Matthew S. Cook

1.7k total citations
18 papers, 1.2k citations indexed

About

Matthew S. Cook is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, Matthew S. Cook has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Immunology and 4 papers in Surgery. Recurrent topics in Matthew S. Cook's work include Epigenetics and DNA Methylation (4 papers), Renal and related cancers (4 papers) and Immunotherapy and Immune Responses (4 papers). Matthew S. Cook is often cited by papers focused on Epigenetics and DNA Methylation (4 papers), Renal and related cancers (4 papers) and Immunotherapy and Immune Responses (4 papers). Matthew S. Cook collaborates with scholars based in United States, United Kingdom and Australia. Matthew S. Cook's co-authors include Blanche Capel, Deborah A. Lewinsohn, David Lewinsohn, Gwendolyn Swarbrick, Megan Null, Meghan Cansler, Marielle C. Gold, Joseph H. Nadeau, Susan Smyk‐Pearson and John W. Stiller and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS ONE.

In The Last Decade

Matthew S. Cook

17 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew S. Cook United States 14 559 553 231 201 181 18 1.2k
Rachel Guiton France 16 329 0.6× 842 1.5× 118 0.5× 92 0.5× 48 0.3× 26 1.3k
Oya Cingöz United States 12 274 0.5× 297 0.5× 147 0.6× 196 1.0× 81 0.4× 18 842
L Bergeron United States 10 790 1.4× 347 0.6× 214 0.9× 160 0.8× 274 1.5× 15 1.3k
Doris Apt United States 11 450 0.8× 123 0.2× 249 1.1× 120 0.6× 100 0.6× 20 866
Julie Nieminen Canada 8 503 0.9× 685 1.2× 46 0.2× 68 0.3× 50 0.3× 8 913
Mary K. Short United States 13 330 0.6× 155 0.3× 123 0.5× 119 0.6× 124 0.7× 24 709
Stephen Pacchione United States 10 587 1.1× 202 0.4× 81 0.4× 168 0.8× 126 0.7× 15 831
Tania Gourley United States 14 360 0.6× 701 1.3× 163 0.7× 54 0.3× 85 0.5× 16 1.1k
William R. Addison Canada 14 379 0.7× 203 0.4× 626 2.7× 103 0.5× 142 0.8× 24 1.3k
Keh-Chuang Chin Singapore 12 622 1.1× 959 1.7× 191 0.8× 77 0.4× 205 1.1× 14 1.6k

Countries citing papers authored by Matthew S. Cook

Since Specialization
Citations

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

Fields of papers citing papers by Matthew S. Cook

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew S. Cook. 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 Matthew S. Cook. The network helps show where Matthew S. Cook may publish in the future.

Co-authorship network of co-authors of Matthew S. Cook

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

All Works

18 of 18 papers shown
1.
Cook, Matthew S., Sean Lal, & Robert D. Hume. (2025). Transcriptional, proteomic and metabolic drivers of cardiac regeneration. Heart. 111(18). 851–858.
2.
Freimer, Jacob W., Raga Krishnakumar, Matthew S. Cook, & Robert Blelloch. (2018). Expression of Alternative Ago2 Isoform Associated with Loss of microRNA-Driven Translational Repression in Mouse Oocytes. Current Biology. 28(2). 296–302.e3. 18 indexed citations
3.
Pierpont, Timothy M., Qiming Jin, Elizabeth S. Moore, et al.. (2017). Chemotherapy-Induced Depletion of OCT4-Positive Cancer Stem Cells in a Mouse Model of Malignant Testicular Cancer. Cell Reports. 21(7). 1896–1909. 43 indexed citations
4.
Cook, Matthew S., et al.. (2017). Neutral Competition forDrosophilaFollicle and Cyst Stem Cell Niches Requires Vesicle Trafficking Genes. Genetics. 206(3). 1417–1428. 9 indexed citations
6.
Bustamante-Marin, Ximena M., et al.. (2015). Left-Biased Spermatogenic Failure in 129/SvJ Dnd1Ter/+ Mice Correlates with Differences in Vascular Architecture, Oxygen Availability, and Metabolites1. Biology of Reproduction. 93(3). 78–78. 9 indexed citations
7.
Šušor, Andrej, Denisa Jansová, Martin Anger, et al.. (2015). Temporal and spatial regulation of translation in the mammalian oocyte via the mTOR–eIF4F pathway. Nature Communications. 6(1). 79 indexed citations
8.
Cook, Matthew S. & Robert Blelloch. (2012). Small RNAs in Germline Development. Current topics in developmental biology. 102. 159–205. 34 indexed citations
9.
Gold, Marielle C., Stefania Cerri, Susan Smyk‐Pearson, et al.. (2010). Human Mucosal Associated Invariant T Cells Detect Bacterially Infected Cells. PLoS Biology. 8(6). e1000407–e1000407. 493 indexed citations
10.
Cook, Matthew S., Steven C. Munger, Joseph H. Nadeau, & Blanche Capel. (2010). Regulation of male germ cell cycle arrest and differentiation by DND1 is modulated by genetic background. Development. 138(1). 23–32. 83 indexed citations
11.
Cook, Matthew S., Steven C. Munger, Joseph H. Nadeau, & Blanche Capel. (2010). Regulation of male germ cell cycle arrest and differentiation by DND1 is modulated by genetic background. Journal of Cell Science. 124(1). e1–e1. 1 indexed citations
12.
Cook, Matthew S., et al.. (2009). BAX-mediated cell death affects early germ cell loss and incidence of testicular teratomas in Dnd1 mice. Developmental Biology. 328(2). 377–383. 63 indexed citations
13.
Krentz, Anthony D., Mark W. Murphy, Shinseog Kim, et al.. (2009). The DM domain protein DMRT1 is a dose-sensitive regulator of fetal germ cell proliferation and pluripotency. Proceedings of the National Academy of Sciences. 106(52). 22323–22328. 154 indexed citations
14.
Gold, Marielle C., Matthew S. Cook, Susan Smyk‐Pearson, et al.. (2008). Human Innate Mycobacterium tuberculosis–Reactive αβTCR+ Thymocytes. PLoS Pathogens. 4(2). e39–e39. 19 indexed citations
15.
Lewinsohn, Deborah A., Gwendolyn Swarbrick, Matthew S. Cook, et al.. (2007). Immunodominant Tuberculosis CD8 Antigens Preferentially Restricted by HLA-B. PLoS Pathogens. 3(9). e127–e127. 112 indexed citations
16.
Gold, Marielle C., et al.. (2007). Human Neonatal Dendritic Cells Are Competent in MHC Class I Antigen Processing and Presentation. PLoS ONE. 2(9). e957–e957. 17 indexed citations
17.
Gold, Marielle C., et al.. (2006). Purified Neonatal Plasmacytoid Dendritic Cells Overcome Intrinsic Maturation Defect with TLR Agonist Stimulation. Pediatric Research. 60(1). 34–37. 17 indexed citations
18.
Stiller, John W. & Matthew S. Cook. (2004). Functional Unit of the RNA Polymerase II C-Terminal Domain Lies within Heptapeptide Pairs. Eukaryotic Cell. 3(3). 735–740. 56 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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