Yichuan Liu
scholar.google.com
0000-0003-2023-072X
Drexel University
64 papers found
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Mitochondrial DNA Haplogroup K Is Protective Against Autism Spectrum Disorder Risk in Populations of European Ancestry
A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder–Associated Copy Number Variations
Genomic information of children with malignant brain tumors for the prediction of length of hospitalization
Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders
Genetic architecture of asthma in African American patients
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic Target
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study
Association of Inherited Copy Number Variation in ADAM3A and ADAM5 Pseudogenes with Oropharynx Cancer Risk and Outcome
Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing
ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies
Identification of novel loci in obstructive sleep apnea in European American and African American children
Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing
Saudi Arabian CML patient with a novel four‐way translocation at t(9;22;5;2)(q34;q11.2;p13;q44)
Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data
A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci
Identification of Mitochondrial DNA Variants Associated With Risk of Neuroblastoma
Improved genetic risk scoring algorithm for type 1 diabetes prediction
Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients
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