The DISC1 Pathway Modulates Expression of Neurodevelopmental, Synaptogenic and Sensory Perception Genes

por Hennah, William, Porteous, David
Publicado 2009

DISC1-binding proteins in neural development, signalling and schizophrenia

por Bradshaw, Nicholas J., Porteous, David J.
Publicado 2012

Generation Scotland participant survey on data collection

por Edwards, Rachel, Campbell, Archie, Porteous, David
Publicado 2019

DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder?

por Boxall, Ruth, Porteous, David J., Thomson, Pippa A.
Publicado 2011

Genetic parameters for periodontal disease: an analysis of electronic dental treatment records linked to pedigree, genomic, sociodemographic and clinical data

por Bermingham, Mairead, Campbell, Archie, Porteous, David, Walls, Angus
Publicado 2017

Generation Scotland - Using Electronic Health Records for Research.

por Campbell, Archie, Flaig, Robin, Porteous, David, Sudlow, Cathie
Publicado 2022

Twin peaks: the draft human genome sequence

por Semple, Colin AM, Evans, Kathryn L, Porteous, David J
Publicado 2001

DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness

por Soares, Dinesh C., Carlyle, Becky C., Bradshaw, Nicholas J., Porteous, David J.
Publicado 2011

DISC1 variants 37W and 607F disrupt its nuclear targeting and regulatory role in ATF4-mediated transcription

por Malavasi, Elise L.V., Ogawa, Fumiaki, Porteous, David J., Millar, J. Kirsty
Publicado 2012

Speeding disease gene discovery by sequence based candidate prioritization

por Adie, Euan A, Adams, Richard R, Evans, Kathryn L, Porteous, David J, Pickard, Ben S
Publicado 2005

SuRFing the genomics wave: an R package for prioritising SNPs by functionality

por Ryan, Niamh M, Morris, Stewart W, Porteous, David J, Taylor, Martin S, Evans, Kathryn L
Publicado 2014

Structural Models of Human eEF1A1 and eEF1A2 Reveal Two Distinct Surface Clusters of Sequence Variation and Potential Differences in Phosphorylation

por Soares, Dinesh C., Barlow, Paul N., Newbery, Helen J., Porteous, David J., Abbott, Catherine M.
Publicado 2009

Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course

por Marioni, Riccardo E, Campbell, Archie, Scotland, Generation, Hayward, Caroline, Porteous, David J, Deary, Ian J
Publicado 2016

NDE1 and NDEL1: Multimerisation, alternate splicing and DISC1 interaction

por Bradshaw, Nicholas J., Christie, Sheila, Soares, Dinesh C., Carlyle, Becky C., Porteous, David J., Millar, J. Kirsty
Publicado 2009

Contribution of common risk variants to multiple sclerosis in Orkney and Shetland

por Barnes, Catriona L. K., Hayward, Caroline, Porteous, David J., Campbell, Harry, Joshi, Peter K., Wilson, James F.
Publicado 2021

Disc1 Variation Leads to Specific Alterations in Adult Neurogenesis

por Chandran, Jayanth S., Kazanis, Ilias, Clapcote, Steven J., Ogawa, Fumiaki, Millar, J. Kirsty, Porteous, David J., ffrench-Constant, Charles
Publicado 2014

Electronic health record and genome-wide genetic data in Generation Scotland participants

por Kerr, Shona M., Campbell, Archie, Marten, Jonathan, Vitart, Veronique, McIntosh, Andrew M, Porteous, David J., Hayward, Caroline
Publicado 2017

Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study

por Meijsen, Joeri J., Campbell, Archie, Hayward, Caroline, Porteous, David J., Deary, Ian J., Marioni, Riccardo E., Nicodemus, Kristin K.
Publicado 2018

Generation Scotland: Donor DNA Databank; A control DNA resource

por Kerr, Shona M, Liewald, David CM, Campbell, Archie, Taylor, Kerrie, Wild, Sarah H, Newby, David, Turner, Marc, Porteous, David J
Publicado 2010