F. Barichard
Impact in
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
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- Renal and related cancers 5
- Epigenetics and DNA Methylation 4
- Hedgehog Signaling Pathway Studies 3
- DNA Repair Mechanisms 1
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- Prenatal Screening and Diagnostics 4
- Co-authors
- Isabelle Henry (10 shared papers)Claudine Junien (11 shared papers)Marc Jeanpierre (6 shared papers)P. Couillin (4 shared papers)Thomas Gläser (1 shared paper)S Grandjouan (2 shared papers)Thierry Philip (1 shared paper)J. L. Chaussain (1 shared paper)
- Journals
- Human Genetics (5 papers)Proceedings of the National Academy of Sciences (1 paper)Genomics (1 paper)Genes Chromosomes and Cancer (1 paper)Cytogenetics and Cell Genetics (2 papers)
- Partner nations
- FranceTunisiaUnited States
In The Last Decade
F. Barichard
11 papers receiving 284 citations
Peers
Comparison fields: 5 of 39
- Genetics 101
- Pediatrics, Perinatology and Child Health 63
- Molecular Biology 208
- Cancer Research 41
- Immunology and Allergy 14
Countries citing papers authored by F. Barichard
This map shows the geographic impact of F. Barichard'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 F. Barichard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Barichard more than expected).
Fields of papers citing papers by F. Barichard
This network shows the impact of papers produced by F. Barichard. 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 F. Barichard. The network helps show where F. Barichard may publish in the future.
Co-authors
The 25 scholars most cited alongside F. Barichard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1989 | 119 | |
| 2 | 1989 | 69 | |
| 3 | 1989 | 18 | |
| 4 | 1988 | 17 | |
| 5 | 1987 | 14 | |
| 6 | 1985 | 12 | |
| 7 | 1994 | 11 | |
| 8 | 1993 | 10 | |
| 9 | Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome. | 1988 | 9 |
| 10 | 2008 | 7 | |
| 11 | [Antenatal diagnosis of structural chromosome anomalies. 226 cases (author's transl)]. | 1981 | 1 |
| 12 | 2008 | 0 |
About F. Barichard
F. Barichard is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Oncology and Surgery, having authored 12 papers that have together received 287 indexed citations. Recurring topics across this work include Renal and related cancers (5 papers), Epigenetics and DNA Methylation (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetic Syndromes and Imprinting (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Cancer-related Molecular Pathways (2 papers), DNA Repair Mechanisms (1 paper) and Osteoarthritis Treatment and Mechanisms (1 paper). The work is most often cited by research in Genetics (101 citations), Pediatrics, Perinatology and Child Health (63 citations), Molecular Biology (208 citations), Cancer Research (41 citations) and Immunology and Allergy (14 citations). F. Barichard has collaborated with scholars based in France, Tunisia and United States. Frequent co-authors include Isabelle Henry, Claudine Junien, Marc Jeanpierre, P. Couillin, Thomas Gläser, S Grandjouan, Thierry Philip, J. L. Chaussain, Gilbert Lenoir and C Turleau. Their work appears in journals such as Human Genetics, Proceedings of the National Academy of Sciences, Genomics, Genes Chromosomes and Cancer and Cytogenetics and Cell 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.