Simone I. Schroder
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Academic and Historical Perspectives in Psychology 3
- Genetics 8
- Genetic and Kidney Cyst Diseases 5
- Genomics and Rare Diseases 2
- Co-authors
- Knut Brockmann (11 shared papers)Hermann Wätzig (4 shared papers)Reinhard Kolb (3 shared papers)U Gebhardt (3 shared papers)Lothar Jänsch (1 shared paper)Birgit Zirn (2 shared papers)Claus Zabel (1 shared paper)Edward S. Yeung (1 shared paper)
- Journals
- Neuropediatrics (6 papers)Orphanet Journal of Rare Diseases (2 papers)Genetics in Medicine (2 papers)Electrophoresis (2 papers)Journal of Proteome Research (1 paper)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Simone I. Schroder
32 papers receiving 399 citations
Peers
Comparison fields: 5 of 82
- Genetics 150
- Aging 5
- Endocrinology, Diabetes and Metabolism 42
- Developmental Neuroscience 10
- Molecular Biology 152
Countries citing papers authored by Simone I. Schroder
This map shows the geographic impact of Simone I. Schroder'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 I. Schroder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone I. Schroder more than expected).
Fields of papers citing papers by Simone I. Schroder
This network shows the impact of papers produced by Simone I. Schroder. 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 I. Schroder. The network helps show where Simone I. Schroder may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone I. Schroder, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 74 | |
| 2 | 2015 | 52 | |
| 3 | 2007 | 49 | |
| 4 | 2008 | 33 | |
| 5 | 2021 | 28 | |
| 6 | 2019 | 21 | |
| 7 | 2016 | 18 | |
| 8 | 2020 | 16 | |
| 9 | 2020 | 16 | |
| 10 | 2018 | 15 | |
| 11 | 2011 | 13 | |
| 12 | 2017 | 11 | |
| 13 | 2011 | 9 | |
| 14 | 2009 | 9 | |
| 15 | 2019 | 8 | |
| 16 | 2017 | 7 | |
| 17 | 2020 | 6 | |
| 18 | 2015 | 4 | |
| 19 | 2008 | 4 | |
| 20 | 2008 | 3 |
About Simone I. Schroder
Simone I. Schroder is a scholar working on General Psychology, Genetics, Spectroscopy, Clinical Biochemistry and Molecular Biology, having authored 36 papers that have together received 412 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (5 papers), Advanced Proteomics Techniques and Applications (4 papers), Academic and Historical Perspectives in Psychology (3 papers), Mass Spectrometry Techniques and Applications (2 papers), Growth Hormone and Insulin-like Growth Factors (2 papers), Genomics and Rare Diseases (2 papers), Metabolism and Genetic Disorders (2 papers) and Pituitary Gland Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (150 citations), Aging (5 citations), Endocrinology, Diabetes and Metabolism (42 citations), Developmental Neuroscience (10 citations) and Molecular Biology (152 citations). Simone I. Schroder has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Knut Brockmann, Hermann Wätzig, Reinhard Kolb, U Gebhardt, Lothar Jänsch, Birgit Zirn, Claus Zabel, Edward S. Yeung, Ernst W. Hanisch and Natalie Sorensen. Their work appears in journals such as Neuropediatrics, Orphanet Journal of Rare Diseases, Genetics in Medicine, Electrophoresis and Journal of Proteome Research.
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.