Jianfen Man

545 total citations
11 papers, 370 citations indexed

About

Jianfen Man is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Jianfen Man has authored 11 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Jianfen Man's work include Genomic variations and chromosomal abnormalities (4 papers), Hormonal and reproductive studies (3 papers) and Genomics and Rare Diseases (3 papers). Jianfen Man is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Hormonal and reproductive studies (3 papers) and Genomics and Rare Diseases (3 papers). Jianfen Man collaborates with scholars based in China, Denmark and United Kingdom. Jianfen Man's co-authors include Yangyu Huang, Zhou Gong, Yanjie Wang, Yi Xiao, Yunjie Zhao, Graham Jackson, H Solomon, Anthony S. Wierzbicki, Timothy O’Brien and P Lumb and has published in prestigious journals such as PLoS ONE, Scientific Reports and Medicine.

In The Last Decade

Jianfen Man

10 papers receiving 360 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jianfen Man China 8 204 99 97 42 32 11 370
Sergio G. Moreira United States 6 126 0.6× 135 1.4× 128 1.3× 64 1.5× 55 1.7× 8 403
Dan Glass United Kingdom 5 106 0.5× 88 0.9× 21 0.2× 36 0.9× 8 0.3× 6 228
Jasmin Katrin Badawi Germany 10 92 0.5× 20 0.2× 26 0.3× 132 3.1× 16 0.5× 25 326
Tamotsu Kiya Japan 11 86 0.4× 8 0.1× 53 0.5× 8 0.2× 34 1.1× 20 468
Ziva Ben Neriah Israel 9 156 0.8× 18 0.2× 20 0.2× 19 0.5× 66 2.1× 11 364
Anna Karin Lind Sweden 7 66 0.3× 15 0.2× 42 0.4× 3 0.1× 22 0.7× 11 367
R Prager-Lewin Israel 12 170 0.8× 12 0.1× 100 1.0× 16 0.4× 116 3.6× 28 314
Marion Depenbusch Germany 9 215 1.1× 14 0.1× 182 1.9× 11 0.3× 137 4.3× 20 448
Federica Moffa Italy 11 217 1.1× 32 0.3× 11 0.1× 9 0.2× 49 1.5× 16 744
Wen Ying Chen Hong Kong 5 139 0.7× 13 0.1× 10 0.1× 9 0.2× 50 1.6× 5 469

Countries citing papers authored by Jianfen Man

Since Specialization
Citations

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

Fields of papers citing papers by Jianfen Man

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jianfen Man

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

All Works

11 of 11 papers shown
1.
Tang, Fei, Zhonghua Wang, Yan Sun, et al.. (2024). Recurrent neural network for predicting absence of heterozygosity from low pass WGS with ultra-low depth. BMC Genomics. 25(1). 470–470. 2 indexed citations
2.
Guo, Xueqin, Linlin Fan, Yaoshen Wang, et al.. (2023). Accuracy and depth evaluation of clinical low pass genome sequencing in the detection of mosaic aneuploidies and CNVs. BMC Medical Genomics. 16(1). 294–294. 3 indexed citations
3.
Liu, Yanqiu, Hui Huang, Wei Li, et al.. (2023). Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform. Human Genome Variation. 10(1).
4.
Mughal, Maleeha, et al.. (2021). ‘Fat chance’: a review of adipose tissue engineering and its role in plastic and reconstructive surgery. Annals of The Royal College of Surgeons of England. 103(4). 245–249. 13 indexed citations
5.
Sun, Yan, Jing Yuan, Limin Wu, et al.. (2019). Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform. Medicine. 98(12). e14860–e14860. 15 indexed citations
6.
Sun, Yan, Jianfen Man, Long Li, et al.. (2018). Targeted next-generation sequencing as a comprehensive test for Mendelian diseases: a cohort diagnostic study. Scientific Reports. 8(1). 11646–11646. 15 indexed citations
7.
Liu, Yanqiu, Xiaoming Wei, Xueqin Guo, et al.. (2015). Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases. PLoS ONE. 10(8). e0133636–e0133636. 28 indexed citations
8.
Zhao, Yunjie, Yangyu Huang, Zhou Gong, et al.. (2012). Automated and fast building of three-dimensional RNA structures. Scientific Reports. 2(1). 734–734. 168 indexed citations
9.
Solomon, H, Yohan Samarasinghe, Michael Feher, et al.. (2006). Erectile dysfunction and statin treatment in high cardiovascular risk patients. International Journal of Clinical Practice. 60(2). 141–145. 57 indexed citations
10.
Solomon, H, Jianfen Man, Anthony S. Wierzbicki, Timothy O’Brien, & Graham Jackson. (2003). ERECTILE DYSFUNCTION: CARDIOVASCULAR RISK AND THE ROLE OF THE CARDIOLOGIST. International Journal of Clinical Practice. 57(2). 96–99. 49 indexed citations
11.
Solomon, H, Jianfen Man, Jesjeet Singh Gill, & Graham Jackson. (2002). VIAGRA ON THE INTERNET: UNSAFE SEXUAL PRACTICE. International Journal of Clinical Practice. 56(5). 403–404. 20 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.

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