Shujia Huang

Latest

Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Genetic study of intrahepatic cholestasis of pregnancy in Chinese women unveils East Asian etiology linked to historic HBV epidemic
Utilizing non-invasive prenatal test sequencing data for human genetic investigation
Genome-wide association and Mendelian randomisation analysis among 30,699 Chinese pregnant women identifies novel genetic and molecular risk factors for gestational diabetes and glycaemic traits
The Born in Guangzhou Cohort Study enables generational genetic discoveries
Patent: BASE MUTATION DETECTION METHOD AND APPARATUS BASED ON SEQUENCING DATA, AND STORAGE MEDIUM
CMDB: the comprehensive population genome variation database of China
Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
Next-generation recurrent network models for cognitive neuroscience
国家专利（已授权）：一种基于基因组组装的变异检测方法和装置
Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History
Assembly and analysis of 100 full MHC haplotypes from the Danish population
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Stochastic anomaly of methylome but persistent SRY hypermethylation in disorder of sex development in canine somatic cell nuclear transfer
Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale
De novo assembly of a haplotype-resolved human genome
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios
Bisulfite sequencing reveals that Aspergillus flavus holds a hollow in DNA methylation
Systematic assessment of reduced representation bisulfite sequencing to human blood samples: A promising method for large-sample-scale epigenomic studies