Yousheng Yan

505 total citations
46 papers, 322 citations indexed

About

Yousheng Yan is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Yousheng Yan has authored 46 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Clinical Biochemistry. Recurrent topics in Yousheng Yan's work include Metabolism and Genetic Disorders (8 papers), RNA modifications and cancer (5 papers) and Genomics and Rare Diseases (4 papers). Yousheng Yan is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), RNA modifications and cancer (5 papers) and Genomics and Rare Diseases (4 papers). Yousheng Yan collaborates with scholars based in China, Japan and Pakistan. Yousheng Yan's co-authors include Yaguang Hu, Hongmei Yu, Qian Liu, Min Zhang, Ge Li, Chuan Zhang, Xiaohua Jin, Xu Ma, Xuan Feng and Yongqing Sun and has published in prestigious journals such as Analytical Chemistry, Molecular Psychiatry and Journal of Medical Internet Research.

In The Last Decade

Yousheng Yan

38 papers receiving 318 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yousheng Yan China	10	181	68	60	39	37	46	322
Mohammad Miryounesi Iran	10	191 1.1×	83 1.2×	63 1.1×	25 0.6×	22 0.6×	70	337
Tommaso Biagini Italy	14	328 1.8×	74 1.1×	111 1.9×	17 0.4×	26 0.7×	46	499
Johanna C. Herkert Netherlands	12	194 1.1×	156 2.3×	43 0.7×	47 1.2×	20 0.5×	16	432
Mohammad Yahya Vahidi Mehrjardi Iran	13	184 1.0×	68 1.0×	122 2.0×	22 0.6×	9 0.2×	38	323
Julie A. Jurgens United States	11	148 0.8×	124 1.8×	23 0.4×	32 0.8×	17 0.5×	14	298
Petr Jira Netherlands	10	412 2.3×	122 1.8×	43 0.7×	35 0.9×	23 0.6×	19	585
Khalid Al‐Thihli Oman	13	219 1.2×	116 1.7×	21 0.3×	58 1.5×	135 3.6×	50	456
Natsuko Arai‐Ichinoi Japan	10	160 0.9×	94 1.4×	14 0.2×	58 1.5×	107 2.9×	18	398
Péter Gergics Hungary	14	209 1.2×	134 2.0×	73 1.2×	28 0.7×	9 0.2×	29	501
Emma M. Lessieur United States	10	150 0.8×	37 0.5×	18 0.3×	12 0.3×	20 0.5×	13	293

Countries citing papers authored by Yousheng Yan

Since Specialization

Citations

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

Fields of papers citing papers by Yousheng Yan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yousheng Yan

This figure shows the co-authorship network connecting the top 25 collaborators of Yousheng Yan. A scholar is included among the top collaborators of Yousheng Yan 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 Yousheng Yan. Yousheng Yan 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

Wang, Jingjing, et al.. (2025). Analysis of Ultrasound Findings and Outcomes in Fetuses with Suspected Congenital Heart Disease at Less than 14 Weeks’ Gestation Compared to Later Gestations. Fetal Diagnosis and Therapy. 52(4). 346–355.

Yan, Yousheng, et al.. (2025). Identification of a novel AGO2 variant causing LESKRES in a Chinese family with intellectual disability. Frontiers in Genetics. 16. 1598462–1598462. 1 indexed citations

Sun, Lijuan, et al.. (2024). Role of copy number variation analysis in prenatally diagnosed Blake’s pouch cyst. BMC Pregnancy and Childbirth. 24(1). 842–842.

Hu, Huaying, et al.. (2024). Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B). Molecular Genetics & Genomic Medicine. 12(3). e2401–e2401. 1 indexed citations

Zhang, Enjie, Rong Zhao, Shen Gao, et al.. (2024). The association between dyslipidaemia in the first trimester and adverse pregnancy outcomes in pregnant women with subclinical hypothyroidism: a cohort study. Lipids in Health and Disease. 23(1). 13–13. 7 indexed citations

Yang, Kai, Yingyi Luan, Shan Wang, et al.. (2024). SGMS1 facilitates osteogenic differentiation of MSCs and strengthens osteogenesis-angiogenesis coupling by modulating Cer/PP2A/Akt pathway. iScience. 27(4). 109358–109358. 4 indexed citations

Sun, Pei, Zicheng Zhao, Yousheng Yan, et al.. (2023). Identify gestational diabetes mellitus by deep learning model from cell-free DNA at the early gestation stage. Briefings in Bioinformatics. 25(1). 7 indexed citations

Zhang, Chuan, Yousheng Yan, Yupei Wang, et al.. (2023). Identification of deep intronic variants of PAH in phenylketonuria using full-length gene sequencing. Orphanet Journal of Rare Diseases. 18(1). 128–128. 3 indexed citations

Meng, Tian, Haofeng Huang, Hao Liu, et al.. (2023). ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular Psychiatry. 28(3). 1219–1231. 12 indexed citations

10.

Yang, Kai, Jue Wu, Shan Wang, et al.. (2023). NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway. Cell Death Discovery. 9(1). 404–404. 25 indexed citations

11.

Ma, Qiang, Chunyan Zheng, Yanxia Huang, et al.. (2022). Identification of novel heterozygous missense variant in the COL11A1 causing fetal craniofacial anomalies. All Life. 15(1). 240–246. 1 indexed citations

12.

Yang, Kai, Huaying Hu, Yazhuo Li, et al.. (2021). Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis. Frontiers in Genetics. 12. 763467–763467. 7 indexed citations

13.

Huang, Yanxia, Chunyan Gao, Chunyan Zheng, et al.. (2021). Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis. Frontiers in Genetics. 12. 688241–688241. 12 indexed citations

14.

Yang, Kai, Huaying Hu, Jing Zhang, et al.. (2021). Metabolic and biophysical study of the MFN2^Ile213Thr mutant causing Hereditary Motor and Sensory Neuropathy (HMSN).. American Journal of Translational Research. 13(10). 11501–11512. 1 indexed citations

15.

Jin, Xiaohua, Qian Liu, Qinhua Zhang, et al.. (2020). Compound heterozygous variants of the FBXO7 gene resulting in infantile‐onset Parkinsonian‐pyramidal syndrome in siblings of a Chinese family. Journal of Clinical Laboratory Analysis. 34(8). 6 indexed citations

16.

Tan, Ya, Qian Liu, Zhi Li, et al.. (2020). A novel frameshift variant in SON causes Zhu‐Tokita‐Takenouchi‐Kim Syndrome. Journal of Clinical Laboratory Analysis. 34(8). e23326–e23326. 7 indexed citations

17.

Zhang, Chuan, Yousheng Yan, Qinghua Zhang, et al.. (2020). Mutation Analysis of 63 Northwest Chinese Probands with Oculocutaneous Albinism. Current Eye Research. 46(1). 140–143. 6 indexed citations

18.

Liu, Chunlian, et al.. (2020). [Identification of a novel c.1A>G variant of GDAP1 gene in a pedigree affected with autosomal recessive fibula atrophy].. PubMed. 37(11). 1244–1246. 1 indexed citations

19.

Yan, Yousheng, Chuan Zhang, Xiaohua Jin, et al.. (2019). Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants. Metabolic Brain Disease. 34(3). 733–745. 13 indexed citations

20.

Yan, Yousheng, Fengxia Yao, Lei Zheng, et al.. (2014). [The mutation analysis of PAH gene and prenatal diagnosis in classical phenylketonuria family].. PubMed. 31(6). 686–92.

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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