P.-M. Sinet

1.6k total citations
27 papers, 1.4k citations indexed

About

P.-M. Sinet is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, P.-M. Sinet has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Physiology. Recurrent topics in P.-M. Sinet's work include Genomic variations and chromosomal abnormalities (7 papers), Mitochondrial Function and Pathology (5 papers) and Alzheimer's disease research and treatments (5 papers). P.-M. Sinet is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Mitochondrial Function and Pathology (5 papers) and Alzheimer's disease research and treatments (5 papers). P.-M. Sinet collaborates with scholars based in France, United States and Belgium. P.-M. Sinet's co-authors include Gerald Cohen, Richard E. Heikkila, Annie Nicole, I. Ceballos, J Lejeune, P. Kamoun, H Jérôme, A.M. Michelson, Jean‐Louis Blouin and Jean‐Maurice Delabar and has published in prestigious journals such as Brain Research, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

P.-M. Sinet

26 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P.-M. Sinet France 18 532 249 221 206 199 27 1.4k
Jannike Mørch Andersen Norway 18 512 1.0× 242 1.0× 121 0.5× 119 0.6× 145 0.7× 52 1.8k
Annie Nicole France 29 1.4k 2.7× 532 2.1× 309 1.4× 317 1.5× 304 1.5× 53 2.6k
Laura Lucchi Italy 26 558 1.0× 188 0.8× 131 0.6× 90 0.4× 95 0.5× 64 1.6k
José M. Medina Spain 24 852 1.6× 500 2.0× 157 0.7× 74 0.4× 76 0.4× 55 2.0k
Daniela Ortiz United States 20 363 0.7× 376 1.5× 133 0.6× 60 0.3× 64 0.3× 32 1.4k
Ardesio Floridi Italy 19 427 0.8× 255 1.0× 325 1.5× 63 0.3× 46 0.2× 35 1.7k
Zbigniew Binienda United States 26 777 1.5× 305 1.2× 98 0.4× 64 0.3× 78 0.4× 72 1.9k
H. J. Armbrecht United States 31 709 1.3× 664 2.7× 501 2.3× 480 2.3× 71 0.4× 86 2.8k
Alain Minn France 28 530 1.0× 289 1.2× 186 0.8× 41 0.2× 43 0.2× 53 1.9k
Antonio Iradi Spain 23 537 1.0× 387 1.6× 208 0.9× 50 0.2× 186 0.9× 35 1.8k

Countries citing papers authored by P.-M. Sinet

Since Specialization
Citations

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

Fields of papers citing papers by P.-M. Sinet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P.-M. Sinet. 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 P.-M. Sinet. The network helps show where P.-M. Sinet may publish in the future.

Co-authorship network of co-authors of P.-M. Sinet

This figure shows the co-authorship network connecting the top 25 collaborators of P.-M. Sinet. A scholar is included among the top collaborators of P.-M. Sinet 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 P.-M. Sinet. P.-M. Sinet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dauphinot, Luce, Robert Lyle, Isabelle Rivals, et al.. (2004). The cerebellar transcriptome during postnatal development of the Ts1Cje mouse, a segmental trisomy model for Down syndrome. Human Molecular Genetics. 14(3). 373–384. 69 indexed citations
2.
Vialard, François, Stefan Taudien, André Rosenthal, et al.. (2000). Characterization of a Novel Gene, C21orf6, Mapping to a Critical Region of Chromosome 21q22.1 Involved in the Monosomy 21 Phenotype and of Its Murine Ortholog, orf5. Genomics. 64(2). 203–210. 2 indexed citations
3.
Gosset, Philippe, Ghania Ait‐Ghezala, P.-M. Sinet, & Nicole Créau. (1999). Isolation and analysis of chromosome 21 genes potentially involved in Down Syndrome. PubMed. 57. 197–209. 5 indexed citations
4.
5.
Paly, Evelyne, et al.. (1995). Genomic Organization of the Human Cystathionine β-Synthase Gene: Evidence for Various cDNAs. Biochemical and Biophysical Research Communications. 211(3). 826–832. 20 indexed citations
6.
Chettouh, Zoubida, M. F. Croquette, B Delobel, et al.. (1995). Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.. PubMed. 57(1). 62–71. 66 indexed citations
7.
Ceballos-Picot, Irène, Annie Nicole, P.-M. Sinet, et al.. (1993). Symposium on free radicals. Mediators of Inflammation. 2(2). 153–170.
8.
Gosset, Philippe, Didier Theophile, Martine Duterque‐Coquillaud, et al.. (1993). Mapping the Down Syndrome Chromosome Region. European Journal of Human Genetics. 1(1). 51–63. 24 indexed citations
9.
Venault, Patrice, Irène Ceballos-Picot, Annie Nicole, et al.. (1993). Hippocampal mossy fiber changes in mice transgenic for the human copper-zinc superoxide dismutase gene. Neuroscience Letters. 160(1). 24–28. 13 indexed citations
10.
Ceballos, I., Annie Nicole, Pascale Briand, et al.. (1991). Expression of Human Cu-Zn Superoxide Dismutase Gene in Transgenic Mice: Model for Gene Dosage Effect in Down Syndrome. Free Radical Research Communications. 13(1). 581–589. 32 indexed citations
11.
Ceballos-Picot, Irène, Annie Nicole, Pascale Briand, et al.. (1991). Neuronal-specific expression of human copper-zinc superoxide dismutase gene in transgenic mice: animal model of gene dosage effects in Down's syndrome. Brain Research. 552(2). 198–214. 81 indexed citations
12.
Ceballos, I., F. Javoy‐Agid, A. Delacourte, et al.. (1991). Neuronal Localization of Copper-Zinc Superoxide Dismutase Protein and mRNA within the Human Hippocampus from Control and Alzheimer'S Disease Brains. Free Radical Research Communications. 13(1). 571–580. 32 indexed citations
13.
Blouin, Jean‐Louis, Zohra Rahmani, Zoubida Chettouh, et al.. (1990). Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.. PubMed. 46(3). 518–26. 17 indexed citations
14.
Ceballos, I., France Javoy‐Agid, Étienne C. Hirsch, et al.. (1989). Localization of copper-zinc superoxide dismutase mRNA in human hippocampus by in situ hybridization. Neuroscience Letters. 105(1-2). 41–46. 18 indexed citations
15.
Ceballos, I., Jean‐Maurice Delabar, Annie Nicole, et al.. (1988). Expression of transfected human CuZn superoxide dismutase gene in mouse L cells and NS20Y neuroblastoma cells induces enhancement of glutathione peroxidase activity. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 949(1). 58–64. 80 indexed citations
16.
Sinet, P.-M., et al.. (1983). Selenium-dependent and non-selenium-dependent glutathione peroxidases in human tissue extracts. Biochimica et Biophysica Acta (BBA) - General Subjects. 759(1-2). 49–57. 160 indexed citations
17.
Sinet, P.-M.. (1982). Metabolism of Oxygen Derivatives in Down's Syndrome*. Annals of the New York Academy of Sciences. 396(1). 83–94. 169 indexed citations
18.
Cohen, Gerald, et al.. (1981). Oxygen consumption during the fenton-type reaction between hydrogen peroxide and a ferrous-chelate (Fe2+-DTPA). Journal of Inorganic Biochemistry. 15(2). 143–151. 22 indexed citations
19.
Sinet, P.-M., Richard E. Heikkila, & Gerald Cohen. (1980). Hydrogen Peroxide Production by Rat Brain In Vivo. Journal of Neurochemistry. 34(6). 1421–1428. 178 indexed citations
20.
Sinet, P.-M., et al.. (1975). Increase in glutathione peroxidase activity in erythrocytes from trisomy 21 subjects. Biochemical and Biophysical Research Communications. 67(3). 910–915. 102 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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