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Immunology

D-Index
59
Citations
11572
World Ranking
3440
National Ranking
297

Overview

Mary Slatter is affiliated with Newcastle University in the United Kingdom. Their work primarily spans the fields of Medicine and Immunology and Microbiology, with a substantial focus on Immunology and Hematology as key subfields. Their research contributions also cover Genetics, Epidemiology, and Infectious Diseases.

Slatter's research interests center on topics including Immunodeficiency and Autoimmune Disorders, Hematopoietic Stem Cell Transplantation, Blood disorders and treatments, Cytomegalovirus and herpesvirus research, Immune Cell Function and Interaction, Parvovirus B19 Infection Studies, and Neutrophil, Myeloperoxidase and Oxidative Mechanisms.

The scientist has published extensively in several prominent journals. Frequent publication venues include:

  • Journal of Clinical Immunology
  • Blood
  • Journal of Allergy and Clinical Immunology
  • Blood Advances
  • Clinical Immunology

Among recent papers, notable publications include:

  • EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity, 2021, Bone Marrow Transplantation
  • Hematopoietic cell transplantation in chronic granulomatous disease: a study of 712 children and adults, 2020, Blood
  • Hematopoietic cell transplantation in severe combined immunodeficiency: The SCETIDE 2006-2014 European cohort, 2021, Journal of Allergy and Clinical Immunology
  • Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey, 2020, Frontiers in Immunology
  • Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysis, 2022, Blood

Slatter collaborates frequently with several researchers. Their frequent co-authors include:

  • Andrew R. Gennery
  • Su Han Lum
  • Zohreh Nademi
  • Sophie Hambleton
  • Eleri Williams

Best Publications

  • Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: Entering a new century, do we do better?

    Andrew R. Gennery;Andrew R. Gennery;Mary A. Slatter;Mary A. Slatter;Laure Grandin;Pierre Taupin

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

    Charlotte Schwab;Annemarie Gabrysch;Peter Olbrich;Virginia Patiño

  • Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study

    Daniele Moratto;Silvia Giliani;Carmem Bonfim;Evelina Mazzolari

  • 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

  • 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

  • Neonatal Diagnosis of Severe Combined Immunodeficiency Leads to Significantly Improved Survival Outcome: The Case for Newborn Screening

    Lucinda Brown;Jinhua Xu-Bayford;Zoe Allwood;Mary Slatter

  • Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening

    Lucinda Brown;Jinhua Xu-Bayford;Zoe Allwood;Mary Slatter

  • Long-term outcome following hematopoietic stem-cell transplantation in Wiskott-Aldrich syndrome: collaborative study of the European Society for Immunodeficiencies and European Group for Blood and Marrow Transplantation.

    Hulya Ozsahin;Marina Cavazzana-Calvo;Luigi D Notarangelo;Ansgar Schulz

  • BCG vaccination in patients with severe combined immunodeficiency: Complications, risks, and vaccination policies

    Beatriz E. Marciano;Chiung Yu Huang;Gyan Joshi;Nima Rezaei

  • Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study

    Federica Barzaghi;Laura Cristina Amaya Hernandez;Benedicte Neven;Silvia Ricci

  • Association of busulfan exposure with survival and toxicity after haemopoietic cell transplantation in children and young adults: a multicentre, retrospective cohort analysis

    Imke H. Bartelink;Arief Lalmohamed;Elisabeth M L van Reij;Christopher C. Dvorak

  • Jakinibs for the treatment of immune dysregulation in patients with gain-of-function signal transducer and activator of transcription 1 (STAT1) or STAT3 mutations.

    Lisa R. Forbes;Tiphanie P. Vogel;Megan A. Cooper;Johana Castro-Wagner

  • Clinical Features That Identify Children With Primary Immunodeficiency Diseases

    Anbezhil Subbarayan;Gloria Colarusso;Stephen M. Hughes;Andrew R. Gennery

  • 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

  • Outcome of hematopoietic stem cell transplantation for adenosine deaminase–deficient severe combined immunodeficiency

    Amel Hassan;Claire Booth;Alex Brightwell;Zoe Allwood

  • Unrelated donor and HLA-identical sibling haematopoietic stem cell transplantation cure chronic granulomatous disease with good long-term outcome and growth

    Elena Soncini;Mary A. Slatter;Laura B. K. R. Jones;Stephen Hughes

  • EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity.

    A. C. Lankester;M. H. Albert;C. Booth;A. R. Gennery

  • Multicenter experience in hematopoietic stem cell transplantation for serious complications of common variable immunodeficiency

    Claudia Wehr;Andrew R. Gennery;Caroline Lindemans;Ansgar Schulz

  • Treosulfan-based conditioning for allogeneic HSCT in children with chronic granulomatous disease: a multicenter experience

    Beatriz Morillo-Gutierrez;Rita Beier;Kanchan Rao;Lauri Burroughs;Lauri Burroughs

  • Treosulfan-based conditioning regimens for hematopoietic stem cell transplantation in children with primary immunodeficiency: United Kingdom experience

    Mary A. Slatter;Kanchan Rao;Persis Amrolia;Terry Flood

  • Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations

    Jennifer W. Leiding;Satoshi Okada;David Hagin;Mario Abinun;Mario Abinun

  • Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF-syndrome)

    M M Hagleitner;A Lankester;P Maraschio;M Hultén

  • Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.

    A R Gennery;M A Slatter;J Rice;L H Hoefsloot

Frequent Co-Authors

Andrew R. Gennery
Andrew R. Gennery Newcastle University
Andrew J. Cant
Andrew J. Cant Newcastle University
Mario Abinun
Mario Abinun Newcastle University
Sophie Hambleton
Sophie Hambleton Newcastle University
Paul Veys
Paul Veys Great Ormond Street Hospital
Persis Amrolia
Persis Amrolia Great Ormond Street Hospital
Bénédicte Neven
Bénédicte Neven Université Paris Cité
Robbert G. M. Bredius
Robbert G. M. Bredius Leiden University Medical Center
Alain Fischer
Alain Fischer Collège de France
Arjan C. Lankester
Arjan C. Lankester Leiden University Medical Center

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