Ene‐Choo Tan

3.2k total citations
89 papers, 1.8k citations indexed

About

Ene‐Choo Tan is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ene‐Choo Tan has authored 89 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 30 papers in Genetics and 12 papers in Surgery. Recurrent topics in Ene‐Choo Tan's work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Pain Management and Opioid Use (8 papers). Ene‐Choo Tan is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (10 papers) and Pain Management and Opioid Use (8 papers). Ene‐Choo Tan collaborates with scholars based in Singapore, United States and Canada. Ene‐Choo Tan's co-authors include Eileen C.P. Lim, Yvonne Lim, Siow‐Ann Chong, Yik‐Ying Teo, Alex Sia, Hai‐Yang Law, Saumya Shekhar Jamuar, Alex Tiong Heng Sia, Eric P.H. Yap and Ruth Landau and has published in prestigious journals such as Journal of Biological Chemistry, Biological Psychiatry and Pain.

In The Last Decade

Ene‐Choo Tan

85 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ene‐Choo Tan Singapore 24 396 392 391 315 306 89 1.8k
Daisuke Nishizawa Japan 18 368 0.9× 203 0.5× 244 0.6× 102 0.3× 146 0.5× 80 1.1k
Inna E. Tchivileva United States 15 111 0.3× 131 0.3× 401 1.0× 165 0.5× 277 0.9× 23 1.5k
Philip H. Heller United States 24 277 0.7× 167 0.4× 892 2.3× 189 0.6× 141 0.5× 40 2.5k
Katherine Beebe United States 17 134 0.3× 95 0.2× 372 1.0× 281 0.9× 160 0.5× 28 2.0k
Masahiko Fujinaga United States 25 350 0.9× 292 0.7× 723 1.8× 145 0.5× 49 0.2× 74 2.0k
Richard Berkowitz United States 20 113 0.3× 358 0.9× 168 0.4× 183 0.6× 67 0.2× 55 1.5k
Cynthia L. Renn United States 21 97 0.2× 115 0.3× 182 0.5× 35 0.1× 117 0.4× 57 1.3k
Constantine Sarantopoulos United States 29 542 1.4× 166 0.4× 324 0.8× 24 0.1× 157 0.5× 90 2.6k
Michael Soyka Switzerland 26 69 0.2× 133 0.3× 298 0.8× 49 0.2× 96 0.3× 126 3.0k
Costanzo Moretti Italy 30 33 0.1× 147 0.4× 661 1.7× 212 0.7× 243 0.8× 91 3.2k

Countries citing papers authored by Ene‐Choo Tan

Since Specialization
Citations

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

Fields of papers citing papers by Ene‐Choo Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ene‐Choo Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Ene‐Choo Tan. A scholar is included among the top collaborators of Ene‐Choo 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 Ene‐Choo Tan. Ene‐Choo 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.
Lim, Jiin Ying, et al.. (2025). A Novel GATAD2B Frameshift Variant Causes GATAD2B-Associated Neurodevelopmental Disorder with Camptodactyly. Molecular Syndromology. 17(1). 54–58. 1 indexed citations
2.
Tan, Ene‐Choo, et al.. (2023). Phenotype and genotype correlation of inherited epidermolysis bullosa in Indonesia. Australasian Journal of Dermatology. 64(4). e327–e332. 1 indexed citations
3.
Yu, Junhong, Iris Rawtaer, Lei Feng, et al.. (2021). Mindfulness intervention for mild cognitive impairment led to attention-related improvements and neuroplastic changes: Results from a 9-month randomized control trial. Journal of Psychiatric Research. 135. 203–211. 34 indexed citations
4.
Ng, Ted Kheng Siang, Lei Feng, Johnson Fam, et al.. (2021). Mindfulness Awareness Practice (MAP) to Prevent Dementia in Older Adults with Mild Cognitive Impairment: Protocol of a Randomized Controlled Trial and Implementation Outcomes. International Journal of Environmental Research and Public Health. 18(19). 10205–10205. 6 indexed citations
5.
Haag, Natja, Ene‐Choo Tan, Matthias Begemann, et al.. (2021). Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European Journal of Human Genetics. 29(11). 1663–1668. 6 indexed citations
6.
Lai, Angeline, et al.. (2020). Coffin-Siris Syndrome-1: Report of five cases from Asian populations with truncating mutations in the ARID1B gene. Journal of the Neurological Sciences. 414. 116819–116819. 4 indexed citations
7.
Tan, Howe‐Siang, Ene‐Choo Tan, Sanjanaa Nagarajan, et al.. (2020). Association of renin-angiotensin-aldosterone system genetic polymorphisms with maternal hypotension during spinal anaesthesia for caesarean delivery: a retrospective cohort study. International Journal of Obstetric Anesthesia. 44. 3–12. 1 indexed citations
8.
Loke, Mun Fai, et al.. (2019). <p>Deep sequencing analysis to identify novel and rare variants in pain-related genes in patients with acute postoperative pain and high morphine use</p>. Journal of Pain Research. Volume 12. 2755–2770. 3 indexed citations
9.
Koh, Mark Jean Aan, et al.. (2018). Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation. JAAD Case Reports. 4(4). 318–321. 2 indexed citations
10.
Hande, M. Prakash, et al.. (2017). Correlation of cord blood telomere length with birth weight. BMC Research Notes. 10(1). 469–469. 25 indexed citations
11.
Sng, Ban Leong, Helen Chen, Pryseley Nkouibert Assam, et al.. (2016). Investigating analgesic and psychological factors associated with risk of postpartum depression development: a case&ndash;control study. Neuropsychiatric Disease and Treatment. 12. 1333–1333. 38 indexed citations
12.
Jamuar, Saumya Shekhar & Ene‐Choo Tan. (2015). Clinical application of next-generation sequencing for Mendelian diseases. Human Genomics. 9(1). 10–10. 65 indexed citations
13.
Tan, Ene‐Choo, Eileen C.P. Lim, & Seng-Teik Lee. (2013). De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus. Molecular Cytogenetics. 6(1). 31–31. 12 indexed citations
14.
Sia, Alex Tiong Heng, Ban Leong Sng, Eileen C.P. Lim, Hai‐Yang Law, & Ene‐Choo Tan. (2010). The influence of ATP-binding cassette sub-family B member -1 (ABCB1) genetic polymorphisms on acute and chronic pain after intrathecal morphine for caesarean section: a prospective cohort study. International Journal of Obstetric Anesthesia. 19(3). 254–260. 57 indexed citations
16.
Tan, Ene‐Choo, et al.. (2008). Ethnic Differences in Pain Perception and Patient-Controlled Analgesia Usage for Postoperative Pain. Journal of Pain. 9(9). 849–855. 74 indexed citations
17.
Tan, Ene‐Choo & Poh San Lai. (2005). Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions. Expert Review of Molecular Diagnostics. 5(1). 101–109. 10 indexed citations
18.
Tan, Ene‐Choo, Siow‐Ann Chong, Lionel Lim, et al.. (2004). Genetic analysis of the thermolabile methylenetetrahydrofolate reductase variant in schizophrenia and mood disorders. Psychiatric Genetics. 14(4). 227–231. 46 indexed citations
19.
Tan, Ene‐Choo, et al.. (2003). Mu opioid receptor gene polymorphisms and heroin dependence in Asian populations. Neuroreport. 14(4). 569–572. 146 indexed citations
20.
Tan, Ene‐Choo & Suyinn Chong. (2000). Identification of Genes for Schizophrenia Susceptibility. Annals of the Academy of Medicine Singapore. 29(3). 305–305. 2 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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