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Immunology

D-Index
72
Citations
23295
World Ranking
2182
National Ranking
14

Overview

Amos Etzioni is affiliated with the Technion - Israel Institute of Technology in Israel. Their research spans several areas within biomedical sciences, focusing primarily on immunology and microbiology, with significant contributions to medicine and biochemistry, genetics, and molecular biology.

The scientist has published extensively in the field of immunology, covering topics such as immunodeficiency and autoimmune disorders, blood disorders and treatments, neutrophil and oxidative mechanisms, tumors and oncological cases, immune responses and vaccinations, cystic fibrosis research, and clinical studies related to COVID-19.

  • Immunodeficiency and Autoimmune Disorders
  • Blood disorders and treatments
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Tumors and Oncological Cases
  • Immune responses and vaccinations
  • Cystic Fibrosis Research Advances
  • COVID-19 Clinical Research Studies

Their work is distributed among leading journals, including the Journal of Clinical Immunology, Frontiers in Immunology, The Journal of Allergy and Clinical Immunology In Practice, Acta Haematologica, and Blood. The most frequent publication venues are:

  • Journal of Clinical Immunology (3 papers)
  • Frontiers in Immunology (1 paper)
  • The Journal of Allergy and Clinical Immunology In Practice (1 paper)
  • Acta Haematologica (1 paper)
  • Blood (1 paper)

Amos Etzioni's recent publications include the following:

  • "Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee" (2020), Journal of Clinical Immunology
  • "Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification" (2020), Journal of Clinical Immunology
  • "Minor Clinical Impact of COVID-19 Pandemic on Patients With Primary Immunodeficiency in Israel" (2021), Frontiers in Immunology
  • "Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee" (2020), Journal of Clinical Immunology
  • "Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in Israel" (2022), The Journal of Allergy and Clinical Immunology In Practice

They have collaborated with multiple researchers, frequently co-authoring with the following:

  • Jean-Laurent Casanova (5 coauthored papers)
  • Charlotte Cunningham-Rundles (4 coauthored papers)
  • Steven M. Holland (4 coauthored papers)
  • Éric Oksenhendler (4 coauthored papers)
  • Capucine Pïcard (4 coauthored papers)

Amos Etzioni's primary fields of study are divided as follows:

  • Immunology and Microbiology (13 publications)
  • Medicine (9 publications)
  • Biochemistry, Genetics and Molecular Biology (5 publications)

Their more focused subfields include:

  • Immunology (13 publications)
  • Genetics (5 publications)
  • Infectious Diseases (3 publications)
  • Pathology and Forensic Medicine (2 publications)
  • Pulmonary and Respiratory Medicine (2 publications)

Best Publications

  • Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies).

    Mary Ellen Conley;Luigi D. Notarangelo;Amos Etzioni

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

    Stuart G. Tangye;Waleed Al-Herz;Aziz Bousfiha;Talal Chatila

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

    Luyan Liu;Satoshi Okada;Xiao Fei Kong;Alexandra Y. Kreins

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

    Capucine Picard;Waleed Al-Herz;Aziz Bousfiha;Jean Laurent Casanova

  • Clinical spectrum of X-linked hyper-IgM syndrome

    Jacov Levy;Teresa Espanol-Boren;Carolin Thomas;Alain Fischer

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

    Waleed Al-Herz;Aziz Bousfiha;Jean-Laurent Casanova;Jean-Laurent Casanova;Helen Chapel

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

    Aziz Bousfiha;Leila Jeddane;Capucine Picard;Waleed Al-Herz

  • Recurrent severe infections caused by a novel leukocyte adhesion deficiency

    A Etzioni;M Frydman;S Pollack;I Avidor

  • Primary immunodeficiencies: 2009 update

    Luigi D. Notarangelo;Alain Fischer;Raif S. Geha;Jean-Laurent Casanova

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

    Gabriela Lopez-Herrera;Giacomo Tampella;Qiang Pan-Hammarström;Peer Herholz

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

    Markus G. Seidel;Gerhard Kindle;Benjamin Gathmann;Isabella Quinti

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

    Julie Toubiana;Satoshi Okada;Satoshi Okada;Julia Hiller;Matias Oleastro

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

    Torben Lübke;Thorsten Marquardt;Amos Etzioni;Enno Hartmann

  • The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

    Aziz Bousfiha;Leïla Jeddane;Waleed Al-Herz;Fatima Ailal

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

    U H von Andrian;E M Berger;L Ramezani;J D Chambers

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

    Karin R. Engelhardt;Karin R. Engelhardt;Karin R. Engelhardt;Michael E. Gertz;Sevgi Keles;Sevgi Keles;Alejandro A. Schäffer

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

    Silvia Giliani;Luigi Mori;Geneviève de Saint Basile;Francoise Le Deist

  • A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets

    Ronit Pasvolsky;Sara W. Feigelson;Sara Sebnem Kilic;Amos J. Simon

  • Adhesion molecules--their role in health and disease.

    Amos Etzioni

  • Of Man and Mouse: Leukocyte and Endothelial Adhesion Molecule Deficiencies

    Amos Etzioni;Claire M. Doerschuk;John M. Harlan

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

    Ziv Shulman;Shmuel J Cohen;Ben Roediger;Vyacheslav Kalchenko

Frequent Co-Authors

Jean-Laurent Casanova
Jean-Laurent Casanova The University of Texas Southwestern Medical Center
Ruth Gershoni-Baruch
Ruth Gershoni-Baruch Rambam Health Care Campus
Hans D. Ochs
Hans D. Ochs University of Washington
Ronen Alon
Ronen Alon Weizmann Institute of Science
Luigi D. Notarangelo
Luigi D. Notarangelo National Institutes of Health
Alain Fischer
Alain Fischer Collège de France
Laurent Abel
Laurent Abel Université Paris Cité
Raif S. Geha
Raif S. Geha Boston Children's Hospital
Bodo Grimbacher
Bodo Grimbacher University of Freiburg
Mary Ellen Conley
Mary Ellen Conley Rockefeller University

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