Juan Geng

1.2k total citations
43 papers, 856 citations indexed

About

Juan Geng is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Juan Geng has authored 43 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 17 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Juan Geng's work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (7 papers) and Prenatal Screening and Diagnostics (6 papers). Juan Geng is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (7 papers) and Prenatal Screening and Diagnostics (6 papers). Juan Geng collaborates with scholars based in China, United States and Ecuador. Juan Geng's co-authors include Carl Nathan, Neio Boéchat, Richard A. Mumford, William N. Rom, John L. Ho, José Roberto Lapa e Silva, Jeffrey R. Weidner, Q W Xie, Maria da Glória Bonecini-Almeida and Jimmy Calaycay and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Immunology and PLoS ONE.

In The Last Decade

Juan Geng

38 papers receiving 839 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Juan Geng China 14 329 209 199 168 154 43 856
Darko Richter Germany 19 328 1.0× 102 0.5× 187 0.9× 86 0.5× 252 1.6× 75 1.1k
Elsa Zotta Argentina 19 615 1.9× 350 1.7× 71 0.4× 228 1.4× 174 1.1× 77 1.5k
Lei Hou China 18 491 1.5× 252 1.2× 147 0.7× 194 1.2× 233 1.5× 46 1.1k
Jinsheng He China 20 362 1.1× 83 0.4× 286 1.4× 283 1.7× 126 0.8× 64 1.1k
Deepa Machiah United States 12 304 0.9× 126 0.6× 110 0.6× 92 0.5× 208 1.4× 18 765
Ferenc Somogyvári Hungary 17 252 0.8× 73 0.3× 129 0.6× 88 0.5× 101 0.7× 60 909
Hailiang Liu China 18 340 1.0× 166 0.8× 65 0.3× 134 0.8× 102 0.7× 37 968
Jessica G. Moreland United States 22 613 1.9× 88 0.4× 139 0.7× 91 0.5× 632 4.1× 42 1.4k

Countries citing papers authored by Juan Geng

Since Specialization
Citations

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

Fields of papers citing papers by Juan Geng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juan Geng

This figure shows the co-authorship network connecting the top 25 collaborators of Juan Geng. A scholar is included among the top collaborators of Juan Geng 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 Juan Geng. Juan Geng 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.
2.
Xie, Yaqi, Zijie Li, Juan Geng, et al.. (2024). Effectiveness of EV-A71 Vaccine and Its Impact on the Incidence of Hand, Foot and Mouth Disease: A Systematic Review. Vaccines. 12(9). 1028–1028. 5 indexed citations
3.
Wang, Yunan, et al.. (2023). Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review. Frontiers in Pediatrics. 11. 1141665–1141665. 2 indexed citations
4.
5.
Liang, Fei, Juan Geng, Min Zhang, et al.. (2021). SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients. eLife. 10. 11 indexed citations
6.
Adzika, Gabriel Komla, Qi Wu, Tongtong Ma, et al.. (2021). Estrogen Attenuates Chronic Stress-Induced Cardiomyopathy by Adaptively Regulating Macrophage Polarizations via β2-Adrenergic Receptor Modulation. Frontiers in Cell and Developmental Biology. 9. 737003–737003. 18 indexed citations
7.
He, Xiaomin, Hui Jing, Xiaoyang Zhang, et al.. (2019). Rare Copy Number Variations Might Not be Involved in the Molecular Pathogenesis of PA–IVS in an Unselected Chinese Cohort. Pediatric Cardiology. 40(4). 762–767. 3 indexed citations
8.
Adzika, Gabriel Komla, Jeremiah Ong’achwa Machuki, Tongtong Ma, et al.. (2019). Pathological cardiac hypertrophy: the synergy of adenylyl cyclases inhibition in cardiac and immune cells during chronic catecholamine stress. Journal of Molecular Medicine. 97(7). 897–907. 22 indexed citations
9.
Xu, Mingyu, et al.. (2018). Clinical Application of Chromosome Microarray Analysis in Han Chinese Children with Neurodevelopmental Disorders. Neuroscience Bulletin. 34(6). 981–991. 7 indexed citations
10.
Geng, Juan, Liqun Li, Qian Lv, et al.. (2017). TaGW2-6A allelic variation contributes to grain size possibly by regulating the expression of cytokinins and starch-related genes in wheat. Planta. 246(6). 1153–1163. 34 indexed citations
11.
Zhang, Xiaoqing, Yuejuan Xu, Deyuan Liu, et al.. (2015). A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease. BMC Genomics. 16(1). 364–364. 41 indexed citations
12.
Wang, Zhigang, Jian Wang, Yuchan Li, et al.. (2014). Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients. Clinica Chimica Acta. 433. 195–199. 17 indexed citations
13.
Kerns, Sarah L., Jaime Guevara‐Aguirre, Shayne F. Andrew, et al.. (2014). A Novel Variant inCDKN1CIs Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes. The Journal of Clinical Endocrinology & Metabolism. 99(10). E2117–E2122. 39 indexed citations
14.
Yang, Haiou, Xiaoqing Zhang, Juan Geng, Zhaojing Zheng, & Qihua Fu. (2014). Toll-like Receptor 6 V327M Polymorphism Is Associated with an Increased Risk of Klebsiella pneumoniae Infection. The Pediatric Infectious Disease Journal. 33(11). e310–e315. 3 indexed citations
15.
16.
Yao, Ruen, Yongguo Yu, Juan Geng, et al.. (2013). Application of MLPA technology in molecular diagnosis of three inherited diseases. Zhonghua jianyan yixue zazhi. 36(2). 136–141. 1 indexed citations
17.
Zheng, Zhaojing, Juan Geng, Ruen Yao, et al.. (2013). Molecular defects identified by whole exome sequencing in a child with Fanconi anemia. Gene. 530(2). 295–300. 17 indexed citations
18.
Yang, Haiou, Lili Wang, Juan Geng, et al.. (2013). Characterization of Six Missense Mutations in the Tissue-Nonspecific Alkaline Phosphatase (TNSALP) Gene in Chinese Children with Hypophosphatasia. Cellular Physiology and Biochemistry. 32(3). 635–644. 13 indexed citations
19.
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
20.
Nicholson, Susan, Maria da Glória Bonecini-Almeida, José Roberto Lapa e Silva, et al.. (1996). Inducible nitric oxide synthase in pulmonary alveolar macrophages from patients with tuberculosis.. The Journal of Experimental Medicine. 183(5). 2293–2302. 388 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Darko Richter Breakdown of academic impact, for papers by Elsa Zotta Breakdown of academic impact, for papers by Lei Hou Breakdown of academic impact, for papers by Jinsheng He Breakdown of academic impact, for papers by Deepa Machiah Breakdown of academic impact, for papers by Ferenc Somogyvári Breakdown of academic impact, for papers by Hailiang Liu Breakdown of academic impact, for papers by Jessica G. Moreland
Rankless by CCL
2026