Merridee A. Wouters

3.0k total citations
44 papers, 2.2k citations indexed

About

Merridee A. Wouters is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Merridee A. Wouters has authored 44 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Merridee A. Wouters's work include Redox biology and oxidative stress (10 papers), Protein Structure and Dynamics (9 papers) and Bioinformatics and Genomic Networks (8 papers). Merridee A. Wouters is often cited by papers focused on Redox biology and oxidative stress (10 papers), Protein Structure and Dynamics (9 papers) and Bioinformatics and Genomic Networks (8 papers). Merridee A. Wouters collaborates with scholars based in Australia, United States and United Kingdom. Merridee A. Wouters's co-authors include Naomi L. Haworth, Paul M. G. Curmi, Sally L. Dunwoodie, Duncan B. Sparrow, Ahsan Husain, K. Mohanasundaram, Tamsyn M. Crowley, Lina Feng, Andrzej Gościński and Diane Fatkin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Merridee A. Wouters

44 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Merridee A. Wouters Australia 25 1.4k 330 203 202 160 44 2.2k
Wolfgang Rist Germany 23 1.4k 1.0× 279 0.8× 191 0.9× 128 0.6× 188 1.2× 38 1.9k
Choel Kim United States 27 2.0k 1.4× 238 0.7× 235 1.2× 173 0.9× 94 0.6× 56 2.6k
Mary F. Lopez United States 33 2.2k 1.5× 211 0.6× 127 0.6× 141 0.7× 145 0.9× 86 3.6k
Mario A. Pagano Italy 29 1.9k 1.3× 198 0.6× 311 1.5× 114 0.6× 206 1.3× 70 2.8k
Bettina Sarg Austria 32 2.0k 1.3× 147 0.4× 238 1.2× 126 0.6× 191 1.2× 105 3.1k
Emily S. Boja United States 28 1.6k 1.1× 188 0.6× 221 1.1× 124 0.6× 151 0.9× 48 2.4k
Shunsuke Imai Japan 29 1.4k 0.9× 290 0.9× 154 0.8× 105 0.5× 269 1.7× 138 2.5k
Jörg Reinders Germany 27 2.2k 1.5× 178 0.5× 251 1.2× 76 0.4× 165 1.0× 74 3.2k
Domenico Bordo Italy 28 1.5k 1.1× 162 0.5× 264 1.3× 117 0.6× 237 1.5× 57 2.6k
Barbara Spolaore Italy 25 1.5k 1.1× 126 0.4× 331 1.6× 171 0.8× 127 0.8× 45 2.2k

Countries citing papers authored by Merridee A. Wouters

Since Specialization
Citations

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

Fields of papers citing papers by Merridee A. Wouters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Merridee A. Wouters. 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 Merridee A. Wouters. The network helps show where Merridee A. Wouters may publish in the future.

Co-authorship network of co-authors of Merridee A. Wouters

This figure shows the co-authorship network connecting the top 25 collaborators of Merridee A. Wouters. A scholar is included among the top collaborators of Merridee A. Wouters 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 Merridee A. Wouters. Merridee A. Wouters 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.
Young, Neil D., Tiffany J. Harris, Marco Evangelista, et al.. (2020). Diversity in the intrinsic apoptosis pathway of nematodes. Communications Biology. 3(1). 478–478. 2 indexed citations
2.
Eissmann, Moritz F., Christine D. Dijkstra, Merridee A. Wouters, et al.. (2018). Interleukin 33 Signaling Restrains Sporadic Colon Cancer in an Interferon-γ–Dependent Manner. Cancer Immunology Research. 6(4). 409–421. 34 indexed citations
3.
4.
Mohanasundaram, K., et al.. (2017). Mapping genotype-phenotype associations of nsSNPs in coiled-coil oligomerization domains of the human proteome. Human Mutation. 38(10). 1378–1393. 1 indexed citations
5.
Bouveret, Romaric, Ashley J. Waardenberg, Nicole Schönrock, et al.. (2015). NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets. eLife. 4. 58 indexed citations
6.
Ballouz, Sara, K. Mohanasundaram, Richard A. George, et al.. (2015). Novel therapeutics for coronary artery disease from genome-wide association study data. BMC Medical Genomics. 8(S2). S1–S1. 27 indexed citations
7.
Mohanasundaram, K., et al.. (2015). Potential role of glutathione in evolution of thiol-based redox signaling sites in proteins. Frontiers in Pharmacology. 6. 1–1. 284 indexed citations
8.
Mann, Stefan A., Robyn Otway, Guanglan Guo, et al.. (2012). Epistatic Effects of Potassium Channel Variation on Cardiac Repolarization and Atrial Fibrillation Risk. Journal of the American College of Cardiology. 59(11). 1017–1025. 47 indexed citations
9.
Ballouz, Sara, Jason Y. Liu, Martin Oti, et al.. (2011). Analysis of genome-wide association study data using the protein knowledge base. BMC Genetics. 12(1). 98–98. 8 indexed citations
10.
Chiu, Joyce, et al.. (2010). Cell Cycle Sensing of Oxidative Stress in Saccharomyces cerevisiae by Oxidation of a Specific Cysteine Residue in the Transcription Factor Swi6p. Journal of Biological Chemistry. 286(7). 5204–5214. 27 indexed citations
11.
Sparrow, Duncan B., David Sillence, Merridee A. Wouters, Peter D. Turnpenny, & Sally L. Dunwoodie. (2010). Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis. European Journal of Human Genetics. 18(6). 674–679. 42 indexed citations
12.
Wouters, Merridee A., et al.. (2009). Disulfides as Redox Switches: From Molecular Mechanisms to Functional Significance. Antioxidants and Redox Signaling. 12(1). 53–91. 188 indexed citations
13.
George, R. A., Tim D. Smith, Steve Callaghan, et al.. (2007). General mutation databases: analysis and review. Journal of Medical Genetics. 45(2). 65–70. 24 indexed citations
14.
George, Richard A., Jason Y. Liu, Lina Feng, et al.. (2006). Analysis of protein sequence and interaction data for candidate disease gene prediction. Nucleic Acids Research. 34(19). e130–e130. 118 indexed citations
15.
Sparrow, Duncan B., Gavin Chapman, Merridee A. Wouters, et al.. (2005). Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype. The American Journal of Human Genetics. 78(1). 28–37. 182 indexed citations
16.
Whittock, Neil V., Duncan B. Sparrow, Merridee A. Wouters, et al.. (2004). Mutated MESP2 Causes Spondylocostal Dysostosis in Humans. The American Journal of Human Genetics. 74(6). 1249–1254. 119 indexed citations
17.
Wouters, Merridee A., et al.. (2003). A Despecialization Step Underlying Evolution of a Family of Serine Proteases. Molecular Cell. 12(2). 343–354. 58 indexed citations
18.
Iismaa, Siiri E., Sara Holman, Merridee A. Wouters, et al.. (2003). Evolutionary specialization of a tryptophan indole group for transition-state stabilization by eukaryotic transglutaminases. Proceedings of the National Academy of Sciences. 100(22). 12636–12641. 45 indexed citations
19.
Liu, Xifu, et al.. (2001). Arg1098 Is Critical for the Chloride Dependence of Human Angiotensin I-converting Enzyme C-domain Catalytic Activity. Journal of Biological Chemistry. 276(36). 33518–33525. 49 indexed citations
20.
Wouters, Merridee A. & Paul M. G. Curmi. (1995). An analysis of side chain interactions and pair correlations within antiparallel β‐sheets: The differences between backbone hydrogen‐bonded and non‐hydrogen‐bonded residue pairs. Proteins Structure Function and Bioinformatics. 22(2). 119–131. 215 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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