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Replication of previous autism-GWAS hits suggests the association between NAA1, SORCS3, and GSDME and autism in the Han Chinese population
Results of neonatal screening for congenital hypothyroidism and hyperphenylalaninemia in Zhejiang province from 1999 to 2022
Evaluating the regulatory function of non‐coding autism‐associated single nucleotide polymorphisms on gene expression in human brain tissue
Childhood maltreatment, multilocus HPA-axis genetic variation and adolescent comorbidity profiles of depressive and anxiety symptoms
The interaction of RELN–DNMT genes involving in neurotrophin signaling pathway contributes to schizophrenia susceptibility
Genetic association study of TERT gene variants with chronic kidney disease susceptibility in the Chinese population
Genetic polymorphisms in CYP2B6 may be associated with lung cancer risk in the Chinese Han population
Association of SOX6 gene polymorphisms with Kashin-Beck disease risk in the Chinese Han population
Association of HTR1A Gene Polymorphisms with Efficacy and Plasma Concentrations of Atypical Antipsychotics in the Treatment of Male Patients with Schizophrenia
SOWAHB polymorphisms affect thyroid cancer risk in the Chinese Han population