Fang‐Ting Kuo

548 total citations
12 papers, 388 citations indexed

About

Fang‐Ting Kuo is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Fang‐Ting Kuo has authored 12 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Public Health, Environmental and Occupational Health and 4 papers in Genetics. Recurrent topics in Fang‐Ting Kuo's work include FOXO transcription factor regulation (7 papers), Reproductive Biology and Fertility (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Fang‐Ting Kuo is often cited by papers focused on FOXO transcription factor regulation (7 papers), Reproductive Biology and Fertility (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Fang‐Ting Kuo collaborates with scholars based in United States, Taiwan and South Korea. Fang‐Ting Kuo's co-authors include Margareta D. Pisarska, Gillian M. Barlow, Salma Khan, Hua‐Wen Fu, Te‐Ling Lu, JoAnne S. Richards, Tomoko Kawai, Zhilin Liu, Kenneth L. Fan and Masayuki Shimada and has published in prestigious journals such as FEBS Letters, Endocrinology and American Journal of Physiology-Endocrinology and Metabolism.

In The Last Decade

Fang‐Ting Kuo

12 papers receiving 386 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fang‐Ting Kuo United States	10	205	145	136	96	48	12	388
Hajime Oishi Japan	10	107 0.5×	98 0.7×	73 0.5×	158 1.6×	28 0.6×	27	442
Man‐Xi Jiang China	13	388 1.9×	271 1.9×	94 0.7×	118 1.2×	17 0.4×	44	543
Hanni Ke China	14	322 1.6×	369 2.5×	181 1.3×	252 2.6×	43 0.9×	22	747
Cheryl A. Nechamen United States	11	327 1.6×	125 0.9×	188 1.4×	320 3.3×	28 0.6×	12	576
Y. Sangeeta Devi United States	11	113 0.6×	64 0.4×	105 0.8×	91 0.9×	15 0.3×	14	348
Iris Keren-Tal Israel	9	179 0.9×	236 1.6×	126 0.9×	190 2.0×	14 0.3×	12	460
Heli Jokela Finland	9	132 0.6×	32 0.2×	130 1.0×	53 0.6×	44 0.9×	10	320
Anita Weinberg Australia	9	147 0.7×	180 1.2×	162 1.2×	227 2.4×	13 0.3×	10	538
Nicholas M. Robert Canada	12	261 1.3×	100 0.7×	290 2.1×	92 1.0×	11 0.2×	18	503
Marie-Charlotte Meinsohn United States	12	161 0.8×	163 1.1×	121 0.9×	106 1.1×	8 0.2×	15	369

Countries citing papers authored by Fang‐Ting Kuo

Since Specialization

Citations

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

Fields of papers citing papers by Fang‐Ting Kuo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fang‐Ting Kuo

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

All Works

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12 of 12 papers shown

Kuo, Fang‐Ting, et al.. (2019). Endocytosis‐dependent lysosomal degradation of Src induced by protease‐activated receptor 1. FEBS Letters. 593(5). 504–517. 1 indexed citations

Richards, JoAnne S., Zhilin Liu, Tomoko Kawai, et al.. (2012). Adiponectin and its receptors modulate granulosa cell and cumulus cell functions, fertility, and early embryo development in the mouse and human. Fertility and Sterility. 98(2). 471–479.e1. 73 indexed citations

Kuo, Fang‐Ting, et al.. (2012). Mouse forkhead L2 maintains repression of FSH-dependent genes in the granulosa cell. Reproduction. 144(4). 485–494. 26 indexed citations

Kuo, Fang‐Ting, et al.. (2011). Relative expression of genes encoding SMAD signal transduction factors in human granulosa cells is correlated with oocyte quality. Journal of Assisted Reproduction and Genetics. 28(10). 931–938. 22 indexed citations

Kuo, Fang‐Ting, et al.. (2011). Mutant Forkhead L2 (FOXL2) Proteins Associated with Premature Ovarian Failure (POF) Dimerize with Wild-Type FOXL2, Leading to Altered Regulation of Genes Associated with Granulosa Cell Differentiation. Endocrinology. 152(10). 3917–3929. 38 indexed citations

Pisarska, Margareta D., Gillian M. Barlow, & Fang‐Ting Kuo. (2011). Minireview: Roles of the Forkhead Transcription Factor FOXL2 in Granulosa Cell Biology and Pathology. Endocrinology. 152(4). 1199–1208. 84 indexed citations

Pisarska, Margareta D., et al.. (2010). LATS1 phosphorylates forkhead L2 and regulates its transcriptional activity. American Journal of Physiology-Endocrinology and Metabolism. 299(1). E101–E109. 44 indexed citations

Kuo, Fang‐Ting, et al.. (2009). Sumoylation of Forkhead L2 by Ubc9 is required for its activity as a transcriptional repressor of the Steroidogenic Acute Regulatory gene. Cellular Signalling. 21(12). 1935–1944. 33 indexed citations

Pisarska, Margareta D., et al.. (2008). Expression of forkhead transcription factors in human granulosa cells. Fertility and Sterility. 91(4). 1392–1394. 28 indexed citations

10.

Pisarska, Margareta D., et al.. (2007). Forkhead L2 (FOXL2), a gene associated with premature ovarian failure is likely regulated through phosphorylation. Fertility and Sterility. 88. S168–S168. 1 indexed citations

11.

Kuo, Fang‐Ting, Te‐Ling Lu, & Hua‐Wen Fu. (2006). Opposing effects of β-arrestin1 and β-arrestin2 on activation and degradation of Src induced by protease-activated receptor 1. Cellular Signalling. 18(11). 1914–1923. 21 indexed citations

12.

Lu, Te‐Ling, et al.. (2006). Negative regulation of protease-activated receptor 1-induced Src kinase activity by the association of phosphocaveolin-1 with Csk. Cellular Signalling. 18(11). 1977–1987. 17 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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