Latest Research in Hemoglobinopathies and Related Disorders

34 research papers · 2026 median publication year

Top Research Topics in Hemoglobinopathies and Related Disorders

Highest-Cited Papers

  1. A phase 4, open-label efficacy and safety study of methotrexate and monthly pegloticase co-administration in patients with uncontrolled gout
  2. Community-based approach for thalassemia patients: a perspective from Bangladesh
  3. Human platelet 5-hydroxyindoleacetic acid concentrations are meager and unlikely to be physiologically active or play a role in inflammation
  4. Cumulative Stress Measured by Allostatic Load is Associated with Vaso-Occlusive Episodes in Sickle Cell Disease
  5. Exploratory investigation of hemodialysis membrane–induced differential DNA methylation in patient blood
  6. Hidden crystals in the heart: A rare case of tophaceous aortic valve gout
  7. Gout: Contemporary Approaches to Diagnosis, Treatment, and Long-Term Management
  8. Gout: Contemporary Approaches to Diagnosis, Treatment, and Long-Term Management
  9. Comparison of hematological parameters in adults with and without jaundice
  10. Factors Contributing to Improved Bone Mineral Density in Patients With Transfusion‐Dependent Thalassemia
  11. Pancreatic iron overload as a marker of endocrine complications in transfusion‐dependent thalassaemia: A multicentre study
  12. DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET
  13. DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET
  14. DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET
  15. Endocrine dysfunctions in patients with beta thalassemia major: a single-center retrospective study from Basrah
  16. DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET
  17. Hypophosphataemia in adults: approach to diagnosis and management
  18. Global burden of thalassemia by socio-demographic index, 1990–2023: trends, disparities, and future implications
  19. Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease
  20. Age-Related Patterns of Organ-Specific Iron Distribution in Non-Transfusion-Dependent Thalassemia: A Multicenter MRI Study
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L3 Region - - 2026 Sep Q3

Hemoglobinopathies and Related Disorders

34 papers

Top Topics (10)

Hemoglobinopathies and Related Disorders19
Gout, Hyperuricemia, Uric Acid5
Platelet Disorders and Treatments1
Dialysis and Renal Disease Management1
Neonatal Health and Biochemistry1
Parathyroid Disorders and Treatments1
Malaria Research and Control1
Biomedical Research and Pathophysiology1
Erythrocyte Function and Pathophysiology1
Erythropoietin and Anemia Treatment1

Top Publications (20)

1.A phase 4, open-label efficacy and safety study of methotrexate and monthly pegloticase co-administration in patients with uncontrolled gout2.Community-based approach for thalassemia patients: a perspective from Bangladesh3.Human platelet 5-hydroxyindoleacetic acid concentrations are meager and unlikely to be physiologically active or play a role in inflammation4.Cumulative Stress Measured by Allostatic Load is Associated with Vaso-Occlusive Episodes in Sickle Cell Disease5.Exploratory investigation of hemodialysis membrane–induced differential DNA methylation in patient blood6.Hidden crystals in the heart: A rare case of tophaceous aortic valve gout7.Gout: Contemporary Approaches to Diagnosis, Treatment, and Long-Term Management8.Gout: Contemporary Approaches to Diagnosis, Treatment, and Long-Term Management9.Comparison of hematological parameters in adults with and without jaundice10.Factors Contributing to Improved Bone Mineral Density in Patients With Transfusion‐Dependent Thalassemia11.Pancreatic iron overload as a marker of endocrine complications in transfusion‐dependent thalassaemia: A multicentre study12.DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET13.DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET14.DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET15.Endocrine dysfunctions in patients with beta thalassemia major: a single-center retrospective study from Basrah16.DISCRIMINATIVE PERFORMANCE OF HEMATOLOGICAL PARAMETERS FOR IDENTIFYING Β-THALASSEMIA CARRIERS: A SECONDARY ANALYSIS OF AN OPEN-ACCESS SCREENING DATASET17.Hypophosphataemia in adults: approach to diagnosis and management18.Global burden of thalassemia by socio-demographic index, 1990–2023: trends, disparities, and future implications19.Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease20.Age-Related Patterns of Organ-Specific Iron Distribution in Non-Transfusion-Dependent Thalassemia: A Multicenter MRI Study
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