALLY SCORED DAY-5 EMBRYOS VIA NGS.

ASSESSING CONCORDANCE OF GENETIC PARAMETERS BETWEEN TROPHECTODERM AND INNER CELL MASS IN MORPHOLOGICALLY SCORED DAY-5 EMBRYOS VIA NGS.

Journal: Reproduction & fertility

Published: October 03, 2025

Insights into Fanconi Anemia Based on Molecular and Clinical Characteristics: A Multicentre Study of 13 Patients.

Insights into Fanconi Anemia Based on Molecular and Clinical Characteristics: A Multicentre Study of 13 Patients.

Journal: Children (Basel, Switzerland)

Published: May 22, 2025

Reproductive Choices in Haemoglobinopathies: The Role of Preimplantation Genetic Testing.

Reproductive Choices in Haemoglobinopathies: The Role of Preimplantation Genetic Testing.

Journal: Genes

Published: January 31, 2025

Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family.

Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family.

Journal: American journal of ophthalmology

Published: September 07, 2024

The current clinical applications of preimplantation genetic testing (PGT): acknowledging the limitations of biology and technology.

The current clinical applications of preimplantation genetic testing (PGT): acknowledging the limitations of biology and technology.

Journal: Expert review of molecular diagnostics

Published: August 07, 2024

Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children.

Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children.

Journal: Genes

Published: July 08, 2024

Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia.

Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia.

Journal: International journal of molecular sciences

Published: July 04, 2024

ENaC gene variants and their involvement in Covid‑19 severity.

ENaC gene variants and their involvement in Covid‑19 severity.

Journal: Biomedical reports

Published: April 19, 2024

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion.

Nablus mask-like facial syndrome: Report of an atypical case with 8q21.3-q22.1 deletion.

Journal: American journal of medical genetics. Part A

Published: April 18, 2024

Showing 1-12 of 78

Last Updated: 09/26/2026