Research map: KLF1 mutation-associated congenital dyserythropoietic anemia type IV: a case report and literature review

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  1. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin · Joseph Borg · 2010 · 381 citations · Cited by this paper
  2. Clinical features and nonoperative strategy for first-time infected urachal cysts in infants · 2026 · Related
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  5. A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia · Lionel Arnaud · 2010 · 202 citations · Cited by this paper
  6. Risk factors and a predictive model for delayed extubation in children undergoing primary repair of tetralogy of Fallot: a retrospective cohort study with rigorous methodological validation · 2026 · Related
  7. KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia · Dun Liu · 2014 · 158 citations · Cited by this paper
  8. Correlation analysis of cyclosporine A trough concentration with hematological and biochemical parameters: a retrospective study in pediatric aplastic anemia · 2026 · Related
  9. Congenital dyserythropoietic anemias · Achille Iolascon · 2020 · 118 citations · Cited by this paper
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  11. Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression · Vip Viprakasit · 2014 · 97 citations · Cited by this paper
  12. Retrospective analysis of the clinical value of targeted nursing using a game-based model in children undergoing auricular reconstruction for congenital microtia · 2026 · Related
  13. Diagnosis and management of congenital dyserythropoietic anemias · Antonella Gambale · 2015 · 89 citations · Cited by this paper
  14. Clinical application value of metagenomic next-generation sequencing in children with fever of unknown origin · 2026 · Related
  15. Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: Review of all reported cases and development of a clinical diagnostic paradigm · Julie Jaffray · 2013 · 80 citations · Cited by this paper
  16. Multimodal quantitative characterization and mechanistic exploration of paraspinal muscle groups in adolescent idiopathic scoliosis · 2026 · Related
  17. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin · S. Satta · 2011 · 76 citations · Cited by this paper
  18. Precision minimally invasive strategy for Hirschsprung’s disease: from anatomical resection to whole-cycle functional management—a review · 2026 · Related
  19. Congenital dyserythropoietic anemias · Achille Iolascon · 2011 · 68 citations · Cited by this paper
  20. Analysis of the interventional effects of ambroxol hydrochloride and ontelukast sodium combined with azithromycin on immune function and C-reactive protein serum expression in children with severe Mycoplasma pneumoniae pneumonia · 2026 · Related
  21. KLF1 directly activates expression of the novel fetal globin repressor ZBTB7A/LRF in erythroid cells · Laura J. Norton · 2017 · 64 citations · Cited by this paper
  22. Genetic disruption of the KLF1 gene to overexpress the γ‐globin gene using the CRISPR/Cas9 system · Laleh Shariati · 2016 · 49 citations · Cited by this paper
  23. Molecular Analysis of the Rare In(Lu) Blood Type: Toward Decoding the Phenotypic Outcome of Haploinsufficiency for the Transcription Factor KLF1 · Virginie Helias · 2012 · 42 citations · Cited by this paper
  24. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin · Jiwei Huang · 2015 · 37 citations · Cited by this paper
  25. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders · Priya Hariharan · 2018 · 32 citations · Cited by this paper
  26. Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin · Milena Radmilovic · 2012 · 24 citations · Cited by this paper
  27. The congenital dyserythropoieitic anemias: genetics and pathophysiology · Richard A. King · 2021 · 24 citations · Cited by this paper
  28. A Very Rare Congenital Dyserythropoietic Anemia Variant—Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature · Tugba Belgemen‐Ozer · 2020 · 16 citations · Cited by this paper
  29. Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review · Linlin Xu · 2021 · 16 citations · Cited by this paper
  30. KLF1Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin · Ting Wang · 2013 · 14 citations · Cited by this paper
  31. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene · Manuel Méndez · 2020 · 11 citations · Cited by this paper
  32. A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor · Takenori Nitta · 2015 · 10 citations · Cited by this paper
  33. Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia · Chattree Hantaweepant · 2023 · 9 citations · Cited by this paper
  34. Novel human cellular model of CDA IV enables comprehensive analysis revealing molecular basis of disease phenotype · Ivan Ferrer Vicens · 2023 · 6 citations · Cited by this paper
  35. A KLF 1 gene mutation causes β‐thalassemia minor in a Chinese family · Limin Huang · 2018 · 3 citations · Cited by this paper

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