344  A maternal-effect selfish genetic element in Caenorhabditis elegans.

343  Structural variants caused by Alu insertions are associated with risks for many human diseases.

342  Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.

341  Male sex in houseflies is determined by Mdmd, a paralog of the generic splice factor gene CWC22.

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.

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