Genome scans and microarrays: converging on genes for schizophrenia?

by Williams, Nigel M, O'Donovan, Michael C, Owen, Michael J
Published 2002

Schizophrenia Genetics: Building the Foundations of the Future

by Tansey, Katherine E., Owen, Michael J., O’Donovan, Michael C.
Published 2015

Pooled DNA genotyping on Affymetrix SNP genotyping arrays

by Kirov, George, Nikolov, Ivan, Georgieva, Lyudmila, Moskvina, Valentina, Owen, Michael J, O'Donovan, Michael C
Published 2006

Neurodevelopmental hypothesis of schizophrenia

by Owen, Michael J., O’Donovan, Michael C., Thapar, Anita, Craddock, Nicholas
Published 2011

Factor Structure of Autistic Traits in Children with ADHD

by Martin, Joanna, Hamshere, Marian L., O’Donovan, Michael C., Rutter, Michael, Thapar, Anita
Published 2013

Neurocognitive abilities in the general population and composite genetic risk scores for attention-deficit hyperactivity disorder

by Martin, Joanna, Hamshere, Marian L, Stergiakouli, Evangelia, O'Donovan, Michael C, Thapar, Anita
Published 2015

Genetic Risk for Attention-Deficit/Hyperactivity Disorder Contributes to Neurodevelopmental Traits in the General Population

by Martin, Joanna, Hamshere, Marian L., Stergiakouli, Evangelia, O’Donovan, Michael C., Thapar, Anita
Published 2014

Association of Genetic Risk for Schizophrenia With Nonparticipation Over Time in a Population-Based Cohort Study

by Martin, Joanna, Tilling, Kate, Hubbard, Leon, Stergiakouli, Evie, Thapar, Anita, Davey Smith, George, O'Donovan, Michael C., Zammit, Stanley
Published 2016

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

by Escott-Price, Valentina, Kirov, George, Rees, Elliott, Isles, Anthony R., Owen, Michael J., O’Donovan, Michael C.
Published 2015

Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals

by Crawford, Andrew A., Lewis, Sarah, Nutt, David, Peters, Tim J., Cowen, Philip, O’Donovan, Michael C., Wiles, Nicola, Lewis, Glyn
Published 2014

No evidence for association between polymorphisms in GRM3 and schizophrenia

by Norton, Nadine, Williams, Hywel J, Dwyer, Sarah, Ivanov, Dobril, Preece, Anna C, Gerrish, Amy, Williams, Nigel M, Yerassimou, Pamela, Zammit, Stanley, O'Donovan, Michael C, Owen, Michael J
Published 2005

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study

by Mills, Sophie, Langley, Kate, Van den Bree, Marianne, Street, Eddy, Turic, Darko, Owen, Michael J, O'Donovan, Michael C, Thapar, Anita
Published 2004

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

by Grozeva, Detelina, Conrad, Donald F., Barnes, Chris P., Hurles, Matthew, Owen, Michael J., O'Donovan, Michael C., Craddock, Nick, Kirov, George
Published 2012

Identifying mechanisms that underlie links between COMT genotype and aggression in male adolescents with ADHD

by van Goozen, Stephanie H.M., Langley, Kate, Northover, Clare, Hubble, Kelly, Rubia, Katya, Schepman, Karen, O'Donovan, Michael C., Thapar, Anita
Published 2015

Gender differences in CNV burden do not confound schizophrenia CNV associations

by Han, Jun, Walters, James T. R., Kirov, George, Pocklington, Andrew, Escott-Price, Valentina, Owen, Michael J., Holmans, Peter, O’Donovan, Michael C., Rees, Elliott
Published 2016

A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents

by Zammit, Stanley, Hamshere, Marian, Dwyer, Sarah, Georgiva, Lyudmila, Timpson, Nic, Moskvina, Valentina, Richards, Alexander, Evans, David M, Lewis, Glyn, Jones, Peter, Owen, Michael J., O’Donovan, Michael C.
Published 2014

Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals

by Lancaster, Thomas M., Ihssen, Niklas, Brindley, Lisa M., Tansey, Katherine E., Mantripragada, Kiran, O'Donovan, Michael C., Owen, Michael J., Linden, David E.J.
Published 2015

All SNPs Are Not Created Equal: Genome-Wide Association Studies Reveal a Consistent Pattern of Enrichment among Functionally Annotated SNPs

by Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helena, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M.
Published 2013

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

by Chapman, Jade, Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, Paul, Stretton, Alexandra, Holmans, Peter, Owen, Michael J., O'Donovan, Michael C., Williams, Julie, Kirov, George
Published 2013

Analysis of copy number variations at 15 schizophrenia-associated loci

by Rees, Elliott, Walters, James T. R., Georgieva, Lyudmila, Isles, Anthony R., Chambert, Kimberly D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J., Kirov, George
Published 2014