Andreas Schedl
Impact in
- Developmental Neuroscience top 0.5%
- Genetics top 0.2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
- Genetics 52
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 32
- Animal Genetics and Reproduction 12
- Genetic and Kidney Cyst Diseases 8
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- Renal and related cancers 51
- Sexual Differentiation and Disorders 15
- Pluripotent Stem Cells Research 13
- Wnt/β-catenin signaling in development and cancer 8
- Co-authors
- Marie‐Christine ChaboissierValérie VidalHaruhiko AkiyamaBenoît De CrombruggheJames F. MartinDirk G. de RooijNicholas D. HastieJames Briscoe
- Journals
- Genes & Development (5 papers)Development (5 papers)Human Molecular Genetics (5 papers)Kidney International (5 papers)Cell Reports (4 papers)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Andreas Schedl
114 papers receiving 13.2k citations
Hit Papers
Peers
Comparison fields: 5 of 148
- Developmental Neuroscience 713
- Genetics 4.3k
- Molecular Biology 9.6k
- Reproductive Medicine 1.0k
- Cell Biology 1.8k
Countries citing papers authored by Andreas Schedl
This map shows the geographic impact of Andreas Schedl'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 Andreas Schedl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Schedl more than expected).
Fields of papers citing papers by Andreas Schedl
This network shows the impact of papers produced by Andreas Schedl. 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 Andreas Schedl. The network helps show where Andreas Schedl may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Schedl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2023 | 8 | |
| 3 | 2023 | 20 | |
| 4 | 2023 | 7 | |
| 5 | 2020 | 31 | |
| 6 | 2020 | 16 | |
| 7 | 2020 | 22 | |
| 8 | 2020 | 13 | |
| 9 | 2018 | 10 | |
| 10 | 2018 | 15 | |
| 11 | 2015 | 38 | |
| 12 | 2012 | 168 | |
| 13 | 2009 | 39 | |
| 14 | 2008 | 1 | |
| 15 | 2004 | 450 | |
| 16 | 2004 | 76 | |
| 17 | The Sox9 transcription factor determines glial fate choice in the developing spinal cord Hit paper breakdown → | 2003 | 509 |
| 18 | WT1 is a key regulator of podocyte function | 2002 | 2 |
| 19 | 2002 | 128 | |
| 20 | 1998 | 34 |
About Andreas Schedl
Andreas Schedl is a scholar working on Genetics, Molecular Biology, Urology, Reproductive Medicine and Developmental Neuroscience, having authored 116 papers that have together received 13.4k indexed citations. Recurring topics across this work include Renal and related cancers (51 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (32 papers), Sexual Differentiation and Disorders (15 papers), Renal cell carcinoma treatment (14 papers), Pluripotent Stem Cells Research (13 papers), Animal Genetics and Reproduction (12 papers), Genetic and Kidney Cyst Diseases (8 papers) and Wnt/β-catenin signaling in development and cancer (8 papers). The work is most often cited by research in Developmental Neuroscience (713 citations), Genetics (4.3k citations), Molecular Biology (9.6k citations), Reproductive Medicine (1.0k citations) and Cell Biology (1.8k citations). Andreas Schedl has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Marie‐Christine Chaboissier, Valérie Vidal, Haruhiko Akiyama, Benoît De Crombrugghe, James F. Martin, Dirk G. de Rooij, Nicholas D. Hastie, James Briscoe, Veronica van Heyningen and Kay‐Dietrich Wagner. Their work appears in journals such as Genes & Development, Development, Human Molecular Genetics, Kidney International and Cell Reports.
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.