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Association of ACYP2 and TSPYL6 Genetic Polymorphisms with Risk of Ischemic Stroke in Han Chinese Population
Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis
Regional analysis and genetic association of nigrostriatal degeneration in Lewy body disease
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration
Polymorphisms of insulin receptor substrate 2 are putative biomarkers for pediatric medulloblastoma: considering the genetic susceptibility and pathological diagnoses
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Decreased gene expression of CD2AP in Chinese patients with sporadic Alzheimer’s disease
Genetic association study between RIT2 and Parkinson’s disease in a Han Chinese population
Genetic analysis of FGF20 in Chinese patients with Parkinson’s disease
SNPs in Aβ clearance proteins: Lower CSF Aβ1-42 levels and earlier onset of dementia in PD