Guoying Chang

427 total citations
41 papers, 258 citations indexed

About

Guoying Chang is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Guoying Chang has authored 41 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 20 papers in Molecular Biology and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Guoying Chang's work include Genetic Syndromes and Imprinting (7 papers), Genomics and Rare Diseases (6 papers) and Growth Hormone and Insulin-like Growth Factors (6 papers). Guoying Chang is often cited by papers focused on Genetic Syndromes and Imprinting (7 papers), Genomics and Rare Diseases (6 papers) and Growth Hormone and Insulin-like Growth Factors (6 papers). Guoying Chang collaborates with scholars based in China, United States and Australia. Guoying Chang's co-authors include Yu Ding, Niu Li, Jian Wang, Xiumin Wang, Yiping Shen, Tingting Yu, Ruen Yao, Xiumin Wang, Xin Li and Yufei Xu and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Guoying Chang

35 papers receiving 253 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guoying Chang China 10 157 117 35 30 27 41 258
Tinka Hovnik Slovenia 10 132 0.8× 91 0.8× 81 2.3× 30 1.0× 9 0.3× 25 290
Adam C. Gunning United Kingdom 7 179 1.1× 151 1.3× 24 0.7× 17 0.6× 36 1.3× 12 291
Sandra Corbani Lebanon 10 225 1.4× 163 1.4× 63 1.8× 88 2.9× 29 1.1× 23 387
Zhangzhang Lan China 8 202 1.3× 103 0.9× 11 0.3× 14 0.5× 33 1.2× 16 304
Adi Har‐Zahav Israel 8 139 0.9× 65 0.6× 11 0.3× 54 1.8× 26 1.0× 14 256
Rana Chakrabarti Canada 5 146 0.9× 25 0.2× 16 0.5× 41 1.4× 39 1.4× 7 227
Arístides López‐Márquez Spain 6 197 1.3× 67 0.6× 158 4.5× 29 1.0× 38 1.4× 14 321
Ellen Schofield United Kingdom 7 105 0.7× 148 1.3× 17 0.5× 33 1.1× 22 0.8× 12 256
Danielle Gattis United States 9 247 1.6× 30 0.3× 20 0.6× 21 0.7× 59 2.2× 9 383
Ruqaiah Altassan Saudi Arabia 10 142 0.9× 63 0.5× 8 0.2× 24 0.8× 13 0.5× 24 229

Countries citing papers authored by Guoying Chang

Since Specialization
Citations

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

Fields of papers citing papers by Guoying Chang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guoying Chang

This figure shows the co-authorship network connecting the top 25 collaborators of Guoying Chang. A scholar is included among the top collaborators of Guoying Chang 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 Guoying Chang. Guoying Chang 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.
Ding, Yu, Shiyang Gao, Guoying Chang, et al.. (2025). Focusing on Rare Variants Related to Maturity‐Onset Diabetes of the Young in Children. Pediatric Diabetes. 2025(1). 8155443–8155443.
2.
Baig, Shanat, Gabriela da Silva Xavier, Charlotte Dawson, et al.. (2025). Defining Puberty and Spectrum of Hypogonadism in Alström Syndrome. The Journal of Clinical Endocrinology & Metabolism. 111(1). 33–44.
3.
Gao, Shiyang, et al.. (2024). Obesity-Related Ciliopathies: Focus on Advances of Biomarkers. International Journal of Molecular Sciences. 25(15). 8484–8484. 1 indexed citations
4.
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
5.
Ying, Lingwen, Fan Yang, Xin Li, et al.. (2024). Screening/diagnosis of pediatric endocrine disorders through the artificial intelligence model in different language settings. European Journal of Pediatrics. 183(6). 2655–2661. 5 indexed citations
6.
7.
Xu, Lei, Yirou Wang, Qianwen Zhang, et al.. (2023). [Clinical characteristics and genetic analysis of a patient with STISS syndrome due to variant of PSMD12 gene].. PubMed. 40(3). 349–353. 1 indexed citations
8.
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
9.
Yang, Fan, et al.. (2023). Clinical and Molecular Characterization of a Patient with Generalized Arterial Calcification of Infancy Caused by Rare ABCC6 Mutation. Journal of Personalized Medicine. 14(1). 54–54. 1 indexed citations
10.
Chang, Guoying, Yijun Tang, Yu Ding, et al.. (2023). Genotypic and phenotypic features of dyslipidemia in a sample of pediatric patients in China. BMC Pediatrics. 23(1).
11.
Chang, Guoying, Xin Li, Yijun Tang, et al.. (2022). A novel CEP57 variant associated with mosaic variegated aneuploidy syndrome in a Chinese female presenting with short stature, microcephaly, brachydactyly, and small teeth. Molecular Genetics & Genomic Medicine. 10(6). e1951–e1951. 4 indexed citations
12.
Chang, Guoying, Xin Li, Jian Wang, et al.. (2022). Diagnosis of patients with mucopolysaccharidosis type II via RNA sequencing. Clinica Chimica Acta. 537. 38–45. 1 indexed citations
13.
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
14.
Ding, Yu, Niu Li, Dan Lou, et al.. (2020). Clinical and genetic analysis in a Chinese cohort of children and adolescents with diabetes/persistent hyperglycemia. Journal of Diabetes Investigation. 12(1). 48–62. 7 indexed citations
15.
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
16.
Li, Xin, Ruen Yao, Xin Tan, et al.. (2019). Molecular and Phenotypic Spectrum of Noonan Syndrome in Chinese Patients. 2 indexed citations
17.
18.
Chang, Guoying, Juan Li, Jian Wang, et al.. (2017). Novel compound heterozygous mutations of the PCNT gene in one Chinese boy with microcephalic osteodysplastic primordial dwarfism type II: case report and literature review. Zhonghua neifenmi daixie zazhi. 33(1). 47–51. 1 indexed citations
19.
Chang, Guoying, Rui Yang, Yanan Cao, et al.. (2016). SIDT2 is involved in the NAADP-mediated release of calcium from insulin secretory granules. Journal of Molecular Endocrinology. 56(3). 249–259. 14 indexed citations
20.
Yu, Tingting, J Li, Yu Ding, et al.. (2016). Obesity and developmental delay in a patient with uniparental disomy of chromosome 2. International Journal of Obesity. 40(12). 1935–1941. 11 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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