Haimei OuYang

639 total citations
9 papers, 158 citations indexed

About

Haimei OuYang is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Haimei OuYang has authored 9 papers receiving a total of 158 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Haimei OuYang's work include Hormonal and reproductive studies (1 paper), Genetic Syndromes and Imprinting (1 paper) and RNA modifications and cancer (1 paper). Haimei OuYang is often cited by papers focused on Hormonal and reproductive studies (1 paper), Genetic Syndromes and Imprinting (1 paper) and RNA modifications and cancer (1 paper). Haimei OuYang collaborates with scholars based in China. Haimei OuYang's co-authors include Xiaofei Lv, Haishan Peng, Yaping Hou, Hailiang Liu, Jie Li, Qun Wang, Qingqing He, Aihua Yin, Shu Liu and Weihong Zeng and has published in prestigious journals such as Endocrinology, Gene and BioMed Research International.

In The Last Decade

Haimei OuYang

9 papers receiving 156 citations

Peers

Countries citing papers authored by Haimei OuYang

Since Specialization

Citations

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

Fields of papers citing papers by Haimei OuYang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haimei OuYang

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Distinct Lipids Profiles and Associations With Clinical Indicators and Gut Microbiota in Children With Prader–Willi Syndrome 2023 ·Endocrinology ·Yaping Hou, (unknown), Jia Guo, Lijuan Lv, Haimei OuYang, Xingwang Wang, (unknown), Xiuwen Chen, Fanghua Wang	3
2	Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene 2022 ·Frontiers in Pediatrics ·Shu Liu, Zhiqing Wang, (unknown), Ye Zhang, (unknown), Haimei OuYang, (unknown), Nuan Chen, Weihong Zeng, Jian‐Hui Jiang	2
3	Severe forms of Johanson-Blizzard syndrome caused by two novel compound heterozygous variants in UBR1: Clinical manifestations, imaging findings and molecular genetics 2020 ·Pancreatology ·Shu Liu, Zhiqing Wang, Jian‐Hui Jiang, (unknown), (unknown), Ye Zhang, Haimei OuYang, (unknown), (unknown), Nuan Chen, Weihong Zeng	8
4	Severe forms of complete androgen insensitivity syndrome caused by a p.Q65X novel mutation in androgen receptor: Clinical manifestations, imaging findings and molecular genetics 2019 ·Steroids ·Shu Liu, Zhiqing Wang, Jian‐Hui Jiang, Haimei OuYang, Sisi Wei, (unknown), Nuan Chen, Weihong Zeng, Liying Chen, (unknown)	2
5	Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review 2018 ·Cytogenetic and Genome Research ·Shu Liu, Zhiqing Wang, Sisi Wei, (unknown), Nuan Chen, Haimei OuYang, Weihong Zeng, Liying Chen, (unknown), Jian‐Hui Jiang	4
6	Human Gut Microbiota Associated with Obesity in Chinese Children and Adolescents 2017 ·BioMed Research International ·Yaping Hou, Qingqing He, Haimei OuYang, Haishan Peng, Qun Wang, Jie Li, Xiaofei Lv, (unknown), (unknown), Hailiang Liu, Aihua Yin	118
7	Two novel mutations in the glycine decarboxylase gene in a boy with classic nonketotic hyperglycinemia: case report 2017 ·Archivos Argentinos de Pediatria ·Shu Liu, Zhiqing Wang, (unknown), Nuan Chen, Haimei OuYang, Weihong Zeng, Liying Chen, (unknown), Jian‐Hui Jiang	9
8	The association between the polymorphism rs2231142 in the ABCG2 gene and gout risk: a meta-analysis 2014 ·Clinical Rheumatology ·Xiaofei Lv, Yuan Zhang, Fangfang Zeng, Aihua Yin, Ning Ye, Haimei OuYang, Dan Feng, Dan Li, Wenhua Ling, Xiaozhuang Zhang	10
9	Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans 2013 ·Gene ·Xiaofei Lv, Yuan Zhang, Shaoqi Rao, Dongfang Su, Dan Feng, Min Wang, Xinrui Li, Dan Li, Honghui Guo, Xiaoyu Zuo, Min Xia, Haimei OuYang, Wenhua Ling, Jian Qiu	2

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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