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T. Abshire · SciRah

Researcher profile · Semantic Scholar

T. Abshire

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T. Abshire — researcher profile on SciRah

h-index: 38
Works: 142
Citations: 5,764

Most-cited papers

ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
F. Rodeghiero, A. Tosetto, T. Abshire, D. Arnold +4 more
2010Journal of Thrombosis and Haemostasis801 citations Open access
Semantic Scholar
Inhibitors of Factor VIII in Black Patients with Hemophilia
K. Viel, A. Ameri, T. Abshire, R. Iyer +10 more
2009New England Journal of Medicine209 citations Open access
Semantic Scholar
Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor.
V. Flood, J. Gill, P. Morateck, P. Christopherson +12 more
2010Blood188 citations Open access
Semantic Scholar
Outcomes after HLA-matched sibling transplantation or chemotherapy in children with B-precursor acute lymphoblastic leukemia in a second remission: a collaborative study of the Children's Oncology Group and the Center for International Blood and Marrow Transplant Research.
M. Eapen, E. Raetz, Mei-Jie Zhang, C. Muehlenbein +7 more
2005Blood168 citations Open access
Semantic Scholar
Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura.
C. Bennett, Z. Rogers, D. Kinnamon, J. Bussel +14 more
2006Blood146 citations Open access
Semantic Scholar
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.
V. Flood, P. Christopherson, J. Gill, K. Friedman +21 more
2016Blood118 citations Open access
Semantic Scholar
Prophylaxis in severe forms of von Willebrand’s disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)
T. Abshire, A. Federici, M. T. Alvarez, J. Bowen +11 more
2012Haemophilia117 citations Open access
Semantic Scholar
VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.
D. Bellissimo, P. Christopherson, V. Flood, J. Gill +9 more
2012Blood111 citations Open access
Semantic Scholar
Safety update on the use of recombinant factor VIIa and the treatment of congenital and acquired deficiency of factor VIII or IX with inhibitors
T. Abshire, G. Kenet
2008Haemophilia104 citations
Semantic Scholar
Evaluation for Bleeding Disorders in Suspected Child Abuse
J. Anderst, S. Carpenter, T. Abshire, J. Hord +12 more
2013Pediatrics100 citations
Semantic Scholar
The safety and efficacy of recombinant human blood coagulation factor IX in previously untreated patients with severe or moderately severe hemophilia B.
A. Shapiro, J. Di Paola, A. Cohen, K. Pasi +8 more
2005Blood98 citations
Semantic Scholar
Clinical evaluation of moroctocog alfa (AF‐CC), a new generation of B‐domain deleted recombinant factor VIII (BDDrFVIII) for treatment of haemophilia A: demonstration of safety, efficacy, and pharmacokinetic equivalence to full‐length recombinant factor VIII
M. Recht, L. Nemes, M. Matysiak, M. Manco-Johnson +10 more
2009Haemophilia90 citations
Semantic Scholar
In non-severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case–control study
C. Kempton, J. M. Soucie, C. Miller, C. Hooper +5 more
2010Journal of Thrombosis and Haemostasis73 citations Open access
Semantic Scholar
Fresh frozen plasma prepared with amotosalen HCl (S‐59) photochemical pathogen inactivation: transfusion of patients with congenital coagulation factor deficiencies
P. D. de Alarcón, R. Benjamin, M. Dugdale, C. Kessler +12 more
2005Transfusion70 citations
Semantic Scholar
Effect of Anticoagulant Therapy for 6 Weeks vs 3 Months on Recurrence and Bleeding Events in Patients Younger Than 21 Years of Age With Provoked Venous Thromboembolism: The Kids-DOTT Randomized Clinical Trial.
N. Goldenberg, J. Kittelson, T. Abshire, M. Bonaca +11 more
2022Journal of the American Medical Association (JAMA)68 citations Open access
Semantic Scholar
Evaluating for Suspected Child Abuse: Conditions That Predispose to Bleeding
S. Carpenter, T. Abshire, Emily Killough, J. Anderst
2013Pediatrics66 citations
Semantic Scholar
Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates
C. Kempton, J. M. Soucie, T. Abshire
2006Journal of Thrombosis and Haemostasis66 citations Open access
Semantic Scholar
Changes in bleeding patterns in von Willebrand disease after institution of long-term replacement therapy: results from the von Willebrand Disease Prophylaxis Network
E. Holm, T. Abshire, J. Bowen, M. A. Teresa Álvarez +18 more
2015Blood Coagulation and Fibrinolysis57 citations Open access
Semantic Scholar
Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment
S. Meeks, T. Abshire
2008Haemophilia55 citations Open access
Semantic Scholar
The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease
M. Makris, A. Federici, P. M. Mannucci, P. Bolton-Maggs +3 more
2015Haemophilia52 citations
Semantic Scholar
TEXTBOOK OF HEMOPHILIA
T. Abshire
200545 citations
Semantic Scholar
Initial Results of a Randomized, Prospective Trial of Prophylaxis To Prevent Joint Disease in Young Children with Factor VIII (FVIII) Deficiency.
M. Manco-Johnson, T. Abshire, Deborah L. Brown, G. Buchanan +10 more
200544 citations
Semantic Scholar
Transfusion Medicine and Hemostasis
B. Shaz, C. Hillyer, C. Abrams, M. Roshal +2 more
200938 citations
Semantic Scholar
A Study of Prospective Surveillance for Inhibitors among Persons with Haemophilia in the United States
J. M. Soucie, C. Miller, F. M. Kelly, Amanda B. Payne +21 more
2013Haemophilia37 citations Open access
Semantic Scholar
No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation.
V. Flood, K. Friedman, J. Gill, S. Haberichter +13 more
2013Blood33 citations Open access
Semantic Scholar
Comparison of the anticoagulant effect of a direct thrombin inhibitor and a low molecular weight heparin in an acquired antithrombin deficiency in children with acute lymphoblastic leukaemia treated with l‐asparaginase: an in vitro study
S. Kuhle, A. Lau, L. Bajzar, P. Vegh +9 more
2006British Journal of Haematology29 citations Open access
Semantic Scholar
Low VWF levels in children and lack of association with bleeding in children undergoing tonsillectomy.
J. Gill, S. Conley, Victoria P. Johnson, P. Christopherson +8 more
2020Blood Advances28 citations Open access
Semantic Scholar
The "parallel-cohort RCT": Novel design aspects and application in the Kids-DOTT trial of pediatric venous thromboembolism.
N. Goldenberg, M. Tripputi, M. Crowther, T. Abshire +3 more
2010Contemporary Clinical Trials28 citations
Semantic Scholar
Current Issues in Prophylactic Therapy for Persons with Hemophilia
A. Dunn, T. Abshire
2006Acta Haematologica24 citations
Semantic Scholar
Safety update on recombinant factor VIIa in the treatment of congenital and acquired hemophilia.
T. Abshire
2008Seminars in hematology (Print)21 citations
Semantic Scholar
Von Willebrand disease in the United States: perspective from the Zimmerman program
V. Flood, T. Abshire, P. Christopherson, K. Friedman +3 more
2018Annals of Blood18 citations Open access
Semantic Scholar
The von Willebrand disease prophylaxis network (vWD PN): exploring a treatment concept.
E. Berntorp, T. Abshire
2006Thrombosis Research18 citations
Semantic Scholar
Laboratory Variability in the Diagnosis of Type 2 VWD Variants
S. Digiandomenico, P. Christopherson, S. Haberichter, T. Abshire +47 more
2020Journal of Thrombosis and Haemostasis16 citations Open access
Semantic Scholar
The role of prophylaxis in the management of von Willebrand disease: today and tomorrow.
T. Abshire
2009Thrombosis Research15 citations
Semantic Scholar
Evaluation of factor VIII pharmacokinetics and anti‐factor VIII antibodies in four boys with haemophilia A and a poor clinical response to factor VIII
C. L. Kempton, S. Meeks, R. D. Harvey, T. Abshire
2011Haemophilia14 citations
Semantic Scholar
Recombinant tissue plasminogen activator may reduce frequency of central venous access device infection in hemophilia patients undergoing immune tolerance therapy
A. L. Dunn, T. Abshire
2008Pediatric Blood & Cancer14 citations
Semantic Scholar
Clinical uses of plasma and plasma fractions: plasma-derived products for hemophilias A and B, and for von Willebrand disease.
C. Josephson, T. Abshire
2006Baillière's Best Practice & Research: Clinical Haematology14 citations
Semantic Scholar
CONSENSUS ON A CORE CURRICULUM IN AMERICAN TRAINING PROGRAMS IN PEDIATRIC HEMATOLOGY–ONCOLOGY: A Report from the ASPHO Training Committee
C. Hastings, D. Wechsler, K. Stine, D. Graham +1 more
2007Pediatric Hematology & Oncology13 citations
Semantic Scholar
A community-based partnership to promote information infrastructure for bleeding disorders.
D. Aschman, T. Abshire, A. Shapiro, J. Lusher +2 more
2011American Journal of Preventive Medicine12 citations
Semantic Scholar
The Complete Type I VWD Cohort Of The Zimmerman Program For The Molecular and Clinical Biology Of VWD - Phenotypic Assignment, Mutation Frequency, and Bleeding Assessment
P. Christopherson, D. Bellissimo, J. Gill, S. Haberichter +12 more
201311 citations
Semantic Scholar
Prophylaxis and von Willebrand's disease (vWD).
T. Abshire
2006Thrombosis Research11 citations
Semantic Scholar
Ristocetin dependent cofactor activity in von Willebrand disease diagnosis: Limitations of relying on a single measure
P. Christopherson, S. Haberichter, V. Flood, Ursula Sicking +23 more
2022Research and Practice in Thrombosis and Haemostasis10 citations Open access
Semantic Scholar
Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score
M. Lavin, P. Christopherson, J. Grabell, T. Abshire +6 more
2022Journal of Thrombosis and Haemostasis10 citations Open access
Semantic Scholar
Guidelines for the Management of von Willebrand Disease 2021
Willebrand, V. Willebrand, Fviii Vwf, W. Nichols +496 more
2021Japanese Journal of Thrombosis and Hemostasis10 citations Open access
Semantic Scholar
Treatment of Relapsed Precursor-B Acute Lymphoblastic Leukemia With Intensive Chemotherapy: POG (Pediatric Oncology Group) Study 9411 (SIMAL 9)
M. Kelly, Xiao-Min Lu, M. Devidas, B. Camitta +6 more
2013Journal of pediatric hematology/oncology10 citations Open access
Semantic Scholar
Unraveling hemophilic arthropathy.
T. Abshire
2011Blood8 citations
Semantic Scholar
Von Willebrand factor mutations and new sequence variations identified in healthy controls are more frequent in the African American population
D. Bellissimo, P. Christopherson, V. Flood, J. Gill +9 more
20118 citations
Semantic Scholar
Factor VIII Prophylaxis Effects Outweigh Other Hemostasis Contributors in Predicting Severe Hemophilia A Joint Outcomes
B. Warren, L. Jacobson, C. Kempton, G. Buchanan +27 more
2019Haemophilia7 citations Open access
Semantic Scholar
rFIXFc for Immune Tolerance Induction in a Severe Hemophilia B Patient with an Inhibitor and Prior History of ITI Related Nephrotic Syndrome
L. Malec, T. Abshire, S. Jobe, G. White
2018Haemophilia7 citations
Semantic Scholar
Regular Replacement Therapy as Prophylaxis In Severe Forms of Von Willebrand Disease: Initial Results From the Von Willebrand Disease Prophylaxis Network (VWD PN) Study Group
E. Berntorp, T. Abshire, A. Federici
20103 citations
Semantic Scholar

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