S. Todd
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
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- RNA modifications and cancer 5
- RNA and protein synthesis mechanisms 3
- Epigenetics and DNA Methylation 2
- Genomics and Chromatin Dynamics 2
- CRISPR and Genetic Engineering 2
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- Neonatal Respiratory Health Research 2
- Co-authors
- Susan L. Naylor (9 shared papers)Harry A. Drabkin (6 shared papers)Robert M. Gemmill (6 shared papers)A.Y. Sakaguchi (3 shared papers)Lisa Hahner (3 shared papers)Joëlle Roche (2 shared papers)Jennifer C. Fung (1 shared paper)Jonathan S. Wiest (2 shared papers)
- Journals
- Genomics (4 papers)Nucleic Acids Research (3 papers)Human Molecular Genetics (1 paper)Biochemical and Biophysical Research Communications (1 paper)Journal of Clinical Pathology (1 paper)
- Partner nations
- United StatesFranceSwitzerland
In The Last Decade
S. Todd
17 papers receiving 349 citations
Peers
Comparison fields: 5 of 53
- Genetics 160
- Cancer Research 57
- Molecular Biology 242
- Clinical Biochemistry 14
- Oncology 51
Countries citing papers authored by S. Todd
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
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-authors
The 25 scholars most cited alongside S. Todd, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 116 | |
| 2 | Homozygous deletions of human chromosome 3p in lung tumors. | 1997 | 73 |
| 3 | 1991 | 48 | |
| 4 | 1989 | 21 | |
| 5 | 1986 | 16 | |
| 6 | Dinucleotide repeat polymorphism in the human surfactant-associated protein 3 gene (SFTP3). | 1991 | 16 |
| 7 | 1997 | 16 | |
| 8 | 1995 | 13 | |
| 9 | 1991 | 13 | |
| 10 | 1985 | 7 | |
| 11 | 1993 | 6 | |
| 12 | 1992 | 6 | |
| 13 | 1974 | 5 | |
| 14 | 1994 | 3 | |
| 15 | 1996 | 2 | |
| 16 | 1991 | 1 | |
| 17 | 1991 | 1 |
About S. Todd
S. Todd is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Genetics, Biochemistry and Surgery, having authored 17 papers that have together received 363 indexed citations. Recurring topics across this work include RNA modifications and cancer (5 papers), RNA and protein synthesis mechanisms (3 papers), Amino Acid Enzymes and Metabolism (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers), Genomics and Chromatin Dynamics (2 papers), Neonatal Respiratory Health Research (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Genetics (160 citations), Cancer Research (57 citations), Molecular Biology (242 citations), Clinical Biochemistry (14 citations) and Oncology (51 citations). S. Todd has collaborated with scholars based in United States, France and Switzerland. Frequent co-authors include Susan L. Naylor, Harry A. Drabkin, Robert M. Gemmill, A.Y. Sakaguchi, Lisa Hahner, Joëlle Roche, Jennifer C. Fung, Jonathan S. Wiest, Carl Hilliker and Wilbur A. Franklin. Their work appears in journals such as Genomics, Nucleic Acids Research, Human Molecular Genetics, Biochemical and Biophysical Research Communications and Journal of Clinical Pathology.
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.