Scott Smemo
Impact in
- Cancer Research top 10%
- Cancer-related molecular mechanisms research
- Molecular Biology top 10%
- RNA modifications and cancer
- Congenital heart defects research
- Cancer-related gene regulation
- RNA Research and Splicing
- Epigenetics and DNA Methylation
- RNA and protein synthesis mechanisms
Papers in
-
- Congenital heart defects research 3
- RNA Research and Splicing 1
- Amyloidosis: Diagnosis, Treatment, Outcomes 1
- Gene expression and cancer classification 1
- Genomics and Chromatin Dynamics 1
- Genetics 3
- Genetic Associations and Epidemiology 2
- Co-authors
- Marcelo A. Nóbrega (4 shared papers)Ivan P. Moskowitz (2 shared papers)Guifang Jia (1 shared paper)Keli Han (1 shared paper)Ye Fu (1 shared paper)Qing Dai (1 shared paper)Xiao Wang (1 shared paper)Qiang Cui (1 shared paper)
- Journals
- Journal of Clinical Investigation (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)Molecular Neurodegeneration (1 paper)Human Molecular Genetics (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesChinaBrazil
In The Last Decade
Scott Smemo
8 papers receiving 863 citations
Peers
Comparison fields: 5 of 67
- Cancer Research 176
- Molecular Biology 733
- Cardiology and Cardiovascular Medicine 103
- Epidemiology 84
- Genetics 74
Countries citing papers authored by Scott Smemo
This map shows the geographic impact of Scott Smemo'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 Scott Smemo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott Smemo more than expected).
Fields of papers citing papers by Scott Smemo
This network shows the impact of papers produced by Scott Smemo. 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 Scott Smemo. The network helps show where Scott Smemo may publish in the future.
Co-authors
The 25 scholars most cited alongside Scott Smemo, 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 | 2013 | 392 | |
| 2 | 2012 | 161 | |
| 3 | 2011 | 115 | |
| 4 | 2012 | 110 | |
| 5 | 2007 | 73 | |
| 6 | 2002 | 11 | |
| 7 | 2007 | 8 | |
| 8 | 2007 | 5 |
About Scott Smemo
Scott Smemo is a scholar working on Molecular Biology, Genetics, Surgery, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 8 papers that have together received 875 indexed citations. Recurring topics across this work include Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (2 papers), RNA Research and Splicing (1 paper), Alzheimer's disease research and treatments (1 paper), Amyloidosis: Diagnosis, Treatment, Outcomes (1 paper), Gene expression and cancer classification (1 paper), Genomics and Chromatin Dynamics (1 paper) and Cholesterol and Lipid Metabolism (1 paper). The work is most often cited by research in Cancer Research (176 citations), Molecular Biology (733 citations), Cardiology and Cardiovascular Medicine (103 citations), Epidemiology (84 citations) and Genetics (74 citations). Scott Smemo has collaborated with scholars based in United States, China and Brazil. Frequent co-authors include Marcelo A. Nóbrega, Ivan P. Moskowitz, Guifang Jia, Keli Han, Ye Fu, Qing Dai, Xiao Wang, Qiang Cui, Chuan He and Xueqin Pang. Their work appears in journals such as Journal of Clinical Investigation, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Molecular Neurodegeneration, Human Molecular Genetics and PLoS ONE.
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.