Christian Staufner

2.9k total citations
27 papers, 688 citations indexed

About

Christian Staufner is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Christian Staufner has authored 27 papers receiving a total of 688 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Christian Staufner's work include Metabolism and Genetic Disorders (13 papers), Neonatal Health and Biochemistry (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Christian Staufner is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Neonatal Health and Biochemistry (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Christian Staufner collaborates with scholars based in Germany, United States and Netherlands. Christian Staufner's co-authors include Verena Peters, Jenny Marzahn, Chrysanthy Ikonomidou, Andrzej Stepulak, Harald Luksch, Katja Brocke, Georg F. Hoffmann, Stefan Kölker, Ortrud Uckermann and Marco Sifringer and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and PEDIATRICS.

In The Last Decade

Christian Staufner

25 papers receiving 676 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian Staufner Germany 13 371 165 158 98 96 27 688
Hendrik Rosewich Germany 18 567 1.5× 137 0.8× 71 0.4× 55 0.6× 120 1.3× 34 857
Chandree L. Beaulieu Canada 20 645 1.7× 107 0.6× 127 0.8× 54 0.6× 459 4.8× 33 1.1k
David Bargiela United Kingdom 17 412 1.1× 59 0.4× 150 0.9× 42 0.4× 95 1.0× 30 855
K Naess Sweden 15 740 2.0× 466 2.8× 76 0.5× 37 0.4× 112 1.2× 41 974
Mauro Scarpelli Italy 17 535 1.4× 312 1.9× 85 0.5× 29 0.3× 42 0.4× 34 796
Diana Ballhausen Switzerland 19 546 1.5× 356 2.2× 58 0.4× 52 0.5× 167 1.7× 46 1.1k
Daria Diodato Italy 18 868 2.3× 535 3.2× 84 0.5× 43 0.4× 89 0.9× 44 1.2k
Ángeles García‐Cazorla Spain 16 550 1.5× 616 3.7× 119 0.8× 50 0.5× 204 2.1× 37 1.1k
Johan Van Hove United States 10 531 1.4× 290 1.8× 38 0.2× 23 0.2× 75 0.8× 17 733
Luc Régal Belgium 15 336 0.9× 84 0.5× 51 0.3× 32 0.3× 117 1.2× 33 689

Countries citing papers authored by Christian Staufner

Since Specialization
Citations

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

Fields of papers citing papers by Christian Staufner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Staufner

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Staufner. A scholar is included among the top collaborators of Christian Staufner 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 Christian Staufner. Christian Staufner 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.
Staufner, Christian, René G. Feichtinger, Johannes Häberle, et al.. (2025). Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency ( DLDD ): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients. Journal of Inherited Metabolic Disease. 48(3). e70035–e70035.
2.
Mendes, Marisa I., Nicole I. Wolf, Joëlle Rudinger‐Thirion, et al.. (2024). Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS. Nucleic Acids Research. 52(22). e107–e107. 1 indexed citations
3.
Staufner, Christian, et al.. (2024). Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiency. Journal of Inherited Metabolic Disease. 48(1). e12707–e12707. 3 indexed citations
4.
Schröter, Julian, Jennifer Hüllein, Vincent Heuveline, et al.. (2023). aRgus: Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment. Computational and Structural Biotechnology Journal. 21. 1077–1083. 6 indexed citations
5.
Regenbogen, Christina, Martin Merkel, Eugen Mengel, et al.. (2023). Management, vaccination status and COVID-19 morbidity of patients with Gaucher disease in Germany during the COVID-19 pandemic. Zeitschrift für Gastroenterologie. 61(4). 375–380.
6.
Lenz, Dominic, et al.. (2023). Pregnancy, delivery, and postpartum period in infantile liver failure syndrome type 2 due to variants in NBAS. JIMD Reports. 64(3). 246–251. 1 indexed citations
7.
Kovacevic, Alexander, Sven F. Garbade, Friederike Hörster, et al.. (2022). Detection of early cardiac disease manifestation in propionic acidemia – Results of a monocentric cross-sectional study. Molecular Genetics and Metabolism. 137(4). 349–358. 5 indexed citations
8.
Schröter, Julian, Heiko Brennenstuhl, Dominic Lenz, et al.. (2022). Genotypic and phenotypic spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency. Molecular Genetics and Metabolism. 137(1-2). 18–25. 7 indexed citations
9.
Lenz, Dominic, Mirjam Stahl, Elias Seidl, et al.. (2020). Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants. Pediatric Pulmonology. 55(11). 3057–3066. 19 indexed citations
10.
Garbade, Sven F., Matthias Zielonka, Konstantin Mechler, et al.. (2020). FDA orphan drug designations for lysosomal storage disorders – a cross-sectional analysis. PLoS ONE. 15(4). e0230898–e0230898. 23 indexed citations
11.
Kovacevic, Alexander, Sven F. Garbade, Georg F. Hoffmann, et al.. (2020). Cardiac phenotype in propionic acidemia – Results of an observational monocentric study. Molecular Genetics and Metabolism. 130(1). 41–48. 14 indexed citations
12.
Lenz, Dominic, Christian Staufner, Gudrun Göhring, et al.. (2019). Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-A. Stem Cell Research. 35. 101398–101398. 1 indexed citations
13.
Lenz, Dominic, Christian Staufner, Gudrun Göhring, et al.. (2019). Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1. Stem Cell Research. 37. 101428–101428. 8 indexed citations
14.
Evers, Christina, Christian Staufner, Martin Granzow, et al.. (2017). Impact of clinical exomes in neurodevelopmental and neurometabolic disorders. Molecular Genetics and Metabolism. 121(4). 297–307. 34 indexed citations
15.
Staufner, Christian, Henk J. Blom, Carlo Dionisi‐Vici, et al.. (2016). MRI and 1H-MRS in adenosine kinase deficiency. Neuroradiology. 58(7). 697–703. 11 indexed citations
16.
Staufner, Christian, Martin Lindner, Carlo Dionisi‐Vici, et al.. (2015). Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options. Journal of Inherited Metabolic Disease. 39(2). 273–283. 48 indexed citations
17.
Staufner, Christian, Olaf Sommerburg, & Stefan Holland‐Cunz. (2012). Algorithm for early diagnosis in nontuberculous mycobacterial lymphadenitis. Acta Paediatrica. 101(8). e382–5. 11 indexed citations
18.
Danhauser, Katharina, Sven W. Sauer, Tobias B. Haack, et al.. (2012). DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria. The American Journal of Human Genetics. 91(6). 1082–1087. 79 indexed citations
19.
Brocke, Katja, Christian Staufner, Harald Luksch, et al.. (2010). Glutamate receptors in pediatric tumors of the central nervous system. Cancer Biology & Therapy. 9(6). 455–468. 62 indexed citations
20.
Stepulak, Andrzej, Harald Luksch, Christine Gebhardt, et al.. (2009). Expression of glutamate receptor subunits in human cancers. Histochemistry and Cell Biology. 132(4). 435–445. 154 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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