C. Mignon
Impact in
-
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
-
- Epigenetics and DNA Methylation
- Ion Transport and Channel Regulation
Papers in
- Genetics 9
- Genetic Syndromes and Imprinting 5
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
-
- Epigenetics and DNA Methylation 4
- Genomics and Chromatin Dynamics 2
- Glycosylation and Glycoproteins Research 1
- Co-authors
- Marie‐Geneviève Mattéi (13 shared papers)Danielle Depetris (4 shared papers)Nathalie Roëckel (3 shared papers)Carlos Cardoso (1 shared paper)Laurence Colleaux (1 shared paper)Michel Fontés (1 shared paper)Gilles Hetet (1 shared paper)Anne Moncla (3 shared papers)
- Journals
- Genomics (3 papers)European Journal of Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Chromosome Research (2 papers)Mammalian Genome (2 papers)
- Partner nations
- FranceUnited StatesGabon
In The Last Decade
C. Mignon
14 papers receiving 430 citations
Peers
Comparison fields: 5 of 54
- Genetics 178
- Molecular Biology 302
- Pediatrics, Perinatology and Child Health 71
- Immunology 66
- Sensory Systems 12
Countries citing papers authored by C. Mignon
This map shows the geographic impact of C. Mignon'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 C. Mignon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Mignon more than expected).
Fields of papers citing papers by C. Mignon
This network shows the impact of papers produced by C. Mignon. 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 C. Mignon. The network helps show where C. Mignon may publish in the future.
Co-authors
The 25 scholars most cited alongside C. Mignon, 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 | 2000 | 81 | |
| 2 | 1995 | 67 | |
| 3 | 1996 | 63 | |
| 4 | 1997 | 61 | |
| 5 | The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region. | 1998 | 35 |
| 6 | 1997 | 30 | |
| 7 | 1999 | 28 | |
| 8 | 1995 | 19 | |
| 9 | 1995 | 15 | |
| 10 | 2000 | 15 | |
| 11 | 1998 | 13 | |
| 12 | 1997 | 7 | |
| 13 | 2008 | 5 | |
| 14 | 1996 | 5 |
About C. Mignon
C. Mignon is a scholar working on Genetics, Molecular Biology, Cancer Research, Oncology and Hematology, having authored 14 papers that have together received 444 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Epigenetics and DNA Methylation (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers), Genomics and Chromatin Dynamics (2 papers) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (178 citations), Molecular Biology (302 citations), Pediatrics, Perinatology and Child Health (71 citations), Immunology (66 citations) and Sensory Systems (12 citations). C. Mignon has collaborated with scholars based in France, United States and Gabon. Frequent co-authors include Marie‐Geneviève Mattéi, Danielle Depetris, Nathalie Roëckel, Carlos Cardoso, Laurence Colleaux, Michel Fontés, Gilles Hetet, Anne Moncla, Michel L.P. Monsigny and Françoise Watrin. Their work appears in journals such as Genomics, European Journal of Human Genetics, Journal of Medical Genetics, Chromosome Research and Mammalian Genome.
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.