Vincent Cantagrel

3.0k total citations
15 papers, 456 citations indexed

About

Vincent Cantagrel is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Vincent Cantagrel has authored 15 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Vincent Cantagrel's work include Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Vincent Cantagrel is often cited by papers focused on Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Vincent Cantagrel collaborates with scholars based in France, United States and Egypt. Vincent Cantagrel's co-authors include Dirk J. Lefeber, Joseph G. Gleeson, William B. Dobyns, Hudson H. Freeze, Janice Zunich, Karl Hackmann, Melanie A. Jones, Shruti Bhide, Amy S. Paller and Madhuri Hegde and has published in prestigious journals such as The American Journal of Human Genetics, eLife and Journal of Medical Genetics.

In The Last Decade

Vincent Cantagrel

12 papers receiving 452 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Cantagrel France 10 281 176 79 53 45 15 456
Rachel Flomen United Kingdom 12 370 1.3× 180 1.0× 48 0.6× 114 2.2× 67 1.5× 17 583
Lauren Brady Canada 17 360 1.3× 120 0.7× 57 0.7× 32 0.6× 48 1.1× 40 558
Elisa Giorgio Italy 16 413 1.5× 177 1.0× 60 0.8× 59 1.1× 21 0.5× 46 622
David A. Keays United Kingdom 14 589 2.1× 149 0.8× 95 1.2× 33 0.6× 13 0.3× 20 726
Pascal Joset Switzerland 14 412 1.5× 245 1.4× 61 0.8× 23 0.4× 31 0.7× 26 640
Michael R. Huff United States 5 234 0.8× 58 0.3× 43 0.5× 122 2.3× 50 1.1× 10 440
Sophie Currier United States 7 682 2.4× 156 0.9× 122 1.5× 94 1.8× 21 0.5× 7 811
Sabine Endele Germany 14 701 2.5× 309 1.8× 51 0.6× 45 0.8× 31 0.7× 22 908
Michelle Ulrich United States 11 381 1.4× 65 0.4× 27 0.3× 32 0.6× 24 0.5× 29 777
Michael A. Pickart United States 10 312 1.1× 89 0.5× 159 2.0× 23 0.4× 18 0.4× 18 471

Countries citing papers authored by Vincent Cantagrel

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Cantagrel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Cantagrel

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

All Works

15 of 15 papers shown
1.
Siquier-Pernet, Karine, Geoffroy Delplancq, Marlène Rio, et al.. (2025). Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech. Molecular Autism. 16(1). 10–10.
2.
Siquier-Pernet, Karine, Pauline Marzin, Christine Bôle‐Feysot, et al.. (2024). LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy. Human Genetics and Genomics Advances. 6(1). 100372–100372.
3.
Fedeli, Valeria, Jingyi Wang, Vincent Cantagrel, & Adolfo Saiardi. (2024). Human plasma inositol hexakisphosphate (InsP6) phosphatase identified as the Multiple Inositol Polyphosphate Phosphatase 1 (MINPP1). PubMed. 2024. 1 indexed citations
4.
Siquier-Pernet, Karine, Pierre Blanc, Arnold Münnich, et al.. (2023). A non-coding variant in the Kozak sequence of RARS2 strongly decreases protein levels and causes pontocerebellar hypoplasia. BMC Medical Genomics. 16(1). 143–143. 1 indexed citations
5.
6.
Siquier-Pernet, Karine, Marlène Rio, Anne Guimier, et al.. (2022). 16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing. European Journal of Human Genetics. 30(6). 712–720. 9 indexed citations
7.
Nguyen, Lam Son, Michaël Nicouleau, Joanna Lipecka, et al.. (2018). High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect. eLife. 7. 41 indexed citations
8.
Megahed, Hisham, Michaël Nicouleau, Giulia Barcia, et al.. (2016). Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population. Orphanet Journal of Rare Diseases. 11(1). 57–57. 24 indexed citations
9.
Thomas, Sophie, Vincent Cantagrel, Laura Mariani, et al.. (2014). Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity. European Journal of Human Genetics. 23(5). 621–627. 43 indexed citations
10.
Radmanesh, Farid, Ahmet Okay Çağlayan, Jennifer L. Silhavy, et al.. (2013). Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities. The American Journal of Human Genetics. 92(3). 468–474. 80 indexed citations
11.
Ng, Bobby G., Karl Hackmann, Melanie A. Jones, et al.. (2012). Mutations in the Glycosylphosphatidylinositol Gene PIGL Cause CHIME Syndrome. The American Journal of Human Genetics. 90(4). 685–688. 90 indexed citations
12.
Cantagrel, Vincent & Dirk J. Lefeber. (2011). From glycosylation disorders to dolichol biosynthesis defects: a new class of metabolic diseases. Journal of Inherited Metabolic Disease. 34(4). 859–867. 64 indexed citations
13.
Cantagrel, Vincent, Philippe Ciofi, Anne-Marie Lossi, et al.. (2009). Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation. Gene Expression Patterns. 9(6). 423–429. 19 indexed citations
14.
Cantagrel, Vincent, Steven Lisgo, Chantal Missirian, et al.. (2006). Truncation ofNHEJ1 in a patient with polymicrogyria. Human Mutation. 28(4). 356–364. 28 indexed citations
15.
Cantagrel, Vincent, et al.. (2004). Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males. Journal of Medical Genetics. 41(10). 736–742. 56 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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