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Immunology

D-Index
107
Citations
44970
World Ranking
545
National Ranking
326

Research.com Recognitions

  • 2011 - Distinguished Service Award, Clinical Immunology Society

Overview

Kathleen E. Sullivan is affiliated with the Children's Hospital of Philadelphia in the United States. Their research primarily focuses on fields including Medicine, Immunology and Microbiology, and Biochemistry, Genetics and Molecular Biology. Key subfields of study encompass Immunology, Genetics, Molecular Biology, Epidemiology, and Pulmonary and Respiratory Medicine.

The scientist's work covers several main topics such as Immunodeficiency and Autoimmune Disorders, Immune Cell Function and Interaction, Congenital heart defects research, Cystic Fibrosis Research Advances, Blood disorders and treatments, Chronic Lymphocytic Leukemia Research, and Autoimmune and Inflammatory Disorders Research.

Recent notable 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: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee (2022, Journal of Clinical Immunology)
  • Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification (2020, Journal of Clinical Immunology)
  • The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity (2022, Journal of Clinical Immunology)
  • Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2 (2020, Journal of Clinical Investigation)

Frequent co-authors include Edward M. Behrens, Kelly Maurer, Jennifer M. Puck, Ramsay Fuleihan, and Charlotte Cunningham-Rundles.

The scientist's publications are frequently found in the following venues:

  • Journal of Allergy and Clinical Immunology (28 publications)
  • Journal of Clinical Immunology (27 publications)
  • Journal of Human Immunity (9 publications)
  • Clinical Immunology (8 publications)
  • Genetics in Medicine (7 publications)

Kathleen E. Sullivan has contributed to book publications, including a book published by Elsevier BV titled "Stiehm's Immune Deficiencies" in 2020.

Award recognition includes the Distinguished Service Award from the Clinical Immunology Society in 2011.

Best Publications

  • 22q11.2 deletion syndrome

    Donna M. McDonald-McGinn;Kathleen E. Sullivan;Bruno Marino;Nicole Philip

  • 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

  • New insights into the immunopathogenesis of systemic lupus erythematosus

    George C. Tsokos;Mindy S. Lo;Patricia Costa Reis;Kathleen E. Sullivan

  • 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

  • A multiinstitutional survey of the Wiskott-Aldrich syndrome

    Kathleen E. Sullivan;Craig A. Mullen;R.Michael Blaese;Jerry A. Winkelstein

  • 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

  • Transplantation Outcomes for Severe Combined Immunodeficiency, 2000–2009

    Sung Yun Pai;Brent R. Logan;Linda M. Griffith;Rebecca H. Buckley

  • Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

    Lisa J Kobrynski;Kathleen E Sullivan

  • Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources

    Sebastian Köhler;Leigh Carmody;Nicole A. Vasilevsky;Julius O. B. Jacobsen

  • 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

  • Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity.

    Jörn Drappa;Akshay K. Vaishnaw;Kathleen E. Sullivan;Jia Li Chu

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

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

  • Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

    Anne S Bassett;Donna M McDonald-McGinn;Koenraad Devriendt;Maria Cristina Digilio

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

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

  • The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.

    Aziz Bousfiha;Leïla Jeddane;Capucine Picard;Fatima Ailal

  • Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

    Donna M. McDonald-McGinn;Kathleen E. Sullivan

  • The Philadelphia story: the 22q11.2 deletion: report on 250 patients

    McDonald-McGinn Dm;Kirschner R;Goldmuntz E;Sullivan K

  • ATM stabilizes DNA double-strand-break complexes during V(D)J recombination.

    Andrea L. Bredemeyer;Girdhar G. Sharma;Ching Yu Huang;Beth A. Helmink

  • Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects

    Charlotte Schwab;Annemarie Gabrysch;Peter Olbrich;Virginia Patiño

  • Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2.

    Caroline Diorio;Sarah E. Henrickson;Laura A. Vella;Kevin O. McNerney

  • Coronavirus Disease 2019 in patients with inborn errors of immunity: an international study.

    Isabelle Meyts;Giorgia Bucciol;Isabella Quinti;Bénédicte Neven

  • Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

    Abbas F. Jawad;Donna M. McDonald-McGinn;Elaine Zackai;Kathleen E. Sullivan

  • Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

    Mary Beth Fasano;Kathleen E. Sullivan;Kathleen E. Sullivan;Sampson B. Sarpong;Sampson B. Sarpong;Robert A. Wood

  • The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies

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

  • Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

    Yun R Li;Jin Li;Sihai D Zhao;Sihai D Zhao;Jonathan P Bradfield

  • Chromosome 22q11.2 Deletion Syndrome: DiGeorge Syndrome/Velocardiofacial Syndrome

    Kathleen E. Sullivan;Kathleen E. Sullivan

Frequent Co-Authors

Donna M. McDonald-McGinn
Donna M. McDonald-McGinn Children's Hospital of Philadelphia
Elaine H. Zackai
Elaine H. Zackai Children's Hospital of Philadelphia
Charlotte Cunningham-Rundles
Charlotte Cunningham-Rundles Icahn School of Medicine at Mount Sinai
Jordan S. Orange
Jordan S. Orange University of Pennsylvania
Jerry A. Winkelstein
Jerry A. Winkelstein Johns Hopkins University School of Medicine
Beverly S. Emanuel
Beverly S. Emanuel Children's Hospital of Philadelphia
Michelle Petri
Michelle Petri Johns Hopkins University School of Medicine
Eline T. Luning Prak
Eline T. Luning Prak University of Pennsylvania
Hans D. Ochs
Hans D. Ochs University of Washington
Howard M. Lederman
Howard M. Lederman Johns Hopkins University

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