Scott Smemo

3.2k citations
8 papers · 833 · h-index 7

Impact in

    • Cancer-related molecular mechanisms research
    • RNA modifications and cancer
    • Cancer-related gene regulation
    • Congenital heart defects research
    • RNA Research and Splicing
    • Epigenetics and DNA Methylation
    • RNA and protein synthesis mechanisms

Papers in

    • Congenital heart defects research 3
    • RNA and protein synthesis mechanisms 1
    • Genetic Associations and Epidemiology 2

Scott Smemo

8 papers receiving 827 citations

Peers

Scott Smemo
Comparison fields: 5 of 71
  • Cancer Research 182
  • Molecular Biology 718
  • Cardiology and Cardiovascular Medicine 112
  • Genetics 84
  • Epidemiology 92
Replace Peiyee Lee with:
Peiyee Lee United States
Sahana Suresh Babu United States
Christine Wahlquist United States
Przemek A. Gorski United States
Giuseppe D’Agostino United Kingdom
Andrea Lim Singapore
Víctor M. Campa Spain
Qiong Gong China
Stefania Monterisi United Kingdom
Peter J. Belmont United States
Scott Smemo relative to Peiyee Lee United States Peiyee Lee's profile →
Citations per field
00.5×4.5×
Peiyee Lee · 1×
Citations per year

Countries citing papers authored by Scott Smemo

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Scott Smemo Line = papers co-authored together Scott Smemo links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1 2013374
2 2012155
3 2011113
4 201299
5 200769
6 200211
7 20077
8 20075

About Scott Smemo

Scott Smemo is a scholar working on Molecular Biology, Genetics, Surgery, Physiology and Neurology, having authored 8 papers that have together received 833 indexed citations. Recurring topics across this work include Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (2 papers), Alzheimer's disease research and treatments (2 papers), Neurological diseases and metabolism (1 paper), Cholesterol and Lipid Metabolism (1 paper), RNA and protein synthesis mechanisms (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper) and Tissue Engineering and Regenerative Medicine (1 paper). The work is most often cited by research in Cancer Research (182 citations), Molecular Biology (718 citations), Cardiology and Cardiovascular Medicine (112 citations), Genetics (84 citations) and Epidemiology (92 citations). Scott Smemo has collaborated with scholars based in United States, Brazil and China. Frequent co-authors include Marcelo A. Nóbrega, Ivan P. Moskowitz, Qiang Cui, Chuan He, Qing Dai, Keli Han, Guifang Jia, Ye Fu, Xiao Wang and Xueqin Pang. Their work appears in journals such as Journal of Clinical Investigation, Molecular Neurodegeneration, Neurology, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Nature Communications.

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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