Rodolphe Dard

578 total citations
19 papers, 233 citations indexed

About

Rodolphe Dard is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Rodolphe Dard has authored 19 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Rodolphe Dard's work include Down syndrome and intellectual disability research (5 papers), Renal and related cancers (3 papers) and Metabolism and Genetic Disorders (3 papers). Rodolphe Dard is often cited by papers focused on Down syndrome and intellectual disability research (5 papers), Renal and related cancers (3 papers) and Metabolism and Genetic Disorders (3 papers). Rodolphe Dard collaborates with scholars based in France, Tunisia and Italy. Rodolphe Dard's co-authors include François Vialard, Fanny Mochel, Alexandra Dürr, Nathalie Janel, Cyril Mignot, Emmanuel Roze, Gaëtan Lesca, Damien Sanlaville, Delphine Fauvert and Radia Boudjenah and has published in prestigious journals such as Brain, Journal of Neurophysiology and Cellular and Molecular Life Sciences.

In The Last Decade

Rodolphe Dard

17 papers receiving 230 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rodolphe Dard France 6 113 67 63 30 28 19 233
Asude Durmaz Türkiye 11 100 0.9× 22 0.3× 92 1.5× 8 0.3× 14 0.5× 60 334
Rosetta Marotta Australia 9 252 2.2× 34 0.5× 42 0.7× 15 0.5× 22 0.8× 13 363
E. Feyereisen France 9 58 0.5× 156 2.3× 45 0.7× 139 4.6× 21 0.8× 17 289
Kuan-Wen Wang Canada 9 130 1.2× 42 0.6× 35 0.6× 4 0.1× 10 0.4× 22 340
Aida Rodríguez‐Nuevo Spain 4 158 1.4× 78 1.2× 19 0.3× 40 1.3× 2 0.1× 5 284
Jennifer Karmouch France 9 176 1.6× 32 0.5× 13 0.2× 11 0.4× 13 0.5× 11 312
Joachim Wölfle Germany 10 116 1.0× 13 0.2× 155 2.5× 42 1.4× 27 1.0× 24 335
Maria Grazia Patricelli Italy 10 176 1.6× 19 0.3× 185 2.9× 34 1.1× 10 0.4× 21 322
Siew L. Wong Australia 6 96 0.8× 121 1.8× 12 0.2× 58 1.9× 58 2.1× 9 329
Ana Marcuello Spain 7 239 2.1× 15 0.2× 70 1.1× 13 0.4× 11 0.4× 7 343

Countries citing papers authored by Rodolphe Dard

Since Specialization
Citations

This map shows the geographic impact of Rodolphe Dard'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 Rodolphe Dard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rodolphe Dard more than expected).

Fields of papers citing papers by Rodolphe Dard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rodolphe Dard. 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 Rodolphe Dard. The network helps show where Rodolphe Dard may publish in the future.

Co-authorship network of co-authors of Rodolphe Dard

This figure shows the co-authorship network connecting the top 25 collaborators of Rodolphe Dard. A scholar is included among the top collaborators of Rodolphe Dard 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 Rodolphe Dard. Rodolphe Dard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Moreau, Manon, Rodolphe Dard, Norma B. Romero, et al.. (2025). Neonatal obstructive sleep apneas in a mouse model of Down syndrome. Journal of Neurophysiology. 133(5). 1551–1557. 1 indexed citations
2.
Molina‐Gomes, Denise, Bérénice Herve, Marion Gauthier‐Villars, et al.. (2024). The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling. Molecular Genetics & Genomic Medicine. 12(4). e2437–e2437. 2 indexed citations
3.
Moreau, Manon, Rodolphe Dard, Nadim Kassis, et al.. (2024). Prenatal treatment with preimplantation factor improves early postnatal neurogenesis and cognitive impairments in a mouse model of Down syndrome. Cellular and Molecular Life Sciences. 81(1). 215–215. 1 indexed citations
4.
Buffet, Alexandre, Alexandra Bruel, Rodolphe Dard, et al.. (2024). X-linked transient antenatal Bartter syndrome related to MAGED2 gene: Enriching the phenotypic description and pathophysiologic investigation. Genetics in Medicine. 27(2). 101217–101217. 1 indexed citations
5.
Spaggiari, Emmanuel, et al.. (2023). Prenatal Diagnosis of Primrose Syndrome. Journal of Ultrasound in Medicine. 43(2). 411–414.
6.
7.
Egloff, Matthieu, Jonathan Lévy, Nicolas Chatron, et al.. (2023). 2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review. European Journal of Human Genetics. 31(8). 895–904. 1 indexed citations
8.
Tessier, Aude, et al.. (2023). Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case report. BMC Cardiovascular Disorders. 23(1). 116–116. 1 indexed citations
9.
Pujol, Claire, Élise Lebigot, Pauline Gaignard, et al.. (2022). MPC2variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy. Brain. 146(3). 858–864. 5 indexed citations
10.
Moreau, Manon, Rodolphe Dard, Stéfania Tolu, et al.. (2021). Metabolic Diseases and Down Syndrome: How Are They Linked Together?. Biomedicines. 9(2). 221–221. 37 indexed citations
11.
Dard, Rodolphe, et al.. (2021). Effects of the implementation of second-line prenatal cell-free DNA testing on termination of pregnancy in a French perinatal network. European Journal of Obstetrics & Gynecology and Reproductive Biology. 267. 36–41. 1 indexed citations
12.
Dard, Rodolphe, Manon Moreau, Nadim Kassis, et al.. (2021). DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of Spermatogenesis. Genes. 12(11). 1800–1800. 4 indexed citations
13.
Dard, Rodolphe, Nathalie Janel, & François Vialard. (2020). COVID-19 and Down’s syndrome: are we heading for a disaster?. European Journal of Human Genetics. 28(11). 1477–1478. 10 indexed citations
14.
Dard, Rodolphe, et al.. (2019). Down syndrome and infertility: what support should we provide?. Journal of Assisted Reproduction and Genetics. 36(6). 1063–1067. 20 indexed citations
15.
Khelifa, Mariem Ben, Radia Boudjenah, Delphine Fauvert, et al.. (2018). A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family. Human Reproduction. 33(6). 1034–1037. 46 indexed citations
16.
Dard, Rodolphe, Valérie Touitou, Giovanni Stévanin, et al.. (2017). Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation. European Journal of Medical Genetics. 60(12). 639–642. 23 indexed citations
17.
Herve, Bérénice, Delphine Fauvert, Rodolphe Dard, et al.. (2016). The emerging microduplication 3q13.31: Expanding the genotype-phenotype correlations of the reciprocal microdeletion 3q13.31 syndrome. European Journal of Medical Genetics. 59(9). 463–469. 4 indexed citations
18.
Dard, Rodolphe, Bérénice Herve, Thierry Leblanc, et al.. (2016). DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype. Pediatric Allergy and Immunology. 28(3). 298–303. 5 indexed citations
19.
Dard, Rodolphe, Cyril Mignot, Alexandra Dürr, et al.. (2015). Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation. Developmental Medicine & Child Neurology. 57(12). 1183–1186. 71 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Asude Durmaz Breakdown of academic impact, for papers by Rosetta Marotta Breakdown of academic impact, for papers by E. Feyereisen Breakdown of academic impact, for papers by Kuan-Wen Wang Breakdown of academic impact, for papers by Aida Rodríguez‐Nuevo Breakdown of academic impact, for papers by Jennifer Karmouch Breakdown of academic impact, for papers by Joachim Wölfle Breakdown of academic impact, for papers by Maria Grazia Patricelli Breakdown of academic impact, for papers by Siew L. Wong Breakdown of academic impact, for papers by Ana Marcuello
Rankless by CCL
2026