Kenny Nguyen

479 total citations
22 papers, 163 citations indexed

About

Kenny Nguyen is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Kenny Nguyen has authored 22 papers receiving a total of 163 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Kenny Nguyen's work include Attention Deficit Hyperactivity Disorder (3 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Kenny Nguyen is often cited by papers focused on Attention Deficit Hyperactivity Disorder (3 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Kenny Nguyen collaborates with scholars based in United States, Iceland and China. Kenny Nguyen's co-authors include Håkon Håkonarson, Patrick Sleiman, Yichuan Liu, Hui‐Qi Qu, Joseph Glessner, Xiao Chang, Lifeng Tian, Frank Mentch, Michael March and Seema S. Aceves and has published in prestigious journals such as Nature Communications, JNCI Journal of the National Cancer Institute and Journal of Allergy and Clinical Immunology.

In The Last Decade

Kenny Nguyen

20 papers receiving 157 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kenny Nguyen United States 9 64 36 31 24 21 22 163
Rogelio Simón Spain 9 41 0.6× 41 1.1× 31 1.0× 14 0.6× 33 1.6× 19 192
Charles‐Joris Roux France 9 60 0.9× 30 0.8× 27 0.9× 9 0.4× 15 0.7× 39 220
Erica A. Peterson Canada 8 165 2.6× 20 0.6× 77 2.5× 8 0.3× 17 0.8× 19 504
Yann Grattau France 5 112 1.8× 100 2.8× 28 0.9× 15 0.6× 16 0.8× 5 323
Hatice Mutlu Albayrak Türkiye 7 67 1.0× 41 1.1× 14 0.5× 13 0.5× 9 0.4× 26 147
Ehud Banne Israel 9 95 1.5× 78 2.2× 20 0.6× 6 0.3× 12 0.6× 16 201
Isabelle Marey France 8 54 0.8× 31 0.9× 6 0.2× 12 0.5× 13 0.6× 15 139
David Skidmore Canada 9 112 1.8× 93 2.6× 29 0.9× 12 0.5× 6 0.3× 17 339
Ruđer Novak Croatia 7 95 1.5× 23 0.6× 18 0.6× 9 0.4× 7 0.3× 16 221
Rodolphe Dard France 6 113 1.8× 63 1.8× 12 0.4× 8 0.3× 15 0.7× 19 233

Countries citing papers authored by Kenny Nguyen

Since Specialization
Citations

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

Fields of papers citing papers by Kenny Nguyen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kenny Nguyen

This figure shows the co-authorship network connecting the top 25 collaborators of Kenny Nguyen. A scholar is included among the top collaborators of Kenny Nguyen 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 Kenny Nguyen. Kenny Nguyen 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.
Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2025). Deep learning algorithms reveal genomic markers for anxiety disorder in a large cohort of children with down syndrome. Molecular Psychiatry. 30(10). 4710–4719. 1 indexed citations
2.
Nguyen, Kenny, et al.. (2025). Downstream Effects of Omission of Axillary Surgery in Older Adults with Early-Stage HR+/HER2− Breast Cancer. Annals of Surgical Oncology. 32(7). 4838–4846. 2 indexed citations
3.
Qu, Hui‐Qi, Xiao Chang, Nolan Williams, et al.. (2025). The genetic landscape of pediatric postural orthostatic tachycardia syndrome. Clinical Autonomic Research. 35(3). 431–451.
4.
Qu, Hui‐Qi, Chethan Gangireddy, Anjali Vaidya, et al.. (2024). Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry. Journal of Molecular Medicine. 103(2). 175–185. 1 indexed citations
5.
March, Michael, Frank Mentch, Hui‐Qi Qu, et al.. (2024). Genetic modifiers of asthma response to air pollution in children: An African ancestry GWAS and PM2.5 polygenic risk score study. Environmental Research. 267. 120666–120666. 2 indexed citations
6.
Nguyen, Kenny, et al.. (2023). Impact of a near-peer teaching program within a college of pharmacy on interest in mentoring roles. Currents in Pharmacy Teaching and Learning. 15(4). 408–413. 5 indexed citations
7.
Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2022). Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing. Human Molecular Genetics. 31(22). 3769–3776. 6 indexed citations
8.
Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2022). Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population. Respiratory Research. 23(1). 116–116. 6 indexed citations
9.
Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2022). Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing. Biomarker Research. 10(1). 84–84.
10.
Liu, Yichuan, Hui‐Qi Qu, Frank Mentch, et al.. (2022). Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients. Molecular Psychiatry. 27(3). 1469–1478. 16 indexed citations
11.
Qu, Hui‐Qi, Xiao Chang, Frank Mentch, et al.. (2022). Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap. Lara D. Veeken. 61(8). 3497–3501. 3 indexed citations
12.
Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2021). Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variation. Experimental Biology and Medicine. 246(21). 2317–2323. 13 indexed citations
13.
Chang, Xiao, Yun Li, Kenny Nguyen, et al.. (2021). Genetic correlations between COVID-19 and a variety of traits and diseases. The Innovation. 2(2). 100112–100112. 5 indexed citations
14.
Chang, Xiao, Michael March, Frank Mentch, et al.. (2021). A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci. Journal of Allergy and Clinical Immunology. 149(3). 988–998. 30 indexed citations
15.
March, Michael, Álvaro Gutiérrez-Uzquiza, Kenny Nguyen, et al.. (2021). NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patients. Nature Communications. 12(1). 1827–1827. 10 indexed citations
16.
Chang, Xiao, Yichuan Liu, Frank Mentch, et al.. (2020). Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans. Translational Psychiatry. 10(1). 370–370. 13 indexed citations
17.
Chang, Xiao, Marina Bakay, Yichuan Liu, et al.. (2020). Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma. JNCI Journal of the National Cancer Institute. 112(12). 1259–1266. 9 indexed citations
18.
Liu, Yichuan, Xiao Chang, Joseph Glessner, et al.. (2019). Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios. Frontiers in Genetics. 10. 819–819. 19 indexed citations
19.
20.
Liu, Yichuan, Yun Li, Michael March, et al.. (2015). Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments. Human Genomics. 9(1). 31–31. 8 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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