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Lack of association of bone morphogenetic protein 2 gene haplotypes with bone mineral density, bone loss, or risk of fractures in men
APOE Genotype-Function Relationship: Evidence of 2491 A/T Promoter Polymorphism Modifying Transcription Control but Not Type 2 Diabetes Risk
Mendelian Randomization Study of B-Type Natriuretic Peptide and Type 2 Diabetes: Evidence of Causal Association from Population Studies
Genetic Association of Multiple Sclerosis with the Marker rs391745 near the Endogenous Retroviral Locus HERVFc1: Analysis of Disease Subtypes
Exome-Sequencing Confirms DNAJC5 Mutations as Cause of Adult Neuronal Ceroid-Lipofuscinosis
Interactions between Genetic Variants in the Adiponectin, Adiponectin Receptor 1 and Environmental Factors on the Risk of Colorectal Cancer
The role of toll-like receptor variants in acute anterior uveitis
Perspectives on the Use of Multiple Sclerosis Risk Genes for Prediction
Genome-Wide Association Study in Bipolar Patients Stratified by Co-Morbidity
Common Variation in Vitamin D Pathway Genes Predicts Circulating 25-Hydroxyvitamin D Levels among African Americans