Christopher Tan

824 total citations
24 papers, 483 citations indexed

About

Christopher Tan is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Christopher Tan has authored 24 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Epidemiology. Recurrent topics in Christopher Tan's work include Genomics and Rare Diseases (4 papers), Congenital Heart Disease Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Christopher Tan is often cited by papers focused on Genomics and Rare Diseases (4 papers), Congenital Heart Disease Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Christopher Tan collaborates with scholars based in United States, Canada and Australia. Christopher Tan's co-authors include Aurora M. Nedelcu, John W. Moore, Daniel S. Levi, Junya Fujimoto, Alexander Augustyn, Patrick Dospoy, Jill E. Larsen, Melanie H. Cobb, Chunli Shao and James P. Sullivan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gene and Journal of Magnetic Resonance Imaging.

In The Last Decade

Christopher Tan

23 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Tan United States 12 251 171 146 92 74 24 483
Hilda Tateossian United Kingdom 11 227 0.9× 105 0.6× 74 0.5× 100 1.1× 48 0.6× 17 515
Sara Franceschi Italy 14 236 0.9× 102 0.6× 43 0.3× 68 0.7× 105 1.4× 35 521
Cecilia Surace Italy 12 328 1.3× 68 0.4× 40 0.3× 201 2.2× 58 0.8× 33 595
Maia V. Ouspenskaia United States 14 622 2.5× 77 0.5× 126 0.9× 267 2.9× 63 0.9× 16 876
David Bourn United Kingdom 13 132 0.5× 37 0.2× 130 0.9× 60 0.7× 67 0.9× 33 604
Christopher Flerin United States 2 505 2.0× 120 0.7× 31 0.2× 43 0.5× 80 1.1× 2 745
Bernd Auber Germany 13 194 0.8× 41 0.2× 33 0.2× 223 2.4× 47 0.6× 48 492
Pascal J. Lafontant United States 9 299 1.2× 56 0.3× 75 0.5× 36 0.4× 50 0.7× 16 404
Tanya M. McLaughlin United States 8 317 1.3× 37 0.2× 75 0.5× 75 0.8× 87 1.2× 9 712
Álvaro González-Rajal Australia 11 462 1.8× 36 0.2× 73 0.5× 48 0.5× 74 1.0× 14 633

Countries citing papers authored by Christopher Tan

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Tan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Tan. A scholar is included among the top collaborators of Christopher 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 Christopher Tan. Christopher 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.
Manders, Toby, Christopher Tan, Yuya Kobayashi, et al.. (2025). Harnessing genotype and phenotype data for population-scale variant classification using large language models and bayesian inference. Human Genetics. 144(6). 605–614.
2.
Padigepati, Samskruthi Reddy, David Stafford, Christopher Tan, et al.. (2024). Scalable approaches for generating, validating and incorporating data from high-throughput functional assays to improve clinical variant classification. Human Genetics. 143(8). 995–1004. 3 indexed citations
3.
Roggenbuck, Jennifer, Ana Morales, Christopher Tan, et al.. (2024). Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy. Journal of the Peripheral Nervous System. 29(3). 363–367. 1 indexed citations
4.
Singh, Kathryn, et al.. (2023). Non-mosaic trisomy 22 and congenital heart surgery using the shared decision making model: a case report. BMC Pediatrics. 23(1). 122–122. 1 indexed citations
5.
Bowen, B.M., Rebecca Truty, Swaroop Aradhya, et al.. (2021). SMA Identified: Clinical and Molecular Findings From a Sponsored Testing Program for Spinal Muscular Atrophy in More Than 2,000 Individuals. Frontiers in Neurology. 12. 663911–663911. 8 indexed citations
6.
Tan, Christopher, M. Jody Westbrook, Rebecca Truty, et al.. (2020). Incorporating Spinal Muscular Atrophy Analysis by Next-Generation Sequencing into a Comprehensive Multigene Panel for Neuromuscular Disorders. Genetic Testing and Molecular Biomarkers. 24(10). 616–624. 11 indexed citations
7.
Roggenbuck, Jennifer, Kelly Rich, Ana Morales, et al.. (2019). A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathy. Molecular Genetics & Genomic Medicine. 7(11). e924–e924. 5 indexed citations
8.
Cohen, Stephanie A., et al.. (2016). An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report. Frontiers in Genetics. 7. 36–36. 3 indexed citations
9.
Tan, Christopher, M. Jody Westbrook, Keith Nykamp, et al.. (2016). Autosomal recessive MFN2‐related Charcot‐Marie‐Tooth disease with diaphragmatic weakness: Case report and literature review. American Journal of Medical Genetics Part A. 170(6). 1580–1584. 14 indexed citations
10.
11.
Bhoj, Elizabeth, Sara Halbach, Donna M. McDonald‐McGinn, et al.. (2013). Expanding the spectrum of microdeletion 4q21 syndrome: A partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and pierre robin sequence. American Journal of Medical Genetics Part A. 161(9). 2327–2333. 19 indexed citations
12.
Tan, Christopher, et al.. (2013). The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing. Brain and Development. 36(4). 351–355. 25 indexed citations
13.
Pfau, Ruthann, Devon Lamb Thrush, Dennis Bartholomew, et al.. (2013). MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation. European Journal of Medical Genetics. 56(11). 609–613. 9 indexed citations
14.
Tan, Christopher, Kelly Arndt, Dorothy K. Grange, et al.. (2013). Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion. Molecular Genetics & Genomic Medicine. 2(2). 115–123. 7 indexed citations
15.
Waggoner, Darrel & Christopher Tan. (2011). Expanding newborn screening for lysosomal disorders: Opportunities and challenges. PubMed. 17(1). 9–14. 9 indexed citations
16.
Ordovás, Karen, Christopher Tan, Gautham P. Reddy, et al.. (2007). Disparity between ratios of diameters and blood flows in central pulmonary arteries in postoperative congenital heart disease using MRI. Journal of Magnetic Resonance Imaging. 25(4). 721–726. 8 indexed citations
17.
Nedelcu, Aurora M. & Christopher Tan. (2007). Early diversification and complex evolutionary history of the p53 tumor suppressor gene family. Development Genes and Evolution. 217(11-12). 801–806. 49 indexed citations
18.
Pujadas, Sandra, Gautham P. Reddy, O. Weber, et al.. (2006). Phase contrast MR imaging to measure changes in collateral blood flow after stenting of recurrent aortic coarctation: Initial experience. Journal of Magnetic Resonance Imaging. 24(1). 72–76. 14 indexed citations
19.
Tan, Christopher, Daniel S. Levi, & John W. Moore. (2005). Percutaneous closure of perimembranous ventricular septal defect associated with a ventricular septal aneurysm using the Amplatzer ductal occluder. Catheterization and Cardiovascular Interventions. 66(3). 427–431. 20 indexed citations
20.
Tan, Christopher, Daniel S. Levi, & John W. Moore. (2005). Embolization and Transcatheter Retrieval of Coils and Devices. Pediatric Cardiology. 26(3). 267–274. 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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