Seminars in Hematology

Papers
(The median citation count of Seminars in Hematology is 2. 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 2020-04-01 to 2024-04-01.)
ArticleCitations
Memory-like natural killer cells for cancer immunotherapy48
Iron metabolism in infections: Focus on COVID-1947
Toward a pathophysiology inspired treatment of VEXAS syndrome39
Treatment of vaccine-induced immune thrombotic thrombocytopenia (VITT)31
Epidemiology of VITT30
Aplastic anemia: Pathophysiology30
Pathogenesis of vaccine-induced immune thrombotic thrombocytopenia (VITT)28
Characteristic bone marrow findings in patients with UBA1 somatic mutations and VEXAS syndrome26
Platelet-activating anti-PF4 disorders: An overview26
Mechanisms of cellular iron sensing, regulation of erythropoiesis and mitochondrial iron utilization24
Thrombotic manifestations of VEXAS syndrome24
Genetics of somatic auto-inflammatory disorders22
VEXAS within the spectrum of rheumatologic disease22
Clonal hematopoiesis and VEXAS syndrome: survival of the fittest clones?22
Improving CAR T cell therapy by optimizing critical quality attributes22
Modulating NK cell metabolism for cancer immunotherapy20
Monitoring MRD in ALL: Methodologies, technical aspects and optimal time points for measurement19
Genetic and epigenetic modification of human primary NK cells for enhanced antitumor activity16
20 years of Hepcidin: How far we have come16
Recent advances in use of fresh frozen plasma, cryoprecipitate, immunoglobulins, and clotting factors for transfusion support in patients with hematologic disease15
Platelet transfusion: Alloimmunization and refractoriness13
Improving CAR T-cells: The next generation13
VEXAS syndrome: An inflammatory and hematologic disease13
Shaping the bone through iron and iron-related proteins12
Laboratory testing for VITT antibodies11
Natural killer cell engineering – a new hope for cancer immunotherapy11
Role of blinatumomab, inotuzumab, and CAR T-cells: Which to choose and how to sequence for patients with relapsed disease11
NK cells as adoptive cellular therapy for hematological malignancies: Advantages and hurdles10
Longitudinal Aspects of VITT10
Immunosuppressive therapy in severe aplastic anemia9
TET-dioxygenase deficiency in oncogenesis and its targeting for tumor-selective therapeutics9
Looking beyond VEXAS: Coexistence of undifferentiated systemic autoinflammatory disease and myelodysplastic syndrome9
Applications of virus-specific T cell therapies post-BMT9
Pharmacogenomics and ALL treatment: How to optimize therapy9
Transfusion support in patients with sickle cell disease8
DNA methylation inhibition in myeloma: Experience from a phase 1b study of low-dose continuous azacitidine in combination with lenalidomide and low-dose dexamethasone in relapsed or refractory multipl8
Selection of allogeneic hematopoietic cell transplant donors to optimize natural killer cell alloreactivity8
Clonality in immune aplastic anemia: Mechanisms of immune escape or malignant transformation8
The spectrum of somatic mutations in large granular lymphocyte leukemia, rheumatoid arthritis, and Felty's syndrome7
Report of consensus Panel 4 from the 11th International Workshop on Waldenstrom's macroglobulinemia on diagnostic and response criteria7
Philadelphia chromosome positive acute lymphoblastic leukemia in adults: Therapeutic options and dilemmas in 20207
The evolution of epigenetic therapy in myelodysplastic syndromes and acute myeloid leukemia7
A pilot clinical trial of oral tetrahydrouridine/decitabine for noncytotoxic epigenetic therapy of chemoresistant lymphoid malignancies7
Optimal approach to the treatment of young adults with acute lymphoblastic leukemia in 20206
Diagnosis and management of adult T-cell leukemia/lymphoma6
The challenge to further improvements in survival of patients with T-ALL: Current treatments and new insights from disease pathogenesis5
Advances in understanding the crosstalk between mother and fetus on iron utilization5
Iron and erythropoiesis: A mutual alliance5
Hemolytic paroxysmal nocturnal hemoglobinuria: 20 years of medical progress5
Place of care manufacturing of chimeric antigen receptor cells: Opportunities and challenges5
SARS-CoV-2 vaccine-induced humoral and cellular immunity in patients with hematologic malignancies5
Report of consensus panel 1 from the 11th International Workshop on Waldenstrom's Macroglobulinemia on management of symptomatic, treatment-naïve patients5
Aplastic anemia: Quo vadis?4
Clinical picture of VITT4
Somatic mutations in VEXAS Syndrome and Erdheim-Chester disease: Inflammatory myeloid diseases4
The role of viruses in HIV-associated lymphomas4
Advances in gene therapy for hematologic disease and considerations for transfusion medicine4
Gene editing for sickle cell disease and transfusion dependent thalassemias- A cure within reach4
Vaccine-induced immune thrombotic thrombocytopenia (VITT)4
Epigenetic modifier directed therapeutics to unleash healthy genes in unhealthy cells4
The epidemiology of Waldenström macroglobulinemia4
Novel therapies targeting cutaneous T cell lymphomas and their microenvironment4
Management of Angioimmunoblastic T-Cell Lymphoma (AITL) and other T Follicular Helper Cell lymphomas (TFH PTCL)4
Management of ALCL and other CD30+ peripheral T-cell lymphomas with a focus on Brentuximab vedotin4
Extranodal natural killer/T-cell lymphoma: An overview on pathology and clinical management4
Epigenetic activities in erythroid cell gene regulation4
Somatic mutations in acquired pure red cell aplasia4
Somatic mutations and clonal expansions in paroxysmal nocturnal hemoglobinuria4
Cell senescence and malignant transformation in the inherited bone marrow failure syndromes: Overlapping pathophysiology with therapeutic implications4
Mendelian inheritance of anemia due to disturbed iron homeostasis3
Somatic compensation of inherited bone marrow failure3
Clonal dynamics of hematopoietic stem cell compartment in aplastic anemia3
The evolution of NK cell immunotherapy for hematologic malignancies: A historical and contemporary perspective3
Challenges and opportunities of CAR T-cell therapies for CLL3
Hepatitis C virus-associated B-cell lymphomas: The importance of the new direct antiviral agent therapy3
Prognosis and risk stratification of peripheral T-cell lymphomas3
New approaches to the treatment of older adults with acute lymphoblastic leukemia3
Transfusion support for stem cell transplant recipients3
Report of Consensus Panel 3 from the 11th International workshop on Waldenström's Macroglobulinemia: Recommendations for molecular diagnosis in Waldenström's Macroglobulinemia3
Clinical manifestations of clonal hematopoiesis: What has SF3B1-mutant MDS taught us?3
Primary and secondary central nervous system mature T- and NK-cell lymphomas3
Report of consensus panel 5 from the 11th international workshop on Waldenstrom's macroglobulinemia on COVID-19 prophylaxis and management3
Infectious complications of chimeric antigen receptor (CAR) T-cell therapies2
Palliative care needs of patients with hematologic malignancies and family caregivers and challenges of palliative care provision in Asia: A review of evidence2
Transfusion support: Considerations in pediatric populations2
Access to essential therapy for sickle cell disease in Africa: Experience from a national program in Ghana2
The psychiatric and psychological sequelae of vaccine-induced immune thrombotic thrombocytopenia (VITT)2
DLBCL arising from indolent lymphomas: How are they different?2
The natural killer cell immunotherapy platform: An overview of the landscape of clinical trials in liquid and solid tumors2
Epidemiology and etiology of diffuse large B-cell lymphoma2
Molecularly targeted therapies for relapsed and refractory peripheral T-cell lymphomas2
Highlights of the 11th International Workshop on Waldenstrom's Macroglobulinemia: What we learned, and how it will impact scientific discovery and patient care2
Clinical applications of circulating tumor DNA in central nervous system lymphoma2
Current challenges and new approaches to implementing optimal management of sickle cell disease in sub-Saharan Africa2
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