Todd Richmond

20.6k total citations · 4 hit papers
69 papers, 8.5k citations indexed

About

Todd Richmond is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Todd Richmond has authored 69 papers receiving a total of 8.5k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 35 papers in Plant Science and 20 papers in Genetics. Recurrent topics in Todd Richmond's work include Chromosomal and Genetic Variations (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genomics and Phylogenetic Studies (10 papers). Todd Richmond is often cited by papers focused on Chromosomal and Genetic Variations (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genomics and Phylogenetic Studies (10 papers). Todd Richmond collaborates with scholars based in United States, Switzerland and United Kingdom. Todd Richmond's co-authors include Roland D. Green, Shauna Somerville, Rebecca R. Selzer, Jonathan P. Anderson, Kemal Kazan, Peer M. Schenk, Iain W. Wilson, John M. Manners, Chris Somerville and Jeffrey A. Jeddeloh and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Todd Richmond

67 papers receiving 8.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Coordinated plant defense responses in Arabidopsis revealed by microarray analysis

2000 1.1k citations Peer M. Schenk, Kemal Kazan et al. Proceedings of the National Academy of Sciences profile →
Chromosome Conformation Capture Carbon Copy (5C): A massively parallel solution for mapping interactions between genomic elements

2006 858 citations Todd Richmond, Rebecca R. Selzer et al. Genome Research profile →
A high-resolution map of active promoters in the human genome

2005 726 citations Todd Richmond, Roland D. Green et al. profile →
Somatic retrotransposition alters the genetic landscape of the human brain

2011 517 citations Daniel J. Gerhardt, Todd Richmond et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Todd Richmond United States	39	5.4k	4.0k	2.3k	476	260	69	8.5k
Marjori Matzke Austria	60	10.5k 2.0×	10.7k 2.7×	1.3k 0.6×	1.4k 3.0×	226 0.9×	141	15.4k
Dana Carroll United States	44	8.4k 1.6×	1.9k 0.5×	2.1k 0.9×	206 0.4×	482 1.9×	116	9.2k
Mary Lou Pardue United States	50	7.3k 1.4×	3.1k 0.8×	1.9k 0.8×	280 0.6×	395 1.5×	100	8.9k
Vincenzo Pirrotta United States	66	13.1k 2.4×	4.0k 1.0×	2.9k 1.2×	474 1.0×	221 0.8×	136	14.4k
Gregory J. Cost United States	27	7.5k 1.4×	1.7k 0.4×	1.7k 0.7×	222 0.5×	105 0.4×	45	8.4k
Fyodor D. Urnov United States	39	11.6k 2.2×	1.4k 0.3×	3.6k 1.5×	304 0.6×	272 1.0×	84	13.4k
Rajinder Kaul United States	39	5.0k 0.9×	865 0.2×	2.9k 1.3×	324 0.7×	61 0.2×	65	7.2k
Peter B. Becker Germany	64	13.0k 2.4×	2.4k 0.6×	2.4k 1.0×	716 1.5×	162 0.6×	191	14.7k
Scott E. Devine United States	28	4.0k 0.8×	1.9k 0.5×	1.4k 0.6×	314 0.7×	39 0.1×	36	5.3k

Countries citing papers authored by Todd Richmond

Since Specialization

Citations

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

Fields of papers citing papers by Todd Richmond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Todd Richmond

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mills, Lauren J., Milcah C. Scott, Pankti Shah, et al.. (2020). Comparative analysis of genome-wide DNA methylation identifies patterns that associate with conserved transcriptional programs in osteosarcoma. Bone. 158. 115716–115716. 9 indexed citations

Gardiner, Laura‐Jayne, Thomas Brabbs, Katherine W. Jordan, et al.. (2019). Integrating genomic resources to present full gene and putative promoter capture probe sets for bread wheat. GigaScience. 8(4). 16 indexed citations

Baalsrud, Helle Tessand, Ave Tooming‐Klunderud, Morten Skage, et al.. (2018). Long‐read sequence capture of the haemoglobin gene clusters across codfish species. Molecular Ecology Resources. 19(1). 245–259. 4 indexed citations

Li, Qing, Masako Suzuki, Jennifer Wendt, et al.. (2015). Post-conversion targeted capture of modified cytosines in mammalian and plant genomes. Nucleic Acids Research. 43(12). e81–e81. 42 indexed citations

Tan, John C., et al.. (2015). Targeted LncRNA Sequencing with the SeqCap RNA Enrichment System. Methods in molecular biology. 1402. 73–100. 2 indexed citations

Li, Qing, Steven R. Eichten, Peter J. Hermanson, et al.. (2014). Genetic Perturbation of the Maize Methylome. The Plant Cell. 26(12). 4602–4616. 139 indexed citations

Forsström, Björn, Klaus‐Peter Stengele, Thomas J. Albert, et al.. (2014). Proteome-wide Epitope Mapping of Antibodies Using Ultra-dense Peptide Arrays. Molecular & Cellular Proteomics. 13(6). 1585–1597. 100 indexed citations

Liu, Sanzhen, Kai Ying, Cheng‐Ting Yeh, et al.. (2012). Changes in genome content generated via segregation of non‐allelic homologs. The Plant Journal. 72(3). 390–399. 16 indexed citations

Haun, William J., David L. Hyten, Wayne Wenzhong Xu, et al.. (2010). The Composition and Origins of Genomic Variation among Individuals of the Soybean Reference Cultivar Williams 82 . PLANT PHYSIOLOGY. 155(2). 645–655. 106 indexed citations

10.

Bainbridge, Matthew N., Min Wang, Daniel L. Burgess, et al.. (2010). Whole exome capture in solution with 3 Gbp of data. Genome biology. 11(6). R62–R62. 120 indexed citations

11.

Springer, Nathan M., Kai Ying, Yan Fu, et al.. (2009). Maize Inbreds Exhibit High Levels of Copy Number Variation (CNV) and Presence/Absence Variation (PAV) in Genome Content. PLoS Genetics. 5(11). e1000734–e1000734. 378 indexed citations

12.

Flibotte, Stéphane, Mark L. Edgley, Rebecca R. Selzer, et al.. (2007). Efficient high-resolution deletion discovery in Caenorhabditis elegans by array comparative genomic hybridization. Genome Research. 17(3). 337–347. 78 indexed citations

13.

Selzer, Rebecca R., et al.. (2007). Methods in High-Resolution, Array-Based Comparative Genomic Hybridization. 189–211. 6 indexed citations

14.

Albert, Thomas J., Michael Molla, Donna M. Muzny, et al.. (2007). Direct selection of human genomic loci by microarray hybridization. Nature Methods. 4(11). 903–905. 468 indexed citations

15.

Khulan, Batbayar, Reid F. Thompson, Kenny Ye, et al.. (2006). Comparative isoschizomer profiling of cytosine methylation: The HELP assay. Genome Research. 16(8). 1046–1055. 287 indexed citations

16.

Sharp, Andrew J., Rebecca R. Selzer, Ze Cheng, et al.. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nature Genetics. 38(9). 1038–1042. 429 indexed citations

17.

Rice, Gregory M., et al.. (2006). Microdissection‐based high‐resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes. American Journal of Medical Genetics Part A. 140A(15). 1637–1643. 11 indexed citations

18.

Schenk, Peer M., Kemal Kazan, Iain W. Wilson, et al.. (2000). Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. Proceedings of the National Academy of Sciences. 97(21). 11655–11660. 1073 indexed citations breakdown →

19.

Richmond, Todd. (2000). Gene recognition via spliced alignment. Genome biology. 1(1). 17 indexed citations

20.

Richmond, Todd. (2000). A simple modular architecture research tool for the identification of signaling domains. Genome biology. 1(1). 7 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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