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Immunology

D-Index
74
Citations
26520
World Ranking
2035
National Ranking
997

Overview

Elaine F. Remmers is affiliated with the National Institutes of Health in the United States. Their research focuses primarily on medicine, with significant contributions in rheumatology, molecular biology, immunology, hematology, and physiology. The scientist's work covers multiple facets of immune-related disorders and genetic factors influencing inflammatory conditions.

The main topics of their research include:

  • Inflammasome and immune disorders
  • Autoimmune and inflammatory disorders research
  • Immune response and inflammation
  • Eosinophilic disorders and syndromes
  • Drug-induced adverse reactions
  • Autoimmune and inflammatory disorders
  • Interferon and immune responses

Elaine F. Remmers has contributed to publications in several distinguished venues. Notable frequent venues include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Immunology
  • Proceedings of the National Academy of Sciences
  • Annals of the Rheumatic Diseases
  • New England Journal of Medicine

Recent papers authored or co-authored by Elaine F. Remmers include:

  • "Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis," 2020, Nature Immunology
  • "Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis," 2020, Proceedings of the National Academy of Sciences
  • "Severe delayed hypersensitivity reactions to IL-1 and IL-6 inhibitors link to common HLA-DRB1*15 alleles," 2021, Annals of the Rheumatic Diseases
  • "De novoCIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): A new member of the expanding family of pyrin-associated autoinflammatory diseases," 2020, UNC Libraries
  • "Variant STAT4 and Response to Ruxolitinib in an Autoinflammatory Syndrome," 2023, New England Journal of Medicine

The scientist frequently collaborates with other researchers. Among the most frequent co-authors are:

  • Daniel L. Kastner
  • Karyl S. Barron
  • Amanda K. Ombrello
  • Ivona Aksentijevich
  • Jae Jin Chae

Best Publications

  • A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

    Ann B. Begovich;Victoria E H Carlton;Lee A. Honigberg;Steven J. Schrodi

  • Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

    Eli A Stahl;Soumya Raychaudhuri;Soumya Raychaudhuri;Elaine F Remmers;Gang Xie

  • STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

    Elaine F. Remmers;Robert M. Plenge;Annette T. Lee;Robert R. Graham;Robert R. Graham

  • An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist

    Ivona Aksentijevich;Seth L. Masters;Polly J. Ferguson;Paul Dancey

  • TRAF1–C5 as a Risk Locus for Rheumatoid Arthritis — A Genomewide Study

    Robert M. Plenge;Mark Seielstad;Leonid Padyukov;Annette T. Lee

  • De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases.

    Ivona Aksentijevich;Miroslawa Nowak;Mustapha Mallah;Jae Jin Chae

  • Cyclooxygenase-1 and -2 expression in rheumatoid synovial tissues. Effects of interleukin-1 beta, phorbol ester, and corticosteroids.

    Leslie J. Crofford;Ronald L. Wilder;Ari P. Ristimaki;Hajime Sano

  • Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

    Qing Zhou;Dan Yang;Amanda K Ombrello;Andrey V Zavialov

  • Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease

    Elaine F. Remmers;Fulya Cosan;Yohei Kirino;Michael J. Ombrello

  • Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

    Robert M Plenge;Robert M Plenge;Robert M Plenge;Chris Cotsapas;Chris Cotsapas;Leela Davies;Alkes L Price;Alkes L Price

  • Common variants at CD40 and other loci confer risk of rheumatoid arthritis

    Soumya Raychaudhuri;Soumya Raychaudhuri;Soumya Raychaudhuri;Elaine F Remmers;Annette T Lee;Rachel Hackett

  • Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

    Yohei Kirino;George Bertsias;George Bertsias;Yoshiaki Ishigatsubo;Nobuhisa Mizuki

  • Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.

    Robert M. Plenge;Leonid Padyukov;Elaine F. Remmers;Shaun Purcell

  • Anchorage-independent growth of synoviocytes from arthritic and normal joints. Stimulation by exogenous platelet-derived growth factor and inhibition by transforming growth factor-beta and retinoids.

    R Lafyatis;E F Remmers;A B Roberts;D E Yocum

  • The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model.

    Ivona Aksentijevich;Christopher D. Putnam;Elaine F. Remmers;James L. Mueller

  • Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.

    Michael J. Ombrello;Elaine F. Remmers;Guangping Sun;Alexandra F. Freeman

  • Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

    Alexandra Zhernakova;Alexandra Zhernakova;Alexandra Zhernakova;Eli A. Stahl;Eli A. Stahl;Gosia Trynka;Soumya Raychaudhuri

  • Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk

    Soumya Raychaudhuri;Soumya Raychaudhuri;Soumya Raychaudhuri;Brian P Thomson;Elaine F Remmers;Stephen Eyre

  • REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.

    Peter K Gregersen;Chistopher I Amos;Annette T Lee;Yue Lu

  • Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production

    Anja Brehm;Yin Liu;Afzal Sheikh;Bernadette Marrero

  • Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

    Alexandra Zhernakova;Alexandra Zhernakova;Alexandra Zhernakova;Eli A. Stahl;Eli A. Stahl;Gosia Trynka;Soumya Raychaudhuri;Soumya Raychaudhuri

Frequent Co-Authors

Ronald L. Wilder
Ronald L. Wilder National Institutes of Health
Daniel L. Kastner
Daniel L. Kastner National Institutes of Health
Ahmet Gül
Ahmet Gül Istanbul University
Robert M. Plenge
Robert M. Plenge Bristol Myers Squibb
Peter K. Gregersen
Peter K. Gregersen Feinstein Institute for Medical Research
Lindsey A. Criswell
Lindsey A. Criswell National Institutes of Health
Ivona Aksentijevich
Ivona Aksentijevich National Institutes of Health
Leslie J. Crofford
Leslie J. Crofford Vanderbilt University Medical Center
Michael F. Seldin
Michael F. Seldin University of California, Davis
Annette T. Lee
Annette T. Lee Northwell Health

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