Angeliki Balassopoulou

Laiko General Hospital of Athens — Greece

Medicine · Health Sciences

11h-index533citations22works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(10), Cystic Fibrosis Research Advances(10), Neonatal Respiratory Health Research(8), Iron Metabolism and Disorders(7), Tracheal and airway disorders(5)

Publications22 total

Hb Thessaloniki, a Novel, Hyperunstable, Alpha Globin Variant Detected in Northern Greece
Hematology Reports·2026Open Access
PB2240: SILENT GLOBIN MUTATIONS. 10 YEARS REFERRALS FOR GENETIC COUNSELING.
HemaSphere·2022Open Access
Rare Pathogenic β<sup>0</sup>-Thalassemia Mutation, Codon 7 (<i>G</i>AG&gt;<i>T</i>AG) (<i>HBB</i>: c.22G&gt;T). Report of the First Two Cases in Albanian Immigrants of Northern Greece
Hemoglobin·2022
A New Hemoglobin Variant, Hb Natal (<i>HBA1</i>: c.423C&gt;A), Found in a Greek Family
Hemoglobin·2022· 2 cited
Droplet Digital PCR for Non-Invasive Prenatal Detection of Fetal Single-Gene Point Mutations in Maternal Plasma
International Journal of Molecular Sciences·2022· 29 citedOpen Access
First Report of a Coincidental Discovery of Hb Antibes-Juan-Les-Pins (<i>HBB</i>: c.349_350insGTGTGCTGGCCC) in a Greek Woman
Hemoglobin·2020
Coinheritance of Triplicated Alpha-Globin Gene and Beta-Thalassemia Mutations in Adulthood: Ten Years of Referrals in Northern Greece
Journal of Pediatric Hematology/Oncology·2020· 11 cited
Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor
Sensors and Actuators B Chemical·2019· 19 citedOpen Access
Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and Migrants
Hemoglobin·2018· 30 cited
Development of a High-Resolution Melting Approach for Scanning Beta Globin Gene Point Mutations in the Greek and Other Mediterranean Populations
PLoS ONE·2016· 7 citedOpen Access
Pregnancy in beta‐thalassemia intermedia: 20‐year experience of a Greek thalassemia center
European Journal Of Haematology·2014· 33 cited
Longitudinal Follow‐Up of Exocrine Pancreatic Function in Pancreatic Sufficient Cystic Fibrosis Patients Using the Fecal Elastase‐1 Test
Journal of Pediatric Gastroenterology and Nutrition·2003· 14 cited
Longitudinal Follow-Up of Exocrine Pancreatic Function in Pancreatic Sufficient Cystic Fibrosis Patients Using the Fecal Elastase-1 Test
Journal of Pediatric Gastroenterology and Nutrition·2003· 56 cited
A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q.
Journal of Medical Genetics·1998· 4 citedOpen Access
Double mutant alleles: are they rare?
Human Molecular Genetics·1995· 63 cited
A novel nonsense mutation identified in the first nucleotide binding fold of the CFTR gene in a Greek patient
Human Molecular Genetics·1994· 1 cited
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene
Human Genetics·1992· 79 cited
of the N1303K mutation of the cystic fibrosis (CFTR) gene
1992
Analysis of 14 cystic fibrosis mutations in five South European populations
Human Genetics·1991· 55 cited
Cystic fibrosis in Greece: Typing with DNA probes and identification of the common molecular defect
Human Genetics·1990· 11 cited
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Frequent Co-authors

Effrossyni Boutou(10), Ersi Voskaridou(6), Stamatia Theodoridou(5), Virginia Nunes(4), Paolo Gasparini(4), Xavier Estivill(4), Bruno Dallapiccola(4), Teresa Casals(4), Eleni Yfanti(4), Αikaterini Teli(4), Brigitte Simon‐Bouy(3), M. Schwartz(3), Milan Maçek(3), Giuseppe Novelli(3), Luba Kalaydjieva(3), P. F. Pignatti(3), Dora Angelicheva(3), A. Bonizzato(3), Dimitris Loukopoulos(3), Timoleon‐Achilleas Vyzantiadis(3)