Nathalie Roëckel
- Genetics top 5%
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 2
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- Galectins and Cancer Biology 3
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- Epigenetics and DNA Methylation 5
- Glycosylation and Glycoproteins Research 4
- RNA and protein synthesis mechanisms 4
- RNA Research and Splicing 3
- Molecular Biology Techniques and Applications 2
- Co-authors
- Marie‐Geneviève MattéiFrançoise MuscatelliFrançoise WatrinM. LalandeHeather R. Glatt-DeeleyIrène BoccaccioPerrine MalzacDanielle Pham-Dinh
- Cited by
- GeneticsImmunologyMolecular Biology
- Journals
- Genomics (7 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Nathalie Roëckel
21 papers receiving 929 citations
Peers
Comparison fields: 5 of 77
- Genetics 422
- Immunology 195
- Molecular Biology 592
- Developmental Neuroscience 34
- Pediatrics, Perinatology and Child Health 134
Countries citing papers authored by Nathalie Roëckel
This map shows the geographic impact of Nathalie Roëckel'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 Nathalie Roëckel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nathalie Roëckel more than expected).
Fields of papers citing papers by Nathalie Roëckel
This network shows the impact of papers produced by Nathalie Roëckel. 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 Nathalie Roëckel. The network helps show where Nathalie Roëckel may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Nathalie Roëckel, 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 | 2009 | 44 | |
| 2 | 2005 | 30 | |
| 3 | 1999 | 151 | |
| 4 | 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 | 34 |
| 5 | 1997 | 14 | |
| 6 | 1997 | 205 | |
| 7 | 1997 | 25 | |
| 8 | 1997 | 29 | |
| 9 | 1996 | 54 | |
| 10 | 1996 | 20 | |
| 11 | 1994 | 1 | |
| 12 | 1994 | 20 | |
| 13 | 1994 | 29 | |
| 14 | 1993 | 4 | |
| 15 | 1993 | 27 | |
| 16 | 1992 | 6 | |
| 17 | 1992 | 30 | |
| 18 | 1991 | 14 | |
| 19 | 1991 | 9 | |
| 20 | 1990 | 28 |
About Nathalie Roëckel
Nathalie Roëckel is a scholar working on Immunology, Genetics, Molecular Biology, Cancer Research and Immunology and Allergy, having authored 21 papers that have together received 946 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (5 papers), Glycosylation and Glycoproteins Research (4 papers), RNA and protein synthesis mechanisms (4 papers), RNA Research and Splicing (3 papers), Galectins and Cancer Biology (3 papers), Molecular Biology Techniques and Applications (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (422 citations), Immunology (195 citations), Molecular Biology (592 citations), Developmental Neuroscience (34 citations) and Pediatrics, Perinatology and Child Health (134 citations). Nathalie Roëckel has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Marie‐Geneviève Mattéi, Françoise Muscatelli, Françoise Watrin, M. Lalande, Heather R. Glatt-Deeley, Irène Boccaccio, Perrine Malzac, Danielle Pham-Dinh, Philippe Berta and J.L. Nussbaum. Their work appears in journals such as Genomics, Human Molecular Genetics, European Journal of Human Genetics, Human Genetics and Nature 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.