Wen‐Hann Tan

6.1k total citations
81 papers, 2.1k citations indexed

About

Wen‐Hann Tan is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wen‐Hann Tan has authored 81 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 44 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wen‐Hann Tan's work include Genetic Syndromes and Imprinting (28 papers), Epigenetics and DNA Methylation (22 papers) and Prenatal Screening and Diagnostics (12 papers). Wen‐Hann Tan is often cited by papers focused on Genetic Syndromes and Imprinting (28 papers), Epigenetics and DNA Methylation (22 papers) and Prenatal Screening and Diagnostics (12 papers). Wen‐Hann Tan collaborates with scholars based in United States, China and United Kingdom. Wen‐Hann Tan's co-authors include Lynne M. Bird, Dongxin Lin, Xiaoping Miao, Deyin Xing, Tong Sun, Peiyu Xiong, Xun Zhang, De‐Chen Lin, Qingyi Wei and Ronald L. Thibert and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and JNCI Journal of the National Cancer Institute.

In The Last Decade

Wen‐Hann Tan

79 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wen‐Hann Tan United States 27 1.3k 928 294 269 224 81 2.1k
Ann Nordgren Sweden 29 1.1k 0.9× 997 1.1× 391 1.3× 217 0.8× 63 0.3× 134 2.6k
Hennie T. Brüggenwirth Netherlands 25 1.3k 1.1× 786 0.8× 183 0.6× 255 0.9× 126 0.6× 73 2.1k
Lisa Edelmann United States 31 1.8k 1.5× 1.5k 1.6× 344 1.2× 195 0.7× 74 0.3× 79 3.3k
Maha S. Zaki Egypt 27 1.2k 0.9× 679 0.7× 388 1.3× 85 0.3× 127 0.6× 147 2.4k
Maja Di Rocco Italy 34 1.5k 1.2× 860 0.9× 350 1.2× 305 1.1× 778 3.5× 147 3.6k
Kanya Suphapeetiporn Thailand 23 804 0.6× 714 0.8× 138 0.5× 142 0.5× 403 1.8× 131 2.0k
Felicitas Lacbawan United States 21 931 0.7× 565 0.6× 170 0.6× 101 0.4× 84 0.4× 50 1.8k
Majid Alfadhel Saudi Arabia 28 1.4k 1.1× 920 1.0× 301 1.0× 60 0.2× 254 1.1× 157 2.5k
Mirella Filocamo Italy 34 1.9k 1.5× 431 0.5× 153 0.5× 148 0.6× 547 2.4× 158 4.3k
Hiroshi Kawame Japan 23 1.1k 0.9× 634 0.7× 253 0.9× 163 0.6× 139 0.6× 66 2.1k

Countries citing papers authored by Wen‐Hann Tan

Since Specialization
Citations

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

Fields of papers citing papers by Wen‐Hann Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wen‐Hann Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Wen‐Hann Tan. A scholar is included among the top collaborators of Wen‐Hann 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 Wen‐Hann Tan. Wen‐Hann Tan 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.
Wang, Ziteng, Wen‐Hann Tan, Jiali Huang, et al.. (2024). Small intestinal bacterial overgrowth and metabolic dysfunction-associated steatotic liver disease. Frontiers in Nutrition. 11. 1502151–1502151. 2 indexed citations
2.
Thomas, Janet, Wen‐Hann Tan, Aneal Khan, et al.. (2024). Long-term safety and efficacy of DTX301 in adults with late-onset ornithine transcarbamylase (OTC) deficiency: A Phase 1/2 trial. Molecular Genetics and Metabolism. 141(4). 108266–108266. 1 indexed citations
3.
Moore, Amanda, et al.. (2024). Community‐Sourced Reporting of Mortalities in Angelman Syndrome (1979–2022). American Journal of Medical Genetics Part A. 197(4). e63961–e63961. 1 indexed citations
4.
Khan, Nasreen, Raquel Cabo, Rebecca D. Burdine, et al.. (2023). Health-related quality of life and medication use among individuals with Angelman syndrome. Quality of Life Research. 32(7). 2059–2067. 3 indexed citations
5.
Keary, Christopher J., Lynne M. Bird, Marie‐Claire Y. de Wit, et al.. (2023). Gaboxadol in angelman syndrome: A double-blind, parallel-group, randomized placebo-controlled phase 3 study. European Journal of Paediatric Neurology. 47. 6–12. 6 indexed citations
6.
Gold, Nina B., Ian M. Campbell, Sarah E. Sheppard, & Wen‐Hann Tan. (2021). Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization. Scientific Reports. 11(1). 19791–19791. 5 indexed citations
7.
Hipp, Joerg F., Joel Frohlich, Marius Keute, Wen‐Hann Tan, & Lynne M. Bird. (2021). Electrophysiological Abnormalities in Angelman Syndrome Correlate With Symptom Severity. SHILAP Revista de lepidopterología. 1(3). 201–209. 17 indexed citations
8.
Kantaputra, Piranit Nik, et al.. (2020). Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutation. Archives of Oral Biology. 116. 104735–104735. 7 indexed citations
9.
Wojcik, Monica H., Katherine R. Chao, Julia K. Goodrich, et al.. (2019). Genome Sequencing Identifies the Pathogenic Variant Missed by Prior Testing in an Infant with Marfan Syndrome. The Journal of Pediatrics. 213. 235–240. 5 indexed citations
10.
Gold, Nina B., Ann Wessel, Deborah R. Stein, et al.. (2018). Acute Pancreatitis in a Patient with Maple Syrup Urine Disease: A Management Paradox. The Journal of Pediatrics. 198. 313–316. 1 indexed citations
11.
Rodan, Lance H., Maureen M. Jonas, Janet S. Soul, et al.. (2017). Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old Female. JIMD Reports. 40. 17–22. 5 indexed citations
12.
Tan, Wen‐Hann & Lynne M. Bird. (2016). Angelman syndrome: Current and emerging therapies in 2016. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 172(4). 384–401. 42 indexed citations
13.
Tan, Wen‐Hann, Lynne M. Bird, Ronald L. Thibert, & Charles A. Williams. (2014). If not Angelman, what is it? a review of Angelman‐like syndromes. American Journal of Medical Genetics Part A. 164(4). 975–992. 79 indexed citations
14.
Gentile, Jennifer, Wen‐Hann Tan, Lucia T. Horowitz, et al.. (2010). A Neurodevelopmental Survey of Angelman Syndrome With Genotype-Phenotype Correlations. Journal of Developmental & Behavioral Pediatrics. 31(7). 592–601. 117 indexed citations
15.
Mochida, Ganeshwaran H., Vijay Ganesh, Jillian M. Felie, et al.. (2010). A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts. The American Journal of Human Genetics. 87(6). 882–889. 64 indexed citations
16.
Manzini, M. Chiara, Anna Rajab, Thomas M. Maynard, et al.. (2009). Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67(4). 516–525. 27 indexed citations
17.
Yang, Ming, Yongchun Guo, Xiaojie Zhang, et al.. (2007). Interaction of P53 Arg72Pro and MDM2 T309G polymorphisms and their associations with risk of gastric cardia cancer. Carcinogenesis. 28(9). 1996–2001. 66 indexed citations
18.
Tan, Wen‐Hann, Hagit Baris, Caroline D. Robson, & Virginia Kimonis. (2005). Cockayne syndrome: The developing phenotype. American Journal of Medical Genetics Part A. 135A(2). 214–216. 10 indexed citations
19.
Tan, Wen‐Hann, Xiaoping Miao, Li Wang, et al.. (2005). Significant increase in risk of gastroesophageal cancer is associated with interaction between promoter polymorphisms in thymidylate synthase and serum folate status. Carcinogenesis. 26(8). 1430–1435. 34 indexed citations
20.
Sun, Tong, Xiaoping Miao, Xun Zhang, et al.. (2004). Polymorphisms of Death Pathway Genes FAS and FASL in Esophageal Squamous-Cell Carcinoma. JNCI Journal of the National Cancer Institute. 96(13). 1030–1036. 176 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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