Sean McGee

3.9k total citations
5 papers, 446 citations indexed

About

Sean McGee is a scholar working on Pharmacology, Hematology and Molecular Biology. According to data from OpenAlex, Sean McGee has authored 5 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Pharmacology, 2 papers in Hematology and 1 paper in Molecular Biology. Recurrent topics in Sean McGee's work include Blood groups and transfusion (2 papers), Pharmacogenetics and Drug Metabolism (2 papers) and Genomics and Rare Diseases (1 paper). Sean McGee is often cited by papers focused on Blood groups and transfusion (2 papers), Pharmacogenetics and Drug Metabolism (2 papers) and Genomics and Rare Diseases (1 paper). Sean McGee collaborates with scholars based in United States, Canada and South Korea. Sean McGee's co-authors include Eden R. Martin, Jill D. Siegfried, Jorge Gonzalez‐Quintana, Libin Wang, Duanxiang Li, Mark J. Rieder, Stephan Züchner, Jochen Reiser, Nadine Norton and Ray E. Hershberger and has published in prestigious journals such as Blood, The American Journal of Human Genetics and Genetics in Medicine.

In The Last Decade

Sean McGee

5 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sean McGee United States	5	194	168	130	91	43	5	446
Mehri Khatami Iran	13	267 1.4×	63 0.4×	54 0.4×	7 0.1×	22 0.5×	58	438
Chunyan Luo China	11	149 0.8×	79 0.5×	39 0.3×	13 0.1×	14 0.3×	17	271
Frank Rühle Germany	15	211 1.1×	36 0.2×	66 0.5×	4 0.0×	48 1.1×	28	366
Amira Turki Tunisia	11	124 0.6×	42 0.3×	87 0.7×	6 0.1×	6 0.1×	16	308
Tatsuo Shinagawa United States	10	209 1.1×	180 1.1×	18 0.1×	8 0.1×	9 0.2×	15	455
Andrea M. Douglas Australia	8	155 0.8×	45 0.3×	28 0.2×	37 0.4×	6 0.1×	8	366
Stephen Archacki United States	13	291 1.5×	83 0.5×	58 0.4×	3 0.0×	34 0.8×	20	487
Editha Andres Saudi Arabia	10	237 1.2×	141 0.8×	70 0.5×	4 0.0×	6 0.1×	20	393
Todd A. Fredrickson United States	11	360 1.9×	57 0.3×	45 0.3×	5 0.1×	6 0.1×	15	485
Mengdan Yan China	12	154 0.8×	19 0.1×	40 0.3×	18 0.2×	6 0.1×	43	346

Countries citing papers authored by Sean McGee

Since Specialization

Citations

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

Fields of papers citing papers by Sean McGee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sean McGee

This figure shows the co-authorship network connecting the top 25 collaborators of Sean McGee. A scholar is included among the top collaborators of Sean McGee 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 Sean McGee. Sean McGee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

5 of 5 papers shown

1.

Venner, Eric, Karynne Patterson, Divya Kalra, et al.. (2024). The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities. Communications Biology. 7(1). 174–174. 25 indexed citations

2.

Gaedigk, Andrea, Erin C. Boone, Steven E. Scherer, et al.. (2022). CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis. Journal of Molecular Diagnostics. 24(4). 337–350. 28 indexed citations

3.

Lee, Seung‐been, Marsha M. Wheeler, Karynne Patterson, et al.. (2018). Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model. Genetics in Medicine. 21(2). 361–372. 81 indexed citations

4.

Johnsen, Jill M., Paul L. Auer, Alanna C. Morrison, et al.. (2013). Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood. 122(4). 590–597. 50 indexed citations

5.

Norton, Nadine, Duanxiang Li, Mark J. Rieder, et al.. (2011). Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy. The American Journal of Human Genetics. 88(3). 273–282. 262 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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