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Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis

Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations

Genes involved in the WNT and vesicular trafficking pathways are associated with melanoma predisposition

Reduced efficiency of sarcolipin-dependent respiration in myocytes from humans with severe obesity

Deubiquitinating enzyme CYLD mediates pressure overload-induced cardiac maladaptive remodeling and dysfunction via downregulating Nrf2

Data in support of the comparative genome analysis of Lysinibacillus B1-CDA, a bacterium that accumulates arsenics

Draft sequencing and assembly of the genome of the world’s largest fish, the whale shark: Rhincodon typus Smith 1828

Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness

Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes

Characterization of a Proposed Dichorhavirus Associated withthe Citrus Leprosis Disease and Analysis of the Host Response