Gregory E. Rice

16.0k total citations
316 papers, 13.1k citations indexed

About

Gregory E. Rice is a scholar working on Obstetrics and Gynecology, Molecular Biology and Epidemiology. According to data from OpenAlex, Gregory E. Rice has authored 316 papers receiving a total of 13.1k indexed citations (citations by other indexed papers that have themselves been cited), including 108 papers in Obstetrics and Gynecology, 100 papers in Molecular Biology and 75 papers in Epidemiology. Recurrent topics in Gregory E. Rice's work include Pregnancy and preeclampsia studies (93 papers), Preterm Birth and Chorioamnionitis (63 papers) and Reproductive System and Pregnancy (60 papers). Gregory E. Rice is often cited by papers focused on Pregnancy and preeclampsia studies (93 papers), Preterm Birth and Chorioamnionitis (63 papers) and Reproductive System and Pregnancy (60 papers). Gregory E. Rice collaborates with scholars based in Australia, United States and Chile. Gregory E. Rice's co-authors include Martha Lappas, Michael Permezel, Carlos Salomón, Murray D. Mitchell, Harry M. Georgiou, Nuzhat Ahmed, Sebastián E. Illanes, M P Bevilacqua, Miharu Kobayashi and Katherin Scholz‐Romero and has published in prestigious journals such as The Journal of Experimental Medicine, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Gregory E. Rice

312 papers receiving 12.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gregory E. Rice Australia 60 5.1k 4.4k 3.6k 2.2k 2.1k 316 13.1k
D. Stephen Charnock‐Jones United Kingdom 76 6.7k 1.3× 8.5k 2.0× 5.1k 1.4× 1.1k 0.5× 1.3k 0.6× 308 18.8k
Yoel Sadovsky United States 69 5.8k 1.1× 5.0k 1.1× 2.9k 0.8× 1.7k 0.8× 2.3k 1.1× 227 14.2k
Hiroshi Kobayashi Japan 57 5.0k 1.0× 2.5k 0.6× 1.7k 0.5× 542 0.2× 1.6k 0.8× 530 12.1k
Jerome F. Strauss United States 83 9.5k 1.9× 3.9k 0.9× 3.6k 1.0× 3.5k 1.6× 1.3k 0.6× 385 26.7k
Yuji Taketani Japan 59 2.8k 0.5× 3.9k 0.9× 3.6k 1.0× 1.6k 0.7× 756 0.4× 345 12.9k
Markku Seppälä Finland 64 3.1k 0.6× 2.4k 0.6× 4.3k 1.2× 966 0.4× 666 0.3× 372 14.3k
Murray D. Mitchell United States 73 4.5k 0.9× 5.2k 1.2× 7.2k 2.0× 6.6k 2.9× 1.7k 0.8× 614 21.8k
Wei Wang China 50 5.0k 1.0× 927 0.2× 2.2k 0.6× 1.2k 0.5× 2.2k 1.1× 403 10.5k
Robert N. Taylor United States 76 3.1k 0.6× 12.3k 2.8× 9.4k 2.7× 1.1k 0.5× 758 0.4× 267 21.0k
Søren K. Moestrup Denmark 85 7.7k 1.5× 343 0.1× 3.9k 1.1× 2.2k 1.0× 2.1k 1.0× 246 20.0k

Countries citing papers authored by Gregory E. Rice

Since Specialization
Citations

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

Fields of papers citing papers by Gregory E. Rice

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory E. Rice. 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 Gregory E. Rice. The network helps show where Gregory E. Rice may publish in the future.

Co-authorship network of co-authors of Gregory E. Rice

This figure shows the co-authorship network connecting the top 25 collaborators of Gregory E. Rice. A scholar is included among the top collaborators of Gregory E. Rice 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 Gregory E. Rice. Gregory E. Rice 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.
Rice, Gregory E. & Carlos Salomón. (2024). IFPA Joan Hunt Senior Award in Placentology lecture: Extracellular vesicle signalling and pregnancy. Placenta. 157. 5–13.
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Monteiro, Lara J., et al.. (2019). Vesículas extracelulares como predictores tempranos de diabetes gestacional. Revista médica de Chile. 147(12). 1503–1509. 11 indexed citations
4.
Salomón, Carlos, Dominic Guanzon, Katherin Scholz‐Romero, et al.. (2017). Placental Exosomes as Early Biomarker of Preeclampsia: Potential Role of Exosomal MicroRNAs Across Gestation. The Journal of Clinical Endocrinology & Metabolism. 102(9). 3182–3194. 240 indexed citations
5.
Salomón, Carlos & Gregory E. Rice. (2017). Role of Exosomes in Placental Homeostasis and Pregnancy Disorders. Progress in molecular biology and translational science. 145. 163–179. 89 indexed citations
6.
Rice, Gregory E., Katherin Scholz‐Romero, Emma L. Sweeney, et al.. (2015). The effect of glucose on the release and bioactivity of exosomes from first trimester trophoblast cells. Queensland's institutional digital repository (The University of Queensland).
7.
Salomón, Carlos, Suchismita Sarker, Gregory Duncombe, et al.. (2015). Placenta-derived exosomes promote trophoblast invasion and spiral arterial remodeling - A possible role in the physiopathology of preeclampsia. Queensland's institutional digital repository (The University of Queensland). 1 indexed citations
8.
Lim, Ratana, Martha Lappas, Clyde Riley, et al.. (2013). Investigation of human cationic antimicrobial protein-18 (hCAP-18), lactoferrin and CD163 as potential biomarkers for ovarian cancer. Journal of Ovarian Research. 6(1). 5–5. 17 indexed citations
9.
Liong, Stella, Megan K. W. Di Quinzio, Yujing J. Heng, et al.. (2012). Proteomic analysis of human cervicovaginal fluid collected before preterm premature rupture of the fetal membranes. Reproduction. 145(2). 137–147. 21 indexed citations
10.
Eisenhardt, Steffen U., Jonathon Habersberger, Karen Oliva, et al.. (2011). A proteomic analysis of C-reactive protein stimulated THP-1 monocytes. Proteome Science. 9(1). 1–1. 54 indexed citations
11.
Riley, Clyde, et al.. (2010). Expression of Foxo4 in Human Placenta and Fetal Membranes: Effect of Human Labour At Term. Placenta. 31(9). 1 indexed citations
12.
Holdsworth‐Carson, Sarah J., Ratana Lim, Clare Whitehead, et al.. (2010). Peroxisome proliferator-activated receptors are altered in pathologies of the human placenta: Gestational diabetes mellitus, intrauterine growth restriction and preeclampsia. Placenta. 31(3). 222–229. 126 indexed citations
13.
Holdsworth‐Carson, Sarah J., Michael Permezel, Gregory E. Rice, & Martha Lappas. (2009). Preterm and infection-driven preterm labor: the role of peroxisome proliferator-activated receptors and retinoid X receptor. Reproduction. 137(6). 1007–1015. 28 indexed citations
14.
Lappas, Martha, et al.. (2008). Pre-labour Fetal Membranes Overlying the Cervix Display Alterations in Inflammation and NF-κB Signalling Pathways. Placenta. 29(12). 995–1002. 54 indexed citations
15.
White, Anthony J., Sean Duffy, Antony Walton, et al.. (2007). Matrix metalloproteinase-3 and coronary remodelling: Implications for unstable coronary disease. Cardiovascular Research. 75(4). 813–820. 35 indexed citations
16.
Lappas, Martha, Michael Permezel, & Gregory E. Rice. (2004). Release of Proinflammatory Cytokines and 8-Isoprostane from Placenta, Adipose Tissue, and Skeletal Muscle from Normal Pregnant Women and Women with Gestational Diabetes Mellitus. The Journal of Clinical Endocrinology & Metabolism. 89(11). 5627–5633. 110 indexed citations
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Moseley, Jane M., et al.. (1997). Vascular effects of PTHrP (1–34) and PTH (1–34) in the human fetal-placental circulation. Placenta. 18(7). 587–592. 23 indexed citations
20.
Briscoe, David M., Frederick J. Schoen, Gregory E. Rice, et al.. (1991). Induced expression of endothelial-leukocyte adhesion molecules in human cardiac allografts.. PubMed. 51(2). 537–9. 111 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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