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 2021-04-01 to 2025-04-01.)
ArticleCitations
Relapsed disease: off-the-shelf immunotherapies vs customized engineered products57
Clots in unusual places: lots of stress, limited data, critical decisions54
The range of haploidentical transplant protocols in sickle cell disease: all haplos are not created equally49
Acute GVHD: think before you treat34
Provoked vs minimally provoked vs unprovoked VTE: does it matter?33
Thrombocytopenia in pregnancy31
How do we optimally utilize factor concentrates in persons with hemophilia?31
Evidence-Based Minireview: How to utilize new therapies for sickle cell disease29
Recognizing, defining, and managing CAR-T hematologic toxicities27
Optimal approach to T-cell ALL25
The future paradigm of HMA + VEN or targeted inhibitor approaches: sequencing or triplet combinations in AML therapy24
Should older patients with low weight and CKD receive full-dose DOACs for treatment of acute proximal DVT?24
When should gene therapy be considered for transfusion-dependent β-thalassemia patients?23
What factors guide treatment selection in mycosis fungoides and Sezary syndrome?22
Diagnosis and therapeutic decision-making for the neutropenic patient21
Mastocytosis demystified21
Hematopoietic cell transplantation for sickle cell disease: updates and future directions21
Controversies in the management of early-stage Hodgkin lymphoma21
Evidence-Based Minireview: Strategies to manage a severely HLA-alloimmunized patient with refractory thrombocytopenia20
The dos, don'ts, and nuances of thrombophilia testing18
Evidence-Based Minireview: Clinical utilization of panel-based molecular testing for patients with AML18
AL amyloidosis: untangling new therapies17
Dual-targeted regimens for the frontline treatment of CLL17
Relapsed ALL: CAR T vs transplant vs novel therapies17
Bispecific antibody therapies17
Lifelong TKI therapy: how to manage cardiovascular and other risks17
Evidence-Based Minireview: For overweight or obese persons with hemophilia A, should factor VIII dosing be based on ideal or actual body weight?16
Optimal strategies for carrier screening and prenatal diagnosis of α- and β-thalassemia16
What have we learned about the patient's experience of von Willebrand disease? A focus on women16
Biology of follicular lymphoma: insights and windows of clinical opportunity16
Pyruvate kinase activators: targeting red cell metabolism in sickle cell disease16
Modern management of Fanconi anemia16
Smoldering multiple myeloma: evolving diagnostic criteria and treatment strategies16
Cytoreduction for ET and PV: who, what, when, and how?16
Labor and delivery: DIC, HELLP, preeclampsia16
Burnett AE, Ragheb B, Kaatz S. Perioperative consultative hematology: can you clear my patient for a procedure? Hematology Am Soc Hematol Educ Program. 2021;2021:521-528.15
Intravenous iron therapy in pediatrics: who should get it and when is the right time?15
Novel platelet products including cold-stored platelets15
Management of Fanconi anemia beyond childhood15
Quantifying menorrhagia and overview of nonsurgical management of heavy menstrual bleeding15
Your chemo is no good here: management of high-risk MCL14
Novel conditioning and prophylaxis regimens for relapse prevention14
Treatment of VTE in the thrombocytopenic cancer patient14
Risk-stratification in frontline CLL therapy: standard of care13
Mutations and MRD: clinical implications of clonal ontogeny13
On the horizon: upcoming new agents for the management of ITP13
Inherited thrombophilia and recurrent miscarriage: is there a role for anticoagulation during pregnancy?13
New definitions for antiphospholipid syndrome: ready for clinical use?13
Neurological manifestations of MGUS13
Catastrophic antiphospholipid syndrome: a CAPS-tivating hematologic disease13
The POD24 challenge: where do we go from here for early progressors?13
To prophylax or not, and how much and how long? Controversies in VTE prevention for medical inpatients, including COVID-19 inpatients12
Diagnosis and management of hereditary hemochromatosis: lifestyle modification, phlebotomy, and blood donation12
Gene therapy for hemophilia12
Pegylated interferon: the who, why, and how12
Anticoagulation at the end of life: whether, when, and how to treat12
Dyskeratosis congenita and telomere biology disorders11
Novel immunotherapies in the treatment of AML: is there hope?11
Inpatient recognition and management of HLH11
How to evaluate the patient with a suspected mast cell disorder and how/when to manage symptoms11
T-cell–based therapies for treating relapsed or refractory mantle cell lymphoma10
Managing pregnancy in patients with sickle cell disease from a transfusion perspective10
To consolidate or not to consolidate: the role of autologous stem cell transplantation in MCL10
Iron overload in acquired sideroblastic anemias and MDS: pathophysiology and role of chelation and luspatercept10
Diagnostic pitfalls and conundrums in type 1 von Willebrand disease10
Hormone-related thrombosis: duration of anticoagulation, risk of recurrence, and the role of hypercoagulability testing10
Has PD-1 blockade changed the standard of care for cHL?10
Challenges in hospice and end-of-life care in the transfusion-dependent patient9
Large granular lymphocyte leukemia: a clonal disorder with autoimmune manifestations9
Updates on strategies to integrate palliative care in hematologic malignancy9
Givosiran: a targeted treatment for acute intermittent porphyria9
In pursuit of a functional cure for follicular lymphoma9
Patient-reported outcomes after CAR T-cell therapy in patients with hematological malignancies9
Targeted medical therapies for vascular anomalies9
What is the ideal approach—doublet, triplet, or quadruplet(s)?9
Atypical hemolytic uremic syndrome: diagnosis, management, and discontinuation of therapy9
Modified T cells as therapeutic agents8
Should posttransplant cyclophosphamide be considered standard of care for pediatric transplantation of acute leukemia?8
Have we reached a molecular era in myelodysplastic syndromes?8
Mutation- and MRD-informed treatment decisions for the transplant-eligible AML patient8
What makes a pediatric or young adult patient an appropriate transplant candidate?8
Individualized patient care in nodular lymphocyte-predominant Hodgkin lymphoma8
Biology of post-transplant relapse: actionable features8
Pregnancy in special populations: challenges and solutions practical aspects of managing von Willebrand disease in pregnancy8
Updates in infant acute lymphoblastic leukemia and the potential for targeted therapy7
Novel approaches to acute graft-versus-host disease prevention7
Passive immune therapies: another tool against COVID-197
Clinical manifestations of telomere biology disorders in adults7
Options at the time of relapse after anti-BCMA therapy7
Beyond the cell: novel noncellular immunotherapy approaches to multiple myeloma7
Using disease-modifying therapies in sickle cell disease7
What is the role of up-front autologous stem cell transplantation in mantle cell lymphoma?7
Resistance mutations in CML and how we approach them7
Amyloid consults do not have to be vexing7
Pyruvate kinase activators for treatment of pyruvate kinase deficiency7
Multiple myeloma: a paradigm for blending community and academic care7
Evidence-Based Minireview: In young children with severe sickle cell disease, do the benefits of HLA-identical sibling donor HCT outweigh the risks?7
How to avoid early mortality in acute promyelocytic leukemia7
Logistics, risks, and benefits of automated red blood cell exchange for patients with sickle cell disease7
Thrombosis and anticoagulation: clinical issues of special importance to hematologists who practice in Asia7
T-cell lymphopenia in frequent volunteer platelet donors7
β-Thalassemia: evolving treatment options beyond transfusion and iron chelation7
Molecular prognostication in Ph-negative MPNs in 20227
Upfront therapy: the case for continuous treatment7
Evolving landscape of JAK inhibition in myelofibrosis: monotherapy and combinations7
Identifying and treating iron deficiency anemia in pregnancy6
Williams KM. Noninfectious complications of hematopoietic cell transplantation. Hematology Am Soc Hematol Educ Program. 2021;2021:578-586.6
Novel therapies and combinations in CLL refractory to BTK inhibitors and venetoclax6
Selection of bispecific antibody therapies or CAR-T cell therapy in relapsed lymphomas6
Platelet components and bacterial contamination: hospital perspective 20226
Allogeneic transplantation for advanced acute leukemia6
Evidence-based management of pregnant women with sickle cell disease in high-income countries6
Cold AIHA and the best treatment strategies6
Next-generation therapy for lower-risk MDS6
Fitness and frailty in myeloma6
Beyond FAScinating: advances in diagnosis and management of autoimmune lymphoproliferative syndrome and activated PI3 kinase δ syndrome6
Diagnosis and laboratory monitoring of acquired hemophilia A6
Medical consult: aHUS, TTP? How to distinguish and what to do6
Perioperative consultative hematology: can you clear my patient for a procedure?6
Double-refractory Hodgkin lymphoma: tackling relapse after brentuximab vedotin and checkpoint inhibitors6
Fungal diagnostic testing and therapy: navigating the neutropenic period in children with high-risk leukemia6
Long-term health outcomes following curative therapies for sickle cell disease6
Thrombopoietin receptor agonists for chemotherapy-induced thrombocytopenia: a new solution for an old problem6
The optimal management of relapsed and refractory Hodgkin lymphoma: post–brentuximab and checkpoint inhibitor failure6
Evidence-Based Minireview: Molecular precision and clinical uncertainty: should molecular profiling be routinely used to guide risk stratification in MDS?6
Ph− ALL: immunotherapy in upfront treatment6
Heparin-induced thrombocytopenia and cardiovascular surgery6
Divergent paths: management of early relapsed follicular lymphoma5
Managing side effects: guidance for use of immunotherapies in multiple myeloma5
MPN and thrombosis was hard enough . . . now there's COVID-19 thrombosis too5
How old is too old? Frailty and geriatric assessments of older patients undergoing allogeneic HCT5
Inflamed—HLH, MAS, or something else?5
Prevention, diagnosis, and management of PE and DVT in pregnant women5
Whom should we treat with novel agents? Specific indications for specific and challenging populations5
The first relapse in multiple myeloma: how to pick the next best thing5
Selecting initial therapy in CLL5
Optimal approach to T-cell ALL5
How to assess hemostasis in patients with severe liver disease5
When to consider inherited marrow failure syndromes in adults5
Evidence-Based Minireview: When should autologous transplant or cellular therapy be considered for follicular lymphoma?5
Evidence-based obstetric management of women with sickle cell disease in low-income countries5
Mutational screening to improve the transplantation decision-making process in MDS5
Management of aggressive lymphoma after CAR T-cell therapy failure5
Approaches to optimize outcomes in transplant recipients5
Pyruvate kinase activators: targeting red cell metabolism in thalassemia5
Frontline treatment in CLL: the case for time-limited treatment4
How to recognize and manage COVID-19-associated coagulopathy4
Gene therapy for sickle cell disease4
TKI discontinuation in CML: how do we make more patients eligible? How do we increase the chances of a successful treatment-free remission?4
Long-term follow-up of CD19-CAR T-cell therapy in children and young adults with B-ALL4
New approaches to tackle cytopenic myelofibrosis4
Mitigating the risk of venous thromboembolism in patients with multiple myeloma receiving immunomodulatory-based therapy4
MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?4
Achieving MRD negativity in AML: how important is this and how do we get there?4
Clonal evolution in inherited marrow failure syndromes predicts disease progression4
Novel therapies upon failure of HMA plus venetoclax4
The evolution of targeted therapy in pediatric AML: gemtuzumab ozogamicin, FLT3/IDH/BCL2 inhibitors, and other therapies4
Diagnosis and clinical management of red cell membrane disorders4
Novel therapies vs hematopoietic cell transplantation in myelofibrosis: who, when, how?4
Current use of CAR T cells to treat multiple myeloma4
Advances in MGUS diagnosis, risk stratification, and management: introducing myeloma-defining genomic events4
Hitting the brakes on accelerated and blast-phase myeloproliferative neoplasms: current and emerging concepts4
Advances in the management of α-thalassemia major: reasons to be optimistic4
Optimizing outcomes in secondary AML4
Through thick and thin: confronting the aggressive cutaneous T-cell lymphomas3
Do all patients with primary refractory/first relapse of HL need autologous stem cell transplant?3
COVID-19 and thrombosis: searching for evidence3
BV and beyond: how to incorporate novel agents into PTCL management3
Incorporating gonadal health counseling into pediatric care of sickle cell patients3
IgG4-related disease for the hematologist3
Hypoxia-inducible factor activators: a novel class of oral drugs for the treatment of anemia of chronic kidney disease3
The role of stem cell transplant (auto and allo) in PTCL and CTCL3
Troubleshooting heparin resistance3
The intersection of sickle cell disease, stigma, and pain in Africa3
Chronic thromboembolic pulmonary hypertension: anticoagulation and beyond3
Practical guide for disease-modifying medication management of children and adolescents with sickle cell disease3
Treatment of Richter's syndrome3
Transplant in myeloma: who, when, and why?3
Renal manifestations of MGUS3
Increasing access to allogeneic hematopoietic cell transplant: an international perspective3
When to use stem cell transplantation for classical Hodgkin lymphoma3
Should we use bisphosphonates to treat bone complications in sickle cell disease?3
Newborn screening initiatives for sickle cell disease in Africa3
Sequencing bispecific antibodies and CAR T cells for FL3
Minimal intensity conditioning strategies for bone marrow failure: is it time for “preventative” transplants?3
Supportive care in myeloma—when treating the clone alone is not enough3
MGCS: where do we stand today?3
Does MRD have a role in the management of iNHL?3
Newly diagnosed multiple myeloma: making sense of the menu2
Planning GvHD preemptive therapy: risk factors, biomarkers, and prognostic scores2
Evidence-Based Minireview: Full dose, modified dose, or no anticoagulation for patients with cancer and acute VTE and thrombocytopenia2
MRD-directed therapy in CLL: ready for prime time?2
Blast and accelerated phase CML: room for improvement2
Chronic GVHD: review advances in prevention, novel endpoints, and targeted strategies2
Acute lymphoblastic leukemia in older adults: curtain call for conventional chemotherapy?2
Diamond-Blackfan anemia2
How to manage hemostasis in patients with liver disease during interventions2
Stem cell transplantation for ALL: you've always got a donor, why not always use it?2
Treatment of older adult or frail patients with multiple myeloma2
Acute pain episodes, acute chest syndrome, and pulmonary thromboembolism in pregnancy2
Incorporating novel agents into frontline treatment of Hodgkin lymphoma2
Approach to the patient with suspected hypereosinophilic syndrome2
Transplant for TP53-mutated MDS and AML: because we can or because we should?2
The burden of myeloma: novel approaches to disease assessment2
Risk factors and screening for neurocognitive impacts of therapy2
Mitigating, monitoring, and managing long-term chemotherapy- and radiation-induced cardiac toxicity2
The 5 most frequently asked questions about factor Xa inhibitors2
How to diagnose and manage antiphospholipid syndrome2
CHIP: is clonal hematopoiesis a surrogate for aging and other disease?2
What else do I need to worry about when treating graft-versus-host disease?2
Incidence, mechanism, and consequences of IV iron–induced hypophosphatemia2
New investigational combinations for higher-risk MDS2
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