László Orbán

5.4k total citations
116 papers, 3.9k citations indexed

About

László Orbán is a scholar working on Genetics, Molecular Biology and Aquatic Science. According to data from OpenAlex, László Orbán has authored 116 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Genetics, 54 papers in Molecular Biology and 21 papers in Aquatic Science. Recurrent topics in László Orbán's work include Genetic diversity and population structure (27 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers) and Animal Genetics and Reproduction (24 papers). László Orbán is often cited by papers focused on Genetic diversity and population structure (27 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers) and Animal Genetics and Reproduction (24 papers). László Orbán collaborates with scholars based in Singapore, Hungary and United States. László Orbán's co-authors include Gen Hua Yue, Woei Chang Liew, Richárd Bártfai, Rajini Sreenivasan, Per‐Erik Olsson, Andreas Chrambach, Balázs Kovács, Ferenc Müller, Alan Christoffels and Mohammad Sorowar Hossain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

László Orbán

112 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Orbán Singapore 37 2.3k 1.4k 1.1k 849 537 116 3.9k
Øivind Andersen Norway 32 1.1k 0.5× 922 0.7× 812 0.8× 969 1.1× 470 0.9× 104 3.3k
Rolf B. Edvardsen Norway 29 998 0.4× 1.2k 0.8× 472 0.4× 562 0.7× 461 0.9× 74 2.8k
Joan Cerdà Spain 42 1.6k 0.7× 1.5k 1.0× 2.7k 2.6× 2.0k 2.3× 879 1.6× 156 5.5k
Zuoyan Zhu China 39 2.2k 1.0× 3.2k 2.3× 749 0.7× 734 0.9× 269 0.5× 274 6.2k
Ronald B. Walter United States 30 998 0.4× 1.3k 0.9× 372 0.4× 301 0.4× 335 0.6× 130 3.2k
Julien Bobe France 35 1.9k 0.8× 1.0k 0.7× 3.0k 2.8× 2.2k 2.6× 1.1k 2.1× 116 5.2k
Masakane Yamashita Japan 40 1.7k 0.7× 2.3k 1.6× 1.7k 1.6× 768 0.9× 358 0.7× 156 5.4k
Deshou Wang China 40 4.3k 1.8× 1.7k 1.2× 2.7k 2.5× 988 1.2× 311 0.6× 177 5.7k
David J. Penman United Kingdom 40 3.3k 1.4× 853 0.6× 1.7k 1.6× 1.7k 2.0× 712 1.3× 117 4.6k
Changwei Shao China 25 1.5k 0.7× 926 0.7× 492 0.5× 600 0.7× 195 0.4× 134 2.7k

Countries citing papers authored by László Orbán

Since Specialization
Citations

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

Fields of papers citing papers by László Orbán

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Orbán

This figure shows the co-authorship network connecting the top 25 collaborators of László Orbán. A scholar is included among the top collaborators of László Orbán 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 László Orbán. László Orbán 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.
Fodor, Erika, Nóra Szabó, Ildikó Szeverényi, et al.. (2024). The reference genome of Macropodus opercularis (the paradise fish). Scientific Data. 11(1). 540–540. 2 indexed citations
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Li, Jia, Chao Bian, Yinchang Hu, et al.. (2016). A chromosome-level genome assembly of the Asian arowana, Scleropages formosus. Scientific Data. 3(1). 160105–160105. 12 indexed citations
5.
Jiang, Junhui, et al.. (2014). Small-scale transcriptomics reveals differences among gonadal stages in Asian seabass (Lates calcarifer). Reproductive Biology and Endocrinology. 12(1). 5–5. 38 indexed citations
6.
Sreenivasan, Rajini, Junhui Jiang, Xingang Wang, et al.. (2013). Gonad Differentiation in Zebrafish Is Regulated by the Canonical Wnt Signaling Pathway1. Biology of Reproduction. 90(2). 45–45. 82 indexed citations
7.
Pradhan, Ajay, Hazem Khalaf, Scott A. Ochsner, et al.. (2012). Activation of NF-κB Protein Prevents the Transition from Juvenile Ovary to Testis and Promotes Ovarian Development in Zebrafish. Journal of Biological Chemistry. 287(45). 37926–37938. 56 indexed citations
8.
Ács, Zoltán, Dragan Chobanov, Kirill Márk Orci, et al.. (2012). Re-Visiting Phylogenetic and Taxonomic Relationships in the Genus Saga (Insecta: Orthoptera). PLoS ONE. 7(8). e42229–e42229. 8 indexed citations
9.
Hossain, Mohammad Sorowar, Anders Larsson, Nikolai Scherbak, Per‐Erik Olsson, & László Orbán. (2007). Zebrafish Androgen Receptor: Isolation, Molecular, and Biochemical Characterization1. Biology of Reproduction. 78(2). 361–369. 105 indexed citations
10.
Li, Yang, Richárd Bártfai, Alan Christoffels, et al.. (2004). Comparative analysis of the testis and ovary transcriptomes in zebrafish by combining experimental and computational tools: Research Articles. Comparative and Functional Genomics. 5(5). 403–418. 3 indexed citations
11.
Bártfai, Richárd & László Orbán. (2003). The vasa Locus in Zebrafish: Multiple RGG Boxes from Duplications. DNA and Cell Biology. 22(1). 47–54. 20 indexed citations
12.
Yue, Gen Hua, et al.. (2002). Comparison of three DNA marker systems for assessing genetic diversity in Asian arowana (Scleropages formosus). Electrophoresis. 23(7-8). 1025–1032. 32 indexed citations
13.
Yue, Gen Hua, et al.. (2000). Rapid isolation and characterization of microsatellites from the genome of Asian arowana (Scleropages formosus, Osteoglossidae, Pisces). Molecular Ecology. 9(7). 1007–1009. 83 indexed citations
14.
Zsolnai, Attila & László Orbán. (1999). Accelerated separation of random complex DNA patterns in gels: Comparing the performance of discontinuous and continuous buffers. Electrophoresis. 20(7). 1462–1468. 12 indexed citations
15.
Müller, Ferenc, Darren W. Williams, Julianna Kobolák, et al.. (1997). Activator effect of coinjected enhancers on the muscle-specific expression of promoters in zebrafish embryos. Molecular Reproduction and Development. 47(4). 404–412. 51 indexed citations
16.
Williams, Darren W., et al.. (1996). High transgene activity in the yolk syncytial layer affects quantitative transient expression assays in zebrafish (Danio rerio) embryos. Transgenic Research. 5(6). 433–442. 36 indexed citations
17.
Wheeler, David, László Orbán, Mark M. Garner, & Andreas Chrambach. (1992). Computer-aided analysis of DNA curves on transverse gradient gels. Journal of Biochemical and Biophysical Methods. 24(3-4). 171–180. 11 indexed citations
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Orbán, László, et al.. (1989). A thin-layer multistrip agarose gel electrophoresis apparatus for Ferguson plot analysis at the sub-microgram load level. Journal of Biochemical and Biophysical Methods. 19(1). 105–120. 3 indexed citations
20.
Orbán, László, et al.. (1988). An improved voltage measurement device for gel electrophoresis in tube apparatus. Electrophoresis. 9(1). 32–36. 19 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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