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Immunology

D-Index
61
Citations
15972
World Ranking
3208
National Ranking
275

Overview

Kimberly Gilmour is affiliated with Great Ormond Street Hospital in the United Kingdom. Their research spans multiple fields within medicine, with a particular focus on immunodeficiency, autoimmune disorders, gene therapy, and CAR-T cell therapies.

Gilmour's main fields of study include Medicine and Biochemistry, Genetics and Molecular Biology. Within these broad fields, their subfields of interest cover Infectious Diseases, Immunology, Genetics, Oncology, and Molecular Biology.

Their work addresses key topics such as Immunodeficiency and Autoimmune Disorders, CAR-T cell therapy research, SARS-CoV-2 and COVID-19 Research, COVID-19 Clinical Research Studies, Virus-based gene therapy research, Immune Cell Function and Interaction, and SARS-CoV-2 detection and testing.

Key recent publications by Gilmour include:

  • Genome-edited, donor-derived allogeneic anti-CD19 chimeric antigen receptor T cells in paediatric and adult B-cell acute lymphoblastic leukaemia: results of two phase 1 studies (2020, The Lancet)
  • The Human Phenotype Ontology in 2024: phenotypes around the world (2023, Nucleic Acids Research)
  • Base-Edited CAR7 T Cells for Relapsed T-Cell Acute Lymphoblastic Leukemia (2023, New England Journal of Medicine)
  • Lentiviral gene therapy for X-linked chronic granulomatous disease (2020, Nature Medicine)
  • Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency (2021, New England Journal of Medicine)

Frequent co-authors collaborating with Gilmour include Stuart Adams, Louis Grandjean, Matthew Buckland, Claire Booth, and Adrian J. Thrasher. These collaborations reflect a strong network in clinical and translational immunology and gene therapy research.

Gilmour has published extensively in prominent journals and venues, notably:

  • Blood
  • New England Journal of Medicine
  • Journal of Clinical Immunology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications

Best Publications

  • Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

    Steven J. Howe;Marc R. Mansour;Kerstin Schwarzwaelder;Cynthia Bartholomae

  • Engineered bacteriophages for treatment of a patient with a disseminated drug-resistant Mycobacterium abscessus

    Rebekah M. Dedrick;Carlos A. Guerrero-Bustamante;Rebecca A. Garlena;Daniel A. Russell

  • Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells

    Waseem Qasim;Hong Zhan;Sujith Samarasinghe;Stuart Adams

  • Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

    H Bobby Gaspar;Kathryn L Parsley;Steven Howe;Doug King

  • Enhanced CAR T cell expansion and prolonged persistence in pediatric patients with ALL treated with a low-affinity CD19 CAR.

    Sara Ghorashian;Anne Marijn Kramer;Shimobi Onuoha;Gary Wright

  • Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome

    Salima Hacein-Bey Abina;H. Bobby Gaspar;Johanna Blondeau;Laure Caccavelli

  • Whole-genome sequencing of patients with rare diseases in a national health system

    Ernest Turro;William J Astle;Karyn Megy;Stefan Graf

  • Hematopoietic Stem Cell Gene Therapy for Adenosine Deaminase–Deficient Severe Combined Immunodeficiency Leads to Long-Term Immunological Recovery and Metabolic Correction

    H. Bobby Gaspar;H. Bobby Gaspar;Samantha Cooray;Samantha Cooray;Kimberly C. Gilmour;Kimberly C. Gilmour;Kathryn L. Parsley;Kathryn L. Parsley

  • X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management, and outcome of the disease

    Claire Booth;Kimberly C. Gilmour;Paul Veys;Andrew R. Gennery

  • A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.

    Yenan T. Bryceson;Daniela Pende;Andrea Maul-Pavicic;Kimberly C. Gilmour

  • Successful reconstitution of immunity in ADA-SCID by stem cell gene therapy following cessation of PEG-ADA and use of mild preconditioning.

    H. Bobby Gaspar;H. Bobby Gaspar;Emma Bjorkegren;Kate Parsley;Kate Parsley;Kimberly C. Gilmour;Kimberly C. Gilmour

  • Long-Term Persistence of a Polyclonal T Cell Repertoire After Gene Therapy for X-Linked Severe Combined Immunodeficiency

    H. Bobby Gaspar;Samantha Cooray;Samantha Cooray;Kimberly C. Gilmour;Kimberly C. Gilmour;Kathryn L. Parsley;Kathryn L. Parsley

  • Gammaretrovirus-mediated correction of SCID-X1 is associated with skewed vector integration site distribution in vivo

    Kerstin Schwarzwaelder;Steven J. Howe;Manfred Schmidt;Manfred Schmidt;Martijn H. Brugman

  • Whole-genome sequencing of a sporadic primary immunodeficiency cohort

    Thaventhiran Jed.;H Lango Allen;O S Burren;W Rae

  • Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis

    Nichola Cooper;Kanchan Rao;Kimberly Gilmour;Lema Hadad

  • Lentiviral gene therapy for X-linked chronic granulomatous disease.

    Donald B. Kohn;Claire Booth;Elizabeth M. Kang;Sung-Yun Pai

  • Immunotherapy of HCC metastases with autologous T cell receptor redirected T cells, targeting HBsAg in a liver transplant patient

    Waseem Qasim;Maurizia Brunetto;Adam J. Gehring;Shao-An Xue

  • Impact of thymoglobulin prior to pediatric unrelated umbilical cord blood transplantation on immune reconstitution and clinical outcome.

    Caroline A. Lindemans;Robert Chiesa;Persis J. Amrolia;Kanchan Rao

  • Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency.

    Donald B. Kohn;Claire Booth;Kit L. Shaw;Jinhua Xu-Bayford

  • The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

    Sebastian Fn Bode;Sandra Ammann;Waleed Al-Herz;Mihaela Bataneant

  • Antitumor activity without on-target off-tumor toxicity of GD2–chimeric antigen receptor T cells in patients with neuroblastoma

    Karin Straathof;Barry Flutter;Rebecca Wallace;Neha Jain

  • Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management

    C. Gholam;S. Grigoriadou;K. C. Gilmour;K. C. Gilmour;H. B. Gaspar;H. B. Gaspar

Frequent Co-Authors

Adrian J. Thrasher
Adrian J. Thrasher University College London
Siobhan O. Burns
Siobhan O. Burns University College London
Paul Veys
Paul Veys Great Ormond Street Hospital
Persis Amrolia
Persis Amrolia Great Ormond Street Hospital
Christine Kinnon
Christine Kinnon University College London
Austen Worth
Austen Worth Great Ormond Street Hospital
Nigel Klein
Nigel Klein University College London
H. Bobby Gaspar
H. Bobby Gaspar Great Ormond Street Hospital
Andrew R. Gennery
Andrew R. Gennery Newcastle University
David M. Sansom
David M. Sansom University College London

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