Christian M. Shaffer

8.8k total citations · 1 hit paper
52 papers, 1.4k citations indexed

About

Christian M. Shaffer is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Christian M. Shaffer has authored 52 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cardiology and Cardiovascular Medicine, 15 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in Christian M. Shaffer's work include Cardiac electrophysiology and arrhythmias (9 papers), Genetic Associations and Epidemiology (9 papers) and Ion channel regulation and function (5 papers). Christian M. Shaffer is often cited by papers focused on Cardiac electrophysiology and arrhythmias (9 papers), Genetic Associations and Epidemiology (9 papers) and Ion channel regulation and function (5 papers). Christian M. Shaffer collaborates with scholars based in United States, Denmark and France. Christian M. Shaffer's co-authors include Dan M. Roden, Jonathan D. Mosley, Joshua C. Denny, Quinn S. Wells, Jason H. Karnes, Jessica Delaney, Sara L. Van Driest, Josiane E. Eid, Jason H. Moore and Andrew M. Glazer and has published in prestigious journals such as JAMA, Circulation and Nature Communications.

In The Last Decade

Christian M. Shaffer

51 papers receiving 1.4k citations

Hit Papers

Predictive Accuracy of a Polygenic Risk Score Compared Wi... 2020 2026 2022 2024 2020 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian M. Shaffer United States 22 457 395 328 197 154 52 1.4k
Jonathan D. Mosley United States 24 725 1.6× 436 1.1× 444 1.4× 268 1.4× 167 1.1× 91 2.0k
Yozo Ohnishi Japan 15 612 1.3× 422 1.1× 467 1.4× 242 1.2× 407 2.6× 28 1.9k
Chun‐Gyoo Ihm South Korea 23 421 0.9× 211 0.5× 136 0.4× 261 1.3× 264 1.7× 56 1.5k
Kimihiko Kato Japan 26 829 1.8× 376 1.0× 406 1.2× 289 1.5× 167 1.1× 83 1.9k
Gopala K. Rangan Australia 22 751 1.6× 126 0.3× 558 1.7× 281 1.4× 235 1.5× 85 2.2k
Axel Muendlein Austria 24 615 1.3× 299 0.8× 227 0.7× 255 1.3× 128 0.8× 124 1.7k
Hideki Oka Japan 18 692 1.5× 338 0.9× 328 1.0× 338 1.7× 124 0.8× 87 1.8k
R Thomas Lumbers United Kingdom 17 481 1.1× 377 1.0× 245 0.7× 153 0.8× 56 0.4× 30 1.3k
Raghu Durvasula United States 20 542 1.2× 216 0.5× 296 0.9× 164 0.8× 202 1.3× 26 1.8k
Joseph F. Solus United States 29 714 1.6× 659 1.7× 180 0.5× 211 1.1× 486 3.2× 58 2.7k

Countries citing papers authored by Christian M. Shaffer

Since Specialization
Citations

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

Fields of papers citing papers by Christian M. Shaffer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christian M. Shaffer. 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 Christian M. Shaffer. The network helps show where Christian M. Shaffer may publish in the future.

Co-authorship network of co-authors of Christian M. Shaffer

This figure shows the co-authorship network connecting the top 25 collaborators of Christian M. Shaffer. A scholar is included among the top collaborators of Christian M. Shaffer 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 Christian M. Shaffer. Christian M. Shaffer 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.
Ullah, Rizwan, Matthew J. O’Neill, Giovanni Davogustto, et al.. (2025). Generation of human induced pluripotent stem cell (hiPSC) lines from patients with extreme high and low polygenic scores for QT interval. Stem Cell Research. 84. 103691–103691.
2.
Liu, Ge, Lan Jiang, V. Eric Kerchberger, et al.. (2023). The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach. Clinical and Translational Science. 16(3). 489–501. 5 indexed citations
3.
Jiang, Lan, V. Eric Kerchberger, Christian M. Shaffer, et al.. (2022). Genome-wide association analyses of common infections in a large practice-based biobank. BMC Genomics. 23(1). 672–672. 6 indexed citations
4.
Wada, Yuko, Tao Yang, Christian M. Shaffer, et al.. (2022). Common Ancestry-Specific Ion Channel Variants Predispose to Drug-Induced Arrhythmias. Circulation. 145(4). 299–308. 13 indexed citations
5.
Wells, Quinn S., Minoo Bagheri, Aaron W. Aday, et al.. (2021). Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults. Circulation Genomic and Precision Medicine. 14(5). e003341–e003341. 14 indexed citations
6.
Zheng, Neil S., Cosby A. Stone, Lan Jiang, et al.. (2021). High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. PLoS Genetics. 17(6). e1009593–e1009593. 7 indexed citations
7.
Mosley, Jonathan D., Deepak K. Gupta, Jingyi Tan, et al.. (2020). Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease. JAMA. 323(7). 627–627. 186 indexed citations breakdown →
8.
Bajaj, Archna, Chengxiang Qiu, Aeron Small, et al.. (2020). Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways. Kidney International. 97(5). 1032–1041. 17 indexed citations
9.
Bretagne, Marie, Bénédicte Lebrun‐Vignes, Alexandre Pariente, et al.. (2019). Heart failure and atrial tachyarrhythmia on abiraterone: A pharmacovigilance study. Archives of cardiovascular diseases. 113(1). 9–21. 31 indexed citations
10.
Feng, QiPing, Wei‐Qi Wei, Sandip Chaugai, et al.. (2019). A Genetic Approach to the Association Between PCSK9 and Sepsis. JAMA Network Open. 2(9). e1911130–e1911130. 22 indexed citations
11.
Karnes, Jason H., Lisa Bastarache, Christian M. Shaffer, et al.. (2017). Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants. Science Translational Medicine. 9(389). 74 indexed citations
12.
Karnes, Jason H., Christian M. Shaffer, Lisa Bastarache, et al.. (2017). Comparison of HLA allelic imputation programs. PLoS ONE. 12(2). e0172444–e0172444. 44 indexed citations
13.
Stroud, Dina Myers, Tao Yang, Kevin Bersell, et al.. (2016). Contrasting Nav1.8 Activity in Scn10a −/− Ventricular Myocytes and the Intact Heart. Journal of the American Heart Association. 5(11). 21 indexed citations
14.
McGeachie, Michael J., Ann Chen Wu, Sze Man Tse, et al.. (2015). CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies. Journal of Allergy and Clinical Immunology. 136(6). 1503–1510. 34 indexed citations
15.
Karnes, Jason H., Robert M. Cronin, Jérôme Rollin, et al.. (2014). A genome-wide association study of heparin-induced thrombocyto - penia using an electronic medical record. Thrombosis and Haemostasis. 113(4). 772–781. 42 indexed citations
16.
Weeke, Peter, Raafia Muhammad, Jessica Delaney, et al.. (2014). Whole-exome sequencing in familial atrial fibrillation. European Heart Journal. 35(36). 2477–2483. 31 indexed citations
17.
McElroy, Jude J., Christian M. Shaffer, Tamara Busch, et al.. (2013). Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. Human Genetics. 132(8). 935–942. 35 indexed citations
18.
Ramirez, Andrea H., Christian M. Shaffer, Jessica Delaney, et al.. (2012). Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes. The Pharmacogenomics Journal. 13(4). 325–329. 48 indexed citations
19.
Guo, Yan, Qiuyin Cai, David C. Samuels, et al.. (2012). The use of next generation sequencing technology to study the effect of radiation therapy on mitochondrial DNA mutation. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 744(2). 154–160. 39 indexed citations
20.
Fox, Rebecca M., Stephen E. Von Stetina, Christian M. Shaffer, et al.. (2005). A gene expression fingerprint of C. elegans embryonic motor neurons. BMC Genomics. 6(1). 42–42. 105 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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