Pao‐Lin Kuo

4.7k total citations
178 papers, 3.4k citations indexed

About

Pao‐Lin Kuo is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Pao‐Lin Kuo has authored 178 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Genetics, 58 papers in Molecular Biology and 56 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Pao‐Lin Kuo's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (40 papers), Sperm and Testicular Function (40 papers) and Prenatal Screening and Diagnostics (30 papers). Pao‐Lin Kuo is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (40 papers), Sperm and Testicular Function (40 papers) and Prenatal Screening and Diagnostics (30 papers). Pao‐Lin Kuo collaborates with scholars based in Taiwan, United States and India. Pao‐Lin Kuo's co-authors include Ying‐Hung Lin, Po‐Chin Huang, Chao‐Chin Hsu, Yung-Ming Lin, Yen‐Ni Teng, Mei‐Tsz Su, Mei-Tsz Su, Yue Leon Guo, Pao‐Chi Liao and Yung‐Che Kuo and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Pao‐Lin Kuo

175 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pao‐Lin Kuo Taiwan 32 1.1k 1.1k 1.0k 743 602 178 3.4k
Patrick Fénichel France 38 1.2k 1.1× 713 0.7× 1.1k 1.1× 725 1.0× 359 0.6× 142 4.0k
Sarah Kimmins Canada 30 2.2k 2.0× 871 0.8× 873 0.9× 790 1.1× 552 0.9× 67 4.0k
Y. Taketani Japan 34 1.1k 1.0× 499 0.5× 1.1k 1.1× 753 1.0× 328 0.5× 148 4.4k
Richard G. Lea United Kingdom 38 685 0.6× 456 0.4× 702 0.7× 824 1.1× 1.2k 2.0× 88 4.0k
Margrit Urbanek United States 37 1.1k 1.0× 1.2k 1.1× 2.1k 2.1× 1.7k 2.3× 335 0.6× 72 4.6k
Serdar Coşkun Saudi Arabia 27 627 0.6× 463 0.4× 980 1.0× 1.2k 1.6× 781 1.3× 82 2.3k
Takahiro Arima Japan 34 2.4k 2.1× 1.2k 1.1× 639 0.6× 847 1.1× 1.8k 2.9× 137 4.4k
Haengseok Song South Korea 29 989 0.9× 444 0.4× 1.3k 1.3× 897 1.2× 352 0.6× 102 3.5k
Isao Tamura Japan 29 806 0.7× 323 0.3× 1.0k 1.0× 717 1.0× 393 0.7× 100 2.7k
S. Hamamah France 40 1.8k 1.6× 770 0.7× 2.7k 2.6× 2.7k 3.7× 1.3k 2.2× 216 5.7k

Countries citing papers authored by Pao‐Lin Kuo

Since Specialization
Citations

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

Fields of papers citing papers by Pao‐Lin Kuo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pao‐Lin Kuo

This figure shows the co-authorship network connecting the top 25 collaborators of Pao‐Lin Kuo. A scholar is included among the top collaborators of Pao‐Lin 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 Pao‐Lin Kuo. Pao‐Lin Kuo 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.
Wang, Han‐Yu, et al.. (2025). SEPT14 complexes maintain sperm morphogenesis and function. The FASEB Journal. 39(4). e70414–e70414. 1 indexed citations
2.
Chou, Yen‐Yin, Pao‐Lin Kuo, Hui‐Pin Hsiao, et al.. (2024). Syndromic ciliopathy: a taiwanese single-center study. BMC Medical Genomics. 17(1). 106–106. 1 indexed citations
3.
Chang, Kung‐Chao, Yi‐Shan Tsai, Yao‐Jong Yang, et al.. (2021). Variants in Maternal Effect Genes and Relaxed Imprinting Control in a Special Placental Mesenchymal Dysplasia Case with Mild Trophoblast Hyperplasia. Biomedicines. 9(5). 544–544. 6 indexed citations
4.
Chang, Wei‐Hsiang, Wei‐Chun Chou, Alexander Waits, et al.. (2021). Cumulative risk assessment of phthalates exposure for recurrent pregnancy loss in reproductive-aged women population using multiple hazard indices approaches. Environment International. 154. 106657–106657. 21 indexed citations
5.
Waits, Alexander, Hsin‐Chang Chen, Pao‐Lin Kuo, et al.. (2020). Urinary phthalate metabolites are associated with biomarkers of DNA damage and lipid peroxidation in pregnant women – Tainan Birth Cohort Study (TBCS). Environmental Research. 188. 109863–109863. 38 indexed citations
6.
Wang, Chia‐Yih, Pei‐Yin Tsai, Ting‐Yu Chen, et al.. (2019). Elevated miR‐200a and miR‐141 inhibit endocrine gland‐derived vascular endothelial growth factor expression and ciliogenesis in preeclampsia. The Journal of Physiology. 597(12). 3069–3083. 41 indexed citations
7.
Kuo, Pao‐Lin, et al.. (2014). Prenatal diagnosis of Prader–Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11‐q13. International Journal of Gynecology & Obstetrics. 125(1). 18–21. 5 indexed citations
8.
Lai, Yi-Chun, et al.. (2012). Human sex ratio at amniocentesis and at birth in Taiwan. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 572–575. 7 indexed citations
9.
Su, Mei‐Tsz, et al.. (2010). Gestational diabetes and central pontine myelinolysis with quadriplegia: A case report. The Journal of Maternal-Fetal & Neonatal Medicine. 23(7). 728–731. 8 indexed citations
10.
Lin, Ying‐Hung, Yung-Ming Lin, Yayun Wang, et al.. (2009). The Expression Level of Septin12 Is Critical for Spermiogenesis. American Journal Of Pathology. 174(5). 1857–1868. 80 indexed citations
11.
Teng, Yen‐Ni, et al.. (2009). Histone gene expression profile during spermatogenesis. Fertility and Sterility. 93(7). 2447–2449. 7 indexed citations
12.
Kuo, Pao‐Lin, et al.. (2008). Association of Extremely Skewed X-chromosome Inactivation with Taiwanese Women Presenting with Recurrent Pregnancy Loss. Journal of the Formosan Medical Association. 107(4). 340–343. 13 indexed citations
13.
Kuo, Pao‐Lin, William J. Huang, Han‐Sun Chiang, et al.. (2007). Partial duplication atAZFcon the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan. Human Mutation. 28(5). 486–494. 83 indexed citations
14.
Kuo, Pao‐Lin, Chao‐Chin Hsu, P. H. Vogt, et al.. (2005). Polymorphisms associated with the DAZ genes on the human Y chromosome. Genomics. 86(4). 431–438. 34 indexed citations
15.
16.
Kuo, Pao‐Lin, Shan‐Tair Wang, Yung-Ming Lin, et al.. (2004). Expression profiles of the DAZ gene family in human testis with and without spermatogenic failure. Fertility and Sterility. 81(4). 1034–1040. 32 indexed citations
17.
Kuo, Pao‐Lin, et al.. (2003). Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations. Prenatal Diagnosis. 23(2). 134–137. 12 indexed citations
18.
Chang, Kong‐Chao, et al.. (2002). Adrenal myelolipoma with translocation (3;21)(q25;p11). Cancer Genetics and Cytogenetics. 134(1). 77–80. 66 indexed citations
19.
Tzeng, Cherng-Chyi, et al.. (2001). An Effective Strategy of Using Molecular Testing to Screen Mentally Retarded Individuals for Fragile X Syndrome. Diagnostic Molecular Pathology. 10(1). 34–40. 6 indexed citations
20.
Wu, Meng‐Hsing, Pao‐Lin Kuo, & Shio‐Jean Lin. (1995). Prenatal diagnosis of recurrence of short rib‐polydactyly syndrome. American Journal of Medical Genetics. 55(3). 279–284. 14 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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