Catherine Dodé
Impact in
- Reproductive Medicine top 0.2%
- Hypothalamic control of reproductive hormones
- Ovarian function and disorders
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hemoglobinopathies and Related Disorders
Papers in
-
- Inflammasome and immune disorders 26
- Receptor Mechanisms and Signaling 4
-
- Hypothalamic control of reproductive hormones 24
- Co-authors
- Jean‐Pierre Hardelin (19 shared papers)Marc Delpech (22 shared papers)Jacques Young (11 shared papers)Jean-Pierre Hardelin (3 shared papers)Gilles Grateau (21 shared papers)Christophe Pécheux (11 shared papers)Philippe Rondard (3 shared papers)Rajagopal Krishnamoorthy (2 shared papers)
- Journals
- The Journal of Clinical Endocrinology & Metabolism (6 papers)European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (3 papers)Human Mutation (3 papers)British Journal of Haematology (2 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Catherine Dodé
88 papers receiving 4.8k citations
Catherine Dodé's Hit Papers
Peers
Comparison fields: 5 of 105
- Reproductive Medicine 1.6k
- Genetics 531
- Hematology 470
- Genetics 1.1k
- Molecular Biology 2.7k
Countries citing papers authored by Catherine Dodé
This map shows the geographic impact of Catherine Dodé'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 Catherine Dodé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine Dodé more than expected).
Fields of papers citing papers by Catherine Dodé
This network shows the impact of papers produced by Catherine Dodé. 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 Catherine Dodé. The network helps show where Catherine Dodé may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine Dodé, 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 93 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment Hit paper breakdown → | 2015 | 584 |
| 2 | 2006 | 361 | |
| 3 | 2004 | 253 | |
| 4 | 2007 | 234 | |
| 5 | 2002 | 234 | |
| 6 | 1999 | 213 | |
| 7 | 2002 | 164 | |
| 8 | 2008 | 160 | |
| 9 | 2013 | 156 | |
| 10 | 1990 | 144 | |
| 11 | 2008 | 132 | |
| 12 | 1993 | 127 | |
| 13 | 2006 | 127 | |
| 14 | 2004 | 124 | |
| 15 | 2011 | 108 | |
| 16 | 2008 | 103 | |
| 17 | 2007 | 103 | |
| 18 | 2007 | 96 | |
| 19 | 2016 | 94 | |
| 20 | Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever. | 2000 | 91 |
About Catherine Dodé
Catherine Dodé is a scholar working on Molecular Biology, Reproductive Medicine, Genetics, Genetics and Cellular and Molecular Neuroscience, having authored 93 papers that have together received 5.1k indexed citations. Recurring topics across this work include Inflammasome and immune disorders (26 papers), Hypothalamic control of reproductive hormones (24 papers), Hemoglobinopathies and Related Disorders (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital Ear and Nasal Anomalies (7 papers), Genetic Neurodegenerative Diseases (6 papers), Receptor Mechanisms and Signaling (4 papers) and IL-33, ST2, and ILC Pathways (4 papers). The work is most often cited by research in Reproductive Medicine (1.6k citations), Genetics (531 citations), Hematology (470 citations), Genetics (1.1k citations) and Molecular Biology (2.7k citations). Catherine Dodé has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Jean‐Pierre Hardelin, Marc Delpech, Jacques Young, Jean-Pierre Hardelin, Gilles Grateau, Christophe Pécheux, Philippe Rondard, Rajagopal Krishnamoorthy, Corinne Fouveaut and Laurence Cuisset. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, European Journal of Human Genetics, The American Journal of Human Genetics, Human Mutation and British Journal of Haematology.
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.