Frédéric Brioude
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 40
- Genetic Syndromes and Imprinting 35
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
-
- Epigenetics and DNA Methylation 23
- Renal and related cancers 4
- Co-authors
- Irène Netchine (32 shared papers)Yves Le Bouc (19 shared papers)Éloïse Giabicani (11 shared papers)Sylvie Rossignol (8 shared papers)Salah Azzi (11 shared papers)Madeleine D. Harbison (6 shared papers)Walid Abi Habib (5 shared papers)Jérôme Bouligand (3 shared papers)
- Journals
- European Journal of Endocrinology (3 papers)Human Mutation (3 papers)Clinical Epigenetics (2 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Frédéric Brioude
47 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 69
- Genetics 796
- Pediatrics, Perinatology and Child Health 462
- Reproductive Medicine 181
- Molecular Biology 772
- Endocrinology, Diabetes and Metabolism 138
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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 99 | |
| 2 | 2012 | 99 | |
| 3 | 2017 | 98 | |
| 4 | 2013 | 89 | |
| 5 | 2010 | 73 | |
| 6 | 2014 | 70 | |
| 7 | 2022 | 57 | |
| 8 | 2019 | 56 | |
| 9 | 2015 | 56 | |
| 10 | 2014 | 51 | |
| 11 | 2013 | 38 | |
| 12 | 2013 | 37 | |
| 13 | 2017 | 34 | |
| 14 | 2019 | 33 | |
| 15 | 2017 | 32 | |
| 16 | 2014 | 31 | |
| 17 | 2017 | 27 | |
| 18 | 2018 | 24 | |
| 19 | 2016 | 23 | |
| 20 | 2018 | 22 |
About Frédéric Brioude
Frédéric Brioude is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Endocrinology, Diabetes and Metabolism and Reproductive Medicine, having authored 49 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (35 papers), Epigenetics and DNA Methylation (23 papers), Prenatal Screening and Diagnostics (19 papers), Renal and related cancers (4 papers), Hypothalamic control of reproductive hormones (4 papers), Tumors and Oncological Cases (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Birth, Development, and Health (3 papers). The work is most often cited by research in Genetics (796 citations), Pediatrics, Perinatology and Child Health (462 citations), Reproductive Medicine (181 citations), Molecular Biology (772 citations) and Endocrinology, Diabetes and Metabolism (138 citations). Frédéric Brioude has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Irène Netchine, Yves Le Bouc, Éloïse Giabicani, Sylvie Rossignol, Salah Azzi, Madeleine D. Harbison, Walid Abi Habib, Jérôme Bouligand, Bruno Francou and Jacques Young. Their work appears in journals such as European Journal of Endocrinology, Human Mutation, Clinical Epigenetics, European Journal of Human Genetics and Journal of Medical Genetics.
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.