Hematology-American Society of Hematology Education Program

Papers
(The TQCC of Hematology-American Society of Hematology Education Program is 12. 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 2021-12-01 to 2025-12-01.)
ArticleCitations
Inherited thrombophilia and recurrent miscarriage: is there a role for anticoagulation during pregnancy?82
Your chemo is no good here: management of high-risk MCL80
When should gene therapy be considered for transfusion-dependent β-thalassemia patients?70
Bispecific antibody therapies52
Labor and delivery: DIC, HELLP, preeclampsia50
Hematopoietic cell transplantation for sickle cell disease: updates and future directions41
Neurological manifestations of MGUS41
Anticoagulation at the end of life: whether, when, and how to treat39
On the horizon: upcoming new agents for the management of ITP38
Mastocytosis demystified36
Diagnosis and therapeutic decision-making for the neutropenic patient35
Inpatient recognition and management of HLH33
Recognizing, defining, and managing CAR-T hematologic toxicities33
Individualized patient care in nodular lymphocyte-predominant Hodgkin lymphoma32
Has PD-1 blockade changed the standard of care for cHL?31
Mutation- and MRD-informed treatment decisions for the transplant-eligible AML patient28
To consolidate or not to consolidate: the role of autologous stem cell transplantation in MCL27
Logistics, risks, and benefits of automated red blood cell exchange for patients with sickle cell disease27
Divergent paths: management of early relapsed follicular lymphoma26
Double-refractory Hodgkin lymphoma: tackling relapse after brentuximab vedotin and checkpoint inhibitors26
Selecting initial therapy in CLL26
T-cell–based therapies for treating relapsed or refractory mantle cell lymphoma26
Minimal intensity conditioning strategies for bone marrow failure: is it time for “preventative” transplants?25
Incidence, mechanism, and consequences of IV iron–induced hypophosphatemia24
How to recognize and manage COVID-19-associated coagulopathy24
New approaches to tackle cytopenic myelofibrosis24
Hypoxia-inducible factor activators: a novel class of oral drugs for the treatment of anemia of chronic kidney disease23
Increasing access to allogeneic hematopoietic cell transplant: an international perspective23
Advances in MGUS diagnosis, risk stratification, and management: introducing myeloma-defining genomic events23
Fitness and frailty in myeloma23
Optimizing outcomes in secondary AML22
BV and beyond: how to incorporate novel agents into PTCL management22
MGCS: where do we stand today?22
Chronic GVHD: review advances in prevention, novel endpoints, and targeted strategies22
How to assess hemostasis in patients with severe liver disease21
Running interferon interference in treating PV/ET: meeting unmet needs21
What is the optimal strategy for secondary prevention after venous thromboembolism in polycythemia vera?21
Incorporating novel agents into frontline treatment of Hodgkin lymphoma21
Troubleshooting heparin resistance21
How to manage hemostasis in patients with liver disease during interventions21
The sum of the parts: what we can and cannot learn from comorbidity scores in allogeneic transplantation20
CHIP: is clonal hematopoiesis a surrogate for aging and other disease?20
Consumptive coagulopathy in the ICU20
Planning GvHD preemptive therapy: risk factors, biomarkers, and prognostic scores20
Management of TKI-resistant chronic phase CML19
Demystifying autoimmune HIT: what it is, when to test, and how to treat19
Mitigating, monitoring, and managing long-term chemotherapy- and radiation-induced cardiac toxicity19
Atypical CML: diagnosis and treatment19
Hematology 2022—what is complete HLA match in 2022?19
Hemophilia gene therapy: ushering in a new treatment paradigm?19
How to diagnose and manage antiphospholipid syndrome19
How to manage bleeding disorders in aging patients needing surgery18
What to use to treat AML: the role of emerging therapies18
Special considerations in GI bleeding in VWD patients18
Management of limited-stage Hodgkin lymphoma18
Evaluating patients with autoimmune hemolytic anemia in the transfusion service and immunohematology reference laboratory: pretransfusion testing challenges and best transfusion-management strategies18
Managing therapy-associated neurotoxicity in children with ALL17
Management of marginal zone lymphomas17
Infectious complications and vaccines17
Approaches to management of HIT in complex scenarios, including cardiac surgery17
Thrombosis questions from the inpatient wards17
Identifying Castleman disease from non-clonal inflammatory causes of generalized lymphadenopathy16
Lower risk but high risk16
Transplant in AML with measurable residual disease: proceed or defer?15
The evolving frontline management of CLL: are triplets better than doublets? How will we find out?15
CNS prophylaxis in aggressive B-cell lymphoma15
Nontransplant treatment approaches for myeloid neoplasm with mutated TP5315
Targeting hardship: poverty as a modifiable risk factor in childhood leukemia and lymphoma treatment15
Organ function indications and potential improvements following curative therapy for sickle cell disease15
Adolescents and young adults (AYAs) vs pediatric patients: survival, risks, and barriers to enrollment15
Alloimmunization and hyperhemolysis in sickle cell disease15
Pyruvate kinase activators: targeting red cell metabolism in sickle cell disease14
What makes a pediatric or young adult patient an appropriate transplant candidate?14
Thrombocytopenia in pregnancy14
When does a PNH clone have clinical significance?14
Treatment of VTE in the thrombocytopenic cancer patient14
How to evaluate the patient with a suspected mast cell disorder and how/when to manage symptoms14
Pegylated interferon: the who, why, and how14
Relapsed disease: off-the-shelf immunotherapies vs customized engineered products14
Should older patients with low weight and CKD receive full-dose DOACs for treatment of acute proximal DVT?14
Cytoreduction for ET and PV: who, what, when, and how?14
Next-generation therapy for lower-risk MDS13
What is the ideal approach—doublet, triplet, or quadruplet(s)?13
β-Thalassemia: evolving treatment options beyond transfusion and iron chelation13
Ph− ALL: immunotherapy in upfront treatment13
What is the role of up-front autologous stem cell transplantation in mantle cell lymphoma?13
Clinical manifestations of telomere biology disorders in adults13
Managing pregnancy in patients with sickle cell disease from a transfusion perspective13
Novel therapies and combinations in CLL refractory to BTK inhibitors and venetoclax13
Approach to the patient with suspected hypereosinophilic syndrome12
Novel therapies upon failure of HMA plus venetoclax12
Should we use bisphosphonates to treat bone complications in sickle cell disease?12
Frontline treatment in CLL: the case for time-limited treatment12
The role of stem cell transplant (auto and allo) in PTCL and CTCL12
MRD in adult Ph/BCR-ABL-negative ALL: how best to eradicate?12
Sequencing bispecific antibodies and CAR T cells for FL12
Managing side effects: guidance for use of immunotherapies in multiple myeloma12
Whom should we treat with novel agents? Specific indications for specific and challenging populations12
What else do I need to worry about when treating graft-versus-host disease?12
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