Citation Impact
Citing Papers
The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis
2009 Standout
Alloimmunization in Sickle Cell Anemia and Transfusion of Racially Unmatched Blood
1990
The β-Thalassemias
1999 Standout
Down's syndrome: A pathology involving the lack of balance of reactive oxygen species
1988
Ursolic acid: An anti‐ and pro‐inflammatory triterpenoid
2008 Standout
Glucose-6-Phosphate Dehydrogenase Deficiency
1991
Additional red blood cell alloantibodies after blood transfusions in a nonhematologic alloimmunized patient cohort: is it time to take precautionary measures?
2006
Molecular Heterogeneity of the Glucose-6-Phosphate Dehydrogenase Deficiency in the Hellenic Population
2000
Evaluation of glucose-6-phosphate dehydrogenase activity in two different ethnic groups using a kit employing the haemoglobin normalization procedure
2003
A mouse model for Down syndrome exhibits learning and behaviour deficits
1995 Standout
Methemoglobinemia: Etiology, Pharmacology, and Clinical Management
1999 Standout
Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography
1998 Standout
Sickle-cell disease
2010 Standout
Bone disease in children with homozygous β-thalassemia
1990
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Antigen‐matched donor blood in the transfusion management of patients with sickle cell disease
1994
7 Increased HbF in adult life
1993
Role of Free Radicals in the Neurodegenerative Diseases
2001 Standout
Screening for glucose-6-phosphate dehydrogenase deficiency as a preventive measure: Prevalence among 1,286,000 Greek newborn infants
1991
Glucose-6-Phosphate Dehydrogenase Deficiency
2016
Neonatal Hyperbilirubinemia
2001 Standout
Superoxide Dismutases: Role in Redox Signaling, Vascular Function, and Diseases
2011 Standout
α‐Chain and Globin: Intermediates in the Synthesis of Rabbit Hemoglobin
1967
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
Predictive Ability of a Predischarge Hour-specific Serum Bilirubin for Subsequent Significant Hyperbilirubinemia in Healthy Term and Near-term Newborns
1999 Standout
Prevalence of Sickle-Cell Trait and Glucose-6-Phosphate Dehydrogenase Deficiency
1970
Fetal Hemoglobin Variants in Mice
1968 StandoutScienceNobel
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
Haemoglobin Miyada, a β—δ Fusion Peptide (Anti-Lepore) Type discovered in a Japanese Family
1971
Breastfeeding and the Use of Human Milk
2012 Standout
Human Haemoglobins
1965
Human DR (Ia-Like) Antigens: Biological and Molecular Profile
1978 StandoutNobel
Overproduction of human Cu/Zn-superoxide dismutase in transfected cells: extenuation of paraquat-mediated cytotoxicity and enhancement of lipid peroxidation.
1986
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
1997
Racial variability in the UDP-glucuronosyltransferase 1 ( UGT1A1 ) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
1998 Standout
Antibody Induction and Tolerance
1965 StandoutScienceNobel
Hemoglobins Lepore and Anti-Lepore
1978
Glucose-6-phosphate dehydrogenase deficiency
1994
[1] Role of free radicals and catalytic metal ions in human disease: An overview
1990 Standout
Does Hyperbilirubinemia Damage the Brain of Healthy Full-Term Infants?
1990
Serum Copper Is Decreased in Premature Newborns and Increased in Newborns with Hemolytic Jaundice
2004
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia.
1966
Transfusion-related mortality: the ongoing risks of allogeneic blood transfusion and the available strategies for their prevention
2009 Standout
The Concentration of Micronutrients and Heavy Metals in Maternal Serum, Placenta, and Cord Blood: A Cross-Sectional Study in Preterm Birth
2019 Standout
THE FUSION OF TWO PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION
1962
Exaggerated Jaundice in Navajo Neonates
1986
Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation
1994 StandoutScience
Sickle cell disease and stroke
2009
Gene duplication as the basis for amino acid ambiguity in the alpha-chain polypeptides of mouse hemoglobins.
1968
THE CONTROL OF GLOBIN SYNTHESIS IN RABBIT RETICULOCYTES *
1974 StandoutNobel
Human immunoglobulin subclasses. Partial amino acid sequence of the constant region of a γ4 chain
1970 StandoutNobel
Reduced oxygen species, mutation, induction and cancer initiation
1987
Thalassemia: The consequences of unbalanced hemoglobin synthesis
1966
Erythrocyte Enzymopathies in the Newborn
1981
The Kenya Form of Hereditary Persistence of Fetal Haemoglobin: Structural Studies and Evidence for Homogeneous Distribution of Haemoglobin F using Fluorescent Anti‐haemoglobin F Antibodies
1976
X-chromosome instability in pluripotential stem cell lines derived from parthenogenetic embryos
1983 StandoutNobel
Glucose-6-Phosphate Dehydrogenase Deficiency and Hyperbilirubinemia in the Newborn
1971
Studies on the activity of the X chromosomes in female teratocarcinoma cells in culture
1976
Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease
1990
Directed blood donor program decreases donor exposure for children with sickle cell disease requiring chronic transfusion
2012 StandoutNobel
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Genetic Control of Hemoglobin Synthesis
1963 Science
Severe Neonatal Hyperbilirubinemia: A Potential Complication of Glucose-6-Phosphate Dehydrogenase Deficiency
1998
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
2014 Standout
Free Radicals in the Physiological Control of Cell Function
2002 Standout
The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece.
1966
Lactic Dehydrogenase: Genetic Control in Man
1963 StandoutScienceNobel
Unexpected relationships between four large deletions in the human β-globin gene cluster
1983 StandoutNobel
cGMP-dependent protein kinase, a chimeric protein homologous with two separate protein families
1984 StandoutNobel
Control of haemoglobin synthesis: Rate of translation of the messenger RNA for the α and β chains
1969 StandoutNobel
Works of A Karaklis being referenced
A simple index for initiating transfusion treatment in thalassaemia intermedia
1987
RISK OF SEVERE JAUNDICE IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY OF THE NEWBORN
1964
Hemoglobin "Pylos": Study of a Hemoglobinopathy Resembling Thalassemia in the Heterozygous, Homozygous and Double Heterozygous State
1962
Incidence and Mechanism of Neonatal Jaundice Related to Glucose-6-Phosphate Dehydrogenase Deficiency
1969
Alloimmunization to Red Cell Antigens in Thalassemia:Comparative Study of Usual versus Better-Match TransfusionProgrammes
1987
The Normal Minor Components of Human Foetal Haemoglobin
1963
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks
1986
Alloimmunization to Red Cell Antigens in Thalassemia: Comparative Study of Usual versus Better‐Match Transfusion Programmes
1987
Red cell enzymes in trisomy 21.
1970