Damien Lederer
Impact in
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 6
- Cleft Lip and Palate Research 2
- Genetic Syndromes and Imprinting 2
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- Hedgehog Signaling Pathway Studies 2
- RNA modifications and cancer 2
- Co-authors
- Isabelle Maystadt (12 shared papers)Valérie Benoît (10 shared papers)Christine Verellen‐Dumoulin (4 shared papers)Bernard Grisart (2 shared papers)Bruno Dallapiccola (1 shared paper)S. Ghariani (1 shared paper)M. Cristina Digilio (1 shared paper)Shane McKee (2 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)Epileptic Disorders (2 papers)European Journal of Paediatric Neurology (2 papers)Epilepsia (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- BelgiumUnited KingdomFrance
In The Last Decade
Damien Lederer
25 papers receiving 811 citations
Peers
Comparison fields: 5 of 66
- Genetics 505
- Pharmacy 23
- Molecular Biology 336
- Psychiatry and Mental health 65
- Aging 6
Countries citing papers authored by Damien Lederer
This map shows the geographic impact of Damien Lederer'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 Damien Lederer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Damien Lederer more than expected).
Fields of papers citing papers by Damien Lederer
This network shows the impact of papers produced by Damien Lederer. 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 Damien Lederer. The network helps show where Damien Lederer may publish in the future.
Co-authors
The 25 scholars most cited alongside Damien Lederer, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 269 | |
| 2 | 2014 | 93 | |
| 3 | 2015 | 85 | |
| 4 | 2021 | 50 | |
| 5 | 2016 | 43 | |
| 6 | 2016 | 42 | |
| 7 | 2014 | 35 | |
| 8 | 2019 | 33 | |
| 9 | 2015 | 29 | |
| 10 | 2017 | 26 | |
| 11 | 2015 | 25 | |
| 12 | 2012 | 15 | |
| 13 | 2016 | 13 | |
| 14 | 2018 | 12 | |
| 15 | 2016 | 10 | |
| 16 | 2018 | 8 | |
| 17 | 2023 | 7 | |
| 18 | 2017 | 7 | |
| 19 | 2019 | 6 | |
| 20 | 2018 | 5 |
About Damien Lederer
Damien Lederer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cell Biology and Psychiatry and Mental health, having authored 25 papers that have together received 824 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Cleft Lip and Palate Research (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Epilepsy research and treatment (2 papers), Genetic Syndromes and Imprinting (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Genetics (505 citations), Pharmacy (23 citations), Molecular Biology (336 citations), Psychiatry and Mental health (65 citations) and Aging (6 citations). Damien Lederer has collaborated with scholars based in Belgium, United Kingdom and France. Frequent co-authors include Isabelle Maystadt, Valérie Benoît, Christine Verellen‐Dumoulin, Bernard Grisart, Bruno Dallapiccola, S. Ghariani, M. Cristina Digilio, Shane McKee, Stéphanie Moortgat and Marie‐Cécile Nassogne. Their work appears in journals such as European Journal of Medical Genetics, Epileptic Disorders, European Journal of Paediatric Neurology, Epilepsia and European Journal of Human 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.