In April 2016 Manchester eScholar was replaced by the University of Manchester’s new Research Information Management System, Pure. In the autumn the University’s research outputs will be available to search and browse via a new Research Portal. Until then the University’s full publication record can be accessed via a temporary portal and the old eScholar content is available to search and browse via this archive.

Related resources

Full-text held externally

A role for noncoding variation in schizophrenia.

Roussos, Panos; Mitchell, Amanda C; Voloudakis, Georgios; Fullard, John F; Pothula, Venu M; Tsang, Jonathan; Stahl, Eli A; Georgakopoulos, Anastasios; Ruderfer, Douglas M; Charney, Alexander; Okada, Yukinori; Siminovitch, Katherine A; Worthington, Jane; Padyukov, Leonid; Klareskog, Lars; Gregersen, Peter K; Plenge, Robert M; Raychaudhuri, Soumya; Fromer, Menachem; Purcell, Shaun M; Brennand, Kristen J; Robakis, Nikolaos K; Schadt, Eric E; Akbarian, Schahram; Sklar, Pamela

Cell reports. 2014;9(4):1417-29.

Access to files

Full-text and supplementary files are not available from Manchester eScholar. Full-text is available externally using the following links:

Full-text held externally

Abstract

A large portion of common variant loci associated with genetic risk for schizophrenia reside within noncoding sequence of unknown function. Here, we demonstrate promoter and enhancer enrichment in schizophrenia variants associated with expression quantitative trait loci (eQTL). The enrichment is greater when functional annotations derived from the human brain are used relative to peripheral tissues. Regulatory trait concordance analysis ranked genes within schizophrenia genome-wide significant loci for a potential functional role, based on colocalization of a risk SNP, eQTL, and regulatory element sequence. We identified potential physical interactions of noncontiguous proximal and distal regulatory elements. This was verified in prefrontal cortex and -induced pluripotent stem cell-derived neurons for the L-type calcium channel (CACNA1C) risk locus. Our findings point to a functional link between schizophrenia-associated noncoding SNPs and 3D genome architecture associated with chromosomal loopings and transcriptional regulation in the brain.

Bibliographic metadata

Type of resource:
Content type:
Publication status:
Published
Publication type:
Publication form:
Published date:
Language:
eng
Journal title:
Abbreviated journal title:
ISSN:
Place of publication:
United States
Volume:
9
Issue:
4
Pagination:
1417-29
Digital Object Identifier:
10.1016/j.celrep.2014.10.015
Pubmed Identifier:
25453756
Pii Identifier:
S2211-1247(14)00869-9
Funder acknowledgement:
Attached files embargo period:
Immediate release
Attached files release date:
10th April, 2015
Access state:
Active

Institutional metadata

University researcher(s):
Academic department(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:262595
Created by:
Ingram, Mary
Created:
10th April, 2015, 09:39:15
Last modified by:
Ingram, Mary
Last modified:
10th April, 2015, 09:49:03

Can we help?

The library chat service will be available from 11am-3pm Monday to Friday (excluding Bank Holidays). You can also email your enquiry to us.