Virginie Steunou

1.9k total citations
16 papers, 1.1k citations indexed

About

Virginie Steunou is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Virginie Steunou has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Virginie Steunou's work include Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (10 papers) and Prenatal Screening and Diagnostics (7 papers). Virginie Steunou is often cited by papers focused on Genetic Syndromes and Imprinting (11 papers), Epigenetics and DNA Methylation (10 papers) and Prenatal Screening and Diagnostics (7 papers). Virginie Steunou collaborates with scholars based in France, Australia and Belgium. Virginie Steunou's co-authors include Yves Le Bouc, Christine Gicquel, Irène Netchine, Sylvie Rossignol, Nathalie Thibaud, Fabienne Danton, Sylvie Cabrol, Salah Azzi, Martine Le Merrer and Muriel Houang and has published in prestigious journals such as Nature Genetics, PLoS ONE and Oncogene.

In The Last Decade

Virginie Steunou

15 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Virginie Steunou France 12 850 815 636 71 59 16 1.1k
Johanne M D Hahnemann Denmark 15 861 1.0× 766 0.9× 604 0.9× 62 0.9× 121 2.1× 19 1.3k
Agostina De Crescenzo Italy 17 681 0.8× 728 0.9× 470 0.7× 13 0.2× 65 1.1× 19 885
Rosanna Weksberg Canada 5 466 0.5× 533 0.7× 410 0.6× 41 0.6× 55 0.9× 5 742
Beike Leegte Netherlands 11 428 0.5× 189 0.2× 118 0.2× 10 0.1× 91 1.5× 15 531
Maria Vernucci Italy 8 353 0.4× 590 0.7× 205 0.3× 24 0.3× 244 4.1× 9 678
G. Bourrouillou France 14 398 0.5× 279 0.3× 146 0.2× 28 0.4× 7 0.1× 40 587
Elena Barbacci Italy 7 262 0.3× 388 0.5× 42 0.1× 93 1.3× 21 0.4× 7 654
Philip N. Mowrey United States 11 232 0.3× 162 0.2× 134 0.2× 17 0.2× 33 0.6× 22 436
Qun Fang China 15 152 0.2× 176 0.2× 359 0.6× 8 0.1× 55 0.9× 65 582
B. A. J. Ponder United Kingdom 10 594 0.7× 275 0.3× 28 0.0× 70 1.0× 171 2.9× 15 822

Countries citing papers authored by Virginie Steunou

Since Specialization
Citations

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

Fields of papers citing papers by Virginie Steunou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Virginie Steunou

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

All Works

16 of 16 papers shown
1.
Steunou, Virginie, Marie‐Laure Sobrier, Luciana Ribeiro Montenegro, et al.. (2020). SUN-090 Investigation of Imprinting Defects in MKRN3 and DLK1 in Children with Idiopathic Central Precocious Puberty Through Specific DNA Methylation Analysis. Journal of the Endocrine Society. 4(Supplement_1).
2.
Canton, Ana Pinheiro Machado, Ana Cristina Victorino Krepischi, Luciana Ribeiro Montenegro, et al.. (2020). Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction. 36(2). 506–518. 21 indexed citations
3.
Habib, Walid Abi, Frédéric Brioude, Salah Azzi, et al.. (2019). Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders. Science Advances. 5(2). eaau9425–eaau9425. 33 indexed citations
4.
Habib, Walid Abi, Salah Azzi, Frédéric Brioude, et al.. (2014). Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome. Human Molecular Genetics. 23(21). 5763–5773. 51 indexed citations
5.
Azzi, Salah, Virginie Steunou, Jörg Tost, et al.. (2014). Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome. Journal of Medical Genetics. 52(1). 53–60. 11 indexed citations
6.
Guillaud-Bataille, Marine, Bruno Ragazzon, Aurélien de Reyniès, et al.. (2014). IGF2 Promotes Growth of Adrenocortical Carcinoma Cells, but Its Overexpression Does Not Modify Phenotypic and Molecular Features of Adrenocortical Carcinoma. PLoS ONE. 9(8). e103744–e103744. 43 indexed citations
7.
Azzi, Salah, Annick Blaise, Virginie Steunou, et al.. (2014). Complex Tissue-Specific Epigenotypes in Russell-Silver Syndrome Associated with 11p15 ICR1 Hypomethylation. Human Mutation. 35(10). 1211–1220. 31 indexed citations
8.
9.
Bouc, Yves Le, Sylvie Rossignol, Salah Azzi, et al.. (2010). Epigenetics, genomic imprinting and assisted reproductive technology. Annales d Endocrinologie. 71(3). 237–238. 33 indexed citations
10.
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Steunou, Virginie, Céline Chalas, Antoine Kerjean, et al.. (2006). The epigenetic imprinting defect of patients with Beckwith—Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. Journal of Medical Genetics. 43(12). 902–907. 170 indexed citations
13.
Gicquel, Christine, Sylvie Rossignol, Sylvie Cabrol, et al.. (2005). Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nature Genetics. 37(9). 1003–1007. 379 indexed citations
14.
Steunou, Virginie, et al.. (2003). Altered transcription of the stem cell leukemia gene in myelofibrosis with myeloid metaplasia. Leukemia. 17(10). 1998–2006. 6 indexed citations
15.
Steunou, Virginie, et al.. (2000). Lack of interferon‐α‐induced tyrosine phosphorylation of Vav proto‐oncogene in patients with myelofibrosis with myeloid metaplasia. British Journal of Haematology. 110(2). 362–369. 3 indexed citations
16.

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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