Nancy Berliner

ORCID: 0000-0001-7502-6895
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About
Contact & Profiles
Research Areas
  • Acute Myeloid Leukemia Research
  • Retinoids in leukemia and cellular processes
  • Autoimmune and Inflammatory Disorders Research
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Blood disorders and treatments
  • Parvovirus B19 Infection Studies
  • Immune Cell Function and Interaction
  • Hematological disorders and diagnostics
  • Chronic Lymphocytic Leukemia Research
  • Cell Adhesion Molecules Research
  • Hemoglobinopathies and Related Disorders
  • Erythrocyte Function and Pathophysiology
  • Immunodeficiency and Autoimmune Disorders
  • RNA modifications and cancer
  • Acute Lymphoblastic Leukemia research
  • Lymphoma Diagnosis and Treatment
  • Platelet Disorders and Treatments
  • Hematopoietic Stem Cell Transplantation
  • Protein Degradation and Inhibitors
  • Iron Metabolism and Disorders
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Venous Thromboembolism Diagnosis and Management
  • RNA Interference and Gene Delivery
  • Heparin-Induced Thrombocytopenia and Thrombosis
  • Protease and Inhibitor Mechanisms

Brigham and Women's Hospital
2015-2024

Harvard University
2014-2023

American Association of Blood Banks
2022

Massachusetts General Hospital
2006-2016

Harvard University Press
2015

Dana-Farber Cancer Institute
2006-2014

Nirma (India)
2012

University of Missouri
2012

Yale University
1999-2008

Baptist Medical Center Jacksonville
2006

Background: Low-dose methotrexate (LD-MTX) is the most commonly used drug for systemic rheumatic diseases worldwide and recommended first-line agent rheumatoid arthritis. Despite extensive clinical use more than 30 years, few data on adverse event (AE) rates derive from randomized, placebo-controlled trials, where both causality magnitude of risk can be inferred. Objective: To investigate AE rates, risk, differences comparing LD-MTX versus placebo. Design: Prespecified secondary analyses a...

10.7326/m19-3369 article EN Annals of Internal Medicine 2020-02-17

Clonal hematopoiesis of indeterminate potential (CHIP) and clonal cytopenia undetermined significance (CCUS) are defined by somatic mutations in genes associated with myeloid neoplasms (MN) at a variant allele fraction (VAF) ≥ 0.02, the absence presence cytopenia, respectively. CHIP/CCUS is highly prevalent adults defining predictors MN risk would aid clinical management research.

10.1056/evidoa2200310 article EN NEJM Evidence 2023-04-25

T cell-mediated hyperinflammatory responses, such as cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity (ICANS), are now well-established toxicities of chimeric antigen receptor (CAR) cell therapy. As the field CAR cells advances, however, there is increasing recognition that hemophagocytic lymphohistiocytosis (HLH)-like following infusion occurring broadly across patient populations constructs. Importantly, these HLH-like often not directly associated with CRS...

10.1016/j.jtct.2023.03.006 article EN cc-by-nc-nd Transplantation and Cellular Therapy 2023-03-09
Ayalew Tefferi Hagop Kantarjian S. Vincent Rajkumar Lawrence Baker Jan L. Abkowitz and 95 more John W. Adamson Ranjana H. Advani James P. Allison Karen H. Antman Robert C. Bast John M. Bennett Edward J. Benz Nancy Berliner Joseph Bertino Ravi Bhatia Smita Bhatia Deepa Bhojwani Charles D. Blanke Clara D. Bloomfield Linda D. Bosserman Hal E. Broxmeyer John C. Byrd Fernando Cabanillas George P. Canellos Bruce A. Chabner Asher Chanan‐Khan Bruce D. Cheson Bayard D. Clarkson Susan L. Cohn Gerardo Colón‐Otero Jorge E. Cortés Steven Coutré Massimo Cristofanilli Walter J. Curran George Q. Daley Daniel J. DeAngelo H. Joachim Deeg Lawrence H. Einhorn Harry P. Erba Francisco J. Esteva Elihu H. Estey Isaiah J. Fidler James M. Foran Stephen J. Forman Emil J. Freireich Charles S. Fuchs James N. George Morie A. Gertz Sergio Giralt Harvey M. Golomb Peter L. Greenberg Jordan U. Gutterman Robert I. Handin Samuel Hellmän Paulo M. Hoff Ronald Hoffman Waun Ki Hong Mary M. Horowitz Gabriel N. Hortobágyi Clifford A. Hudis Jean‐Pierre J. Issa Bruce E. Johnson Philip W. Kantoff Kenneth Kaushansky David Khayat Fadlo R. Khuri Thomas J. Kipps Margaret L. Kripke Robert A. Kyle Richard A. Larson Theodore S. Lawrence Ross L. Levine Michael P. Link Scott M. Lippman Sagar Lonial Gary H. Lyman Maurie Markman John Mendelsohn Neal J. Meropol Yoav H. Messinger Therese M. Mulvey Susan O’Brien Román Pérez-Soler Raphael E. Pollock Josef T. Prchal Oliver W. Press Jerald P. Radich R. Kanti Saul A. Rosenberg Jacob M. Rowe Hope Rugo Carolyn D. Runowicz Brenda M. Sandmaier Alan Saven Andrew I. Schafer Charles A. Schiffer Mikkael A. Sekeres Richard T. Silver Lillian L. Siu David P. Steensma

10.1016/j.mayocp.2015.06.001 article EN Mayo Clinic Proceedings 2015-07-23

Summary Haemophagocytic lymphohistiocytosis ( HLH ) is a syndrome of uncontrolled immune activation that has gained increasing attention over the past decade. Although classically known as familial disorder children caused by mutations affect cytotoxic T‐cell function, an acquired form in adults now widely recognized. This often seen setting malignancy, infection or rheumatological disorders. We performed retrospective review across 3 tertiary care centres and identified 68 with . The...

10.1111/bjh.13837 article EN British Journal of Haematology 2015-11-05

Recent molecular studies of myeloid differentiation have utilized several in vitro models myelopoiesis. Hematopoietic progenitors expressing the CD34+ antigen can be induced a process that recapitulates normal development. Two human leukemic cell lines, NB-4 and HL-60, been demonstrated to undergo retinoic acid-induced development, however, both lines exhibit defects upregulation late-expressed neutrophil-specific genes. In contrast, two murine factor-dependent myelopoiesis express full...

10.1002/0471142735.im22f05s104 article EN Current Protocols in Immunology 2014-02-01

Abstract Anemia is a significant problem in elderly patients. Although many anemic patients can be diagnosed with nutritional deficiency, anemia of chronic inflammation or comorbid diseases that explain their decreased hematocrit, the etiology fraction remains obscure. There evidence to suggest hematopoietic stem cell displays increasing erythropoietin (EPO) resistance age. EPO levels rise elderly, nonanemic patients, and it hypothesized there an interplay between this rising demand for...

10.1182/asheducation-2010.1.271 article EN Hematology 2010-12-04
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