Human coding synonymous single nucleotide polymorphisms at ramp regions of mRNA translation. by Quan Li, Hui-Qi Qu

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Navigating Complexity in Postural Orthostatic Tachycardia Syndrome by Hui-Qi Qu, Hakon Hakonarson

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Genetics of BAG3: A Paradigm for Developing Precision Therapies for Dilated Cardiomyopathies by Hui‐Qi Qu, Arthur M. Feldman, Hakon Hakonarson

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Trans‐ethnic polygenic risk scores for body mass index by Hui‐Qi Qu, John J Connolly, Hakon Hakonarson

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Expression Pattern of the SARS-CoV-2 Entry Genes <i>ACE2</i> and <i>TMPRSS2</i> in the Respiratory Tract by Yichuan Liu, Hui-Qi Qu, Jingchun Qu, Lifeng Tian, Hakon Hakonarson

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COVID-19: Look to the Future, Learn from the Past by Zhangkai J. Cheng, Hui-Qi Qu, Lifeng Tian, Zhifeng Duan, Hakon Hakonarson

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Gene-specific function prediction for non-synonymous mutations in monogenic diabetes genes. by Quan Li, Xiaoming Liu, Richard A Gibbs, Eric Boerwinkle, Constantin Polychronakos, Hui-Qi Qu

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Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries by Hui-Qi Qu, James Snyder, John Connolly, Joseph Glessner, Charlly Kao, Patrick Sleiman, Hakon Hakonarson

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The definition of insulin resistance using HOMA-IR for Americans of Mexican descent using machine learning. by Hui-Qi Qu, Quan Li, Anne R Rentfro, Susan P Fisher-Hoch, Joseph B McCormick

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Copy number variations contribute to malignant tumor development in children with serious birth defects by Yichuan Liu, Joseph Glessner, Hui‐Qi Qu, Xiao Chang, Haijun Qiu, Tiancheng Wang, Frank D. Mentch, Hakon Hakonarson

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Prevalence of metabolic syndrome and risks of abnormal serum alanine aminotransferase in Hispanics: a population-based study. by Jen-Jung Pan, Hui-Qi Qu, Anne Rentfro, Joseph B McCormick, Susan P Fisher-Hoch, Michael B Fallon

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Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans by Hui-Qi Qu, Joseph Glessner, Jingchun Qu, Steven Gilhool, Frank Mentch, Ian Campbell, Patrick Sleiman, John J. Connolly, Hakon Hakonarson

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Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator by Christopher J. Cardinale, Xiao Chang, Xiao Chang, Zhi Wei, Hui-Qi Qu, Jonathan P. Bradfield, Constantin Polychronakos, Hakon Hakonarson, Hakon Hakonarson

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Deciphering protective genomic factors of tumor development in pediatric Down syndrome via deep learning approach to whole genome and RNA sequencing by Yichuan Liu, Hui‐Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Kayleigh Ostberg, Tiancheng Wang, Joseph Glessner, Hakon Hakonarson

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Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development by Yichuan Liu, Hui-Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson

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Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population by Yichuan Liu, Hui-Qi Qu, Jingchun Qu, Xiao Chang, Frank D. Mentch, Kenny Nguyen, Lifeng Tian, Joseph Glessner, Patrick M. A. Sleiman, Hakon Hakonarson

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Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing by Yichuan Liu, Hui-Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson

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Genomic information of children with malignant brain tumors for the prediction of length of hospitalization by Yichuan Liu, Hui‐Qi Qu, Xiao Chang, Frank D Mentch, Haijun Qiu, Kenny Nguyen, Xiang Wang, Amir Hossein Saeidian, Deborah Watson, Joseph Glessner, Hakon Hakonarson

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Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients by Jingchun Qu, Hui-Qi Qu, Jonathan P. Bradfield, Joseph T. Glessner, Xiao Chang, Lifeng Tian, Michael March, John J. Connolly, Jeffrey D. Roizen, Patrick M. A. Sleiman, Hakon Hakonarson

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Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci by Hui-Qi Qu, Jingchun Qu, Jonathan Bradfield, Luc Marchand, Joseph Glessner, Xiao Chang, Michael March, Jin Li, John J. Connolly, Jeffrey D. Roizen, Patrick Sleiman, Constantin Polychronakos, Hakon Hakonarson

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