Hematology-American Society of Hematology Education Program

Papers
(The median citation count of Hematology-American Society of Hematology Education Program is 3. 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 2021-05-01 to 2025-05-01.)
ArticleCitations
Diagnosis and therapeutic decision-making for the neutropenic patient61
When should gene therapy be considered for transfusion-dependent β-thalassemia patients?58
Your chemo is no good here: management of high-risk MCL54
Inherited thrombophilia and recurrent miscarriage: is there a role for anticoagulation during pregnancy?36
Neurological manifestations of MGUS35
On the horizon: upcoming new agents for the management of ITP33
Anticoagulation at the end of life: whether, when, and how to treat33
Labor and delivery: DIC, HELLP, preeclampsia30
Mastocytosis demystified29
Recognizing, defining, and managing CAR-T hematologic toxicities26
Inpatient recognition and management of HLH26
Hematopoietic cell transplantation for sickle cell disease: updates and future directions26
Bispecific antibody therapies25
Has PD-1 blockade changed the standard of care for cHL?25
Individualized patient care in nodular lymphocyte-predominant Hodgkin lymphoma24
Mutation- and MRD-informed treatment decisions for the transplant-eligible AML patient24
T-cell–based therapies for treating relapsed or refractory mantle cell lymphoma23
Double-refractory Hodgkin lymphoma: tackling relapse after brentuximab vedotin and checkpoint inhibitors22
To consolidate or not to consolidate: the role of autologous stem cell transplantation in MCL22
Logistics, risks, and benefits of automated red blood cell exchange for patients with sickle cell disease22
Selecting initial therapy in CLL21
Divergent paths: management of early relapsed follicular lymphoma21
Hypoxia-inducible factor activators: a novel class of oral drugs for the treatment of anemia of chronic kidney disease20
New approaches to tackle cytopenic myelofibrosis19
Advances in MGUS diagnosis, risk stratification, and management: introducing myeloma-defining genomic events19
MGCS: where do we stand today?18
Chronic GVHD: review advances in prevention, novel endpoints, and targeted strategies18
Increasing access to allogeneic hematopoietic cell transplant: an international perspective18
How to recognize and manage COVID-19-associated coagulopathy18
Fitness and frailty in myeloma18
BV and beyond: how to incorporate novel agents into PTCL management17
Incidence, mechanism, and consequences of IV iron–induced hypophosphatemia17
How to assess hemostasis in patients with severe liver disease17
Optimizing outcomes in secondary AML17
How to manage hemostasis in patients with liver disease during interventions17
Troubleshooting heparin resistance17
How to diagnose and manage antiphospholipid syndrome17
Minimal intensity conditioning strategies for bone marrow failure: is it time for “preventative” transplants?17
Incorporating novel agents into frontline treatment of Hodgkin lymphoma16
Mitigating, monitoring, and managing long-term chemotherapy- and radiation-induced cardiac toxicity16
Planning GvHD preemptive therapy: risk factors, biomarkers, and prognostic scores16
Hemophilia gene therapy: ushering in a new treatment paradigm?16
Running interferon interference in treating PV/ET: meeting unmet needs16
Management of TKI-resistant chronic phase CML16
The sum of the parts: what we can and cannot learn from comorbidity scores in allogeneic transplantation16
What is the optimal strategy for secondary prevention after venous thromboembolism in polycythemia vera?16
CHIP: is clonal hematopoiesis a surrogate for aging and other disease?15
Hematology 2022—what is complete HLA match in 2022?15
Consumptive coagulopathy in the ICU15
Special considerations in GI bleeding in VWD patients14
Management of limited-stage Hodgkin lymphoma14
Evaluating patients with autoimmune hemolytic anemia in the transfusion service and immunohematology reference laboratory: pretransfusion testing challenges and best transfusion-management strategies13
What to use to treat AML: the role of emerging therapies13
Demystifying autoimmune HIT: what it is, when to test, and how to treat13
Managing therapy-associated neurotoxicity in children with ALL13
Management of marginal zone lymphomas13
Atypical CML: diagnosis and treatment13
How to manage bleeding disorders in aging patients needing surgery13
Targeting hardship: poverty as a modifiable risk factor in childhood leukemia and lymphoma treatment12
Nontransplant treatment approaches for myeloid neoplasm with mutated TP5312
Infectious complications and vaccines12
Identifying Castleman disease from non-clonal inflammatory causes of generalized lymphadenopathy12
Thrombosis questions from the inpatient wards12
Approaches to management of HIT in complex scenarios, including cardiac surgery12
Organ function indications and potential improvements following curative therapy for sickle cell disease11
Adolescents and young adults (AYAs) vs pediatric patients: survival, risks, and barriers to enrollment11
Alloimmunization and hyperhemolysis in sickle cell disease11
Relapsed disease: off-the-shelf immunotherapies vs customized engineered products11
The evolving frontline management of CLL: are triplets better than doublets? How will we find out?11
Lower risk but high risk11
When does a PNH clone have clinical significance?11
Transplant in AML with measurable residual disease: proceed or defer?11
CNS prophylaxis in aggressive B-cell lymphoma11
Thrombocytopenia in pregnancy11
Cytoreduction for ET and PV: who, what, when, and how?10
How to evaluate the patient with a suspected mast cell disorder and how/when to manage symptoms10
What makes a pediatric or young adult patient an appropriate transplant candidate?10
Should older patients with low weight and CKD receive full-dose DOACs for treatment of acute proximal DVT?10
Treatment of VTE in the thrombocytopenic cancer patient10
Pyruvate kinase activators: targeting red cell metabolism in sickle cell disease10
Pegylated interferon: the who, why, and how10
What is the ideal approach—doublet, triplet, or quadruplet(s)?10
What is the role of up-front autologous stem cell transplantation in mantle cell lymphoma?10
Novel therapies and combinations in CLL refractory to BTK inhibitors and venetoclax9
Managing pregnancy in patients with sickle cell disease from a transfusion perspective9
MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?9
Novel therapies upon failure of HMA plus venetoclax9
β-Thalassemia: evolving treatment options beyond transfusion and iron chelation9
Clinical manifestations of telomere biology disorders in adults9
Frontline treatment in CLL: the case for time-limited treatment9
Whom should we treat with novel agents? Specific indications for specific and challenging populations9
Next-generation therapy for lower-risk MDS9
Ph− ALL: immunotherapy in upfront treatment9
Managing side effects: guidance for use of immunotherapies in multiple myeloma9
IV iron formulations and use in adults8
Treatment of older adult or frail patients with multiple myeloma8
The role of stem cell transplant (auto and allo) in PTCL and CTCL8
Approach to the patient with suspected hypereosinophilic syndrome8
Sequencing bispecific antibodies and CAR T cells for FL8
Thrombocytopenia and liver disease: pathophysiology and periprocedural management8
In 2022, which is preferred: haploidentical or cord transplant?8
Should we use bisphosphonates to treat bone complications in sickle cell disease?8
Warm autoimmune hemolytic anemia and the best treatment strategies8
Barriers to accessing cellular therapy for patients receiving care in community practices8
Diamond-Blackfan anemia8
Stem cell transplantation for ALL: you've always got a donor, why not always use it?8
What else do I need to worry about when treating graft-versus-host disease?8
Porphyria cutanea tarda: a unique iron-related disorder8
The approach of HMA plus VEN with or without BMT for all patients with AML7
Luspatercept: a treatment for ineffective erythropoiesis in thalassemia7
Understanding differential technologies for detection of MRD and how to incorporate into clinical practice7
Long-term prophylaxis: what are our options and how to define success?7
Evidence-Based Minireview: How to utilize new therapies for sickle cell disease7
How to classify risk based on clinical and molecular modeling: integrating molecular markers in the risk assessment of myelodysplastic syndrome7
Immunology 101: fundamental immunology for the practicing hematologist7
When should we use it? The role of brentuximab vedotin in 20247
Diagnosis and clinical management of enzymopathies7
Psychosocial and financial issues after hematopoietic cell transplantation7
Clonal hematopoiesis in frequent whole blood donors7
von Willebrand disease and heavy menstrual bleeding: when and how to test7
Are transplant indications changing for myelofibrosis?7
The spectrum of Ph-negative disease: CNL and CSF3R-related disorders7
Sequencing therapy in relapsed DLBCL7
Posttransplant complications in patients with marrow failure syndromes: are we improving long-term outcomes?7
Hitting the brakes on accelerated and blast-phase myeloproliferative neoplasms: current and emerging concepts6
Diagnosis and clinical management of red cell membrane disorders6
Heparin-induced thrombocytopenia and cardiovascular surgery6
Multiple myeloma: a paradigm for blending community and academic care6
Risk-stratification in frontline CLL therapy: standard of care6
Evolving landscape of JAK inhibition in myelofibrosis: monotherapy and combinations6
Intravenous iron therapy in pediatrics: who should get it and when is the right time?6
COVID-19 and thrombosis: searching for evidence6
The intersection of sickle cell disease, stigma, and pain in Africa6
New definitions for antiphospholipid syndrome: ready for clinical use?6
Hormone-related thrombosis: duration of anticoagulation, risk of recurrence, and the role of hypercoagulability testing6
Management of Fanconi anemia beyond childhood6
Selection of bispecific antibody therapies or CAR-T cell therapy in relapsed lymphomas6
MPN and thrombosis was hard enough . . . now there's COVID-19 thrombosis too6
Newborn screening initiatives for sickle cell disease in Africa6
Novel platelet products including cold-stored platelets6
Amyloid consults do not have to be vexing6
Using disease-modifying therapies in sickle cell disease6
Acute lymphoblastic leukemia in young adults: which up-front treatment?5
No crystal stair: supporting fertility care and the pursuit of pregnancy in women with sickle cell disease5
Clonal evolution in inherited marrow failure syndromes predicts disease progression5
Maintenance strategies for relapse prevention and treatment5
Prevention and management of venous thromboembolism in pregnancy: cutting through the practice variation5
Potential and emerging therapeutics for HHT5
Management of hemolytic transfusion reactions5
Mitigating and managing infection risk in adults treated with CAR T-cell therapy5
Renal manifestations of MGUS5
New investigational combinations for higher-risk MDS5
When to consider inherited marrow failure syndromes in adults5
Knowledge to date on secondary malignancy following hematopoietic cell transplantation for sickle cell disease5
Challenges to successful outcomes in AYAs with ALL and potential solutions5
Cryptogenic oozers and bruisers5
Novel clinical care models for patients with sickle cell disease5
Molina JC, Rotz S. Acute lymphoblastic leukemia in young adults: which up-front treatment? Hematology Am Soc Hematol Educ Program. 2023;2023(1):573-580.5
The first relapse in multiple myeloma: how to pick the next best thing5
Evidence-Based Minireview: Full dose, modified dose, or no anticoagulation for patients with cancer and acute VTE and thrombocytopenia5
Double-hit lymphoma: optimizing therapy5
Novel investigational approaches for high-risk genetic subsets of AML: TP53, KMT2A, FLT35
Sharing is caring: a network collaborative approach to identify and address barriers in accessing clinical trials in adolescents and young adults with leukemia and lymphoma5
Transplantation in CML in the TKI era: who, when, and how?5
Thilagar B, Beidoun M, Rhoades R, Kaatz S. COVID-19 and thrombosis: searching for evidence. Hematology Am Soc Hematol Educ Program. 2021;2021:621-627.4
Cellular therapy for multiple myeloma: what's now and what's next4
Ph+ ALL in 2022: is there an optimal approach?4
Quantifying menorrhagia and overview of nonsurgical management of heavy menstrual bleeding4
Epidemiology and treatment of priapism in sickle cell disease4
Late complications and long-term care of adult CAR T-cell patients4
Platton S, Sivapalaratnam S, Raheja P. Diagnosis and laboratory monitoring of acquired hemophilia A. Hematology Am Soc Hematol Educ Program. 2023;2023(1):11-18.4
How immunodeficiency can lead to malignancy4
End-of-life care for people with sickle cell disease: barriers to and facilitators of high-quality care4
High-risk multiple myeloma: how to treat at diagnosis and relapse?4
Current use of bispecific antibodies to treat multiple myeloma4
The range of haploidentical transplant protocols in sickle cell disease: all haplos are not created equally4
Considerations for next therapy after anti-CD38 monoclonal antibodies used as first line4
How to manage ITP with life-threatening bleeding4
Ph+ ALL: new approaches for upfront therapy4
Sickle cell disease in India: the journey and hope for the future4
Sex, lies, and iron deficiency: a call to change ferritin reference ranges4
Unexplained arterial thrombosis: approach to diagnosis and treatment4
Optimal strategies for carrier screening and prenatal diagnosis of α- and β-thalassemia4
Should posttransplant cyclophosphamide be considered standard of care for pediatric transplantation of acute leukemia?3
Acute GVHD: think before you treat3
Iron overload in acquired sideroblastic anemias and MDS: pathophysiology and role of chelation and luspatercept3
Passive immune therapies: another tool against COVID-193
Pyruvate kinase activators: targeting red cell metabolism in thalassemia3
Mutational screening to improve the transplantation decision-making process in MDS3
Beyond FAScinating: advances in diagnosis and management of autoimmune lymphoproliferative syndrome and activated PI3 kinase δ syndrome3
Givosiran: a targeted treatment for acute intermittent porphyria3
Patient-reported outcomes after CAR T-cell therapy in patients with hematological malignancies3
Optimal approach to T-cell ALL3
Catastrophic antiphospholipid syndrome: a CAPS-tivating hematologic disease3
Perioperative consultative hematology: can you clear my patient for a procedure?3
Thrombopoietin receptor agonists for chemotherapy-induced thrombocytopenia: a new solution for an old problem3
Identifying and treating iron deficiency anemia in pregnancy3
Platelet components and bacterial contamination: hospital perspective 20223
AL amyloidosis: untangling new therapies3
Dual-targeted regimens for the frontline treatment of CLL3
Thrombosis and anticoagulation: clinical issues of special importance to hematologists who practice in Asia3
Approaches to optimize outcomes in transplant recipients3
Novel approaches to acute graft-versus-host disease prevention3
Modified T cells as therapeutic agents3
0.085319042205811