Chau‐Ti Ting

3.1k total citations
30 papers, 2.0k citations indexed

About

Chau‐Ti Ting is a scholar working on Genetics, Ecology, Evolution, Behavior and Systematics and Molecular Biology. According to data from OpenAlex, Chau‐Ti Ting has authored 30 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Ecology, Evolution, Behavior and Systematics and 9 papers in Molecular Biology. Recurrent topics in Chau‐Ti Ting's work include Genetic diversity and population structure (11 papers), Plant and animal studies (9 papers) and Animal Behavior and Reproduction (6 papers). Chau‐Ti Ting is often cited by papers focused on Genetic diversity and population structure (11 papers), Plant and animal studies (9 papers) and Animal Behavior and Reproduction (6 papers). Chau‐Ti Ting collaborates with scholars based in Taiwan, United States and Russia. Chau‐Ti Ting's co-authors include Chung‐I Wu, Shun-Chern Tsaur, Hope Hollocher, Aya Takahashi, Sha Sun, Chung-I Wu, Leonie C. Moyle, Kyoichi Sawamura, Artyom Kopp and Cheng‐Ruei Lee and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and PLoS ONE.

In The Last Decade

Chau‐Ti Ting

30 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chau‐Ti Ting Taiwan 17 1.4k 703 700 411 289 30 2.0k
James R. Walters United States 25 1.3k 0.9× 608 0.9× 613 0.9× 377 0.9× 510 1.8× 44 1.9k
Marta L. Wayne United States 20 1.1k 0.8× 748 1.1× 477 0.7× 308 0.7× 314 1.1× 58 2.0k
Colin D. Meiklejohn United States 23 1.6k 1.1× 1.2k 1.7× 559 0.8× 422 1.0× 314 1.1× 26 2.5k
José M. Ranz United States 18 1.4k 1.0× 1.2k 1.7× 450 0.6× 732 1.8× 301 1.0× 42 2.2k
John E. Pool United States 27 1.6k 1.1× 776 1.1× 621 0.9× 401 1.0× 438 1.5× 48 2.4k
Raymond Tobler Australia 19 1.1k 0.8× 512 0.7× 337 0.5× 276 0.7× 200 0.7× 32 1.8k
Brian A. Counterman United States 22 1.4k 1.0× 523 0.7× 1.1k 1.6× 299 0.7× 180 0.6× 44 2.0k
Tim Connallon Australia 28 1.5k 1.1× 456 0.6× 1.1k 1.5× 251 0.6× 254 0.9× 73 2.2k
Shun-Chern Tsaur Taiwan 11 885 0.6× 448 0.6× 507 0.7× 219 0.5× 285 1.0× 22 1.3k
Hope Hollocher United States 19 771 0.5× 329 0.5× 563 0.8× 227 0.6× 299 1.0× 48 1.3k

Countries citing papers authored by Chau‐Ti Ting

Since Specialization
Citations

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

Fields of papers citing papers by Chau‐Ti Ting

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chau‐Ti Ting. 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 Chau‐Ti Ting. The network helps show where Chau‐Ti Ting may publish in the future.

Co-authorship network of co-authors of Chau‐Ti Ting

This figure shows the co-authorship network connecting the top 25 collaborators of Chau‐Ti Ting. A scholar is included among the top collaborators of Chau‐Ti Ting 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 Chau‐Ti Ting. Chau‐Ti Ting 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.
Lin, Ya‐Ping, Hung‐Wei Chen, Juan Li, et al.. (2023). Demographic history and distinct selection signatures of two domestication genes in mungbean. PLANT PHYSIOLOGY. 193(2). 1197–1212. 10 indexed citations
2.
Lin, Ya‐Ping, Hung‐Wei Chen, М. О. Burlyaeva, et al.. (2023). Environment as a limiting factor of the historical global spread of mungbean. eLife. 12. 13 indexed citations
3.
Lee, Cheng‐Ruei, Chau‐Ti Ting, Roland Schafleitner, et al.. (2021). Modeling of Flowering Time in Vigna radiata with Approximate Bayesian Computation. Agronomy. 11(11). 2317–2317. 2 indexed citations
4.
Kozlov, Konstantin, Cheng‐Ruei Lee, Chau‐Ti Ting, et al.. (2020). Dynamical climatic model for time to flowering in Vigna radiata. BMC Plant Biology. 20(S1). 202–202. 7 indexed citations
5.
Burlyaeva, М. О., M. A. Vishnyаkova, Cheng‐Ruei Lee, et al.. (2019). Collections of Mungbean [Vigna radiata) (L.) R. Wilczek] and urdbean [V. mungo (L.) Hepper] in Vavilov Institute (VIR): traits diversity and trends in the breeding process over the last 100 years. Genetic Resources and Crop Evolution. 66(4). 767–781. 11 indexed citations
6.
Chen, Chih-Kuan, Chun-Ping Yu, Sung‐Chou Li, et al.. (2017). Identification and evolutionary analysis of long non-coding RNAs in zebra finch. BMC Genomics. 18(1). 117–117. 11 indexed citations
7.
Chen, Chih-Kuan, Chen Siang Ng, Ping Wu, et al.. (2016). Regulatory Differences in Natal Down Development between Altricial Zebra Finch and Precocial Chicken. Molecular Biology and Evolution. 33(8). 2030–2043. 13 indexed citations
8.
Chang, Chia‐Chen, et al.. (2014). The Persistence of Facultative Parthenogenesis in Drosophila albomicans. PLoS ONE. 9(11). e113275–e113275. 16 indexed citations
9.
Yang, Haiwang, Bin He, Shun-Chern Tsaur, et al.. (2014). Expression Profile and Gene Age Jointly Shaped the Genome-Wide Distribution of Premature Termination Codons in a Drosophila melanogaster Population. Molecular Biology and Evolution. 32(1). 216–228. 15 indexed citations
10.
Sawamura, Kyoichi, Chau‐Ti Ting, Artyom Kopp, & Leonie C. Moyle. (2012). Mechanisms of Speciation. PubMed. 2012. 1–2. 64 indexed citations
11.
Poh, Yu-Ping, Chau‐Ti Ting, Hua‐Wen Fu, Charles H. Langley, & David J Begun. (2012). Population Genomic Analysis of Base Composition Evolution in Drosophila melanogaster. Genome Biology and Evolution. 4(12). 1245–1255. 15 indexed citations
12.
Lu, Xuemei, Joshua A. Shapiro, Chau‐Ti Ting, et al.. (2010). Genome-wide misexpression of X-linked versus autosomal genes associated with hybrid male sterility. Genome Research. 20(8). 1097–1102. 31 indexed citations
13.
Fang, Shu, et al.. (2009). Molecular Evolution and Functional Diversification of Fatty Acid Desaturases after Recurrent Gene Duplication in Drosophila. Molecular Biology and Evolution. 26(7). 1447–1456. 48 indexed citations
14.
Ting, Chau‐Ti, Shun-Chern Tsaur, Sha Sun, et al.. (2004). Gene duplication and speciation in Drosophila : Evidence from the Odysseus locus. Proceedings of the National Academy of Sciences. 101(33). 12232–12235. 62 indexed citations
15.
Takahashi, Aya & Chau‐Ti Ting. (2004). Genetic Basis of Sexual Isolation in Drosophila melanogaster. Genetica. 120(1-3). 273–284. 18 indexed citations
16.
Wu, Chung‐I & Chau‐Ti Ting. (2004). Genes and speciation. Nature Reviews Genetics. 5(2). 114–122. 386 indexed citations
17.
Tsaur, Shun-Chern, Chau‐Ti Ting, & Chung-I Wu. (2001). Sex in Drosophila mauritiana: A Very High Level of Amino Acid Polymorphism in a Male Reproductive Protein Gene, Acp26Aa. Molecular Biology and Evolution. 18(1). 22–26. 33 indexed citations
18.
Ting, Chau‐Ti, Aya Takahashi, & Chung‐I Wu. (2001). Incipient speciation by sexual isolation in Drosophila : Concurrent evolution at multiple loci. Proceedings of the National Academy of Sciences. 98(12). 6709–6713. 114 indexed citations
19.
Tsaur, Shun-Chern, Chau‐Ti Ting, & Chung‐I Wu. (1998). Positive selection driving the evolution of a gene of male reproduction, Acp26Aa, of Drosophila: II. Divergence versus polymorphism. Molecular Biology and Evolution. 15(8). 1040–1046. 120 indexed citations
20.
Hollocher, Hope, et al.. (1997). INCIPIENT SPECIATION BY SEXUAL ISOLATION INDROSOPHILA MELANOGASTER: VARIATION IN MATING PREFERENCE AND CORRELATION BETWEEN SEXES. Evolution. 51(4). 1175–1181. 85 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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