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Additional Evidence Supports Association of Common Variants in COL11A1 with Increased Risk of Hip Osteoarthritis Susceptibility
Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations
The RAD51C exonic splice-site mutations c. 404G> C and c. 404G> T are associated with familial breast and ovarian cancer
Replicative Analysis Of 30 Snps In Russian Patients With Alzheimer’s Disease
Damaging Missense De Novo Coding Mutations Contribute To Schizophrenia Risk
Association of polymorphism in the dopamine receptors and transporter genes with hyperprolactinemia in patients with schizophrenia
Influence of serotonergic gene variants on serotonin transporter binding in ADHD
Dopamine receptors genes polymorphisms in Parkinson patients with levodopa-induced dyskinesia
MDR1 and CYP3A4 genes variants association with clinical response measured on a five-factor model in multiepisodic schizophrenia and related …
Association between prolactin gene polymorphism (–1149 G/T) and hyperprolactinemia in anti-psychotic treated patients with schizophrenia