Stefanie Sander

1.1k total citations
28 papers, 793 citations indexed

About

Stefanie Sander is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Stefanie Sander has authored 28 papers receiving a total of 793 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Clinical Biochemistry, 15 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Stefanie Sander's work include Metabolism and Genetic Disorders (21 papers), Mitochondrial Function and Pathology (6 papers) and Neonatal Health and Biochemistry (5 papers). Stefanie Sander is often cited by papers focused on Metabolism and Genetic Disorders (21 papers), Mitochondrial Function and Pathology (6 papers) and Neonatal Health and Biochemistry (5 papers). Stefanie Sander collaborates with scholars based in Germany, United States and Switzerland. Stefanie Sander's co-authors include Nils Janzen, Johannes Sander, Michael Peter, Michael Terhardt, Ulrike Steuerwald, Anibh M. Das, Ute Holtkamp, Jörn Oliver Sass, Iris Marquardt and Thomas Lücke and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Agricultural and Food Chemistry.

In The Last Decade

Stefanie Sander

28 papers receiving 780 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefanie Sander Germany 18 419 418 254 106 82 28 793
M. Mathieu France 16 320 0.8× 267 0.6× 70 0.3× 73 0.7× 53 0.6× 61 771
Pedro Ruiz‐Sala Spain 13 302 0.7× 223 0.5× 39 0.2× 67 0.6× 47 0.6× 34 514
Françoise Fouque France 15 306 0.7× 128 0.3× 93 0.4× 28 0.3× 44 0.5× 26 654
Norman R. Marquis United States 10 451 1.1× 511 1.2× 99 0.4× 61 0.6× 23 0.3× 15 1.0k
Ellen S. Kang United States 18 324 0.8× 393 0.9× 42 0.2× 87 0.8× 58 0.7× 51 811
H.M. Hegarty United States 10 246 0.6× 587 1.4× 241 0.9× 38 0.4× 64 0.8× 13 949
Gitten Cederblad Sweden 13 362 0.9× 736 1.8× 116 0.5× 156 1.5× 13 0.2× 22 1.0k
Naomi van Vlies Netherlands 21 443 1.1× 265 0.6× 40 0.2× 84 0.8× 43 0.5× 46 1.1k
Philip J. Snodgrass United States 21 404 1.0× 499 1.2× 77 0.3× 127 1.2× 68 0.8× 32 1.0k
E A Burgess United Kingdom 13 331 0.8× 380 0.9× 71 0.3× 95 0.9× 171 2.1× 25 786

Countries citing papers authored by Stefanie Sander

Since Specialization
Citations

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

Fields of papers citing papers by Stefanie Sander

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Sander

This figure shows the co-authorship network connecting the top 25 collaborators of Stefanie Sander. A scholar is included among the top collaborators of Stefanie Sander 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 Stefanie Sander. Stefanie Sander 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.
Sander, Johannes, et al.. (2019). A new method for quantifying causative and diagnostic markers of methylenecyclopropylglycine poisoning. Toxicology Reports. 6. 803–808. 8 indexed citations
2.
Sander, Johannes, Joerg Ziegler, Michael Terhardt, et al.. (2019). Detection of MCPG metabolites in horses with atypical myopathy. PLoS ONE. 14(2). e0211698–e0211698. 21 indexed citations
3.
Sander, Johannes, Michael Terhardt, Stefanie Sander, & Nils Janzen. (2018). Use of a Standard Newborn Screening Test for the Rapid Diagnosis of Inhibited ß-Oxidation in Atypical Myopathy in Horses. Journal of Equine Veterinary Science. 67. 71–74. 4 indexed citations
4.
Sander, Johannes, Michael Terhardt, Stefanie Sander, & Nils Janzen. (2016). Quantification of hypoglycin A as butyl ester. Journal of Chromatography B. 1029-1030. 169–173. 13 indexed citations
5.
Janzen, Nils, Michael Terhardt, Stefanie Sander, et al.. (2013). Towards newborn screening for ornithine transcarbamylase deficiency: Fast non-chromatographic orotic acid quantification from dried blood spots by tandem mass spectrometry. Clinica Chimica Acta. 430. 28–32. 14 indexed citations
6.
Janzen, Nils, Ulrike Steuerwald, Stefanie Sander, et al.. (2013). UPLC–MS/MS analysis of C5-acylcarnitines in dried blood spots. Clinica Chimica Acta. 421. 41–45. 17 indexed citations
7.
Janzen, Nils, Felix G. Riepe, Michael Peter, et al.. (2012). Neonatal Screening: Identification of Children with 11β-Hydroxylase Deficiency by Second-Tier Testing. Hormone Research in Paediatrics. 77(3). 195–199. 23 indexed citations
8.
Illsinger, Sabine, Nils Janzen, Stefanie Sander, et al.. (2011). Energy metabolism in umbilical endothelial cells from preterm and term neonates. Journal of Perinatal Medicine. 39(5). 587–93. 3 indexed citations
9.
Janzen, Nils, Stefanie Sander, Michael Terhardt, et al.. (2011). Rapid steroid hormone quantification for congenital adrenal hyperplasia (CAH) in dried blood spots using UPLC liquid chromatography–tandem mass spectrometry. Steroids. 76(13). 1437–1442. 46 indexed citations
10.
Sander, Johannes, Nils Janzen, Michael Terhardt, et al.. (2010). Monitoring tyrosinaemia type I: Blood spot test for nitisinone (NTBC). Clinica Chimica Acta. 412(1-2). 134–138. 23 indexed citations
11.
Janzen, Nils, Stefanie Sander, Michael Terhardt, et al.. (2010). Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serum. Journal of Lipid Research. 51(6). 1591–1598. 21 indexed citations
12.
Illsinger, Sabine, Nils Janzen, Stefanie Sander, et al.. (2010). Preeclampsia and HELLP Syndrome: Impaired Mitochondrial Function in Umbilical Endothelial Cells. Reproductive Sciences. 17(3). 219–226. 34 indexed citations
13.
Peter, Michael, Nils Janzen, Stefanie Sander, et al.. (2008). A Case of 11β-Hydroxylase Deficiency Detected in a Newborn Screening Program by Second-Tier LC-MS/MS. Hormone Research in Paediatrics. 69(4). 253–256. 19 indexed citations
14.
Janzen, Nils, Stefanie Sander, Michael Terhardt, Michael Peter, & Johannes Sander. (2007). Fast and direct quantification of adrenal steroids by tandem mass spectrometry in serum and dried blood spots. Journal of Chromatography B. 861(1). 117–122. 94 indexed citations
15.
Janzen, Nils, Michael Peter, Stefanie Sander, et al.. (2007). Newborn Screening for Congenital Adrenal Hyperplasia: Additional Steroid Profile using Liquid Chromatography-Tandem Mass Spectrometry. The Journal of Clinical Endocrinology & Metabolism. 92(7). 2581–2589. 164 indexed citations
16.
Sander, Johannes, Stefanie Sander, Ulrike Steuerwald, et al.. (2005). Neonatal screening for defects of the mitochondrial trifunctional protein. Molecular Genetics and Metabolism. 85(2). 108–114. 56 indexed citations
17.
Lücke, Thomas, Celia Pérez‐Cerdá, Matthias R. Baumgartner, et al.. (2004). Propionic acidemia: unusual course with late onset and fatal outcome. Metabolism. 53(6). 809–810. 32 indexed citations
18.
Sander, Johannes, Nils Janzen, Stefanie Sander, et al.. (2003). Neonatal screening for citrullinaemia. European Journal of Pediatrics. 162(6). 417–420. 32 indexed citations
19.
Weber, Bernhard H. F., et al.. (1995). X-linked juvenile retinoschisis (RS) maps between DXS987 and DXS443. Cytogenetic and Genome Research. 69(1-2). 35–37. 12 indexed citations
20.
Sander, Stefanie, et al.. (1980). Piperacillin in the Treatment of Urinary Tract Infections. Chemotherapy. 26(2). 141–144. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by M. Mathieu Breakdown of academic impact, for papers by Pedro Ruiz‐Sala Breakdown of academic impact, for papers by Françoise Fouque Breakdown of academic impact, for papers by Norman R. Marquis Breakdown of academic impact, for papers by Ellen S. Kang Breakdown of academic impact, for papers by H.M. Hegarty Breakdown of academic impact, for papers by Gitten Cederblad Breakdown of academic impact, for papers by Naomi van Vlies Breakdown of academic impact, for papers by Philip J. Snodgrass Breakdown of academic impact, for papers by E A Burgess
Rankless by CCL
2026