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Amos Etzioni

Researcher Next ID · RN-042179

Researcher · Biochemistry, Genetics and Molecular Biology

Technion – Israel Institute of Technology

Haifa, Israel

Accepting doctoral researchersFunding unknown
Works count
473
Citation count
19,874
H-index
66
i10-index
159

Research interests

Biochemistry, Genetics and Molecular Biology
Immunology and Microbiology
Medicine
Immunodeficiency and Autoimmune Disorders
Cell Adhesion Molecules Research
Blood disorders and treatments
Platelet Disorders and Treatments
Immune Cell Function and Interaction

Publications

  • Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

    Journal of Clinical Immunology · 2020 · https://doi.org/10.1007/s10875-019-00737-x

  • Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification

    Journal of Clinical Immunology · 2020 · 10.1007/s10875-020-00758-x

  • The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

    The Journal of Allergy and Clinical Immunology In Practice · 2019 · https://doi.org/10.1016/j.jaip.2019.02.004

  • ZNF341 controls STAT3 expression and thereby immunocompetence

    Science Immunology · 2018 · https://doi.org/10.1126/sciimmunol.aat4941

  • The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

    Journal of Clinical Immunology · 2017 · 10.1007/s10875-017-0465-8

  • International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

    Journal of Clinical Immunology · 2017 · https://doi.org/10.1007/s10875-017-0464-9

  • Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

    Blood · 2016 · https://doi.org/10.1182/blood-2015-11-679902

  • The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

    Journal of Clinical Immunology · 2015 · 10.1007/s10875-015-0198-5

  • Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015

    Journal of Clinical Immunology · 2015 · https://doi.org/10.1007/s10875-015-0201-1

  • The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

    Journal of Allergy and Clinical Immunology · 2015 · 10.1016/j.jaci.2014.12.1945

  • Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency

    Frontiers in Immunology · 2014 · https://doi.org/10.3389/fimmu.2014.00162

  • TLR3 deficiency in herpes simplex encephalitis

    Neurology · 2014 · https://doi.org/10.1212/wnl.0000000000000999

  • Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

    The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.04.015

  • Alopecia Areata

    New England Journal of Medicine · 2012 · 10.1056/nejmra1103442

  • Leukocyte adhesion deficiencies

    Annals of the New York Academy of Sciences · 2012 · 10.1111/j.1749-6632.2011.06389.x

  • Transendothelial migration of lymphocytes mediated by intraendothelial vesicle stores rather than by extracellular chemokine depots

    Nature Immunology · 2011 · 10.1038/ni.2173

  • Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis

    The Journal of Experimental Medicine · 2011 · https://doi.org/10.1084/jem.20110958

  • Primary immunodeficiencies: 2009 update

    Journal of Allergy and Clinical Immunology · 2009 · 10.1016/j.jaci.2009.10.013

  • Interleukin‐7 receptor α (IL‐7Rα) deficiency: cellular and molecular bases. Analysis of clinical, immunological, and molecular features in 16 novel patients

    Immunological Reviews · 2005 · 10.1111/j.0105-2896.2005.00234.x

  • Fatal varicella associated with selective natural killer cell deficiency

    The Journal of Pediatrics · 2005 · 10.1016/j.jpeds.2004.11.022

  • Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency

    Nature Genetics · 2001 · 10.1038/ng0501-73

  • Cholangiopathy and tumors of the pancreas, liver, and biliary tree in boys with X-linked immunodeficiency with hyper-IgM

    The Journal of Immunology · 1997 · 10.4049/jimmunol.158.2.977

  • Clinical spectrum of X-linked hyper-IgM syndrome

    The Journal of Pediatrics · 1997 · 10.1016/s0022-3476(97)70123-9

  • Adhesion Molecules-Their Role in Health and Disease

    Pediatric Research · 1996 · 10.1203/00006450-199602000-00001

  • In vivo behavior of neutrophils from two patients with distinct inherited leukocyte adhesion deficiency syndromes.

    Journal of Clinical Investigation · 1993 · 10.1172/jci116535

  • Recurrent Severe Infections Caused by a Novel Leukocyte Adhesion Deficiency

    New England Journal of Medicine · 1992 · 10.1056/nejm199212173272505

Current projects

    No projects listed.