Scott Smemo

3.2k total citations
8 papers, 833 citations indexed

About

Scott Smemo is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Scott Smemo has authored 8 papers receiving a total of 833 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Scott Smemo's work include Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (2 papers) and Alzheimer's disease research and treatments (2 papers). Scott Smemo is often cited by papers focused on Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (2 papers) and Alzheimer's disease research and treatments (2 papers). Scott Smemo collaborates with scholars based in United States, Brazil and China. Scott Smemo's co-authors include Marcelo A. Nóbrega, Ivan P. Moskowitz, Xiao Wang, Xueqin Pang, Ye Fu, Qiang Cui, Qing Dai, Chuan He, Guifang Jia and Keli Han and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and PLoS ONE.

In The Last Decade

Scott Smemo

8 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Scott Smemo United States 7 718 182 112 92 84 8 833
Sahana Suresh Babu United States 13 381 0.5× 166 0.9× 107 1.0× 54 0.6× 28 0.3× 15 620
Christine Wahlquist United States 8 605 0.8× 309 1.7× 176 1.6× 26 0.3× 34 0.4× 9 784
Przemek A. Gorski United States 12 506 0.7× 119 0.7× 240 2.1× 34 0.4× 25 0.3× 17 682
Peter J. Belmont United States 9 406 0.6× 48 0.3× 67 0.6× 289 3.1× 30 0.4× 11 796
Claudine Grépin Canada 9 685 1.0× 27 0.1× 189 1.7× 54 0.6× 141 1.7× 10 790
Feiya Li Canada 15 1.0k 1.4× 759 4.2× 47 0.4× 31 0.3× 14 0.2× 29 1.2k
Naser Jaleel United States 9 615 0.9× 28 0.2× 353 3.2× 49 0.5× 27 0.3× 11 854
David Y. Chiang United States 18 839 1.2× 79 0.4× 1.0k 9.0× 26 0.3× 36 0.4× 38 1.3k
Andrea Lim Singapore 11 283 0.4× 66 0.4× 23 0.2× 126 1.4× 33 0.4× 15 474
Priyanka Madireddi United States 6 648 0.9× 58 0.3× 26 0.2× 84 0.9× 24 0.3× 6 750

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-authorship network of co-authors of Scott Smemo

This figure shows the co-authorship network connecting the top 25 collaborators of Scott Smemo. A scholar is included among the top collaborators of Scott Smemo 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 Scott Smemo. Scott Smemo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
Fu, Ye, Guifang Jia, Xueqin Pang, et al.. (2013). FTO-mediated formation of N6-hydroxymethyladenosine and N6-formyladenosine in mammalian RNA. Nature Communications. 4(1). 1798–1798. 374 indexed citations
2.
Arnolds, David E., Fang Liu, John Fahrenbach, et al.. (2012). TBX5 drives Scn5a expression to regulate cardiac conduction system function. Journal of Clinical Investigation. 122(7). 2509–2518. 99 indexed citations
3.
Smemo, Scott, Luciene Cristina Gastalho Campos, Ivan P. Moskowitz, et al.. (2012). Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Human Molecular Genetics. 21(14). 3255–3263. 155 indexed citations
4.
Shen, Tao, Ivy Aneas, Noboru J. Sakabe, et al.. (2011). Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function. Journal of Clinical Investigation. 121(12). 4640–4654. 113 indexed citations
5.
Smemo, Scott & Justin Borevitz. (2007). Redundancy in Genotyping Arrays. PLoS ONE. 2(3). e287–e287. 5 indexed citations
6.
Wahrle, Suzanne E., Aarti R. Shah, Anne M. Fagan, et al.. (2007). Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1polymorphisms. Molecular Neurodegeneration. 2(1). 7–7. 69 indexed citations
7.
Nowotny, Petra, Sarah Bertelsen, Anthony L. Hinrichs, et al.. (2007). Association studies testing for risk for late‐onset Alzheimer's disease with common variants in the β‐amyloid precursor protein (APP). American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(4). 469–474. 7 indexed citations
8.
Racette, Brad A., Melissa M. Rundle, Alison Goate, et al.. (2002). A multi-incident, Old-Order Amish family with PD. Neurology. 58(4). 568–574. 11 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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