z-logo
open-access-imgOpen Access
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders
Author(s) -
A. Jeremy Willsey,
Montana T. Morris,
Sheng Wang,
Helen Rankin Willsey,
Nawei Sun,
Nia Teerikorpi,
Tierney Baum,
Gerard Cagney,
Kevin J. Bender,
Tejal A. Desai,
Deepak Srivastava,
Graeme W. Davis,
Jennifer A. Doudna,
Edward F. Chang,
Vikaas S. Sohal,
Daniel H. Lowenstein,
Hao Li,
David A. Agard,
Michael J. Keiser,
Brian K. Shoichet,
Mark von Zastrow,
Lennart Mucke,
Steven Finkbeiner,
Li Gan,
Nenad Šestan,
Michael E. Ward,
Ruth Hüttenhain,
Tomasz J. Nowakowski,
Hugo J. Bellen,
Loren M. Frank,
Mustafa K. Khokha,
Richard P. Lifton,
Martin Kampmann,
Trey Ideker,
Matthew W. State,
Nevan J. Krogan
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.06.016
Subject(s) - biology , key (lock) , neuroscience , computational biology , ecology
Although gene discovery in neuropsychiatric disorders, including autism spectrum disorder, intellectual disability, epilepsy, schizophrenia, and Tourette disorder, has accelerated, resulting in a large number of molecular clues, it has proven difficult to generate specific hypotheses without the corresponding datasets at the protein complex and functional pathway level. Here, we describe one path forward-an initiative aimed at mapping the physical and genetic interaction networks of these conditions and then using these maps to connect the genomic data to neurobiology and, ultimately, the clinic. These efforts will include a team of geneticists, structural biologists, neurobiologists, systems biologists, and clinicians, leveraging a wide array of experimental approaches and creating a collaborative infrastructure necessary for long-term investigation. This initiative will ultimately intersect with parallel studies that focus on other diseases, as there is a significant overlap with genes implicated in cancer, infectious disease, and congenital heart defects.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom