Beth McGee

2.2k total citations · 1 hit paper
19 papers, 1.6k citations indexed

About

Beth McGee is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Beth McGee has authored 19 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Hematology. Recurrent topics in Beth McGee's work include Platelet Disorders and Treatments (4 papers), Erythrocyte Function and Pathophysiology (4 papers) and Complement system in diseases (4 papers). Beth McGee is often cited by papers focused on Platelet Disorders and Treatments (4 papers), Erythrocyte Function and Pathophysiology (4 papers) and Complement system in diseases (4 papers). Beth McGee collaborates with scholars based in United States, Canada and Germany. Beth McGee's co-authors include David Siemieniak, Han‐Mou Tsai, Ralph A. Gruppo, Eric E. Bouhassira, David Ginsburg, Gallia G. Levy, Ravi Sarode, Jeanette N. McClintick, Sally P. Stabler and Angela Yang and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

Beth McGee

15 papers receiving 1.6k citations

Hit Papers

Mutations in a member of the ADAMTS gene family cause thr... 2001 2026 2009 2017 2001 400 800 1.2k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
    2001 1.3k citations Gallia G. Levy, William C. Nichols et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beth McGee United States 11 1.1k 876 454 373 260 19 1.6k
Kenji Soejima Japan 21 1.5k 1.4× 1.2k 1.4× 566 1.2× 603 1.6× 237 0.9× 52 2.2k
Ara Metjian United States 14 617 0.6× 447 0.5× 281 0.6× 219 0.6× 310 1.2× 40 1.2k
Saskia Langemeijer Netherlands 16 578 0.5× 877 1.0× 280 0.6× 445 1.2× 976 3.8× 51 1.9k
CE van der Schoot Netherlands 12 617 0.6× 391 0.4× 103 0.2× 144 0.4× 186 0.7× 23 1.2k
Susan A. Boackle United States 18 1.3k 1.2× 183 0.2× 260 0.6× 102 0.3× 271 1.0× 37 1.8k
D Raum United States 22 1.2k 1.1× 522 0.6× 82 0.2× 307 0.8× 287 1.1× 37 1.8k
Ghislaine Bernard France 20 523 0.5× 110 0.1× 392 0.9× 86 0.2× 511 2.0× 28 1.5k
A Bybee United Kingdom 20 671 0.6× 231 0.3× 326 0.7× 85 0.2× 1.4k 5.4× 35 1.9k
V C Broudy United States 14 603 0.6× 1.1k 1.2× 39 0.1× 329 0.9× 323 1.2× 19 1.8k
A J Fish United States 21 274 0.3× 189 0.2× 387 0.9× 211 0.6× 251 1.0× 33 1.1k

Countries citing papers authored by Beth McGee

Since Specialization
Citations

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

Fields of papers citing papers by Beth McGee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beth McGee

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

All Works

19 of 19 papers shown
1.
Drysdale, Claire, Lei Yu, Beth McGee, et al.. (2025). p27Kip1 regulates γ-globin production. Blood. 147(9). 973–986.
2.
Underwood, Mary, Ayse Bilge Ozel, Beth McGee, et al.. (2025). Genome-wide association and linkage analysis of histidine-rich glycoprotein identifies common variants associated with plasma histidine-rich glycoprotein concentrations. Research and Practice in Thrombosis and Haemostasis. 9(5). 102955–102955.
3.
Everett, Lesley, Ann Friedman, Vi T. Tang, et al.. (2024). LMAN1 serves as a cargo receptor for thrombopoietin. JCI Insight. 9(24).
4.
McGee, Beth, Richard A. King, Claire Drysdale, et al.. (2023). Identifying Novel Regulators of γ-Globin Expression Using a Genome-Scale CRISPR Activation Screen. Blood. 142(Supplement 1). 1100–1100. 1 indexed citations
5.
McGee, Beth, Claire Drysdale, Ann Friedman, et al.. (2023). The CDK-Inhibitor p27 Kip1 Regulates Fetal Hemoglobin Expression. Blood. 142(Supplement 1). 556–556. 2 indexed citations
6.
King, Richard A., Ann Friedman, Guojing Zhu, et al.. (2021). SEC23A rescues SEC23B-deficient congenital dyserythropoietic anemia type II. Science Advances. 7(48). eabj5293–eabj5293. 13 indexed citations
7.
King, Richard A., Vi T. Tang, Ann Friedman, et al.. (2020). The Endoplasmic Reticulum Cargo Receptor SURF4 Facilitates Efficient Erythropoietin Secretion. Molecular and Cellular Biology. 40(23). 22 indexed citations
8.
Khoriaty, Rami, Geoffrey G. Hesketh, Amélie Bernard, et al.. (2018). Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo. Proceedings of the National Academy of Sciences. 115(33). E7748–E7757. 58 indexed citations
9.
Ma, Qianyi, Paula M. Jacobi, Brian T. Emmer, et al.. (2017). Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels. Blood Advances. 1(15). 1037–1046. 17 indexed citations
10.
Khoriaty, Rami, Angela C. Weyand, Geoffrey G. Hesketh, et al.. (2017). Overlap of SEC23A and SEC23B Function Suggests a Novel Therapeutic Approach for Congenital Dyserythropoietic Anemia Type II. Blood. 130(Suppl_1). 80–80.
11.
Ozel, Ayse Bilge, Beth McGee, D. R. Siemieniak, et al.. (2016). Genome‐wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance. Journal of Thrombosis and Haemostasis. 14(9). 1888–1898. 13 indexed citations
12.
Yee, Andrew, Robert Gildersleeve, Shufang Gu, et al.. (2014). A von Willebrand factor fragment containing the D′D3 domains is sufficient to stabilize coagulation factor VIII in mice. Blood. 124(3). 445–452. 55 indexed citations
13.
Ma, Qianyi, Ayse Bilge Ozel, Shweta Ramdas, et al.. (2014). Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels. Blood. 124(20). 3155–3164. 20 indexed citations
14.
Staubach, Fabian, Sven Künzel, Andrea C. Baines, et al.. (2012). Expression of the blood-group-related glycosyltransferase B4galnt2 influences the intestinal microbiota in mice. The ISME Journal. 6(7). 1345–1355. 54 indexed citations
15.
Johnsen, Jill M., Meike Teschke, Pavlos Pavlidis, et al.. (2008). Selection on cis-Regulatory Variation at B4galnt2 and Its Influence on von Willebrand Factor in House Mice. Molecular Biology and Evolution. 26(3). 567–578. 18 indexed citations
16.
Buchner, David A., Fengyun Su, Makoto Kamei, et al.. (2007). pak2a mutations cause cerebral hemorrhage in redhead zebrafish. Proceedings of the National Academy of Sciences. 104(35). 13996–14001. 78 indexed citations
17.
Buchner, David A., Jordan A. Shavit, Fengyun Su, et al.. (2006). pak2a Mutations Cause Cerebral Hemorrhage in Redhead Zebrafish.. Blood. 108(11). 142–142. 3 indexed citations
18.
Motto, David G., et al.. (2003). ADAMTS13 mutations identified in familial TTP patients result in loss of VWF‐cleaving protease activity. Deep Blue (University of Michigan). 10 indexed citations
19.
Levy, Gallia G., William C. Nichols, Eric C.‐Y. Lian, et al.. (2001). Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 413(6855). 488–494. 1254 indexed citations breakdown →

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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