Arnold S.C. Tan

469 total citations
17 papers, 91 citations indexed

About

Arnold S.C. Tan is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Arnold S.C. Tan has authored 17 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 8 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Arnold S.C. Tan's work include Prenatal Screening and Diagnostics (11 papers), Hemoglobinopathies and Related Disorders (7 papers) and Parvovirus B19 Infection Studies (4 papers). Arnold S.C. Tan is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Hemoglobinopathies and Related Disorders (7 papers) and Parvovirus B19 Infection Studies (4 papers). Arnold S.C. Tan collaborates with scholars based in Singapore, China and Vietnam. Arnold S.C. Tan's co-authors include Samuel S. Chong, Felicia S.H. Cheah, Boran Jiang, Eng Leng Saw, Min Chen, Hai‐Yang Law, Indhu‐Shree Rajan‐Babu, Anupriya Agarwal, P.C. Wong and Wendy S.W. Wong and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Clinical Chemistry.

In The Last Decade

Arnold S.C. Tan

16 papers receiving 89 citations

Peers

Countries citing papers authored by Arnold S.C. Tan

Since Specialization

Citations

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

Fields of papers citing papers by Arnold S.C. Tan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnold S.C. Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Arnold S.C. Tan. A scholar is included among the top collaborators of Arnold S.C. 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 Arnold S.C. Tan. Arnold S.C. 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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17 of 17 papers shown

#	Work	Indexed citations
1	A Strategy Potentially Suitable for Combined Preimplantation Genetic Testing of Aneuploidy and Monogenic Disease That Permits Direct Detection of Pathogenic Variants Including Repeat Expansions and Gene Deletions 2025 ·International Journal of Molecular Sciences ·(unknown), Ying Liang, Arnold S.C. Tan, S. M. Wong, (unknown), P. H. Chua, Caroline Lee, Mahesh Choolani, Dang Tien Truong, Samuel S. Chong	0
2	Preimplantation Genetic Testing of Spinocerebellar Ataxia Type 3/Machado–Joseph Disease—Robust Tools for Direct and Indirect Detection of the ATXN3 (CAG)n Repeat Expansion 2024 ·International Journal of Molecular Sciences ·(unknown), (unknown), (unknown), (unknown), (unknown), Arnold S.C. Tan, Shilin Liu, Caroline Lee, Samuel S. Chong	2
3	Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion 2023 ·Thrombosis Journal ·Minh Tam Nguyen, Thanh Tùng Nguyễn, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Arnold S.C. Tan, Samuel S. Chong, (unknown)	1
4	Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances 2023 ·Clinical Chemistry ·(unknown), Timing Liu, (unknown), (unknown), Arnold S.C. Tan, S. M. Wong, Chiea Chuen Khor, Henry Yang, Caroline Lee, Zhongwei Huang, Mahesh Choolani, Samuel S. Chong	5
5	Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy 2019 ·Frontiers in Genetics ·(unknown), (unknown), Felicia S.H. Cheah, Arnold S.C. Tan, Anupriya Agarwal, Samuel S. Chong	4
6	Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping 2019 ·Scientific Reports ·(unknown), Felicia S.H. Cheah, Arnold S.C. Tan, (unknown), (unknown), Anupriya Agarwal, Samuel S. Chong	5
7	Single‐tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A 2017 ·Journal of Thrombosis and Haemostasis ·Manman Zhao, Mark Chen, Arnold S.C. Tan, (unknown), (unknown), P.C. Wong, Samuel S. Chong	7
8	FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome 2017 ·Expert Reviews in Molecular Medicine ·Indhu‐Shree Rajan‐Babu, (unknown), Felicia S.H. Cheah, Min Chen, Arnold S.C. Tan, (unknown), (unknown), Samuel S. Chong	12
9	Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome 2015 ·Prenatal Diagnosis ·Min Chen, Jerry Kok Yen Chan, (unknown), Arnold S.C. Tan, (unknown), (unknown), Eng Leng Saw, (unknown), Wendy S.W. Wong, Felicia S.H. Cheah, Hai‐Yang Law, (unknown), Samuel S. Chong	12
10	Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single‐tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta‐thalassemia 2015 ·Electrophoresis ·Min Chen, Arnold S.C. Tan, Felicia S.H. Cheah, Eng Leng Saw, Samuel S. Chong	6
11	Evidence of differential selection for the −α^3.7 and −α^4.2 single‐α‐globin gene deletions within the same population 2013 ·European Journal Of Haematology ·(unknown), (unknown), (unknown), Arnold S.C. Tan, Samuel S. Chong	3
12	Molecular strategies for pre-implantation genetic diagnosis of single gene and chromosomal disorders 2012 ·Best Practice & Research Clinical Obstetrics & Gynaecology ·Boran Jiang, Arnold S.C. Tan, Samuel S. Chong	5
13	Preimplantation genetic diagnosis of chromosome translocations by analysis of polymorphic short tandem repeats. 2012 ·PubMed ·(unknown), (unknown), Boran Jiang, (unknown), Arnold S.C. Tan, (unknown), (unknown), (unknown), (unknown), Mahesh Choolani, (unknown), Samuel S. Chong	2
14	Simplified PGD of common determinants of haemoglobin Bart’s hydrops fetalis syndrome using multiplex-microsatellite PCR 2010 ·Reproductive BioMedicine Online ·Wen Wang, (unknown), (unknown), Arnold S.C. Tan, (unknown), (unknown), (unknown), (unknown), Boran Jiang, (unknown), (unknown), Angela Ho, (unknown), (unknown), Mahesh Choolani, Samuel S. Chong	11
15	Successful preimplantation genetic diagnosis of Hb Bart's hydrops fetalis in Singapore after fresh and frozen embryo replacement cycles. 2009 ·PubMed ·(unknown), Wen Wang, Arnold S.C. Tan, (unknown), (unknown), Samuel S. Chong	4
16	First successful preimplantation genetic diagnosis in Singapore--avoidance of beta-thalassaemia major. 2009 ·PubMed ·(unknown), Arnold S.C. Tan, Wen Wang, (unknown), Samuel S. Chong	5
17	Rapid carrier screening for β-thalassemia by single-step allele-specific PCR and detection 2007 ·Clinical Biochemistry ·(unknown), (unknown), (unknown), Arnold S.C. Tan, (unknown), Ivy Ng, Hai‐Yang Law, Samuel S. Chong	7

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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