Julien Van‐Gils

1.7k total citations
19 papers, 155 citations indexed

About

Julien Van‐Gils is a scholar working on Developmental Biology, Genetics and Molecular Biology. According to data from OpenAlex, Julien Van‐Gils has authored 19 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Developmental Biology, 8 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Julien Van‐Gils's work include Congenital limb and hand anomalies (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Orthopedic Surgery and Rehabilitation (4 papers). Julien Van‐Gils is often cited by papers focused on Congenital limb and hand anomalies (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Orthopedic Surgery and Rehabilitation (4 papers). Julien Van‐Gils collaborates with scholars based in France, Belgium and South Africa. Julien Van‐Gils's co-authors include Didier Lacombe, Patricia Fergelot, Frédérique Magdinier, Cyril Goizet, Aurélien Trimouille, Florence Riant, Elisabeth Tournier‐Lasserve, Pierre‐Simon Jouk, Sébastien Moutton and Patrice Ménégon and has published in prestigious journals such as The Journal of Pediatrics, Journal of Autism and Developmental Disorders and Journal of Medical Genetics.

In The Last Decade

Julien Van‐Gils

16 papers receiving 150 citations

Peers

Julien Van‐Gils

GENET

NEURO

SURGE

Anne Chun‐Hui Tsai United States

Lorella Caffi Italy

Martha Schatz United States

Michèle Mathieu‐Dramard France

Raoul C. M. Hennekam Netherlands

J A Hurst United Kingdom

Lisa Robertson United Kingdom

Ping Yee Billie Au Canada

Asım Cenani Türkiye

Heba Y. El Khashab Saudi Arabia

Anne Chun‐Hui Tsai United States

Julien Van‐Gils

126 ×1.8

117 ×1.7

GENET

32 ×0.9

8 ×0.3

NEURO

37 ×1.9

SURGE

Citations per year, relative to Julien Van‐Gils Julien Van‐Gils (= 1×) peers Anne Chun‐Hui Tsai

Countries citing papers authored by Julien Van‐Gils

Since Specialization

Citations

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

Fields of papers citing papers by Julien Van‐Gils

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julien Van‐Gils. 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 Julien Van‐Gils. The network helps show where Julien Van‐Gils may publish in the future.

Co-authorship network of co-authors of Julien Van‐Gils

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

All Works

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19 of 19 papers shown

Van‐Gils, Julien, Stéphane Claverol, Caroline Tokarski, et al.. (2024). Transcriptome and acetylome profiling identify crucial steps of neuronal differentiation in Rubinstein-Taybi syndrome. Communications Biology. 7(1). 1331–1331. 2 indexed citations

Guyader, Gwenaël Le, et al.. (2024). Care pathways in childhood neurodevelopmental disorders: Toward greater awareness of KBG syndrome among pediatricians. Archives de Pédiatrie. 31(5). 320–325.

Brunelle, Perrine, Geneviève Baujat, Caroline Michot, et al.. (2024). Clinical spectrum of rare bone fragility disorders and response to bisphosphonate treatment: a retrospective study. European Journal of Human Genetics. 32(12). 1559–1566.

Marzin, Pauline, Sophie Rondeau, Jean‐Luc Alessandri, et al.. (2023). Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature. Journal of Medical Genetics. 61(2). 109–116. 7 indexed citations

Van‐Gils, Julien, et al.. (2022). Rubinstein-Taybi Syndrome: Presentation in the First Month of Life. The Journal of Pediatrics. 249. 106–110. 1 indexed citations

Lacombe, Didier, Julien Van‐Gils, Marine Lebrun, et al.. (2022). Hemidystonia with polymicrogyria is part of ATP1A3-related disorders. Brain and Development. 44(8). 567–570.

Magdinier, Frédérique, et al.. (2022). Chromatin Structure and Dynamics: Focus on Neuronal Differentiation and Pathological Implication. Genes. 13(4). 639–639. 11 indexed citations

Elalaoui, Siham Chafai, Julien Van‐Gils, Patricia Fergelot, et al.. (2021). Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome. African Health Sciences. 21(2). 960–967. 1 indexed citations

Van‐Gils, Julien, Kelley Kaye, Romuald Blanc, et al.. (2021). A comparative study of cognitive and socio-emotional development in children with Rubinstein-Taybi syndrome and children with Autism Spectrum Disorder associated with a severe intellectual disability, and in young typically developing children with matched developmental ages. Research in Developmental Disabilities. 116. 104029–104029. 11 indexed citations

10.

Van‐Gils, Julien, Frédérique Magdinier, Patricia Fergelot, & Didier Lacombe. (2021). Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder. Genes. 12(7). 968–968. 38 indexed citations

11.

Crombé, Amandine, Vincent Jecko, P. Bessou, et al.. (2020). Magnetic resonance imaging diagnosis of subependymal giant cell astrocytomas in follow-up of children with tuberous sclerosis complex: should we always use contrast enhancement?. Pediatric Radiology. 50(10). 1397–1408. 5 indexed citations

12.

Van‐Gils, Julien, et al.. (2020). Early-onset epileptic encephalopathy related to germline PIGA mutations: A series of 5 cases. European Journal of Paediatric Neurology. 28. 214–220. 4 indexed citations

13.

Lacombe, Didier, et al.. (2020). Psychomotor, cognitive, and socio-emotional developmental profiles of children with Rubinstein-Taybi Syndrome and a severe intellectual disability. Journal of Intellectual & Developmental Disability. 46(1). 80–89. 10 indexed citations

14.

Michaud, Vincent, Julien Van‐Gils, Claudio Plaisant, et al.. (2020). Triple diagnosis of Wiedemann‐Steiner, Waardenburg and DLG3‐related intellectual disability association found by WES: A case report. The Journal of Gene Medicine. 22(8). e3197–e3197. 7 indexed citations

15.

Van‐Gils, Julien, Sophie Naudion, Jérôme Toutain, et al.. (2019). Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations. Clinical Genetics. 95(3). 420–426. 8 indexed citations

16.

Van‐Gils, Julien, Cécile Zordan, Julie Tinat, et al.. (2019). Coexistence of schwannomatosis and glioblastoma in two families. European Journal of Medical Genetics. 62(8). 103680–103680. 7 indexed citations

17.

Van‐Gils, Julien, Antoine Bigourdan, Pierre‐Simon Jouk, et al.. (2018). Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant. European Journal of Medical Genetics. 62(6). 103530–103530. 30 indexed citations

18.

Cazalets, Jean‐René, Anouck Amestoy, Manuel Bouvard, et al.. (2017). Evaluation of Motor Skills in Children with Rubinstein–Taybi Syndrome. Journal of Autism and Developmental Disorders. 47(11). 3321–3332. 7 indexed citations

19.

Van‐Gils, Julien, Jérôme Harambat, Charlotte Jubert, et al.. (2014). Atypical hematologic and renal manifestations in Neurofibromatosis type I: Coincidence or pathophysiological link?. European Journal of Medical Genetics. 57(11-12). 639–642. 6 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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