Scott C. Smith

550 total citations
23 papers, 353 citations indexed

About

Scott C. Smith is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Scott C. Smith has authored 23 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Genetics. Recurrent topics in Scott C. Smith's work include DNA Repair Mechanisms (4 papers), Glioma Diagnosis and Treatment (3 papers) and Neuroblastoma Research and Treatments (3 papers). Scott C. Smith is often cited by papers focused on DNA Repair Mechanisms (4 papers), Glioma Diagnosis and Treatment (3 papers) and Neuroblastoma Research and Treatments (3 papers). Scott C. Smith collaborates with scholars based in United States, Netherlands and Australia. Scott C. Smith's co-authors include Ingrid E. Scheffer, Mary Connolly, K Farrell, Lynette G. Sadleir, Michal Hetman, Theo Hagg, Cynthia Gomes, Irene Litvan, Pierre Champy and Frederick A. Luzzio and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Neurology.

In The Last Decade

Scott C. Smith

20 papers receiving 347 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 C. Smith United States 9 176 92 91 60 45 23 353
Maria Stella Vari Italy 13 202 1.1× 111 1.2× 56 0.6× 23 0.4× 126 2.8× 31 453
Jonathan van Eyll Belgium 9 289 1.6× 53 0.6× 69 0.8× 7 0.1× 77 1.7× 14 434
Yoshitaka Furuta Japan 8 123 0.7× 72 0.8× 49 0.5× 10 0.2× 106 2.4× 15 366
Paul J. Tolentino United States 10 187 1.1× 51 0.6× 123 1.4× 16 0.3× 34 0.8× 14 485
Sabrina Petri United States 7 256 1.5× 37 0.4× 58 0.6× 12 0.2× 78 1.7× 8 361
Jimmy El Hokayem United States 11 297 1.7× 14 0.2× 44 0.5× 36 0.6× 78 1.7× 16 395
Han Zhou China 9 144 0.8× 16 0.2× 83 0.9× 17 0.3× 14 0.3× 23 339
William Craigen United States 9 290 1.6× 15 0.2× 34 0.4× 10 0.2× 81 1.8× 13 443
Daniel Ye United States 11 213 1.2× 36 0.4× 67 0.7× 11 0.2× 26 0.6× 14 435
Fabien Dachet United States 10 277 1.6× 60 0.7× 85 0.9× 27 0.5× 40 0.9× 15 412

Countries citing papers authored by Scott C. Smith

Since Specialization
Citations

This map shows the geographic impact of Scott C. Smith'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 C. Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott C. Smith more than expected).

Fields of papers citing papers by Scott C. Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Scott C. Smith. 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 C. Smith. The network helps show where Scott C. Smith may publish in the future.

Co-authorship network of co-authors of Scott C. Smith

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

All Works

20 of 20 papers shown
1.
2.
Lebel, Robert Roger, et al.. (2025). Proximal Deletions of 14q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic Features. American Journal of Medical Genetics Part A. 197(7). e64042–e64042.
3.
4.
Cooley, Linda D., John Herriges, Lei Zhang, et al.. (2023). Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours. Cancer Genetics. 274-275. 10–20. 2 indexed citations
5.
Miller, Eric, Scott W. Riddell, Frank A. Middleton, et al.. (2022). Development and Validation of Two RT-qPCR Diagnostic Assays for Detecting Severe Acute Respiratory Syndrome Coronavirus 2 Genomic Targets across Two Specimen Types. Journal of Molecular Diagnostics. 24(4). 294–308. 5 indexed citations
6.
Smith, Scott C., et al.. (2020). The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3. American Journal of Medical Genetics Part A. 182(9). 2161–2167. 4 indexed citations
7.
Smith, Scott C., et al.. (2020). MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular review. Leukemia Research. 95. 106387–106387. 2 indexed citations
8.
Smith, Scott C., et al.. (2020). Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus Assay. Journal of Molecular Diagnostics. 23(1). 29–37. 3 indexed citations
9.
Smith, Scott C., Pamela A. Althof, Bhavana J. Davé, & Jennifer N. Sanmann. (2020). High‐risk cytogenetics in multiple myeloma: Further scrutiny of deletions within the IGH gene region enhances risk stratification. Genes Chromosomes and Cancer. 59(10). 569–574. 8 indexed citations
10.
Smith, Scott C., et al.. (2019). Maintaining a methods database to optimize solid tumor tissue culture: Review of a 15-year database from a single institution. Cancer Genetics. 233-234. 96–101. 5 indexed citations
11.
Hackett, Simon & Scott C. Smith. (2018). Young people who engage in child sexual exploitation behaviours : an exploratory study.. Durham Research Online (Durham University). 1 indexed citations
12.
Vashishta, Aruna, Łukasz P. Słomnicki, Maciej Pietrzak, et al.. (2018). RNA Polymerase 1 Is Transiently Regulated by Seizures and Plays a Role in a Pharmacological Kindling Model of Epilepsy. Molecular Neurobiology. 55(11). 8374–8387. 10 indexed citations
13.
Warner, Dennis, et al.. (2016). Inhibition of p300 histone acetyltransferase activity in palate mesenchyme cells attenuates Wnt signaling via aberrant E-cadherin expression. Experimental Cell Research. 342(1). 32–38. 15 indexed citations
14.
Słomnicki, Łukasz P., et al.. (2016). Proapoptotic Requirement of Ribosomal Protein L11 in Ribosomal Stress-Challenged Cortical Neurons. Molecular Neurobiology. 55(1). 538–553. 10 indexed citations
15.
Smith, Scott C., Aleksandra V. Petrova, Matthew Z. Madden, et al.. (2014). A gemcitabine sensitivity screen identifies a role for NEK9 in the replication stress response. Nucleic Acids Research. 42(18). 11517–11527. 32 indexed citations
16.
Smith, Scott C., Andria R. Robinson, Laura J. Niedernhofer, & Michal Hetman. (2011). Downregulation of cholesterol biosynthesis genes in the forebrain of ERCC1-deficient mice. Neurobiology of Disease. 45(3). 1136–1144. 8 indexed citations
17.
Pietrzak, Maciej, et al.. (2011). Nucleolar disruption and apoptosis are distinct neuronal responses to etoposide‐induced DNA damage. Journal of Neurochemistry. 117(6). 1033–1046. 21 indexed citations
18.
Smith, Scott C. & Michal Hetman. (2011). ATM is a Novel Regulator of Nucleolar Transcription. The FASEB Journal. 25(S1). 1 indexed citations
19.
Luzzio, Frederick A., et al.. (2011). Annonacin in Asimina triloba fruit: Implication for neurotoxicity. NeuroToxicology. 33(1). 53–58. 46 indexed citations
20.
Gomes, Cynthia, et al.. (2010). RNA Polymerase 1-driven Transcription as a Mediator of BDNF-induced Neurite Outgrowth. Journal of Biological Chemistry. 286(6). 4357–4363. 46 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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