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Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease
Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson’s Disease
Genetic Diagnosis of Deafness
Genetic effect of MTHFR C677T polymorphism on the structural covariance network and white-matter integrity in Alzheimer’s disease
Genetic modifiers of multiple sclerosis progression, severity and onset
Genetic polymorphisms of C-type lectin receptors in Behcet’s disease in a Chinese Han population
Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population
Family history of type 1 and type 2 diabetes and risk of latent autoimmune diabetes in adults (LADA)
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
Filaggrin gene polymorphism associated with Epstein–Barr virus-associated tumors in China