Arnaud Gos
Impact in
- Physiology top 2%
- Adenosine and Purinergic Signaling
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
Papers in
-
- Protein Tyrosine Phosphatases 2
- Genomics and Chromatin Dynamics 2
- Epigenetics and DNA Methylation 2
- Genetics 7
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2
- Co-authors
- Michael A. Morris (12 shared papers)Stylianos E. Antonarakis (14 shared papers)Maria Karayiorgou (1 shared paper)Paula Wolyniec (1 shared paper)Rosalie Goldberg (1 shared paper)Julian Borrow (1 shared paper)Gerald Nestadt (1 shared paper)Virginia K. Lasseter (1 shared paper)
- Journals
- Human Mutation (4 papers)Genomics (3 papers)Human Genetics (2 papers)Experimental Cell Research (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- SwitzerlandUnited StatesNetherlands
In The Last Decade
Arnaud Gos
18 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 84
- Physiology 184
- Genetics 464
- Endocrine and Autonomic Systems 61
- Molecular Biology 617
- Speech and Hearing 34
Countries citing papers authored by Arnaud Gos
This map shows the geographic impact of Arnaud Gos'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 Arnaud Gos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arnaud Gos more than expected).
Fields of papers citing papers by Arnaud Gos
This network shows the impact of papers produced by Arnaud Gos. 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 Arnaud Gos. The network helps show where Arnaud Gos may publish in the future.
Co-authors
The 25 scholars most cited alongside Arnaud Gos, 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 | 1995 | 462 | |
| 2 | Characterization and chromosomal localization of a human P2X receptor from the urinary bladder. | 1995 | 102 |
| 3 | 2008 | 90 | |
| 4 | Gene structure and chromosomal localization of the human P2X7 receptor. | 1998 | 89 |
| 5 | 1999 | 63 | |
| 6 | 1999 | 55 | |
| 7 | 2014 | 37 | |
| 8 | 1997 | 30 | |
| 9 | A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. | 1995 | 29 |
| 10 | 1997 | 25 | |
| 11 | 1992 | 23 | |
| 12 | 1996 | 11 | |
| 13 | 1997 | 10 | |
| 14 | 1996 | 10 | |
| 15 | 1999 | 8 | |
| 16 | 1996 | 7 | |
| 17 | 1999 | 6 | |
| 18 | 1997 | 2 |
About Arnaud Gos
Arnaud Gos is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Immunology, having authored 18 papers that have together received 1.1k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Protein Tyrosine Phosphatases (2 papers), Genomics and Chromatin Dynamics (2 papers), Epigenetics and DNA Methylation (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Physiology (184 citations), Genetics (464 citations), Endocrine and Autonomic Systems (61 citations), Molecular Biology (617 citations) and Speech and Hearing (34 citations). Arnaud Gos has collaborated with scholars based in Switzerland, United States and Netherlands. Frequent co-authors include Michael A. Morris, Stylianos E. Antonarakis, Maria Karayiorgou, Paula Wolyniec, Rosalie Goldberg, Julian Borrow, Gerald Nestadt, Virginia K. Lasseter, Bernice E. Morrow and Robert J. Shprintzen. Their work appears in journals such as Human Mutation, Genomics, Human Genetics, Experimental Cell Research and Journal of Medical 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.