Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice

by Doherty, Joanne L, Owen, Michael J
Published 2014

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

Schizophrenia

by Owen, Michael J, Sawa, Akira, Mortensen, Preben B
Published 2016

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

Lymphocyte Migration in Lymphocyte Function-associated Antigen (LFA)-1–deficient Mice

by Berlin-Rufenach, Cornelia, Otto, Florian, Mathies, Meg, Westermann, Juergen, Owen, Michael J., Hamann, Alf, Hogg, Nancy
Published 1999

Protein Kinase Cε Is Required for Macrophage Activation and Defense Against Bacterial Infection

by Castrillo, Antonio, Pennington, Daniel J., Otto, Florian, Parker, Peter J., Owen, Michael J., Boscá, Lisardo
Published 2001

Neurodevelopmental hypothesis of schizophrenia

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

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

by Heyes, Samuel, Pratt, Wendy S., Rees, Elliott, Dahimene, Shehrazade, Ferron, Laurent, Owen, Michael J., Dolphin, Annette C.
Published 2015

The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome

by Niarchou, Maria, Martin, Joanna, Thapar, Anita, Owen, Michael J., van den Bree, Marianne B. M.
Published 2015

γδ T Cells from Tolerized αβ T Cell Receptor (TCR)–deficient Mice Inhibit Contact Sensitivity-Effector T Cells In Vivo, and Their Interferon-γ Production In Vitro

by Szczepanik, Marian, Anderson, Laurel R., Ushio, Hiroko, Ptak, Wlodzimierz, Owen, Michael J., Hayday, Adrian C., Askenase, Philip W.
Published 1996

The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS)☆

by van den Bree, Marianne B.M., Miller, Gregory, Mansell, Elizabeth, Thapar, Anita, Flinter, Frances, Owen, Michael J.
Published 2013

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

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

The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder

by Economou, Alexis, Grey, Michelle, McGregor, Joanna, Craddock, Nick, Lyons, Ronan A, Owen, Michael J, Price, Vaughn, Thomson, Sue, Walters, James TR, Lloyd, Keith
Published 2012

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

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia†

by Hamshere, Marian L., Stergiakouli, Evangelia, Langley, Kate, Martin, Joanna, Holmans, Peter, Kent, Lindsey, Owen, Michael J., Gill, Michael, Thapar, Anita, O’Donovan, Mick, Craddock, Nick
Published 2013

Psychopathology and cognition in children with 22q11.2 deletion syndrome

by Niarchou, Maria, Zammit, Stanley, van Goozen, Stephanie H. M., Thapar, Anita, Tierling, Hayley M., Owen, Michael J., van den Bree, Marianne B. M.
Published 2014

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD

by Stergiakouli, Evangelia, Hamshere, Marian, Holmans, Peter, Langley, Kate, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel, Owen, Michael J., O'Donovan, Michael, Thapar, Anita
Published 2012