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Prenatal organophosphorus pesticide exposure and executive function in preschool-aged children in the Norwegian Mother, Father and Child Cohort Study (MoBa)
Gender differences of genetic etiology in the incidence of major depressive disorder among Han freshmen
Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia
CYP2S1 gene methylation among High-altitude pulmonary edema
RORA polymorphisms are risk factors for allergic rhinitis susceptibility in the Shaanxi Han population
A SNP in the 5′ flanking region of the SAA1 gene is associated with serum levels of serum amyloid A and cardiovascular risk factors
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study
Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy
Ischemic Postconditioning Protects against Aged Myocardial Ischemia/Reperfusion Injury by Transcriptional and Epigenetic Regulation of miR-181a-2-3p
Molecular Signatures of KRAS-Mutated Lung Adenocarcinoma: Analysis of Concomitant EGFR, ALK, STK11, and PD-L1 Status