Meihua Tan

3.7k total citations
24 papers, 636 citations indexed

About

Meihua Tan is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Meihua Tan has authored 24 papers receiving a total of 636 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Meihua Tan's work include Prenatal Screening and Diagnostics (4 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Cancer-related molecular mechanisms research (4 papers). Meihua Tan is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Cancer-related molecular mechanisms research (4 papers). Meihua Tan collaborates with scholars based in China, United States and United Kingdom. Meihua Tan's co-authors include Xin Zhou, Min Tang, Shanlin Liu, Guanliang Meng, Xu Su, Qiong Wu, Yiyuan Li, Wenhui Song, Ai‐bing Zhang and Chloe J. Hardman and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Meihua Tan

22 papers receiving 628 citations

Peers

Countries citing papers authored by Meihua Tan

Since Specialization

Citations

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

Fields of papers citing papers by Meihua Tan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meihua Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Meihua Tan. A scholar is included among the top collaborators of Meihua Tan 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 Meihua Tan. Meihua Tan 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	The lncRNA SENCR knockdown alleviates vascular calcification via miR-4731-5p by suppressing endoplasmic reticulum stress 2025 ·PLoS ONE ·(unknown), Wei Zhan, (unknown), Meihua Tan, Li Wu, Shihao Wu	0
2	Loss of BACH1 improves osteogenic differentiation in glucocorticoid-induced hBMSCs through restoring autophagy 2024 ·BMC Musculoskeletal Disorders ·(unknown), (unknown), Meihua Tan, Wenjun Liu, Wenjin Li	1
3	An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing 2024 ·npj Genomic Medicine ·(unknown), Meihua Tan, Jiao Liu, Yanmei Yang, Jialing Yu, Lijuan He, (unknown), Yixi Sun, Yeqing Qian, Kai Yan, Minyue Dong	2
4	Retrospective study revealed integration of CNV-seq and karyotype analysis is an effective strategy for prenatal diagnosis of chromosomal abnormalities 2024 ·Frontiers in Genetics ·Yunsheng Ge, Jiayan Chen, Yanru Huang, Ди Шао, Ruikang K. Wang, (unknown), Meihua Tan, Jian Zhang	3
5	A novel PLS1 c.981+ 1G >A variant causes autosomal‐dominant hereditary hearing loss in a family 2022 ·Clinical Genetics ·Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, (unknown), Yanhong Zhang, Wei Li, (unknown), Meihua Tan, (unknown), Meihuan Chen, (unknown), Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao	2
6	Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease 2022 ·Frontiers in Genetics ·Meihua Tan, Xinrui Wang, Hongjie Liu, Xiaoyan Peng, (unknown), (unknown), Liangpu Xu, Jia Li, Hua Cao	11
7	Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing 2022 ·Gene ·Liu Ya, Meihua Tan, (unknown), (unknown), Qingqing Chen, Wei Chen, Hang Yang, Yaping Xu	5
8	Two Novel Pathogenic Variants of TJP2 Gene and the Underlying Molecular Mechanisms in Progressive Familial Intrahepatic Cholestasis Type 4 Patients 2021 ·Frontiers in Cell and Developmental Biology ·Jia Tang, Meihua Tan, Yihui Deng, Hui Tang, (unknown), Mingzhen Li, Wei Ma, Li Jia, Hongzheng Dai, Jianli Li, Shengmei Zhou, (unknown), Fengxiang Wei, Xiaofen Ma, (unknown)	8
9	Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases 2021 ·BMC Medical Genomics ·Yunsheng Ge, Jia Li, (unknown), Jian Zhang, Yanru Huang, Meihua Tan, Wei Li, Jiayan Chen, Yulin Zhou	24
10	Identification of copy number variants by NGS-based NIPT at low sequencing depth 2020 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Xiaoqing Ye, (unknown), (unknown), Meihua Tan, Jia Li, Jiayan Wang, (unknown), Huimin Zhang, Shaoying Li, Dunjin Chen, Min Chen	15
11	Effect of Multi-Directional Nursing Intervention on the Prognosis and Quality Of Life in Patients with Type 2 Diabetes 2020 ·Indian Journal of Pharmaceutical Sciences ·(unknown), Meihua Tan, (unknown)	1
12	Abstract 3407: A high performance target-enrichment strategy for liquid biopsy 2018 ·Cancer Research ·Jilong Liu, Yan Song, Lei Liu, Meihua Tan, (unknown), Jingjing Wang, Mingzhi Ye	5
13	Heteroplasmy and Copy Number Variations of Mitochondria in 88 Hepatocellular Carcinoma Individuals 2017 ·Journal of Cancer ·Weiyang Li, Yanwei Qi, Xiaofang Cui, Yuhui Sun, Qing Huo, Yan Yang, (unknown), Meihua Tan, (unknown), Huali Zhang, Meng Zhang, Chuanxin Liu, Qingsheng Kong	9
14	Mitochondrial genome of Hylaeus dilatatus (Hymenoptera: Colletidae) 2015 ·Mitochondrial DNA Part A ·Meihua Tan, Rui Zhang, Chloe J. Hardman, Xin Zhou	14
15	The mitochondrial genome of the winter stonefly Apteroperla tikumana (Plecoptera, Capniidae) 2015 ·Mitochondrial DNA Part A ·Chengran Zhou, Meihua Tan, (unknown), Rui Zhang, Ryuichiro Machida, Xin Zhou	8
16	Mitochondrial capture enriches mito‐DNA 100 fold, enabling PCR‐free mitogenomics biodiversity analysis 2015 ·Molecular Ecology Resources ·Shanlin Liu, Xin Wang, Lin Xie, Meihua Tan, Zhenyu Li, Xu Su, Hao Zhang, Bernhard Misof, Karl M. Kjer, Min Tang, Oliver Niehuis, Hui Jiang, Xin Zhou	63
17	High‐throughput monitoring of wild bee diversity and abundance via mitogenomics 2015 ·Methods in Ecology and Evolution ·Min Tang, Chloe J. Hardman, Yinqiu Ji, Guanliang Meng, Shanlin Liu, Meihua Tan, (unknown), Ellen Moss, Jiaxin Wang, Chenxue Yang, (unknown), (unknown), Simon G. Potts, Xin Zhou, Douglas W. Yu	102
18	The complete mitochondrial genome of the pumpkin fruit fly, Bactrocera tau (Diptera: Tephritidae) 2015 ·Mitochondrial DNA Part A ·Meihua Tan, Rui Zhang, (unknown), Xin Zhou	17
19	Multiplex sequencing of pooled mitochondrial genomes—a crucial step toward biodiversity analysis using mito-metagenomics 2014 ·Nucleic Acids Research ·Min Tang, Meihua Tan, Guanliang Meng, (unknown), Xu Su, Shanlin Liu, Wenhui Song, Yiyuan Li, Qiong Wu, Ai‐bing Zhang, Xin Zhou	237
20	Utility of the Health Belief Model in predicting compliance of screening in patients with chronic hepatitis B 2005 ·Alimentary Pharmacology & Therapeutics ·Chun Tao Wai, Michelle Wong, S.C. Ng, (unknown), Meihua Tan, Wei Jin Chua, (unknown), Myat Oo Aung, Seng Gee Lim	53

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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