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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
Genome-wide genotype-based risk model for survival in acute myeloid leukaemia patients with normal karyotype
Human Candidate Polymorphisms in Sympatric Ethnic Groups Differing in Malaria Susceptibility in Mali
Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study
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)