Sophie Scheidecker
Impact in
- Genetics top 5%
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
-
- Hedgehog Signaling Pathway Studies
- Ubiquitin and proteasome pathways
- Retinal Development and Disorders
Papers in
- Genetics 25
- Genetic and Kidney Cyst Diseases 12
- Genomics and Rare Diseases 9
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
-
- Hedgehog Signaling Pathway Studies 7
- Renal and related cancers 3
- Genomics and Phylogenetic Studies 2
- Co-authors
- Hélène Dollfus (15 shared papers)Véronique Geoffroy (9 shared papers)Jean Muller (11 shared papers)Corinne Stoetzel (11 shared papers)Élise Schaefer (7 shared papers)Christelle Etard (4 shared papers)Uwe Straehle (4 shared papers)Vincent Marion (3 shared papers)
- Journals
- Human Mutation (6 papers)Clinical Genetics (3 papers)The American Journal of Human Genetics (2 papers)Nucleic Acids Research (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- FranceGermanyUnited States
In The Last Decade
Sophie Scheidecker
35 papers receiving 909 citations
Peers
Comparison fields: 5 of 77
- Genetics 498
- Molecular Biology 540
- Cell Biology 94
- Cellular and Molecular Neuroscience 78
- Psychiatry and Mental health 54
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
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 111 | |
| 2 | 2018 | 102 | |
| 3 | 2017 | 77 | |
| 4 | 2016 | 61 | |
| 5 | 2015 | 53 | |
| 6 | 2017 | 51 | |
| 7 | 2016 | 49 | |
| 8 | 2018 | 48 | |
| 9 | 2021 | 48 | |
| 10 | 2020 | 47 | |
| 11 | 2014 | 33 | |
| 12 | 2020 | 29 | |
| 13 | 2015 | 28 | |
| 14 | 2020 | 22 | |
| 15 | 2019 | 21 | |
| 16 | 2015 | 20 | |
| 17 | 2019 | 20 | |
| 18 | 2018 | 19 | |
| 19 | 2020 | 14 | |
| 20 | HCN1 mutation spectrum: From neonatal epileptic encephalopathy to benign generalized epilepsy and beyond | 2018 | 13 |
About Sophie Scheidecker
Sophie Scheidecker is a scholar working on Genetics, Molecular Biology, Cell Biology, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 938 indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Genomics and Rare Diseases (9 papers), Hedgehog Signaling Pathway Studies (7 papers), Genetic Syndromes and Imprinting (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Renal and related cancers (3 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Genetics (498 citations), Molecular Biology (540 citations), Cell Biology (94 citations), Cellular and Molecular Neuroscience (78 citations) and Psychiatry and Mental health (54 citations). Sophie Scheidecker has collaborated with scholars based in France, Germany and United States. Frequent co-authors include Hélène Dollfus, Véronique Geoffroy, Jean Muller, Corinne Stoetzel, Élise Schaefer, Christelle Etard, Uwe Straehle, Vincent Marion, Valérie Pelletier and Kirsley Chennen. Their work appears in journals such as Human Mutation, Clinical Genetics, The American Journal of Human Genetics, Nucleic Acids Research and Journal of Medical Genetics.
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.