Corinne Gemperle-Britschgi

456 total citations
8 papers, 152 citations indexed

About

Corinne Gemperle-Britschgi is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Corinne Gemperle-Britschgi has authored 8 papers receiving a total of 152 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 2 papers in Rheumatology. Recurrent topics in Corinne Gemperle-Britschgi's work include Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Mitochondrial Function and Pathology (4 papers). Corinne Gemperle-Britschgi is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Mitochondrial Function and Pathology (4 papers). Corinne Gemperle-Britschgi collaborates with scholars based in Switzerland, Germany and United Kingdom. Corinne Gemperle-Britschgi's co-authors include Véronique Rüfenacht, Johannes Häberle, Marta Spodenkiewicz, Carmen Dı́ez-Fernández, Jörn Oliver Sass, Beat Thöny, Stephanie Oerum, Louis Droogmans, Alain Fouilhoux and Wyatt W. Yue and has published in prestigious journals such as Gene, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Journal of Medical Genetics.

In The Last Decade

Corinne Gemperle-Britschgi

7 papers receiving 151 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinne Gemperle-Britschgi Switzerland 6 87 62 26 22 22 8 152
Jozef Hertecant United Arab Emirates 5 61 0.7× 62 1.0× 36 1.4× 20 0.9× 11 0.5× 7 120
Benjamin O’Callaghan United Kingdom 7 81 0.9× 59 1.0× 13 0.5× 16 0.7× 19 0.9× 11 162
Yun Jin Pai United Kingdom 5 112 1.3× 69 1.1× 19 0.7× 14 0.6× 28 1.3× 6 210
Ramona Salvarinova Canada 8 109 1.3× 80 1.3× 40 1.5× 46 2.1× 16 0.7× 18 202
Celia Medrano Spain 7 100 1.1× 38 0.6× 67 2.6× 30 1.4× 12 0.5× 9 191
Monique Albersen Netherlands 12 109 1.3× 154 2.5× 20 0.8× 50 2.3× 39 1.8× 17 292
Elisenda Cortès‐Saladelafont Spain 9 99 1.1× 111 1.8× 47 1.8× 47 2.1× 36 1.6× 21 231
Loreta Cimbalistienė Lithuania 11 121 1.4× 60 1.0× 53 2.0× 79 3.6× 21 1.0× 22 233
Varunvenkat M. Srinivasan India 8 51 0.6× 39 0.6× 13 0.5× 11 0.5× 7 0.3× 36 113
Kamil S. Sitarz United Kingdom 7 176 2.0× 79 1.3× 18 0.7× 13 0.6× 4 0.2× 9 225

Countries citing papers authored by Corinne Gemperle-Britschgi

Since Specialization
Citations

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

Fields of papers citing papers by Corinne Gemperle-Britschgi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Corinne Gemperle-Britschgi. 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 Corinne Gemperle-Britschgi. The network helps show where Corinne Gemperle-Britschgi may publish in the future.

Co-authorship network of co-authors of Corinne Gemperle-Britschgi

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

All Works

8 of 8 papers shown
1.
Grünert, Sarah C., Anke Schumann, Allan M. Lund, et al.. (2021). Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease. Biochimie. 183. 55–62. 9 indexed citations
2.
Benson, Matthew D., Paul R. Freund, James R. Lewis, et al.. (2020). Severe retinal degeneration in a patient with Canavan disease. Ophthalmic Genetics. 42(1). 75–78. 5 indexed citations
3.
Canda, Ebru, Havva Yazıcı, Sema Kalkan Uçar, et al.. (2018). Recurrent ketoacidosis: Is it a ketone metabolism disorder?. Journal of Dr Behcet Uz Children s Hospital.
4.
Oerum, Stephanie, Martine Roovers, Michael Leichsenring, et al.. (2017). Novel patient missense mutations in the HSD17B10 gene affect dehydrogenase and mitochondrial tRNA modification functions of the encoded protein. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(12). 3294–3302. 34 indexed citations
5.
Spronsen, Francjan J. van, Nastassja Himmelreich, Véronique Rüfenacht, et al.. (2017). Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability. Journal of Medical Genetics. 55(4). 249–253. 37 indexed citations
6.
Spodenkiewicz, Marta, Carmen Dı́ez-Fernández, Véronique Rüfenacht, Corinne Gemperle-Britschgi, & Johannes Häberle. (2016). Minireview on Glutamine Synthetase Deficiency, an Ultra-Rare Inborn Error of Amino Acid Biosynthesis. Biology. 5(4). 40–40. 45 indexed citations
7.
Sass, Jörn Oliver, Corinne Gemperle-Britschgi, Cathérine C.S. Delnooz, et al.. (2015). Expanding the phenotype in aminoacylase 1 (ACY1) deficiency: characterization of the molecular defect in a 63-year-old woman with generalized dystonia. Metabolic Brain Disease. 31(3). 587–592. 12 indexed citations
8.
Gemperle-Britschgi, Corinne, et al.. (2015). A novel common large genomic deletion and two new missense mutations identified in the Romanian phenylketonuria population. Gene. 576(1). 182–188. 10 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