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Immunology

D-Index
76
Citations
23821
World Ranking
1890
National Ranking
131

Overview

Bernd H. Belohradsky is affiliated with Ludwig-Maximilians-Universität München in Germany. Their research primarily spans the fields of Medicine and Immunology and Microbiology, with specific subfield contributions in Immunology, Infectious Diseases, Genetics, and Pulmonary and Respiratory Medicine.

The scientist's work addresses multiple topics including Immunodeficiency and Autoimmune Disorders, Parvovirus B19 Infection Studies, Blood disorders and treatments, and Cystic Fibrosis Research Advances.

Recent publications by Bernd H. Belohradsky include:

  • Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations, 2021, Journal of Allergy and Clinical Immunology
  • Inborn errors of immunity: Manifestation, treatment, and outcome-an ESID registry 1994-2024 report on 30,628 patients, 2025, Journal of Human Immunity

Bernd H. Belohradsky has collaborated frequently with several co-authors, including:

  • Gerhard Kindle
  • Alexandra Nieters
  • Stephan Rusch
  • Mikko Seppänen
  • Alain Fischer

Their research has been published mainly in the following venues:

  • Journal of Allergy and Clinical Immunology
  • Journal of Human Immunity

Best Publications

  • Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

    Salima Hacein-Bey-Abina;Alexandrine Garrigue;Gary P. Wang;Jean Soulier

  • 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

  • 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

  • Chronic Granulomatous Disease: The European Experience

    J. Merlijn van den Berg;Elsbeth van Koppen;Anders Åhlin;Bernd H. Belohradsky

  • Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency

    Salima Hacein-Bey-Abina;Julia Hauer;Annick Lim;Capucine Picard

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

    Benjamin Gathmann;Nizar Mahlaoui;Laurence Gérard;Eric Oksenhendler

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

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

  • Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4

    Bodo Grimbacher;Alejandro A. Schäffer;Steven M. Holland;Joie Davis

  • Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study

    Tayfun Güngör;Pierre Teira;Mary Slatter;Georg Stussi

  • Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

    Eleonore D. Renner;Jennifer M. Puck;Steven M. Holland;Markus Schmitt

  • ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia

    Christie-Ann McCarl;Christie-Ann McCarl;Capucine Picard;Capucine Picard;Sara Khalil;Takumi Kawasaki

  • Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome.

    Ellen D. Renner;Ellen D. Renner;Stacey Rylaarsdam;Stephanie Aňover-Sombke;Anita L. Rack

  • DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

    Susanne E. Aydin;Sara Sebnem Kilic;Caner Aytekin;Ashish Kumar

  • Treatment of chronic granulomatous disease with myeloablative conditioning and an unmodified hemopoietic allograft: a survey of the European experience, 1985-2000.

    Reinhard A. Seger;Tayfun Gungor;Bernd H. Belohradsky;Stephane Blanche

  • The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency

    Laura Gámez-Díaz;Dietrich August;Polina Stepensky;Shoshana Revel-Vilk

  • Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.

    Ulrich Salzer;Chiara Bacchelli;Sylvie Buckridge;Qiang Pan-Hammarström

  • CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation

    Veronica Marcos;Zhe Zhou;Ali Önder Yildirim;Alexander Bohla

  • Long-term follow-up and outcome of 39 patients with chronic granulomatous disease.

    Johannes Liese;Sibylle Kloos;Verena Jendrossek;Theoni Petropoulou

  • ICOS deficiency in patients with common variable immunodeficiency

    Ulrich Salzer;Andrea Maul-Pavicic;Charlotte Cunningham-Rundles;Simon Urschel

  • Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

    Guillaume Vogt;Ariane Chapgier;Kun Yang;Kun Yang;Nadia Chuzhanova

  • Relevance of biallelic vs monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

    U S Salzer;C Bacchelli;S Buckridge;Q Pan-Hammar-Strom

Frequent Co-Authors

Bodo Grimbacher
Bodo Grimbacher University of Freiburg
Hans D. Ochs
Hans D. Ochs University of Washington
Andrew R. Gennery
Andrew R. Gennery Newcastle University
Troy R. Torgerson
Troy R. Torgerson Allen Institute
Dominik Hartl
Dominik Hartl Novartis (Switzerland)
Michael Borte
Michael Borte Leipzig University
klaus schwarz
klaus schwarz University of Ulm
Alain Fischer
Alain Fischer Collège de France
Dirk Roos
Dirk Roos University of Amsterdam
Capucine Picard
Capucine Picard Université Paris Cité

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