World's Best Scientists 2026 revealed!
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Immunology
New Zealand
2026

D-Index & Metrics

Immunology

D-Index
52
Citations
13396
World Ranking
4032
National Ranking
3

Research.com Recognitions

  • 2026 - Research.com Immunology in New Zealand Leader Award

Overview

Hilary Longhurst is affiliated with the Auckland District Health Board in New Zealand. Their research primarily focuses on hereditary angioedema, genetics, and immunology within the broader field of medicine.

The scientist's recent publications include:

  • CRISPR-Cas9 In Vivo Gene Editing of KLKB1 for Hereditary Angioedema, 2024, New England Journal of Medicine
  • The international WAO/EAACI guideline for the management of hereditary angioedema-The 2021 revision and update, 2022, Allergy
  • The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update, 2022, World Allergy Organization Journal
  • Assessment and management of disease burden and quality of life in patients with hereditary angioedema: a consensus report, 2021, Allergy Asthma and Clinical Immunology
  • Consensus on treatment goals in hereditary angioedema: A global Delphi initiative, 2021, Journal of Allergy and Clinical Immunology

Longhurst's frequent co-authors include:

  • Rohan Ameratunga
  • Marcus Maurer
  • Timothy Craig
  • Teresa Caballero
  • Markus Magerl

The most common publication venues for Longhurst's work are:

  • Journal of Allergy and Clinical Immunology
  • Clinical Reviews in Allergy & Immunology
  • The Journal of Allergy and Clinical Immunology In Practice
  • Allergy Asthma and Clinical Immunology
  • Allergy

They have published books through Frontiers Media, including C1 Inhibitor Deficiency and Angioedema (2022).

The main fields of study represented in Longhurst's body of work are medicine and its related subfields, including:

  • Genetics
  • Immunology
  • Hematology
  • Pathology and Forensic Medicine
  • Infectious Diseases

Longhurst's research topics cover various aspects of hereditary angioedema and related conditions, specifically:

  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Urticaria and Related Conditions
  • Autoimmune Bullous Skin Diseases
  • Hemophilia Treatment and Research
  • Immunodeficiency and Autoimmune Disorders
  • COVID-19 Clinical Research Studies
  • SARS-CoV-2 and COVID-19 Research

Best Publications

  • Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.

    Angelo Agostoni;Emel Aygören-Pürsün;Karen E. Binkley;Alvaro Blanch

  • Clinical picture and treatment of 2212 patients with common variable immunodeficiency

    Benjamin Gathmann;Nizar Mahlaoui;Laurence Gérard;Eric Oksenhendler

  • 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema

    Tom Bowen;Marco Cicardi;Henriette Farkas;Konrad Bork

  • C1 inhibitor deficiency: consensus document

    M. M. Gompels;R. J. Lock;M. Abinun;C. A. Bethune

  • The international WAO/EAACI guideline for the management of hereditary angioedema—The 2017 revision and update

    M. Maurer;M. Magerl;I. Ansotegui;E. Aygören-Pürsün

  • WAO Guideline for the Management of Hereditary Angioedema

    Timothy Craig;Emel A.ygören Pürsün;Konrad Bork;Tom Bowen

  • Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.

    Tanya I Coulter;Anita Chandra;Chris M Bacon;Judith Babar

  • The international WAO/EAACI guideline for the management of hereditary angioedema – the 2017 revision and update

    Marcus Maurer;Markus Magerl;Ignacio Ansotegui;Emel Aygören-Pürsün

  • Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary C1 inhibitor deficiency: Consensus report of an International Working Group

    M. Cicardi;K. Bork;T. Caballero;T. Craig

  • International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency.

    Teresa Caballero;Henriette Farkas;Laurence Bouillet;Tom Bowen

  • Autoantibodies to interferon-gamma in a patient with selective susceptibility to mycobacterial infection and organ-specific autoimmunity.

    Rainer Döffinger;Matthew R. Helbert;Gabriela Barcenas-Morales;Kun Yang

  • Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema

    Tom Bowen;Marco Cicardi;Konrad Bork;Bruce Zuraw

  • Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor

    Hilary Longhurst;Marco Cicardi;Timothy Craig;Konrad Bork

  • Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

    Paul Tuijnenburg;Hana Lango Allen;Hana Lango Allen;Siobhan O. Burns;Daniel Greene;Daniel Greene

  • Disease expression in women with hereditary angioedema.

    Laurence Bouillet;Hilary Longhurst;Isabelle Boccon-Gibod;Konrad Bork

  • International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency

    H Farkas;I Martinez-Saguer;K Bork;T Bowen

  • Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

    Maria Elena Maccari;Hassan Abolhassani;Hassan Abolhassani;Asghar Aghamohammadi;Alessandro Aiuti

  • HAE international home therapy consensus document.

    Hilary J. Longhurst;Henriette Farkas;Timothy Craig;Emel Aygören-Pürsün

  • The International/Canadian Hereditary Angioedema Guideline

    Stephen Betschel;Jacquie Badiou;Karen Binkley;Rozita Borici-Mazi

  • British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders

    John R. Hurst;Nisha Verma;David Lowe;Helen E. Baxendale

Frequent Co-Authors

Marcus Maurer
Marcus Maurer Charité - University Medicine Berlin
Marco Cicardi
Marco Cicardi University of Milan
Werner Aberer
Werner Aberer University of Graz
Timothy J. Craig
Timothy J. Craig Pennsylvania State University
Bruce L. Zuraw
Bruce L. Zuraw University of California, San Diego
Jonathan A. Bernstein
Jonathan A. Bernstein University of Cincinnati Medical Center
Stephen Jolles
Stephen Jolles University Hospital of Wales
Jacques Hébert
Jacques Hébert Université Laval
Klaus Warnatz
Klaus Warnatz University of Freiburg
George Füst
George Füst Semmelweis University

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