Robert Feil

21.5k citations
130 papers · 17.1k · 6 hit papers · h-index 57

Impact in

  • Genetics top 0.2%
    • Genetic Syndromes and Imprinting
    • Epigenetics and DNA Methylation
    • Genomics and Chromatin Dynamics
    • Pluripotent Stem Cells Research

Papers in

    • Genetic Syndromes and Imprinting 87
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • Genomic variations and chromosomal abnormalities 4
    • Animal Genetics and Reproduction 4
    • Epigenetics and DNA Methylation 18
    • Genomics and Chromatin Dynamics 17

Robert Feil

129 papers receiving 16.6k citations

Robert Feil's Hit Papers

Genomic Imprinting and Physiological Processes in Mammals 2019 · 392 citations
3920+11+22Years since publication1k2k3k4k

Peers

Robert Feil
Comparison fields: 5 of 148
  • Genetics 5k
  • Molecular Biology 8.4k
  • Clinical Biochemistry 628
  • Cancer Research 990
  • Pediatrics, Perinatology and Child Health 876
Replace Christine M. Distèche with:
Christine M. Distèche United States
Christian Gilissen Netherlands
Alexander Hoischen Netherlands
André Reis Germany
Fowzan Sami Alkuraya Saudi Arabia
Niels Tommerup Denmark
Joris Andre Veltman Netherlands
Mariano Rocchi Italy
Charles E. Schwartz United States
Richard Alan Lewis United States
Robert Feil relative to Christine M. Distèche United States Christine M. Distèche's profile →
Citations per field
00.5×1.5×2.1×
Christine M. Distèche · 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 130 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 →
20064267
2
Epigenetics and the environment: emerging patterns and implications
Hit paper breakdown →
20121503
3
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Hit paper breakdown →
19931023
4
The Air Noncoding RNA Epigenetically Silences Transcription by Targeting G9a to Chromatin
Hit paper breakdown →
2008756
5
Child Health, Developmental Plasticity, and Epigenetic Programming
Hit paper breakdown →
2010514
6 2001470
7
Genomic Imprinting and Physiological Processes in Mammals
Hit paper breakdown →
2019392
8 2004356
9 2004337
10 1998315
11 2004296
12 2016281
13 1994230
14 1997218
15 2007216
16 2006209
17 2005208
18 2010202
19 2001199
20 2006188

About Robert Feil

Robert Feil is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Reproductive Medicine, having authored 130 papers that have together received 17.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (87 papers), Epigenetics and DNA Methylation (18 papers), Genomics and Chromatin Dynamics (17 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Animal Genetics and Reproduction (4 papers) and Birth, Development, and Health (4 papers). The work is most often cited by research in Genetics (5k citations), Molecular Biology (8.4k citations), Clinical Biochemistry (628 citations), Cancer Research (990 citations) and Pediatrics, Perinatology and Child Health (876 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, Bradley Bernstein, Alexander Meissner, James A. Cuff, Eric S. Lander, Ben Fry, Tarjei S. Mikkelsen and Dana J. Huebert. Their work appears in journals such as Nucleic Acids Research, Cell Reports, The EMBO Journal, Molecular and Cellular Biology 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.

Explore authors with similar magnitude of impact