Hematology-American Society of Hematology Education Program

Papers
(The median citation count of Hematology-American Society of Hematology Education Program 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 2021-02-01 to 2025-02-01.)
ArticleCitations
Relapsed disease: off-the-shelf immunotherapies vs customized engineered products43
Clots in unusual places: lots of stress, limited data, critical decisions40
The range of haploidentical transplant protocols in sickle cell disease: all haplos are not created equally34
Acute GVHD: think before you treat27
Evidence-Based Minireview: How to utilize new therapies for sickle cell disease26
Optimal approach to T-cell ALL26
The future paradigm of HMA + VEN or targeted inhibitor approaches: sequencing or triplet combinations in AML therapy24
The dos, don'ts, and nuances of thrombophilia testing23
Hematopoietic cell transplantation for sickle cell disease: updates and future directions22
Controversies in the management of early-stage Hodgkin lymphoma22
Mastocytosis demystified22
Diagnosis and therapeutic decision-making for the neutropenic patient21
Evidence-Based Minireview: Strategies to manage a severely HLA-alloimmunized patient with refractory thrombocytopenia21
Evidence-Based Minireview: Clinical utilization of panel-based molecular testing for patients with AML20
Inpatient recognition and management of HLH20
To prophylax or not, and how much and how long? Controversies in VTE prevention for medical inpatients, including COVID-19 inpatients20
Should older patients with low weight and CKD receive full-dose DOACs for treatment of acute proximal DVT?18
When should gene therapy be considered for transfusion-dependent β-thalassemia patients?18
Lifelong TKI therapy: how to manage cardiovascular and other risks17
What factors guide treatment selection in mycosis fungoides and Sezary syndrome?17
AL amyloidosis: untangling new therapies17
Dual-targeted regimens for the frontline treatment of CLL17
Relapsed ALL: CAR T vs transplant vs novel therapies16
Diagnostic pitfalls and conundrums in type 1 von Willebrand disease16
Labor and delivery: DIC, HELLP, preeclampsia16
Optimal strategies for carrier screening and prenatal diagnosis of α- and β-thalassemia16
Bispecific antibody therapies15
Cytoreduction for ET and PV: who, what, when, and how?15
Provoked vs minimally provoked vs unprovoked VTE: does it matter?15
How do we optimally utilize factor concentrates in persons with hemophilia?14
Evidence-Based Minireview: For overweight or obese persons with hemophilia A, should factor VIII dosing be based on ideal or actual body weight?13
Thrombocytopenia in pregnancy13
What have we learned about the patient's experience of von Willebrand disease? A focus on women13
Pyruvate kinase activators: targeting red cell metabolism in sickle cell disease13
Smoldering multiple myeloma: evolving diagnostic criteria and treatment strategies13
Novel immunotherapies in the treatment of AML: is there hope?13
How to evaluate the patient with a suspected mast cell disorder and how/when to manage symptoms12
Management of Fanconi anemia beyond childhood12
Novel platelet products including cold-stored platelets12
Biology of follicular lymphoma: insights and windows of clinical opportunity12
Modern management of Fanconi anemia12
Intravenous iron therapy in pediatrics: who should get it and when is the right time?11
Burnett AE, Ragheb B, Kaatz S. Perioperative consultative hematology: can you clear my patient for a procedure? Hematology Am Soc Hematol Educ Program. 2021;2021:521-528.11
Recognizing, defining, and managing CAR-T hematologic toxicities11
Dyskeratosis congenita and telomere biology disorders11
Gene therapy for hemophilia11
Inherited thrombophilia and recurrent miscarriage: is there a role for anticoagulation during pregnancy?10
Catastrophic antiphospholipid syndrome: a CAPS-tivating hematologic disease10
Quantifying menorrhagia and overview of nonsurgical management of heavy menstrual bleeding10
On the horizon: upcoming new agents for the management of ITP10
Neurological manifestations of MGUS10
Novel conditioning and prophylaxis regimens for relapse prevention10
Mutations and MRD: clinical implications of clonal ontogeny10
The POD24 challenge: where do we go from here for early progressors?10
New definitions for antiphospholipid syndrome: ready for clinical use?10
Your chemo is no good here: management of high-risk MCL10
Treatment of VTE in the thrombocytopenic cancer patient10
What makes a pediatric or young adult patient an appropriate transplant candidate?9
Diagnosis and management of hereditary hemochromatosis: lifestyle modification, phlebotomy, and blood donation9
Should posttransplant cyclophosphamide be considered standard of care for pediatric transplantation of acute leukemia?9
Pegylated interferon: the who, why, and how9
Modified T cells as therapeutic agents9
Anticoagulation at the end of life: whether, when, and how to treat9
Risk-stratification in frontline CLL therapy: standard of care9
Thrombopoietin receptor agonists for chemotherapy-induced thrombocytopenia: a new solution for an old problem8
Using disease-modifying therapies in sickle cell disease8
Managing pregnancy in patients with sickle cell disease from a transfusion perspective8
Pregnancy in special populations: challenges and solutions practical aspects of managing von Willebrand disease in pregnancy8
Evidence-Based Minireview: In young children with severe sickle cell disease, do the benefits of HLA-identical sibling donor HCT outweigh the risks?8
Platelet components and bacterial contamination: hospital perspective 20228
Options at the time of relapse after anti-BCMA therapy8
Novel approaches to acute graft-versus-host disease prevention7
Upfront therapy: the case for continuous treatment7
Thrombosis and anticoagulation: clinical issues of special importance to hematologists who practice in Asia7
Passive immune therapies: another tool against COVID-197
What is the role of up-front autologous stem cell transplantation in mantle cell lymphoma?7
Pyruvate kinase activators for treatment of pyruvate kinase deficiency7
Amyloid consults do not have to be vexing7
Beyond the cell: novel noncellular immunotherapy approaches to multiple myeloma7
β-Thalassemia: evolving treatment options beyond transfusion and iron chelation7
Heparin-induced thrombocytopenia and cardiovascular surgery7
Long-term health outcomes following curative therapies for sickle cell disease7
T-cell lymphopenia in frequent volunteer platelet donors7
Individualized patient care in nodular lymphocyte-predominant Hodgkin lymphoma7
How to avoid early mortality in acute promyelocytic leukemia7
Updates in infant acute lymphoblastic leukemia and the potential for targeted therapy7
Identifying and treating iron deficiency anemia in pregnancy7
Next-generation therapy for lower-risk MDS7
The optimal management of relapsed and refractory Hodgkin lymphoma: post–brentuximab and checkpoint inhibitor failure7
Novel therapies and combinations in CLL refractory to BTK inhibitors and venetoclax7
Molecular prognostication in Ph-negative MPNs in 20226
Multiple myeloma: a paradigm for blending community and academic care6
Williams KM. Noninfectious complications of hematopoietic cell transplantation. Hematology Am Soc Hematol Educ Program. 2021;2021:578-586.6
Givosiran: a targeted treatment for acute intermittent porphyria6
What is the ideal approach—doublet, triplet, or quadruplet(s)?6
Hormone-related thrombosis: duration of anticoagulation, risk of recurrence, and the role of hypercoagulability testing6
Logistics, risks, and benefits of automated red blood cell exchange for patients with sickle cell disease6
Have we reached a molecular era in myelodysplastic syndromes?6
Clinical manifestations of telomere biology disorders in adults6
Double-refractory Hodgkin lymphoma: tackling relapse after brentuximab vedotin and checkpoint inhibitors6
Targeted medical therapies for vascular anomalies6
Has PD-1 blockade changed the standard of care for cHL?6
Fungal diagnostic testing and therapy: navigating the neutropenic period in children with high-risk leukemia6
Evidence-based management of pregnant women with sickle cell disease in high-income countries6
Cold AIHA and the best treatment strategies6
To consolidate or not to consolidate: the role of autologous stem cell transplantation in MCL6
Challenges in hospice and end-of-life care in the transfusion-dependent patient6
In pursuit of a functional cure for follicular lymphoma6
Patient-reported outcomes after CAR T-cell therapy in patients with hematological malignancies5
Selection of bispecific antibody therapies or CAR-T cell therapy in relapsed lymphomas5
Perioperative consultative hematology: can you clear my patient for a procedure?5
Optimal approach to T-cell ALL5
Diagnosis and laboratory monitoring of acquired hemophilia A5
Beyond FAScinating: advances in diagnosis and management of autoimmune lymphoproliferative syndrome and activated PI3 kinase δ syndrome5
Biology of post-transplant relapse: actionable features5
Iron overload in acquired sideroblastic anemias and MDS: pathophysiology and role of chelation and luspatercept5
Evolving landscape of JAK inhibition in myelofibrosis: monotherapy and combinations5
Evidence-Based Minireview: Molecular precision and clinical uncertainty: should molecular profiling be routinely used to guide risk stratification in MDS?5
Evidence-Based Minireview: When should autologous transplant or cellular therapy be considered for follicular lymphoma?5
Updates on strategies to integrate palliative care in hematologic malignancy5
Ph− ALL: immunotherapy in upfront treatment5
Large granular lymphocyte leukemia: a clonal disorder with autoimmune manifestations5
T-cell–based therapies for treating relapsed or refractory mantle cell lymphoma5
Resistance mutations in CML and how we approach them5
New investigational combinations for higher-risk MDS5
Do all patients with primary refractory/first relapse of HL need autologous stem cell transplant?5
Atypical hemolytic uremic syndrome: diagnosis, management, and discontinuation of therapy5
Mutation- and MRD-informed treatment decisions for the transplant-eligible AML patient5
Transplant in myeloma: who, when, and why?4
Should we use bisphosphonates to treat bone complications in sickle cell disease?4
Increasing access to allogeneic hematopoietic cell transplant: an international perspective4
Long-term follow-up of CD19-CAR T-cell therapy in children and young adults with B-ALL4
Newborn screening initiatives for sickle cell disease in Africa4
Troubleshooting heparin resistance4
The first relapse in multiple myeloma: how to pick the next best thing4
Allogeneic transplantation for advanced acute leukemia4
Whom should we treat with novel agents? Specific indications for specific and challenging populations4
Sequencing bispecific antibodies and CAR T cells for FL4
The role of stem cell transplant (auto and allo) in PTCL and CTCL4
Practical guide for disease-modifying medication management of children and adolescents with sickle cell disease4
BV and beyond: how to incorporate novel agents into PTCL management4
MGCS: where do we stand today?4
New approaches to tackle cytopenic myelofibrosis4
Divergent paths: management of early relapsed follicular lymphoma4
Renal manifestations of MGUS4
The intersection of sickle cell disease, stigma, and pain in Africa4
IgG4-related disease for the hematologist4
Hypoxia-inducible factor activators: a novel class of oral drugs for the treatment of anemia of chronic kidney disease4
Supportive care in myeloma—when treating the clone alone is not enough4
Through thick and thin: confronting the aggressive cutaneous T-cell lymphomas4
Evidence-based obstetric management of women with sickle cell disease in low-income countries4
Current use of CAR T cells to treat multiple myeloma4
When to use stem cell transplantation for classical Hodgkin lymphoma4
Medical consult: aHUS, TTP? How to distinguish and what to do3
Advances in the management of α-thalassemia major: reasons to be optimistic3
Novel therapies vs hematopoietic cell transplantation in myelofibrosis: who, when, how?3
Advances in MGUS diagnosis, risk stratification, and management: introducing myeloma-defining genomic events3
Management of aggressive lymphoma after CAR T-cell therapy failure3
Hitting the brakes on accelerated and blast-phase myeloproliferative neoplasms: current and emerging concepts3
Treatment of Richter's syndrome3
How old is too old? Frailty and geriatric assessments of older patients undergoing allogeneic HCT3
Minimal intensity conditioning strategies for bone marrow failure: is it time for “preventative” transplants?3
MPN and thrombosis was hard enough . . . now there's COVID-19 thrombosis too3
Mitigating the risk of venous thromboembolism in patients with multiple myeloma receiving immunomodulatory-based therapy3
Selecting initial therapy in CLL3
Pyruvate kinase activators: targeting red cell metabolism in thalassemia3
Diagnosis and clinical management of red cell membrane disorders3
Achieving MRD negativity in AML: how important is this and how do we get there?3
Approaches to optimize outcomes in transplant recipients3
Acute lymphoblastic leukemia in older adults: curtain call for conventional chemotherapy?3
Novel therapies upon failure of HMA plus venetoclax3
The evolution of targeted therapy in pediatric AML: gemtuzumab ozogamicin, FLT3/IDH/BCL2 inhibitors, and other therapies3
Inflamed—HLH, MAS, or something else?3
When to consider inherited marrow failure syndromes in adults3
Fitness and frailty in myeloma3
Incidence, mechanism, and consequences of IV iron–induced hypophosphatemia3
How to assess hemostasis in patients with severe liver disease3
Does MRD have a role in the management of iNHL?2
Managing side effects: guidance for use of immunotherapies in multiple myeloma2
Prevention, diagnosis, and management of PE and DVT in pregnant women2
MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?2
Frontline treatment in CLL: the case for time-limited treatment2
Approach to the patient with suspected hypereosinophilic syndrome2
Allogeneic hematopoietic cell transplantation for older patients2
How to manage hemostasis in patients with liver disease during interventions2
Chronic GVHD: review advances in prevention, novel endpoints, and targeted strategies2
COVID-19 and thrombosis: searching for evidence2
Mutational screening to improve the transplantation decision-making process in MDS2
Chronic thromboembolic pulmonary hypertension: anticoagulation and beyond2
Transplant for TP53-mutated MDS and AML: because we can or because we should?2
Incorporating gonadal health counseling into pediatric care of sickle cell patients2
The sum of the parts: what we can and cannot learn from comorbidity scores in allogeneic transplantation2
Risk factors and screening for neurocognitive impacts of therapy2
TKI discontinuation in CML: how do we make more patients eligible? How do we increase the chances of a successful treatment-free remission?2
Gene therapy for sickle cell disease2
Optimizing outcomes in secondary AML2
Clonal evolution in inherited marrow failure syndromes predicts disease progression2
How to recognize and manage COVID-19-associated coagulopathy2
What else do I need to worry about when treating graft-versus-host disease?2
Incorporating novel agents into frontline treatment of Hodgkin lymphoma2
Mitigating, monitoring, and managing long-term chemotherapy- and radiation-induced cardiac toxicity2
The burden of myeloma: novel approaches to disease assessment2
Blast and accelerated phase CML: room for improvement2
Newly diagnosed multiple myeloma: making sense of the menu2
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