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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
Phylogenetic Distinctiveness of Middle Eastern and Southeast Asian Village Dog Y Chromosomes Illuminates Dog Origins
DNA Methylation Profiling of Embryonic Stem Cell Differentiation into the Three Germ Layers
The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
Genotyping Performance Assessment of Whole Genome Amplified DNA with Respect to Multiplexing Level of Assay and Its Period of Storage
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