World's Best Scientists 2026 revealed!

D-Index & Metrics

Immunology

D-Index
122
Citations
56624
World Ranking
317
National Ranking
201

Medicine

D-Index
122
Citations
56984
World Ranking
3464
National Ranking
1903

Research.com Recognitions

  • 2009 - Presidential Award, Clinical Immunology Society

Overview

Hans D. Ochs is affiliated with the University of Washington in the United States. Their research primarily focuses on medicine with a strong emphasis on immunology and microbiology. The major subfields of study include immunology, infectious diseases, genetics, hematology, and molecular biology.

The scientist has contributed extensively to topics related to immunodeficiency and autoimmune disorders, COVID-19 clinical research, SARS-CoV-2 and COVID-19 research, blood disorders and treatments, long-term effects of COVID-19, chronic lymphocytic leukemia research, and diabetes along with associated disorders.

Hans D. Ochs has published multiple papers in notable venues, including the Journal of Clinical Immunology, bioRxiv (Cold Spring Harbor Laboratory), Clinical Immunology, Frontiers in Immunology, and the Journal of Allergy and Clinical Immunology. Their most recent papers include:

  • 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)
  • The urgent need for integrated science to fight COVID-19 pandemic and beyond (2020, Journal of Translational Medicine)
  • Autoantibodies targeting GPCRs and RAS-related molecules associate with COVID-19 severity (2022, Nature Communications)
  • Excellent outcomes following hematopoietic cell transplantation for Wiskott-Aldrich syndrome: a PIDTC report (2020, Blood)

The scientist has coauthored work with several frequent collaborators, including Otávio Cabral-Marques, Igor Salerno Filgueiras, Lena F. Schimke, Paula Paccielli Freire, and Dennyson Leandro M. Fonseca.

In recognition of their contributions, Hans D. Ochs received the Presidential Award from the Clinical Immunology Society in 2009.

Best Publications

  • The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.

    Craig L. Bennett;Jacinda Christie;Fred Ramsdell;Mary E. Brunkow

  • Chronic granulomatous disease. Report on a national registry of 368 patients.

    Jerry A. Winkelstein;Mary C. Marino;Richard B. Johnston;John Boyle

  • Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

    Jonathan M.J. Derry;Hans D. Ochs;Uta Francke;Uta Francke

  • 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

  • The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

    Alejandro Aruffo;Alejandro Aruffo;Mary Farrington;Diane Hollenbaugh;Xu Li

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

    Capucine Picard;H. Bobby Gaspar;Waleed Al-Herz;Aziz Bousfiha

  • 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

  • Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis.

    Eleonora Gambineri;Troy R. Torgerson;Hans D. Ochs

  • Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity

    Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe

  • CTLA4Ig-mediated blockade of T cell costimulation in patients with psoriasis vulgaris

    Judith R. Abrams;Mark G. Lebwohl;Cynthia A. Guzzo;Brian V. Jegasothy

  • Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.

    Kohsuke Imai;Geir Slupphaug;Wen I. Lee;Wen I. Lee;Patrick Revy

  • X-Linked Lymphoproliferative Disease 2b4 Molecules Displaying Inhibitory Rather than Activating Function Are Responsible for the Inability of Natural Killer Cells to Kill Epstein-Barr Virus–Infected Cells

    Silvia Parolini;Cristina Bottino;Michela Falco;Raffaella Augugliaro

  • 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

  • X-linked agammaglobulinemia: report on a United States registry of 201 patients.

    Jerry A. Winkelstein;Mary C. Marino;Howard M. Lederman;Stacie M. Jones

  • Primary immunodeficiencies: 2009 update

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

  • Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

    Raif S. Geha;Luigi D. Notarangelo;Jean Laurent Casanova;Helen Chapel

  • Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

    Louis M. Kunkel;Anthony P. Monaco;William Middlesworth;Hans D. Ochs

  • Transcellular Diapedesis Is Initiated by Invasive Podosomes

    Christopher V. Carman;Peter T. Sage;Tracey E. Sciuto;Miguel A. de la Fuente

  • 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

  • The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.

    Aziz Bousfiha;Leïla Jeddane;Capucine Picard;Fatima Ailal

Frequent Co-Authors

Troy R. Torgerson
Troy R. Torgerson Allen Institute
Shigeaki Nonoyama
Shigeaki Nonoyama National Defense Medical College
Luigi D. Notarangelo
Luigi D. Notarangelo National Institutes of Health
Charlotte Cunningham-Rundles
Charlotte Cunningham-Rundles Icahn School of Medicine at Mount Sinai
David J. Rawlings
David J. Rawlings Seattle Children's Hospital
Jean-Laurent Casanova
Jean-Laurent Casanova The University of Texas Southwestern Medical Center
Jennifer M. Puck
Jennifer M. Puck University of California, San Francisco
Alejandro Aruffo
Alejandro Aruffo Syngenta (United States)
Antonio Condino-Neto
Antonio Condino-Neto Universidade de São Paulo
Bernd H. Belohradsky
Bernd H. Belohradsky Ludwig-Maximilians-Universität München

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