Fernande Barichard
Impact in
-
- Prenatal Screening and Diagnostics
-
- Genetic Syndromes and Imprinting
Papers in
-
- Renal and related cancers 5
- Epigenetics and DNA Methylation 4
- Hedgehog Signaling Pathway Studies 3
- RNA modifications and cancer 1
-
- Prenatal Screening and Diagnostics 3
- Co-authors
- Claudine Junien (11 shared papers)Isabelle Marie Henry (10 shared papers)Marc Jeanpierre (6 shared papers)Philippe Couillin (4 shared papers)Thomas M Glaser (1 shared paper)Sophie Grandjouan (2 shared papers)Thierry O. Philip (1 shared paper)J. L. Chaussain (1 shared paper)
- Journals
- Human Genetics (5 papers)Genomics (1 paper)Genes Chromosomes and Cancer (1 paper)Proceedings of the National Academy of Sciences (1 paper)PubMed (1 paper)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Fernande Barichard
10 papers receiving 311 citations
Peers
Comparison fields: 5 of 39
- Pediatrics, Perinatology and Child Health 76
- Genetics 117
- Immunology and Allergy 20
- Cancer Research 47
- Molecular Biology 234
Countries citing papers authored by Fernande Barichard
This map shows the geographic impact of Fernande 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 Fernande Barichard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernande Barichard more than expected).
Fields of papers citing papers by Fernande Barichard
This network shows the impact of papers produced by Fernande 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 Fernande Barichard. The network helps show where Fernande Barichard may publish in the future.
Co-authors
The 25 scholars most cited alongside Fernande 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 | 132 | |
| 2 | 1989 | 80 | |
| 3 | 1988 | 25 | |
| 4 | 1989 | 21 | |
| 5 | 1985 | 13 | |
| 6 | Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome. | 1988 | 13 |
| 7 | 1987 | 12 | |
| 8 | 1994 | 12 | |
| 9 | 1993 | 11 | |
| 10 | 2008 | 8 | |
| 11 | 2008 | 0 |
About Fernande Barichard
Fernande Barichard is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics, Urology and Immunology and Allergy, having authored 11 papers that have together received 327 indexed citations. Recurring topics across this work include Renal and related cancers (5 papers), Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (3 papers), Prenatal Screening and Diagnostics (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Cancer-related Molecular Pathways (2 papers), Cell Adhesion Molecules Research (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (76 citations), Genetics (117 citations), Immunology and Allergy (20 citations), Cancer Research (47 citations) and Molecular Biology (234 citations). Fernande Barichard has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Claudine Junien, Isabelle Marie Henry, Marc Jeanpierre, Philippe Couillin, Thomas M Glaser, Sophie Grandjouan, Thierry O. Philip, J. L. Chaussain, Gilbert Lenoir and CATHERINE TURLEAU. Their work appears in journals such as Human Genetics, Genomics, Genes Chromosomes and Cancer, Proceedings of the National Academy of Sciences and PubMed.
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.