Daniel G. Stetka

1.1k total citations
21 papers, 963 citations indexed

About

Daniel G. Stetka is a scholar working on Molecular Biology, Plant Science and Cancer Research. According to data from OpenAlex, Daniel G. Stetka has authored 21 papers receiving a total of 963 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Plant Science and 9 papers in Cancer Research. Recurrent topics in Daniel G. Stetka's work include Carcinogens and Genotoxicity Assessment (9 papers), DNA Repair Mechanisms (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Daniel G. Stetka is often cited by papers focused on Carcinogens and Genotoxicity Assessment (9 papers), DNA Repair Mechanisms (7 papers) and DNA and Nucleic Acid Chemistry (6 papers). Daniel G. Stetka collaborates with scholars based in United States and Poland. Daniel G. Stetka's co-authors include Sheldon Wolff, A.V. Carrano, J.L. Minkler, J.A. Mazrimas, Dan H. Moore, Larry H. Thompson, Susan Fong, Nicos Skordis, Saul P. Greenfield and Margaret H. MacGillivray and has published in prestigious journals such as The Journal of Pediatrics, Experimental Cell Research and Radiation Research.

In The Last Decade

Daniel G. Stetka

20 papers receiving 873 citations

Peers

Daniel G. Stetka
D.S. Rupa India
M. L. O'RIORDAN United Kingdom
J.G. Brewen United States
C. C. Huang United States
John D. Gingerich Canada
Carole Bradt United States
Baldev K. Vig United States
K.T. Cain United States
J. Schöneich Germany
D. Włodek Poland
D.S. Rupa India
Daniel G. Stetka
Citations per year, relative to Daniel G. Stetka Daniel G. Stetka (= 1×) peers D.S. Rupa

Countries citing papers authored by Daniel G. Stetka

Since Specialization
Citations

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

Fields of papers citing papers by Daniel G. Stetka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel G. Stetka. 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 Daniel G. Stetka. The network helps show where Daniel G. Stetka may publish in the future.

Co-authorship network of co-authors of Daniel G. Stetka

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel G. Stetka. A scholar is included among the top collaborators of Daniel G. Stetka 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 Daniel G. Stetka. Daniel G. Stetka 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.
Verma, Ram S., et al.. (1997). Centromeric alphoid DNA heteromorphisms of chromosome 21 revealed by FISH‐technique. Clinical Genetics. 51(2). 91–93. 9 indexed citations
2.
Stetka, Daniel G., et al.. (1994). Alphoid DNA diversity of a so-called monocentric Robertsonian fusion. Chromosome Research. 2(1). 73–75. 3 indexed citations
3.
Nolin, Sarah L., Edmund C. Jenkins, Michael S. Krawczun, et al.. (1991). Fragile X screening program in New York State. American Journal of Medical Genetics. 38(2-3). 251–255. 29 indexed citations
4.
McPherson, Elspeth & Daniel G. Stetka. (1990). Trisomy 22 in a liveborn infant with multiple congenital anomalies. American Journal of Medical Genetics. 36(1). 11–14. 23 indexed citations
5.
Skordis, Nicos, Daniel G. Stetka, Margaret H. MacGillivray, & Saul P. Greenfield. (1987). Familial 46,XX males coexisting with familial 46,XX true hermaphrodites in same pedigree. The Journal of Pediatrics. 110(2). 244–248. 52 indexed citations
6.
Stetka, Daniel G., et al.. (1985). SCE induction is uncoupled from mutation induction in mammalian cells following exposure to ethylnitrosourea (ENU). Environmental Mutagenesis. 7(2). 233–243. 9 indexed citations
7.
Stetka, Daniel G., et al.. (1984). SCEs are induced by replication of BrdU-substituted DNA templates, but not by incorporation of BrdU into nascent DNA. Mutation Research Letters. 140(1). 33–42. 16 indexed citations
8.
Brusick, David, et al.. (1980). Genetic activity of para formaldehyde in the ames assay the l 5178y mouse lymphoma assay the cho sister chromatid exchange assay and in an in vitro cho chromosome analysis. Environmental Mutagenesis. 2(2). 253. 1 indexed citations
9.
Carrano, A.V., J.L. Minkler, Daniel G. Stetka, & Dan H. Moore. (1980). Variation in the baseline sister chromatid exchange frequency in human lymphocytes. Environmental Mutagenesis. 2(3). 325–337. 81 indexed citations
10.
Carrano, A.V., Larry H. Thompson, Daniel G. Stetka, et al.. (1979). DNA crosslinking, sister-chromatid exchange and specific-locus mutations. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 63(1). 175–188. 121 indexed citations
11.
Stetka, Daniel G.. (1979). Further analysis of the replication bypass model for sister chromatid exchange. Human Genetics. 49(1). 63–69. 29 indexed citations
12.
Minkler, J.L., et al.. (1978). An ultraviolet light source for consistent differential staining of sister chromatids.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 53(6). 359–60. 37 indexed citations
13.
Stetka, Daniel G., J.L. Minkler, & A.V. Carrano. (1978). Induction of long-lived chromosome damage, as manifested by sister-chromatid exchange, in lymphocytes of animals exposed to mitomycin-C. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 51(3). 383–396. 75 indexed citations
14.
Mazrimas, J.A. & Daniel G. Stetka. (1978). Direct evidence for the role of incorporated BUdR in the induction of sister chromatid exchanges. Experimental Cell Research. 117(1). 23–30. 99 indexed citations
15.
Stetka, Daniel G. & A.V. Carrano. (1978). The interaction of Hoechst 33258 and BrdU-substituted DNA in the formation of sister chromatid exchanges. Mutation Research/Environmental Mutagenesis and Related Subjects. 53(1). 75–76. 1 indexed citations
16.
Stetka, Daniel G. & Peter L. Webster. (1977). Recovery of Pisum Root Meristems after Mitotic-inhibitory Treatments with 3 H-thymidine. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine. 31(4). 321–334. 1 indexed citations
17.
Stetka, Daniel G. & A.V. Carrano. (1977). The interaction of Hoechst 33258 and BrdU substituted DNA in the formation of sister chromatid exchanges. Chromosoma. 63(1). 21–31. 65 indexed citations
18.
Stetka, Daniel G. & Sheldon Wolff. (1976). Sister chromatid exchange as an assay for genetic damage induced by mutagen-carcinogens. I. In vivo test for compounds requiring metabolic activation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 41(2-3). 333–342. 111 indexed citations
19.
Stetka, Daniel G. & Sheldon Wolff. (1976). Sister chromatid exchange as an assay for genetic damage induced by mutagen-carcinogens. II. In vitro test for compounds requiring metabolic activation. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 41(2-3). 343–349. 180 indexed citations
20.
Stetka, Daniel G. & Peter L. Webster. (1975). Tritiated-Thymidine Induced Changes in Cell Population Kinetics in Root Meristems of Pisum sativum. Radiation Research. 64(3). 475–475. 6 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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