Keith F. Schertz

1.8k total citations
17 papers, 939 citations indexed

About

Keith F. Schertz is a scholar working on Plant Science, Genetics and Molecular Biology. According to data from OpenAlex, Keith F. Schertz has authored 17 papers receiving a total of 939 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Plant Science, 9 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Keith F. Schertz's work include Genetic Mapping and Diversity in Plants and Animals (9 papers), Bioenergy crop production and management (4 papers) and Wheat and Barley Genetics and Pathology (3 papers). Keith F. Schertz is often cited by papers focused on Genetic Mapping and Diversity in Plants and Animals (9 papers), Bioenergy crop production and management (4 papers) and Wheat and Barley Genetics and Pathology (3 papers). Keith F. Schertz collaborates with scholars based in United States, China and Australia. Keith F. Schertz's co-authors include John Doebley, Andrew H. Paterson, Yann‐Rong Lin, Zhikang Li, Sin‐Chieh Liu, J. E. Irvine, J. W. Stansel, Shannon R. M. Pinson, Jeffrey L. Bennetzen and Wenpeng Yang and has published in prestigious journals such as Science, The Plant Journal and Theoretical and Applied Genetics.

In The Last Decade

Keith F. Schertz

17 papers receiving 853 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keith F. Schertz United States 11 702 445 311 133 110 17 939
Youliang Zheng China 19 1.1k 1.6× 429 1.0× 240 0.8× 118 0.9× 157 1.4× 80 1.2k
Esteban Bortiri United States 10 685 1.0× 291 0.7× 396 1.3× 109 0.8× 223 2.0× 13 867
D. González de León France 10 856 1.2× 411 0.9× 166 0.5× 126 0.9× 39 0.4× 13 962
Jianzhong Wu Japan 22 1.2k 1.8× 542 1.2× 480 1.5× 109 0.8× 46 0.4× 41 1.4k
Sandra E. Harrington United States 11 1.6k 2.3× 922 2.1× 422 1.4× 65 0.5× 55 0.5× 16 1.7k
K. Tsunewaki Japan 23 1.5k 2.1× 436 1.0× 629 2.0× 91 0.7× 165 1.5× 57 1.7k
Alexandra M. Allen United Kingdom 16 1.4k 2.0× 610 1.4× 435 1.4× 128 1.0× 221 2.0× 23 1.6k
A. E. Van Deynze United States 13 1.5k 2.1× 754 1.7× 310 1.0× 87 0.7× 67 0.6× 15 1.6k
Héctor Sánchez‐Villeda United States 11 1.0k 1.5× 779 1.8× 287 0.9× 72 0.5× 31 0.3× 15 1.3k
G. M. M. Bredemeijer Netherlands 14 803 1.1× 302 0.7× 387 1.2× 35 0.3× 150 1.4× 33 952

Countries citing papers authored by Keith F. Schertz

Since Specialization
Citations

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

Fields of papers citing papers by Keith F. Schertz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keith F. Schertz

This figure shows the co-authorship network connecting the top 25 collaborators of Keith F. Schertz. A scholar is included among the top collaborators of Keith F. Schertz 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 Keith F. Schertz. Keith F. Schertz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Xin, Zhanguo, Gloria Burow, Cleve D. Franks, et al.. (2012). Registration of a Diverse Collection of Sorghum Genetic Stocks. Journal of Plant Registrations. 7(1). 119–124. 1 indexed citations
2.
Nagy, É., Wusirika Ramakrishna, Zi‐jun Xu, et al.. (2007). Fine mapping of the Pc locus of Sorghum bicolor, a gene controlling the reaction to a fungal pathogen and its host-selective toxin. Theoretical and Applied Genetics. 114(6). 961–970. 28 indexed citations
3.
Lin, Yann‐Rong, Li Zhu, Shuxin Ren, et al.. (1999). Lin, Y. et al. A Sorghum propinquum BAC library, suitable for cloning genes associated with loss-of-function mutations during crop domestication. Mol. Breed. 5, 511-520. 9 indexed citations
4.
Lin, Yann‐Rong, Li Zhu, Shuxin Ren, et al.. (1999). A Sorghum propinquum BAC library, suitable for cloning genes associated with loss-of-function mutations during crop domestication. Molecular Breeding. 5(6). 511–520. 32 indexed citations
5.
Islam‐Faridi, M. Nurul, Sung‐Sick Woo, Michael S. Zwick, et al.. (1997). FISH of a maizesh2-selected sorghum BAC to chromosomes ofSorghum bicolor. Genome. 40(4). 475–478. 17 indexed citations
6.
Tang, Hoang V., et al.. (1996). Transcript processing internal to a mitochondrial open reading frame is correlated with fertility restoration in male‐sterile sorghum. The Plant Journal. 10(1). 123–133. 90 indexed citations
7.
Yang, Wenpeng, Antônio Costa de Oliveira, Ian D. Godwin, Keith F. Schertz, & Jeffrey L. Bennetzen. (1996). Comparison of DNA Marker Technologies in Characterizing Plant Genome Diversity: Variability in Chinese Sorghums. Crop Science. 36(6). 1669–1676. 167 indexed citations
8.
Schertz, Keith F., et al.. (1995). Characterization and expression of rpoC2 in CMS and fertile lines of sorghum. Plant Molecular Biology. 28(5). 799–809. 14 indexed citations
9.
Paterson, Andrew H., Yann‐Rong Lin, Zhikang Li, et al.. (1995). Convergent Domestication of Cereal Crops by Independent Mutations at Corresponding Genetic Loci. Science. 269(5231). 1714–1718. 433 indexed citations
10.
Woo, Sung‐Sick, Vipin K. Rastogi, Hong-Bin Zhang, et al.. (1995). Isolation of megabase-size DNA from sorghum and applications for physical mapping and bacterial and yeast artificial chromosome library construction. Plant Molecular Biology Reporter. 13(1). 82–94. 10 indexed citations
11.
Muthukrishnan, Subbaratnam, et al.. (1993). A chloroplast DNA deletion located in RNA polymerase gene rpoC2 in CMS lines of sorghum. Molecular and General Genetics MGG. 236-236(2-3). 251–259. 35 indexed citations
12.
Morden, Clifford W., John Doebley, & Keith F. Schertz. (1989). ALLOZYME VARIATION IN OLD WORLD RACES OF SORGHUM BICOLOR (POACEAE). American Journal of Botany. 76(2). 247–255. 49 indexed citations
13.
Morden, Clifford W., John Doebley, & Keith F. Schertz. (1989). Allozyme Variation in Old World Races of Sorghum bicolor (Poaceae). American Journal of Botany. 76(2). 247–247. 9 indexed citations
14.
Dunkle, Larry D., et al.. (1988). Pathotoxin‐Induced Alteration in Protein Synthesis Associated with Susceptibility of Sorghum to Milo Disease. Crop Science. 28(4). 615–617. 4 indexed citations
15.
Doebley, John, Clifford W. Morden, & Keith F. Schertz. (1986). A gene modifying mitochondrial malate dehydrogenase isozymes inSorghum (Gramineae). Biochemical Genetics. 24(11-12). 813–819. 8 indexed citations
16.
Bhaskaran, Shyamala, Roberta H. Smith, & Keith F. Schertz. (1986). Progeny Screening of Sorghum Plants Regenerated from Sodium chloride-selected Callus for Salt Tolerance. Journal of Plant Physiology. 122(3). 205–210. 9 indexed citations
17.
Bhaskaran, Shyamala, Roberta H. Smith, & Keith F. Schertz. (1983). Sodium Chloride Tolerant Callus of Sorghum bicolor (L.) Moench.. Zeitschrift für Pflanzenphysiologie. 112(5). 459–463. 24 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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