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Riten Kumar, M.B.,B.S.

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Biography
Medical College, University of Calcutta, Kolkata, WB, IndiaMBBS02/2004Medicine
State University of New York, Downstate Campus, Brooklyn, NY, USA06/2008Residency, Pediatrics
Mayo Clinic, Rochester, MN, USA06/2011Fellowship, Pediatric Hematology/Oncology
Mayo Clinic, Rochester, MN, USAMSc05/2011Clinical and Translational Sciences
Hospital for Sick Children, University of Toronto, Toronto, ON, Canada10/2013Fellowship Pediatric Thrombosis/Hemostasis
2018 - 2019
Faculty Award for Clinical and Translational Sciences
2016 - 2019
Pediatric/Neonatal SSC Research Award
2016 - 2019
Mentored Research Award
2015 - 2016
Faculty Award for Teaching
2015 - 2016
Clinical Research Training Institute (CRTI) participant
2014 - 2015
Faculty Award for Citizenship
2014 - 2015
Eberhard F. Mammen Young Investigator Award
2014 - 2015
Young Researcher Award
2007 - 2008
Peter H. Karl Award (Research)

Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Young G, Lensing AWA, Monagle P, Male C, Thelen K, Willmann S, Palumbo JS, Kumar R, Nurmeev I, Hege K, Bajolle F, Connor P, Hooimeijer HL, Torres M, Chan AKC, Kenet G, Holzhauer S, Santamaría A, Amedro P, Beyer-Westendorf J, Martinelli I, Massicotte MP, Smith WT, Berkowitz SD, Schmidt S, Price V, Prins MH, Kubitza D. Rivaroxaban for treatment of pediatric venous thromboembolism. An Einstein-Jr phase 3 dose-exposure-response evaluation. J Thromb Haemost. 2020 07; 18(7):1672-1685. PMID: 32246743.
    Citations: 2     Fields:    
  2. Belsky J, Warren P, Stanek J, Kumar R. Catheter-directed thrombolysis for submassive pulmonary embolism in children: A case series. Pediatr Blood Cancer. 2020 04; 67(4):e28144. PMID: 31876109.
    Citations:    Fields:    Translation:Humans
  3. Male C, Lensing AWA, Palumbo JS, Kumar R, Nurmeev I, Hege K, Bonnet D, Connor P, Hooimeijer HL, Torres M, Chan AKC, Kenet G, Holzhauer S, Santamaría A, Amedro P, Chalmers E, Simioni P, Bhat RV, Yee DL, Lvova O, Beyer-Westendorf J, Biss TT, Martinelli I, Saracco P, Peters M, Kállay K, Gauger CA, Massicotte MP, Young G, Pap AF, Majumder M, Smith WT, Heubach JF, Berkowitz SD, Thelen K, Kubitza D, Crowther M, Prins MH, Monagle P. Rivaroxaban compared with standard anticoagulants for the treatment of acute venous thromboembolism in children: a randomised, controlled, phase 3 trial. Lancet Haematol. 2020 Jan; 7(1):e18-e27. PMID: 31699660.
    Citations: 5     Fields:    Translation:HumansCTClinical Trials
  4. Kumar R, Warren P, Mannava K. Popliteal Artery Entrapment Syndrome Presenting with Critical Limb Ischemia in an Adolescent. J Pediatr. 2020 02; 217:215-215.e1. PMID: 31606150.
    Citations:    Fields:    Translation:Humans
  5. Monagle P, Lensing AWA, Thelen K, Martinelli I, Male C, Santamaría A, Samochatova E, Kumar R, Holzhauer S, Saracco P, Simioni P, Robertson J, Grangl G, Halton J, Connor P, Young G, Molinari AC, Nowak-Göttl U, Kenet G, Kapsa S, Willmann S, Pap AF, Becka M, Twomey T, Beyer-Westendorf J, Prins MH, Kubitza D. Bodyweight-adjusted rivaroxaban for children with venous thromboembolism (EINSTEIN-Jr): results from three multicentre, single-arm, phase 2 studies. Lancet Haematol. 2019 Oct; 6(10):e500-e509. PMID: 31420317.
    Citations: 3     Fields:    Translation:HumansCTClinical Trials
  6. Kumar R, Dawson J, Varga E, Canini JT, Monda KL, Dunn AL. Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male. Pediatr Blood Cancer. 2019 09; 66(9):e27832. PMID: 31131962.
    Citations:    Fields:    Translation:HumansCells
  7. Kumar R, Vidaurre J, Gedela S. Valproic Acid-Induced Coagulopathy. Pediatr Neurol. 2019 09; 98:25-30. PMID: 31201069.
    Citations:    Fields:    Translation:Humans
  8. Saini S, Folta AN, Harsh KL, Stanek JR, Dunn AL, O'Brien SH, Kumar R. Anti-Factor Xa-Based Monitoring of Unfractionated Heparin: Clinical Outcomes in a Pediatric Cohort. J Pediatr. 2019 06; 209:212-219.e1. PMID: 30961988.
    Citations:    Fields:    Translation:Humans
  9. Sharma R, Woods GM, Creary S, O'Brien S, Stanek J, Hor K, Gallagher C, Dunn AL, Kumar R. Impact of erythrocytapheresis on natural anticoagulant levels in children with sickle cell disease: A pilot study. Pediatr Blood Cancer. 2019 04; 66(4):e27588. PMID: 30548773.
    Citations:    Fields:    Translation:Humans
  10. Kumar R, Harsh K, Saini S, O'Brien SH, Stanek J, Warren P, Giver J, Go MR, Kerlin BA. Treatment-Related Outcomes in Paget-Schroetter Syndrome-A Cross-Sectional Investigation. J Pediatr. 2019 04; 207:226-232.e1. PMID: 30528572.
    Citations:    Fields:    Translation:Humans
  11. Valasek AE, Warren P, Kumar R. Klinefelter syndrome as a risk factor for recurrent deep vein thrombosis in an adolescent male: Significance of a thorough physical examination. Pediatr Blood Cancer. 2018 08; 65(8):e27080. PMID: 29633496.
    Citations: 1     Fields:    Translation:Humans
  12. Woods GM, Sharma R, Creary S, O'Brien S, Stanek J, Hor K, Young J, Dunn AL, Kumar R. Venous Thromboembolism in Children with Sickle Cell Disease: A Retrospective Cohort Study. J Pediatr. 2018 06; 197:186-190.e1. PMID: 29605397.
    Citations: 4     Fields:    Translation:Humans
  13. Kumar R, Stanek J, Creary S, Dunn A, O'Brien SH. Prevalence and risk factors for venous thromboembolism in children with sickle cell disease: an administrative database study. Blood Adv. 2018 02 13; 2(3):285-291. PMID: 29431623.
    Citations: 8     Fields:    Translation:Humans
  14. Bhat R, Kumar R, Kwon S, Murthy K, Liem RI. Risk Factors for Neonatal Venous and Arterial Thromboembolism in the Neonatal Intensive Care Unit-A Case Control Study. J Pediatr. 2018 04; 195:28-32. PMID: 29398052.
    Citations: 1     Fields:    Translation:Humans
  15. Wedekind MF, Warren P, Shah S, Kumar R. Mesoaortic compression of a left-sided inferior vena-cava presenting as recurrent pulmonary embolism in a child-a novel anatomic thrombophilia? Pediatr Blood Cancer. 2018 06; 65(6):e26986. PMID: 29350462.
    Citations:    Fields:    Translation:Humans
  16. Rangarajan HG, Stanek JR, Abu-Arja R, Bajwa RPS, Auletta JJ, Lee DA, O'Brien SH, Kumar R. Venous Thromboembolism in Pediatric Hematopoietic Cell Transplant: A Multicenter Cohort Study. Biol Blood Marrow Transplant. 2018 02; 24(2):337-342. PMID: 29128552.
    Citations:    Fields:    Translation:Humans
  17. Woods GM, Stanek J, Harrison S, Texter K, Kerlin BA, Dunn AL, Kumar R. Activated Partial Thromboplastin Time versus Anti-Factor Xa Levels for Monitoring Unfractionated Heparin Therapy in Children: An Institutional Experience. J Pediatr Hematol Oncol. 2017 10; 39(7):576-577. PMID: 28902081.
    Citations: 1     Fields:    Translation:Humans
  18. Kumar R, Kerlin BA. Thrombosis of the Abdominal Veins in Childhood. Front Pediatr. 2017; 5:188. PMID: 28929091.
    Citations: 1     
  19. Tarango C, Kumar R, Patel M, Blackmore A, Warren P, Palumbo JS. Inferior vena cava atresia predisposing to acute lower extremity deep vein thrombosis in children: A descriptive dual-center study. Pediatr Blood Cancer. 2018 Feb; 65(2). PMID: 28853209.
    Citations: 1     Fields:    Translation:HumansCTClinical Trials
  20. Lo WD, Kumar R. Arterial Ischemic Stroke in Children and Young Adults. Continuum (Minneap Minn). 2017 02; 23(1, Cerebrovascular Disease):158-180. PMID: 28157749.
    Citations: 1     Fields:    Translation:Humans
  21. Kumar R, Creary S, Varga EA, Kahwash SB. Thrombocytopenia Pitfalls: Misdiagnosing Type 2B von Willebrand Disease as Ethylenediaminetetraacetic Acid-Dependent Pseudothrombocytopenia. J Pediatr. 2016 Aug; 175:238-238.e1. PMID: 27215777.
    Citations: 2     Fields:    Translation:Humans
  22. Wang TF, Dawson JE, Forman-Kay JD, Kahr WHA, Williams S, Chan AK, Kumar R. Molecular structural analysis of a novel and de-novo mutation in the SERPINC1 gene associated with type 1 antithrombin deficiency. Br J Haematol. 2017 05; 177(4):654-656. PMID: 27098850.
    Citations: 2     Fields:    Translation:HumansCells
  23. Kumar R, Bouskill V, Schneiderman JE, Pluthero FG, Kahr WH, Craik A, Clark D, Whitney K, Zhang C, Rand ML, Carcao M. Impact of aerobic exercise on haemostatic indices in paediatric patients with haemophilia. Thromb Haemost. 2016 06 02; 115(6):1120-8. PMID: 26917411.
    Citations:    Fields:    Translation:Humans
  24. Kumar R, Dunn A, Carcao M. Changing Paradigm of Hemophilia Management: Extended Half-Life Factor Concentrates and Gene Therapy. Semin Thromb Hemost. 2016 Feb; 42(1):18-29. PMID: 26771678.
    Citations: 4     Fields:    Translation:Humans
  25. Kumar R, O'Brien SH. aPTT in children receiving UFH: time for a change? Blood. 2015 Oct 29; 126(18):2075-6. PMID: 26516213.
    Citations: 1     Fields:    Translation:Humans
  26. Kumar R, Dawson JE, Chan AK, Forman-Kay JD, Kahr WH, Williams S. c.1058C>T variant in the SERPINC1 gene is pathogenic for antithrombin deficiency. Br J Haematol. 2015 Jul; 170(1):123-5. PMID: 25522812.
    Citations:    Fields:    Translation:HumansCells
  27. Kumar R, Rodriguez V, Matsumoto JM, Khan SP, Weaver AL, McBane RD, Beebe TJ, Heit JA. Prevalence and risk factors for post thrombotic syndrome after deep vein thrombosis in children: a cohort study. Thromb Res. 2015 Feb; 135(2):347-51. PMID: 25528070.
    Citations: 2     Fields:    Translation:Humans
  28. Kottschade LA, Grotz TE, Dronca RS, Salomao DR, Pulido JS, Wasif N, Jakub JW, Bagaria SP, Kumar R, Kaur JS, Morita SY, Moran SL, Nguyen JT, Nguyen EC, Hand JL, Erickson LA, Brewer JD, Baum CL, Miller RC, Swanson DL, Lowe V, Markovic SN. Rare presentations of primary melanoma and special populations: a systematic review. Am J Clin Oncol. 2014 Dec; 37(6):635-41. PMID: 23563206.
    Citations: 8     Fields:    Translation:Humans
  29. Kumar R, Chan AK, Dawson JE, Forman-Kay JD, Kahr WH, Williams S. Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study. Br J Haematol. 2014 Jul; 166(1):130-9. PMID: 24684277.
    Citations: 2     Fields:    Translation:Humans
  30. Kumar R, Rodriguez V, Matsumoto JM, Khan SP, Weaver AL, McBane RD, Beebe TJ, Heit JA. Health-related quality of life in children and young adults with post-thrombotic syndrome: results from a cross-sectional study. Pediatr Blood Cancer. 2014 Mar; 61(3):546-51. PMID: 24347376.
    Citations: 3     Fields:    Translation:Humans
  31. Kumar R, Carcao M. Inherited abnormalities of coagulation: hemophilia, von Willebrand disease, and beyond. Pediatr Clin North Am. 2013 Dec; 60(6):1419-41. PMID: 24237980.
    Citations: 3     Fields:    Translation:Humans
  32. Kumar R, Kahr WH. Congenital thrombocytopenia: clinical manifestations, laboratory abnormalities, and molecular defects of a heterogeneous group of conditions. Hematol Oncol Clin North Am. 2013 Jun; 27(3):465-94. PMID: 23714308.
    Citations: 5     Fields:    Translation:Humans
  33. Kumar R, Stain AM, Hilliard P, Carcao M. Consequences of delayed therapy for sports-related bleeds in patients with mild-to-moderate haemophilia and type 3 von Willebrand's disease not on prophylaxis. Haemophilia. 2013 Jul; 19(4):e264-7. PMID: 23647798.
    Citations: 1     Fields:    Translation:Humans
  34. Kumar R, Moharir M, Yau I, Williams S. A novel mutation in the SerpinC1 gene presenting as unprovoked neonatal cerebral sinus venous thrombosis in a kindred. Pediatr Blood Cancer. 2013 Jan; 60(1):133-6. PMID: 22997155.
    Citations:    Fields:    Translation:Humans
  35. Warad D, Kumar R, Rodriguez V. Treatment of Hodgkin's lymphoma in a patient with type III von Willebrand's disease. Haemophilia. 2012 Sep; 18(5):e378-9. PMID: 22757977.
    Citations:    Fields:    Translation:Humans
  36. Nageswara Rao AA, Kumar R, Altaf S, Gourde JA, Rodriguez V, Khan SP. Pretransplant conditioning with Campath-1H (alemtuzumab) in pediatric matched unrelated hematopoietic stem cell transplants: an institutional experience. J Pediatr Hematol Oncol. 2012 Mar; 34(2):96-100. PMID: 22146532.
    Citations:    Fields:    Translation:Humans
  37. Kumar R, Rodriguez V, Matsumoto JM, Khan SP, Weaver AL, McBane RD, Heit JA. Development and initial validation of a questionnaire to diagnose the presence and severity of post-thrombotic syndrome in children. Pediatr Blood Cancer. 2012 Apr; 58(4):643-4. PMID: 22190414.
    Citations: 2     Fields:    Translation:HumansCTClinical Trials
  38. Kumar R, Rodriguez V, Khan SP, Laack NN, Arndt CA. Postradiation dermatofibrosarcoma protuberans in a patient with Wilms tumor. J Pediatr Hematol Oncol. 2011 Dec; 33(8):635-6. PMID: 21423044.
    Citations:    Fields:    Translation:Humans
  39. Kumar R, Galardy PJ, Dogan A, Rodriguez V, Khan SP. Rituximab in combination with multiagent chemotherapy for pediatric follicular lymphoma. Pediatr Blood Cancer. 2011 Aug; 57(2):317-20. PMID: 21462303.
    Citations: 3     Fields:    Translation:Humans
  40. Kumar R, Pruthi RK, Kobrinsky N, Shaughnessy WJ, McKusick MA, Rodriguez V. Pelvic pseudotumor and pseudoaneurysm in a pediatric patient with moderate hemophilia B: successful management with arterial embolization and surgical excision. Pediatr Blood Cancer. 2011 Mar; 56(3):484-7. PMID: 21105052.
    Citations:    Fields:    Translation:Humans
  41. Kumar R, Khan SP, Joshi DD, Shaw GR, Ketterling RP, Feldman AL. Pediatric histiocytic sarcoma clonally related to precursor B-cell acute lymphoblastic leukemia with homozygous deletion of CDKN2A encoding p16INK4A. Pediatr Blood Cancer. 2011 Feb; 56(2):307-10. PMID: 20973102.
    Citations: 12     Fields:    Translation:Humans
  42. Oliveira JL, Kumar R, Khan SP, Law ME, Erickson-Johnson M, Oliveira AM, Ketterling RP, Dogan A. Successful treatment of a child with T/myeloid acute bilineal leukemia associated with TLX3/BCL11B fusion and 9q deletion. Pediatr Blood Cancer. 2011 Mar; 56(3):467-9. PMID: 21225930.
    Citations: 7     Fields:    Translation:HumansCells
  43. Kumar R, Qureshi S, Mohanty P, Rao SP, Miller ST. A short course of prednisone in the management of acute chest syndrome of sickle cell disease. J Pediatr Hematol Oncol. 2010 Apr; 32(3):e91-4. PMID: 20216237.
    Citations: 6     Fields:    Translation:Humans
  44. Riten K, Shahina Q, Jeannette J, Palma-Diaz MF. A severe case of acute generalized exanthematous pustulosis (AGEP) in a child after the administration of amoxicillin-clavulanic acid: brief report. Pediatr Dermatol. 2009 Sep-Oct; 26(5):623-5. PMID: 19840330.
    Citations:    Fields:    Translation:Humans
  45. Rao AA, Kumar R, Arteaga GM, Galardy PJ, Rodriguez V. Non-catheter related internal jugular vein thrombosis in a patient with severe haemophilia A. Haemophilia. 2009 Nov; 15(6):1339-40. PMID: 19702884.
    Citations:    Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.