Damien Lederer

3.6k citations
25 papers · 824 · h-index 13

Impact in

  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
  • Pharmacy top 10%

Papers in

    • 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
    • Hedgehog Signaling Pathway Studies 2
    • RNA modifications and cancer 2

Damien Lederer

25 papers receiving 811 citations

Peers

Damien Lederer
Comparison fields: 5 of 66
  • Genetics 505
  • Pharmacy 23
  • Molecular Biology 336
  • Psychiatry and Mental health 65
  • Aging 6
Replace Isabelle Maystadt with:
Isabelle Maystadt Belgium
A. Moncla France
S. Ghariani Belgium
Fanny Kortüm Germany
Sofia Douzgou United Kingdom
Dominique Martin‐Coignard France
I. van der Bürgt Netherlands
Rasim Özgür Rosti United States
F. George Otieno United States
Lamei Yuan China
Damien Lederer relative to Isabelle Maystadt Belgium Isabelle Maystadt's profile →
Citations per field
00.5×4.6×
Isabelle Maystadt · 1×
Citations per year

Countries citing papers authored by Damien Lederer

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Damien Lederer Line = papers co-authored together Damien Lederer links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2011269
2 201493
3 201585
4 202150
5 201643
6 201642
7 201435
8 201933
9 201529
10 201726
11 201525
12 201215
13 201613
14 201812
15 201610
16 20188
17 20237
18 20177
19 20196
20 20185

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.

Explore authors with similar magnitude of impact