Thierry Seroz

800 citations
8 papers · 705 · h-index 7

Impact in

    • DNA Repair Mechanisms
    • RNA modifications and cancer
    • Genomics and Chromatin Dynamics
    • RNA Research and Splicing
    • Epigenetics and DNA Methylation
  • Genetics top 10%
    • Neurogenetic and Muscular Disorders Research

Papers in

    • RNA modifications and cancer 6
    • DNA Repair Mechanisms 5
    • Genomics and Chromatin Dynamics 2
    • Epigenetics and DNA Methylation 2
    • Ion channel regulation and function 1
    • Muscle Physiology and Disorders 1
    • Cancer-related Molecular Pathways 2

Thierry Seroz

8 papers receiving 682 citations

Peers

Thierry Seroz
Comparison fields: 5 of 54
  • Molecular Biology 622
  • Genetics 84
  • Oncology 178
  • Cell Biology 102
  • Virology 28
Replace Catherine Denicourt with:
Catherine Denicourt United States
Marta Sanz-García Spain
Angélica Romero United States
Thomas Metz Germany
Elke Will Germany
Niels‐Bjarne Woods Sweden
Greg Conway United States
Ruchika Gupta United States
Androniki Kretsovali Greece
John A. Schmiesing United States
Thierry Seroz relative to Catherine Denicourt United States Catherine Denicourt's profile →
Citations per field
00.5×3.5×
Catherine Denicourt · 1×
Citations per year

Countries citing papers authored by Thierry Seroz

Since Specialization
Citations

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

Fields of papers citing papers by Thierry Seroz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

8 of 8 papers shown
#Work
1 1994388
2
The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.
199790
3 199676
4 199556
5 200039
6 200232
7 200022
8 19982

About Thierry Seroz

Thierry Seroz is a scholar working on Molecular Biology, Oncology, Surgery, Genetics and Cell Biology, having authored 8 papers that have together received 705 indexed citations. Recurring topics across this work include RNA modifications and cancer (6 papers), DNA Repair Mechanisms (5 papers), Genomics and Chromatin Dynamics (2 papers), Epigenetics and DNA Methylation (2 papers), Cancer-related Molecular Pathways (2 papers), Congenital Anomalies and Fetal Surgery (1 paper), Ion channel regulation and function (1 paper) and Muscle Physiology and Disorders (1 paper). The work is most often cited by research in Molecular Biology (622 citations), Genetics (84 citations), Oncology (178 citations), Cell Biology (102 citations) and Virology (28 citations). Thierry Seroz has collaborated with scholars based in France, Netherlands and Belgium. Frequent co-authors include Jan H.J. Hoeijmakers, Wim Vermeulen, Jean‐Marc Egly, Laurent Schaeffer, Jean‐Pierre Tassan, Erich A. Nigg, J P Adamczewski, Richard Roy, Jae Ryoung Hwang and Jean‐Marc Egly. Their work appears in journals such as Journal of Biological Chemistry, Nucleic Acids Research, Gene, EMBO Reports and Cell.

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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