Andrea Schlune

835 total citations
24 papers, 319 citations indexed

About

Andrea Schlune is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Andrea Schlune has authored 24 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Clinical Biochemistry, 10 papers in Molecular Biology and 7 papers in Biochemistry. Recurrent topics in Andrea Schlune's work include Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (6 papers) and Mitochondrial Function and Pathology (4 papers). Andrea Schlune is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (6 papers) and Mitochondrial Function and Pathology (4 papers). Andrea Schlune collaborates with scholars based in Germany, United States and Austria. Andrea Schlune's co-authors include Regina Ensenauer, Ertan Mayatepek, Dieter Häussinger, Hans Oberleithner, Stephan vom Dahl, Victor Shahin, Timm Danker, Claudia Schäfer, Eva Thimm and Chris Mühlhausen and has published in prestigious journals such as Journal of Cellular Biochemistry, The Journal of Membrane Biology and Amino Acids.

In The Last Decade

Andrea Schlune

20 papers receiving 313 citations

Peers

Andrea Schlune
Uta Meyer Germany
Sandesh C.S. Nagamani United States
Sravan Jaggumantri Canada
Stefan Koelker Germany
Cristiana Artiola Italy
James R. Bonham United Kingdom
Serap Sivri Türkiye
Cynthia Le Mons United States
Marina Morath Germany
Helen Prunty United Kingdom
Uta Meyer Germany
Andrea Schlune
Citations per year, relative to Andrea Schlune Andrea Schlune (= 1×) peers Uta Meyer

Countries citing papers authored by Andrea Schlune

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Schlune

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Schlune

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Schlune. A scholar is included among the top collaborators of Andrea Schlune 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 Andrea Schlune. Andrea Schlune 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.
Schlune, Andrea & Regina Ensenauer. (2024). Beikost und Übergang zur Familienkost: Wann? Was? Wie?. OpenAgrar. 19(3). 229–243.
2.
Brettschneider, Anna-Kristin, Andrea Schlune, Thorsten Heuer, et al.. (2024). Unfavorable food consumption in children up to school entry age: results from the nationwide German KiESEL study. Frontiers in Nutrition. 11. 1335934–1335934. 3 indexed citations
3.
Ensenauer, Regina, Andrea Schlune, & Jens H. Stupin. (2023). Perinatale metabolische Programmierung. Pädiatrie. 35(S1). 30–33. 1 indexed citations
4.
Taylan, Christina, Andrea Schlune, Thomas Meißner, et al.. (2016). Disease control via intensified lipoprotein apheresis in three siblings with familial hypercholesterolemia. Journal of clinical lipidology. 10(6). 1303–1310. 6 indexed citations
5.
Landolt, Markus A., Matthias R. Baumgartner, Julia Quitmann, et al.. (2016). Living with Intoxication-Type Inborn Errors of Metabolism: A Qualitative Analysis of Interviews with Paediatric Patients and Their Parents. JIMD Reports. 31. 1–9. 21 indexed citations
6.
Huemer, Martina, Daniel R. Carvalho, Jaime Moritz Brum, et al.. (2016). Clinical phenotype, biochemical profile, and treatment in 19 patients with arginase 1 deficiency. Journal of Inherited Metabolic Disease. 39(3). 331–340. 30 indexed citations
7.
Schlune, Andrea, Stephan vom Dahl, Dieter Häussinger, Regina Ensenauer, & Ertan Mayatepek. (2015). Hyperargininemia due to arginase I deficiency: the original patients and their natural history, and a review of the literature. Amino Acids. 47(9). 1751–1762. 51 indexed citations
8.
Schlune, Andrea, et al.. (2015). Arginase 1 deficiency: long-term follow-up of the original patients. Zeitschrift für Gastroenterologie. 53(12). 2 indexed citations
9.
Baertling, Fabian, Ertan Mayatepek, Eva Thimm, et al.. (2014). Malonic aciduria: long-term follow-up of new patients detected by newborn screening. European Journal of Pediatrics. 173(12). 1719–1722. 12 indexed citations
10.
Schlune, Andrea, Sebastian Kummer, & Thomas Meißner. (2014). Hypoglykämien im Kindesalter. Monatsschrift Kinderheilkunde. 162(9). 811–825.
11.
Kummer, Sebastian, et al.. (2013). Synergistic mutations in SLC3A1 and SLC7A9 leading to heterogeneous cystinuria phenotypes: pitfalls in the diagnostic workup. Pediatric Nephrology. 29(1). 155–159. 4 indexed citations
12.
El‐Gharbawy, Areeg, Jennifer Goldstein, David S. Millington, et al.. (2013). Elevation of guanidinoacetate in newborn dried blood spots and impact of early treatment in GAMT deficiency. Molecular Genetics and Metabolism. 109(2). 215–217. 34 indexed citations
13.
Baertling, Fabian, Ertan Mayatepek, Patrick Gerner, et al.. (2013). Liver cirrhosis in glycogen storage disease Ib. Molecular Genetics and Metabolism. 108(3). 198–200. 5 indexed citations
14.
Kölker, Stefan, Jana Herınger, Edith Müller, et al.. (2012). Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I — A decade of experience. Molecular Genetics and Metabolism. 107(1-2). 72–80. 38 indexed citations
15.
Schlune, Andrea, Eva Thimm, Diran Herebıan, & Ute Spiekerkoetter. (2012). Single dose NTBC‐treatment of hereditary tyrosinemia type I. Journal of Inherited Metabolic Disease. 35(5). 831–836. 18 indexed citations
16.
Schlune, Andrea, et al.. (2006). Plugs in nuclear pores: Transcripts in early oocyte development identified with nanotechniques. Journal of Cellular Biochemistry. 98(3). 567–576. 7 indexed citations
17.
Buchholz, Ina, et al.. (2004). Transient Permeability Leak of Nuclear Envelope Induced by Aldosterone. The Journal of Membrane Biology. 199(3). 135–141. 7 indexed citations
18.
Danker, Timm, et al.. (2003). Passive Transport of Macromolecules through Xenopus laevis Nuclear Envelope. The Journal of Membrane Biology. 196(3). 147–155. 15 indexed citations
19.
Danker, Timm, Victor Shahin, Andrea Schlune, Claudia Schäfer, & Hans Oberleithner. (2001). Electrophoretic Plugging of Nuclear Pores by Using the Nuclear Hourglass Technique. The Journal of Membrane Biology. 184(2). 91–99. 19 indexed citations
20.
Oberleithner, Hans, Claudia Schäfer, Victor Shahin, et al.. (2001). Nuclear Plug Harvesting Using Atomic Force Microscopy. 2(2). 117–120. 7 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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