Antonio Vitobello

4.6k total citations
36 papers, 595 citations indexed

About

Antonio Vitobello is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Antonio Vitobello has authored 36 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Antonio Vitobello's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Ubiquitin and proteasome pathways (4 papers). Antonio Vitobello is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Ubiquitin and proteasome pathways (4 papers). Antonio Vitobello collaborates with scholars based in France, Switzerland and Italy. Antonio Vitobello's co-authors include Filippo M. Rijli, Nathalie Vilain, Sébastien Ducret, Taro Kitazawa, Hubertus Kohler, Maryline Minoux, Michael Stadler, Laurence Faivre, Christophe Philippe and Elisabetta Ferretti and has published in prestigious journals such as Science, Developmental Cell and Stem Cells.

In The Last Decade

Antonio Vitobello

34 papers receiving 587 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antonio Vitobello France 13 446 212 79 71 48 36 595
Pascal Joset Switzerland 14 412 0.9× 245 1.2× 78 1.0× 35 0.5× 61 1.3× 26 640
Carmelo Ferrai Italy 14 528 1.2× 114 0.5× 63 0.8× 53 0.7× 83 1.7× 18 670
Susan Reijntjes United Kingdom 10 411 0.9× 118 0.6× 114 1.4× 27 0.4× 82 1.7× 12 521
Chen Khuan Wong United States 10 278 0.6× 72 0.3× 43 0.5× 94 1.3× 57 1.2× 11 457
Gladys Alfama France 10 340 0.8× 187 0.9× 61 0.8× 63 0.9× 28 0.6× 12 572
Lauren Gehman United States 7 716 1.6× 107 0.5× 129 1.6× 100 1.4× 41 0.9× 11 938
Lohith Madireddy United States 12 272 0.6× 69 0.3× 133 1.7× 48 0.7× 59 1.2× 15 594
Erik Engelen Netherlands 8 471 1.1× 141 0.7× 48 0.6× 38 0.5× 35 0.7× 8 627
Keith J. Jenné United States 5 374 0.8× 99 0.5× 105 1.3× 48 0.7× 41 0.9× 9 532
Christopher M. LaCoursiere United States 6 315 0.7× 324 1.5× 93 1.2× 42 0.6× 61 1.3× 7 584

Countries citing papers authored by Antonio Vitobello

Since Specialization
Citations

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

Fields of papers citing papers by Antonio Vitobello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Vitobello

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Vitobello. A scholar is included among the top collaborators of Antonio Vitobello 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 Antonio Vitobello. Antonio Vitobello 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.
Vitobello, Antonio, Bekim Sadiković, Juliette Albuisson, et al.. (2025). Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype. American Journal of Medical Genetics Part A. 197(7). e64043–e64043. 1 indexed citations
2.
Strong, Alanna, Caoimhe McKenna, Karen Stals, et al.. (2025). Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay. American Journal of Medical Genetics Part A. 197(10). e64119–e64119. 1 indexed citations
3.
Haghshenas, Sadegheh, Michael A. Levy, Raissa Relator, et al.. (2025). Identification of an episignature for the MEF2C-associated syndrome. European Journal of Human Genetics. 34(1). 53–60.
4.
5.
Oleari, Roberto, Antonella Lettieri, Stefano Manzini, et al.. (2023). Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency. Disease Models & Mechanisms. 16(3). 8 indexed citations
6.
Taylor, James R., Antonio Vitobello, Christophe Philippe, et al.. (2022). Expanding the phenotype of HNRNPU‐related neurodevelopmental disorder with emphasis on seizure phenotype and review of literature. American Journal of Medical Genetics Part A. 188(5). 1497–1514. 12 indexed citations
7.
Chevarin, Martin, Antonio Vitobello, Cyril Fournier, et al.. (2022). A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European Journal of Human Genetics. 31(7). 761–768. 6 indexed citations
8.
Thomas, Quentin, Céline Verstuyft, Émilie Tisserant, et al.. (2022). Exome sequencing allows detection of relevant pharmacogenetic variants in epileptic patients. The Pharmacogenomics Journal. 22(5-6). 258–263. 1 indexed citations
9.
Mallet, Delphine, Florence Roucher‐Boulez, Marie Bournez, et al.. (2022). Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants. American Journal of Medical Genetics Part A. 188(12). 3540–3545. 2 indexed citations
10.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
11.
Mau‐Them, Frédéric Tran, Yannis Duffourd, Antonio Vitobello, et al.. (2021). Interest of exome sequencing trio‐like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases. Molecular Genetics & Genomic Medicine. 9(12). e1836–e1836. 4 indexed citations
12.
Ebstein, Frédéric, Geoffroy Delplancq, Stéphane Auvin, et al.. (2020). Report of the first patient with a homozygous OTUD7A variant responsible for epileptic encephalopathy and related proteasome dysfunction. Clinical Genetics. 97(4). 567–575. 18 indexed citations
13.
Assoum, Mirna, Ange‐Line Bruel, Melissa Crenshaw, et al.. (2020). NovelKIAA1033/WASHC4mutations in three patients with syndromic intellectual disability and a review of the literature. American Journal of Medical Genetics Part A. 182(4). 792–797. 10 indexed citations
14.
Delplancq, Geoffroy, Antonio Vitobello, Sophie Nambot, et al.. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 129–135. 15 indexed citations
15.
Bruel, Ange‐Line, Antonio Vitobello, Frédéric Tran Mau‐Them, et al.. (2020). Next‐generation sequencing approaches and challenges in the diagnosis of developmental anomalies and intellectual disability. Clinical Genetics. 98(5). 433–444. 11 indexed citations
16.
Vitobello, Antonio, Juliane Perner, Jiang Zhu, et al.. (2019). Drug-induced chromatin accessibility changes associate with sensitivity to liver tumor promotion. Life Science Alliance. 2(5). e201900461–e201900461. 9 indexed citations
17.
Bris, Céline, Vincent Procaccio, Patrizia Amati‐Bonneau, et al.. (2019). Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light. Human Mutation. 40(12). 2430–2443. 7 indexed citations
18.
Bruel, Ange‐Line, Sophie Nambot, Antonio Vitobello, et al.. (2019). Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing. European Journal of Human Genetics. 27(10). 1519–1531. 39 indexed citations
19.
Moutton, Sébastien, Ange‐Line Bruel, Mirna Assoum, et al.. (2018). Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Clinical Genetics. 93(6). 1172–1178. 17 indexed citations
20.
Minoux, Maryline, Antonio Vitobello, Taro Kitazawa, et al.. (2017). Gene bivalency at Polycomb domains regulates cranial neural crest positional identity. Science. 355(6332). 95 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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