Arnaud Gos

27.4k total citations
18 papers, 1.1k citations indexed

About

Arnaud Gos is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Arnaud Gos has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Plant Science. Recurrent topics in Arnaud Gos's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). Arnaud Gos is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). Arnaud Gos collaborates with scholars based in Switzerland, United States and Netherlands. Arnaud Gos's co-authors include Michael A. Morris, Stylianos E. Antonarakis, Paula Wolyniec, Gerald Nestadt, Julian Borrow, Robert J. Shprintzen, Bernice E. Morrow, Maria Karayiorgou, Virginia K. Lasseter and Rosalie Goldberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical and Biophysical Research Communications and Experimental Cell Research.

In The Last Decade

Arnaud Gos

18 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Arnaud Gos Switzerland 12 617 464 184 88 77 18 1.1k
Mario Plaas Estonia 17 404 0.7× 204 0.4× 46 0.3× 82 0.9× 134 1.7× 43 870
James Hewinson United Kingdom 18 484 0.8× 116 0.3× 104 0.6× 91 1.0× 178 2.3× 23 1.2k
Tarja Joensuu Finland 19 670 1.1× 344 0.7× 32 0.2× 77 0.9× 158 2.1× 31 1.3k
Hiroaki Kanki Japan 13 592 1.0× 145 0.3× 43 0.2× 91 1.0× 231 3.0× 15 890
Gareth Elvidge United Kingdom 13 511 0.8× 265 0.6× 46 0.3× 52 0.6× 30 0.4× 15 911
Lucie Vérot France 10 337 0.5× 180 0.4× 121 0.7× 36 0.4× 106 1.4× 11 1.0k
Nathalie Suarez-Huerta Belgium 8 966 1.6× 236 0.5× 342 1.9× 190 2.2× 274 3.6× 9 1.8k
Lourdes Hontecillas‐Prieto Spain 13 362 0.6× 55 0.1× 127 0.7× 69 0.8× 124 1.6× 29 698
Gretel Beck United States 8 837 1.4× 362 0.8× 23 0.1× 106 1.2× 166 2.2× 8 1.4k
Sebok K. Halder Japan 18 345 0.6× 144 0.3× 28 0.2× 118 1.3× 69 0.9× 45 829

Countries citing papers authored by Arnaud Gos

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Arnaud Gos

This figure shows the co-authorship network connecting the top 25 collaborators of Arnaud Gos. A scholar is included among the top collaborators of Arnaud Gos based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Arnaud Gos. Arnaud Gos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Famiglietti, Maria Livia, Anne Estreicher, Arnaud Gos, et al.. (2014). Genetic Variations and Diseases in UniProtKB/Swiss‐Prot: The Ins and Outs of Expert Manual Curation. Human Mutation. 35(8). 927–935. 37 indexed citations
2.
Yip, Yum L., Maria Livia Famiglietti, Arnaud Gos, et al.. (2008). Annotating single amino acid polymorphisms in the UniProt/Swiss-Prot knowledgebase. Human Mutation. 29(3). 361–366. 90 indexed citations
3.
4.
Mittaz, Lauréane, Colette Rossier, Maarit Heino, et al.. (1999). Isolation and Characterization of the MouseAireGene. Biochemical and Biophysical Research Communications. 255(2). 483–490. 55 indexed citations
5.
Bartoloni, Lucia, Julie Blouin, Amanda Sainsbury, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping. Cytogenetic and Genome Research. 84(3-4). 188–189. 6 indexed citations
6.
7.
Buell, Gary, et al.. (1998). Gene structure and chromosomal localization of the human P2X7 receptor.. PubMed. 5(6). 347–54. 89 indexed citations
8.
Eliez, Stéphan, Michael A. Morris, C.D. DeLozier-Blanchet, et al.. (1997). Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13. American Journal of Medical Genetics. 70(3). 222–228. 10 indexed citations
9.
Morris, Michael A., J. Chabod, Arnaud Gos, et al.. (1997). Fortuitous detection of uniparental isodisomy of chromosome 6.. Journal of Medical Genetics. 34(1). 77–78. 30 indexed citations
10.
Villard, Jean, Walter Reith, Emmanuèle Barras, et al.. (1997). Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency. Human Mutation. 10(6). 430–435. 25 indexed citations
11.
Villard, Jean, Walter Reith, Emmanuèle Barras, et al.. (1997). Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency. Human Mutation. 10(6). 430–435. 2 indexed citations
12.
Blouin, Jean‐Louis, Haiming Chen, Arnaud Gos, et al.. (1996). Mapping of the Gene for the p60 Subunit of the Human Chromatin Assembly Factor (CAF1A) to the Down Syndrome Region of Chromosome 21. Genomics. 33(2). 309–312. 11 indexed citations
13.
Lalioti, Maria D., Arnaud Gos, Michael R. Green, et al.. (1996). The Gene for Human U2 snRNP Auxiliary Factor Small 35-kDa Subunit (U2AF1) Maps to the Progressive Myoclonus Epilepsy (EPM1) Critical Region on Chromosome 21q22.3. Genomics. 33(2). 298–300. 10 indexed citations
14.
Chen, Haiming, Arnaud Gos, Michael A. Morris, & Stylianos E. Antonarakis. (1996). Localization of a Human Homolog of the Mouse Pericentrin Gene (PCNT) to Chromosome 21qter. Genomics. 35(3). 620–624. 7 indexed citations
15.
Christie, Derek Pierre, Arnaud Gos, Audrey Lynn, et al.. (1995). A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.. PubMed. 57(2). 388–94. 29 indexed citations
16.
Karayiorgou, Maria, Michael A. Morris, Bernice E. Morrow, et al.. (1995). Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.. Proceedings of the National Academy of Sciences. 92(17). 7612–7616. 462 indexed citations
17.
Valera, Soledad, R J Evans, Arnaud Gos, et al.. (1995). Characterization and chromosomal localization of a human P2X receptor from the urinary bladder.. PubMed. 3(4). 283–9. 102 indexed citations
18.
Ragno, Pia, Anne Estreicher, Arnaud Gos, et al.. (1992). Polarized secretion of urokinase-type plasminogen activator by epithelial cells. Experimental Cell Research. 203(1). 236–243. 23 indexed citations

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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