Pierre Miniou
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
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- RNA modifications and cancer
- Epigenetics and DNA Methylation
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 3
- Neurogenetic and Muscular Disorders Research 3
-
- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 3
- CRISPR and Genetic Engineering 2
- Retinal Development and Disorders 2
- Co-authors
- E. Viégas-Pèquignot (7 shared papers)Marc Jeanpierre (4 shared papers)Judith Melki (2 shared papers)Véronique Blanquet (2 shared papers)Deborah Bartholdi (1 shared paper)Andoni Echaniz‐Laguna (1 shared paper)Déborah Bourc’his (3 shared papers)Alain Niveleau (1 shared paper)
- Journals
- Genomics (3 papers)Human Genetics (2 papers)Human Molecular Genetics (1 paper)The American Journal of Human Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Pierre Miniou
15 papers receiving 740 citations
Peers
Comparison fields: 5 of 65
- Genetics 168
- Molecular Biology 588
- Genetics 172
- Cellular and Molecular Neuroscience 90
- Immunology 78
Countries citing papers authored by Pierre Miniou
This map shows the geographic impact of Pierre Miniou'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 Pierre Miniou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pierre Miniou more than expected).
Fields of papers citing papers by Pierre Miniou
This network shows the impact of papers produced by Pierre Miniou. 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 Pierre Miniou. The network helps show where Pierre Miniou may publish in the future.
Co-authors
The 25 scholars most cited alongside Pierre Miniou, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 177 | |
| 2 | 1994 | 118 | |
| 3 | The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease. | 1997 | 89 |
| 4 | 1999 | 72 | |
| 5 | 1997 | 70 | |
| 6 | Baculovirus recombinant expressing a secreted form of a transmembrane carcinoma-associated antigen. | 1992 | 61 |
| 7 | 1997 | 39 | |
| 8 | 1999 | 33 | |
| 9 | 2022 | 30 | |
| 10 | 1995 | 21 | |
| 11 | 1994 | 20 | |
| 12 | 2008 | 14 | |
| 13 | 1996 | 13 | |
| 14 | 2021 | 12 | |
| 15 | 1995 | 1 | |
| 16 | 2025 | 0 |
About Pierre Miniou
Pierre Miniou is a scholar working on Genetics, Genetics, Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience, having authored 16 papers that have together received 770 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Genomic variations and chromosomal abnormalities (3 papers), RNA modifications and cancer (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), CRISPR and Genetic Engineering (2 papers), Monoclonal and Polyclonal Antibodies Research (2 papers), Retinal Development and Disorders (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (168 citations), Molecular Biology (588 citations), Genetics (172 citations), Cellular and Molecular Neuroscience (90 citations) and Immunology (78 citations). Pierre Miniou has collaborated with scholars based in France, United States and Italy. Frequent co-authors include E. Viégas-Pèquignot, Marc Jeanpierre, Judith Melki, Véronique Blanquet, Deborah Bartholdi, Andoni Echaniz‐Laguna, Déborah Bourc’his, Alain Niveleau, Catherine Herbelin and Alain Fischer. Their work appears in journals such as Genomics, Human Genetics, Human Molecular Genetics, The American Journal of Human Genetics and Cytogenetic and Genome 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.