Blood Cells Molecules and Diseases

Papers
(The median citation count of Blood Cells Molecules and Diseases is 1. 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 2021-06-01 to 2025-06-01.)
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 thrombocytopenia20
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 monother16
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 applications14
Commentary on “unmasking the morphological alteration of erythrocytes among women suffering from PCOS”12
Malignant histiocytosis with a Langerhans cell subtype: A report on the diagnostic and therapeutic challenge11
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)10
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant10
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 mutations10
Editorial Board9
Editorial Board9
Characterization of peripheral T helper 17 (Th17) cells phenotype in postmenopausal women with estrogen insufficiency9
Editorial Board9
Rare bleeding disorders: Real-world data from a Spanish tertiary hospital9
Editorial Board9
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
Systemic corticosteroids in the treatment of warm autoimmune hemolytic anemia: A clinical setting perspective8
Drinking recommended daily water significantly alters haemato-biochemical parameters in prospective blood donors; a one-center quasi-experimental study in a tropical setting8
Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-198
Artefactual decrease in the fluorescence intensity of hereditary spherocytosis EMA test related to statins8
LXRβ is involved in the control of platelet production from megakaryocytes7
Mitapivat increases ATP and decreases oxidative stress and erythrocyte mitochondria retention in a SCD mouse model7
Up-regulation of microRNA 101-3p during erythropoiesis in β-thalassemia/HbE7
Outpatient ATG-free hematopoietic transplantation for aplastic anemia in limited-resource environments offers excellent results: Data from a single LATAM center6
Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France6
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
Prognostic factors associated with COVID-19 related severity in sickle cell disease6
Prognostic significance of CD45 antigen expression in pediatric acute lymphoblastic leukemia6
Indices of iron homeostasis in asymptomatic subjects with HFE mutations and moderate ferritin elevation during iron removal treatment6
The inhibitor of MyoD Family A (I-MFA) regulates megakaryocyte lineage commitment and terminal differentiation6
Extreme γ′ fibrinogen levels in COVID-19 patients5
Hypoferremia of inflammation: Innate host defense against infections5
Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress5
Editorial Board5
PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants5
Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing5
Daucosterol regulates JAK2-STAT3 signaling pathway to promote megakaryocyte differentiation5
Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?5
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
Isolated central nervous system relapse of acute promyelocytic leukemia with altered morphology in an asymptomatic patient4
Performance of serum procalcitonin as a biochemical predictor of death in hematology patients with febrile neutropenia4
Hematologically important mutations: Leukocyte adhesion deficiency (second update)4
Mechanism of the apoptosis of bone marrow erythroblasts in rats under hypobaric hypoxia3
Corrigendum to “Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy” [Blood Cells Mol. Dis. 99 (2023) 102727]3
Discovery of seven hox genes in zebrafish thrombopoiesis3
Blood cells molecules and diseases in 2022: A fountain of youth3
Bone marrow burden score is not useful as a follow-up parameter in stable patients with type 1 Gaucher disease after 5 years of treatment3
Early iron supplementation and iron sufficiency at one month of age in NICU patients at-risk for iron deficiency3
Retraction notice to “MZF1 regulates α-globin gene transcription via long-range interactions in erythroid differentiation” [Blood Cells, Mol. Dis., Volume 87, March 2021, 102533]3
Liver kinase B1 (LKB1) in murine erythroid progenitors modulates erythropoietin setpoint in association with maturation control3
Bio-net dataset: AI-based diagnostic solutions using peripheral blood smear images3
Decreasing circ_0014614 promotes the differentiation of bone marrow flineage cells into megakaryocytes in essential thrombocythemia via activiation of miR-138-5p/caspase3 axis3
Growth hormone is involved in GATA1 gene expression via STAT5B in human erythroleukemia and monocytic cell lines2
Analysis of baseline characteristics, disease burden and long-term follow-up of 167 patients with Paroxysmal Nocturnal Hemoglobinuria at a single center in Brazil2
Editorial Board2
A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosis2
Corrigendum to “Clinical utility of relative telomere length analysis in pediatric bone marrow failure” [Blood Cells Mol. Dis. 109 (2024) 102882]2
Further biological characterization of small molecules UM171 and SR1: In vitro effects on three hematopoietic cell populations from human cord blood2
Telomere shortening correlates with disease severity in hemoglobin H disease patients2
The significance of surface neutrophilic MPO expression level in NETosis and NETosis-associated coagulopathies in covid-19 infected patients2
Identification of Nfel1a and Nfel3 as novel regulators for zebrafish thrombopoiesis2
Thirty-five males with severe (Class 1) G6PD deficiency (c.637G>T) in a North American family of European ancestry2
Whole exome sequencing of a breast tumor in a patient with Diamond Blackfan anemia2
Editorial Board2
Platelet activation and blood extracellular vesicles: The influence of venepuncture and short blood storage2
Co-morbidities and mortality in patients with sickle cell disease in England: A 10-year cohort analysis using hospital episodes statistics (HES) data2
Molecular and biochemical evaluation of oxidative effects of cord blood CD34+ MPs on hematopoietic cells2
Immunodeficiency in children with Diamond Blackfan and Diamond Blackfan like anemia2
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort2
Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studies2
Editorial Board2
Two new mutations in the GLRX5 gene cause sideroblastic anemia2
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Rheumatological manifestations of chronic graft versus host disease - Case series2
Red cell anarchy. Evidence of neoplastic dyserythropoiesis2
Impact of CD34 positive cell dose in donor graft on the outcomes after haploidentical peripheral blood stem cell transplantation with post-transplant cyclophosphamide – A retrospective single-center s2
Anti-TFPI for hemostasis induction in patients with rare bleeding disorders, an ex vivo thrombin generation (TG) guided pilot study1
Severe immune thrombocytopenia after COVID-19 vaccination: Report of four cases and review of the literature1
Monoclonal IgM gammopathy in adult acquired pure red cell aplasia: culprit or innocent bystander?1
Immunological profile in a pediatric population of patients with spherocytosis. A single-center experience1
Plasma immune mediators as laboratorial biomarkers for Sickle Cell Disease patients according to the hydroxyurea therapy and disease severity1
Outcome of first or second transplantation using unrelated umbilical cord blood without ATG conditioning regimen for pediatric bone marrow failure disorders1
Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy1
Daratumumab as a novel treatment option in refractory ITP1
Platelet counts on peripheral blood and Mean Platelet Volume as markers of clinical severity in Sickle Cell Disease1
Identification of TCR repertoires in asymptomatic COVID-19 patients by single-cell T-cell receptor sequencing1
Reliability of different estimated glomerular filtration rate as measures of renal function in children with sickle cell disease1
Mouse models of sickle cell disease: Imperfect and yet very informative1
Sickle cell disease in Indian tribal population: Findings of a multi-centre Indian SCD registry1
Editorial Board1
Effects of d-ribose on human erythrocytes: Non-enzymatic glycation of hemoglobin, eryptosis, oxidative stress and energy metabolism1
Clinical characteristics, laboratory features and genetic profile of hemoglobin E (HBB:c.79 G > A)/β (nucleotide -28 A > G) (HBB:c.-78 A > G) -thalassemia subjects identified from community- 1
Regarding γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity1
Clonal hematopoiesis and acquired genetic abnormalities of the red cell: An historical review1
Bach1 inhibitor HPP-D mediates γ-globin gene activation in sickle erythroid progenitors1
Editorial Board1
Effect of voxelotor on murine bone marrow and peripheral blood with hematopoietic progenitor cell mobilization for gene therapy of sickle cell disease1
COVID-19 induces proatherogenic alterations in moderate to severe non-comorbid patients: A single-center observational study1
Good treatment-free survival of monoclonal gammopathy of undetermined significance associated pure red cell aplasia after bortezomib plus dexamethasone1
Surgical procedures and complications in placement of totally implantable venous access port in pediatric hemophilia patients: A retrospective analysis1
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