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Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
NAT2 acetylator phenotype, occupation and bladder cancer risk: Results from the EPIC cohort
Nonsynonymous polymorphisms of the PDLIM5 gene association with the occurrence of both bipolar disorder and schizophrenia
Novel A18T and pA29S substitutions in ?-synuclein may be associated with sporadic Parkinson’s disease
Novel associations of UDP-glucuronosyltransferase 2B gene variants with prostate cancer risk in a multiethnic study
Novel single nucleotide polymorphisms in interleukin 6 affect tacrolimus metabolism in liver transplant patients
IL10 polymorphisms associated with BehÃ§et’s disease in Chinese Han
Impact of COMT genotype on serotonin-1A receptor binding investigated with PET
Inherited common variants in mitochondrial DNA and invasive serous epithelial ovarian cancer risk
Innate Immunity Pathways and Breast Cancer Risk in African American and European-American Women in the Womenâ€™s Circle of Health Study (WCHS)