Renata Collard

470 total citations
7 papers, 198 citations indexed

About

Renata Collard is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Renata Collard has authored 7 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Rheumatology. Recurrent topics in Renata Collard's work include Metabolism and Genetic Disorders (3 papers), Folate and B Vitamins Research (3 papers) and Mitochondrial Function and Pathology (2 papers). Renata Collard is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Folate and B Vitamins Research (3 papers) and Mitochondrial Function and Pathology (2 papers). Renata Collard collaborates with scholars based in United States, Czechia and Canada. Renata Collard's co-authors include Jan P. Kraus, Tomáš Majtán, Adam J. Guenzel, Robert H. Allen, Michael A. Barry, Sally P. Stabler, Viktor Kožich, Dietrich Matern, Robert A. Hegele and In-Sun Park and has published in prestigious journals such as Molecular and Cellular Biology, Proteins Structure Function and Bioinformatics and Human Gene Therapy.

In The Last Decade

Renata Collard

7 papers receiving 198 citations

Peers

Renata Collard
Hümeyra Karacal United States
Patrick Forny Switzerland
Leighton LeGros United States
W.G. Ng United States
Hümeyra Karacal United States
Renata Collard
Citations per year, relative to Renata Collard Renata Collard (= 1×) peers Hümeyra Karacal

Countries citing papers authored by Renata Collard

Since Specialization
Citations

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

Fields of papers citing papers by Renata Collard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renata Collard

This figure shows the co-authorship network connecting the top 25 collaborators of Renata Collard. A scholar is included among the top collaborators of Renata Collard 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 Renata Collard. Renata Collard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
1.
Collard, Renata & Tomáš Majtán. (2023). Genetic and Pharmacological Modulation of Cellular Proteostasis Leads to Partial Functional Rescue of Homocystinuria-Causing Cystathionine-Beta Synthase Variants. Molecular and Cellular Biology. 43(12). 664–674. 6 indexed citations
2.
Collard, Renata, Tomáš Majtán, In-Sun Park, & Jan P. Kraus. (2018). Import of TAT-Conjugated Propionyl Coenzyme A Carboxylase Using Models of Propionic Acidemia. Molecular and Cellular Biology. 38(6). 11 indexed citations
3.
Simon, Mariella, Bobby G. Ng, Marisa W. Friederich, et al.. (2017). Activation of a cryptic splice site in the mitochondrial elongation factor GFM1 causes combined OXPHOS deficiency. Mitochondrion. 34. 84–90. 17 indexed citations
4.
Guenzel, Adam J., Renata Collard, Jan P. Kraus, Dietrich Matern, & Michael A. Barry. (2015). Long-Term Sex-Biased Correction of Circulating Propionic Acidemia Disease Markers by Adeno-Associated Virus Vectors. Human Gene Therapy. 26(3). 153–160. 32 indexed citations
5.
Maclean, Kenneth N., Jakub Sikora, Viktor Kožich, et al.. (2010). A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment. Molecular Genetics and Metabolism. 101(2-3). 153–162. 55 indexed citations
6.
Kraus, Jan P., Jindřich Hašek, Viktor Kožich, et al.. (2009). Cystathionine γ-lyase: Clinical, metabolic, genetic, and structural studies. Molecular Genetics and Metabolism. 97(4). 250–259. 50 indexed citations
7.
Král, Vlastimil, P. Mäder, Renata Collard, et al.. (2007). Stabilization of antibody structure upon association to a human carbonic anhydrase IX epitope studied by X‐ray crystallography, microcalorimetry, and molecular dynamics simulations. Proteins Structure Function and Bioinformatics. 71(3). 1275–1287. 27 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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2026