Damien Lederer

3.5k total citations
25 papers, 771 citations indexed

About

Damien Lederer is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Damien Lederer has authored 25 papers receiving a total of 771 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in Damien Lederer's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (7 papers). Damien Lederer is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (7 papers). Damien Lederer collaborates with scholars based in Belgium, United Kingdom and France. Damien Lederer's co-authors include Isabelle Maystadt, Valérie Benoît, Christine Verellen‐Dumoulin, Bernard Grisart, Bruno Dallapiccola, S. Ghariani, M. Cristina Digilio, Shane McKee, Stéphanie Moortgat and Deborah Shears and has published in prestigious journals such as The American Journal of Human Genetics, Epilepsia and Journal of Medical Genetics.

In The Last Decade

Damien Lederer

25 papers receiving 765 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Damien Lederer Belgium 13 518 359 78 62 59 25 771
Zöe Powis United States 15 562 1.1× 387 1.1× 88 1.1× 60 1.0× 31 0.5× 34 873
Marion Gérard France 14 386 0.7× 436 1.2× 46 0.6× 47 0.8× 51 0.9× 29 837
Fabienne Giuliano France 17 549 1.1× 698 1.9× 71 0.9× 31 0.5× 118 2.0× 38 1.1k
Krzysztof Szczałuba Poland 15 369 0.7× 328 0.9× 40 0.5× 31 0.5× 28 0.5× 57 638
Angela Peron Italy 18 365 0.7× 261 0.7× 114 1.5× 37 0.6× 29 0.5× 54 827
Alexandra Afenjar France 16 621 1.2× 521 1.5× 127 1.6× 19 0.3× 96 1.6× 42 1.0k
Kyle Retterer United States 24 906 1.7× 681 1.9× 193 2.5× 67 1.1× 56 0.9× 37 1.4k
Karen Buysse Belgium 15 633 1.2× 456 1.3× 64 0.8× 32 0.5× 66 1.1× 19 959
Kate Pope Australia 17 392 0.8× 567 1.6× 147 1.9× 26 0.4× 53 0.9× 28 867
Isabelle Maystadt Belgium 14 516 1.0× 514 1.4× 16 0.2× 55 0.9× 86 1.5× 32 946

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-authorship network of co-authors of Damien Lederer

This figure shows the co-authorship network connecting the top 25 collaborators of Damien Lederer. A scholar is included among the top collaborators of Damien Lederer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Damien Lederer. Damien Lederer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lederer, Damien, et al.. (2023). Precision medicine: Vinpocetine as a potential treatment for GABRG2‐related epilepsy. Epileptic Disorders. 25(3). 383–389. 4 indexed citations
2.
Ochoa, Eguzkine, Magdalena Badura‐Stronka, Deirdre Donnelly, et al.. (2023). Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics. 31(9). 1040–1047. 5 indexed citations
3.
Destrèe, Anne, Marie Deprez, Hazim Kadhim, et al.. (2022). ASC1 complex related conditions: Two novel paediatric patients with TRIP4 pathogenic variants and review of literature. European Journal of Medical Genetics. 65(4). 104469–104469. 1 indexed citations
4.
Vel, Anouk Van de, et al.. (2019). The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures. European Journal of Paediatric Neurology. 24. 148–153. 5 indexed citations
5.
Benoît, Valérie, et al.. (2018). Case report: An infantile lethal form of Albright hereditary osteodystrophy due to a GNAS mutation. Clinical Case Reports. 6(10). 1933–1940. 5 indexed citations
6.
Moortgat, Stéphanie, Damien Lederer, Marie Deprez, et al.. (2018). Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia. European Journal of Medical Genetics. 61(8). 442–450. 8 indexed citations
7.
Moortgat, Stéphanie, et al.. (2018). Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. Yearbook of pediatric endocrinology. 12 indexed citations
8.
Lehalle, Daphné, Umut Altunoğlu, Ange‐Line Bruel, et al.. (2017). Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients. American Journal of Medical Genetics Part A. 173(12). 3136–3142. 5 indexed citations
9.
Régal, Luc, Isabelle Maystadt, Nicol C. Voermans, et al.. (2017). PREPL deficiency: delineation of the phenotype and development of a functional blood assay. Genetics in Medicine. 20(1). 109–118. 24 indexed citations
10.
Lederer, Damien, et al.. (2017). Faut-il toujours traiter les convulsions infantiles liées à une mutation de PRRT2  ?. Archives de Pédiatrie. 24(10). 1010–1012. 2 indexed citations
11.
Moortgat, Stéphanie, Julie Désir, Valérie Benoît, et al.. (2016). Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. American Journal of Medical Genetics Part A. 170(11). 2927–2933. 41 indexed citations
12.
Lambert, Sophie, Isabelle Maystadt, Pascal Vrielynck, et al.. (2016). Expanding phenotype of p.Ala140Val mutation in MECP2 in a 4 generation family with X-linked intellectual disability and spasticity. European Journal of Medical Genetics. 59(10). 522–525. 13 indexed citations
13.
Parker, Michael, Alan Fryer, Deborah Shears, et al.. (2015). De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics Part A. 167(10). 2231–2237. 79 indexed citations
14.
Mignot, Cyril, Agnès Guët, Caroline Nava, et al.. (2015). DYRK1A mutations in two unrelated patients. European Journal of Medical Genetics. 58(3). 168–174. 24 indexed citations
15.
Morgan, Angela, Cristina Mei, Damien Lederer, et al.. (2015). Speech and language in a genotyped cohort of individuals with Kabuki syndrome. American Journal of Medical Genetics Part A. 167(7). 1483–1492. 27 indexed citations
16.
Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations
17.
Lederer, Damien, Debbie Shears, Valérie Benoît, Christine Verellen‐Dumoulin, & Isabelle Maystadt. (2014). A three generation X‐linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A. American Journal of Medical Genetics Part A. 164(5). 1289–1292. 32 indexed citations
18.
Lederer, Damien, Brian T. Wilson, Pierre Lefesvre, et al.. (2012). Atypical findings in three patients with Pai syndrome and literature review. American Journal of Medical Genetics Part A. 158A(11). 2899–2904. 14 indexed citations
19.
Lederer, Damien, et al.. (2012). Discordant monozygotic twins for macrocephaly‐capillary malformation. American Journal of Medical Genetics Part A. 158A(6). 1509–1511. 3 indexed citations
20.
Lederer, Damien, Bernard Grisart, M. Cristina Digilio, et al.. (2011). Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome. The American Journal of Human Genetics. 90(1). 119–124. 248 indexed citations

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.

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