Search

Search results

78 results found

About

Our Mission is to understand the causes of serious mental illness and to develop transformative treatments. We study the biological mechanisms underlying psychiatric and neurodegenerative disorders – from the molecular-cellular level to the circuit-systems level in the brain. Our current research...

Laborum Repellendus Est Minima

Qui ut voluptatem voluptatem velit molestias hic ad nihil nostrum.Quis nihil ea veniam labore ducimus velit eos. Natus Eos Sed Maiores In Neque Dolores Et. Minima praesentium repudiandae sed nam qui iusto nulla occaecati tempore. Eos sunt ut repudiandae distinctio. Aspernatur cumque quos ab pariatur...

Turpis cursus in hac habitasse platea dictumst quisque sagittis purus

Semper feugiat nibh sed pulvinar proin gravida hendrerit lectus. Vel orci porta non pulvinar neque. Volutpat lacus laoreet non curabitur gravida arcu. Quis risus sed vulputate odio ut enim. Eu nisl nunc mi ipsum faucibus vitae. Qui minus repellendus libero non rem perferendis. Consectetur magnam...

Group Alumni

Where are they now? Check their career progress on Dr. Cimini's [ CV] Alum Year Role Alice Lucas 2021-2022 Software Engineer Barbara Diaz-Rohrer 2021-2023 Postdoctoral Associate Callum Tromans-Coia 2022-2023 Postdoctoral Associate David Stirling 2019-2021 Postdoctoral Associate Eddy Onyango 2023...

Our Team

The Sheng lab is committed to diversity, equity and inclusion and our lab is dedicated to ensuring a welcoming and safe space for all individuals. We actively work to increase the breadth of our applicant pools to create an environment that supports and retains a richly diverse community...

Merkin Prize Jury

The Merkin Prize Jury is composed of scientific leaders from academia and industry in the US and Europe.

Get in Touch

Powerful websites to share your science story: from team and research to publications and impact.

Limb-Girdle Muscular Dystrophy (LGMD)

The limb-girdle muscular dystrophy (LGMD) branch of the Rare Genomes Project is a partnership with the Muscular Dystrophy Association and the Jain Foundation dedicated to diagnosis and gene discovery through whole genome sequencing for individuals and families with LGMD.