Ruoqian Cheng

415 total citations
26 papers, 272 citations indexed

About

Ruoqian Cheng is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Molecular Biology. According to data from OpenAlex, Ruoqian Cheng has authored 26 papers receiving a total of 272 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Molecular Biology. Recurrent topics in Ruoqian Cheng's work include Diabetes and associated disorders (5 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Genetic Syndromes and Imprinting (4 papers). Ruoqian Cheng is often cited by papers focused on Diabetes and associated disorders (5 papers), Growth Hormone and Insulin-like Growth Factors (5 papers) and Genetic Syndromes and Imprinting (4 papers). Ruoqian Cheng collaborates with scholars based in China, Qatar and Sweden. Ruoqian Cheng's co-authors include Feihong Luo, Miaoying Zhang, Chengjun Sun, Pei Zhou, Lingfeng Cao, Xi Li, Zhongyang Lu, Xiaodong Wang, Xiaojing Li and Jie Lian and has published in prestigious journals such as Fuel, Osteoporosis International and European Journal of Endocrinology.

In The Last Decade

Ruoqian Cheng

23 papers receiving 264 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ruoqian Cheng China	10	130	119	79	70	32	26	272
J. Dennis Wilson Australia	11	205 1.6×	50 0.4×	68 0.9×	374 5.3×	7 0.2×	27	502
J. Guillermo Sanchez United States	7	38 0.3×	18 0.2×	103 1.3×	69 1.0×	58 1.8×	11	240
Travis Beckett United States	10	73 0.6×	20 0.2×	63 0.8×	144 2.1×	16 0.5×	13	478
Asuka Desroches France	7	79 0.6×	35 0.3×	88 1.1×	167 2.4×	13 0.4×	12	413
Takamasa Iwaki Japan	7	67 0.5×	16 0.1×	124 1.6×	35 0.5×	34 1.1×	14	287
Carmela Felz Israel	12	41 0.3×	34 0.3×	263 3.3×	89 1.3×	6 0.2×	13	686
Gavin Anderson United Kingdom	7	197 1.5×	9 0.1×	146 1.8×	60 0.9×	18 0.6×	14	412
Katja Herde Germany	4	50 0.4×	15 0.1×	155 2.0×	109 1.6×	23 0.7×	5	345
Stephen Sullivan United States	12	52 0.4×	8 0.1×	270 3.4×	44 0.6×	43 1.3×	18	409
L Dorantes Mexico	8	238 1.8×	93 0.8×	137 1.7×	319 4.6×	8 0.3×	13	431

Countries citing papers authored by Ruoqian Cheng

Since Specialization

Citations

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

Fields of papers citing papers by Ruoqian Cheng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruoqian Cheng

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

All Works

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20 of 20 papers shown

Wu, Jing, Wei Lü, Chengjun Sun, et al.. (2025). A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody. Calcified Tissue International. 116(1). 65–65.

Guo, Haiyan, Jinrong Fu, Yufeng Zhou, Feihong Luo, & Ruoqian Cheng. (2024). Evaluating the effect of recombinant human growth hormone treatment on sleep-related breathing disorders in toddlers with Prader–Willi syndrome: a one-year retrospective cohort study. BMC Pediatrics. 24(1). 32–32. 1 indexed citations

Yuan, Meng, Yuanyuan Shan, Lin Yang, et al.. (2023). A newborn with a pathogenic variant in ASXL2 expanding the phenotype of SHAPNS: a case report and literature review. Translational Pediatrics. 12(1). 86–96. 3 indexed citations

Cheng, Ruoqian, Yanqin Ying, Zhengqing Qiu, et al.. (2022). Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome. World Journal of Pediatrics. 19(5). 438–449. 9 indexed citations

Cheng, Ruoqian, et al.. (2022). Population pharmacokinetic/pharmacodynamic analysis of PEG-rhGH enhances confidence in exploring dosing schemes with longer intervals. European Journal of Pharmaceutical Sciences. 179. 106304–106304. 2 indexed citations

Yang, Lin, Bo Liu, Xinran Dong, et al.. (2022). Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects. Osteoporosis International. 33(6). 1373–1384. 7 indexed citations

Li, Xiaojing, et al.. (2021). Clinical risk score for central precocious puberty among girls with precocious pubertal development: a cross sectional study. BMC Endocrine Disorders. 21(1). 75–75. 4 indexed citations

Lu, Wei, Xi Li, Xiaojing Li, et al.. (2021). Genetic aetiology of primary adrenal insufficiency in Chinese children. BMC Medical Genomics. 14(1). 172–172. 5 indexed citations

Zhang, Miaoying, Chengjun Sun, Renchao Liu, et al.. (2020). Phenotypes and epigenetic errors in patients with Beckwith-Wiedemann syndrome in China. Translational Pediatrics. 9(5). 653–661. 3 indexed citations

10.

Yan, Zhifeng, Jie Lian, Yu Feng, et al.. (2020). A mechanistic insight into glucose conversion in subcritical water: Complex reaction network and the effects of acid-base catalysis. Fuel. 289. 119969–119969. 30 indexed citations

11.

Zhu, Xiaoyi, Wei Lü, Weihua Sun, et al.. (2020). Altered Serum Amino Acid and Acylcarnitine Profiles in Hyperinsulinemic Hypoglycemia and Ketotic Hypoglycemia. Frontiers in Endocrinology. 11. 577373–577373. 3 indexed citations

12.

Ge, Jingjie, Miaoying Zhang, Khalid Hussain, et al.. (2019). Genotype and phenotype analysis of a cohort of patients with congenital hyperinsulinism based on DOPA-PET CT scanning. European Journal of Pediatrics. 178(8). 1161–1169. 14 indexed citations

13.

Cheng, Ruoqian, et al.. (2019). Clinical characteristics and beta-cell function of Chinese children and adolescents with type 2 diabetes from 2009 to 2018. World Journal of Pediatrics. 15(4). 405–411. 9 indexed citations

14.

Zhang, Miaoying, Xiaojing Li, Xi Li, et al.. (2018). Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: A Rare Association in Chinese Children.

15.

Sun, Chengjun, Zeyi Zhou, Bingbing Wu, et al.. (2018). Novel aggrecan variant, p. Gln2364Pro, causes severe familial nonsyndromic adult short stature and poor growth hormone response in Chinese children. BMC Medical Genetics. 19(1). 79–79. 15 indexed citations

16.

Sun, Chengjun, Pei Zhou, Miaoying Zhang, et al.. (2017). Recovered insulin production after thiamine administration in permanent neonatal diabetes mellitus with a novel solute carrier family 19 member 2 (SLC19A2) mutation. Journal of Diabetes. 10(1). 50–58. 7 indexed citations

17.

Sun, Chengjun, Haiyan Wei, Xiuli Chen, et al.. (2016). ERBB3 -rs2292239 as primary type 1 diabetes association locus among non- HLA genes in Chinese. Meta Gene. 9. 120–123. 12 indexed citations

18.

Gao, Lingling, Lingfeng Cao, Yi Yang, et al.. (2011). The growth hormone receptor (GHR) exon 3 polymorphism and its correlation with metabolic profiles in obese Chinese children. Pediatric Diabetes. 12(4pt2). 429–434. 15 indexed citations

19.

Cao, Lingfeng, Wieland Kieß, Rong Ye, et al.. (2007). Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus. European Journal of Endocrinology. 157(6). 783–787. 15 indexed citations

20.

Wu, Xiaoning, et al.. (2004). Cluster Analysis of 12 Chinese Native Chicken Populations Using Microsatellite Markers. Asian-Australasian Journal of Animal Sciences. 17(8). 1047–1052. 28 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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