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CDKN2A(p16) and HRAS are frequently mutated in vulvar squamous cell carcinoma (Oct 2014)
Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC
Insulin family polymorphisms in pregnancies complicated by small for gestational age infants
Association of GWAS-supported loci rs2107595 in HDAC9 gene with ischemic stroke in Southern Han Chinese
A 22-single nucleotide polymorphism Alzheimer risk score correlates with family history, onset age, and cerebrospinal fluid A?42
Linkage of an ABCC transporter to a single QTL that controls Ostrinia nubilalis larval resistance to the Bacillus thuringiensis Cry1Fa toxin
Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role ofÂ LMO1
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-KÃ¼ster-Hauser Syndrome in Chinese Han
HLA-DPB1 variant rs3117242 is associated with anti-neutrophil cytoplasmic antibody-associated vasculitidesÂ in a Han Chinese population
Association of seven thrombotic pathway gene CpG-SNPs with coronary heart disease