Frédéric Brioude

3.5k total citations
49 papers, 1.2k citations indexed

About

Frédéric Brioude is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Frédéric Brioude has authored 49 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 34 papers in Molecular Biology and 24 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Frédéric Brioude's work include Genetic Syndromes and Imprinting (35 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (19 papers). Frédéric Brioude is often cited by papers focused on Genetic Syndromes and Imprinting (35 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (19 papers). Frédéric Brioude collaborates with scholars based in France, United States and United Kingdom. Frédéric Brioude's co-authors include Irène Netchine, Yves Le Bouc, Éloïse Giabicani, Sylvie Rossignol, Salah Azzi, Madeleine D. Harbison, Walid Abi Habib, Jacques Young, Jérôme Bouligand and Bruno Francou and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Science Advances.

In The Last Decade

Frédéric Brioude

47 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frédéric Brioude France 21 796 772 462 181 138 49 1.2k
Salah Azzi France 19 1.0k 1.3× 930 1.2× 681 1.5× 27 0.1× 155 1.1× 28 1.3k
Nico Ruf Germany 13 849 1.1× 1.2k 1.5× 352 0.8× 42 0.2× 82 0.6× 16 1.6k
Sandra Chantot‐Bastaraud France 24 939 1.2× 759 1.0× 404 0.9× 304 1.7× 21 0.2× 67 1.4k
Michael H. Guo United States 20 509 0.6× 603 0.8× 86 0.2× 76 0.4× 174 1.3× 33 1.2k
Albert de la Chapelle Finland 13 477 0.6× 544 0.7× 86 0.2× 407 2.2× 133 1.0× 15 1.3k
Susana Fernandes Portugal 17 827 1.0× 800 1.0× 239 0.5× 550 3.0× 27 0.2× 58 1.3k
J.H.A.M. Tuerlings Netherlands 18 453 0.6× 440 0.6× 145 0.3× 210 1.2× 45 0.3× 49 880
Véronique Gaston France 14 616 0.8× 681 0.9× 450 1.0× 114 0.6× 252 1.8× 22 1.4k
Juan J. Heinrich Argentina 17 541 0.7× 469 0.6× 122 0.3× 111 0.6× 805 5.8× 35 1.5k
J. Barra France 7 281 0.4× 635 0.8× 55 0.1× 106 0.6× 253 1.8× 10 1.1k

Countries citing papers authored by Frédéric Brioude

Since Specialization
Citations

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

Fields of papers citing papers by Frédéric Brioude

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédéric Brioude

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Brioude. A scholar is included among the top collaborators of Frédéric Brioude 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 Frédéric Brioude. Frédéric Brioude 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.
Nguyen‐Khoa, Thao, Caroline Moreau, Jean Fiet, et al.. (2025). Advances in congenital adrenal hyperplasia newborn screening: 11-ketotestosterone and 21-deoxycortisone as additional discriminatory biomarkers. European Journal of Endocrinology. 193(6). 677–686.
2.
Jonard, Laurence, Natalie Loundon, Laurence Heidet, et al.. (2024). HDR syndrome: Large cohort and systematic review. Clinical Genetics. 106(5). 564–573. 2 indexed citations
3.
Brioude, Frédéric, et al.. (2022). IGF2: Development, Genetic and Epigenetic Abnormalities. Cells. 11(12). 1886–1886. 57 indexed citations
4.
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
5.
Brioude, Frédéric, et al.. (2019). Overgrowth syndromes — clinical and molecular aspects and tumour risk. Nature Reviews Endocrinology. 15(5). 299–311. 56 indexed citations
6.
Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Alessandra Baumer, et al.. (2019). CUGC for Simpson-Golabi-Behmel syndrome (SGBS). European Journal of Human Genetics. 27(4). 663–668. 10 indexed citations
7.
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
8.
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
9.
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
10.
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
11.
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
12.
Giabicani, Éloïse, Frédéric Brioude, Yves Le Bouc, & Irène Netchine. (2017). Imprinted disorders and growth. Annales d Endocrinologie. 78(2). 112–113. 5 indexed citations
13.
Habib, Walid Abi, Frédéric Brioude, Thomas Édouard, et al.. (2017). Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction. Genetics in Medicine. 20(2). 250–258. 98 indexed citations
14.
Chantot‐Bastaraud, Sandra, Frédéric Brioude, Matthias Begemann, et al.. (2017). Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 10(1). 28–28. 20 indexed citations
15.
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
16.
Dufourg, Marie‐Noëlle, Laurence Périn, Muriel Houang, et al.. (2015). Silver Russell syndrome: A Cause of Partial IGF1 Resistance?. 84. 1 indexed citations
17.
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
18.
Brioude, Frédéric, Jérôme Bouligand, Bruno Francou, et al.. (2013). Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Novel Mutation. PLoS ONE. 8(1). e53896–e53896. 37 indexed citations
19.
Bouc, Yves Le & Frédéric Brioude. (2012). Existe-t-il une relation entre la dose d'hormone de croissance et d'éventuelles complications tumorales ou cardiovasculaires ?. Bulletin de l Académie Nationale de Médecine. 196(1). 127–137. 2 indexed citations
20.
Brioude, Frédéric, Jérôme Bouligand, Séverine Trabado, et al.. (2010). Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype–phenotype relationships. European Journal of Endocrinology. 162(5). 835–851. 73 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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