Dean H. Betts

4.0k total citations
99 papers, 3.0k citations indexed

About

Dean H. Betts is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Physiology. According to data from OpenAlex, Dean H. Betts has authored 99 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 30 papers in Public Health, Environmental and Occupational Health and 25 papers in Physiology. Recurrent topics in Dean H. Betts's work include Pluripotent Stem Cells Research (43 papers), Reproductive Biology and Fertility (28 papers) and Telomeres, Telomerase, and Senescence (22 papers). Dean H. Betts is often cited by papers focused on Pluripotent Stem Cells Research (43 papers), Reproductive Biology and Fertility (28 papers) and Telomeres, Telomerase, and Senescence (22 papers). Dean H. Betts collaborates with scholars based in Canada, United States and Denmark. Dean H. Betts's co-authors include Thomas G. Koch, W.A. King, W.A. King, Pavneesh Madan, Andrew J. Watson, Preben D. Thomsen, Lise Charlotte Berg, Laura A. Favetta, Steven D. Perrault and Mark Westhusin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Dean H. Betts

98 papers receiving 2.9k citations

Peers

Dean H. Betts

PHEOH

GENET

SURGE

GENET

María P. De Miguel Spain

Kwang Yul South Korea

Jinlian Hua China

Jae Ho Lee South Korea

Shin Yong Moon South Korea

Rehannah Borup Denmark

Guangxiu Lu China

Timo Tuuri Finland

Pradeep Reddy United States

Maria Giulia Minasi Italy

María P. De Miguel Spain

Dean H. Betts

1.1k ×0.7

599 ×0.5

PHEOH

427 ×0.8

GENET

559 ×1.0

SURGE

597 ×1.2

GENET

Citations per year, relative to Dean H. Betts Dean H. Betts (= 1×) peers María P. De Miguel

Countries citing papers authored by Dean H. Betts

Since Specialization

Citations

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

Fields of papers citing papers by Dean H. Betts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dean H. Betts. 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 Dean H. Betts. The network helps show where Dean H. Betts may publish in the future.

Co-authorship network of co-authors of Dean H. Betts

This figure shows the co-authorship network connecting the top 25 collaborators of Dean H. Betts. A scholar is included among the top collaborators of Dean H. Betts 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 Dean H. Betts. Dean H. Betts 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

Betts, Dean H., et al.. (2024). Flexible learning dimensions in higher education: aligning students’ and educators’ perspectives for more inclusive practices. Frontiers in Education. 9. 5 indexed citations

Watson, Andrew J., et al.. (2023). Selecting Normalizers for MicroRNA RT-qPCR Expression Analysis in Murine Preimplantation Embryos and the Associated Conditioned Culture Media. Journal of Developmental Biology. 11(2). 17–17. 3 indexed citations

Kiser, Patti, et al.. (2023). Deletion of p66Shc Dysregulates ERK and STAT3 Activity in Mouse Embryonic Stem Cells, Enhancing Their Naive-Like Self-Renewal in the Presence of Leukemia Inhibitory Factor. Stem Cells and Development. 32(15-16). 434–449.

Russell, Keith A., et al.. (2023). Opening the “Black Box” Underlying Barriers to the Use of Canine Induced Pluripotent Stem Cells: A Narrative Review. Stem Cells and Development. 32(11-12). 271–291. 2 indexed citations

Ait‐Aissa, Karima, William E. Hughes, Joseph C. Hockenberry, et al.. (2022). Noncanonical Role of Telomerase in Regulation of Microvascular Redox Environment With Implications for Coronary Artery Disease. Function. 3(5). zqac043–zqac043. 13 indexed citations

Watson, Andrew J., et al.. (2022). Modulation of PKM1/2 Levels by Steric Blocking Morpholinos Alters the Metabolic and Pluripotent State of Murine Pluripotent Stem Cells. Stem Cells and Development. 31(11-12). 278–295. 2 indexed citations

Arzi, Boaz, Tracy L. Webb, Thomas G. Koch, et al.. (2021). Cell Therapy in Veterinary Medicine as a Proof-of-Concept for Human Therapies: Perspectives From the North American Veterinary Regenerative Medicine Association. Frontiers in Veterinary Science. 8. 779109–779109. 13 indexed citations

Watson, Andrew J., et al.. (2018). Knockdown of p66Shc Alters Lineage-Associated Transcription Factor Expression in Mouse Blastocysts. Stem Cells and Development. 27(21). 1479–1493. 3 indexed citations

Cumming, Robert C., et al.. (2018). Metabolic plasticity during transition to naïve-like pluripotency in canine embryo-derived stem cells. Stem Cell Research. 30. 22–33. 7 indexed citations

10.

Teichroeb, Jonathan H., et al.. (2016). Small-Molecule Induction of Canine Embryonic Stem Cells Toward Naïve Pluripotency. Stem Cells and Development. 25(16). 1208–1222. 10 indexed citations

11.

Teichroeb, Jonathan H., Dean H. Betts, & Homayoun Vaziri. (2011). Suppression of the Imprinted Gene NNAT and X-Chromosome Gene Activation in Isogenic Human iPS Cells. PLoS ONE. 6(10). e23436–e23436. 16 indexed citations

12.

Wilcox, Jared T., E. Semple, Cathy Gartley, et al.. (2009). Characterization of Canine Embryonic Stem Cell Lines Derived From Different Niche Microenvironments. Stem Cells and Development. 18(8). 1167–1178. 42 indexed citations

13.

Watson, Jenny, Chris Watson, Kathryn Woodfine, et al.. (2009). Generation of an epigenetic signature by chronic hypoxia in prostate cells. Human Molecular Genetics. 18(19). 3594–3604. 84 indexed citations

14.

Koch, Thomas G., Preben D. Thomsen, & Dean H. Betts. (2009). Improved isolation protocol for equine cord blood-derived mesenchymal stromal cells. Cytotherapy. 11(4). 443–447. 39 indexed citations

15.

Jeon, Byeong-Gyun, Gianfranco Coppola, Steven D. Perrault, et al.. (2008). S -adenosylhomocysteine treatment of adult female fibroblasts alters X-chromosome inactivation and improves in vitro embryo development after somatic cell nuclear transfer. Reproduction. 135(6). 815–828. 40 indexed citations

16.

Rho, Gyu‐Jin, Gianfranco Coppola, R. Kasimanickam, et al.. (2007). Use of Somatic Cell Nuclear Transfer to Study Meiosis in Female Cattle Carrying A Sex-Dependent Fertility-Impairing X-Chromosome Abnormality. Cloning and Stem Cells. 9(1). 118–129. 10 indexed citations

17.

Betts, Dean H., et al.. (2000). Apoptosis in the early bovine embryo. Zygote. 8(1). 57–68. 148 indexed citations

18.

MacPhee, Daniel J., Doug Jones, Kevin Barr, et al.. (2000). Differential Involvement of Na+,K+-ATPase Isozymes in Preimplantation Development of the Mouse. Developmental Biology. 222(2). 486–498. 47 indexed citations

19.

Betts, Dean H. & W.A. King. (1999). Telomerase activity and telomere detection during early bovine development. Developmental Genetics. 25(4). 397–403. 70 indexed citations

20.

Betts, Dean H., Daniel J. MacPhee, Gerald M. Kidder, & Andrew J. Watson. (1997). Ouabain sensitivity and expression of Na/K-ATPase α- and β-subunit isoform genes during bovine early development. Molecular Reproduction and Development. 46(2). 114–126. 49 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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