World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
59
Citations
14282
World Ranking
12418
National Ranking
5318

Overview

Terri Gelbart is affiliated with the Scripps Research Institute in the United States and conducts research primarily in the field of Medicine. Their work spans several important subfields including Infectious Diseases, Genetics, Radiology, Nuclear Medicine and Imaging, Obstetrics and Gynecology, as well as Public Health, Environmental and Occupational Health.

The scientist's research topics cover a range of areas with a significant focus on SARS-CoV-2 and COVID-19, which is reflected in their publications. Additional areas of study include Monoclonal and Polyclonal Antibodies, Diabetes and associated disorders, COVID-19 Impact on Reproduction, Mosquito-borne diseases and control, Insect symbiosis and bacterial influences, and Viral Infections and Vectors.

Gelbart's recent papers demonstrate ongoing contributions to the scientific understanding of infectious diseases and immune responses. Notable publications include:

  • Early non-neutralizing, afucosylated antibody responses are associated with COVID-19 severity (2022, Science Translational Medicine)
  • Antibodies elicited by SARS-CoV-2 infection or mRNA vaccines have reduced neutralizing activity against Beta and Omicron pseudoviruses (2022, Science Translational Medicine)
  • Structural basis of Zika virus NS1 multimerization and human antibody recognition (2024, npj Viruses)
  • Persistent immune and clotting dysfunction detected in saliva and blood plasma after COVID-19 (2023, Heliyon)
  • Structurally and functionally distinct early antibody responses predict COVID-19 disease trajectory and mRNA vaccine response (2021, bioRxiv [Cold Spring Harbor Laboratory])

Their work has appeared extensively in venues such as bioRxiv (Cold Spring Harbor Laboratory), Science Translational Medicine, npj Viruses, Heliyon, and STAR Protocols. The highest number of publications comes from bioRxiv with three contributions.

Gelbart has collaborated frequently with several researchers, including:

  • Gene S. Tan
  • Benjamín L. Sievers
  • Saborni Chakraborty
  • Joseph C. González
  • Arianna G. Cassidy

Best Publications

  • Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?

    Ernest Beutler;Terri Gelbart;Anna Demina

  • Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA

    Ernest Beutler;Vincent J Felitti;James A Koziol;Ngoc J Ho

  • Regulation of hepcidin transcription by interleukin-1 and interleukin-6

    Pauline Lee;Hongfan Peng;Terri Gelbart;Lei Wang

  • The serine protease TMPRSS6 is required to sense iron deficiency.

    Xin Du;Ellen She;Terri Gelbart;Jaroslav Truksa

  • Mutation Analysis in Hereditary Hemochromatosis

    Ernest Beutler;Terri Gelbart;Carol West;Pauline Lee

  • The human glucocerebrosidase gene and pseudogene : structure and evolution

    Mia Horowitz;Sylvia Wilder;Zeev Horowitz;Orly Reiner

  • Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patients.

    Ari Zimran;Andrea Kay;Terri Gelbart;Paul Garver

  • The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.

    Pauline L. Lee;Terri Gelbart;Carol West;Carol Halloran

  • The Effect of HFE Genotypes on Measurements of Iron Overload in Patients Attending a Health Appraisal Clinic

    Ernest Beutler;Vincent Felitti;Terri Gelbart;Ngoc Ho

  • Hematologically important mutations: Gaucher disease.

    Ernest Beutler;Terri Gelbart

  • The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE-, transferrin receptor 2-, and β2-microglobulin-deficient hepatocytes

    Pauline Lee;Hongfan Peng;Terri Gelbart;Ernest Beutler

  • Gaucher disease : gene frequencies in the Ashkenazi Jewish population

    E Beutler;N J Nguyen;M W Henneberger;J M Smolec

  • Molecular characterization of a case of atransferrinemia.

    Ernest Beutler;Terri Gelbart;Terri Gelbart;Pauline Lee;Pauline Lee;Reneé Trevino;Reneé Trevino

  • Evolution of the genome and the genetic code: selection at the dinucleotide level by methylation and polyribonucleotide cleavage

    Ernest Beutler;Terri Gelbart;Jiahuai Han;James A. Koziol

  • High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews.

    A Zimran;T Gelbart;B Westwood;G A Grabowski

  • A less costly regimen of alglucerase to treat Gaucher's disease.

    Michael L. Figueroa;Barry E. Rosenbloom;Andrea C. Kay;Paul Garver

  • Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state

    E Beutler;T Gelbart;W Kuhl;J Sorge

  • Mutations in Jewish Patients With Gaucher Disease

    E Beutler;T Gelbart;W Kuhl;A Zimran

  • Understanding and predicting suicidality using a combined genomic and clinical risk assessment approach

    A B Niculescu;D F Levey;P L Phalen;H Le-Niculescu

  • Estimating the prevalence of pyruvate kinase deficiency from the gene frequency in the general white population

    Ernest Beutler;Terri Gelbart

Frequent Co-Authors

Ernest Beutler
Ernest Beutler Scripps Research Institute
Vincent J. Felitti
Vincent J. Felitti University of California, San Diego
Michael Abecassis
Michael Abecassis University of Arizona
James A. Koziol
James A. Koziol Scripps Research Institute
Bruce Beutler
Bruce Beutler The University of Texas Southwestern Medical Center
Steven R. Head
Steven R. Head Scripps Research Institute
Nicholas J. Schork
Nicholas J. Schork Translational Genomics Research Institute
Anantha Shekhar
Anantha Shekhar Indiana University
Lei Wang
Lei Wang University of California, San Francisco
Henry A. Erlich
Henry A. Erlich UCSF Benioff Children's Hospital

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