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Meta-analysis identifies BACH2 and RAD51B as rheumatoid arthritis susceptibility loci
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
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
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