Match tier
Listed
Presence
Current · Arkansas
Last published
2025
Sources
OpenAlex · ORCID
Refreshed
2026-08-15
S
Susie L. Brown
Researcher
Also affiliated: Program for Appropriate Technology in Health (1985); University of Kentucky (1987); University of Washington (1985)
Faculty Researcher
7 h-index
9 pubs
348 cited
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Susie L. Brown's research investigates immunological memory, particularly in the context of malaria. Her work explores the heterogeneity of memory B cell populations, specifically IgM+ and IgM– memory B cells, and their capacity to produce class-switched antibodies and germinal center B cells upon rechallenge with Plasmodium yoelii. Brown also studies the role of non-canonical DNA structures, such as G-quadruplex and i-motif DNA, in gene regulation, examining their formation in the promoter region of MYD88, a key innate immune adaptor. Her research network includes collaborators Jason S. Stumhofer, Jonathan J. Bauer, Juhyung Lee, and Enatha Ntirandekura, all from the University of Arkansas for Medical Sciences, with whom she has co-authored multiple publications. Brown's scholarly output includes 9 publications with an h-index of 6 and 337 total citations.
Metrics
- h-index: 7
- Publications: 9
- Citations: 348
Selected Publications
-
G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88 (2025)
-
IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i> (2022)
-
IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i> (2021)
-
The i-Motif as a Molecular Target: More Than a Complementary DNA Secondary Structure (2021)
-
NK1.1 Expression Defines a Population of CD4+ Effector T Cells Displaying Th1 and Tfh Cell Properties That Support Early Antibody Production During Plasmodium yoelii Infection (2018)
-
IL-17 Promotes Differentiation of Splenic LSK− Lymphoid Progenitors into B Cells following <i>Plasmodium yoelii</i> Infection (2017)
Collaboration Network
Top Collaborators
Samantha Kendrick
University of Arkansas for Medical Sciences
2 shared publications
In database
- The i-Motif as a Molecular Target: More Than a Complementary DNA Secondary Structure
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Jonathan J. Bauer
University of Arkansas for Medical Sciences
2 shared publications
In database
- IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i>
- IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i>
Juhyung Lee
University of Arkansas for Medical Sciences
2 shared publications
In database
- IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i>
- IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i>
Enatha Ntirandekura
University of Arkansas for Medical Sciences
2 shared publications
In database
- IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i>
- IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i>
Jason S. Stumhofer
University of Arkansas for Medical Sciences
2 shared publications
In database
- IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i>
- IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i>
Kennith Swafford
University of Arkansas for Medical Sciences
1 shared publication
In database
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Mason McCrury
University of Arkansas for Medical Sciences
1 shared publication
In database
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Farhana Nasrin
University of Arkansas for Medical Sciences
1 shared publication
In database
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Carlon Q Gragg
University of Arkansas for Medical Sciences
1 shared publication
In database
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Ameya Chavan
1 shared publication
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Samrat Roy Choudhury
1 shared publication
In database
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Jonathan Dickerhoff
Purdue University West Lafayette (US)
1 shared publication
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Danzhou Yang
Purdue University West Lafayette (US)
1 shared publication
- G-quadruplex and i-motif DNA structures form in the promoter of the key innate immune adaptor MYD88
Similar Researchers
Based on overlapping research topics
K K Laffoon
University of Arkansas for Medical Sciences
Immune Response and Inflammation
Disease Mechanisms Research
Microbial infections and disease research
Carlon Q Gragg
University of Arkansas for Medical Sciences
Immune Response and Inflammation
Disease Mechanisms Research
Molecular Biology Techniques and Applications
Hayden Roys
University of Arkansas for Medical Sciences
Immune Response and Inflammation
Disease Mechanisms Research
Microbial infections and disease research
Rachel S. Palmer
University of Arkansas for Medical Sciences
Immune Response and Inflammation
Disease Mechanisms Research
Microbial infections and disease research
Jeffrey D. Robertson
University of Arkansas for Medical Sciences
Disease Mechanisms Research
Microbial infections and disease research
Molecular Biology Techniques and Applications
Tiffany Weinkopff
University of Arkansas for Medical Sciences
Immune Response and Inflammation
Disease Mechanisms Research
Microbial infections and disease research