Irène Netchine

8.2k total citations
101 papers, 3.9k citations indexed

About

Irène Netchine is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Irène Netchine has authored 101 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Genetics, 80 papers in Molecular Biology and 45 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Irène Netchine's work include Genetic Syndromes and Imprinting (77 papers), Epigenetics and DNA Methylation (55 papers) and Prenatal Screening and Diagnostics (39 papers). Irène Netchine is often cited by papers focused on Genetic Syndromes and Imprinting (77 papers), Epigenetics and DNA Methylation (55 papers) and Prenatal Screening and Diagnostics (39 papers). Irène Netchine collaborates with scholars based in France, United Kingdom and United States. Irène Netchine's co-authors include Yves Le Bouc, Salah Azzi, Sylvie Rossignol, Nathalie Thibaud, Frédéric Brioude, Marie‐Laure Sobrier, Christine Gicquel, Serge Amselem, Virginie Steunou and Sylvie Cabrol and has published in prestigious journals such as Nature Genetics, PLoS ONE and Endocrine Reviews.

In The Last Decade

Irène Netchine

97 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Irène Netchine France 34 2.6k 2.4k 1.5k 993 327 101 3.9k
Alexander A.L. Jorge Brazil 36 1.7k 0.7× 2.0k 0.9× 330 0.2× 1.5k 1.5× 467 1.4× 185 3.8k
Koji Muroya Japan 28 1.9k 0.7× 1.9k 0.8× 301 0.2× 719 0.7× 377 1.2× 119 3.1k
Trevor Cole United Kingdom 31 1.7k 0.7× 1.7k 0.7× 489 0.3× 258 0.3× 386 1.2× 62 3.2k
Barto J. Otten Netherlands 37 2.0k 0.8× 2.7k 1.1× 563 0.4× 1.5k 1.5× 488 1.5× 74 3.8k
Peter Wieacker Germany 35 1.6k 0.6× 2.4k 1.0× 397 0.3× 255 0.3× 191 0.6× 141 3.8k
Dvorah Abeliovich Israel 31 1.4k 0.5× 1.5k 0.6× 450 0.3× 148 0.1× 340 1.0× 98 3.0k
Dieter Kotzot Austria 29 1.9k 0.7× 1.3k 0.6× 1.1k 0.8× 123 0.1× 188 0.6× 100 2.9k
Masayo Kagami Japan 28 1.8k 0.7× 1.6k 0.7× 1.1k 0.8× 89 0.1× 128 0.4× 106 2.5k
Christine Gicquel France 38 1.9k 0.7× 2.3k 1.0× 1.5k 1.0× 1.4k 1.4× 2.2k 6.8× 78 5.3k
Sarina G. Kant Netherlands 26 1.3k 0.5× 1.4k 0.6× 325 0.2× 451 0.5× 193 0.6× 70 2.7k

Countries citing papers authored by Irène Netchine

Since Specialization
Citations

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

Fields of papers citing papers by Irène Netchine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irène Netchine

This figure shows the co-authorship network connecting the top 25 collaborators of Irène Netchine. A scholar is included among the top collaborators of Irène Netchine 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 Irène Netchine. Irène Netchine 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.
Busiah, Kanetee, Célina Roda, Anaïs Brassier, et al.. (2024). Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study. Molecular Genetics and Metabolism. 141(3). 108123–108123. 1 indexed citations
2.
Lacroix, Agnès, R. Coutant, Bruno Donadille, et al.. (2023). Executive functioning in adolescents and adults with Silver-Russell syndrome. PLoS ONE. 18(1). e0279745–e0279745. 1 indexed citations
3.
Mitanchez, Delphine, Anne Forhan, Laurence Périn, et al.. (2022). Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth. Frontiers in Endocrinology. 13. 836731–836731. 4 indexed citations
4.
Giabicani, Éloïse, Vincent Fontaine, Frédéric Brioude, et al.. (2022). Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells. Clinical Epigenetics. 14(1). 190–190. 4 indexed citations
5.
Brioude, Frédéric, et al.. (2022). IGF2: Development, Genetic and Epigenetic Abnormalities. Cells. 11(12). 1886–1886. 57 indexed citations
6.
Sobrier, Marie‐Laure, et al.. (2021). Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants. European Journal of Human Genetics. 29(12). 1756–1761. 3 indexed citations
7.
Mackay, Deborah, Jet Bliek, Maria Lombardi, et al.. (2019). Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes. Genetics Research. 101. e3–e3. 16 indexed citations
8.
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
9.
Giabicani, Éloïse, Michèle Boulé, Guillaume Aubertin, et al.. (2019). Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome. Sleep Medicine. 64. 23–29. 5 indexed citations
10.
Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Jean‐Luc Alessandri, et al.. (2018). Mutation update for theGPC3gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Human Mutation. 39(6). 790–805. 22 indexed citations
11.
Stoupa, Athanasia, Isabelle Flechtner, Graziella Pinto, et al.. (2018). Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation due to Severe Primary IGF1 Deficiency (GROWPATI Study). HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
12.
Heide, Solveig, Sandra Chantot‐Bastaraud, Boris Keren, et al.. (2017). Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences. Journal of Medical Genetics. 55(3). 205–213. 34 indexed citations
13.
Giabicani, Éloïse, Frédéric Brioude, Yves Le Bouc, & Irène Netchine. (2017). Imprinted disorders and growth. Annales d Endocrinologie. 78(2). 112–113. 5 indexed citations
14.
Canton, Ana Pinheiro Machado, Frédéric Brioude, & Irène Netchine. (2016). Silver-Russell Syndrome with 11p15 Epimutation: Clinical Analysis of Adrenarche, Central Puberty and Body Mass Index in a Cohort of French Children. 86. 1 indexed citations
15.
Mackay, Deborah, Thomas Eggermann, Karin Buiting, et al.. (2015). Multilocus methylation defects in imprinting disorders. BioMolecular Concepts. 6(1). 47–57. 28 indexed citations
16.
Giabicani, Éloïse, et al.. (2015). Sleep Apneas in Silver Russell Syndrome: A Constant Finding. 84. 2 indexed citations
17.
Dufourg, Marie‐Noëlle, Laurence Périn, Muriel Houang, et al.. (2015). Silver Russell syndrome: A Cause of Partial IGF1 Resistance?. 84. 1 indexed citations
18.
Rossignol, Sylvie, et al.. (2014). Prevalence and management of gastrointestinal manifestations in Silver–Russell syndrome. Archives of Disease in Childhood. 100(4). 353–358. 21 indexed citations
19.
Vallette-Kasic, Sophie, Irène Netchine, Rachel Reynaud, et al.. (2002). Causes génétiques de déficit en hormone de croissance. 4(1). 15–22. 1 indexed citations
20.
Saal, Howard M., Madeleine D. Harbison, & Irène Netchine. (1978). [Silver Russell's syndrome].. PubMed. 148(5). 527–30. 3 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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