Cynthia F. Bartels

6.1k total citations
58 papers, 4.0k citations indexed

About

Cynthia F. Bartels is a scholar working on Molecular Biology, Pharmacology and Computational Theory and Mathematics. According to data from OpenAlex, Cynthia F. Bartels has authored 58 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 26 papers in Pharmacology and 17 papers in Computational Theory and Mathematics. Recurrent topics in Cynthia F. Bartels's work include Cholinesterase and Neurodegenerative Diseases (25 papers), Computational Drug Discovery Methods (17 papers) and Genomics and Chromatin Dynamics (6 papers). Cynthia F. Bartels is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (25 papers), Computational Drug Discovery Methods (17 papers) and Genomics and Chromatin Dynamics (6 papers). Cynthia F. Bartels collaborates with scholars based in United States, France and Canada. Cynthia F. Bartels's co-authors include Oksana Lockridge, Bert N. La Du, Patrick Masson, Peter C. Scacheri, Cheng Kit Wong, Linda L. Johnson, Sheila Norton, Marie-Thérèse Froment, Thomas LaFramboise and Lawrence M. Schopfer and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Cynthia F. Bartels

58 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cynthia F. Bartels United States 35 2.0k 1.7k 1.1k 766 454 58 4.0k
Vincenzo Nicola Talesa Italy 30 946 0.5× 537 0.3× 223 0.2× 240 0.3× 77 0.2× 98 2.5k
Scott W. Rowlinson United States 30 1.3k 0.6× 1.6k 0.9× 173 0.2× 64 0.1× 536 1.2× 55 3.7k
Charles L. Bisgaier United States 29 1.4k 0.7× 465 0.3× 83 0.1× 676 0.9× 100 0.2× 57 4.4k
Tiantai Zhang China 31 976 0.5× 437 0.3× 142 0.1× 241 0.3× 36 0.1× 96 2.4k
Cristina M. Rondinone United States 37 2.7k 1.3× 282 0.2× 89 0.1× 141 0.2× 201 0.4× 74 4.8k
Taku Nagao Japan 36 2.6k 1.3× 198 0.1× 156 0.1× 82 0.1× 118 0.3× 188 4.4k
Paul Nioi United States 17 3.1k 1.5× 137 0.1× 73 0.1× 275 0.4× 204 0.4× 33 4.3k
Kyle L. Kolaja United States 30 2.0k 1.0× 102 0.1× 206 0.2× 197 0.3× 124 0.3× 70 3.6k
Ju‐Xian Song Hong Kong 36 1.2k 0.6× 528 0.3× 82 0.1× 152 0.2× 80 0.2× 70 3.3k
Aimee Landar United States 37 3.4k 1.7× 304 0.2× 49 0.0× 96 0.1× 105 0.2× 61 5.1k

Countries citing papers authored by Cynthia F. Bartels

Since Specialization
Citations

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

Fields of papers citing papers by Cynthia F. Bartels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cynthia F. Bartels. 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 Cynthia F. Bartels. The network helps show where Cynthia F. Bartels may publish in the future.

Co-authorship network of co-authors of Cynthia F. Bartels

This figure shows the co-authorship network connecting the top 25 collaborators of Cynthia F. Bartels. A scholar is included among the top collaborators of Cynthia F. Bartels 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 Cynthia F. Bartels. Cynthia F. Bartels 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.
Wang, Ruoyu, et al.. (2023). Epigenetic effects of high-fat diet on intestinal tumorigenesis in C57BL/6J-ApcMin/+ mice. PubMed. 7(1). 3–16. 2 indexed citations
2.
Corradin, Olivia, Richard Sallari, Bibi Kassim, et al.. (2022). Convergence of case-specific epigenetic alterations identify a confluence of genetic vulnerabilities tied to opioid overdose. Molecular Psychiatry. 27(4). 2158–2170. 7 indexed citations
3.
Bayık, Defne, Cynthia F. Bartels, Dionysios C. Watson, et al.. (2022). Distinct Cell Adhesion Signature Defines Glioblastoma Myeloid-Derived Suppressor Cell Subsets. Cancer Research. 82(22). 4274–4287. 17 indexed citations
4.
Hung, Stevephen, Alina Saiakhova, Zachary Faber, et al.. (2019). Mismatch repair-signature mutations activate gene enhancers across human colorectal cancer epigenomes. eLife. 8. 16 indexed citations
5.
Bayles, Ian, Małgorzata Krajewska, William Pontius, et al.. (2019). Ex vivo screen identifies CDK12 as a metastatic vulnerability in osteosarcoma. Journal of Clinical Investigation. 129(10). 4377–4392. 34 indexed citations
6.
Korvala, Johanna, Harald Jüppner, Outi Mäkitie, et al.. (2012). Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Medical Genetics. 13(1). 26–26. 85 indexed citations
7.
Vaisi‐Raygani, Asad, Hori Ghaneialvar, Zohreh Rahimi, et al.. (2011). Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease. Molecular Biology Reports. 38(8). 5421–5428. 26 indexed citations
8.
Bartels, Cynthia F., et al.. (2010). Mutations in the CHD7 Gene: The Experience of a Commercial Laboratory. Genetic Testing and Molecular Biomarkers. 14(6). 881–891. 38 indexed citations
9.
Schnetz, Michael P., Lusy Handoko, Batool Akhtar‐Zaidi, et al.. (2010). CHD7 Targets Active Gene Enhancer Elements to Modulate ES Cell-Specific Gene Expression. PLoS Genetics. 6(7). e1001023–e1001023. 193 indexed citations
10.
Olney, Robert C., Hülya Bükülmez, Cynthia F. Bartels, et al.. (2006). Heterozygous Mutations in Natriuretic Peptide Receptor-B ( NPR2 ) Are Associated with Short Stature. The Journal of Clinical Endocrinology & Metabolism. 91(4). 1229–1232. 134 indexed citations
11.
Rhee, David K., José Roberto Marcelino, Sulaiman M. Al‐Mayouf, et al.. (2005). Consequences of Disease-causing Mutations on Lubricin Protein Synthesis, Secretion, and Post-translational Processing. Journal of Biological Chemistry. 280(35). 31325–31332. 53 indexed citations
12.
Ai, Minrong, et al.. (2005). Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome. The American Journal of Human Genetics. 77(5). 741–753. 134 indexed citations
13.
Duysen, Ellen G., Cynthia F. Bartels, & Oksana Lockridge. (2002). Wild-Type and A328W Mutant Human Butyrylcholinesterase Tetramers Expressed in Chinese Hamster Ovary Cells Have a 16-Hour Half-Life in the Circulation and Protect Mice from Cocaine Toxicity. Journal of Pharmacology and Experimental Therapeutics. 302(2). 751–758. 80 indexed citations
14.
Josse, Denis, Oksana Lockridge, Weihua Xie, et al.. (2001). The active site of human paraoxonase (PON1). Journal of Applied Toxicology. 21(S1). S7–S11. 74 indexed citations
15.
Bartels, Cynthia F., Weihua Xie, Amanda K. Lindholm‐Perry, Lawrence M. Schopfer, & Oksana Lockridge. (2000). Determination of the DNA sequences of acetylcholinesterase and butyrylcholinesterase from cat and demonstration of the existence of both in cat plasma. Biochemical Pharmacology. 60(4). 479–487. 26 indexed citations
16.
Lindholm‐Perry, Amanda K., Elliott Bedows, Cynthia F. Bartels, et al.. (1999). A Naturally Occurring Genetic Variant in the Human Chorionic Gonadotropin-β Gene 5 Is Assembly Inefficient*. Endocrinology. 140(8). 3496–3506. 23 indexed citations
17.
Bartels, Cynthia F., et al.. (1992). DNA mutations associated with the human butyrylcholinesterase J-variant.. PubMed. 50(5). 1104–14. 63 indexed citations
18.
Du, Bert N. La, et al.. (1991). Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing. Cellular and Molecular Neurobiology. 11(1). 79–89. 43 indexed citations
19.
Du, Bert N. La, Cynthia F. Bartels, Cristina Nogueira, et al.. (1990). Phenotypic and molecular biological analysis of human butyrylcholinesterase variants. Clinical Biochemistry. 23(5). 423–431. 59 indexed citations
20.
Nogueira, Cristina, Cynthia F. Bartels, Martine Arpagaus, et al.. (1990). Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).. PubMed. 46(5). 934–42. 55 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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