Marilyn Diaz

2.8k total citations
48 papers, 2.2k citations indexed

About

Marilyn Diaz is a scholar working on Immunology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Marilyn Diaz has authored 48 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Immunology, 22 papers in Molecular Biology and 12 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Marilyn Diaz's work include T-cell and B-cell Immunology (25 papers), Immune Cell Function and Interaction (18 papers) and Monoclonal and Polyclonal Antibodies Research (11 papers). Marilyn Diaz is often cited by papers focused on T-cell and B-cell Immunology (25 papers), Immune Cell Function and Interaction (18 papers) and Monoclonal and Polyclonal Antibodies Research (11 papers). Marilyn Diaz collaborates with scholars based in United States, Japan and Poland. Marilyn Diaz's co-authors include Martin F. Flajnik, Laurent Verkoczy, Igor B. Rogozin, Paolo Casali, Norman R. Klinman, Andrew S. Greenberg, Sukhdev S. Brar, Chuancang Jiang, Mary Ann Watson and Lynn L. Rumfelt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Immunity.

In The Last Decade

Marilyn Diaz

47 papers receiving 2.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marilyn Diaz United States 25 1.2k 966 469 233 223 48 2.2k
Annaiah Cariappa United States 24 2.4k 2.0× 958 1.0× 227 0.5× 133 0.6× 255 1.1× 34 3.3k
Anke Peters Germany 12 1.3k 1.0× 1.2k 1.2× 294 0.6× 62 0.3× 157 0.7× 23 2.5k
Aya Jakobovits United States 20 637 0.5× 1.4k 1.4× 744 1.6× 236 1.0× 369 1.7× 36 2.6k
Robert W. Maul United States 23 972 0.8× 781 0.8× 137 0.3× 99 0.4× 257 1.2× 50 1.8k
H Mostowski United States 16 1.2k 1.0× 443 0.5× 337 0.7× 184 0.8× 142 0.6× 22 1.9k
Maria D. Iglesias-Ussel United States 15 691 0.6× 766 0.8× 142 0.3× 290 1.2× 79 0.4× 25 1.4k
Claude Mawas France 33 2.4k 2.0× 593 0.6× 773 1.6× 171 0.7× 218 1.0× 125 3.2k
Matthew J. Androlewicz United States 19 1.5k 1.2× 935 1.0× 325 0.7× 136 0.6× 112 0.5× 32 2.2k
Donald Pious United States 30 2.5k 2.1× 1.1k 1.1× 683 1.5× 137 0.6× 396 1.8× 78 3.6k
R Jerzy United States 10 1.2k 1.0× 555 0.6× 138 0.3× 105 0.5× 170 0.8× 12 1.8k

Countries citing papers authored by Marilyn Diaz

Since Specialization
Citations

This map shows the geographic impact of Marilyn Diaz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marilyn Diaz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marilyn Diaz more than expected).

Fields of papers citing papers by Marilyn Diaz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marilyn Diaz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marilyn Diaz. The network helps show where Marilyn Diaz may publish in the future.

Co-authorship network of co-authors of Marilyn Diaz

This figure shows the co-authorship network connecting the top 25 collaborators of Marilyn Diaz. A scholar is included among the top collaborators of Marilyn Diaz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marilyn Diaz. Marilyn Diaz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Li, Xiaojun, Dongmei Liao, Zhengyang Li, et al.. (2022). Autoreactivity and broad neutralization of antibodies against HIV-1 are governed by distinct mutations: Implications for vaccine design strategies. Frontiers in Immunology. 13. 977630–977630. 2 indexed citations
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Kang, SunAh, Andrew J. Monteith, Chuancang Jiang, et al.. (2016). Apoptotic Debris Accumulates on Hematopoietic Cells and Promotes Disease in Murine and Human Systemic Lupus Erythematosus. The Journal of Immunology. 196(10). 4030–4039. 18 indexed citations
5.
Verkoczy, Laurent & Marilyn Diaz. (2014). Autoreactivity in HIV-1 broadly neutralizing antibodies. Current Opinion in HIV and AIDS. 9(3). 224–234. 43 indexed citations
6.
Richter, Kathleen, Lauranell H. Burch, David C. Henke, et al.. (2012). Altered Pattern of Immunoglobulin Hypermutation in Mice Deficient in Slip-GC Protein. Journal of Biological Chemistry. 287(38). 31856–31865. 6 indexed citations
7.
Selmi, Carlo, Patrick S.C. Leung, David H. Sherr, et al.. (2012). Mechanisms of environmental influence on human autoimmunity: A national institute of environmental health sciences expert panel workshop. Journal of Autoimmunity. 39(4). 272–284. 122 indexed citations
8.
Verkoczy, Laurent, Marilyn Diaz, T. Matt Holl, et al.. (2009). Autoreactivity in an HIV-1 broadly reactive neutralizing antibody variable region heavy chain induces immunologic tolerance. Proceedings of the National Academy of Sciences. 107(1). 181–186. 131 indexed citations
9.
Zhao, Ming‐Lang, Chuancang Jiang, & Marilyn Diaz. (2009). Amelioration of Lupus Nephritis in MRL/lpr mice by Adoptive Transfer of IgM Anti-dsDNA antibodies (50.28). The Journal of Immunology. 182(Supplement_1). 50.28–50.28. 1 indexed citations
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Ray, Madhumita, et al.. (2007). Known components of the immunoglobulin A:T mutational machinery are intact in Burkitt lymphoma cell lines with G:C bias. Molecular Immunology. 44(10). 2659–2666. 24 indexed citations
12.
Diaz, Marilyn & Christopher W. Lawrence. (2005). An update on the role of translesion synthesis DNA polymerases in Ig hypermutation. Trends in Immunology. 26(4). 215–220. 43 indexed citations
13.
Rumfelt, Lynn L., et al.. (2004). Unprecedented Multiplicity of Ig Transmembrane and Secretory mRNA Forms in the Cartilaginous Fish. The Journal of Immunology. 173(2). 1129–1139. 57 indexed citations
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Diaz, Marilyn, Robyn L. Stanfield, Andrew S. Greenberg, & Martin F. Flajnik. (2002). Structural analysis, selection, and ontogeny of the shark new antigen receptor (IgNAR): identification of a new locus preferentially expressed in early development. Immunogenetics. 54(7). 501–512. 90 indexed citations
17.
Kunkel, Thomas A. & Marilyn Diaz. (2002). Enzymatic Cytosine Deamination. Molecular Cell. 10(5). 962–963. 8 indexed citations
18.
Diaz, Marilyn, Laurent Verkoczy, Martin F. Flajnik, & Norman R. Klinman. (2001). Decreased Frequency of Somatic Hypermutation and Impaired Affinity Maturation but Intact Germinal Center Formation in Mice Expressing Antisense RNA to DNA Polymerase ζ. The Journal of Immunology. 167(1). 327–335. 130 indexed citations
19.
Diaz, Marilyn & Norman R. Klinman. (2000). Relative Roles of Somatic and Darwinian Evolution in Shaping the Antibody Response. Immunologic Research. 21(2-3). 89–102. 9 indexed citations
20.
Diaz, Marilyn, et al.. (1998). Evolution of somatic hypermutation and gene conversion in adaptive immunity. Immunological Reviews. 162(1). 13–24. 78 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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