Robert Feil
- Genetics top 0.1%
- Genetic Syndromes and Imprinting 80
- Genetics and Neurodevelopmental Disorders 6
- Molecular Biology top 0.2%
- Epigenetics and DNA Methylation 89
- Genomics and Chromatin Dynamics 20
- Pluripotent Stem Cells Research 9
- RNA modifications and cancer 7
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- Prenatal Screening and Diagnostics 47
- Cancer Research top 1%
- Aging top 2%
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- Reproductive Biology and Fertility 6
Robert Feil
118 papers receiving 14.9k citations
Hit Papers
Peers
Comparison fields: 5 of 160
- Genetics 5.6k
- Molecular Biology 12.7k
- Pediatrics, Perinatology and Child Health 3.3k
- Cancer Research 1.5k
- Aging 149
Countries citing papers authored by Robert Feil
This map shows the geographic impact of Robert Feil'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 Robert Feil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Feil more than expected).
Fields of papers citing papers by Robert Feil
This network shows the impact of papers produced by Robert Feil. 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 Robert Feil. The network helps show where Robert Feil may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Robert Feil, 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 | 2023 | 40 | |
| 2 | 2023 | 0 | |
| 3 | 2019 | 51 | |
| 4 | 2018 | 30 | |
| 5 | 2018 | 51 | |
| 6 | 2018 | 17 | |
| 7 | 2015 | 36 | |
| 8 | 2015 | 56 | |
| 9 | 2015 | 38 | |
| 10 | 2011 | 19 | |
| 11 | The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatinbreakdown → | 2008 | 732 |
| 12 | 2008 | 73 | |
| 13 | 2007 | 66 | |
| 14 | 2006 | 202 | |
| 15 | 2006 | 54 | |
| 16 | 2006 | 98 | |
| 17 | 2006 | 162 | |
| 18 | 2004 | 332 | |
| 19 | 1996 | 8 | |
| 20 | Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome. | 1990 | 25 |
About Robert Feil
Robert Feil is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 119 papers that have together received 15.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (89 papers), Genetic Syndromes and Imprinting (80 papers), Prenatal Screening and Diagnostics (47 papers), Genomics and Chromatin Dynamics (20 papers), Pluripotent Stem Cells Research (9 papers), RNA modifications and cancer (7 papers), Reproductive Biology and Fertility (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (5.6k citations), Molecular Biology (12.7k citations) and Pediatrics, Perinatology and Child Health (3.3k citations). Robert Feil has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Mario F. Fraga, Alexandre Wagschal, Wolf Reik, Eric S. Lander, Tarjei S. Mikkelsen, Alex Meissner, Ben Fry, Dana J. Huebert, Michael Kamal and Stuart L. Schreiber. Their work appears in journals such as Nucleic Acids Research, Molecular and Cellular Biology, Cell Reports, The EMBO Journal and Proceedings of the National Academy of Sciences.
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.