Matthew Schmerer

928 total citations
26 papers, 526 citations indexed

About

Matthew Schmerer is a scholar working on Microbiology, Physiology and Molecular Biology. According to data from OpenAlex, Matthew Schmerer has authored 26 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Microbiology, 10 papers in Physiology and 6 papers in Molecular Biology. Recurrent topics in Matthew Schmerer's work include Reproductive tract infections research (12 papers), Bacterial Infections and Vaccines (11 papers) and Syphilis Diagnosis and Treatment (9 papers). Matthew Schmerer is often cited by papers focused on Reproductive tract infections research (12 papers), Bacterial Infections and Vaccines (11 papers) and Syphilis Diagnosis and Treatment (9 papers). Matthew Schmerer collaborates with scholars based in United States, France and Denmark. Matthew Schmerer's co-authors include James J. Bull, Ian J. Molineux, Waqas Chaudhry, Christina S. Vegge, Bruce R. Levin, Todd Evans, Daniel I. Bolnick, Marty Shankland, Ellen N. Kersh and Aryeh Warmflash and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Matthew Schmerer

26 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew Schmerer United States 14 242 180 171 75 67 26 526
Donna Perkins-Balding United States 9 96 0.4× 296 1.6× 114 0.7× 141 1.9× 93 1.4× 14 543
Adrian Cantu United States 8 263 1.1× 307 1.7× 34 0.2× 102 1.4× 85 1.3× 10 572
Zuzana Zubáčová Czechia 8 111 0.5× 336 1.9× 93 0.5× 38 0.5× 57 0.9× 8 537
Masato Miyata Japan 13 114 0.5× 174 1.0× 76 0.4× 142 1.9× 44 0.7× 22 758
Agnès Vallier France 23 123 0.5× 310 1.7× 56 0.3× 256 3.4× 254 3.8× 44 1.7k
María del Mar Ortega-Villaizán Spain 20 60 0.2× 204 1.1× 92 0.5× 116 1.5× 23 0.3× 48 905
Patricia M. Gaffney United States 14 141 0.6× 151 0.8× 35 0.2× 130 1.7× 38 0.6× 29 661
Gregory E. Jordan United Kingdom 8 54 0.2× 376 2.1× 47 0.3× 172 2.3× 51 0.8× 9 745
Dubravka Mužinić Croatia 4 74 0.3× 107 0.6× 90 0.5× 96 1.3× 30 0.4× 10 597
Alan Liss United States 13 169 0.7× 133 0.7× 196 1.1× 104 1.4× 179 2.7× 30 536

Countries citing papers authored by Matthew Schmerer

Since Specialization
Citations

This map shows the geographic impact of Matthew Schmerer'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 Matthew Schmerer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthew Schmerer more than expected).

Fields of papers citing papers by Matthew Schmerer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew Schmerer. 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 Matthew Schmerer. The network helps show where Matthew Schmerer may publish in the future.

Co-authorship network of co-authors of Matthew Schmerer

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Schmerer. A scholar is included among the top collaborators of Matthew Schmerer 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 Matthew Schmerer. Matthew Schmerer 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
1.
Reimche, Jennifer L., Sandeep J. Joseph, Matthew Schmerer, et al.. (2023). Genomic analysis of 1710 surveillance-based Neisseria gonorrhoeae isolates from the USA in 2019 identifies predominant strain types and chromosomal antimicrobial-resistance determinants. Microbial Genomics. 9(5). 11 indexed citations
2.
Liu, Hsi, Kevin Tang, Cau D. Pham, et al.. (2022). Characterization of a Neisseria gonorrhoeae Ciprofloxacin panel for an antimicrobial resistant Isolate Bank. PLoS ONE. 17(3). e0264149–e0264149. 3 indexed citations
3.
Reimche, Jennifer L., Matthew Schmerer, Sandeep J. Joseph, et al.. (2021). Genomic Analysis of the Predominant Strains and Antimicrobial Resistance Determinants Within 1479 Neisseria gonorrhoeae Isolates From the US Gonococcal Isolate Surveillance Project in 2018. Sexually Transmitted Diseases. 48(8S). S78–S87. 12 indexed citations
4.
Pham, Cau D., Hsi Liu, Matthew Schmerer, et al.. (2020). Atypical Mutation in Neisseria gonorrhoeae 23S rRNA Associated with High-Level Azithromycin Resistance. Antimicrobial Agents and Chemotherapy. 65(2). 14 indexed citations
5.
Liu, Hsi, et al.. (2020). A Culture Collection of 50 Neisseria gonorrhoeae Isolates. Microbiology Resource Announcements. 9(40). 3 indexed citations
6.
Palavecino, Elizabeth, et al.. (2020). First Case of High-Level Azithromycin-Resistant Neisseria gonorrhoeae in North Carolina. Sexually Transmitted Diseases. 47(5). 326–328. 5 indexed citations
7.
Schmerer, Matthew, et al.. (2019). Synergy with TGFβ ligands switches WNT pathway dynamics from transient to sustained during human pluripotent cell differentiation. Proceedings of the National Academy of Sciences. 116(11). 4989–4998. 46 indexed citations
8.
Kersh, Ellen N., Vanessa Allen, Eric M. Ransom, et al.. (2019). Rationale for a Neisseria gonorrhoeae Susceptible–only Interpretive Breakpoint for Azithromycin. Clinical Infectious Diseases. 70(5). 798–804. 15 indexed citations
9.
Liu, Hsi, Matthew Schmerer, Sancta St. Cyr, et al.. (2019). P861 Novel mutation conferring high-level azithromycin resistance inneisseria gonorrhoeae. Poster presentations. A359.3–A360. 1 indexed citations
10.
Thomas, Jesse C., Sandra Seby, A. Jeanine Abrams, et al.. (2019). Evidence of Recent Genomic Evolution in Gonococcal Strains With Decreased Susceptibility to Cephalosporins or Azithromycin in the United States, 2014–2016. The Journal of Infectious Diseases. 220(2). 294–305. 32 indexed citations
11.
Bolnick, Daniel I., et al.. (2015). Population-Specific Covariation between Immune Function and Color of Nesting Male Threespine Stickleback. PLoS ONE. 10(6). e0126000–e0126000. 15 indexed citations
12.
Stutz, William E., et al.. (2015). Among‐lake reciprocal transplants induce convergent expression of immune genes in threespine stickleback. Molecular Ecology. 24(18). 4629–4646. 29 indexed citations
13.
Bull, James J., Christina S. Vegge, Matthew Schmerer, Waqas Chaudhry, & Bruce R. Levin. (2014). Phenotypic Resistance and the Dynamics of Bacterial Escape from Phage Control. PLoS ONE. 9(4). e94690–e94690. 93 indexed citations
14.
Schmerer, Matthew, et al.. (2014). Challenges in predicting the evolutionary maintenance of a phage transgene. Journal of Biological Engineering. 8(1). 21–21. 18 indexed citations
15.
Schmerer, Matthew, Ian J. Molineux, & James J. Bull. (2014). Synergy as a rationale for phage therapy using phage cocktails. PeerJ. 2. e590–e590. 104 indexed citations
16.
Schmerer, Matthew, Ryan W. Null, & Marty Shankland. (2013). Developmental transition to bilaterally symmetric cell divisions is regulated by Pax-mediated transcription in embryos of the leech Helobdella austinensis. Developmental Biology. 382(1). 149–159. 13 indexed citations
17.
Quigley, Ian K., Matthew Schmerer, & Marty Shankland. (2010). A member of the Six gene family promotes the specification of P cell fates in the O/P equivalence group of the leech Helobdella. Developmental Biology. 344(1). 319–330. 9 indexed citations
18.
Schmerer, Matthew, Robert Savage, & Marty Shankland. (2009). Paxβ: a novel family of lophotrochozoan Pax genes. Evolution & Development. 11(6). 689–696. 12 indexed citations
19.
Yergeau, Donald, Matthew Schmerer, Emin Kuliyev, Todd Evans, & Paul E. Mead. (2005). Cloning and expression pattern of the Xenopus erythropoietin receptor. Gene Expression Patterns. 6(4). 420–425. 4 indexed citations
20.

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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