Jonathan C. Lamb

2.7k total citations
27 papers, 2.0k citations indexed

About

Jonathan C. Lamb is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Jonathan C. Lamb has authored 27 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Plant Science, 14 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Jonathan C. Lamb's work include Chromosomal and Genetic Variations (25 papers), Plant Disease Resistance and Genetics (14 papers) and Plant Virus Research Studies (10 papers). Jonathan C. Lamb is often cited by papers focused on Chromosomal and Genetic Variations (25 papers), Plant Disease Resistance and Genetics (14 papers) and Plant Virus Research Studies (10 papers). Jonathan C. Lamb collaborates with scholars based in United States, China and Japan. Jonathan C. Lamb's co-authors include James A. Birchler, Akio Kato, Fangpu Han, Dorothy E. Shippen, Weichang Yu, Yulia V. Surovtseva, Xiangyu Song, Ross Warrington, Akio Kato and Juan M. Vega and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and Molecular Cell.

In The Last Decade

Jonathan C. Lamb

27 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan C. Lamb United States 23 1.7k 1.1k 342 247 69 27 2.0k
Iva Mozgová Czechia 19 1.1k 0.6× 986 0.9× 54 0.2× 108 0.4× 27 0.4× 35 1.3k
Kiyotaka Nagaki Japan 26 2.7k 1.6× 1.6k 1.4× 356 1.0× 24 0.1× 123 1.8× 58 2.8k
Eugene V. Shakirov Russia 17 601 0.4× 513 0.5× 64 0.2× 403 1.6× 33 0.5× 49 887
Yannick Jacob United States 18 1.4k 0.8× 1.5k 1.4× 104 0.3× 16 0.1× 52 0.8× 44 1.9k
Michael F. Portereiko United States 8 832 0.5× 871 0.8× 60 0.2× 23 0.1× 135 2.0× 8 1.1k
Jaroslav Fulneček Czechia 16 580 0.3× 490 0.4× 99 0.3× 18 0.1× 66 1.0× 30 765
Shumin Li China 16 745 0.4× 324 0.3× 73 0.2× 26 0.1× 67 1.0× 30 924
Wojciech P. Pawlowski United States 26 1.5k 0.9× 1.5k 1.4× 258 0.8× 10 0.0× 50 0.7× 45 1.9k
Francisco Martínez‐Granero Spain 18 560 0.3× 567 0.5× 218 0.6× 28 0.1× 34 0.5× 21 997
Ricardo A. Dante United States 12 828 0.5× 600 0.5× 125 0.4× 9 0.0× 49 0.7× 22 973

Countries citing papers authored by Jonathan C. Lamb

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan C. Lamb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan C. Lamb. 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 Jonathan C. Lamb. The network helps show where Jonathan C. Lamb may publish in the future.

Co-authorship network of co-authors of Jonathan C. Lamb

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan C. Lamb. A scholar is included among the top collaborators of Jonathan C. Lamb 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 Jonathan C. Lamb. Jonathan C. Lamb 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.
Lee, Yang‐Seok, Julius Dürr, Charo I. del Genio, et al.. (2021). A transposon surveillance mechanism that safeguards plant male fertility during stress. Nature Plants. 7(1). 34–41. 32 indexed citations
2.
Han, Fangpu, et al.. (2018). Meiotic Studies on Combinations of Chromosomes With Different Sized Centromeres in Maize. Frontiers in Plant Science. 9. 785–785. 7 indexed citations
3.
Nelson, Andrew D. L., et al.. (2011). Parameters Affecting Telomere-Mediated Chromosomal Truncation in Arabidopsis  . The Plant Cell. 23(6). 2263–2272. 39 indexed citations
4.
Kato, Akio, Jonathan C. Lamb, Patrice S. Albert, et al.. (2010). Chromosome Painting for Plant Biotechnology. Methods in molecular biology. 701. 67–96. 23 indexed citations
5.
Zhang, Peifen, Chuanhe Yu, Jonathan C. Lamb, et al.. (2009). Alternative Ac/Ds transposition induces major chromosomal rearrangements in maize. Genes & Development. 23(6). 755–765. 50 indexed citations
6.
Surovtseva, Yulia V., Dmitri Churikov, Kara A. Boltz, et al.. (2009). Conserved Telomere Maintenance Component 1 Interacts with STN1 and Maintains Chromosome Ends in Higher Eukaryotes. Molecular Cell. 36(2). 207–218. 220 indexed citations
7.
Jin, Weiwei, Jonathan C. Lamb, Wenli Zhang, et al.. (2008). Histone modifications associated with both A and B chromosomes of maize. Chromosome Research. 16(8). 1203–1214. 51 indexed citations
8.
Lamb, Jonathan C., Nicole C. Riddle, Ya-Ming Cheng, James Theuri, & James A. Birchler. (2007). Localization and transcription of a retrotransposon-derived element on the maize B chromosome. Chromosome Research. 15(3). 383–98. 49 indexed citations
9.
Lamb, Jonathan C., et al.. (2007). Distinct chromosomal distributions of highly repetitive sequences in maize. Chromosome Research. 15(1). 33–49. 66 indexed citations
10.
Han, Fangpu, Jonathan C. Lamb, Weichang Yu, Zhi Gao, & James A. Birchler. (2007). Centromere Function and Nondisjunction Are Independent Components of the Maize B Chromosome Accumulation Mechanism. The Plant Cell. 19(2). 524–533. 45 indexed citations
12.
Sampedro, Javier, et al.. (2007). Recent Proliferation and Translocation of Pollen Group 1 Allergen Genes in the Maize Genome. PLANT PHYSIOLOGY. 143(3). 1269–1281. 20 indexed citations
13.
Yu, Weichang, Jonathan C. Lamb, Fangpu Han, & James A. Birchler. (2006). Cytological Visualization of DNA Transposons and Their Transposition Pattern in Somatic Cells of Maize. Genetics. 175(1). 31–39. 26 indexed citations
14.
Yu, Weichang, Jonathan C. Lamb, Fangpu Han, & James A. Birchler. (2006). Telomere-mediated chromosomal truncation in maize. Proceedings of the National Academy of Sciences. 103(46). 17331–17336. 95 indexed citations
15.
Lamb, Jonathan C., et al.. (2006). Cytogenetics and chromosome analytical techniques.. 245–248. 5 indexed citations
16.
Kato, Akio, Donald L. Auger, T. Phelps-Durr, et al.. (2005). Minichromosomes derived from the B chromosome of maize. Cytogenetic and Genome Research. 109(1-3). 156–165. 36 indexed citations
17.
Kato, Akio, Juan M. Vega, Fangpu Han, Jonathan C. Lamb, & James A. Birchler. (2005). Advances in plant chromosome identification and cytogenetic techniques. Current Opinion in Plant Biology. 8(2). 148–154. 68 indexed citations
18.
Lamb, Jonathan C., Akio Kato, & James A. Birchler. (2004). Sequences associated with A chromosome centromeres are present throughout the maize B chromosome. Chromosoma. 113(7). 337–349. 71 indexed citations
19.
Lamb, Jonathan C., James Theuri, & James A. Birchler. (2004). What's in a centromere?. Genome Biology. 5(9). 239–239. 18 indexed citations
20.
Lamb, Jonathan C. & James A. Birchler. (2003). The role of DNA sequence in centromere formation.. Genome Biology. 4(5). 214–214. 29 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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