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 2022-01-01 to 2026-01-01.)
ArticleCitations
A case series of cerebrovascular abnormalities in Townes sickle cell mice visualized with magnetic resonance imaging and angiography31
The role of PKC in X-ray-induced megakaryocyte apoptosis and thrombocytopenia26
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 anaemia23
Targeting of Calbindin 1 rescues erythropoiesis in a human model of Diamond Blackfan anemia18
Erythrocyte deformability correlates with systemic inflammation18
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 monother17
Investigation of the cytotoxicity, genotoxicity and antioxidant prospects of JM-20 on human blood cells: A multi-target compound with potential therapeutic applications17
Commentary on “unmasking the morphological alteration of erythrocytes among women suffering from PCOS”16
First report of a patient with homozygous hemoglobin Ernz: Evidence to support a non-pathogenic variant15
Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)14
γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity14
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Rare bleeding disorders: Real-world data from a Spanish tertiary hospital11
Mitapivat increases ATP and decreases oxidative stress and erythrocyte mitochondria retention in a SCD mouse model9
Characterization of peripheral T helper 17 (Th17) cells phenotype in postmenopausal women with estrogen insufficiency9
Artefactual decrease in the fluorescence intensity of hereditary spherocytosis EMA test related to statins9
Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-198
Drinking recommended daily water significantly alters haemato-biochemical parameters in prospective blood donors; a one-center quasi-experimental study in a tropical setting8
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 center7
Pancytopenia and thrombosis defects in zebrafish mutants of Fanconi anemia genes7
The inhibitor of MyoD Family A (I-MFA) regulates megakaryocyte lineage commitment and terminal differentiation7
Indices of iron homeostasis in asymptomatic subjects with HFE mutations and moderate ferritin elevation during iron removal treatment7
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Acquired elliptocytosis in chronic myeloid neoplasms: An enigmatic relationship to acquired red cell membrane protein and genetic abnormalities6
Extreme γ′ fibrinogen levels in COVID-19 patients6
Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France6
Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing5
Editorial Board5
Mechanism of the apoptosis of bone marrow erythroblasts in rats under hypobaric hypoxia5
Hypoferremia of inflammation: Innate host defense against infections5
Daucosterol regulates JAK2-STAT3 signaling pathway to promote megakaryocyte differentiation5
Manifestation of paroxysmal nocturnal hemoglobinuria after COVID-19 mRNA vaccination5
Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?5
Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress5
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]4
Methodological strategies to study and elucidate RBC properties and their potential clinical impact on transfused patients4
Chronic lymphocytic leukemia with a transient atypical T-cell proliferation raising concern for T-cell lymphoma4
PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants4
Hematologically important mutations: Leukocyte adhesion deficiency (second update)4
Decreasing circ_0014614 promotes the differentiation of bone marrow flineage cells into megakaryocytes in essential thrombocythemia via activiation of miR-138-5p/caspase3 axis4
Blood cells molecules and diseases in 2022: A fountain of youth3
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
Bio-net dataset: AI-based diagnostic solutions using peripheral blood smear images3
Impact of elevated red blood cell membrane cholesterol in sickle cell anemia patients: Effects of BRN-002, a 2-hydroxypropyl-β-cyclodextrin derivate, on red blood cell lipids, deformability, sickling 3
Discovery of seven hox genes in zebrafish thrombopoiesis3
Rheumatological manifestations of chronic graft versus host disease - Case series3
Liver kinase B1 (LKB1) in murine erythroid progenitors modulates erythropoietin setpoint in association with maturation control3
Molecular and biochemical evaluation of oxidative effects of cord blood CD34+ MPs on hematopoietic cells3
Platelet activation and blood extracellular vesicles: The influence of venepuncture and short blood storage2
Further biological characterization of small molecules UM171 and SR1: In vitro effects on three hematopoietic cell populations from human cord blood2
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Thalidomide confers therapeutic benefit in beta thalassemia patients by enhancing hemoglobin and hematopoietic gene expression: A non-randomized clinical trial2
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An analysis of bone marrow burden scores in a retrospective analysis of adult patients with type 1 Gaucher disease2
Immunodeficiency in children with Diamond Blackfan and Diamond Blackfan like anemia2
Corrigendum to “Clinical utility of relative telomere length analysis in pediatric bone marrow failure” [Blood Cells Mol. Dis. 109 (2024) 102882]2
Growth hormone is involved in GATA1 gene expression via STAT5B in human erythroleukemia and monocytic cell lines2
Phenotypic and genotypic evaluation of bleeding diagnostic dilemmas: Two case studies2
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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
Phenotypic screens reveal Plasmodium falciparum genetic factors associated with infection of sickle-trait cells2
Identification of Nfel1a and Nfel3 as novel regulators for zebrafish thrombopoiesis2
The significance of surface neutrophilic MPO expression level in NETosis and NETosis-associated coagulopathies in covid-19 infected patients2
Two new mutations in the GLRX5 gene cause sideroblastic anemia2
Danazol causes significant changes in the cardiometabolic profile of patients with acquired aplastic anaemia1
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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
Identification of TCR repertoires in asymptomatic COVID-19 patients by single-cell T-cell receptor sequencing1
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A case of VEXAS syndrome associated with EBV-associated hemophagocytic lymphohistiocytosis1
Plasma immune mediators as laboratorial biomarkers for Sickle Cell Disease patients according to the hydroxyurea therapy and disease severity1
Effects of d-ribose on human erythrocytes: Non-enzymatic glycation of hemoglobin, eryptosis, oxidative stress and energy metabolism1
Dysmorphic megakaryocytes in TAFRO syndrome: A case series from a single institute1
Effect of voxelotor on murine bone marrow and peripheral blood with hematopoietic progenitor cell mobilization for gene therapy of sickle cell disease1
Immunological profile in a pediatric population of patients with spherocytosis. A single-center experience1
Surgical procedures and complications in placement of totally implantable venous access port in pediatric hemophilia patients: A retrospective analysis1
Editorial Board1
Bach1 inhibitor HPP-D mediates γ-globin gene activation in sickle erythroid progenitors1
Prevalence of multi-organ complications in patients with non-transfusion and neo-transfusion dependent thalassemia: a cross-sectional survey1
Regarding γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity1
Daratumumab as a novel treatment option in refractory ITP1
Culprit or innocent bystander? The case of a new fast-moving hemoglobin J variant in a pregnant woman1
Sickle cell disease in Indian tribal population: Findings of a multi-centre Indian SCD registry1
Hereditary disorders of ineffective erythropoiesis1
A novel ELANE variant causing severe congenital neutropenia diagnosed in adulthood1
Outcome of first or second transplantation using unrelated umbilical cord blood without ATG conditioning regimen for pediatric bone marrow failure disorders1
Mouse models of sickle cell disease: Imperfect and yet very informative1
Clonal hematopoiesis and acquired genetic abnormalities of the red cell: An historical review1
Anti-TFPI for hemostasis induction in patients with rare bleeding disorders, an ex vivo thrombin generation (TG) guided pilot study1
Impact of maternal iron deficiency anemia on fetal iron status and placental iron transporters in human pregnancy1
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