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IRF2BPL Is Associated with Neurological Phenotypes
Single nucleotide polymorphism-mediated translational suppression of endoplasmic reticulum mannosidase I modifies the onset of end-stage liver disease in alpha1-antitrypsin deficiency
Somatic mutations affect key pathways in lung adenocarcinoma
Comparative and demographic analysis of orang-utan genomes
Evolutionary and Biomedical Insights from the Rhesus Macaque Genome
Functional and evolutionary insights from the genomes of three parasitoid Nasonia species
A catalog of reference genomes from the human microbiome
Genome-wide detection and characterization of positive selection in human populations
A second generation human haplotype map of over 3.1 million SNPs
Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy
