Yongjia Yang

775 total citations
49 papers, 465 citations indexed

About

Yongjia Yang is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Yongjia Yang has authored 49 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Genetics and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Yongjia Yang's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Elbow and Forearm Trauma Treatment (4 papers). Yongjia Yang is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Elbow and Forearm Trauma Treatment (4 papers). Yongjia Yang collaborates with scholars based in China, United States and Taiwan. Yongjia Yang's co-authors include Ming Tu, Jihong Guo, Zhao Liu, Liping Li, Yimin Zhu, Yimin Zhu, Haibo Mei, Rui Zhao, Weijian Chen and Yu Zheng and has published in prestigious journals such as Applied Physics Letters, PLoS ONE and Advanced Functional Materials.

In The Last Decade

Yongjia Yang

44 papers receiving 436 citations

Peers

Countries citing papers authored by Yongjia Yang

Since Specialization

Citations

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

Fields of papers citing papers by Yongjia Yang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yongjia Yang

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

#	Work	Indexed citations
1	Penta-channel waveguide-based near-eye display with two-dimensional pupil expansion 2025 ·Displays ·Chao Ping Chen, Xiaojun Wu, Feng Wang, (unknown), Yongjia Yang, Shuxin Liu	2
2	Synostosis of joints caused by mutant FBN2 is linked to the abnormalities and misdifferentiation of articular surface cells 2025 ·Genetics in Medicine ·Mei Deng, Fang Shen, Yu Zheng, Cheng Liu, (unknown), (unknown), Guanghui Zhu, Sha Zhao, (unknown), Yongjia Yang	0
3	Organic acid accumulation pattern and its key genes in Chinese cherry fruits 2025 ·BMC Genomics ·(unknown), (unknown), Xiao‐Cheng Liu, Linlin Hao, Yongjia Yang, (unknown), Hao Wang, Zhenshan Liu, Jing Zhang, (unknown), Yuanxiu Lin, (unknown), Mengyao Li, Yong Zhang, (unknown), (unknown), Qing Chen, Xiaorong Wang	0
4	Roots and rewards: Exploring the symbiotic relationship between familism and Chinese family business philanthropy 2024 ·Finance research letters ·(unknown), Yongjia Yang, (unknown), Yingkai Tang	0
5	An active controllable wide-angle and ultra-wideband terahertz absorber/reflector based on VO₂ metamaterial 2024 ·Physical Chemistry Chemical Physics ·(unknown), Bin Hou, Yongjia Yang, Qianju Song, Zao Yi, Zigang Zhou	8
6	Chinese patients with 3M syndrome: clinical manifestations and two novel pathogenic variants 2023 ·Frontiers in Genetics ·(unknown), (unknown), Yongjia Yang, Xiaoming Li, Yan Zhong	3
7	Case series of congenital pseudarthrosis of the tibia unfulfilling neurofibromatosis type 1 diagnosis: 21% with somatic NF1 haploinsufficiency in the periosteum 2022 ·Human Genetics ·Yu Zheng, Guanghui Zhu, (unknown), Weihua Zhao, Yongjia Yang, (unknown), (unknown), Haibo Mei, Zhengmao Hu	2
8	Mutant B3GALT6 in a Multiplex Family: A Dominant Variant Co-Segregated With Moderate Malformations 2022 ·Frontiers in Genetics ·Fang Shen, Yongjia Yang, Yu Zheng, Ming Tu, Zhao Liu, (unknown), (unknown), Yimin Zhu	2
9	Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E 2022 ·Journal of Clinical Immunology ·Xiaojun Duan, Fang Shen, Yafei Deng, Jin Zhang, (unknown), (unknown), Yanping Chen, Yongjia Yang	2
10	A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis 2021 ·Molecular Genetics & Genomic Medicine ·Fang Shen, Yongjia Yang, Pengcheng Li, Yu Zheng, (unknown), (unknown), Guanghui Zhu, Haibo Mei, (unknown), Yimin Zhu	10
11	Expanding the genotypes and phenotypes for 19 rare diseases by exome sequencing performed in pediatric intensive care unit 2021 ·Human Mutation ·Juan Liu, Yu Zheng, (unknown), Desheng Zhu, (unknown), (unknown), Yongjia Yang, Peng Yu, Zhenghui Xiao, Yimin Zhu, (unknown)	4
12	Genetic and Clinical Analyses of 13 Chinese Families With Cystine Urolithiasis and Identification of 15 Novel Pathogenic Variants in SLC3A1 and SLC7A9 2020 ·Frontiers in Genetics ·Chuangye Li, Yongjia Yang, Yu Zheng, Fang Shen, Li Liu, Yanfang Li, Liping Li, (unknown)	5
13	Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation 2019 ·Frontiers in Pharmacology ·(unknown), Weijian Chen, Liping Li, Xinyuan Zhu, Caizhi Huang, (unknown), Yongjia Yang, (unknown)	7
14	Clinical and Genetic Study of Children With Peutz‐Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation 2018 ·Journal of Pediatric Gastroenterology and Nutrition ·Hongmei Zhao, Yongjia Yang, (unknown), (unknown), Li Liu, (unknown), Zhenghui Xiao, Yu Zheng, Peng Lv, Thomas M. Attard, Ding‐You Li, Jie‐Yu You	11
15	XRCC2 mutation causes meiotic arrest, azoospermia and infertility 2018 ·Journal of Medical Genetics ·Yongjia Yang, Jihong Guo, Lei Dai, Yimin Zhu, Hao Hu, (unknown), Weijian Chen, Desheng Liang, Jingliang He, Ming Tu, (unknown), Lingqian Wu	55
16	First Report of CTNS Mutations in a Chinese Family with Infantile Cystinosis 2015 ·The Scientific World JOURNAL ·Yongjia Yang, Yuan Hu, Rui Zhao, Xinyu He, Zhao Liu, Ming Tu, Lijun Zhou, Jihong Guo, (unknown), Tantai Zhao, Yimin Zhu	5
17	Intragenic and extragenic disruptions of FOXL2 mapped by whole genome low-coverage sequencing in two BPES families with chromosome reciprocal translocation 2014 ·Genomics ·Yongjia Yang, (unknown), Yimin Zhu, Haixiao Chen, Rui Zhao, Xinyu He, (unknown), Pin Wang, Lijun Zhou, Zhao Liu, Ming Tu, Zirui Dong, Hui Chen, Zhiguo Xie	23
18	A family with radio‐ulnar synostosis, scoliosis, and thick vermilion of lips: A novel syndrome or variant of Giuffrè–Tsukahara syndrome? 2012 ·American Journal of Medical Genetics Part A ·Yimin Zhu, Ke Jin, Haibo Mei, Liping Li, Zheng Liu, Yongjia Yang, (unknown), (unknown), Rui Zhao, Xinyu He	4
19	A novel mutation leading to elongation of the deduced α1(X) chain results in Metaphyseal Chondrodysplasia type Schmid 2011 ·Clinica Chimica Acta ·Yimin Zhu, Liping Li, Lijun Zhou, (unknown), Ke Jin, Kun Liu, (unknown), Jinsong Tang, Yongjia Yang, Rui Zhao, (unknown)	9
20	A novel MSH2 mutation in a Chinese family with hereditary non-polyposis colorectal cancer 2007 ·International Journal of Colorectal Disease ·Duo Zheng, Tiegang Li, Xiaoping Liu, Wei‐Xin Hu, Hanchun Chen, Yongjia Yang	3

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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