Christopher Smith

588 total citations
11 papers, 274 citations indexed

About

Christopher Smith is a scholar working on Molecular Biology, Social Psychology and Genetics. According to data from OpenAlex, Christopher Smith has authored 11 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Social Psychology and 3 papers in Genetics. Recurrent topics in Christopher Smith's work include Human-Automation Interaction and Safety (3 papers), Mitochondrial Function and Pathology (2 papers) and ATP Synthase and ATPases Research (2 papers). Christopher Smith is often cited by papers focused on Human-Automation Interaction and Safety (3 papers), Mitochondrial Function and Pathology (2 papers) and ATP Synthase and ATPases Research (2 papers). Christopher Smith collaborates with scholars based in Canada, United Kingdom and Japan. Christopher Smith's co-authors include Jillian S. Parboosingh, A. Micheil Innes, François P. Bernier, Ryan E. Lamont, Siegfried Hekimi, Ying Wang, Aneal Khan, Arif B. Ekici, Hasan Tawamie and Rami Abou Jamra and has published in prestigious journals such as Cancer Research, The American Journal of Human Genetics and Frontiers in Microbiology.

In The Last Decade

Christopher Smith

11 papers receiving 269 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christopher Smith Canada	8	189	45	32	32	23	11	274
Minjae Kwon South Korea	11	158 0.8×	16 0.4×	4 0.1×	23 0.7×	2 0.1×	27	420
Mélanie Marie France	10	145 0.8×	33 0.7×	13 0.4×	5 0.2×	4 0.2×	17	375
Beichen Xie China	9	178 0.9×	26 0.6×	8 0.3×	16 0.5×		20	301
Hilary Holloway New Zealand	10	150 0.8×	24 0.5×	4 0.1×	12 0.4×	12 0.5×	13	341
S. Y. Kim South Korea	10	161 0.9×	115 2.6×	4 0.1×	17 0.5×	3 0.1×	27	552
Coralie Barrau France	6	149 0.8×	4 0.1×	11 0.3×	4 0.1×	8 0.3×	16	329
Zhihao Zhao China	10	154 0.8×	19 0.4×	5 0.2×	7 0.2×	2 0.1×	18	278
Izabela Koszela-Piotrowska Poland	11	321 1.7×	14 0.3×	9 0.3×	14 0.4×		14	400
You‐Kyung Lee South Korea	9	189 1.0×	23 0.5×	9 0.3×	8 0.3×	3 0.1×	20	428
Yuanjun Zhang China	8	97 0.5×	19 0.4×	2 0.1×	8 0.3×	3 0.1×	16	336

Countries citing papers authored by Christopher Smith

Since Specialization

Citations

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

Fields of papers citing papers by Christopher Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Smith

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

All Works

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11 of 11 papers shown

Smith, Christopher, et al.. (2023). Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature. Psychiatric Genetics. 34(1). 1–7. 2 indexed citations

Aranda, Ruth, Laura Waters, Krystal Moya, et al.. (2023). Abstract 2778: A novel MTA-cooperative PRMT5 inhibitor, MRTX1719, stabilizes the ternary MTA-PRMT5 complex and leads to synthetic lethality in MTAP deleted cancers. Cancer Research. 83(7_Supplement). 2778–2778. 1 indexed citations

Smith, Christopher, et al.. (2021). Co-Designing Interactions between Pedestrians in Wheelchairs and Autonomous Vehicles. 339–351. 20 indexed citations

Smith, Christopher, Sowmya Somanath, Ehud Sharlin, & Yoshifumi Kitamura. (2020). Exploring Interactions between Rogue Autonomous Vehicles and People. 453–455. 2 indexed citations

Smith, Christopher, et al.. (2020). Views from the Wheelchair: Understanding Interaction between Autonomous Vehicle and Pedestrians with Reduced Mobility. 1–8. 8 indexed citations

Smith, Christopher, Rasha Sabouny, Tian Zhao, et al.. (2019). The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy. EBioMedicine. 45. 379–392. 33 indexed citations

Smith, Ashley, Rosemary A. Bamford, Christopher Smith, et al.. (2018). The Culture Environment Influences Both Gene Regulation and Phenotypic Heterogeneity in Escherichia coli. Frontiers in Microbiology. 9. 1739–1739. 42 indexed citations

Wang, Ying, Christopher Smith, Jillian S. Parboosingh, et al.. (2017). Pathogenicity of two COQ7 mutations and responses to 2,4‐dihydroxybenzoate bypass treatment. Journal of Cellular and Molecular Medicine. 21(10). 2329–2343. 47 indexed citations

Smith, Christopher, Jillian S. Parboosingh, Kym M. Boycott, et al.. (2016). Expansion of the GLE1‐associated arthrogryposis multiplex congenita clinical spectrum. Clinical Genetics. 91(3). 426–430. 14 indexed citations

10.

Smith, Christopher, Ryan E. Lamont, Andrew Wade, et al.. (2015). A relatively mild skeletal ciliopathy phenotype consistent with cranioectodermal dysplasia is associated with a homozygous nonsynonymous mutation in WDR35. American Journal of Medical Genetics Part A. 170(3). 760–765. 10 indexed citations

11.

Buchert, Rebecca, Hasan Tawamie, Christopher Smith, et al.. (2014). A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency. The American Journal of Human Genetics. 95(5). 602–610. 95 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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