Blood Cells Molecules and Diseases

Papers
(The TQCC of Blood Cells Molecules and Diseases is 4. 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 2021-05-01 to 2025-05-01.)
ArticleCitations
The utility of multiple genomic technologies for interpretation of modern next generation sequencing: A novel case of three FANCA gene variants resulting in autosomal recessive Fanconi anaemia32
Erythrocyte deformability correlates with systemic inflammation32
Evidence for continued dose escalation of plerixafor for hematopoietic progenitor cell collections in sickle cell disease30
Rapid and automated quantitation of dense red blood cells: A robust biomarker of hydroxyurea treatment response25
The role of PKC in X-ray-induced megakaryocyte apoptosis and thrombocytopenia24
Differential effects of iron chelators on iron burden and long-term morbidity and mortality outcomes in a large cohort of transfusion-dependent β-thalassemia patients who remained on the same monother18
Targeting of Calbindin 1 rescues erythropoiesis in a human model of Diamond Blackfan anemia16
Investigation of the cytotoxicity, genotoxicity and antioxidant prospects of JM-20 on human blood cells: A multi-target compound with potential therapeutic applications16
Commentary on “unmasking the morphological alteration of erythrocytes among women suffering from PCOS”14
Malignant histiocytosis with a Langerhans cell subtype: A report on the diagnostic and therapeutic challenge14
Editorial Board12
Is the erythropoietin-erythroferrone-hepcidin axis intact in human neonates?11
A computational study of structural differences of binding of NADP+ and G6P substrates to G6PD Mediterraneanc.563T, G6PD A−c.202A/c.376G, G6PD Cairoc.404C and G6PD Gazac.536A mutations11
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)11
Editorial Board10
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant10
Rare bleeding disorders: Real-world data from a Spanish tertiary hospital10
Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients9
Megakaryocyte-specific knockout of the Mir-99b/let7e/125a cluster lowers platelet count without altering platelet function9
γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity9
Editorial Board9
Characterization of peripheral T helper 17 (Th17) cells phenotype in postmenopausal women with estrogen insufficiency9
Editorial Board9
Systemic corticosteroids in the treatment of warm autoimmune hemolytic anemia: A clinical setting perspective8
Cytogenetic profile and outcome of a pediatric acute promyelocytic leukemia patient presenting with isolated isochromosome 17q in absence of RARA rearrangement8
Drinking recommended daily water significantly alters haemato-biochemical parameters in prospective blood donors; a one-center quasi-experimental study in a tropical setting8
Editorial Board8
Prognostic significance of CD45 antigen expression in pediatric acute lymphoblastic leukemia8
Artefactual decrease in the fluorescence intensity of hereditary spherocytosis EMA test related to statins8
Up-regulation of microRNA 101-3p during erythropoiesis in β-thalassemia/HbE7
LXRβ is involved in the control of platelet production from megakaryocytes7
Outpatient ATG-free hematopoietic transplantation for aplastic anemia in limited-resource environments offers excellent results: Data from a single LATAM center7
Mitapivat increases ATP and decreases oxidative stress and erythrocyte mitochondria retention in a SCD mouse model7
Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-197
Pancytopenia and thrombosis defects in zebrafish mutants of Fanconi anemia genes6
Acquired elliptocytosis in chronic myeloid neoplasms: An enigmatic relationship to acquired red cell membrane protein and genetic abnormalities6
The inhibitor of MyoD Family A (I-MFA) regulates megakaryocyte lineage commitment and terminal differentiation6
Daratumumab for pure red cell aplasia post ABO incompatible allogeneic hematopoietic stem cell transplant for aplastic anemia6
Indices of iron homeostasis in asymptomatic subjects with HFE mutations and moderate ferritin elevation during iron removal treatment6
Daucosterol regulates JAK2-STAT3 signaling pathway to promote megakaryocyte differentiation5
Editorial Board5
Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?5
Clinical and health-related quality of life outcomes of transfusion-dependent thalassaemia patients in Singapore5
Prognostic factors associated with COVID-19 related severity in sickle cell disease5
Extreme γ′ fibrinogen levels in COVID-19 patients5
Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing5
Hypoferremia of inflammation: Innate host defense against infections5
Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France5
Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress5
Friend or foe? The case of Wilms' Tumor 1 (WT1) mutations in acute myeloid leukemia5
Manifestation of paroxysmal nocturnal hemoglobinuria after COVID-19 mRNA vaccination5
Chronic lymphocytic leukemia with a transient atypical T-cell proliferation raising concern for T-cell lymphoma4
Mechanism of the apoptosis of bone marrow erythroblasts in rats under hypobaric hypoxia4
PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants4
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