OOIR: Observatory of International Research

Papers

(The median citation count of Hemoglobin is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-04-01 to 2026-04-01.)

Article	Citations
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation	20
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage	20
Identification of a New δ chain hemoglobin Variant, Hb A2-Malay [δ46(CD5)Gly > Arg, HBD : C.139G > C;316-443A > G]	15
Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia	13
A Novel 5 kb Deletion in theβ-Globin Gene Cluster Identified in a Chinese Patient	10
Strong Positive Dichlorophenolindophenol Precipitation Suggests Hb Dhonburi (or Hb Neapolis) (HBB: c.380T>G) Inheritance in a Couple at Risk for Severe β-Thalassemia	9
Morbidity and Mortality Associated with COVID-19 and Acute Chest Syndrome in Sickle Cell Disease Patients	8
ATG-Thymoglobulin Versus ATG-Fresenius for Conditioning in Thalassemia Patients Who Underwent Allogenic Stem Cell Transplantation from Matched-Sibling Donor: A Tertiary Cancer Care Center Short-Term E	7
A Cross-Sectional Study on Pain and Quality of Life of Adult Patients with Transfusion-Dependent Thalassemia in a Tertiary Hospital In Malaysia	6
A New Case of Hb Headington (HBB: c.217A>C) Due to a New DNA Transversion, Found in a Patient with Type 2 Diabetes Mellitus	6
The First Iranian Case of Unstable Hemoglobin Santa Ana	6
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype	6
Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β ⁰ -Thalassemia	6
Identification of Sickle Cell Disease and Its Associated Other Structural Variants of Hemoglobin Using High Performance Liquid Chromatography and Their Clinical Profiling	6
Coexistence of Mycoplasma Pneumonia and Pulmonary Embolism as a Cause of Acute Chest Syndrome in a Child with Sickle Cell Disease	5
A Triple-Heterozygous β-Thalassemia Patient Demonstrated an Unusual Electrophoresis Pattern Due to a Novel β⁰ Mutation [an IVS-II-654 (C>T) mutation with a Hb Zürich-Langstrasse (HBB<	5
Submitting Novel Globin Gene Variants to Hemoglobin	5
A novel α Globin Gene Cluster Duplication, αααα³⁸⁰ Heterozygous β⁰-Thal Variant, Leading to a Blood Transfusion-Dependent Phenotype	5
Gene Therapies for Hemoglobinopathies: Promises and Challenges	4
Identification of a β-Globin Gene Mutation with the Genotype β-28(A > G), IVS-I-5(G > A)/βCD 71/72(+A) Using Third-Generation Sequencing	4
Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional Study	4
Evaluation of the Function of a Rare Variant in the 3'-Untranslated Region of the β-Globin Gene	4
Comparison of Sickle Solubility Test with Mass Spectrometry for Hemoglobin S Confirmation	4
Effect of Hydroxyurea Therapy on Growth Parameters in Older Children (6-15 Year-Old) with Sickle Cell Disease: Low Dose Versus High Dose	4
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China	4

Two Novel δ-Globin Chain Variants Identified in the Chinese Population	4
Research Progress of Cell-Free Fetal DNA in Non-Invasive Prenatal Diagnosis of Thalassemia	4
A Review of Gene Therapies for Hemoglobinopathies	4
A 6-Year Follow-up of a Chinese Child with Homozygous β ⁰ -Thalaasemia and a Heterozygous KLF1 Mutation	4
Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)	3
The Risk of Rapid Deterioration of Sepsis in the Patient with Non-Transfusion-Dependent Thalassemia: A Case Report	3
Rapid Identification of β-Thalassemia, Hb E, and High Hb F Determinants Using a High-Resolution Melting Analysis: Application in Prenatal Diagnosis in Southern Thailand	3
A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T > C β 68(E12) Leu-Pro]: A First Report in the Chinese Population	3
Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the Gambia	3
The Impact of Region-of-Interest Selection on MRI T ₂ * Quantification of Hepatic Iron Overload in Thalassemia Major	3
A Hemoglobin Variant, Resulting from a Novel Missense Mutation [CD 112(G14) Cys > Ser (TGT > TCT); HBB : C.338G > C], Was Discovered by MALDI-TOF MS	3
Identification of a Rare β-Globin Chain Hemoglobin Variant: HBB : C.24G > C (Glu7Asp)	3
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg, HBD : C.139G > A]	2
Adherence to Iron Chelation Therapy Among Children with Beta Thalassemia Major: A Multicenter Cross-Sectional Study	2
Current Status of β-Thalassemic Burden in India	2
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation	2
Comparative Analysis of Erythroferrone and Hepcidin as Emerging Biomarkers of Iron Homeostasis in Patients with β-Thalassemia Major: A Case-Control Study from Pakistan	2
Difficult Cases in the Diagnosis of Thalassemia Syndromes	2
Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25	2
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning Methods	2
Polyneuropathy Associated with Age of Starting the Transfusion and Serum Ferritin Level in Iranian Patients with Thalassemia Major and Intermedia	2
The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran	2
The Most Common Types of 3.7 Kilobase Deletion in the Iranian Population	2
Prevalence and Spectrum of β-Thalassemia Mutations in Baghdad, Iraq: Data from the Premarital Screening Program	2
Identification of a Novel Mutation in the 3′ Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family	2
Alpha Thalassemia Major: From a Lethal to a Treatable Condition	2
Misdiagnosis of α-Thalassemia Heterozygotes as Homozygotes Due to Base Mutations in the Primer Binding Region	2
Genetically Confirmed Dual Hematologic Disorder: A Case of β-Thalassemia with Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient	2
Hb Huadu [α124(H7)Ser→Thr (TCC>ACC), HBA2: c.373T>A]: A Novel Variant of the α-Globin Gene	2
Hypercoagulability in Sickle Cell Disease: A Thrombo-Inflammatory Mechanism	2
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb Rush	2
High Prevalence of Hb Riccarton Challenges HbA1c Analysis in a Danish Clinical Laboratory Using the Tosoh G11	2
Therapeutic Response to Hydroxyurea in Beta-Thalassemia Intermedia with Rare Mutation: A Case Report	2
Premarital Screening is Pivotal in Reducing the Births of Babies Affected with Thalassemia Major in Iraq	2
Fist Detection of Hb Suqian[β42(CD1) Phe→Leu, HBB:c.129T > A] in Han Chinese	2
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening Program	1
Haplotype-Specific Genetic Epidemiology of Sickle Cell Anemia Patients in Accra, Ghana: Patterns, Clinical Implications, and Public Health Responses	1
Detection of Hb Yulin [β13(A10)Ala→Val, HBB: c.41C>T] by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry	1
A Novel Frameshift Mutation( HBA2 :C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	1
Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas	1
Hb Yongning [β1 (NA1) Val→Leu; HBB :C.4G > C]: A Novel Hemoglobin Variant Causing Significant Interference in Common Glycated Hemoglobin Assays	1
Knowledge of Sickle Cell Disease, Awareness of Sickle Cell Trait Status and Its Impact on Relationships Among Students at a Historically Black College	1
Kinetic Characterisation of the R and R2 Quaternary Structures of Oxyhemoglobins Arising from Different Effects of Inositol Hexakisphosphate on Their Reactions with Ellman’s Reagent	1
A Novel β-Globin Variant, Hb Odder [ HBB : C.316C > G; CD105 (Leu > Val)]	1
Silent Cerebral Infarcts in Iraqi Patients with Sickle Cell Disease	1
Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child	1
A Rare Hemoglobin Variant Detected for the First Time in Türkiye (Hb Iraq-Halabja): Evaluation of the Effect of Variant Hemoglobins on HbA1c Methods	1
Rare Case of Homozygosity for CYB5R3 Variant c.235C > T p.(Arg79Trp) Causing Type II Methemoglobinemia	1
Implementation of a Dedicated Hematopoietic Stem Cell Transplant Program for Sickle Cell Disease in Lagos, Nigeria: Challenges and Opportunities	1
Sickle Cell Disease in Brazil: Current Management	1

The First Compound Heterozygosity for Two Different α-Thalassemia Determinants Causes Hb Bart’s Hydrops Fetalis in a Chinese Family	1
Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]	1
Existing Tubular Injury in β-Thalassemia Major Patients Receiving Iron Chelating Agents with Normal Creatinine Level in East Java, Indonesia	1
A Rare Severe Hemolytic Crisis in Homozygous Hemoglobin E (HbEE)	1
Poor Sleep Quality in Jamaican Adults With Sickle Cell Disease: Prevalence, Risk Factors, and Association With Quality of Life	1
The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (-- ^CR ) Type Deletion with Hb Constant Spring	1
Hb A ₂ -Getafe [δ 132 (H10) Lys > Thr, HBD : c.88C > A]: New Mutation in the δ-Globin Gene in a Spanish Patient	1
Diagnostic Dilemma of Hemoglobinopathies Using High Performance Liquid Chromatography Alone: A Case Report from a Resource-Constrained Setting	1
Pyruvate Kinase Activators for Sickle Cell Disease: An Exploratory Systematic Review and Meta-Analysis	1
The Effect of Single Nucleotide Polymorphisms on Clinical Phenotypes of Sabahan Transfusion-Dependent β-Thalassemia Patients with Homozygous Filipino β ⁰ -Deletion	1
Mild Thalassemic Effect of Heterozygous Hb Sogn in a Large Cohort from Routine Hemoglobinopathy Investigation	1
β ⁰ -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]	1
Hereditary Hemolytic Anemia Due to PIEZO1 Red Blood Cell Membrane Defect	1
KLF1 Knockdown Differentially Regulates γ-Globin Expression: Inhibition in K562 Cells but Reactivation in β-Thalassemia Major Erythrocytes with Erythropoiesis Disruption	1
Identification of a Novel Variant c.163delG in HBB Gene Resulting in a Beta Null Phenotype in a Proband with Thalassemia Intermedia	1
Perspectives of General Hematologists on a Proposed Shared Care Model for HSCT in Sickle Cell Disease	1
HbH Disease in an Elderly Man Due to Compound Heterozygosity for Deletional α-Thalassemia and Hb Dubai ( HBA2 :c.368A > T)	1
Encouraging Outcomes of Hematopoeitic Stem Cell Transplantation in Pediatric Sickle Cell Disease- A Decade-Long Experience from the Developing World	1
A New Hemoglobin Variant: Hb Tangshan [ HBA1 : c.239C > T, CD79(GCG > GTG)(Ala > Val)] Detected by MALDI-TOF MS	1
Rare Coexistence of Hemoglobin D-Iran and Hemoglobin S in a Case from Central India	1
Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload	1
Phenotypic Analysis of the HBA2 : C.95 G > A Mutation in China	1
Hypersplenism Affects Growth and Haematology in HbSS: Observations from the Jamaican Birth Cohort	1
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation	1
β-Thalassemia Trait Caused by a SUPT5H Defect: First Report of an Intragenic Deletion	1
Prevalence and Molecular Characteristics of Hemoglobin Variants in Laibin City, Central Guangxi of Southern China	1
Sociodemographic and Clinical Factors Predictive of Poor Health-Related Quality of Life of Children with Sickle Cell Anemia in The Gambia	1
Ameliorating Mental Health Issues in Sickle Cell Disease Patients: A Viewpoint	1
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing	1
A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient	1
Diagnosis and Treatment of Alpha Thalassemia Major	1
Hb Laibin [β96(FG3)Leu→Arg; HBB: c.290T>G]: A Novel Hemoglobin Variant Described in a Chinese Family	1
Long-Term and Transient Calcium Channel Blockers; A Systematic Review of Their Role in the Management of Cardiomyopathy in Transfusion-Dependent Thalassemia	1
Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report	1
Estimating the Cost of Thalassemia Care across the World: A Thalassemia International Federation Model	1
Risk Factors for Anemia in Silent Carrier or Minor α-Thalassemia	1
Sickling Disorder Caused by Co-Inheritance of Hemoglobin Maputo and Hemoglobin S: Case Report and Review of the Literature	1
Prevalence and Molecular Characterization of β-Thalassemia in Kirkuk Province of Northern Iraq	1
Hb A ₂ -Pontedera [δ93(F9) Cys > Trp; HBD : C.282T > G]: A New δ-Globin Chain Variant Detected by Screening Tests for Hemoglobin	1
When Unstable Hemoglobin Lansing Interacts with Alpha Thalassemia Along with HbS : An Interesting Case with Unique Clinical Presentation	0
Hb A ₂ -Guangxi [δ79 (EF3) Asp→Asn, HBD : C.238G > A] and polyA + 70 ( HBD : C.*200G > A): Two No	0
Treatment Status and Quality-of-Life Assessment of Transfusion-Dependent Thalassemia Managed with Standard-of-Care or Hematopoietic Stem Cell Transplantation in Southern Jiangxi, China: A Cross-Sectio	0
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease	0
Two Novel α-Thalassemia Mutations CD 39 -C [Thr > Pro] and CD 109 ACC > CCC [Thr > Pro] Identified in Two Chinese Families: A Case Report	0
Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation ( HBB :	0
First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation ( HBA2 c.244delT) in a Chinese Family	0
A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn	0
Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary Electrophoresis	0
Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr)	0
Mutation Spectrum of β-Thalassemia in Some Ethnic Groups of North Maharashtra, India	0
CRISPR in Thalassemia: Global Research Trend Analysis	0
Hb Bart’s Disease Due to Uniparental Disomy for Chromosome 16: The Need for Clinical Vigilance in Hydropic Fetuses with Only One Parent Carrying α ⁰	0
Second Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Thalassemia Major after Graft Rejection	0
A Diverse Genetic Landscape: Thalassemia Genotype Patterns in Myanmar and Cambodian Workers in Southern Thailand	0
First Case of Hb City of Hope ( HBB : c.208G > A) in Andalusia. A Molecular Update of β-Thalassemia in Southwestern Spain (Huelva Province)	0
Hereditary Persistence of Fetal Hemoglobin (HPFH): Detection of Unknow ^A γ-Globin Promoter Mutation at the C2H2 Zinc Finger Transcription Factors Binding Sites	0
A Retrospective Study of Unmet Blood Transfusion Needs and Status of Iron Overload in 190 Transfusion-Dependent Thalassemia Patients from Southern China	0
Hemoglobin Oviedo ( c.115A > G; p.T39A ): A Cause of Low Oxygen Saturation	0
β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report	0
Neurological Complications in Sickle Cell Disease: Clinical, Analytical and Radiological Correlations in a Multicentre Cohort	0
Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq	0
Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions	0
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)	0
Misdiagnosis of β-Thalassemia Major Due to Chinese ^G γ+( ^A γδβ) ⁰ -Thalassemia Combined with β	0
Heterozygous Beta Thalassemia with Segmental Duplication of chr16p13.3 Leading to Thalassemia Intermedia Phenotype: A Report of 2 Cases with Review of Literature	0
Anemia in Sri Lanka: A Literature Review	0
Effect of α⁺ Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study	0
Hb Hebei [α20 (B1) His→Leu; HBA2 :C.62A > T]: A Novel Hemoglobin Variant Found during Measurement of Glycated Hemoglobin	0
Hb Mizuho Case Report; Early Genomic Testing Facilitates a Life Changing Diagnosis	0
The Validation of Whole β-Globin Gene Sequencing for Detecting β-Thalassemia Mutations Found in Thailand Using Next-Generation Sequencing (NGS)	0
Editorial	0
Characterization of HbH Disease Caused by Compound Heterozygotes α ⁺ -Thalassemia 3.7 kb Deletion and a Large Novel α ⁰ -Thalassem	0
Association of Micro RNA-155 with Alloimmunization in Transfusion-Dependent Thalassemia Patients	0
Hepatobiliary Manifestations in Thalassemia Patients: A Narrative Review	0
Dysregulated Serum Cytokine Production in Pediatric Patients with β-Thalassemia Major	0
Matched Unrelated Donor (MUD) Transplants Show Promising Outcomes in Thalassemia Patients Aged ≤ 12 Years	0
Alterations in Serum MAO Activity and Tau Levels in β-Thalassemia	0
Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations	0
Prevalence and Associated Factors of Zinc and Vitamin D Deficiencies in Pediatric and Young Adult Patients with Non-Transfusion-Dependent Thalassemia	0
Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D HBA1 : C.119_121delCCA Mutation and	0

α ⁰ -Thalassemia Caused by a Novel α-Globin Gene Cluster Deletion (– ^LB ) Found in a Chinese Family	0
Analysis of Mean Corpuscular Volume and Red Cell Distribution Width in Patients with Aplastic Anemia	0
Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for β-Thalassemia and Sicilian (δβ)⁰-Thalassemia	0
Genotypic Characterization of Thalassemia in Huadu District, Guangzhou, China: A Single-Center Retrospective Study	0
Clinical Implications of HbD-Punjab and HbS co-Inheritance – A Rare Case in South India	0
Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China	0
Influence of Hemoglobin Strasbourg, a Rare High Oxygen Affinity Hemoglobin Variant, on Different Methods of HbA1c Measurement	0
Characterization and Confirmation of Mildly Unstable Hb Pontoise or α1 63(E12) Ala > Asp and Literature Review	0
Identification of a Patient with Transfusion-Dependent β-Thalassemia Caused by Compound Heterozygous Mutations of HBB : C.84_85insC and Common Linked Int	0
Distinguishing the R2 from the R Quaternary Structure of Hemoglobin: Role of the Tertiary Structure Transition Involving the 93β Sulfhydryl Group	0
Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del ( ^A γδβ) ⁰ -Thalassemia, and Thai del-	0
Hemoglobin Dieppe ( HBB:c. 383A > G ): A Rare Dominant β-Thalassemia in an Iraqi Kurdish Family	0
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?	0
Genotype-Phenotype Study of β-Thalassemia Patients in Sabah	0
Characterization of Hemoglobin Malay Phenotypes in Tertiary Hospitals	0
Vitamin B12 Deficiency Does Not Induce Homocysteine Increase in Transfusion-Dependent β-Thalassemia Major Patients Receiving Folic Acid Supplementation	0
De Novo Occurrence of Hb Chile [β28(B10) Leu→Met] in a Korean Boy with Methemoglobinemia	0
Genetic Variants Associated with the Risk of Stroke in Sickle Cell Anemia: Systematic Review and Meta-Analysis	0
First Case in Portugal of a Rare Hemoglobin Variant – Hb Montfermeil: Importance of Laboratory Diagnosis	0
Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life	0
Evaluation of the Neuropathic Component of Pain in Sickle Cell Disease	0
Malaria Infection in Patients with Sickle Cell Disease in Nigeria: Association with Markers of Hyposplenism	0
The Prevalence of Obstructive Sleep Apnea and Associated Symptoms among Patients with Sickle Cell Disease: A Systematic Review and Meta-analysis	0
Identification of a Novel 7-bp Deletion in the α-Globin Gene Cluster in One Chinese Family	0
Long-Term Survival Rates of a Sickle Cell Disease Cohort in Saudi Arabia: A 2009–2023 Observational Study	0
Dynamic Thiol-Disulfide Homeostasis in Children With β-Thalassemia Trait	0
Alloimmunization in β-Thalassemia and Sickle Cell Disease in Middle Eastern Countries: A Systemic Review	0
Molecular Diagnosis and Stability Testing of Hemoglobin Phnom Penh [ HBA1 : C.353_355dup (p.Phe118_Thr119insIle)] – The First Northern Thai Case	0
Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster	0
Venous Thromboembolism in Individuals with Sickle Cell Disease: A Narrative Review	0
Death from S. pneumoniae in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?	0
Elevated Plasma Atherogenic and Triglyceride-Glucose Indices: Markers of Cardiovascular Risk in Transfusion-Dependent Thalassemia	0
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease	0
Analysis of Iron Status in Sickle Cell Disease Patients During Steady State at the Center de Recherche et de Lutte contre la Drépanocytose (CRLD) Bamako	0
Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report	0
A Population-Oriented Genetic Scoring System to Predict Phenotype: A Pathway to Personalized Medicine in Iraqis With β-Thalassemia	0
A Novel Large Deletion Including the Major Regulatory Element Compounded with SEA Deletion Causing Hydrops-Fetalis-Syndrome	0
Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials	0
α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh	0
Evaluating Renal Glomerular Function in Beta-Thalassemia Patients Receiving Deferasirox Using Serum Cystatin-C and Creatinine: A Cross-Sectional Study	0
Treatment with Hydroxyurea Leads to Fetal Hemoglobin Reactivation through CA1 and LIN28B Genes: An In Vitro Study	0
Predicting the Double Heterozygotes of HbE and α-Thalassemia-1 (Southeast Asian Type) Using RapidMiner -Generated Hematologic Algorithm	0
Educational Bias in Cognitive Screening of Adults with Sickle Cell Disease: A Bilingual Multisite Observational Study	0
Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports	0
Unraveling Hemoglobin D’s Influence: A Comprehensive Analysis of Clinicopathological Parameters in Hemoglobin D Patients	0
First Report of an α Chain Variant [Hb Coombe Park (HBA2: c.382A>G)] from India, Coinherited with a Novel SERPINC1 Gene Mutation: A Double Whammy?	0
Identification of Three Families Carrying Hb Anti-Lepore Hong Kong Variant in Guangxi, China, and Analysis of Their Hematological Data	0
Update on Prevention of Hemoglobinopathies in Azerbaijan	0
A Novel β-Globin Variant, Hb Raklev [β 75(E19) HBB :c.227T > A (Leu→Gln)]	0
Investigation of the Distribution of Thalassemia in Children in Jiangxi Province, the People’s Republic of China	0
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature Review	0
A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [β7(A4)Glu→Lys; HBB: c.22G>A] and Hb H Disease	0
First Report of Filipino β ⁰ -Thalassemia/β-Thalassemia in a Chinese Family	0
Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing	0
Factors Associated with Overt Stroke in Children and Adolescents with Sickle Cell Disease: A Retrospective Cohort Study	0
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease	0
COVID-19 and Anemia: What Do We Know So Far?	0
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of α-Thalassemia: A Perspective of the National Reference Laboratory	0
Secretory Phospholipase A2 Levels Are High in Women with Sickle Cell Disease and Menstruation-Induced Vaso-Occlusive Crises	0
Prevalence and Diagnostic Prediction of Hemoglobin Variants in Neonates: A Study from Two Indian Hospitals Using Capillary Electrophoresis and Molecular Sequencing	0
Use of Capillary Electrophoresis Migration Position for the Presumptive Identification of Hemoglobin Variants Prevalent in China	0
Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country	0
HBA2 : C.4delG: A Novel Frameshift Mutation Causing α ⁺ -Thalassemia Found in a Chinese Family	0
Detection of Common α-Hemoglobin Variants in Thailand by Using Real-Time PCR with High Resolution Melting Analysis	0
Novel Double Heterozygosity: HBA2 : c.70G > A (Hb Chad)/ HBB : c.-78A > G and Novel Compound Heterozygosity: HBA2	0
Targeted Next-Generation Sequencing Reveals a Large Novel β-Thalassemia Deletion that Removes the Entire HBB Gene	0
Knowledge and Attitude toward Hemoglobinopathies in Premarital Screening Program among the General Population in the Western Region of Saudi Arabia	0
Two Novel SUPT5H Variants Causing β-Thalassemia Trait Phenotypes	0
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?	0
The Aplastic Crisis in HbSS: Observations from the Jamaican Birth Cohort	0
Genetic Analysis and Clinical Relevance of *HBA1* :c.305T > C (Leu > Pro): A Novel Variant Linked	0
Case Fatality Rate and Severity of COVID-19 among Patients with Sickle Cell Disease: A Systematic Review and Meta-Analysis	0
Therapeutic Plasma Exchange as a Rescue Therapy in Sickle Cell Disease-Associated Fat Embolism Syndrome: Case Series and Literature Review	0
Evaluating Health-Related Quality of Life in Thalassemia: Low-Dose Thalidomide vs. Standard Care—Insights from a Comparative Study	0
Adherence to Iron Chelation Therapy among Adults with Thalassemia: A Systematic Review	0
An HBB Intron 1 Variant (c.92 + 9C > T) Suggestive of β-Thalassemia Trait	0
A Novel Frameshift Mutation of HBB Causing Dominant β-Thalassemia in a Chinese Individual	0
An Expert Overview on Therapies in Non-Transfusion-Dependent Thalassemia: Classical to Cutting Edge in Treatment	0
Prevalence of Hemoglobinopathies in Premarital Screening in the Province of Nigde, Turkey	0
Mutation Spectrum of β-Globin Gene in Patients with β-Thalassemia at Tidar Hospital, Magelang, Central Java, Indonesia	0
Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam	0
Unusual Causes of β Thalassemia Trait: Discovery of another Three Novel SUPT5H Variants	0
Molecular Characterization of Complex Thalassemia with Multiple Variants in β-Globin Gene Cluster and the Identification of a Novel Structural Rearrangement in γ-Globin Gene	0
The Spectrum of α-Thalassemia Mutations in Syrian Patients	0
Prevalence, Severity, and Determinants of Pain in Thalassemia	0
Thalassaemia Registries: A Call for Action. A Position Statement from the Thalassaemia International Federation	0
Hemoglobin Balkh, a Novel Mutation in Codon 132 of α2-Globin Gene [α132(H15) (+T) or HBA2 :C.396dup (p.Val134fs)]: A Case Report and Insight into the Pathophysiology	0
A New α1-Globin Variant, Hb Ormylia [ HBA1 :c.63C > G; p.His21Gln]. Report of Eleven Cases in Northern Greece	0
Ethical and Clinical Considerations in the Use of Hydroxyurea in Pregnant Women with Sickle Cell Disease	0
Consideration of Splenectomy in Unstable Hemoglobinopathy: A Case Report of Hb Hammersmith (HBB: c.128T>C)	0