Margot L. Day

1.6k total citations
51 papers, 1.3k citations indexed

About

Margot L. Day is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Immunology. According to data from OpenAlex, Margot L. Day has authored 51 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 23 papers in Public Health, Environmental and Occupational Health and 13 papers in Immunology. Recurrent topics in Margot L. Day's work include Reproductive Biology and Fertility (22 papers), Reproductive System and Pregnancy (13 papers) and Pluripotent Stem Cells Research (11 papers). Margot L. Day is often cited by papers focused on Reproductive Biology and Fertility (22 papers), Reproductive System and Pregnancy (13 papers) and Pluripotent Stem Cells Research (11 papers). Margot L. Day collaborates with scholars based in Australia, United Kingdom and Ireland. Margot L. Day's co-authors include Martin H. Johnson, David I. Cook, Christopher R. Murphy, Yui Kaneko, Michael B. Morris, Susan J. Pickering, Cecil A. Gibb, Philip Poronnik, Anuwat Dinudom and Sharad Kumar and has published in prestigious journals such as Nature, Journal of Biological Chemistry and The EMBO Journal.

In The Last Decade

Margot L. Day

51 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Margot L. Day Australia 21 711 377 249 207 131 51 1.3k
Albina Jablonka‐Shariff United States 27 526 0.7× 667 1.8× 173 0.7× 537 2.6× 185 1.4× 49 1.9k
Nanami Kawamura Japan 16 475 0.7× 922 2.4× 244 1.0× 603 2.9× 121 0.9× 22 1.4k
William C. Gorospe United States 15 328 0.5× 429 1.1× 377 1.5× 418 2.0× 73 0.6× 26 1.3k
Nobuhiko Yamauchi Japan 23 429 0.6× 518 1.4× 372 1.5× 436 2.1× 31 0.2× 115 1.8k
Ayumi Hasegawa Japan 16 378 0.5× 258 0.7× 82 0.3× 193 0.9× 36 0.3× 48 881
Rüdiger Behr Germany 30 1.5k 2.1× 438 1.2× 118 0.5× 639 3.1× 67 0.5× 95 2.3k
Alina Isakova United States 13 707 1.0× 66 0.2× 305 1.2× 209 1.0× 117 0.9× 18 1.2k
Yoshikatsu Uematsu Japan 9 622 0.9× 254 0.7× 192 0.8× 379 1.8× 48 0.4× 10 1.7k
Takashi Nagashima Japan 20 502 0.7× 214 0.6× 533 2.1× 565 2.7× 38 0.3× 44 1.5k
Haruhiko Kanasaki Japan 22 550 0.8× 248 0.7× 120 0.5× 997 4.8× 301 2.3× 122 1.7k

Countries citing papers authored by Margot L. Day

Since Specialization
Citations

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

Fields of papers citing papers by Margot L. Day

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margot L. Day. 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 Margot L. Day. The network helps show where Margot L. Day may publish in the future.

Co-authorship network of co-authors of Margot L. Day

This figure shows the co-authorship network connecting the top 25 collaborators of Margot L. Day. A scholar is included among the top collaborators of Margot L. Day 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 Margot L. Day. Margot L. Day 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.
2.
Morris, Michael B., et al.. (2023). Glutamine, proline, and isoleucine support maturation and fertilisation of bovine oocytes. Theriogenology. 201. 59–67. 7 indexed citations
4.
Day, Margot L., et al.. (2021). Redox Regulation and Oxidative Stress in Mammalian Oocytes and Embryos Developed In Vivo and In Vitro. International Journal of Environmental Research and Public Health. 18(21). 11374–11374. 64 indexed citations
5.
Morris, Michael B., et al.. (2019). Amino acid supplementation of a simple inorganic salt solution supports efficient in vitro maturation (IVM) of bovine oocytes. Scientific Reports. 9(1). 11739–11739. 19 indexed citations
6.
Day, Margot L., et al.. (2016). Daily & Hourly Adherence. 3211–3218. 10 indexed citations
7.
Hinton, Tina, Pippa Yeoman, Lucila Carvalho, et al.. (2014). Participating in the Communication of Science: Identifying Relationships Between Laboratory Space Designs and Students’ Activities. International Journal of Innovation in Science and Mathematics Education. 22(5). 3 indexed citations
8.
10.
Kaneko, Yui, Christopher R. Murphy, & Margot L. Day. (2013). Calpain 2 activity increases at the time of implantation in rat uterine luminal epithelial cells and administration of calpain inhibitor significantly reduces implantation sites. Histochemistry and Cell Biology. 141(4). 423–430. 8 indexed citations
11.
Day, Margot L., et al.. (2013). Insulin-like growth factor 1 acts as an autocrine factor to improve early embryogenesis in vitro. The International Journal of Developmental Biology. 57(11-12). 837–844. 16 indexed citations
12.
Kaneko, Yui, Margot L. Day, & Christopher R. Murphy. (2012). Uterine epithelial cells: Serving two masters. The International Journal of Biochemistry & Cell Biology. 45(2). 359–363. 14 indexed citations
13.
Kaneko, Yui, Laura Lecce, Margot L. Day, & Christopher R. Murphy. (2011). ß1 and ß3 integrins disassemble from basal focal adhesions and ß3 integrin is later localised to the apical plasma membrane of rat uterine luminal epithelial cells at the time of implantation. Reproduction Fertility and Development. 23(3). 481–495. 39 indexed citations
14.
Kaneko, Yui, Margot L. Day, & Christopher R. Murphy. (2011). Integrin  3 in rat blastocysts and epithelial cells is essential for implantation in vitro: studies with Ishikawa cells and small interfering RNA transfection. Human Reproduction. 26(7). 1665–1674. 43 indexed citations
15.
Day, Margot L., et al.. (2011). Caveolin and Focal Adhesion Proteins Talin and Paxillin During Early Pregnancy in the Rat and in Human Ishikawa Cells.. Biology of Reproduction. 85(Suppl_1). 476–476. 2 indexed citations
16.
Li, Yan, Vashe Chandrakanthan, Margot L. Day, & Chris O’Neill. (2007). Direct Evidence for the Action of Phosphatidylinositol (3,4,5)-Trisphosphate-Mediated Signal Transduction in the 2-Cell Mouse Embryo1. Biology of Reproduction. 77(5). 813–821. 32 indexed citations
17.
Li, Yan, Margot L. Day, & Chris O’Neill. (2007). Autocrine activation of ion currents in the two-cell mouse embryo. Experimental Cell Research. 313(13). 2786–2794. 13 indexed citations
18.
Harding, E. A., Cecil A. Gibb, Martin H. Johnson, David I. Cook, & Margot L. Day. (2002). Developmental Changes in the Management of Acid Loads During Preimplantation Mouse Development1. Biology of Reproduction. 67(5). 1419–1429. 17 indexed citations
19.
Day, Margot L., et al.. (2001). tiK + toK + : an embryonic clock?. Reproduction Fertility and Development. 13(1). 69–79. 18 indexed citations
20.
Day, Margot L., Martin H. Johnson, & David I. Cook. (1998). A cytoplasmic cell cycle controls the activity of a K+ channel in pre-implantation mouse embryos. The EMBO Journal. 17(7). 1952–1960. 39 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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