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Pharmacogenetics and Genomics|October 19, 2018
Leveraging electronic health records to assess the role of ADRB2 single nucleotide polymorphisms in predicting exacerbation frequency in asthma patientsNikita Sood, John J Connolly, Frank D Mentch, et al.
BMC Musculoskeletal Disorders|February 17, 2016
Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variantAkshatha Desai, John J Connolly, Michael March, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2013
Practical challenges in integrating genomic data into the electronic health recordAbel N Kho, Luke V Rasmussen, John J Connolly, et al.
Frontiers in Genetics|March 28, 2014
Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium effortsJohn J Connolly, Joseph T Glessner, Berta Almoguera, et al.
Iscience|July 11, 2022
Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African AmericansHui-Qi Qu, Joseph Glessner, Jingchun Qu, et al.
Journal of Personalized Medicine|December 23, 2022
Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their ChildrenShannon Terek, Maya C Del Rosario, Heather S Hain, et al.
The Journal of Gene Medicine|August 20, 2025
Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells in Patients With Single Ventricle/Hypoplastic Left Heart SyndromeHui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Genes|January 21, 2023
Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood SamplesHui-Qi Qu, Charlly Kao, James Garifallou, et al.
Diabetes Research and Clinical Practice|February 22, 2026
Sex specific genomic insights into type 1 diabetes through GWAS and single cell transcriptome analysisHui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|November 21, 2023
High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number VariationsHui-Qi Qu, Joseph T Glessner, Jingchun Qu, et al.
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