Robert Feil

21.0k citations
125 papers · 16.3k · 5 hit papers · h-index 57

Impact in

  • Genetics top 0.1%
    • Genetic Syndromes and Imprinting
    • Epigenetics and DNA Methylation
    • Genomics and Chromatin Dynamics
    • RNA modifications and cancer
    • Pluripotent Stem Cells Research
    • Cancer-related gene regulation

Papers in

    • Epigenetics and DNA Methylation 91
    • Genomics and Chromatin Dynamics 20
    • Pluripotent Stem Cells Research 11
    • Cancer-related gene regulation 7
    • RNA modifications and cancer 7
    • Genetic Syndromes and Imprinting 85
    • Genetics and Neurodevelopmental Disorders 7

Robert Feil

124 papers receiving 15.9k citations

Robert Feil's Hit Papers

Epigenetics and the environment: emerging patterns and implications 2012 · 1.4k citations
1.4k0+11+22Years since publication10002.0k3.0k4.0k

Peers

Robert Feil
Comparison fields: 5 of 160
  • Genetics 5.8k
  • Molecular Biology 12.8k
  • Pediatrics, Perinatology and Child Health 3.2k
  • Cancer Research 1.5k
  • Aging 155
Replace Gavin Kelsey with:
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Howard Cedar Israel
Timothy H. Bestor United States
Huntington F. Willard United States
Jörn Walter Germany
Alan P. Wolffe United States
Christine M. Distèche United States
Wendy Dean United Kingdom
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Robert Feil relative to Gavin Kelsey United Kingdom Gavin Kelsey's profile →
Citations per field
00.5×1.7×
Gavin Kelsey · 1×
Citations per year

Countries citing papers authored by Robert Feil

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

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.

Border = papers with Robert Feil Line = papers co-authored together Robert Feil links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 125 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
Hit paper breakdown →
20064242
2
Epigenetics and the environment: emerging patterns and implications
Hit paper breakdown →
20121442
3
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Hit paper breakdown →
1993995
4
The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatin
Hit paper breakdown →
2008770
5
Child Health, Developmental Plasticity, and Epigenetic Programming
Hit paper breakdown →
2010499
6 2001469
7 2004364
8 2004349
9 1998324
10 2004310
11 1994237
12 1997224
13 2006214
14 2007214
15 2005207
16 2010201
17 2001197
18 2002185
19 2006184
20 2007175

About Robert Feil

Robert Feil is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Cancer Research, having authored 125 papers that have together received 16.3k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (91 papers), Genetic Syndromes and Imprinting (85 papers), Prenatal Screening and Diagnostics (46 papers), Genomics and Chromatin Dynamics (20 papers), Pluripotent Stem Cells Research (11 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cancer-related gene regulation (7 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Genetics (5.8k citations), Molecular Biology (12.8k citations), Pediatrics, Perinatology and Child Health (3.2k citations), Cancer Research (1.5k citations) and Aging (155 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, B Bernstein, Alex Meissner, Tarjei S. Mikkelsen, Michael Kamal, Eric S. Lander, Rudolf Jaenisch and Xiaohui Xie. Their work appears in journals such as Nucleic Acids Research, Molecular and Cellular Biology, Cell Reports, The EMBO Journal 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.

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