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Methylome analysis for spina bifida shows SOX18 hypomethylation as risk factor with evidence for a complex (epi) genetic interplay to affect neural tube development
Neural substrates of fear conditioning are modulated by GLRB allelic variation: converging evidence from an independent replication
Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations
Genetic 3′ UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight
Congenital skull fracture as a presenting sign of Menkes disease: A case of perinatal diagnosis and early treatment
Whole-genome analysis reveals unexpected dynamics of mutant subclone development in a patient with JAK2-V617F-positive chronic myeloid leukemia
Association of transketolase polymorphisms with measures of polyneuropathy in patients with recently diagnosed diabetes
Tissue-specific methylation profile in obese patients with type 2 diabetes before and after Roux-en-Y gastric bypass
Association between Cullin-3 single-nucleotide polymorphism rs17479770 and essential hypertension in the male Chinese Han population
Association between Two Resistin Gene Polymorphisms and Metabolic Syndrome in Jilin, Northeast China: A Case-Control Study