M. Gené

734 total citations
37 papers, 452 citations indexed

About

M. Gené is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, M. Gené has authored 37 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 15 papers in Molecular Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in M. Gené's work include Forensic and Genetic Research (18 papers), Genetic diversity and population structure (8 papers) and Molecular Biology Techniques and Applications (7 papers). M. Gené is often cited by papers focused on Forensic and Genetic Research (18 papers), Genetic diversity and population structure (8 papers) and Molecular Biology Techniques and Applications (7 papers). M. Gené collaborates with scholars based in Spain, Mexico and Portugal. M. Gené's co-authors include E. Huguet, Jacint Corbella i Corbella, Ester Piqué, Jesús Gómez-Catalán, Jordi To‐Figueras, Alejandro Pérez‐Pérez, Daniel Turbón, C. Barrot, Alexandre Xifró and Ángel Carracedo and has published in prestigious journals such as Cancer Letters, Electrophoresis and European Journal of Epidemiology.

In The Last Decade

M. Gené

36 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Gené Spain 12 266 246 39 38 37 37 452
Rakesh Tamang India 12 199 0.7× 117 0.5× 15 0.4× 21 0.6× 59 1.6× 28 448
Carla Bini Italy 12 280 1.1× 205 0.8× 25 0.6× 35 0.9× 55 1.5× 57 442
Houssein Khodjet‐El‐Khil Tunisia 14 343 1.3× 140 0.6× 15 0.4× 31 0.8× 95 2.6× 32 491
Vânia Pereira Denmark 17 552 2.1× 436 1.8× 11 0.3× 19 0.5× 64 1.7× 60 765
Jiujin Xu China 10 282 1.1× 100 0.4× 8 0.2× 28 0.7× 68 1.8× 13 410
Zheng Ren China 12 215 0.8× 196 0.8× 7 0.2× 51 1.3× 40 1.1× 52 333
E. Huguet Spain 12 258 1.0× 168 0.7× 36 0.9× 19 0.5× 30 0.8× 32 364
Yongli Dong China 10 378 1.4× 136 0.6× 3 0.1× 14 0.4× 145 3.9× 16 519
Uta‐Dorothee Immel Germany 10 130 0.5× 122 0.5× 27 0.7× 41 1.1× 6 0.2× 21 273

Countries citing papers authored by M. Gené

Since Specialization
Citations

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

Fields of papers citing papers by M. Gené

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Gené

This figure shows the co-authorship network connecting the top 25 collaborators of M. Gené. A scholar is included among the top collaborators of M. Gené 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 M. Gené. M. Gené 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.
Barrot, C., et al.. (2013). DNA paternity tests in Spain without the mother's consent: The legal responsibility of the laboratories. Forensic Science International Genetics. 8(1). 33–35. 3 indexed citations
2.
Barrot, C., et al.. (2012). Polimorfismos genéticos como indicadores de la vulnerabilidad individual a la adicción al tabaco. Medicina Clínica. 140(2). 49–52. 2 indexed citations
3.
Barrot, C., Alexandre Xifró, Inmaculada Gómez de Aranda, et al.. (2007). Haplotype frequencies of 16 Y-chromosome STR loci in the Barcelona metropolitan area population using Y-Filer™ kit. Forensic Science International. 172(2-3). 211–217. 23 indexed citations
4.
Barrot, C., Alexandre Xifró, J. Mas, et al.. (2007). Data for Y-chromosome haplotypes in Fang and Bubi populations from Bioko (Equatorial Guinea). Forensic Science International. 168(1). e10–e12. 4 indexed citations
5.
Barrot, C., C. Brandt-Casadevall, Antonio González‐Martín, et al.. (2007). Haplotype Frequencies of Eight Y‐Chromosome Short Tandem Repeats Loci in Four Amerindian Populations (State of Hidalgo, Mexico). Journal of Forensic Sciences. 52(2). 504–506. 5 indexed citations
6.
Gorostiza, Amaya, Antonio González‐Martín, C. Barrot, et al.. (2006). Allele frequencies of the 15 AmpF/Str Identifiler loci in the population of Metztitlán (Estado de Hidalgo), México. Forensic Science International. 166(2-3). 230–232. 20 indexed citations
7.
Gené, M., et al.. (2004). Mitochondrial DNA diversity in the Llanos de Moxos: Moxo, Movima and Yuracare Amerindian populations from Bolivia lowlands. Annals of Human Biology. 31(1). 9–28. 47 indexed citations
8.
Brandt-Casadevall, C., M. Gené, Ester Piqué, et al.. (2003). Presence of two mutations between father and child in two cases of paternity testing. International Congress Series. 1239. S15–S18. 5 indexed citations
9.
Huguet, E. & M. Gené. (2002). La investigación biológica de la paternidad. 40(9). 415–422.
10.
To‐Figueras, Jordi, M. Gené, Jesús Gómez-Catalán, et al.. (2002). Microsomal epoxide hydrolase and glutathione S-transferase polymorphisms in relation to laryngeal carcinoma risk. Cancer Letters. 187(1-2). 95–101. 60 indexed citations
11.
To‐Figueras, Jordi, et al.. (2001). Lung cancer susceptibility in relation to combined polymorphisms of microsomal epoxide hydrolase and glutathione S-transferase P1. Cancer Letters. 173(2). 155–162. 40 indexed citations
12.
Gené, M., Ester Piqué, Alexandre Xifró, et al.. (2000). Population study of Aymara Amerindians for the PCR-DNA polymorphisms HUMTH01, HUMVWA31A, D3S1358, D8S1179, D18S51, D19S253, YNZ22 and HLA-DQα. International Journal of Legal Medicine. 113(2). 126–128. 10 indexed citations
13.
Gené, M., et al.. (1999). Haplotype frequencies of eight Y-chromosome STR loci in Barcelona (North-East Spain). International Journal of Legal Medicine. 112(6). 403–405. 32 indexed citations
14.
Gené, M., et al.. (1998). Catalonian population study of the tetranucleotide repeat loci D3S1358, D8S1179, D18S51 and D19S253. International Journal of Legal Medicine. 112(1). 75–77. 10 indexed citations
15.
Gené, M., et al.. (1997). Population genetics of the D12S391, CSF1PO and TPOX loci in Catalonia (Northeast Spain). International Journal of Legal Medicine. 111(1). 52–54. 15 indexed citations
16.
Gené, M., et al.. (1997). Low apolipoprotein E ε4 allele frequency in the population of Catalonia (spain) determined by Pcr-Rflp and Laser fluorescent sequencer. European Journal of Epidemiology. 13(7). 841–843. 9 indexed citations
17.
Huguet, E., et al.. (1996). Study of three AMPFLPs (D1S80, 3′ApoB and YNZ22) in the population of the North of Portugal. Forensic Science International. 79(1). 23–29. 8 indexed citations
18.
Gené, M., et al.. (1996). Population study of the STRs HUMTH01 (including a new variant) and HUMVWA31A in Catalonia (northeast Spain). International Journal of Legal Medicine. 108(6). 318–320. 9 indexed citations
19.
Queralt, R., Oriol de Fàbregues, M. Gené, et al.. (1993). Direct Sequencing of the Human Protamine P1 Gene and Application in Forensic Medicine. Journal of Forensic Sciences. 38(6). 1491–1501. 7 indexed citations
20.
Carracedo, Ángel, et al.. (1988). Comparison between isoelectric focusing methods for the detection of orosomucoid phenotypes. Electrophoresis. 9(6). 268–272. 13 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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