S. Todd

2.7k total citations
17 papers, 353 citations indexed

About

S. Todd is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, S. Todd has authored 17 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in S. Todd's work include RNA modifications and cancer (5 papers), RNA and protein synthesis mechanisms (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). S. Todd is often cited by papers focused on RNA modifications and cancer (5 papers), RNA and protein synthesis mechanisms (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). S. Todd collaborates with scholars based in United States, France and Japan. S. Todd's co-authors include Susan L. Naylor, Harry A. Drabkin, Robert M. Gemmill, A.Y. Sakaguchi, Lisa Hahner, Joëlle Roche, Wilbur A. Franklin, Jennifer C. Fung, Carl Hilliker and Jonathan S. Wiest and has published in prestigious journals such as Nucleic Acids Research, Biochemical and Biophysical Research Communications and CHEST Journal.

In The Last Decade

S. Todd

17 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. Todd United States 9 252 160 55 53 43 17 353
Shinsuke Ninomiya Japan 14 268 1.1× 210 1.3× 48 0.9× 16 0.3× 43 1.0× 31 444
Bengt Elmfors Sweden 8 151 0.6× 118 0.7× 127 2.3× 50 0.9× 34 0.8× 8 361
Michelle M. Thiaville United States 11 422 1.7× 93 0.6× 77 1.4× 57 1.1× 20 0.5× 14 534
Kanur Srinivasan United States 6 324 1.3× 71 0.4× 33 0.6× 68 1.3× 23 0.5× 7 392
G.N. Hendy United States 6 324 1.3× 131 0.8× 9 0.2× 112 2.1× 26 0.6× 9 465
John D. Ansell United Kingdom 9 283 1.1× 61 0.4× 52 0.9× 62 1.2× 8 0.2× 10 375
Monica Piccini Italy 8 240 1.0× 58 0.4× 63 1.1× 35 0.7× 20 0.5× 8 378
Xiaoyan Zhong China 7 310 1.2× 46 0.3× 94 1.7× 53 1.0× 35 0.8× 10 471
Franck Brunel France 7 238 0.9× 117 0.7× 41 0.7× 46 0.9× 15 0.3× 9 387
Maxine Fico Santoro United States 5 243 1.0× 34 0.2× 83 1.5× 32 0.6× 28 0.7× 7 341

Countries citing papers authored by S. Todd

Since Specialization
Citations

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

Fields of papers citing papers by S. Todd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Todd

This figure shows the co-authorship network connecting the top 25 collaborators of S. Todd. A scholar is included among the top collaborators of S. Todd 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 S. Todd. S. Todd 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.
Boldog, Ferenc, Robert M. Gemmill, James West, et al.. (1997). Chromosome 3p14 Homozygous Deletions and Sequence Analysis of FRA3B. Human Molecular Genetics. 6(2). 193–203. 117 indexed citations
2.
Todd, S., Wilbur A. Franklin, Marileila Varella‐Garcia, et al.. (1997). 613 Homozygous deletions of human chromosome 3p in lung tumors. Lung Cancer. 18. 157–157. 16 indexed citations
3.
Todd, S., Wilbur A. Franklin, M. Varella-Garcia, et al.. (1997). Homozygous deletions of human chromosome 3p in lung tumors.. PubMed. 57(7). 1344–52. 71 indexed citations
4.
Franklin, Wilbur A., S. Todd, Robert M. Gemmill, et al.. (1996). Correlative Assessment of Morphologic, Immunophenotypic, and Genetic Changes in Bronchial Epithelium of Tobacco Smokers. CHEST Journal. 109(3). 26S–26S. 2 indexed citations
5.
Todd, S., et al.. (1995). YAC contigs covering an 8-megabase region of 3p deleted in the small-cell lung cancer cell line U2020. Genomics. 25(1). 19–28. 13 indexed citations
6.
Whisenant, Emily, S. Todd, Robert M. Gemmill, et al.. (1994). Physical and genetic mapping of human chromosome 3 loci containing microsatellite repeats. Chromosome Research. 2(6). 423–427. 3 indexed citations
7.
Todd, S., et al.. (1993). Dinucleotide Repeat Loci Contribute Highly Informative Genetic Markers to the Human Chromosome 2 Linkage Map. Genomics. 16(3). 612–618. 6 indexed citations
8.
Todd, S. & Susan L. Naylor. (1992). New chromosomal mapping assignments for argininosuccinate synthetase pseudogene 1, interferon-?3 gene, and the diazepam binding inhibitor gene. Somatic Cell and Molecular Genetics. 18(4). 381–385. 6 indexed citations
9.
Todd, S. & Susan L. Naylor. (1991). Dinucleotide repeat polymorphism in the human tubulin alpha 1 (testis specific) gene (TUBA1). Nucleic Acids Research. 19(13). 3755–3755. 1 indexed citations
10.
Fung, Jennifer C., et al.. (1991). PCR primers for human chromosomes: Reagents for the rapid analysis of somatic cell hybrids. Genomics. 9(3). 511–516. 47 indexed citations
11.
Todd, S. & Susan L. Naylor. (1991). Dinucleotide repeat polymorphism in the human surfactant-associated protein 3 gene (SFTP3).. PubMed. 19(13). 3756–3756. 12 indexed citations
12.
Todd, S. & Susan L. Naylor. (1991). Dinucleotide repeat polymorphism in the human surfactant-associated protein 3 gene (SFTP3). Nucleic Acids Research. 19(13). 3756–3756. 1 indexed citations
13.
Todd, S. & Susan L. Naylor. (1991). Dinucleotide repeat polymorphism in the human interleukin 1, alpha gene (IL1A). Nucleic Acids Research. 19(13). 3756–3756. 10 indexed citations
14.
Todd, S., et al.. (1989). cDNA Sequence, interspecies comparison, and gene mapping analysis of argininosuccinate lyase. Genomics. 4(1). 53–59. 20 indexed citations
15.
Naylor, Susan L., A.Y. Sakaguchi, L. Clifford McDonald, et al.. (1986). Mapping thyrotropin β subunit gene in man and mouse. Somatic Cell and Molecular Genetics. 12(3). 307–311. 16 indexed citations
16.
Todd, S., Michihiro C. Yoshida, L. Clifford McDonald, et al.. (1985). Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1. Biochemical and Biophysical Research Communications. 131(3). 1175–1180. 7 indexed citations
17.
Montgomery, D. A. D., et al.. (1974). An evaluation of absorbent granule kits for determining serum thyroxine concentration and free thyroxine index in the diagnosis of thyroid function.. Journal of Clinical Pathology. 27(5). 372–376. 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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