Wen‐Lang Fan

2.0k total citations
49 papers, 1.3k citations indexed

About

Wen‐Lang Fan is a scholar working on Molecular Biology, Pharmacology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Wen‐Lang Fan has authored 49 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 6 papers in Pharmacology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Wen‐Lang Fan's work include Drug-Induced Adverse Reactions (4 papers), Genomics and Phylogenetic Studies (4 papers) and Autoimmune Bullous Skin Diseases (3 papers). Wen‐Lang Fan is often cited by papers focused on Drug-Induced Adverse Reactions (4 papers), Genomics and Phylogenetic Studies (4 papers) and Autoimmune Bullous Skin Diseases (3 papers). Wen‐Lang Fan collaborates with scholars based in Taiwan, United States and China. Wen‐Lang Fan's co-authors include Shih‐Chi Su, Shun‐Fa Yang, Wen‐Hung Chung, Chiao‐Wen Lin, Wei‐En Yang, Wen‐Hsiung Li, Shih‐Chi Su, Ya‐Ching Chang, Rosaline Chung‐Yee Hui and Chuang‐Wei Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Wen‐Lang Fan

47 papers receiving 1.3k citations

Peers

Wen‐Lang Fan
Arkadiusz Nawrocki Denmark
André N. Tiaden Switzerland
Peter Korošec Slovenia
Hajime Nakano Japan
Gonzalo Sánchez‐Duffhues Netherlands
Muneharu Maruyama Japan
Masashi Shiina Japan
Yu Sawada Japan
Olga Genina Israel
Arkadiusz Nawrocki Denmark
Wen‐Lang Fan
Citations per year, relative to Wen‐Lang Fan Wen‐Lang Fan (= 1×) peers Arkadiusz Nawrocki

Countries citing papers authored by Wen‐Lang Fan

Since Specialization
Citations

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

Fields of papers citing papers by Wen‐Lang Fan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wen‐Lang Fan. 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 Wen‐Lang Fan. The network helps show where Wen‐Lang Fan may publish in the future.

Co-authorship network of co-authors of Wen‐Lang Fan

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

All Works

20 of 20 papers shown
1.
2.
Chou, I‐Jun, et al.. (2023). Long-Term Outcome of Neonatal Seizure with PACS2 Mutation: Case Series and Literature Review. Children. 10(4). 621–621. 1 indexed citations
3.
Wang, Chih‐Chi, Wen‐Lang Fan, Tingting Liu, et al.. (2023). Impact of Genomic Alterations on the Clinical Outcome of Patients With Hepatitis B-related Hepatocellular Carcinoma Receiving Curative Surgery: A Retrospective Cohort Study. Anticancer Research. 43(10). 4709–4722. 1 indexed citations
4.
Chao, Chih‐Ying, et al.. (2023). Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review. Journal of Movement Disorders. 16(2). 202–206.
5.
Kambe, Naotomo, et al.. (2022). Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome. Pediatric Rheumatology. 20(1). 86–86. 2 indexed citations
6.
Fan, Wen‐Lang, Lan‐Yan Yang, Chia‐Hsun Hsieh, et al.. (2021). Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma. Cancers. 13(11). 2709–2709. 13 indexed citations
7.
Fan, Wen‐Lang, Yuan‐Ming Yeh, Weiming Lin, et al.. (2021). Leptin Is Associated with Poor Clinical Outcomes and Promotes Clear Cell Renal Cell Carcinoma Progression. Biomolecules. 11(3). 431–431. 9 indexed citations
8.
Tseng, Min‐Hua, Shih‐Ming Huang, Martin Konrad, et al.. (2021). Effect of Hydrocortisone on Angiotensinogen (AGT) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis. Cells. 10(4). 782–782. 2 indexed citations
9.
Liao, Chun‐Ta, Lan‐Yan Yang, Li‐Yu Lee, et al.. (2021). Whole-exome sequencing identifies biosignatures that predict adverse survival outcomes in surgically treated patients with oral cavity squamous cell carcinoma. Oral Oncology. 122. 105547–105547. 6 indexed citations
10.
Chao, Chih‐Ying, Chun‐Chieh Wang, Wen‐Lang Fan, et al.. (2021). Association of AXIN1 With Parkinson’s Disease in a Taiwanese Population. Journal of Movement Disorders. 15(1). 33–37. 1 indexed citations
11.
Wu-Chou, Yah-Huei, et al.. (2021). NOTCH1 mutations as prognostic marker in oral squamous cell carcinoma. Pathology - Research and Practice. 223. 153474–153474. 12 indexed citations
12.
Tseng, Min‐Hua, Wen‐Lang Fan, Hsuan Liu, et al.. (2021). Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis. Frontiers in Medicine. 7. 621609–621609. 10 indexed citations
13.
Chiu, Chih‐Yung, Lun‐Ching Chang, Wen‐Lang Fan, et al.. (2020). Integration of metagenomics‐metabolomics reveals specific signatures and functions of airway microbiota in mite‐sensitized childhood asthma. Allergy. 75(11). 2846–2857. 32 indexed citations
14.
Fan, Wen‐Lang, Yu‐De Chu, Kung‐Hao Liang, et al.. (2020). Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands. Frontiers in Genetics. 11. 574943–574943. 7 indexed citations
15.
Su, Shih‐Chi, Chiao‐Wen Lin, Yu‐Fan Liu, et al.. (2017). Exome Sequencing of Oral Squamous Cell Carcinoma Reveals Molecular Subgroups and Novel Therapeutic Opportunities. Theranostics. 7(5). 1088–1099. 111 indexed citations
16.
Chiu, Chih‐Yung, Shih‐Chi Su, Wen‐Lang Fan, et al.. (2017). Whole-Genome Sequencing of a Family with Hereditary Pulmonary Alveolar Proteinosis Identifies a Rare Structural Variant Involving CSF2RA/CRLF2/IL3RA Gene Disruption. Scientific Reports. 7(1). 43469–43469. 8 indexed citations
17.
Ng, Chen Siang, Chih-Kuan Chen, Wen‐Lang Fan, et al.. (2015). Transcriptomic analyses of regenerating adult feathers in chicken. BMC Genomics. 16(1). 756–756. 35 indexed citations
18.
Shiao, Meng‐Shin, Jia‐Ming Chang, Wen‐Lang Fan, et al.. (2015). Expression Divergence of Chemosensory Genes between Drosophila sechellia and Its Sibling Species and Its Implications for Host Shift. Genome Biology and Evolution. 7(10). 2843–2858. 36 indexed citations
19.
Fan, Wen‐Lang, Chen Siang Ng, Chih‐Feng Chen, et al.. (2013). Genome-Wide Patterns of Genetic Variation in Two Domestic Chickens. Genome Biology and Evolution. 5(7). 1376–1392. 61 indexed citations
20.
Chen, Hong-Da, et al.. (2010). Universal Global Imprints of Genome Growth and Evolution – Equivalent Length and Cumulative Mutation Density. PLoS ONE. 5(4). e9844–e9844. 4 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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