| 340 Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.
339 Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.
338 Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI).
337 Common coding variant in SERPINA1 increases the risk for large artery stroke.
336 A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear.
335 Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c.
334 3D structures of individual mammalian genomes studied by single-cell Hi-C.
333 Population genetic analysis of the DARC locus (Duffy) reveals adaptation from standing variation associated with malaria resistance in humans.
332 A technique called genome architecture mapping (GAM) involves sequencing DNA from a large number of thin nuclear cryosections to develop a map of genome organization without the limitations of existing 3C-based methods.
331 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.