David Schorling
Impact in
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Congenital Anomalies and Fetal Surgery
Papers in
-
- RNA modifications and cancer 4
- Muscle Physiology and Disorders 3
- Ion channel regulation and function 1
- Genetics 7
- Neurogenetic and Muscular Disorders Research 7
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Janbernd Kirschner (17 shared papers)Astrid Pechmann (11 shared papers)Thorsten Langer (5 shared papers)Ulrike Schara (4 shared papers)Sibylle Emilie Vogt (2 shared papers)Sabine Stein (2 shared papers)Carsten G. Bönnemann (2 shared papers)Hanns Lochmüller (5 shared papers)
- Journals
- Neuropediatrics (4 papers)Neuromuscular Disorders (3 papers)Journal of Neuromuscular Diseases (2 papers)Neurology (2 papers)Orphanet Journal of Rare Diseases (2 papers)
- Partner nations
- GermanyCanadaUnited States
In The Last Decade
David Schorling
18 papers receiving 527 citations
Peers
Comparison fields: 5 of 54
- Genetics 413
- Surgery 145
- Molecular Biology 242
- Genetics 63
- Speech and Hearing 8
Countries citing papers authored by David Schorling
This map shows the geographic impact of David Schorling'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 David Schorling with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Schorling more than expected).
Fields of papers citing papers by David Schorling
This network shows the impact of papers produced by David Schorling. 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 David Schorling. The network helps show where David Schorling may publish in the future.
Co-authors
The 25 scholars most cited alongside David Schorling, 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 | 2019 | 171 | |
| 2 | 2018 | 105 | |
| 3 | 2019 | 67 | |
| 4 | 2019 | 36 | |
| 5 | 2017 | 28 | |
| 6 | 2017 | 27 | |
| 7 | 2013 | 24 | |
| 8 | 2022 | 21 | |
| 9 | 2017 | 19 | |
| 10 | 2019 | 18 | |
| 11 | 2019 | 7 | |
| 12 | 2020 | 6 | |
| 13 | 2020 | 5 | |
| 14 | Mechanographic analysis of the timed 4 stair climb test - methodology and reference data of healthy children and adolescents. | 2023 | 2 |
| 15 | 2018 | 2 | |
| 16 | 2021 | 1 | |
| 17 | 2017 | 1 | |
| 18 | 2019 | 1 |
About David Schorling
David Schorling is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 541 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (7 papers), RNA modifications and cancer (4 papers), Muscle Physiology and Disorders (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Hemophilia Treatment and Research (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Genetics (413 citations), Surgery (145 citations), Molecular Biology (242 citations), Genetics (63 citations) and Speech and Hearing (8 citations). David Schorling has collaborated with scholars based in Germany, Canada and United States. Frequent co-authors include Janbernd Kirschner, Astrid Pechmann, Thorsten Langer, Ulrike Schara, Sibylle Emilie Vogt, Sabine Stein, Carsten G. Bönnemann, Hanns Lochmüller, Heike Kölbel and Brunhilde Wirth. Their work appears in journals such as Neuropediatrics, Neuromuscular Disorders, Journal of Neuromuscular Diseases, Neurology and Orphanet Journal of Rare Diseases.
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.