Péter L. Nagy

3.9k citations
59 papers · 2.4k · h-index 27

Impact in

  • Neurology top 5%
    • Amyotrophic Lateral Sclerosis Research
    • Genomics and Chromatin Dynamics
    • RNA Research and Splicing
    • Epigenetics and DNA Methylation
    • RNA modifications and cancer
    • Cancer-related gene regulation

Papers in

    • RNA Research and Splicing 11
    • Genomics and Chromatin Dynamics 10
    • Biochemical and Molecular Research 6
    • RNA modifications and cancer 6
    • Epigenetics and DNA Methylation 5
    • Genomics and Rare Diseases 8
    • Genomic variations and chromosomal abnormalities 6
    • Genetics and Neurodevelopmental Disorders 5

Péter L. Nagy

58 papers receiving 2.3k citations

Peers

Péter L. Nagy
Comparison fields: 5 of 117
  • Neurology 330
  • Molecular Biology 1.5k
  • Neurology 152
  • Aging 29
  • Genetics 162
Replace Benoît J. Gentil with:
Benoît J. Gentil Canada
Héctor Sandoval United States
Thomas Floß Germany
Fiona M. Menzies United Kingdom
Holger Hummerich United Kingdom
Usha Narayanan United States
Giuseppe Ronzitti France
Penelope E. Bonnen United States
Rory Kirchner United States
Vincenzo A. Gennarino United States
Péter L. Nagy relative to Benoît J. Gentil Canada Benoît J. Gentil's profile →
Citations per field
00.5×1.5×2.3×
Benoît J. Gentil · 1×
Citations per year

Countries citing papers authored by Péter L. Nagy

Since Specialization
Citations

This map shows the geographic impact of Péter L. Nagy'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 Péter L. Nagy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Péter L. Nagy more than expected).

Fields of papers citing papers by Péter L. Nagy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Péter L. Nagy. 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 Péter L. Nagy. The network helps show where Péter L. Nagy may publish in the future.

Co-authors

The 25 scholars most cited alongside Péter L. Nagy, 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 Péter L. Nagy Line = papers co-authored together Péter L. Nagy links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 59 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2014322
2 2014277
3 2001267
4 2008102
5 200392
6 199586
7 201179
8 201966
9 200262
10 199561
11 201457
12 200252
13 201649
14 201547
15 200946
16 199341
17 201139
18 201638
19 201534
20 199432

About Péter L. Nagy

Péter L. Nagy is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cancer Research, having authored 59 papers that have together received 2.4k indexed citations. Recurring topics across this work include RNA Research and Splicing (11 papers), Genomics and Chromatin Dynamics (10 papers), Genomics and Rare Diseases (8 papers), Biochemical and Molecular Research (6 papers), Genomic variations and chromosomal abnormalities (6 papers), RNA modifications and cancer (6 papers), Epigenetics and DNA Methylation (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Neurology (330 citations), Molecular Biology (1.5k citations), Neurology (152 citations), Aging (29 citations) and Genetics (162 citations). Péter L. Nagy has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Michael L. Cleary, H Zalkin, Roger D. Kornberg, Joachim Griesenbeck, Jimena Baleriola, Carol M. Troy, Ying Y. Jean, Ulrich Hengst, John F. Crary and Hiroshi Mitsumoto. Their work appears in journals such as Journal of Molecular Diagnostics, Neurology Genetics, Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nucleic Acids Research.

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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