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NEDD4 single nucleotide polymorphism rs2271289 is associated with keloids in Chinese Han population
SLC1A2 rs3794087 are associated with susceptibility to Parkinson’s disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population
Role of HIF1A, VEGFA and VEGFR2 SNPs in the Susceptibility and Progression of COPD in a Spanish Population
Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development—Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus
Multiple genetic imaging study of the association between cholesterol metabolism and brain functional alterations in individuals with risk factors for Alzheimer’s disease
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes
The identification of two regulatory ESCC susceptibility genetic variants in the TERT-CLPTM1L loci
MAPK activation and HRAS mutation identified in pituitary spindle cell oncocytoma
Genetic variants of lncRNA HOTAIR and risk of epithelial ovarian cancer among Chinese women
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer
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