Arnaud Wiedemann

1.2k total citations
34 papers, 240 citations indexed

About

Arnaud Wiedemann is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Arnaud Wiedemann has authored 34 papers receiving a total of 240 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Clinical Biochemistry, 11 papers in Molecular Biology and 6 papers in Physiology. Recurrent topics in Arnaud Wiedemann's work include Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (5 papers) and Folate and B Vitamins Research (5 papers). Arnaud Wiedemann is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Diet and metabolism studies (5 papers) and Folate and B Vitamins Research (5 papers). Arnaud Wiedemann collaborates with scholars based in France, Canada and United States. Arnaud Wiedemann's co-authors include François Feillet, Jean‐Louis Guéant, Klaus P. Kohse, Abderrahim Oussalah, Hermann Wisser, D. Ratge, Élise Jeannesson, G. Weryha, B. Dousset and Nicolas Richard and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Bone and Mineral Research.

In The Last Decade

Arnaud Wiedemann

30 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnaud Wiedemann France 9 83 62 47 42 40 34 240
Fatih Kardaş Türkiye 11 87 1.0× 68 1.1× 42 0.9× 22 0.5× 34 0.8× 47 367
İlyas Okur Türkiye 12 124 1.5× 78 1.3× 32 0.7× 86 2.0× 46 1.1× 62 372
Brian J. Shayota United States 10 127 1.5× 109 1.8× 36 0.8× 35 0.8× 68 1.7× 23 321
Mahoko Furujo Japan 10 99 1.2× 59 1.0× 17 0.4× 76 1.8× 28 0.7× 27 319
Lili Tong China 11 114 1.4× 32 0.5× 11 0.2× 17 0.4× 69 1.7× 25 332
Ceren Acar Türkiye 8 62 0.7× 17 0.3× 35 0.7× 48 1.1× 22 0.6× 21 192
Veronica Pagliardini Italy 11 65 0.8× 41 0.7× 61 1.3× 103 2.5× 42 1.1× 16 346
Kevin Martens Belgium 8 96 1.2× 30 0.5× 23 0.5× 35 0.8× 68 1.7× 9 317
Daniela Lapa Italy 8 42 0.5× 21 0.3× 29 0.6× 16 0.4× 72 1.8× 10 352
Angela Lopomo Italy 7 98 1.2× 17 0.3× 21 0.4× 14 0.3× 23 0.6× 10 258

Countries citing papers authored by Arnaud Wiedemann

Since Specialization
Citations

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

Fields of papers citing papers by Arnaud Wiedemann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Wiedemann

This figure shows the co-authorship network connecting the top 25 collaborators of Arnaud Wiedemann. A scholar is included among the top collaborators of Arnaud Wiedemann 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 Arnaud Wiedemann. Arnaud Wiedemann 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.
Wiedemann, Arnaud, et al.. (2025). Risk Factors and Causes of Readmission to the Pediatric Intensive Care Unit After Cardiac Surgery. World Journal for Pediatric and Congenital Heart Surgery. 1938268495–1938268495. 1 indexed citations
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Wiedemann, Arnaud, et al.. (2022). Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis. Cell Reports Medicine. 3(7). 100670–100670. 9 indexed citations
5.
Sindou, M., et al.. (2022). Dorsal rhizotomy in cerebral palsy: How root sectioning is influenced by intraoperative neuromonitoring?. Neurochirurgie. 68(5). e16–e21. 1 indexed citations
6.
Wiedemann, Arnaud, Céline Chéry, Jean‐Marie Ravel, et al.. (2021). Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study. Human Genetics. 141(7). 1269–1278. 12 indexed citations
7.
Wiedemann, Arnaud, Élise Jeannesson, Abderrahim Oussalah, et al.. (2021). Le dépistage de la phénylcétonurie en France. médecine/sciences. 37(5). 468–473. 4 indexed citations
8.
Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations
9.
Oualha, Mehdi, Corinne Levy, Denise Antona, et al.. (2021). Educational Setting and SARS-CoV-2 Transmission Among Children With Multisystem Inflammatory Syndrome: A French National Surveillance System. Frontiers in Pediatrics. 9. 745364–745364. 2 indexed citations
10.
Guéant‐Rodriguez, Rosa‐Maria, Abderrahim Oussalah, Arnaud Wiedemann, et al.. (2021). Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review. Human Genetics. 141(7). 1239–1251. 7 indexed citations
11.
Schweitzer, Cyril, et al.. (2021). How do the FIFA World Cup 2018 and the 2016 UEFA championships impact a pediatric emergency department?. Archives de Pédiatrie. 28(3). 234–237. 1 indexed citations
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Castiglioni, Claudia, François Feillet, Christine Barnérias, et al.. (2020). Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications. Human Mutation. 42(2). 142–149. 13 indexed citations
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Wiedemann, Arnaud, et al.. (2020). La phénylcétonurie. médecine/sciences. 36(8-9). 725–734. 10 indexed citations
15.
Wiedemann, Arnaud, Marc Merten, Élise Jeannesson, et al.. (2019). Efficacy of low dose nitisinone in the management of alkaptonuria. Molecular Genetics and Metabolism. 127(3). 184–190. 19 indexed citations
16.
Ghemrawi, Rose, Carole Arnold, Shyue-Fang Battaglia-Hsu, et al.. (2019). SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders. Metabolism. 101. 153992–153992. 24 indexed citations
17.
Wiedemann, Arnaud, Céline Chéry, David Coelho, et al.. (2019). Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis. Journal of Human Genetics. 65(2). 91–98. 5 indexed citations
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Molin, Arnaud, François Feillet, Arnaud Wiedemann, et al.. (2016). Two French Families with Vitamin D Dependency Rickets Type 1B Harbor Homozygous Recessive Expression Of CYP2R1 Mutations L99P and G42_L46DEL INSR. 86. 1 indexed citations
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Wiedemann, Arnaud, Bruno Leheup, Shyue-Fang Battaglia-Hsu, et al.. (2013). Undiagnosed phenylketonuria in parents of phenylketonuric patients, is it worthwhile to be checked?. Molecular Genetics and Metabolism. 110. S62–S65. 5 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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