Sophie Scheidecker
Impact in
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
-
- Hedgehog Signaling Pathway Studies
- Renal and related cancers
- Retinal Development and Disorders
- Protist diversity and phylogeny
Papers in
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- Hedgehog Signaling Pathway Studies 6
- Renal and related cancers 2
- Mitochondrial Function and Pathology 2
- Genomics and Phylogenetic Studies 2
- Genetics 13
- Genetic and Kidney Cyst Diseases 9
- Genetic Syndromes and Imprinting 5
- Genomics and Rare Diseases 3
- Co-authors
- Hélène Dollfus (15 shared papers)Véronique Geoffroy (9 shared papers)Corinne Stoetzel (11 shared papers)Jean Muller (11 shared papers)Élise Schaefer (7 shared papers)Uwe Strähle (4 shared papers)Christelle Etard (4 shared papers)Vincent Marion (3 shared papers)
- Journals
- Human Mutation (3 papers)European Journal of Medical Genetics (2 papers)Nucleic Acids Research (2 papers)Clinical Genetics (2 papers)Nature Communications (1 paper)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Sophie Scheidecker
19 papers receiving 427 citations
Peers
Comparison fields: 5 of 54
- Genetics 270
- Molecular Biology 279
- Cell Biology 49
- Developmental Biology 5
- Sensory Systems 10
Countries citing papers authored by Sophie Scheidecker
This map shows the geographic impact of Sophie Scheidecker'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 Sophie Scheidecker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sophie Scheidecker more than expected).
Fields of papers citing papers by Sophie Scheidecker
This network shows the impact of papers produced by Sophie Scheidecker. 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 Sophie Scheidecker. The network helps show where Sophie Scheidecker may publish in the future.
Co-authors
The 25 scholars most cited alongside Sophie Scheidecker, 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 | 2013 | 104 | |
| 2 | 2016 | 58 | |
| 3 | 2015 | 51 | |
| 4 | 2016 | 41 | |
| 5 | 2021 | 35 | |
| 6 | 2014 | 28 | |
| 7 | 2015 | 20 | |
| 8 | 2015 | 16 | |
| 9 | 2019 | 16 | |
| 10 | 2019 | 15 | |
| 11 | 2020 | 11 | |
| 12 | 2020 | 10 | |
| 13 | 2023 | 7 | |
| 14 | 2019 | 5 | |
| 15 | 2023 | 5 | |
| 16 | 2016 | 5 | |
| 17 | 2018 | 2 | |
| 18 | 2024 | 1 | |
| 19 | 2022 | 1 | |
| 20 | 2023 | 0 |
About Sophie Scheidecker
Sophie Scheidecker is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Developmental Biology and Cellular and Molecular Neuroscience, having authored 20 papers that have together received 431 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (9 papers), Hedgehog Signaling Pathway Studies (6 papers), Genetic Syndromes and Imprinting (5 papers), Genomics and Rare Diseases (3 papers), Biomedical Research and Pathophysiology (2 papers), Renal and related cancers (2 papers), Mitochondrial Function and Pathology (2 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Genetics (270 citations), Molecular Biology (279 citations), Cell Biology (49 citations), Developmental Biology (5 citations) and Sensory Systems (10 citations). Sophie Scheidecker has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Hélène Dollfus, Véronique Geoffroy, Corinne Stoetzel, Jean Muller, Élise Schaefer, Uwe Strähle, Christelle Etard, Vincent Marion, Valérie Pelletier and Kirsley Chennen. Their work appears in journals such as Human Mutation, European Journal of Medical Genetics, Nucleic Acids Research, Clinical Genetics and Nature Communications.
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.