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Experimental Biology and Medicine (Maywood, N.J.)|September 2, 2025
Natural killer cell subpopulations in the peripheral blood of single ventricle/hypoplastic left heart syndrome patients via single-cell RNA sequencingHui-Qi Qu, Kushagra Goel, Kayleigh Ostberg, et al.
Nucleic Acids Research|February 15, 2011
Ranking causal variants and associated regions in genome-wide association studies by the support vector machine and random forestUsman Roshan, Satish Chikkagoudar, Zhi Wei, et al.
Current Diabetes Reports|November 6, 2019
The Genetic Contribution to Type 1 DiabetesMarina Bakay, Rahul Pandey, Struan F A Grant, et al.
European Journal of Human Genetics : EJHG|December 6, 2017
Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk lociYu Zhang, Lifeng Tian, Patrick Sleiman, et al.
Genome Research|February 27, 2023
Complex hierarchical structures in single-cell genomics data unveiled by deep hyperbolic manifold learningTian Tian, Cheng Zhong, Xiang Lin, et al.
Biological Psychiatry|October 21, 2023
A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number VariationsXiao Chang, Huiqi Qu, Yichuan Liu, et al.
Rheumatology (Oxford, England)|February 16, 2022
Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlapHui-Qi Qu, Jingchun Qu, Courtney Vaccaro, et al.
Nature Communications|March 26, 2021
Model-based deep embedding for constrained clustering analysis of single cell RNA-seq dataTian Tian, Jie Zhang, Xiang Lin, et al.
American Journal of Medical Genetics. Part A|February 6, 2019
Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrumChaya Murali, Dong Li, Katheryn Grand, et al.
Genes|April 28, 2023
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic TargetBrian E White, Yichuan Liu, Hakon Hakonarson, et al.
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