Ruen Yao

1.0k total citations
64 papers, 657 citations indexed

About

Ruen Yao is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Ruen Yao has authored 64 papers receiving a total of 657 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 31 papers in Genetics and 6 papers in Hematology. Recurrent topics in Ruen Yao's work include Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital heart defects research (8 papers). Ruen Yao is often cited by papers focused on Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital heart defects research (8 papers). Ruen Yao collaborates with scholars based in China, United States and United Kingdom. Ruen Yao's co-authors include Niu Li, Jian Wang, Tingting Yu, Yiping Shen, Xiumin Wang, Yufei Xu, Yongguo Yu, Xuyun Hu, Yu Ding and Xiaodong Huang and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ruen Yao

61 papers receiving 648 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruen Yao China 15 385 334 61 55 44 64 657
Erik-Jan Kamsteeg Netherlands 15 425 1.1× 320 1.0× 84 1.4× 60 1.1× 65 1.5× 21 874
Flavio Faletra Italy 15 251 0.7× 267 0.8× 30 0.5× 58 1.1× 59 1.3× 84 649
Sahar Mansour United Kingdom 11 575 1.5× 288 0.9× 47 0.8× 39 0.7× 81 1.8× 15 854
Luitgard Graul‐Neumann Germany 19 539 1.4× 457 1.4× 37 0.6× 31 0.6× 97 2.2× 46 884
Rocío Acuña‐Hidalgo United States 7 443 1.2× 340 1.0× 162 2.7× 77 1.4× 23 0.5× 8 824
Tawfeg Ben‐Omran Qatar 11 353 0.9× 225 0.7× 47 0.8× 19 0.3× 43 1.0× 24 584
Ender Karaca Türkiye 13 265 0.7× 247 0.7× 31 0.5× 63 1.1× 41 0.9× 25 544
Marcello Niceta Italy 18 489 1.3× 304 0.9× 35 0.6× 24 0.4× 60 1.4× 53 810
Pagon Ra United States 6 450 1.2× 260 0.8× 23 0.4× 19 0.3× 55 1.3× 291 791
Meena Balasubramanian United Kingdom 18 310 0.8× 555 1.7× 50 0.8× 45 0.8× 79 1.8× 74 802

Countries citing papers authored by Ruen Yao

Since Specialization
Citations

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

Fields of papers citing papers by Ruen Yao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruen Yao

This figure shows the co-authorship network connecting the top 25 collaborators of Ruen Yao. A scholar is included among the top collaborators of Ruen Yao 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 Ruen Yao. Ruen Yao 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.
Chen, Yiwei, Jinjin Wu, Hao Chen, et al.. (2024). Clinical and Genetic Profile of Chinese Children With Danon Disease: A Single-Center Retrospective Cohort Study. Canadian Journal of Cardiology. 41(1). 89–101.
2.
Gao, Shiyang, Yu Ding, Zhiying Li, et al.. (2024). Molecular and phenotypic characteristics of Bardet-Biedl syndrome in Chinese patients. Orphanet Journal of Rare Diseases. 19(1). 149–149. 2 indexed citations
3.
4.
Yu, Tingting, et al.. (2023). Two patients with KDM3B variants and new presentations of Diets–Jongmans syndrome. Neurogenetics. 24(2). 95–101. 2 indexed citations
5.
Zhang, Jiasheng, et al.. (2023). SINE-VNTR-Alu retrotransposon insertion as a novel mutational event underlying Glanzmann thrombasthenia. Journal of Thrombosis and Haemostasis. 21(12). 3597–3607. 3 indexed citations
6.
Li, Xin, Yirou Wang, Ruen Yao, et al.. (2023). Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients. Orphanet Journal of Rare Diseases. 18(1). 284–284. 3 indexed citations
7.
Li, Xin, Xia Qin, Miao Yan, et al.. (2023). Germline Neurofibromin 1 mutation enhances the anti‐tumour immune response and decreases juvenile myelomonocytic leukaemia tumourigenicity. British Journal of Haematology. 202(2). 328–343. 4 indexed citations
8.
Yao, Ruen, Qun Li, Xin Li, et al.. (2021). A novel homozygous variant of COL2A1 in a Chinese male with type II collagenopathy: a case report. BMC Medical Genomics. 14(1). 201–201. 2 indexed citations
9.
Li, Niu, Jing Wu, Yufen Wu, et al.. (2020). Further delineation of primary B cell immunodeficiency caused by novel variants of the BLNK gene in two Chinese patients. Clinical Immunology. 214. 108387–108387. 2 indexed citations
10.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients. Clinical Genetics. 96(4). 290–299. 32 indexed citations
11.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients. 2 indexed citations
12.
Xu, Yufei, Yirou Wang, Niu Li, et al.. (2019). New insights from unbiased panel and whole-exome sequencing in a large Chinese cohort with disorders of sex development. European Journal of Endocrinology. 181(3). 311–323. 20 indexed citations
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15.
Yao, Ruen, Cheng Zhang, Tingting Yu, et al.. (2017). Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data. Molecular Cytogenetics. 10(1). 30–30. 67 indexed citations
16.
Fan, Yanjie, Lili Wang, Ruen Yao, et al.. (2016). Copy number variations in 119 Chinese children with idiopathic short stature identified by the custom genome-wide microarray. Molecular Cytogenetics. 9(1). 16–16. 13 indexed citations
17.
Yu, Yongguo, Ruen Yao, Lili Wang, et al.. (2015). De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature. BMC Genomics. 16(1). 701–701. 20 indexed citations
18.
Li, Huimin, et al.. (2014). A Novel and a Previously Described Compound HeterozygousPKLRGene Mutations Causing Pyruvate Kinase Deficiency in a Chinese Child. Fetal and Pediatric Pathology. 33(3). 182–190. 5 indexed citations
19.
20.
Geng, Juan, Jian Wang, Ruen Yao, Xiaoqing Liu, & Qihua Fu. (2012). Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease. World Journal of Pediatrics. 9(2). 158–162. 8 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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