S. S. Sommer
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- Cancer-related Molecular Pathways 2
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- Hemophilia Treatment and Research 3
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- Cancer-related gene regulation 2
- Mitochondrial Function and Pathology 1
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- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Qiang LiuBobbie S. GostoutHagen BlaszykJ. S. KovachJinong FengJulie M. CunninghamJennifer J. SchroederRenee M. McGovern
- Cited by
- OncologyCancer ResearchHematology
- Journals
- Nucleic Acids Research (3 papers)Human Molecular Genetics (2 papers)Human Genetics (1 paper)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
S. S. Sommer
8 papers receiving 261 citations
Peers
Comparison fields: 5 of 49
- Oncology 99
- Cancer Research 49
- Hematology 32
- Cellular and Molecular Neuroscience 50
- Molecular Biology 174
Countries citing papers authored by S. S. Sommer
This map shows the geographic impact of S. S. Sommer'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. S. Sommer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. S. Sommer more than expected).
Fields of papers citing papers by S. S. Sommer
This network shows the impact of papers produced by S. S. Sommer. 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. S. Sommer. The network helps show where S. S. Sommer may publish in the future.
Co-authorship network
The 25 scholars most cited alongside S. S. Sommer, 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 | 23 | |
| 2 | 1996 | 21 | |
| 3 | 1996 | 50 | |
| 4 | 1995 | 10 | |
| 5 | p53 gene mutations inside and outside of exons 5-8: the patterns differ in breast and other cancers. | 1995 | 94 |
| 6 | "Cryptic" repeating triplets of purines and pyrimidines (cRRY(i)) are frequent and polymorphic: analysis of coding cRRY(i) in the proopiomelanocortin (POMC) and TATA-binding protein (TBP) genes. | 1993 | 59 |
| 7 | 1991 | 2 | |
| 8 | 1990 | 0 | |
| 9 | 1990 | 6 |
About S. S. Sommer
S. S. Sommer is a scholar working on Hematology, Genetics and Oncology, having authored 9 papers that have together received 265 indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (3 papers), Cancer-related Molecular Pathways (2 papers), Cancer-related gene regulation (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper), Genetic Syndromes and Imprinting (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Oncology (99 citations), Cancer Research (49 citations) and Hematology (32 citations). S. S. Sommer has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Qiang Liu, Bobbie S. Gostout, Hagen Blaszyk, J. S. Kovach, Jinong Feng, Julie M. Cunningham, Jennifer J. Schroeder, Renee M. McGovern, A. Hartmann and Arndt Hartmann. Their work appears in journals such as Nucleic Acids Research, Human Molecular Genetics and Human Genetics.
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.