Hervé Moine

3.8k citations
43 papers · 2.8k · 1 hit paper · h-index 25

Impact in

  • Genetics top 1%
    • Genetics and Neurodevelopmental Disorders
    • RNA and protein synthesis mechanisms
    • RNA modifications and cancer
    • RNA Research and Splicing
    • DNA and Nucleic Acid Chemistry
    • Advanced biosensing and bioanalysis techniques
    • RNA Interference and Gene Delivery

Papers in

    • RNA modifications and cancer 26
    • RNA and protein synthesis mechanisms 20
    • RNA Research and Splicing 16
    • Ubiquitin and proteasome pathways 4
    • DNA and Nucleic Acid Chemistry 4
    • Genetics and Neurodevelopmental Disorders 17
    • Bacterial Genetics and Biotechnology 8

Hervé Moine

42 papers receiving 2.8k citations

Hervé Moine's Hit Papers

Fragile X syndrome 2017 · 486 citations
4860+3+6Years since publication100200300400

Peers

Hervé Moine
Comparison fields: 5 of 105
  • Genetics 1.2k
  • Molecular Biology 2.4k
  • Cognitive Neuroscience 326
  • Genetics 117
  • Developmental Neuroscience 39
Replace Édouard W. Khandjian with:
Édouard W. Khandjian Canada
Peter J. Skene United States
Claire Fraser United States
María Clara Bonaglia Italy
Jacqueline Levilliers France
Claudia M.B. Carvalho United States
Stéphane Blanchard France
Donny D. Licatalosi United States
Edwin Mientjes Netherlands
Victoria Brown United States
Hervé Moine relative to Édouard W. Khandjian Canada Édouard W. Khandjian's profile →
Citations per field
00.5×1.5×1.8×
Édouard W. Khandjian · 1×
Citations per year

Countries citing papers authored by Hervé Moine

Since Specialization
Citations

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

Fields of papers citing papers by Hervé Moine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hervé Moine. 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 Hervé Moine. The network helps show where Hervé Moine may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Fragile X syndrome
Hit paper breakdown →
2017486
2 2012230
3 2011200
4 2013192
5 2009162
6 2008156
7 2003147
8 2005127
9 201996
10 200781
11 200879
12 201671
13 199070
14 198669
15 201362
16 200460
17 199649
18 199445
19 199543
20 198840

About Hervé Moine

Hervé Moine is a scholar working on Molecular Biology, Genetics, Cell Biology, Cognitive Neuroscience and Ecology, having authored 43 papers that have together received 2.8k indexed citations. Recurring topics across this work include RNA modifications and cancer (26 papers), RNA and protein synthesis mechanisms (20 papers), Genetics and Neurodevelopmental Disorders (17 papers), RNA Research and Splicing (16 papers), Bacterial Genetics and Biotechnology (8 papers), Ubiquitin and proteasome pathways (4 papers), DNA and Nucleic Acid Chemistry (4 papers) and Autism Spectrum Disorder Research (3 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (2.4k citations), Cognitive Neuroscience (326 citations), Genetics (117 citations) and Developmental Neuroscience (39 citations). Hervé Moine has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Jean‐Louis Mandel, Stéphan Vagner, Stefania Millevoi, Murugan Subramanian, Bernard Ehresmann, Céline Schaeffer, Chantal Ehresmann, Flora Tassone, Ricardos Tabet and Eric Flatter. Their work appears in journals such as Journal of Molecular Biology, Nucleic Acids Research, Proceedings of the National Academy of Sciences, Biochimie and The EMBO Journal.

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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