Latest Research in Lipid metabolism and disorders

19 research papers · 2026 median publication year

Top Research Topics in Lipid metabolism and disorders

Highest-Cited Papers

  1. Frequencies of Three Targeted HBB Gene Mutations Among Transfusion-Dependent Β-Thalassemia Patients from Southern Punjab, Pakistan
  2. ASSESSMENT OF DNA DAMAGE ENZYME, OXIDATIVE STRESS, INFLAMMATION BIOMARKERS AMONG MALE SCD PATIENTS IN IRRUA, EDO STATE, NIGERIA
  3. Frequencies of Three Targeted HBB Gene Mutations Among Transfusion-Dependent Β-Thalassemia Patients from Southern Punjab, Pakistan
  4. ASSESSMENT OF DNA DAMAGE ENZYME, OXIDATIVE STRESS, INFLAMMATION BIOMARKERS AMONG MALE SCD PATIENTS IN IRRUA, EDO STATE, NIGERIA
  5. Spectrum of α- and β-thalassemia variants in individuals with persistent microcytic hypochromia in Eastern Iran: implications for population genetic screening
  6. Death by Triglycerides
  7. Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia
  8. Long-term longitudinal evaluation of the sele s128r polymorphism and serum E-selectin levels in autosomal dominant polycystic kidney disease
  9. Co-Heredity of (−α)20.5 Deletion and IVS I-1 G > A ( HBB : C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?
  10. Molecular profiling of thalassemia in Southeastern Romania
  11. Molecular genetics analysis of genes BCL11A, HBS1L-MYB , and HBG2 variants association in thalassemic children
  12. Endothelial Dysfunction in β-Thalassemia: Mechanisms, Biomarkers, Vascular Imaging and Therapeutic Perspectives
  13. Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients
  14. Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population
  15. The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection
  16. The molecular spectrum of alpha- and beta-thalassemia pathogenic variants in Indonesia: implications for national screening and prevention
  17. Neutropenia in adult patients with thalassemia receiving deferiprone: a 10-year experience from a large thalassemia cohort
  18. Prevalence and Clinical Characteristics of Patients With Pseudogout and Concomitant Monosodium Urate Crystals
  19. A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China
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L3 Region - - 2026 Sep Q3

Lipid metabolism and disorders

19 papers

Top Topics (5)

Hemoglobinopathies and Related Disorders15
Lipid metabolism and disorders1
Genetic and Kidney Cyst Diseases1
Blood disorders and treatments1
Gout, Hyperuricemia, Uric Acid1

Top Publications (19)

1.Frequencies of Three Targeted HBB Gene Mutations Among Transfusion-Dependent Β-Thalassemia Patients from Southern Punjab, Pakistan2.ASSESSMENT OF DNA DAMAGE ENZYME, OXIDATIVE STRESS, INFLAMMATION BIOMARKERS AMONG MALE SCD PATIENTS IN IRRUA, EDO STATE, NIGERIA3.Frequencies of Three Targeted HBB Gene Mutations Among Transfusion-Dependent Β-Thalassemia Patients from Southern Punjab, Pakistan4.ASSESSMENT OF DNA DAMAGE ENZYME, OXIDATIVE STRESS, INFLAMMATION BIOMARKERS AMONG MALE SCD PATIENTS IN IRRUA, EDO STATE, NIGERIA5.Spectrum of α- and β-thalassemia variants in individuals with persistent microcytic hypochromia in Eastern Iran: implications for population genetic screening6.Death by Triglycerides7.Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia8.Long-term longitudinal evaluation of the sele s128r polymorphism and serum E-selectin levels in autosomal dominant polycystic kidney disease9.Co-Heredity of (−α)20.5 Deletion and IVS I-1 G > A ( HBB : C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?10.Molecular profiling of thalassemia in Southeastern Romania11.Molecular genetics analysis of genes BCL11A, HBS1L-MYB , and HBG2 variants association in thalassemic children12.Endothelial Dysfunction in β-Thalassemia: Mechanisms, Biomarkers, Vascular Imaging and Therapeutic Perspectives13.Hematologic Indices of Hemoglobin D Co-Inheritance with α and β Thalassemia: A Comparative Study of 202 Patients14.Tailoring Genetic Approaches for Easier Detection of Anti-3.7 Alpha-Globin Gene Triplication in the Iranian Population15.The Efficiency of Capillarys 2 Flex Piercing, Premier Resolution-HPLC, and VARIANT II-HPLC for Hemoglobin Constant Spring Detection16.The molecular spectrum of alpha- and beta-thalassemia pathogenic variants in Indonesia: implications for national screening and prevention17.Neutropenia in adult patients with thalassemia receiving deferiprone: a 10-year experience from a large thalassemia cohort18.Prevalence and Clinical Characteristics of Patients With Pseudogout and Concomitant Monosodium Urate Crystals19.A Decade‑Long Genetic Epidemiological Profile of Thalassemia in the Childbearing‑Age Population of Huizhou, a Major Hakka Center in Guangdong, China
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