Céline Bürer

710 total citations
16 papers, 342 citations indexed

About

Céline Bürer is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Céline Bürer has authored 16 papers receiving a total of 342 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 9 papers in Rheumatology. Recurrent topics in Céline Bürer's work include Metabolism and Genetic Disorders (11 papers), Folate and B Vitamins Research (9 papers) and Mitochondrial Function and Pathology (4 papers). Céline Bürer is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Folate and B Vitamins Research (9 papers) and Mitochondrial Function and Pathology (4 papers). Céline Bürer collaborates with scholars based in Switzerland, United Kingdom and Austria. Céline Bürer's co-authors include Matthias R. Baumgartner, Brian Fowler, Patricie Burda, D. Sean Froese, Terttu Suormala, Cecilia Giunta, Wyatt W. Yue, Sarah C. Grünert, Raphael J. Morscher and Marianne Rohrbach and has published in prestigious journals such as Nature Communications, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Biochimie.

In The Last Decade

Céline Bürer

15 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Céline Bürer Switzerland 10 170 151 120 71 35 16 342
Sofía Gouveia Spain 11 152 0.9× 37 0.2× 23 0.2× 114 1.6× 14 0.4× 37 361
Eyby Leon United States 9 263 1.5× 60 0.4× 22 0.2× 104 1.5× 32 0.9× 29 379
Zhengwen He China 11 198 1.2× 32 0.2× 54 0.5× 17 0.2× 11 0.3× 29 370
Esther Vamos Belgium 15 286 1.7× 54 0.4× 30 0.3× 179 2.5× 85 2.4× 21 533
Mohammad Al-Owain Saudi Arabia 10 170 1.0× 41 0.3× 20 0.2× 65 0.9× 24 0.7× 15 264
Leslie A. Bard United States 10 249 1.5× 149 1.0× 32 0.3× 68 1.0× 27 0.8× 11 480
Sara Bertok Slovenia 10 166 1.0× 42 0.3× 25 0.2× 122 1.7× 37 1.1× 35 354
Johji Inazawa Japan 10 308 1.8× 34 0.2× 67 0.6× 54 0.8× 69 2.0× 16 452
Alice Goldenberg France 9 382 2.2× 117 0.8× 22 0.2× 87 1.2× 38 1.1× 12 527
Yu Ding China 12 219 1.3× 38 0.3× 24 0.2× 170 2.4× 19 0.5× 38 359

Countries citing papers authored by Céline Bürer

Since Specialization
Citations

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

Fields of papers citing papers by Céline Bürer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Bürer

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

All Works

16 of 16 papers shown
1.
Bürer, Céline, et al.. (2024). Dynamic inter-domain transformations mediate the allosteric regulation of human 5, 10-methylenetetrahydrofolate reductase. Nature Communications. 15(1). 3248–3248. 7 indexed citations
2.
3.
Ramon, Charlotte, et al.. (2022). Cellular and computational models reveal environmental and metabolic interactions in MMUT‐type methylmalonic aciduria. Journal of Inherited Metabolic Disease. 46(3). 421–435. 5 indexed citations
4.
Forny, Patrick, et al.. (2021). Spectrum and characterization of bi-allelic variants in MMAB causing cblB-type methylmalonic aciduria. Human Genetics. 141(7). 1253–1267. 9 indexed citations
5.
Bezerra, G.A., Kevin G. Hicks, Céline Bürer, et al.. (2021). Identification of small molecule allosteric modulators of 5,10-methylenetetrahydrofolate reductase (MTHFR) by targeting its unique regulatory domain. Biochimie. 183. 100–107. 6 indexed citations
6.
Bürer, Céline, et al.. (2019). Sitosterolemia—10 years observation in two sisters. JIMD Reports. 48(1). 4–10. 9 indexed citations
7.
Bailey, H., Patricie Burda, A. Chaikuad, et al.. (2019). Genetic, structural, and functional analysis of pathogenic variations causing methylmalonyl-CoA epimerase deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1865(6). 1265–1272. 13 indexed citations
8.
Parameswaran, Narayanan, et al.. (2018). Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings. Neuropediatrics. 49(2). 154–157. 12 indexed citations
9.
Bürer, Céline, et al.. (2017). Protein destabilization and loss of protein‐protein interaction are fundamental mechanisms in cblA ‐type methylmalonic aciduria. Human Mutation. 38(8). 988–1001. 19 indexed citations
10.
Mathis, Déborah, Lucia Abela, Monique Albersen, et al.. (2016). The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies. Journal of Inherited Metabolic Disease. 39(5). 733–741. 17 indexed citations
11.
Burda, Patricie, Alice Küster, Ola Hjalmarson, et al.. (2015). Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment. Journal of Inherited Metabolic Disease. 38(5). 863–872. 29 indexed citations
12.
Burda, Patricie, Alexandra Schäfer, Terttu Suormala, et al.. (2015). Insights into Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency: Molecular Genetic and Enzymatic Characterization of 76 Patients. Human Mutation. 36(6). 611–621. 52 indexed citations
13.
Abdalla, Ebtesam, et al.. (2014). Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype. European Journal of Pediatrics. 174(1). 105–112. 17 indexed citations
14.
Rohrbach, Marianne, Helen Spencer, Louise F. Porter, et al.. (2013). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. Molecular Genetics and Metabolism. 109(3). 289–295. 58 indexed citations
15.
Grünert, Sarah C., Martin Stucki, Raphael J. Morscher, et al.. (2012). 3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals. Orphanet Journal of Rare Diseases. 7(1). 31–31. 65 indexed citations
16.
Morscher, Raphael J., Sarah C. Grünert, Céline Bürer, et al.. (2011). A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency. Molecular Genetics and Metabolism. 105(4). 602–606. 24 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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