Craig Harris

2.8k total citations
87 papers, 2.2k citations indexed

About

Craig Harris is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Biochemistry. According to data from OpenAlex, Craig Harris has authored 87 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 28 papers in Pediatrics, Perinatology and Child Health and 17 papers in Biochemistry. Recurrent topics in Craig Harris's work include Sulfur Compounds in Biology (17 papers), Birth, Development, and Health (15 papers) and Glutathione Transferases and Polymorphisms (14 papers). Craig Harris is often cited by papers focused on Sulfur Compounds in Biology (17 papers), Birth, Development, and Health (15 papers) and Glutathione Transferases and Polymorphisms (14 papers). Craig Harris collaborates with scholars based in United States, Cameroon and Japan. Craig Harris's co-authors include Jason M. Hansen, Mont R. Juchau, Kevin L. Stark, Dana C. Dolinoy, Josef M. Miller, Alfred L. Nuttall, Tatsuya Yamasoba, Martin A. Philbert, Yehoash Raphael and Rita Loch‐Caruso and has published in prestigious journals such as Brain Research, Environmental Health Perspectives and Free Radical Biology and Medicine.

In The Last Decade

Craig Harris

83 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Craig Harris United States 27 864 516 429 278 243 87 2.2k
Michel Tauc France 35 1.9k 2.2× 542 1.1× 154 0.4× 130 0.5× 97 0.4× 117 3.7k
Philippe Poujeol France 30 1.5k 1.7× 556 1.1× 138 0.3× 74 0.3× 63 0.3× 99 3.0k
Kirsten Madsen Denmark 38 2.9k 3.3× 110 0.2× 689 1.6× 284 1.0× 103 0.4× 128 4.4k
Si Houn Hahn United States 27 1.2k 1.4× 325 0.6× 226 0.5× 220 0.8× 21 0.1× 81 2.4k
Christophe Duranton France 36 1.7k 1.9× 154 0.3× 624 1.5× 74 0.3× 307 1.3× 75 3.8k
Nils Gunnar Lindquist Sweden 22 400 0.5× 273 0.5× 68 0.2× 70 0.3× 78 0.3× 43 1.5k
Margaret Clagett‐Dame United States 31 2.2k 2.6× 163 0.3× 294 0.7× 31 0.1× 208 0.9× 90 3.7k
Hiroshi Mitsubuchi Japan 23 775 0.9× 86 0.2× 278 0.6× 261 0.9× 55 0.2× 92 2.0k
Jean‐Paul Blondeau France 28 974 1.1× 296 0.6× 179 0.4× 226 0.8× 54 0.2× 58 2.1k
Masato Matsuoka Japan 32 868 1.0× 490 0.9× 40 0.1× 53 0.2× 57 0.2× 127 2.9k

Countries citing papers authored by Craig Harris

Since Specialization
Citations

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

Fields of papers citing papers by Craig Harris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Craig Harris. 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 Craig Harris. The network helps show where Craig Harris may publish in the future.

Co-authorship network of co-authors of Craig Harris

This figure shows the co-authorship network connecting the top 25 collaborators of Craig Harris. A scholar is included among the top collaborators of Craig Harris 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 Craig Harris. Craig Harris 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.
Simon, A., Adam M. Clark, Craig Harris, et al.. (2025). Proton capture on $$^{90}$$Zr revisited. The European Physical Journal A. 61(3).
2.
Bleuel, D. L., N. D. Scielzo, L. A. Bernstein, et al.. (2024). Nuclear level density and γ-decay strength of Sr93. Physical review. C. 109(5). 2 indexed citations
3.
Spyrou, A., P. Mohr, P. A. DeYoung, et al.. (2023). Cross-section measurement of the Kr82(p,γ)Rb83 reaction in inverse kinematics. Physical review. C. 107(3). 4 indexed citations
4.
Spyrou, A., P. A. DeYoung, A. C. Dombos, et al.. (2022). Constraining the astrophysical p process: Cross section measurement of the Kr84(p,γ)Rb85 reaction in inverse kinematics. Physical review. C. 105(6). 7 indexed citations
5.
Loch‐Caruso, Rita, et al.. (2020). Tert-Butyl Hydroperoxide Stimulated Apoptosis Independent of Prostaglandin E2 and IL-6 in the HTR-8/SVneo Human Placental Cell Line. Reproductive Sciences. 27(11). 2104–2114. 6 indexed citations
6.
Hansen, Jason M., Dean P. Jones, & Craig Harris. (2019). The Redox Theory of Development. Antioxidants and Redox Signaling. 32(10). 715–740. 41 indexed citations
7.
Harris, Craig. (2019). Rat Whole Embryo Culture. Methods in molecular biology. 1965. 195–217. 3 indexed citations
8.
Veltman, Karin, et al.. (2018). A mechanistic model for thiol redox dynamics in the organogenesis stage rat conceptus. Reproductive Toxicology. 82. 38–49.
9.
Sant, Karilyn E., Dana C. Dolinoy, Joseph L. Jilek, Brian Shay, & Craig Harris. (2015). Mono-2-ethylhexyl phthalate (MEHP) alters histiotrophic nutrition pathways and epigenetic processes in the developing conceptus. The Journal of Nutritional Biochemistry. 27. 211–218. 17 indexed citations
10.
Giese, Roger W., et al.. (2013). Mono-2-ethylhexyl phthalate induces oxidative stress responses in human placental cells in vitro. Toxicology and Applied Pharmacology. 268(1). 47–54. 125 indexed citations
11.
Harris, Craig. (2012). Overview of In Vitro Models in Developmental Toxicology. Methods in molecular biology. 889. 105–113. 3 indexed citations
12.
Harris, Craig, M.M. Dixon, & Jason M. Hansen. (2004). Glutathione depletion modulates methanol, formaldehyde and formate toxicity in cultured rat conceptuses. Cell Biology and Toxicology. 20(3). 133–145. 34 indexed citations
13.
Hansen, Jason M., et al.. (2002). Thalidomide Modulates Nuclear Redox Status and Preferentially Depletes Glutathione in Rabbit Limb versus Rat Limb. Journal of Pharmacology and Experimental Therapeutics. 300(3). 768–776. 55 indexed citations
14.
Hansen, Jason M., et al.. (2001). Spatial and Temporal Ontogenies of Glutathione Peroxidase and Glutathione Disulfide Reductase During Development of the Prenatal Rat. Journal of Biochemical and Molecular Toxicology. 15(4). 197–206. 27 indexed citations
15.
Harris, Craig, et al.. (1996). Formation of glutathione adducts and 2-aminofluorene from 2-nitrosofluorene in postimplantation rat conceptuses in vitro. Reproductive Toxicology. 10(4). 273–284. 3 indexed citations
16.
Harris, Craig, et al.. (1995). Formation of protein–glutathione mixed disulfides in the developing rat conceptus following diamide treatment in vitro. Teratology. 52(4). 196–204. 16 indexed citations
17.
Harris, Craig, Mont R. Juchau, & Philip E. Mirkes. (1991). Role of glutathione and hsp 70 in the acquisition of thermotolerance in postimplantation rat embryos. Teratology. 43(3). 229–239. 41 indexed citations
18.
Stark, Kevin L., Craig Harris, & Mont R. Juchau. (1989). Modulation of the embryotoxicity and cytotoxicity elicited by 7-hydroxy-2-acetylaminofluorene and acetaminophen via deacetylation. Toxicology and Applied Pharmacology. 97(3). 548–560. 29 indexed citations
19.
Harris, Craig, Kevin L. Stark, Daniel L. Luchtel, & Mont R. Juchau. (1989). Abnormal neurulation induced by 7-hydroxy-2-acetylaminofluorene and acetaminophen: Evidence for catechol metabolites as proximate dysmorphogens. Toxicology and Applied Pharmacology. 101(3). 432–446. 19 indexed citations
20.
Harris, Craig, et al.. (1982). Effective filtration in completion and other wellbore operations can be good investment. Oil & gas journal. 5 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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