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Nima Rezaei

Researcher Next ID · RN-028569

Researcher · Immunology and Microbiology

Education and Research Network

New Delhi, India

Not currently recruitingFunding unknown
Works count
2,063
Citation count
116,660
H-index
119
i10-index
883

Research interests

Immunology and Microbiology
Biochemistry, Genetics and Molecular Biology
Medicine
Immunodeficiency and Autoimmune Disorders
Blood disorders and treatments
Immune Cell Function and Interaction
COVID-19 Clinical Research Studies
Immunotherapy and Immune Responses

Publications

  • Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee

    Journal of Human Immunity · 2025 · 10.70962/jhi.20250003

  • The role of Toll-like receptors and neuroinflammation in Parkinson’s disease

    Journal of Neuroinflammation · 2022 · 10.1186/s12974-022-02496-w

  • Role of Toll‐like receptors in the pathogenesis of COVID‐19

    Journal of Medical Virology · 2021 · 10.1002/jmv.26826

  • COVID-19 and telemedicine: Immediate action required for maintaining healthcare providers well-being

    Journal of Clinical Virology · 2020 · 10.1016/j.jcv.2020.104345

  • The immune system and COVID-19: Friend or foe?

    Life Sciences · 2020 · 10.1016/j.lfs.2020.117900

  • Immune-epidemiological parameters of the novel coronavirus – a perspective

    Expert Review of Clinical Immunology · 2020 · 10.1080/1744666x.2020.1750954

  • Effects of lead and cadmium on the immune system and cancer progression

    Journal of Environmental Health Science and Engineering · 2020 · 10.1007/s40201-020-00455-2

  • Understanding the tumor microenvironment for effective immunotherapy

    Medicinal Research Reviews · 2020 · 10.1002/med.21765

  • Lymphopenia in COVID‐19: Therapeutic opportunities

    Cell Biology International · 2020 · 10.1002/cbin.11403

  • COVID-19: Transmission, prevention, and potential therapeutic opportunities

    Clinica Chimica Acta · 2020 · https://doi.org/10.1016/j.cca.2020.05.044

  • Cytokine Alterations in Schizophrenia: An Updated Review

    Frontiers in Psychiatry · 2019 · 10.3389/fpsyt.2019.00892

  • A meta-analysis of pro-inflammatory cytokines in autism spectrum disorders: Effects of age, gender, and latitude

    Journal of Psychiatric Research · 2019 · 10.1016/j.jpsychires.2019.05.019

  • The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017

    ˜The œLancet. Gastroenterology & hepatology · 2019 · https://doi.org/10.1016/s2468-1253(19)30333-4

  • Alopecia areata: a review of disease pathogenesis

    British Journal of Dermatology · 2018 · 10.1111/bjd.16808

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

    Journal of Allergy and Clinical Immunology · 2016 · 10.1016/j.jaci.2015.09.025

  • PD-1/PD-L and autoimmunity: A growing relationship

    Cellular Immunology · 2016 · 10.1016/j.cellimm.2016.09.009

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

    Journal of Clinical Immunology · 2015 · 10.1007/s10875-014-0126-0

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

    Journal of Allergy and Clinical Immunology · 2014 · 10.1016/j.jaci.2014.02.028

  • Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

    The American Journal of Human Genetics · 2012 · 10.1016/j.ajhg.2012.04.015

  • The phenotype of human STK4 deficiency

    Blood · 2012 · 10.1182/blood-2011-09-378158

  • Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

    Journal of Clinical Investigation · 2011 · 10.1172/jci59259

  • A Homozygous CARD9 Mutation in a Family with Susceptibility to Fungal Infections

    New England Journal of Medicine · 2009 · https://doi.org/10.1056/nejmoa0810719

  • IgA Deficiency: Correlation Between Clinical and Immunological Phenotypes

    Journal of Clinical Immunology · 2008 · 10.1007/s10875-008-9229-9

  • A Syndrome with Congenital Neutropenia and Mutations in G6PC3

    New England Journal of Medicine · 2008 · 10.1056/nejmoa0805051

  • HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

    Nature Genetics · 2006 · 10.1038/ng1940

Current projects

    No projects listed.