Simone Schröder

575 total citations
30 papers, 235 citations indexed

About

Simone Schröder is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Simone Schröder has authored 30 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Simone Schröder's work include Genetic and Kidney Cyst Diseases (5 papers), Advanced Proteomics Techniques and Applications (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Simone Schröder is often cited by papers focused on Genetic and Kidney Cyst Diseases (5 papers), Advanced Proteomics Techniques and Applications (4 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Simone Schröder collaborates with scholars based in Germany, United States and Switzerland. Simone Schröder's co-authors include Hermann Wätzig, Knut Brockmann, R Kolb, Birgit Zirn, N. Sörensen, U Gebhardt, Jutta Gärtner, E. Hanisch, Hermann L. Müller and Matthew Borchers and has published in prestigious journals such as Clinica Chimica Acta, Osteoporosis International and Neurobiology of Disease.

In The Last Decade

Simone Schröder

26 papers receiving 231 citations

Peers

Simone Schröder
Lisa McDougall Switzerland
Masami Togawa Japan
Sorina Mihaela Papuc Romania
W Zaleski Canada
Apeksha Sahu India
Verayuth Praphanphoj Thailand
Anaita Hegde India
Riina Žordania Estonia
Kirsty McWalter United States
Valeria Messina Italy
Lisa McDougall Switzerland
Simone Schröder
Citations per year, relative to Simone Schröder Simone Schröder (= 1×) peers Lisa McDougall

Countries citing papers authored by Simone Schröder

Since Specialization
Citations

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

Fields of papers citing papers by Simone Schröder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Schröder

This figure shows the co-authorship network connecting the top 25 collaborators of Simone Schröder. A scholar is included among the top collaborators of Simone Schröder 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 Simone Schröder. Simone Schröder 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.
2.
Schröder, Simone, Gökhan Yigit, Yun Li, et al.. (2023). The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued. Orphanet Journal of Rare Diseases. 18(1). 101–101. 2 indexed citations
3.
Schröder, Simone, Gökhan Yigit, Eugen Boltshauser, et al.. (2021). Heterozygous Truncating Variants in SUFU Cause Congenital Ocular Motor Apraxia. Neuropediatrics. 52.
4.
Schröder, Simone, Yun Li, Gökhan Yigit, et al.. (2020). Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia. Genetics in Medicine. 23(2). 341–351. 10 indexed citations
5.
Hillebrand, Merle, Simone Schröder, Julia Hofhuis, et al.. (2020). Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity. Neurobiology of Disease. 143. 105012–105012. 10 indexed citations
6.
Schröder, Simone, Britta Wieland, Andreas Ohlenbusch, et al.. (2020). Evidence of pathogenicity for the leaky splice variant c.1066‐6T>G in ATM. American Journal of Medical Genetics Part A. 182(12). 2971–2975. 5 indexed citations
7.
Schröder, Simone, Johannes Buckard, Florian von Deimling, et al.. (2016). Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study. Orphanet Journal of Rare Diseases. 11(1). 104–104. 12 indexed citations
8.
Schröder, Simone, et al.. (2015). Tod zweier Stuten mit Retentio secundinarum. Tierärztliche Praxis Ausgabe G Großtiere / Nutztiere. 43(4). 228–231. 1 indexed citations
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10.
Albers, Lucia, Matthew Borchers, Jutta Gärtner, et al.. (2015). Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life. Clinical Genetics. 89(2). 258–266. 48 indexed citations
11.
Schröder, Simone, et al.. (2011). Quantitative gel electrophoresis: New records in precision by elaborated staining and detection protocols. Electrophoresis. 32(13). 1667–1674. 9 indexed citations
12.
Schröder, Simone, et al.. (2011). The challenge to quantify proteins with charge trains due to isoforms or conformers. Electrophoresis. 33(2). 263–269. 13 indexed citations
13.
Schröder, Simone, et al.. (2009). Improving precision in gel electrophoresis by stepwisely decreasing variance components. Journal of Pharmaceutical and Biomedical Analysis. 50(3). 320–327. 9 indexed citations
14.
Johnson, David E., et al.. (2008). Annotated Bibliography on the Teaching of Psychology: 2007. Teaching of Psychology. 35(4). 376–384. 3 indexed citations
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16.
Müller, Hermann L., U Gebhardt, Simone Schröder, et al.. (2007). First Experiences with Laparoscopic Adjustable Gastric Banding (LAGB) in the Treatment of Patients with Childhood Craniopharyngioma and Morbid Obesity. Klinische Pädiatrie. 219(6). 323–325. 45 indexed citations
17.
Johnson, David E. & Simone Schröder. (2006). Annotated Bibliography on the Teaching of Psychology: 2005. Teaching of Psychology. 33(4). 288–296.
18.
Johnson, David E., et al.. (2005). Annotated Bibliography on the Teaching of Psychology: 2004. Teaching of Psychology. 32(4). 281–287. 2 indexed citations
19.
Johnson, David E. & Simone Schröder. (2000). Annotated Bibliography on the Teaching of Psychology: 1999. Teaching of Psychology. 27(4). 296–303. 1 indexed citations
20.
Rosenquist, Christian, et al.. (1996). Automatic test for measurement of N-MIDTM osteocalcin (OC) in the enzymun-testR-analyser (Es 300 AL). Osteoporosis International. 6(S1). 192–192. 1 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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