Martine Doco‐Fenzy
- Co-authors
- Stéphanie StruskiPascale Cornillet‐LefèbvreDominique GaillardEmilie LandaisAude LallemandCéline PoirsierMarta SpodenkiewiczAnne-Sophie Lèbre
- Topics
- Genomic variations and chromosomal abnormalities (14 papers)Genetics and Neurodevelopmental Disorders (5 papers)Genomics and Rare Diseases (4 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Martine Doco‐Fenzy
28 papers receiving 661 citations
Peers
Comparison fields: 5 of 76
- Molecular Biology 349
- Genetics 302
- Pediatrics, Perinatology and Child Health 80
- Oncology 72
- Plant Science 70
Countries citing papers authored by Martine Doco‐Fenzy
This map shows the geographic impact of Martine Doco‐Fenzy'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 Martine Doco‐Fenzy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martine Doco‐Fenzy more than expected).
Fields of papers citing papers by Martine Doco‐Fenzy
This network shows the impact of papers produced by Martine Doco‐Fenzy. 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 Martine Doco‐Fenzy. The network helps show where Martine Doco‐Fenzy may publish in the future.
Co-authorship network of co-authors of Martine Doco‐Fenzy
This figure shows the co-authorship network connecting the top 25 collaborators of Martine Doco‐Fenzy. A scholar is included among the top collaborators of Martine Doco‐Fenzy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Martine Doco‐Fenzy. Martine Doco‐Fenzy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 3 | |
| 3 | 16 | |
| 4 | 14 | |
| 5 | 55 | |
| 6 | 12 | |
| 7 | 24 | |
| 8 | 21 | |
| 9 | 27 | |
| 10 | 8 | |
| 11 | 21 | |
| 12 | 11 | |
| 13 | 11 | |
| 14 | 62 | |
| 15 | 3 | |
| 16 | 104 | |
| 17 | 15 | |
| 18 | 13 | |
| 19 | 58 | |
| 20 | 15 |
About Martine Doco‐Fenzy
Martine Doco‐Fenzy is a scholar working on Genetics, Genetics and Cancer Research, having authored 29 papers that have together received 690 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (302 citations), Sensory Systems (37 citations) and Molecular Biology (349 citations). Martine Doco‐Fenzy has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Stéphanie Struski, Pascale Cornillet‐Lefèbvre, Dominique Gaillard, Emilie Landais, Aude Lallemand, Céline Poirsier, Marta Spodenkiewicz, Anne-Sophie Lèbre, Anouck Schneider and Jacques Motté. Their work appears in journals such as Human Molecular Genetics, Molecular Biology of the Cell 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.