Andrew M. MacMillan

2.1k total citations
46 papers, 1.7k citations indexed

About

Andrew M. MacMillan is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Andrew M. MacMillan has authored 46 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Andrew M. MacMillan's work include RNA and protein synthesis mechanisms (32 papers), RNA Research and Splicing (23 papers) and RNA modifications and cancer (21 papers). Andrew M. MacMillan is often cited by papers focused on RNA and protein synthesis mechanisms (32 papers), RNA Research and Splicing (23 papers) and RNA modifications and cancer (21 papers). Andrew M. MacMillan collaborates with scholars based in Canada, United States and France. Andrew M. MacMillan's co-authors include Gregory L. Verdine, Matthew J. Schellenberg, Oliver A. Kent, Steven G. Chaulk, Emily M. Gesner, Dustin B. Ritchie, Wen‐Yi Chang, Liuhong Chen, W S Lane and Phillip A. Sharp and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Andrew M. MacMillan

46 papers receiving 1.6k citations

Peers

Andrew M. MacMillan

GENET

ECOLO

Caroline Köhrer United States

Ryohei Ishii Japan

Masayuki Takahashi Japan

Dmitry E. Agafonov Germany

Matthew J. Schellenberg United States

Mikhaïl Grigoriev France

S. Kundhavai Natchiar France

Carilee Denison United States

Etsuko Miyamoto‐Sato Japan

Martin C. Moncrieffe United Kingdom

Caroline Köhrer United States

Andrew M. MacMillan

1.6k ×1.0

326 ×1.9

GENET

153 ×1.3

ECOLO

56 ×0.6

63 ×0.8

Citations per year, relative to Andrew M. MacMillan Andrew M. MacMillan (= 1×) peers Caroline Köhrer

Countries citing papers authored by Andrew M. MacMillan

Since Specialization

Citations

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

Fields of papers citing papers by Andrew M. MacMillan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew M. MacMillan

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

All Works

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20 of 20 papers shown

Black, Corbin, et al.. (2023). Spliceosome assembly and regulation: insights from analysis of highly reduced spliceosomes. RNA. 29(5). 531–550. 9 indexed citations

Kim, Hyeong Jin, M.M. Black, Ross A. Edwards, et al.. (2022). Structural basis for recognition of transcriptional terminator structures by ProQ/FinO domain RNA chaperones. Nature Communications. 13(1). 7076–7076. 8 indexed citations

MacMillan, Andrew M., et al.. (2017). Reversibly constraining spliceosome-substrate complexes by engineering disulfide crosslinks. Methods. 125. 25–35. 1 indexed citations

Kent, Oliver A., et al.. (2017). Radical probing of spliceosome assembly. Methods. 125. 16–24. 1 indexed citations

Schellenberg, Matthew J., Tao Wu, Dustin B. Ritchie, et al.. (2013). A conformational switch in PRP8 mediates metal ion coordination that promotes pre-mRNA exon ligation. Nature Structural & Molecular Biology. 20(6). 728–734. 30 indexed citations

Schellenberg, Matthew J., Emily M. Gesner, J.B. Bonanno, et al.. (2012). Cas5d processes pre-crRNA and is a member of a larger family of CRISPR RNA endonucleases. RNA. 18(11). 2020–2028. 73 indexed citations

Chaulk, Steven G., Oliver A. Kent, Zhizhong Xu, et al.. (2011). Role of pri-miRNA tertiary structure in miR-17~92 miRNA biogenesis. RNA Biology. 8(6). 1105–1114. 82 indexed citations

Schellenberg, Matthew J., Dustin B. Ritchie, & Andrew M. MacMillan. (2008). Pre-mRNA splicing: a complex picture in higher definition. Trends in Biochemical Sciences. 33(6). 243–246. 32 indexed citations

Schellenberg, Matthew J., Ross A. Edwards, Dustin B. Ritchie, et al.. (2006). Crystal structure of a core spliceosomal protein interface. Proceedings of the National Academy of Sciences. 103(5). 1266–1271. 64 indexed citations

10.

Wu, Tao, Chao Liang, Matthew J. Schellenberg, et al.. (2006). FRET Analysis of in Vivo Dimerization by RNA-editing Enzymes. Journal of Biological Chemistry. 281(24). 16530–16535. 56 indexed citations

11.

Kent, Oliver A., Dustin B. Ritchie, & Andrew M. MacMillan. (2004). Characterization of a U2AF-Independent Commitment Complex (E′) in the Mammalian Spliceosome Assembly Pathway. Molecular and Cellular Biology. 25(1). 233–240. 36 indexed citations

12.

Kent, Oliver A. & Andrew M. MacMillan. (2004). RNAi: running interference for the cell. Organic & Biomolecular Chemistry. 2(14). 1957–1957. 13 indexed citations

13.

Kent, Oliver A., et al.. (2003). Structuring of the 3′ Splice Site by U2AF65. Journal of Biological Chemistry. 278(50). 50572–50577. 35 indexed citations

14.

Collins, Cynthia H., et al.. (2002). Adenosine to Inosine Editing by ADAR2 Requires Formation of a Ternary Complex on the GluR-B R/G Site. Journal of Biological Chemistry. 277(40). 37624–37629. 38 indexed citations

15.

Kent, Oliver A. & Andrew M. MacMillan. (2002). Early organization of pre-mRNA during spliceosome assembly. Nature Structural Biology. 9(8). 576–81. 39 indexed citations

16.

Chaulk, Steven G. & Andrew M. MacMillan. (2001). Separation of Spliceosome Assembly from Catalysis with Caged pre-mRNA Substrates. Angewandte Chemie International Edition. 40(11). 2149–2152. 22 indexed citations

17.

Kent, Oliver A., Steven G. Chaulk, & Andrew M. MacMillan. (2000). Kinetic Analysis of the M1 RNA Folding Pathway. Journal of Molecular Biology. 304(5). 699–705. 23 indexed citations

18.

Krummel, Daniel A. Pomeranz, Oliver A. Kent, Andrew M. MacMillan, & Sidney Altman. (2000). Evidence for helical unwinding of an RNA substrate by the RNA enzyme RNase P: use of an interstrand disulfide crosslink in substrate. Journal of Molecular Biology. 295(5). 1113–1118. 21 indexed citations

19.

MacMillan, Andrew M., et al.. (2000). Template-directed interference footprinting for RNA based on inosine-specific cleavage. Bioorganic & Medicinal Chemistry Letters. 10(15). 1633–1635. 1 indexed citations

20.

Chen, Liuhong, et al.. (1991). Direct identification of the active-site nucleophile in a DNA (cytosine-5)-methyltransferase. Biochemistry. 30(46). 11018–11025. 208 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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