Frédéric Brioude
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Papers in
- Genetics 49
- Genetic Syndromes and Imprinting 45
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- Prenatal Screening and Diagnostics 20
- Birth, Development, and Health 3
- Co-authors
- Irène Netchine (34 shared papers)Yves Le Bouc (20 shared papers)Éloïse Giabicani (11 shared papers)Sylvie Rossignol (10 shared papers)Salah Azzi (11 shared papers)Madeleine D. Harbison (6 shared papers)Walid Abi Habib (5 shared papers)Bruno Francou (3 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)Human Mutation (6 papers)Clinical Epigenetics (4 papers)The Journal of Clinical Endocrinology & Metabolism (3 papers)European Journal of Endocrinology (3 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Frédéric Brioude
63 papers receiving 2.5k citations
Frédéric Brioude's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 1.7k
- Pediatrics, Perinatology and Child Health 771
- Reproductive Medicine 205
- Molecular Biology 1.2k
- Endocrinology, Diabetes and Metabolism 257
Countries citing papers authored by Frédéric Brioude
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
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-authors
The 25 scholars most cited alongside Frédéric Brioude, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement Hit paper breakdown → | 2018 | 397 |
| 2 | Diagnosis and management of Silver–Russell syndrome: first international consensus statement Hit paper breakdown → | 2016 | 369 |
| 3 | 2013 | 122 | |
| 4 | 2012 | 112 | |
| 5 | 2017 | 110 | |
| 6 | 2013 | 108 | |
| 7 | 2010 | 87 | |
| 8 | 2014 | 80 | |
| 9 | 2022 | 73 | |
| 10 | 2019 | 69 | |
| 11 | 2015 | 65 | |
| 12 | 2015 | 59 | |
| 13 | 2016 | 58 | |
| 14 | 2014 | 57 | |
| 15 | 2018 | 50 | |
| 16 | 2013 | 46 | |
| 17 | 2015 | 43 | |
| 18 | 2017 | 41 | |
| 19 | 2013 | 38 | |
| 20 | 2017 | 37 |
About Frédéric Brioude
Frédéric Brioude is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Endocrinology, Diabetes and Metabolism and Reproductive Medicine, having authored 66 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (45 papers), Epigenetics and DNA Methylation (23 papers), Prenatal Screening and Diagnostics (20 papers), Growth Hormone and Insulin-like Growth Factors (4 papers), Birth, Development, and Health (3 papers), Hypothalamic control of reproductive hormones (3 papers), Renal and related cancers (3 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (771 citations), Reproductive Medicine (205 citations), Molecular Biology (1.2k citations) and Endocrinology, Diabetes and Metabolism (257 citations). Frédéric Brioude has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Irène Netchine, Yves Le Bouc, Éloïse Giabicani, Sylvie Rossignol, Salah Azzi, Madeleine D. Harbison, Walid Abi Habib, Bruno Francou, Jérôme Bouligand and Jacques Young. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, Clinical Epigenetics, The Journal of Clinical Endocrinology & Metabolism and European Journal of Endocrinology.
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.