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Xin Jin

Utilizing non-invasive prenatal test sequencing data for human genetic investigation
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
Patent: BASE MUTATION DETECTION METHOD AND APPARATUS BASED ON SEQUENCING DATA, AND STORAGE MEDIUM
CMDB: the comprehensive population genome variation database of China
How robust are cross-population signatures of polygenic adaptation in humans?
Genome-wide association study of COVID-19 severity among the Chinese population
Trans-ethnic genome-wide association study of severe COVID-19
Genomic epidemiology of SARS-CoV-2 in the UAE reveals novel virus mutation, patterns of co-infection and tissue specific host immune response
The genetic architecture of sporadic and multiple consecutive miscarriage
Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History

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