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Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies
Kalirin: a novel genetic risk factor for ischemic stroke
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility
Identification of single nucleotide polymorphisms in the p21 (CDKN1A) gene and correlations with longevity in the Italian population
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus
Genetic variation in GIPR influences the glucose and insulin responses to oral glucose challenge
Genetic variation in neuroendocrine genes associates with somatic symptoms in the general population: Results from the EPIFUND study
Interleukin-10 (IL-10) pathway: genetic variants and outcomes of HIV-1 infection in African American adolescents
Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
Lack of association of the CIITA -168A/G promoter SNP with Myasthenia gravis and its role in autoimmunity