cached image

Michael J. Owen, PhD - Publications

Affiliations: 
Psychological Medicine, Neuropsychiatric Genetics and Genomics Cardiff University, Cardiff, Wales, United Kingdom 
Website:
http://conference.iepa.org.au/speakers/professor-michael-j-owen/

441 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Owen MJ, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7  0.76
2019 Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, ... ... Owen MJ, et al. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. PMID 31160808 DOI: 10.1038/S41588-019-0450-7  0.32
2019 Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Owen MJ, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2  0.32
2018 Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, ... ... Owen MJ, et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics. PMID 29483656 DOI: 10.1038/S41588-018-0059-2  0.32
2018 Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, ... ... Owen MJ, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry. 23: 162-163. PMID 29296025 DOI: 10.1038/Mp.2017.214  0.32
2017 Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Owen MJ, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916  0.76
2016 Legge SE, Hamshere ML, Ripke S, Pardinas AF, Goldstein JI, Rees E, Richards AL, Leonenko G, Jorskog LF, Chambert KD, Collier DA, Genovese G, Giegling I, Holmans P, ... ... Owen MJ, et al. Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Molecular Psychiatry. PMID 27400856 DOI: 10.1038/Mp.2016.97  0.76
2016 Legge SE, Hamshere M, Hayes RD, Downs J, O'Donovan MC, Owen MJ, Walters JT, MacCabe JH. Reasons for discontinuing clozapine: A cohort study of patients commencing treatment. Schizophrenia Research. PMID 27211516 DOI: 10.1016/J.Schres.2016.05.002  0.76
2016 Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, ... ... Owen MJ, et al. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. Plos Genetics. 12: e1005993. PMID 27153221 DOI: 10.1371/Journal.Pgen.1005993  0.76
2016 Fry AE, Rees E, Thompson R, Mantripragada K, Blake P, Jones G, Morgan S, Jose S, Mugalaasi H, Archer H, McCann E, Clarke A, Taylor C, Davies S, Gibbon F, ... ... Owen MJ, et al. Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. Bmc Medical Genetics. 17: 34. PMID 27113213 DOI: 10.1186/S12881-016-0294-2  0.76
2016 Jones HJ, Stergiakouli E, Tansey KE, Hubbard L, Heron J, Cannon M, Holmans P, Lewis G, Linden DE, Jones PB, Davey Smith G, O'Donovan MC, Owen MJ, Walters JT, Zammit S. Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population. Jama Psychiatry. PMID 26818099 DOI: 10.1001/Jamapsychiatry.2015.3058  0.76
2016 Owen MJ, Sawa A, Mortensen PB. Schizophrenia. Lancet (London, England). PMID 26777917 DOI: 10.1016/S0140-6736(15)01121-6  0.76
2016 Richards AL, Leonenko G, Walters JT, Kavanagh DH, Rees EG, Evans A, Chambert KD, Moran JL, Goldstein J, Neale BM, McCarroll SA, Pocklington AJ, Holmans PA, Owen MJ, O'Donovan MC. Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics. PMID 26740555 DOI: 10.1093/Hmg/Ddv620  0.76
2016 Harrison JR, Owen MJ. Alzheimer's disease: the amyloid hypothesis on trial. The British Journal of Psychiatry : the Journal of Mental Science. 208: 1-3. PMID 26729836 DOI: 10.1192/Bjp.Bp.115.167569  0.76
2015 Hubbard L, Tansey KE, Rai D, Jones P, Ripke S, Chambert KD, Moran JL, McCarroll SA, Linden DE, Owen MJ, O'Donovan MC, Walters JT, Zammit S. Evidence of Common Genetic Overlap Between Schizophrenia and Cognition. Schizophrenia Bulletin. PMID 26678674 DOI: 10.1093/Schbul/Sbv168  0.76
2015 Collishaw S, Hammerton G, Mahedy L, Sellers R, Owen MJ, Craddock N, Thapar AK, Harold GT, Rice F, Thapar A. Mental health resilience in the adolescent offspring of parents with depression: a prospective longitudinal study. The Lancet. Psychiatry. PMID 26654748 DOI: 10.1016/S2215-0366(15)00358-2  0.76
2015 Escott-Price V, Kirov G, Rees E, Isles AR, Owen MJ, O'Donovan MC. No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci. Plos One. 10: e0144172. PMID 26633303 DOI: 10.1371/Journal.Pone.0144172  0.76
2015 D'Angelo D, Lebon S, Chen Q, Martin-Brevet S, Snyder LG, Hippolyte L, Hanson E, Maillard AM, Faucett WA, Macé A, Pain A, Bernier R, Chawner SJ, David A, Andrieux J, ... ... Owen MJ, et al. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. Jama Psychiatry. 1-11. PMID 26629640 DOI: 10.1001/Jamapsychiatry.2015.2123  0.76
2015 Lancaster TM, Ihssen N, Brindley LM, Tansey KE, Mantripragada K, O'Donovan MC, Owen MJ, Linden DE. Associations between polygenic risk for schizophrenia and brain function during probabilistic learning in healthy individuals. Human Brain Mapping. PMID 26510167 DOI: 10.1002/Hbm.23044  0.76
2015 Hall J, Owen MJ. Psychiatric classification - a developmental perspective. The British Journal of Psychiatry : the Journal of Mental Science. 207: 281-2. PMID 26429678 DOI: 10.1192/Bjp.Bp.114.159996  0.76
2015 Niarchou M, Martin J, Thapar A, Owen MJ, van den Bree MB. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 730-8. PMID 26400629 DOI: 10.1002/Ajmg.B.32378  0.76
2015 Heyes S, Pratt WS, Rees E, Dahimene S, Ferron L, Owen MJ, Dolphin AC. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology. PMID 26386135 DOI: 10.1016/J.Pneurobio.2015.09.002  0.76
2015 Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, ... ... Owen MJ, et al. Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia. Translational Psychiatry. 5: e607. PMID 26196440 DOI: 10.1038/Tp.2015.99  0.76
2015 Klein M, van der Voet M, Harich B, van Hulzen KJ, Onnink AM, Hoogman M, Guadalupe T, Zwiers M, Groothuismink JM, Verberkt A, Nijhof B, Castells-Nobau A, Faraone SV, Buitelaar JK, Schenck A, et al. Converging evidence does not support GIT1 as an ADHD risk gene. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26061966 DOI: 10.1002/Ajmg.B.32327  0.76
2015 Hung CF, Breen G, Czamara D, Corre T, Wolf C, Kloiber S, Bergmann S, Craddock N, Gill M, Holsboer F, Jones L, Jones I, Korszun A, Kutalik Z, Lucae S, ... ... Owen MJ, et al. A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder. Bmc Medicine. 13: 86. PMID 25903154 DOI: 10.1186/S12916-015-0334-3  0.76
2015 Desikan RS, Schork AJ, Wang Y, Witoelar A, Sharma M, McEvoy LK, Holland D, Brewer JB, Chen CH, Thompson WK, Harold D, Williams J, Owen MJ, O'Donovan MC, Pericak-Vance MA, et al. Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Molecular Psychiatry. PMID 25687773 DOI: 10.1038/Mp.2015.6  0.76
2015 Kavanagh DH, Tansey KE, O'Donovan MC, Owen MJ. Schizophrenia genetics: emerging themes for a complex disorder. Molecular Psychiatry. 20: 72-6. PMID 25385368 DOI: 10.1038/Mp.2014.148  0.76
2015 Hall J, Trent S, Thomas KL, O'Donovan MC, Owen MJ. Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity. Biological Psychiatry. 77: 52-8. PMID 25152434 DOI: 10.1016/J.Biopsych.2014.07.011  0.76
2015 Rees E, O'Donovan MC, Owen MJ. Genetics of schizophrenia Current Opinion in Behavioral Sciences. 2: 8-14. DOI: 10.1016/J.Cobeha.2014.07.001  0.76
2014 Lancaster TM, Brindley LM, Tansey KE, Sims RC, Mantripragada K, Owen MJ, Williams J, Linden DE. Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 25496871 DOI: 10.1016/J.Jalz.2014.10.012  0.76
2014 Owen MJ. New approaches to psychiatric diagnostic classification. Neuron. 84: 564-71. PMID 25442935 DOI: 10.1016/J.Neuron.2014.10.028  0.76
2014 Proitsi P, Lupton MK, Velayudhan L, Newhouse S, Fogh I, Tsolaki M, Daniilidou M, Pritchard M, Kloszewska I, Soininen H, Mecocci P, Vellas B, Williams J, et al. Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis. Plos Medicine. 11: e1001713. PMID 25226301 DOI: 10.1371/Journal.Pmed.1001713  0.76
2014 Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine PE, Lynch B, Kirov G, O'Riordan S, ... ... Owen MJ, et al. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. Journal of Neurology. 261: 2296-304. PMID 25209853 DOI: 10.1007/S00415-014-7488-3  0.76
2014 Rees E, Walters JT, Owen MJ, Kirov G. Authors' reply. The British Journal of Psychiatry : the Journal of Mental Science. 205: 78. PMID 24986392 DOI: 10.1192/bjp.205.1.78  0.76
2014 Mullins N, Perroud N, Uher R, Butler AW, Cohen-Woods S, Rivera M, Malki K, Euesden J, Power RA, Tansey KE, Jones L, Jones I, Craddock N, Owen MJ, Korszun A, et al. Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 428-37. PMID 24964207 DOI: 10.1002/Ajmg.B.32247  0.76
2014 Martin J, Cooper M, Hamshere ML, Pocklington A, Scherer SW, Kent L, Gill M, Owen MJ, Williams N, O'Donovan MC, Thapar A, Holmans P. Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 761-70.e26. PMID 24954825 DOI: 10.1016/J.Jaac.2014.03.004  0.76
2014 Doherty JL, Owen MJ. Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. Genome Medicine. 6: 29. PMID 24944580 DOI: 10.1186/Gm546  0.76
2014 Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Owen MJ, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661  0.76
2014 Niarchou M, Zammit S, Escott-Price V, Owen MJ, van den Bree MB. Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 410-20. PMID 24862404 DOI: 10.1002/Ajmg.B.32245  0.76
2014 van Os J, Rutten BP, Myin-Germeys I, Delespaul P, Viechtbauer W, van Zelst C, Bruggeman R, Reininghaus U, Morgan C, Murray RM, Di Forti M, McGuire P, Valmaggia LR, Kempton MJ, ... ... Owen MJ, et al. Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin. 40: 729-36. PMID 24860087 DOI: 10.1093/Schbul/Sbu069  0.76
2014 Hung CF, Rivera M, Craddock N, Owen MJ, Gill M, Korszun A, Maier W, Mors O, Preisig M, Rice JP, Rietschel M, Jones L, Middleton L, Aitchison KJ, Davis OS, et al. Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study. The British Journal of Psychiatry : the Journal of Mental Science. 205: 24-8. PMID 24809401 DOI: 10.1192/Bjp.Bp.113.130419  0.76
2014 Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, ... ... Owen MJ, et al. Copy number variation in schizophrenia in Sweden. Molecular Psychiatry. 19: 762-73. PMID 24776740 DOI: 10.1038/Mp.2014.40  0.76
2014 Pocklington AJ, O'Donovan M, Owen MJ. The synapse in schizophrenia. The European Journal of Neuroscience. 39: 1059-67. PMID 24712986 DOI: 10.1111/Ejn.12489  0.76
2014 Doherty JL, Owen MJ. The Research Domain Criteria: moving the goalposts to change the game. The British Journal of Psychiatry : the Journal of Mental Science. 204: 171-3. PMID 24590970 DOI: 10.1192/Bjp.Bp.113.133330  0.76
2014 Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, et al. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. The American Journal of Psychiatry. 171: 627-39. PMID 24577245 DOI: 10.1176/Appi.Ajp.2013.13070864  0.76
2014 Cardno AG, Owen MJ. Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder. Schizophrenia Bulletin. 40: 504-15. PMID 24567502 DOI: 10.1093/Schbul/Sbu016  0.76
2014 Monks S, Niarchou M, Davies AR, Walters JT, Williams N, Owen MJ, van den Bree MB, Murphy KC. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Schizophrenia Research. 153: 231-6. PMID 24534796 DOI: 10.1016/J.Schres.2014.01.020  0.76
2014 Fromer M, Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S, Gormley P, Georgieva L, Rees E, Palta P, Ruderfer DM, Carrera N, Humphreys I, Johnson JS, Roussos P, Barker DD, ... ... Owen MJ, et al. De novo mutations in schizophrenia implicate synaptic networks. Nature. 506: 179-84. PMID 24463507 DOI: 10.1038/Nature12929  0.76
2014 Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G. Analysis of copy number variations at 15 schizophrenia-associated loci. The British Journal of Psychiatry : the Journal of Mental Science. 204: 108-14. PMID 24311552 DOI: 10.1192/Bjp.Bp.113.131052  0.76
2014 Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, ... ... Owen MJ, et al. Evidence that duplications of 22q11.2 protect against schizophrenia. Molecular Psychiatry. 19: 37-40. PMID 24217254 DOI: 10.1038/Mp.2013.156  0.76
2014 Ferentinos P, Rivera M, Ising M, Spain SL, Cohen-Woods S, Butler AW, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Mors O, et al. Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution. Journal of Affective Disorders. 155: 81-9. PMID 24215895 DOI: 10.1016/J.Jad.2013.10.027  0.76
2014 Zammit S, Hamshere M, Dwyer S, Georgiva L, Timpson N, Moskvina V, Richards A, Evans DM, Lewis G, Jones P, Owen MJ, O'Donovan MC. A population-based study of genetic variation and psychotic experiences in adolescents. Schizophrenia Bulletin. 40: 1254-62. PMID 24174267 DOI: 10.1093/Schbul/Sbt146  0.76
2014 Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, ... ... Owen MJ, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Human Molecular Genetics. 23: 1669-76. PMID 24163246 DOI: 10.1093/Hmg/Ddt540  0.76
2014 Niarchou M, Zammit S, van Goozen SH, Thapar A, Tierling HM, Owen MJ, van den Bree MB. Psychopathology and cognition in children with 22q11.2 deletion syndrome. The British Journal of Psychiatry : the Journal of Mental Science. 204: 46-54. PMID 24115343 DOI: 10.1192/Bjp.Bp.113.132324  0.76
2014 Kirov G, Rees E, Walters JT, Escott-Price V, Georgieva L, Richards AL, Chambert KD, Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ. The penetrance of copy number variations for schizophrenia and developmental delay. Biological Psychiatry. 75: 378-85. PMID 23992924 DOI: 10.1016/J.Biopsych.2013.07.022  0.76
2014 Mulle JG, Pulver AE, McGrath JA, Wolyniec PS, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, ... ... Owen MJ, et al. Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biological Psychiatry. 75: 371-7. PMID 23871472 DOI: 10.1016/J.Biopsych.2013.05.040  0.76
2014 Hamshere ML, Walters JTR, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, ... ... Owen MJ, et al. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC Nature. 508: 708-712.  0.76
2013 Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Owen MJ, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802  0.76
2013 Grozeva D, Kirov G, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N. Reduced burden of very large and rare CNVs in bipolar affective disorder. Bipolar Disorders. 15: 893-8. PMID 24127788 DOI: 10.1111/Bdi.12125  0.76
2013 Mars B, Harold GT, Elam KK, Sellers R, Owen MJ, Craddock N, Thapar AK, Rice F, Collishaw S, Thapar A. Specific parental depression symptoms as risk markers for new-onset depression in high-risk offspring. The Journal of Clinical Psychiatry. 74: 925-31. PMID 24107766 DOI: 10.4088/Jcp.12M08152  0.76
2013 Schosser A, Butler AW, Uher R, Ng MY, Cohen-Woods S, Craddock N, Owen MJ, Korszun A, Gill M, Rice J, Hauser J, Henigsberg N, Maier W, Mors O, Placentino A, et al. Genome-wide association study of co-occurring anxiety in major depression. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 14: 611-21. PMID 24047446 DOI: 10.3109/15622975.2013.782107  0.76
2013 Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, ... ... Owen MJ, ... ... Owen MJ, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics. 45: 1150-9. PMID 23974872 DOI: 10.1038/Ng.2742  0.76
2013 Moskvina V, Harold D, Russo G, Vedernikov A, Sharma M, Saad M, Holmans P, Bras JM, Bettella F, Keller MF, Nicolaou N, Simón-Sánchez J, Gibbs JR, Schulte C, Durr A, ... ... Owen MJ, et al. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. Jama Neurology. 70: 1268-76. PMID 23921447 DOI: 10.1001/Jamaneurol.2013.448  0.76
2013 Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, Moskvina V, Fernández G, Gill M, Corvin A, O'Donovan MC, ... ... Owen MJ, et al. The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up. The American Journal of Psychiatry. 170: 877-85. PMID 23903335 DOI: 10.1176/Appi.Ajp.2013.12020226  0.76
2013 Aberg KA, Liu Y, Bukszár J, McClay JL, Khachane AN, Andreassen OA, Blackwood D, Corvin A, Djurovic S, Gurling H, Ophoff R, Pato CN, Pato MT, Riley B, Webb T, ... ... Owen M, et al. A comprehensive family-based replication study of schizophrenia genes. Jama Psychiatry. 70: 573-81. PMID 23894747 DOI: 10.1001/Jamapsychiatry.2013.288  0.76
2013 Tandon R, Heckers S, Bustillo J, Barch DM, Gaebel W, Gur RE, Malaspina D, Owen MJ, Schultz S, Tsuang M, van Os J, Carpenter W. Catatonia in DSM-5. Schizophrenia Research. 150: 26-30. PMID 23806583 DOI: 10.1016/J.Schres.2013.04.034  0.76
2013 Tandon R, Gaebel W, Barch DM, Bustillo J, Gur RE, Heckers S, Malaspina D, Owen MJ, Schultz S, Tsuang M, Van Os J, Carpenter W. Definition and description of schizophrenia in the DSM-5. Schizophrenia Research. 150: 3-10. PMID 23800613 DOI: 10.1016/J.Schres.2013.05.028  0.76
2013 Tsuang MT, Van Os J, Tandon R, Barch DM, Bustillo J, Gaebel W, Gur RE, Heckers S, Malaspina D, Owen MJ, Schultz S, Carpenter W. Attenuated psychosis syndrome in DSM-5. Schizophrenia Research. 150: 31-5. PMID 23773295 DOI: 10.1016/J.Schres.2013.05.004  0.76
2013 van den Bree MB, Miller G, Mansell E, Thapar A, Flinter F, Owen MJ. The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS). European Journal of Medical Genetics. 56: 439-41. PMID 23707654 DOI: 10.1016/J.Ejmg.2013.05.001  0.76
2013 Malaspina D, Owen MJ, Heckers S, Tandon R, Bustillo J, Schultz S, Barch DM, Gaebel W, Gur RE, Tsuang M, Van Os J, Carpenter W. Schizoaffective Disorder in the DSM-5. Schizophrenia Research. 150: 21-5. PMID 23707642 DOI: 10.1016/J.Schres.2013.04.026  0.76
2013 Heckers S, Barch DM, Bustillo J, Gaebel W, Gur R, Malaspina D, Owen MJ, Schultz S, Tandon R, Tsuang M, Van Os J, Carpenter W. Structure of the psychotic disorders classification in DSM-5. Schizophrenia Research. 150: 11-4. PMID 23707641 DOI: 10.1016/J.Schres.2013.04.039  0.76
2013 Barch DM, Bustillo J, Gaebel W, Gur R, Heckers S, Malaspina D, Owen MJ, Schultz S, Tandon R, Tsuang M, Van Os J, Carpenter W. Logic and justification for dimensional assessment of symptoms and related clinical phenomena in psychosis: relevance to DSM-5. Schizophrenia Research. 150: 15-20. PMID 23706415 DOI: 10.1016/J.Schres.2013.04.027  0.76
2013 Hamshere ML, Stergiakouli E, Langley K, Martin J, Holmans P, Kent L, Owen MJ, Gill M, Thapar A, O'Donovan M, Craddock N. Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 203: 107-11. PMID 23703318 DOI: 10.1192/Bjp.Bp.112.117432  0.76
2013 Niarchou M, Zammit S, Walters J, Lewis G, Owen MJ, van den Bree MB. Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort. The American Journal of Psychiatry. 170: 550-7. PMID 23632836 DOI: 10.1176/Appi.Ajp.2012.12060792  0.76
2013 Power RA, Lecky-Thompson L, Fisher HL, Cohen-Woods S, Hosang GM, Uher R, Powell-Smith G, Keers R, Tropeano M, Korszun A, Jones L, Jones I, Owen MJ, Craddock N, Craig IW, et al. The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression. Journal of Psychiatric Research. 47: 1032-5. PMID 23618376 DOI: 10.1016/J.Jpsychires.2013.03.017  0.76
2013 Hamshere ML, Langley K, Martin J, Agha SS, Stergiakouli E, Anney RJ, Buitelaar J, Faraone SV, Lesch KP, Neale BM, Franke B, Sonuga-Barke E, Asherson P, Merwood A, Kuntsi J, ... ... Owen MJ, et al. High loading of polygenic risk for ADHD in children with comorbid aggression. The American Journal of Psychiatry. 170: 909-16. PMID 23599091 DOI: 10.1176/Appi.Ajp.2013.12081129  0.76
2013 Kavanagh DH, Dwyer S, O'Donovan MC, Owen MJ. The ENCODE project: implications for psychiatric genetics. Molecular Psychiatry. 18: 540-2. PMID 23478746 DOI: 10.1038/Mp.2013.13  0.76
2013 Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Jarlbrzkowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, ... ... Owen MJ, et al. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics. 92: 439-47. PMID 23453669 DOI: 10.1016/J.Ajhg.2013.03.005  0.76
2013 Majounie E, Cross W, Newsway V, Dillman A, Vandrovcova J, Morris CM, Nalls MA, Ferrucci L, Owen MJ, O'Donovan MC, Cookson MR, Singleton AB, de Silva R, Morris HR. Variation in tau isoform expression in different brain regions and disease states. Neurobiology of Aging. 34: 1922.e7-1922.e12. PMID 23428180 DOI: 10.1016/J.Neurobiolaging.2013.01.017  0.76
2013 Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Van Cauwenberghe C, Kolen KV, Geller F, Sottejeau Y, Harold D, Dourlen P, Grenier-Boley B, Kamatani Y, Delepine B, Demiautte F, Zelenika D, ... ... Owen M, et al. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Molecular Psychiatry. 18: 1225-34. PMID 23399914 DOI: 10.1038/Mp.2013.1  0.76
2013 Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, ... ... Owen MJ, et al. SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain : a Journal of Neurology. 136: 294-303. PMID 23365103 DOI: 10.1093/Brain/Aws308  0.76
2013 Williams HJ, Monks S, Murphy KC, Kirov G, O'Donovan MC, Owen MJ. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 177-82. PMID 23335482 DOI: 10.1002/Ajmg.B.32129  0.76
2013 Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, ... ... Owen MJ, et al. Implication of a rare deletion at distal 16p11.2 in schizophrenia. Jama Psychiatry. 70: 253-60. PMID 23325106 DOI: 10.1001/2013.Jamapsychiatry.71  0.76
2013 Ruderfer DM, Chambert K, Moran J, Talkowski M, Chen ES, Gigek C, Gusella JF, Blackwood DH, Corvin A, Gurling HM, Hultman CM, Kirov G, Magnusson P, O'Donovan MC, Owen MJ, et al. Mosaic copy number variation in schizophrenia. European Journal of Human Genetics : Ejhg. 21: 1007-11. PMID 23321615 DOI: 10.1038/Ejhg.2012.287  0.76
2013 Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, et al. Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. Genes, Brain, and Behavior. 12: 203-9. PMID 23320435 DOI: 10.1111/Gbb.12016  0.76
2013 Power RA, Wingenbach T, Cohen-Woods S, Uher R, Ng MY, Butler AW, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, et al. Estimating the heritability of reporting stressful life events captured by common genetic variants. Psychological Medicine. 43: 1965-71. PMID 23237013 DOI: 10.1017/S0033291712002589  0.76
2013 Kim Y, Ripke S, Kirov G, Sklar P, Purcell SM, Owen MJ, O'Donovan MC, Sullivan PF. Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophrenia Research. 143: 11-7. PMID 23177929 DOI: 10.1016/J.Schres.2012.11.002  0.76
2013 Chapman J, Rees E, Harold D, Ivanov D, Gerrish A, Sims R, Hollingworth P, Stretton A, Holmans P, Owen MJ, O'Donovan MC, Williams J, Kirov G. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics. 22: 816-24. PMID 23148125 DOI: 10.1093/Hmg/Dds476  0.76
2013 Green EK, Hamshere M, Forty L, Gordon-Smith K, Fraser C, Russell E, Grozeva D, Kirov G, Holmans P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, Jones L, et al. Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Molecular Psychiatry. 18: 1302-7. PMID 23070075 DOI: 10.1038/mp.2012.142  0.76
2013 Sellers R, Collishaw S, Rice F, Thapar AK, Potter R, Mars B, Harold GT, Smith DJ, Owen MJ, Craddock N, Thapar A. Risk of psychopathology in adolescent offspring of mothers with psychopathology and recurrent depression. The British Journal of Psychiatry : the Journal of Mental Science. 202: 108-14. PMID 23060622 DOI: 10.1192/Bjp.Bp.111.104984  0.76
2013 Fisher HL, Cohen-Woods S, Hosang GM, Korszun A, Owen M, Craddock N, Craig IW, Farmer AE, McGuffin P, Uher R. Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder. Journal of Affective Disorders. 145: 136-41. PMID 22840631 DOI: 10.1016/J.Jad.2012.05.032  0.76
2013 Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill FA, O'Neill T, Kendler KS, Sklar P, ... ... Owen MJ, et al. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry. 18: 708-12. PMID 22614287 DOI: 10.1038/Mp.2012.67  0.76
2013 Green EK, Grozeva D, Forty L, Gordon-Smith K, Russell E, Farmer A, Hamshere M, Jones IR, Jones L, McGuffin P, Moran JL, Purcell S, Sklar P, Owen MJ, O'Donovan MC, et al. Association at SYNE1 in both bipolar disorder and recurrent major depression. Molecular Psychiatry. 18: 614-7. PMID 22565781 DOI: 10.1038/Mp.2012.48  0.76
2013 Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, ... ... Owen M, et al. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry. 18: 461-70. PMID 22430674 DOI: 10.1038/Mp.2012.14  0.76
2013 Rucker JJ, Breen G, Pinto D, Pedroso I, Lewis CM, Cohen-Woods S, Uher R, Schosser A, Rivera M, Aitchison KJ, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, et al. Genome-wide association analysis of copy number variation in recurrent depressive disorder. Molecular Psychiatry. 18: 183-9. PMID 22042228 DOI: 10.1038/Mp.2011.144  0.76
2013 Williams HJ, O'Donovan MC, Craddock N, Owen MJ. Schizophrenia and Bipolar Disorder Genomic and Personalized Medicine. 2: 1051-1058. DOI: 10.1016/B978-0-12-382227-7.00088-4  0.76
2012 Fromer M, Moran JL, Chambert K, Banks E, Bergen SE, Ruderfer DM, Handsaker RE, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, Sullivan PF, Hultman CM, Sklar P, Purcell SM. Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth. American Journal of Human Genetics. 91: 597-607. PMID 23040492 DOI: 10.1016/J.Ajhg.2012.08.005  0.76
2012 Owen MJ. Implications of genetic findings for understanding schizophrenia. Schizophrenia Bulletin. 38: 904-7. PMID 22987847 DOI: 10.1093/Schbul/Sbs103  0.76
2012 Williams HJ, Georgieva L, Dwyer S, Kirov G, Owen MJ, O'Donovan MC. Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample. Schizophrenia Research. 141: 274-6. PMID 22986046 DOI: 10.1016/J.Schres.2012.08.024  0.76
2012 Power RA, Keers R, Ng MY, Butler AW, Uher R, Cohen-Woods S, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Hauser J, et al. Dissecting the genetic heterogeneity of depression through age at onset. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 859-68. PMID 22915352 DOI: 10.1002/Ajmg.B.32093  0.76
2012 Thapar A, Heron J, Jones RB, Owen MJ, Lewis G, Zammit S. Trajectories of change in self-reported psychotic-like experiences in childhood and adolescence. Schizophrenia Research. 140: 104-9. PMID 22789670 DOI: 10.1016/J.Schres.2012.06.024  0.76
2012 Fowler T, Zammit S, Owen MJ, Rasmussen F. A population-based study of shared genetic variation between premorbid IQ and psychosis among male twin pairs and sibling pairs from Sweden. Archives of General Psychiatry. 69: 460-6. PMID 22566578 DOI: 10.1001/Archgenpsychiatry.2011.1370  0.76
2012 HÃ¥vik B, Degenhardt FA, Johansson S, Fernandes CP, Hinney A, Scherag A, Lybæk H, Djurovic S, Christoforou A, Ersland KM, Giddaluru S, O'Donovan MC, Owen MJ, Craddock N, Mühleisen TW, et al. DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. Plos One. 7: e35424. PMID 22539971 DOI: 10.1371/Journal.Pone.0035424  0.76
2012 Owen MJ. Intellectual disability and major psychiatric disorders: a continuum of neurodevelopmental causality. The British Journal of Psychiatry : the Journal of Mental Science. 200: 268-9. PMID 22474230 DOI: 10.1192/Bjp.Bp.111.105551  0.76
2012 Rees E, Kirov G, O'Donovan MC, Owen MJ. De novo mutation in schizophrenia. Schizophrenia Bulletin. 38: 377-81. PMID 22451492 DOI: 10.1093/Schbul/Sbs047  0.76
2012 Hudson G, Sims R, Harold D, Chapman J, Hollingworth P, Gerrish A, Russo G, Hamshere M, Moskvina V, Jones N, Thomas C, Stretton A, Holmans PA, O'Donovan MC, Owen MJ, et al. No consistent evidence for association between mtDNA variants and Alzheimer disease. Neurology. 78: 1038-42. PMID 22442439 DOI: 10.1212/WNL.0b013e31824e8f1d  0.76
2012 Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. The American Journal of Psychiatry. 169: 186-94. PMID 22420046 DOI: 10.1176/Appi.Ajp.2011.11040551  0.76
2012 Economou A, Grey M, McGregor J, Craddock N, Lyons RA, Owen MJ, Price V, Thomson S, Walters JT, Lloyd K. The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder. Bmc Research Notes. 5: 95. PMID 22333117 DOI: 10.1186/1756-0500-5-95  0.76
2012 Moskvina V, Schmidt KM, Vedernikov A, Owen MJ, Craddock N, Holmans P, O'Donovan MC. Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. European Journal of Human Genetics : Ejhg. 20: 890-6. PMID 22317971 DOI: 10.1038/Ejhg.2012.8  0.76
2012 Baig S, Palmer LE, Owen MJ, Williams J, Kehoe PG, Love S. Clusterin mRNA and protein in Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 337-44. PMID 22232000 DOI: 10.3233/Jad-2011-110473  0.76
2012 Grozeva D, Conrad DF, Barnes CP, Hurles M, Owen MJ, O'Donovan MC, Craddock N, Kirov G. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophrenia Research. 135: 1-7. PMID 22130109 DOI: 10.1016/J.Schres.2011.11.004  0.76
2012 Kirov G, Pocklington AJ, Holmans P, Ivanov D, Ikeda M, Ruderfer D, Moran J, Chambert K, Toncheva D, Georgieva L, Grozeva D, Fjodorova M, Wollerton R, Rees E, Nikolov I, ... ... Owen MJ, et al. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry. 17: 142-53. PMID 22083728 DOI: 10.1038/Mp.2011.154  0.76
2012 Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, ... ... Owen MJ, et al. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 377-87. PMID 22027014 DOI: 10.3233/Jad-2011-110824  0.76
2012 Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, ... ... Owen MJ, et al. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry. 17: 1316-27. PMID 22005930 DOI: 10.1016/J.Jalz.2011.05.516  0.76
2012 Fisher HL, Cohen-Woods S, Hosang GM, Uher R, Powell-Smith G, Keers R, Tropeano M, Korszun A, Jones L, Jones I, Owen M, Craddock N, Craig IW, Farmer AE, McGuffin P. Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression. Journal of Affective Disorders. 136: 189-93. PMID 21982504 DOI: 10.1016/J.Jad.2011.09.016  0.76
2012 Doherty JL, O'Donovan MC, Owen MJ. Recent genomic advances in schizophrenia. Clinical Genetics. 81: 103-9. PMID 21895634 DOI: 10.1111/J.1399-0004.2011.01773.X  0.76
2012 Rietschel M, Mattheisen M, Degenhardt F, Mühleisen TW, Kirsch P, Esslinger C, Herms S, Demontis D, Steffens M, Strohmaier J, Haenisch B, Breuer R, Czerski PM, Giegling I, ... ... Owen MJ, et al. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Molecular Psychiatry. 17: 906-17. PMID 21747397 DOI: 10.1038/Mp.2011.80  0.76
2012 Rivera M, Cohen-Woods S, Kapur K, Breen G, Ng MY, Butler AW, Craddock N, Gill M, Korszun A, Maier W, Mors O, Owen MJ, Preisig M, Bergmann S, Tozzi F, et al. Depressive disorder moderates the effect of the FTO gene on body mass index. Molecular Psychiatry. 17: 604-11. PMID 21502950 DOI: 10.1038/Mp.2011.45  0.76
2012 Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR, Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry. 17: 193-201. PMID 21339752 DOI: 10.1038/Mp.2011.11  0.76
2012 Proitsi P, Lupton MK, Reeves SJ, Hamilton G, Archer N, Martin BM, Iyegbe C, Hollingworth P, Lawlor B, Gill M, Brayne C, Rubinsztein DC, Owen MJ, Williams J, Lovestone S, et al. Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia. Neurobiology of Aging. 33: 791-803. PMID 20685009 DOI: 10.1016/J.Neurobiolaging.2010.06.011  0.76
2011 Langley K, Martin J, Agha SS, Davies C, Stergiakouli E, Holmans P, Williams N, Owen M, O'Donovan M, Thapar A. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. The British Journal of Psychiatry : the Journal of Mental Science. 199: 398-403. PMID 22045946 DOI: 10.1192/Bjp.Bp.111.092130  0.76
2011 Hamshere ML, O'Donovan MC, Jones IR, Jones L, Kirov G, Green EK, Moskvina V, Grozeva D, Bass N, McQuillin A, Gurling H, St Clair D, Young AH, Ferrier IN, Farmer A, ... ... Owen MJ, et al. Polygenic dissection of the bipolar phenotype. The British Journal of Psychiatry : the Journal of Mental Science. 198: 284-8. PMID 21972277 DOI: 10.1192/Bjp.Bp.110.087866  0.76
2011 Hamshere ML, Holmans PA, McCarthy GM, Jones LA, Murphy KC, Sanders RD, Gray MY, Zammit S, Williams NM, Norton N, Williams HJ, McGuffin P, O'Donovan MC, Craddock N, Owen MJ, et al. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 929-40. PMID 21960518 DOI: 10.1002/Ajmg.B.31240  0.76
2011 Zammit S, Owen MJ, Evans J, Heron J, Lewis G. Cannabis, COMT and psychotic experiences. The British Journal of Psychiatry : the Journal of Mental Science. 199: 380-5. PMID 21947654 DOI: 10.1192/Bjp.Bp.111.091421  0.76
2011 Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, Chapman J, Jones N, Abraham R, Ivanov D, Pahwa JS, Moskvina V, Dowzell K, Thomas C, Stretton A, Lovestone S, ... ... Owen MJ, et al. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 764-71. PMID 21812096 DOI: 10.1002/Ajmg.B.31216  0.76
2011 Steinberg S, de Jong S, Andreassen OA, Werge T, Børglum AD, Mors O, Mortensen PB, Gustafsson O, Costas J, Pietiläinen OP, Demontis D, Papiol S, Huttenlocher J, Mattheisen M, ... ... Owen MJ, et al. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics. 20: 4076-81. PMID 21791550 DOI: 10.1093/Hmg/Ddr325  0.76
2011 Schosser A, Butler AW, Ising M, Perroud N, Uher R, Ng MY, Cohen-Woods S, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, et al. Genomewide association scan of suicidal thoughts and behaviour in major depression. Plos One. 6: e20690. PMID 21750702 DOI: 10.1371/Journal.Pone.0020690  0.76
2011 Peall KJ, Waite AJ, Blake DJ, Owen MJ, Morris HR. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 1939-42. PMID 21713999 DOI: 10.1002/Mds.23791  0.76
2011 Samaan Z, Gaysina D, Cohen-Woods S, Craddock N, Jones L, Korszun A, Owen M, Mente A, McGuffin P, Farmer A. Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis. Bmc Neurology. 11: 66. PMID 21635773 DOI: 10.1186/1471-2377-11-66  0.76
2011 Schosser A, Gaysina D, Cohen-Woods S, Domenici E, Perry J, Tozzi F, Korszun A, Gunasinghe C, Gray J, Jones L, Binder EB, Holsboer F, Craddock N, Owen MJ, Craig IW, et al. A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 640-50. PMID 21630437 DOI: 10.1002/Ajmg.B.31204  0.76
2011 Boot E, Booij J, Zinkstok JR, Baas F, Swillen A, Owen MJ, Murphy DG, Murphy KC, Linszen DH, Van Amelsvoort TA. COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome. Synapse (New York, N.Y.). 65: 967-70. PMID 21465565 DOI: 10.1002/Syn.20932  0.76
2011 Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, ... ... Owen MJ, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics. 43: 429-35. PMID 21460840 DOI: 10.1038/Ng.803  0.76
2011 Green EK, Grozeva D, Sims R, Raybould R, Forty L, Gordon-Smith K, Russell E, St Clair D, Young AH, Ferrier IN, Kirov G, Jones I, Jones L, Owen MJ, O'Donovan MC, et al. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 490-2. PMID 21445958 DOI: 10.1002/ajmg.b.31187  0.76
2011 Owen MJ, O'Donovan MC, Thapar A, Craddock N. Neurodevelopmental hypothesis of schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 198: 173-5. PMID 21357874 DOI: 10.1192/Bjp.Bp.110.084384  0.76
2011 Cichon S, Mühleisen TW, Degenhardt FA, Mattheisen M, Miró X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Breuer R, ... ... Owen MJ, et al. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics. 88: 372-81. PMID 21353194 DOI: 10.1016/J.Ajhg.2011.01.017  0.76
2011 Belbin O, Brown K, Shi H, Medway C, Abraham R, Passmore P, Mann D, Smith AD, Holmes C, McGuinness B, Craig D, Warden D, Heun R, Kölsch H, Love S, ... ... Owen MJ, et al. A multi-center study of ACE and the risk of late-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 24: 587-97. PMID 21297258 DOI: 10.3233/Jad-2011-101914  0.76
2011 Stergiakouli E, Langley K, Williams H, Walters J, Williams NM, Suren S, Giegling I, Wilkinson LS, Owen MJ, O'Donovan MC, Rujescu D, Thapar A, Davies W. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes, Brain, and Behavior. 10: 334-44. PMID 21255266 DOI: 10.1111/J.1601-183X.2010.00672.X  0.76
2011 Zuliani R, Moorhead TW, Bastin ME, Johnstone EC, Lawrie SM, Brambilla P, O'Donovan MC, Owen MJ, Hall J, McIntosh AM. Genetic variants in the ErbB4 gene are associated with white matter integrity. Psychiatry Research. 191: 133-7. PMID 21232925 DOI: 10.1016/J.Pscychresns.2010.11.001  0.76
2011 Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, ... ... Owen M, et al. Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Archives of Neurology. 68: 99-106. PMID 21220680 DOI: 10.1001/Archneurol.2010.346  0.76
2011 Williams HJ, Craddock N, Russo G, Hamshere ML, Moskvina V, Dwyer S, Smith RL, Green E, Grozeva D, Holmans P, Owen MJ, O'Donovan MC. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics. 20: 387-91. PMID 21037240 DOI: 10.1093/Hmg/Ddq471  0.32
2011 Hollingworth P, Harold D, Jones L, Owen MJ, Williams J. Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry. 26: 793-802. PMID 20957767 DOI: 10.1002/Gps.2628  0.32
2011 Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, et al. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 16: 1117-29. PMID 20838396 DOI: 10.1038/Mp.2010.96  0.76
2011 Ikeda M, Aleksic B, Kinoshita Y, Okochi T, Kawashima K, Kushima I, Ito Y, Nakamura Y, Kishi T, Okumura T, Fukuo Y, Williams HJ, Hamshere ML, Ivanov D, Inada T, ... ... Owen MJ, et al. Genome-wide association study of schizophrenia in a Japanese population. Biological Psychiatry. 69: 472-8. PMID 20832056 DOI: 10.1016/J.Biopsych.2010.07.010  0.76
2011 Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, ... ... Owen MJ, et al. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry. 16: 429-41. PMID 20368704 DOI: 10.1038/Mp.2010.36  0.76
2011 Liu Y, Blackwood DH, Caesar S, de Geus EJ, Farmer A, Ferreira MA, Ferrier IN, Fraser C, Gordon-Smith K, Green EK, Grozeva D, Gurling HM, Hamshere ML, Heutink P, Holmans PA, ... ... Owen MJ, et al. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Molecular Psychiatry. 16: 2-4. PMID 20351715 DOI: 10.1038/Mp.2009.107  0.76
2011 Proitsi P, Hamilton G, Tsolaki M, Lupton M, Daniilidou M, Hollingworth P, Archer N, Foy C, Stylios F, McGuinness B, Todd S, Lawlor B, Gill M, Brayne C, Rubinsztein DC, ... Owen M, et al. A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD). Neurobiology of Aging. 32: 434-42. PMID 19386383 DOI: 10.1016/J.Neurobiolaging.2009.03.005  0.76
2011 Cichon S, Mühleisen TW, Degenhardt FA, Mattheisen M, Miró X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Breuer R, ... ... Owen MJ, et al. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder (The American Journal of Human Genetics (2011) 88, (372-381)) American Journal of Human Genetics. 88: 396. DOI: 10.1016/J.Ajhg.2011.03.001  0.76
2010 Langley K, Heron J, O'Donovan MC, Owen MJ, Thapar A. Genotype link with extreme antisocial behavior: the contribution of cognitive pathways. Archives of General Psychiatry. 67: 1317-23. PMID 21135332 DOI: 10.1001/Archgenpsychiatry.2010.163  0.76
2010 Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, ... ... Owen MJ, et al. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. Plos One. 5: e13950. PMID 21085570 DOI: 10.1371/Journal.Pone.0013950  0.76
2010 Talkowski ME, McCann KL, Chen M, McClain L, Bamne M, Wood J, Chowdari KV, Watson A, Prasad KM, Kirov G, Georgieva L, Toncheva D, Mansour H, Lewis DA, Owen M, et al. Fine-mapping reveals novel alternative splicing of the dopamine transporter. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1434-47. PMID 20957647 DOI: 10.1002/Ajmg.B.31125  0.76
2010 Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K, Magnusson P, Gudmundsson OO, Gustafsson O, Holmans P, Owen MJ, O'Donovan M, Thapar A. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet. 376: 1401-8. PMID 20888040 DOI: 10.1016/S0140-6736(10)61109-9  0.76
2010 Butler AW, Breen G, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton LT, Mors O, Owen MJ, Perry J, Preisig M, Rice JP, Rietschel M, Jones L, et al. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1465-73. PMID 20886545 DOI: 10.1002/Ajmg.B.31127  0.76
2010 Cruchaga C, Kauwe JS, Mayo K, Spiegel N, Bertelsen S, Nowotny P, Shah AR, Abraham R, Hollingworth P, Harold D, Owen MM, Williams J, Lovestone S, Peskind ER, Li G, et al. SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease. Plos Genetics. 6: e1001101. PMID 20862329 DOI: 10.1371/Journal.Pgen.1001101  0.76
2010 Baig S, Joseph SA, Tayler H, Abraham R, Owen MJ, Williams J, Kehoe PG, Love S. Distribution and expression of picalm in Alzheimer disease. Journal of Neuropathology and Experimental Neurology. 69: 1071-7. PMID 20838239 DOI: 10.1097/Nen.0B013E3181F52E01  0.76
2010 Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schäfer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, ... ... Owen M, et al. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 884-97. PMID 20732625 DOI: 10.1016/J.Jaac.2010.06.008  0.76
2010 Zammit S, Owen MJ, Lewis G. Misconceptions about gene-environment interactions in psychiatry. Evidence-Based Mental Health. 13: 65-8. PMID 20682811 DOI: 10.1136/Ebmh.13.3.65  0.76
2010 Walters JT, Corvin A, Owen MJ, Williams H, Dragovic M, Quinn EM, Judge R, Smith DJ, Norton N, Giegling I, Hartmann AM, Möller HJ, Muglia P, Moskvina V, Dwyer S, et al. Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Archives of General Psychiatry. 67: 692-700. PMID 20603450 DOI: 10.1001/Archgenpsychiatry.2010.81  0.76
2010 Green EK, Grozeva D, Moskvina V, Hamshere ML, Jones IR, Jones L, Forty L, Caesar S, Gordon-Smith K, Fraser C, Russell E, St Clair D, Young AH, Ferrier N, Farmer A, ... ... Owen MJ, et al. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1347-9. PMID 20583128 DOI: 10.1002/Ajmg.B.31108  0.76
2010 Cohen-Woods S, Craig I, Gaysina D, Gray J, Gunasinghe C, Craddock N, Elkin A, Jones L, Kennedy J, King N, Korszun A, Knight J, Owen M, Parikh S, Strauss J, et al. The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1298-304. PMID 20552676 DOI: 10.1002/Ajmg.B.31101  0.76
2010 Lewis CM, Ng MY, Butler AW, Cohen-Woods S, Uher R, Pirlo K, Weale ME, Schosser A, Paredes UM, Rivera M, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, et al. Genome-wide association study of major recurrent depression in the U.K. population. The American Journal of Psychiatry. 167: 949-57. PMID 20516156 DOI: 10.1176/Appi.Ajp.2010.09091380  0.76
2010 Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT, ... ... Owen MJ, et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. Jama. 303: 1832-40. PMID 20460622 DOI: 10.1001/Jama.2010.574  0.76
2010 Blake DJ, Forrest M, Chapman RM, Tinsley CL, O'Donovan MC, Owen MJ. TCF4, schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin. 36: 443-7. PMID 20421335 DOI: 10.1093/Schbul/Sbq035  0.76
2010 Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N, et al. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. Archives of General Psychiatry. 67: 318-27. PMID 20368508 DOI: 10.1001/Archgenpsychiatry.2010.25  0.76
2010 Langley K, Fowler T, Ford T, Thapar AK, van den Bree M, Harold G, Owen MJ, O'Donovan MC, Thapar A. Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder. The British Journal of Psychiatry : the Journal of Mental Science. 196: 235-40. PMID 20194547 DOI: 10.1192/Bjp.Bp.109.066274  0.76
2010 Ingason A, Giegling I, Cichon S, Hansen T, Rasmussen HB, Nielsen J, Jürgens G, Muglia P, Hartmann AM, Strengman E, Vasilescu C, Mühleisen TW, Djurovic S, Melle I, Lerer B, ... ... Owen MJ, et al. A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Human Molecular Genetics. 19: 1379-86. PMID 20071346 DOI: 10.1093/Hmg/Ddq009  0.76
2010 Kauwe JS, Bertelsen S, Mayo K, Cruchaga C, Abraham R, Hollingworth P, Harold D, Owen MJ, Williams J, Lovestone S, Morris JC, Goate AM. Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 955-9. PMID 20029940 DOI: 10.1002/Ajmg.B.31053  0.76
2010 Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N. Copy number variation in schizophrenia in the Japanese population. Biological Psychiatry. 67: 283-6. PMID 19880096 DOI: 10.1016/J.Biopsych.2009.08.034  0.76
2010 Dwyer S, Carroll L, Mantripragada KK, Owen MJ, O'Donovan MC, Williams NM. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 766-74. PMID 19859905 DOI: 10.1002/Ajmg.B.31045  0.76
2010 Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, ... ... Owen MJ, et al. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry. 15: 1101-11. PMID 19786960 DOI: 10.1038/Mp.2009.96  0.76
2010 Green EK, Grozeva D, Jones I, Jones L, Kirov G, Caesar S, Gordon-Smith K, Fraser C, Forty L, Russell E, Hamshere ML, Moskvina V, Nikolov I, Farmer A, McGuffin P, ... ... Owen MJ, et al. The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia. Molecular Psychiatry. 15: 1016-22. PMID 19621016 DOI: 10.1038/Mp.2009.49  0.76
2010 Lupton MK, Stahl D, Archer N, Foy C, Poppe M, Lovestone S, Hollingworth P, Williams J, Owen MJ, Dowzell K, Abraham R, Sims R, Brayne C, Rubinsztein D, Gill M, et al. Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. International Journal of Geriatric Psychiatry. 25: 30-6. PMID 19459177 DOI: 10.1002/Gps.2294  0.76
2010 Schosser A, Cohen-Woods S, Gaysina D, Chow PC, Martucci L, Farmer A, Korszun A, Gunashinghe C, Gray J, Jones L, Craddock N, Owen MJ, Craig IW, McGuffin P. NRG1 gene in recurrent major depression: no association in a large-scale case-control association study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 141-7. PMID 19367584 DOI: 10.1002/Ajmg.B.30965  0.76
2010 Schosser A, Gaysina D, Cohen-Woods S, Chow PC, Martucci L, Craddock N, Farmer A, Korszun A, Gunasinghe C, Gray J, Jones L, Tozzi F, Perry J, Muglia P, Owen MJ, et al. Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies. Molecular Psychiatry. 15: 844-9. PMID 19255581 DOI: 10.1038/Mp.2009.21  0.76
2010 Craddock N, Jones L, Jones IR, Kirov G, Green EK, Grozeva D, Moskvina V, Nikolov I, Hamshere ML, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Norton N, ... ... Owen MJ, et al. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype. Molecular Psychiatry. 15: 146-53. PMID 19078961 DOI: 10.1038/Mp.2008.66  0.76
2010 Sims R, Harold D, Gerrish A, Hollingworth P, Abraham R, Donovan MO, Owen M, Williams J. Mitochondrial genome-wide association study of Alzheimer's disease Alzheimers & Dementia. 6: 550. DOI: 10.1016/J.Jalz.2013.05.1070  0.32
2010 Cruchaga C, Kauwe JS, Mayo K, Bertelsen S, Nowotny P, Shah AR, Abraham R, Hollingworth P, Harold D, Owen MJ, Williams J, Lovestone S, Morris JC, Fagan AM, Holtzman DM, et al. SNPs associated with CSF tau levels modify rate of progression in Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.612  0.76
2010 Reitz C, Cheng R, Rogaeva E, Lee J, Tokuhiro S, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Kamboh IM, Prince J, Maier W, Riemenschneider M, Owen M, et al. Meta-analysis of the association between SORL1 variants and Alzheimer's disease Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.351  0.32
2009 Azuma R, Daly EM, Campbell LE, Stevens AF, Deeley Q, Giampietro V, Brammer MJ, Glaser B, Ambery FZ, Morris RG, Williams SC, Owen MJ, Murphy DG, Murphy KC. Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study. Journal of Neurodevelopmental Disorders. 1: 46-60. PMID 21547621 DOI: 10.1007/S11689-009-9008-9  0.76
2009 Carroll LS, Owen MJ. Genetic overlap between autism, schizophrenia and bipolar disorder. Genome Medicine. 1: 102. PMID 19886976 DOI: 10.1186/Gm102  0.76
2009 McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, ... ... Owen MJ, et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics. 41: 1223-7. PMID 19855392 DOI: 10.1038/Ng.474  0.76
2009 Fowler T, Langley K, Rice F, van den Bree MB, Ross K, Wilkinson LS, Owen MJ, O'Donovan MC, Thapar A. Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatric Genetics. 19: 312-9. PMID 19829167 DOI: 10.1097/Ypg.0B013E3283328Df4  0.76
2009 Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Owen MJ, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nature Genetics. 41: 1088-93. PMID 19734902 DOI: 10.1038/Ng.440  0.76
2009 Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Ruderfer DM, McQuillin A, Morris DW, Oĝdushlaine CT, Corvin A, Holmans PA, Oĝdonovan MC, MacGregor S, Gurling H, ... ... Owen MJ, et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature. 460: 748-752. PMID 19571811 DOI: 10.1038/Nature08185  0.76
2009 Hamshere ML, Green EK, Jones IR, Jones L, Moskvina V, Kirov G, Grozeva D, Nikolov I, Vukcevic D, Caesar S, Gordon-Smith K, Fraser C, Russell E, Breen G, St Clair D, ... ... Owen MJ, et al. Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. The British Journal of Psychiatry : the Journal of Mental Science. 195: 23-9. PMID 19567891 DOI: 10.1192/Bjp.Bp.108.061424  0.76
2009 Sims R, Hollingworth P, Moskvina V, Dowzell K, O'Donovan MC, Powell J, Lovestone S, Brayne C, Rubinsztein D, Owen MJ, Williams J, Abraham R. Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease. Neuroscience Letters. 461: 54-9. PMID 19477230 DOI: 10.1016/J.Neulet.2009.05.051  0.76
2009 Metlapally R, Li YJ, Tran-Viet KN, Abbott D, Czaja GR, Malecaze F, Calvas P, Mackey D, Rosenberg T, Paget S, Zayats T, Owen MJ, Guggenheim JA, Young TL. COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Investigative Ophthalmology & Visual Science. 50: 4080-6. PMID 19387081 DOI: 10.1167/Iovs.08-3346  0.76
2009 Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T, Riley B, Paunio T, Pulver AE, Irmansyah, Holmans PA, Escamilla M, Wildenauer DB, Williams NM, Laurent C, ... ... Owen MJ, et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry. 14: 774-85. PMID 19349958 DOI: 10.1038/Mp.2008.135  0.76
2009 Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF. Genomewide association studies: history, rationale, and prospects for psychiatric disorders. The American Journal of Psychiatry. 166: 540-56. PMID 19339359 DOI: 10.1176/Appi.Ajp.2008.08091354  0.76
2009 Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, et al. An international collaborative family-based whole-genome linkage scan for high-grade myopia. Investigative Ophthalmology & Visual Science. 50: 3116-27. PMID 19324860 DOI: 10.1167/Iovs.08-2781  0.76
2009 Abraham R, Sims R, Carroll L, Hollingworth P, O'Donovan MC, Williams J, Owen MJ. An association study of common variation at the MAPT locus with late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1152-5. PMID 19308965 DOI: 10.1002/Ajmg.B.30951  0.32
2009 Ball HA, Samaan Z, Brewster S, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Rice J, Rietschel M, Jones L, et al. Depression, migraine with aura and migraine without aura: their familiality and interrelatedness. Cephalalgia : An International Journal of Headache. 29: 848-54. PMID 19239674 DOI: 10.1111/J.1468-2982.2008.01808.X  0.76
2009 Holmans PA, Riley B, Pulver AE, Owen MJ, Wildenauer DB, Gejman PV, Mowry BJ, Laurent C, Kendler KS, Nestadt G, Williams NM, Schwab SG, Sanders AR, Nertney D, Mallet J, et al. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry. 14: 786-95. PMID 19223858 DOI: 10.1038/Mp.2009.11  0.76
2009 Cohen-Woods S, Gaysina D, Craddock N, Farmer A, Gray J, Gunasinghe C, Hoda F, Jones L, Knight J, Korszun A, Owen MJ, Sterne A, Craig IW, McGuffin P. Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. Human Molecular Genetics. 18: 1504-9. PMID 19181679 DOI: 10.1093/Hmg/Ddp051  0.76
2009 Green EK, Grozeva D, Raybould R, Elvidge G, Macgregor S, Craig I, Farmer A, McGuffin P, Forty L, Jones L, Jones I, O'Donovan MC, Owen MJ, Kirov G, Craddock N. P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1063-9. PMID 19160446 DOI: 10.1002/Ajmg.B.30931  0.76
2009 Carroll LS, Kendall K, O'Donovan MC, Owen MJ, Williams NM. Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 893-9. PMID 19132710 DOI: 10.1002/Ajmg.B.30915  0.76
2009 Fowler T, Langley K, Rice F, Whittinger N, Ross K, van Goozen S, Owen MJ, O'Donovan MC, van den Bree MB, Thapar A. Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder. The British Journal of Psychiatry : the Journal of Mental Science. 194: 62-7. PMID 19118328 DOI: 10.1192/Bjp.Bp.107.046870  0.76
2009 Talkowski ME, McClain L, Allen T, Bradford LD, Calkins M, Edwards N, Georgieva L, Go R, Gur R, Gur R, Kirov G, Chowdari K, Kwentus J, Lyons P, Mansour H, ... ... Owen MJ, et al. Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 560-9. PMID 18937293 DOI: 10.1002/Ajmg.B.30862  0.76
2009 Gerrish A, Williams H, Moskvina V, Owen MJ, O'Donovan MC, Williams NM. An examination of MUTED as a schizophrenia susceptibility gene. Schizophrenia Research. 107: 110-1. PMID 18815010 DOI: 10.1016/j.schres.2008.08.011  0.76
2009 O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, ... ... Owen MJ, et al. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry. 14: 30-6. PMID 18813210 DOI: 10.1038/Mp.2008.108  0.76
2009 Langley K, Fowler TA, Grady DL, Moyzis RK, Holmans PA, van den Bree MB, Owen MJ, O'Donovan MC, Thapar A. Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder. European Child & Adolescent Psychiatry. 18: 26-32. PMID 18563476 DOI: 10.1007/S00787-008-0698-4  0.76
2009 Morgan AR, Hollingworth P, Abraham R, Lovestone S, Brayne C, Rubinsztein DC, Lynch A, Lawlor B, Gill M, O'Donovan MC, Owen MJ, Williams J. Association analysis of dynamin-binding protein (DNMBP) on chromosome 10q with late onset Alzheimer's disease in a large caucasian UK sample. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 61-4. PMID 18452187 DOI: 10.1002/Ajmg.B.30768  0.76
2009 Hayesmoore JB, Bray NJ, Cross WC, Owen MJ, O'Donovan MC, Morris HR. The effect of age and the H1c MAPT haplotype on MAPT expression in human brain. Neurobiology of Aging. 30: 1652-6. PMID 18276036 DOI: 10.1016/J.Neurobiolaging.2007.12.017  0.76
2009 Proitsi P, Lupton M, Reeves S, Hamilton G, Archer N, Martin B, hollingworth P, Lawlord B, Gill M, Owen MJ, Williams J, Lovestone S, Powell J. Genes of the serotonergic and dopaminergic pathways and their interaction affect the expression of Behavioural and Psychological Symptoms in Dementia (BPSD). Nature Precedings. DOI: 10.1038/Npre.2009.3896.1  0.32
2008 Richards AL, Holmans P, O'Donovan MC, Owen MJ, Jones L. A comparison of four clustering methods for brain expression microarray data. Bmc Bioinformatics. 9: 490. PMID 19032745 DOI: 10.1186/1471-2105-9-490  0.76
2008 Kwok JB, Loy CT, Hamilton G, Lau E, Hallupp M, Williams J, Owen MJ, Broe GA, Tang N, Lam L, Powell JF, Lovestone S, Schofield PR. Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease. Annals of Neurology. 64: 446-54. PMID 18991351 DOI: 10.1002/Ana.21476  0.76
2008 Abraham R, Moskvina V, Sims R, Hollingworth P, Morgan A, Georgieva L, Dowzell K, Cichon S, Hillmer AM, O'Donovan MC, Williams J, Owen MJ, Kirov G. A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. Bmc Medical Genomics. 1: 44. PMID 18823527 DOI: 10.1186/1755-8794-1-44  0.32
2008 Craddock N, Antebi D, Attenburrow MJ, Bailey A, Carson A, Cowen P, Craddock B, Eagles J, Ebmeier K, Farmer A, Fazel S, Ferrier N, Geddes J, Goodwin G, Harrison P, ... ... Owen MJ, et al. Wake-up call for British psychiatry. The British Journal of Psychiatry : the Journal of Mental Science. 193: 6-9. PMID 18700211 DOI: 10.1192/Bjp.Bp.108.053561  0.76
2008 Williams NM, Williams H, Majounie E, Norton N, Glaser B, Morris HR, Owen MJ, O'Donovan MC. Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Research. 36: e112. PMID 18697816 DOI: 10.1093/Nar/Gkn495  0.76
2008 O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, ... ... Owen MJ, et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics. 40: 1053-5. PMID 18677311 DOI: 10.1038/Ng.201  0.76
2008 Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, et al. Rare chromosomal deletions and duplications increase risk of schizophrenia Nature. 455: 237-241. PMID 18668038 DOI: 10.1038/Nature07239  0.76
2008 Farmer A, Korszun A, Owen MJ, Craddock N, Jones L, Jones I, Gray J, Williamson RJ, McGuffin P. Medical disorders in people with recurrent depression. The British Journal of Psychiatry : the Journal of Mental Science. 192: 351-5. PMID 18450658 DOI: 10.1192/Bjp.Bp.107.038380  0.76
2008 Krystal JH, Carter CS, Geschwind D, Manji HK, March JS, Nestler EJ, Zubieta JK, Charney DS, Goldman D, Gur RE, Lieberman JA, Roy-Byrne P, Rubinow DR, Anderson SA, Barondes S, ... ... Owen MJ, et al. It is time to take a stand for medical research and against terrorism targeting medical scientists. Biological Psychiatry. 63: 725-7. PMID 18371494 DOI: 10.1016/J.Biopsych.2008.03.005  0.76
2008 Hayesmoore JB, Bray NJ, Owen MJ, O'Donovan MC. DISC1 mRNA expression is not influenced by common Cis-acting regulatory polymorphisms or imprinting. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1065-9. PMID 18270998 DOI: 10.1002/Ajmg.B.30715  0.76
2008 Caspi A, Langley K, Milne B, Moffitt TE, O'Donovan M, Owen MJ, Polo Tomas M, Poulton R, Rutter M, Taylor A, Williams B, Thapar A. A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder. Archives of General Psychiatry. 65: 203-10. PMID 18250258 DOI: 10.1001/Archgenpsychiatry.2007.24  0.76
2008 Bray NJ, Holmans PA, van den Bree MB, Jones L, Elliston LA, Hughes G, Richards AL, Williams NM, Craddock N, Owen MJ, O'Donovan MC. Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Human Molecular Genetics. 17: 1169-74. PMID 18182443 DOI: 10.1093/Hmg/Ddn006  0.76
2008 Morgan AR, Hamilton G, Turic D, Jehu L, Harold D, Abraham R, Hollingworth P, Moskvina V, Brayne C, Rubinsztein DC, Lynch A, Lawlor B, Gill M, O'Donovan M, Powell J, ... ... Owen MJ, et al. Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 727-31. PMID 18163421 DOI: 10.1002/Ajmg.B.30670  0.76
2008 Blom ES, Holmans P, Arepalli S, Adighibe O, Hamshere ML, Gatz M, Pedersen NL, Bergem AL, Owen MJ, Hollingworth P, Goate A, Williams J, Lannfelt L, Hardy J, Wavrant-De Vrièze F, et al. Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 778-83. PMID 18161859 DOI: 10.1002/Ajmg.B.30681  0.76
2008 Li Y, Grupe A, Rowland C, Holmans P, Segurado R, Abraham R, Jones L, Catanese J, Ross D, Mayo K, Martinez M, Hollingworth P, Goate A, Cairns NJ, Racette BA, ... ... Owen MJ, et al. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Human Molecular Genetics. 17: 759-67. PMID 18063669 DOI: 10.1093/Hmg/Ddm348  0.76
2008 Talkowski ME, Kirov G, Bamne M, Georgieva L, Torres G, Mansour H, Chowdari KV, Milanova V, Wood J, McClain L, Prasad K, Shirts B, Zhang J, O'Donovan MC, Owen MJ, et al. A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Human Molecular Genetics. 17: 747-58. PMID 18045777 DOI: 10.1093/Hmg/Ddm347  0.76
2008 Li H, Wetten S, Li L, St Jean PL, Upmanyu R, Surh L, Hosford D, Barnes MR, Briley JD, Borrie M, Coletta N, Delisle R, Dhalla D, Ehm MG, Feldman HH, ... ... Owen MJ, et al. Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Archives of Neurology. 65: 45-53. PMID 17998437 DOI: 10.1001/Archneurol.2007.3  0.76
2008 Kirov G, Gumus D, Chen W, Norton N, Georgieva L, Sari M, O'Donovan MC, Erdogan F, Owen MJ, Ropers HH, Ullmann R. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics. 17: 458-65. PMID 17989066 DOI: 10.1093/Hmg/Ddm323  0.76
2008 Li Y, Rowland C, Catanese J, Morris J, Lovestone S, O'Donovan MC, Goate A, Owen M, Williams J, Grupe A. SORL1 variants and risk of late-onset Alzheimer's disease. Neurobiology of Disease. 29: 293-6. PMID 17949987 DOI: 10.1016/J.Nbd.2007.09.001  0.76
2008 Buxbaum JD, Georgieva L, Young JJ, Plescia C, Kajiwara Y, Jiang Y, Moskvina V, Norton N, Peirce T, Williams H, Craddock NJ, Carroll L, Corfas G, Davis KL, Owen MJ, et al. Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene. Molecular Psychiatry. 13: 162-72. PMID 17579610 DOI: 10.1038/Sj.Mp.4001991  0.76
2008 Langley K, Turic D, Rice F, Holmans P, van den Bree MB, Craddock N, Kent L, Owen MJ, O'Donovan MC, Thapar A. Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 49-53. PMID 17579368 DOI: 10.1002/ajmg.b.30571  0.76
2008 van Amelsvoort T, Zinkstok J, Figee M, Daly E, Morris R, Owen MJ, Murphy KC, De Haan L, Linszen DH, Glaser B, Murphy DG. Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome. Psychological Medicine. 38: 89-100. PMID 17493297 DOI: 10.1017/S0033291707000700  0.76
2008 Sims R, Hollingworth P, Morgan A, Dowzell K, Stretton A, Jones L, Norton N, Williams H, Georgieva L, Moskvina V, Nikolov I, Hamshere M, Holmans P, Lovestone S, Brayne C, ... ... Owen M, et al. P3-265: Testing for association between Alzheimer's disease with psychosis and variants identified as influencing risk of schizophrenia Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1833  0.44
2008 Abraham R, Georgieva L, Sims R, Morgan A, Hollingworth P, Lovestone S, Brayne C, Cichon S, O'Donovan M, Williams J, Owen M, Kirov G. P3-196: A genome-wide association study for late-onset Alzheimer's disease using DNA pooling Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1762  0.32
2007 Nejentsev S, Howson JM, Walker NM, Szeszko J, Field SF, Stevens HE, Reynolds P, Hardy M, King E, Masters J, Hulme J, Maier LM, Smyth D, Bailey R, Cooper JD, et al. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature. 450: 887-92. PMID 18004301 DOI: 10.1038/Nature06406  0.76
2007 Hamilton G, Proitsi P, Williams J, O'Donovan M, Owen M, Powell J, Lovestone S. Complement factor H Y402H polymorphism is not associated with late-onset Alzheimer's disease. Neuromolecular Medicine. 9: 331-4. PMID 17999207 DOI: 10.1007/S12017-007-8013-Y  0.76
2007 Zammit S, Spurlock G, Williams H, Norton N, Williams N, O'Donovan MC, Owen MJ. Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. The British Journal of Psychiatry : the Journal of Mental Science. 191: 402-7. PMID 17978319 DOI: 10.1192/Bjp.Bp.107.036129  0.76
2007 Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, ... ... Owen MJ, et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nature Genetics. 39: 1329-37. PMID 17952073 DOI: 10.1038/Ng.2007.17  0.76
2007 Williams HJ, Norton N, Peirce T, Dwyer S, Williams NM, Moskvina V, Owen MJ, O'Donovan MC. Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia. Schizophrenia Research. 97: 271-6. PMID 17897812 DOI: 10.1016/j.schres.2007.09.004  0.76
2007 Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrièze F, Go R, Fallin D, Lovestone S, Hardy J, ... ... Owen MJ, et al. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Human Molecular Genetics. 16: 2703-12. PMID 17725986 DOI: 10.1093/Hmg/Ddm224  0.76
2007 Owen MJ, Craddock N, Jablensky A. The genetic deconstruction of psychosis. Schizophrenia Bulletin. 33: 905-11. PMID 17551090 DOI: 10.1093/Schbul/Sbm053  0.76
2007 Thapar A, Langley K, Owen MJ, O'Donovan MC. Advances in genetic findings on attention deficit hyperactivity disorder. Psychological Medicine. 37: 1681-92. PMID 17506925 DOI: 10.1017/S0033291707000773  0.76
2007 Hollingworth P, Hamshere ML, Holmans PA, O'Donovan MC, Sims R, Powell J, Lovestone S, Myers A, DeVrieze FW, Hardy J, Goate A, Owen M, Williams J. Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 841-8. PMID 17492769 DOI: 10.1002/Ajmg.B.30515  0.76
2007 Hamilton G, Proitsi P, Jehu L, Morgan A, Williams J, O'Donovan MC, Owen MJ, Powell JF, Lovestone S. Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 508-16. PMID 17440948 DOI: 10.1002/Ajmg.B.30503  0.76
2007 Harold D, Jehu L, Turic D, Hollingworth P, Moore P, Summerhayes P, Moskvina V, Foy C, Archer N, Hamilton BA, Lovestone S, Powell J, Brayne C, Rubinsztein DC, Jones L, ... ... Owen MJ, et al. Interaction between the ADAM12 and SH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 448-52. PMID 17440933 DOI: 10.1002/Ajmg.B.30456  0.76
2007 Morgan AR, Turic D, Jehu L, Hamilton G, Hollingworth P, Moskvina V, Jones L, Lovestone S, Brayne C, Rubinsztein DC, Lawlor B, Gill M, O'Donovan MC, Owen MJ, Williams J. Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 762-70. PMID 17373700 DOI: 10.1002/Ajmg.B.30509  0.76
2007 Grupe A, Abraham R, Li Y, Rowland C, Hollingworth P, Morgan A, Jehu L, Segurado R, Stone D, Schadt E, Karnoub M, Nowotny P, Tacey K, Catanese J, Sninsky J, ... ... Owen MJ, et al. Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Human Molecular Genetics. 16: 865-73. PMID 17317784 DOI: 10.1093/Hmg/Ddm031  0.76
2007 Gaughran F, Blizard R, Mohan R, Zammit S, Owen M. Birth order and the severity of illness in schizophrenia. Psychiatry Research. 150: 205-10. PMID 17292486 DOI: 10.1016/J.Psychres.2006.05.012  0.76
2007 Nicholas B, Rudrasingham V, Nash S, Kirov G, Owen MJ, Wimpory DC. Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis. Molecular Psychiatry. 12: 581-92. PMID 17264841 DOI: 10.1038/sj.mp.4001953  0.76
2007 Gunnell D, Lewis S, Wilkinson J, Georgieva L, Davey GS, Day IN, Holly JM, O'Donovan MC, Owen MJ, Kirov G, Zammit S. IGF1, growth pathway polymorphisms and schizophrenia: a pooling study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 117-20. PMID 17044098 DOI: 10.1002/ajmg.b.30396  0.76
2006 van Amelsvoort T, Schmitz N, Daly E, Deeley Q, Critchley H, Henry J, Robertson D, Owen M, Murphy KC, Murphy DG. Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging. The British Journal of Psychiatry : the Journal of Mental Science. 189: 560-1. PMID 17139043 DOI: 10.1192/Bjp.Bp.105.019876  0.76
2006 Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry. 11: 1085-91, 1061. PMID 17033633 DOI: 10.1038/Sj.Mp.4001904  0.76
2006 Hollingworth P, Hamshere ML, Moskvina V, Dowzell K, Moore PJ, Foy C, Archer N, Lynch A, Lovestone S, Brayne C, Rubinsztein DC, Lawlor B, Gill M, Owen MJ, Williams J. Four components describe behavioral symptoms in 1,120 individuals with late-onset Alzheimer's disease. Journal of the American Geriatrics Society. 54: 1348-54. PMID 16970641 DOI: 10.1111/J.1532-5415.2006.00854.X  0.32
2006 Georgieva L, Moskvina V, Peirce T, Norton N, Bray NJ, Jones L, Holmans P, Macgregor S, Zammit S, Wilkinson J, Williams H, Nikolov I, Williams N, Ivanov D, Davis KL, ... ... Owen MJ, et al. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 103: 12469-74. PMID 16891421 DOI: 10.1073/Pnas.0603029103  0.76
2006 Li Y, Grupe A, Rowland C, Nowotny P, Kauwe JS, Smemo S, Hinrichs A, Tacey K, Toombs TA, Kwok S, Catanese J, White TJ, Maxwell TJ, Hollingworth P, Abraham R, ... ... Owen M, et al. DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. Human Molecular Genetics. 15: 2560-8. PMID 16847012 DOI: 10.1093/Hmg/Ddl178  0.76
2006 Rees MI, Harvey K, Pearce BR, Chung SK, Duguid IC, Thomas P, Beatty S, Graham GE, Armstrong L, Shiang R, Abbott KJ, Zuberi SM, Stephenson JB, Owen MJ, Tijssen MA, et al. Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nature Genetics. 38: 801-6. PMID 16751771 DOI: 10.1038/Ng1814  0.76
2006 Williams NM, O'Donovan MC, Owen MJ. Chromosome 22 deletion syndrome and schizophrenia. International Review of Neurobiology. 73: 1-27. PMID 16737900 DOI: 10.1016/S0074-7742(06)73001-X  0.76
2006 Thapar A, Langley K, O'donovan M, Owen M. Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Molecular Psychiatry. 11: 714-20. PMID 16702977 DOI: 10.1038/Sj.Mp.4001831  0.76
2006 Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, et al. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. Proceedings of the National Academy of Sciences of the United States of America. 103: 7729-34. PMID 16684884 DOI: 10.1073/Pnas.0600206103  0.76
2006 Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, ... ... Owen MJ, et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry. 60: 152-62. PMID 16631129 DOI: 10.1016/J.Biopsych.2006.02.015  0.76
2006 Williams NM, Green EK, Macgregor S, Dwyer S, Norton N, Williams H, Raybould R, Grozeva D, Hamshere M, Zammit S, Jones L, Cardno A, Kirov G, Jones I, O'Donovan MC, ... Owen MJ, et al. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry. 63: 366-73. PMID 16585465 DOI: 10.1001/Archpsyc.63.4.366  0.76
2006 Hamilton G, Samedi F, Knight J, Archer N, Foy C, Walter S, Turic D, Jehu L, Moore P, Hollingworth P, O'Donovan MC, Williams J, Owen MJ, Lovestone S, Powell JF. Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neuroscience Letters. 401: 77-80. PMID 16574322 DOI: 10.1016/J.Neulet.2006.03.021  0.76
2006 Zammit S, Owen MJ. Stressful life events, 5-HTT genotype and risk of depression. The British Journal of Psychiatry : the Journal of Mental Science. 188: 199-201. PMID 16507957 DOI: 10.1192/Bjp.Bp.105.020644  0.76
2006 Harold D, Macgregor S, Patterson CE, Hollingworth P, Moore P, Owen MJ, Williams J, O'Donovan M, Passmore P, McIlroy S, Jones L. A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. Pharmacogenetics and Genomics. 16: 75-7. PMID 16424819 DOI: 10.1097/01.Fpc.0000189799.88596.04  0.76
2006 Blair IP, Chetcuti AF, Badenhop RF, Scimone A, Moses MJ, Adams LJ, Craddock N, Green E, Kirov G, Owen MJ, Kwok JB, Donald JA, Mitchell PB, Schofield PR. Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele. Molecular Psychiatry. 11: 372-83. PMID 16402135 DOI: 10.1002/Ajmg.B.30233  0.76
2006 Peirce TR, Bray NJ, Williams NM, Norton N, Moskvina V, Preece A, Haroutunian V, Buxbaum JD, Owen MJ, O'Donovan MC. Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of General Psychiatry. 63: 18-24. PMID 16389193 DOI: 10.1001/Archpsyc.63.1.18  0.76
2006 Smemo S, Nowotny P, Hinrichs AL, Kauwe JS, Cherny S, Erickson K, Myers AJ, Kaleem M, Marlowe L, Gibson AM, Hollingworth P, O'Donovan MC, Morris CM, Holmans P, Lovestone S, ... ... Owen MJ, et al. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology. 59: 21-6. PMID 16278862 DOI: 10.1002/Ana.20673  0.76
2006 Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer S, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, ... ... Owen MJ, et al. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 96-101. PMID 16249994 DOI: 10.1002/Ajmg.B.30236  0.76
2006 Hamshere ML, Williams NM, Norton N, Williams H, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, Holmans P, O'Donovan MC, Owen MJ, et al. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics. 43: 563-7. PMID 16227524 DOI: 10.1136/Jmg.2005.035345  0.76
2006 Zammit S, Lewis G, Thapar A, Owen R, Jones G, Jones S, Sanders R, Milham C, Mahdi A, O'Donovan MC, Owen MJ. Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophrenia. Journal of Psychiatric Research. 40: 622-6. PMID 16038933 DOI: 10.1016/J.Jpsychires.2005.05.006  0.76
2006 Grupe A, Li Y, Rowland C, Hinrichs T, Holmans P, Hardy J, O'Donovan M, Owen MJ, Williams J, Goate A. Reply to Bertram et al. [2] American Journal of Human Genetics. 79: 183-184. DOI: 10.1086/505033  0.76
2006 Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia Molecular Psychiatry. 11: 1061. DOI: 10.1038/Sj.Mp.4001930  0.76
2006 Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, et al. Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 - Corrigendum Molecular Psychiatry. DOI: 10.1038/Sj.Mp.4001917  0.32
2006 Sims R, Hollingworth P, Cope N, Jehu L, Morgan A, Moskvina V, Lovestone S, Brayne C, Rubinsztein DC, O’Donovan M, Owen M, Williams J, Abraham R. P1-327: Testing for association between Alzheimer’s disease with psychosis and functional gene candidates Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.705  0.32
2006 Proitsi P, Hamilton G, Archer N, Foy C, Hollinworth P, Owen M, Williams J, Lovestone S, Powell J. P1-326: Statistical and genetic studies on the psychosis sub-phenotype in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.704  0.32
2006 Jones L, Harold D, MacGregor S, Patterson CE, Hollingworth P, Owen MJ, Williams J, McIlroy S, Passmore P, O’Donovan M. P1-275: A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.652  0.32
2006 Hoogendoorn B, Turic D, Dudley E, Grassl J, Abraham R, Hollingworth P, Moskvina V, Williams J, Owen MJ, O’Donovan M, Jones L. P1-073: Protein profiling of the hippocampus of the Tg2576 transgenic AD mouse model Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.448  0.32
2006 Li Y, Grupe A, Rowland C, Nowotny P, Kauwe JSK, Smemo S, Hinrichs A, Tacey K, Kwok S, Catanese J, Sninsky J, White TJ, Hollingworth P, Harris SL, Levine A, ... ... Owen M, et al. O2-02-07 Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.117  0.48
2005 Thapar A, O'Donovan M, Owen MJ. The genetics of attention deficit hyperactivity disorder. Human Molecular Genetics. 14: R275-82. PMID 16244326 DOI: 10.1093/Hmg/Ddi263  0.76
2005 Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, ... Owen MJ, et al. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of General Psychiatry. 62: 1081-8. PMID 16203953 DOI: 10.1001/Archpsyc.62.10.1081  0.32
2005 McGuffin P, Knight J, Breen G, Brewster S, Boyd PR, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Reich T, et al. Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics. 14: 3337-45. PMID 16203746 DOI: 10.1093/Hmg/Ddi363  0.76
2005 Ahuja AS, Thapar A, Owen MJ. Genetics of mental retardation. Indian Journal of Medical Sciences. 59: 407-17. PMID 16199928 DOI: 10.4103/0019-5359.16820  0.76
2005 Williams NM, O'Donovan MC, Owen MJ. Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? Schizophrenia Bulletin. 31: 800-5. PMID 16166606 DOI: 10.1093/Schbul/Sbi061  0.76
2005 Williams HJ, Glaser B, Williams NM, Norton N, Zammit S, MacGregor S, Kirov GK, Owen MJ, O'Donovan MC. No association between schizophrenia and polymorphisms in COMT in two large samples. The American Journal of Psychiatry. 162: 1736-8. PMID 16135635 DOI: 10.1176/Appi.Ajp.162.9.1736  0.76
2005 Glaser B, Schumacher J, Williams HJ, Jamra RA, Ianakiev N, Milev R, Ohlraun S, Schulze TG, Czerski PM, Hauser J, Jönsson EG, Sedvall GC, Klopp N, Illig T, Becker T, ... ... Owen MJ, et al. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological Psychiatry. 58: 78-80. PMID 15992527 DOI: 10.1016/J.Biopsych.2005.03.017  0.76
2005 Li Y, Rowland C, Tacey K, Catanese J, Sninsky J, Hardy J, Powell J, Lovestone S, Morris JC, Thal L, Goate A, Owen M, Williams J, Grupe A. The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Molecular Psychiatry. 10: 809-10. PMID 15970929 DOI: 10.1038/Sj.Mp.4001702  0.76
2005 Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, Green E, O'Mahony E, Nikolov I, Mulcahy T, Haque S, Bort S, Bennett P, Norton N, Owen MJ, et al. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular Psychiatry. 10: 831-41. PMID 15940300 DOI: 10.1038/Sj.Mp.4001684  0.32
2005 Glaser B, Kirov G, Bray NJ, Green E, O'Donovan MC, Craddock N, Owen MJ. Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. Molecular Psychiatry. 10: 920-7. PMID 15940297 DOI: 10.1038/Sj.Mp.4001689  0.76
2005 Kent L, Green E, Hawi Z, Kirley A, Dudbridge F, Lowe N, Raybould R, Langley K, Bray N, Fitzgerald M, Owen MJ, O'Donovan MC, Gill M, Thapar A, Craddock N. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry. 10: 939-43. PMID 15940292 DOI: 10.1038/Sj.Mp.4001696  0.76
2005 Bray NJ, Preece A, Williams NM, Moskvina V, Buckland PR, Owen MJ, O'Donovan MC. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics. 14: 1947-54. PMID 15917270 DOI: 10.1093/Hmg/Ddi199  0.76
2005 Norton N, Williams HJ, Dwyer S, Ivanov D, Preece AC, Gerrish A, Williams NM, Yerassimou P, Zammit S, O'Donovan MC, Owen MJ. No evidence for association between polymorphisms in GRM3 and schizophrenia. Bmc Psychiatry. 5: 23. PMID 15892884 DOI: 10.1186/1471-244X-5-23  0.76
2005 Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell T, Holmans P, Hamshere M, Turic D, Jehu L, Hollingworth P, Moore P, Bryden L, Myers A, Doil LM, Tacey KM, ... ... Owen MJ, et al. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 136: 62-8. PMID 15858813 DOI: 10.1002/Ajmg.B.30186  0.76
2005 Holmans P, Hamshere M, Hollingworth P, Rice F, Tunstall N, Jones S, Moore P, Wavrant DeVrieze F, Myers A, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, ... ... Owen M, et al. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 135: 24-32. PMID 15729734 DOI: 10.1002/Ajmg.B.30114  0.76
2005 Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics. 76: 581-91. PMID 15717286 DOI: 10.1086/429131  0.44
2005 Li Y, Hollingworth P, Moore P, Foy C, Archer N, Powell J, Nowotny P, Holmans P, O'Donovan M, Tacey K, Doil L, van Luchene R, Garcia V, Rowland C, Lau K, ... ... Owen M, et al. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation. 25: 270-7. PMID 15714520 DOI: 10.1002/Humu.20138  0.76
2004 Bray NJ, Jehu L, Moskvina V, Buxbaum JD, Dracheva S, Haroutunian V, Williams J, Buckland PR, Owen MJ, O'Donovan MC. Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. Human Molecular Genetics. 13: 2885-92. PMID 15385439 DOI: 10.1093/Hmg/Ddh299  0.76
2004 Li Y, Tacey K, Doil L, van Luchene R, Garcia V, Rowland C, Schrodi S, Leong D, Lau K, Catanese J, Sninsky J, Nowotny P, Holmans P, Hardy J, Powell J, ... ... Owen M, et al. Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study. Neuroscience Letters. 366: 268-71. PMID 15288432 DOI: 10.1016/J.Neulet.2004.05.047  0.76
2004 Cichon S, Buervenich S, Kirov G, Akula N, Dimitrova A, Green E, Schumacher J, Klopp N, Becker T, Ohlraun S, Schulze TG, Tullius M, Gross MM, Jones L, Krastev S, ... ... Owen MJ, et al. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nature Genetics. 36: 783-4; author reply . PMID 15284840 DOI: 10.1038/Ng0804-783  0.76
2004 Harvey K, Duguid IC, Alldred MJ, Beatty SE, Ward H, Keep NH, Lingenfelter SE, Pearce BR, Lundgren J, Owen MJ, Smart TG, Lüscher B, Rees MI, Harvey RJ. The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 5816-26. PMID 15215304 DOI: 10.1523/Jneurosci.1184-04.2004  0.76
2004 Ristevski S, O'Leary DA, Thornell AP, Owen MJ, Kola I, Hertzog PJ. The ETS transcription factor GABPα is essential for early embryogenesis Molecular and Cellular Biology. 24: 5844-5849. PMID 15199140 DOI: 10.1128/Mcb.24.13.5844-5849.2004  0.76
2004 Reid SJ, van Roon-Mom WM, Wood PC, Rees MI, Owen MJ, Faull RL, Dragunow M, Snell RG. TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease. Brain Research. Molecular Brain Research. 125: 120-8. PMID 15193429 DOI: 10.1016/J.Molbrainres.2004.03.018  0.76
2004 Williams NM, Owen MJ. Genetic abnormalities of chromosome 22 and the development of psychosis Current Psychiatry Reports. 6: 176-182. PMID 15142470 DOI: 10.1007/S11920-004-0062-4  0.76
2004 Owen MJ, Williams NM, O'Donovan MC. Dysbindin-1 and chnizophrenia: From genetics to neuropathology Journal of Clinical Investigation. 113: 1255-1257. PMID 15124015 DOI: 10.1172/Jci21470  0.76
2004 Norton N, Williams NM, O'Donovan MC, Owen MJ. DNA pooling as a tool for large-scale association studies in complex traits Annals of Medicine. 36: 146-152. PMID 15119834 DOI: 10.1080/07853890310021724  0.76
2004 Busby V, Goossens S, Nowotny P, Hamilton G, Smemo S, Harold D, Turic D, Jehu L, Myers A, Womick M, Woo D, Compton D, Doil LM, Tacey KM, Lau KF, ... ... Owen MJ, et al. Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Medicine. 5: 133-46. PMID 15075440 DOI: 10.1385/Nmm:5:2:133  0.76
2004 Cook LJ, Ho LW, Taylor AE, Brayne C, Evans JG, Xuereb J, Cairns NJ, Pritchard A, Lemmon H, Mann D, St Clair D, Turic D, Hollingworth P, Moore PJ, Jehu L, ... ... Owen MJ, et al. Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. Neuroscience Letters. 358: 142-6. PMID 15026168 DOI: 10.1016/J.Neulet.2004.01.016  0.76
2004 Mowry BJ, Holmans PA, Pulver AE, Gejman PV, Riley B, Williams NM, Laurent C, Schwab SG, Wildenauer DB, Bauché S, Owen MJ, Wormley B, Sanders AR, Nestadt G, Liang KY, et al. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry. 9: 784-95. PMID 15007391 DOI: 10.1038/Sj.Mp.4001481  0.76
2004 Plomin R, Turic DM, Hill L, Turic DE, Stephens M, Williams J, Owen MJ, O'Donovan MC. A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability. Molecular Psychiatry. 9: 582-6. PMID 14981524 DOI: 10.1038/Sj.Mp.4001441  0.76
2004 Turic D, Langley K, Mills S, Stephens M, Lawson D, Govan C, Williams N, Van Den Bree M, Craddock N, Kent L, Owen M, O'Donovan M, Thapar A. Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Molecular Psychiatry. 9: 169-73. PMID 14966475 DOI: 10.1038/Sj.Mp.4001387  0.76
2004 Bray NJ, Buckland PR, Hall H, Owen MJ, O'Donovan MC. The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain. Molecular Psychiatry. 9: 109-14. PMID 14699448 DOI: 10.1038/Sj.Mp.4001366  0.76
2004 Myers AJ, Marshall H, Holmans P, Compton D, Crook RJ, Mander AP, Nowotny P, Smemo S, Dunstan M, Jehu L, Wang JC, Hamshere M, Morris JC, Norton J, Chakraventy S, ... ... Owen MJ, et al. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 29-37. PMID 14681909 DOI: 10.1002/Ajmg.B.20036  0.76
2004 Owen MJ, Williams NM, O'Donovan MC. The molecular genetics of schizophrenia: New findings promise new insights Molecular Psychiatry. 9: 14-27. PMID 14581932 DOI: 10.1038/Sj.Mp.4001444  0.76
2004 Li Y, Hollingworth P, Moore P, Foy C, Archer N, Nowotny P, Holmans P, Smemo S, Tacey K, Doil L, Luchene Rv, Lau K, Catanese J, Garcia V, Rowland C, ... ... Owen M, et al. P4-122 Genetic association of an APP binding protein gene with late onset Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81680-4  0.48
2004 Doil L, Tacey K, Nowotny P, Luchene Rv, Li Y, Holmans P, Smemo S, Garcia V, Rowland C, Leong D, Gogic G, Cravchik A, Ross D, Lau K, Catanese J, ... ... Owen M, et al. P4-110 A systematic scan of chromosome 10 single nucleotide polymorphisms identifies novel candidate genes showing strong association to Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81668-3  0.48
2004 Lau KF, Rowland C, Tacey K, Doil L, Li Y, Luchene Rv, Nowotny P, Smemo S, Garcia V, Lovestone S, Owen M, Williams J, Grupe A, Goate A. P4-067 Genetic association studies of insulin-degrading enzyme (IDE) with late onset Alzheimer's disease (LOAD) - Equivocal results from two large case-control studies Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81625-7  0.44
2004 Hamilton G, Samadi F, Archer N, Foy C, Walter S, Turic D, Jehu L, Hollingworth P, Jones S, Moore P, Jones L, Williams J, Owen M, Lovestone S, Powell J. P4-058 Searching chromosome 10 for an AD risk factor — Analysis of a positional and biological candidate Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81616-6  0.32
2004 Li Y, Nowotny P, Holmans P, Smemo S, Kawe K, Tacey K, Doil L, Luchene Rv, Garcia V, Rowland C, Schrodi S, Leong D, Chan J, Lau K, Chang S, ... ... Owen M, et al. P4-046 Association of late onset Alzheimer's disease with genetic variation in multiple members of a gene family involved in neuronal apoptosis Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81604-X  0.48
2003 Williams NM, Norton N, Williams H, Ekholm B, Hamshere ML, Lindblom Y, Chowdari KV, Cardno AG, Zammit S, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Jones G, ... ... Owen MJ, et al. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. American Journal of Human Genetics. 73: 1355-67. PMID 14628288 DOI: 10.1086/380206  0.76
2003 O'Donovan MC, Williams NM, Owen MJ. Recent advances in the genetics of schizophrenia Human Molecular Genetics. 12. PMID 12952866 DOI: 10.1093/Hmg/Ddg302  0.76
2003 Norton N, Williams HJ, Williams NM, Spurlock G, Zammit S, Jones G, Jones S, Owen R, O'Donovan MC, Owen MJ. Mutation screening of the Homer gene family and association analysis in schizophrenia American Journal of Medical Genetics - Neuropsychiatric Genetics. 120: 18-21. PMID 12815733 DOI: 10.1002/Ajmg.B.20032  0.76
2003 Williams NM, Preece A, Spurlock G, Norton N, Williams HJ, Zammit S, O'Donovan MC, Owen MJ. Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia. Molecular Psychiatry. 8: 485-7. PMID 12808428 DOI: 10.1038/Sj.Mp.4001348  0.76
2003 Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, ... ... Owen MJ, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics. 73: 34-48. PMID 12802786 DOI: 10.1086/376549  0.76
2003 Bray NJ, Buckland PR, Williams NM, Williams HJ, Norton N, Owen MJ, O'Donovan MC. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. American Journal of Human Genetics. 73: 152-61. PMID 12802784 DOI: 10.1086/376578  0.76
2003 Harold D, Peirce T, Moskvina V, Myers A, Jones S, Hollingworth P, Moore P, Lovestone S, Powell J, Foy C, Archer N, Walter S, Edmonson A, McIlroy S, Craig D, ... ... Owen MJ, et al. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Human Genetics. 113: 258-67. PMID 12759818 DOI: 10.1007/S00439-003-0960-2  0.76
2003 Reid SJ, Rees MI, van Roon-Mom WM, Jones AL, MacDonald ME, Sutherland G, During MJ, Faull RL, Owen MJ, Dragunow M, Snell RG. Molecular investigation of TBP allele length: a SCA17 cellular model and population study. Neurobiology of Disease. 13: 37-45. PMID 12758065 DOI: 10.1016/S0969-9961(03)00014-7  0.76
2003 Edwards D, Burnard P, Owen M, Hannigan B, Fothergill A, Coyle D. A systematic review of the effectiveness of stress-management interventions for mental health professionals Journal of Psychiatric and Mental Health Nursing. 10: 370-371. PMID 12755924 DOI: 10.1046/J.1365-2850.2003.00606.X  0.76
2003 Bray NJ, Buckland PR, Owen MJ, O'Donovan MC. Cis-acting variation in the expression of a high proportion of genes in human brain. Human Genetics. 113: 149-53. PMID 12728311 DOI: 10.1007/S00439-003-0956-Y  0.76
2003 Rees MI, Harvey K, Ward H, White JH, Evans L, Duguid IC, Hsu CC, Coleman SL, Miller J, Baer K, Waldvogel HJ, Gibbon F, Smart TG, Owen MJ, Harvey RJ, et al. Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. The Journal of Biological Chemistry. 278: 24688-96. PMID 12684523 DOI: 10.1074/Jbc.M301070200  0.76
2003 Jönsson EG, Norton N, Forslund K, Mattila-Evenden M, Rylander G, Asberg M, Owen MJ, Sedvall GC. Association between a promoter variant in the monoamine oxidase A gene and schizophrenia. Schizophrenia Research. 61: 31-7. PMID 12648733 DOI: 10.1016/S0920-9964(02)00224-4  0.76
2003 Børglum AD, Kirov G, Craddock N, Mors O, Muir W, Murray V, McKee I, Collier DA, Ewald H, Owen MJ, Blackwood D, Kruse TA. Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 18-22. PMID 12555230 DOI: 10.1002/Ajmg.B.10030  0.76
2002 Bray NJ, Kirov G, Owen RJ, Jacobsen NJ, Georgieva L, Williams HJ, Norton N, Spurlock G, Jones S, Zammit S, O'Donovan MC, Owen MJ. Screening the human protocadherin 8 (PCDH8) gene in schizophrenia. Genes, Brain, and Behavior. 1: 187-91. PMID 12884975 DOI: 10.1034/J.1601-183X.2002.10307.X  0.76
2002 Garpenstrand H, Norton N, Damberg M, Rylander G, Forslund K, Mattila-Evenden M, Gustavsson JP, Ekblom J, Oreland L, Bergman H, Owen MJ, Jönsson EG. A regulatory monoamine oxidase a promoter polymorphism and personality traits. Neuropsychobiology. 46: 190-3. PMID 12566936 DOI: 10.1159/000067804  0.76
2002 Sham P, Bader JS, Craig I, O'Donovan M, Owen M. DNA Pooling: a tool for large-scale association studies. Nature Reviews. Genetics. 3: 862-71. PMID 12415316 DOI: 10.1038/Nrg930  0.76
2002 Williams NM, Bowen T, Spurlock G, Norton N, Williams HJ, Hoogendoorn B, Owen MJ, O'Donovan MC. Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor Molecular Psychiatry. 7: 508-514. PMID 12082569 DOI: 10.1038/Sj.Mp.4001030  0.76
2002 Norton N, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, Hoogendoorn B, Owen MJ, O'Donovan MC. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Human Genetics. 110: 471-8. PMID 12073018 DOI: 10.1007/S00439-002-0706-6  0.76
2002 Williams NM, O'Donovan MC, Owen MJ. Genome scans and microarrays: Converging on genes for schizophrenia? Genome Biology. 3. PMID 11983064 DOI: 10.1186/Gb-2002-3-4-Reviews1011  0.76
2002 Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV, Schwab SG, Williams NM, Owen MJ, Wildenauer DB, Sanders AR, Nestadt G, Mowry BJ, Wormley B, Bauché S, et al. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science (New York, N.Y.). 296: 739-41. PMID 11976456 DOI: 10.1126/Science.1069914  0.76
2002 Rees MI, Lewis TM, Kwok JB, Mortier GR, Govaert P, Snell RG, Schofield PR, Owen MJ. Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB). Human Molecular Genetics. 11: 853-60. PMID 11929858 DOI: 10.1093/Hmg/11.7.853  0.76
2002 Myers A, Wavrant De-Vrieze F, Holmans P, Hamshere M, Crook R, Compton D, Marshall H, Meyer D, Shears S, Booth J, Ramic D, Knowles H, Morris JC, Williams N, Norton N, ... ... Owen MJ, et al. Full genome screen for Alzheimer disease: stage II analysis. American Journal of Medical Genetics. 114: 235-44. PMID 11857588 DOI: 10.1002/Ajmg.10183  0.76
2001 Plomin R, Hill L, Craig IW, McGuffin P, Purcell S, Sham P, Lubinski D, Thompson LA, Fisher PJ, Turic D, Owen MJ. A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behavior Genetics. 31: 497-509. PMID 11838529 DOI: 10.1023/A:1013385125887  0.76
2001 Abraham R, Myers A, Wavrant-DeVrieze F, Hamshere ML, Thomas HV, Marshall H, Compton D, Spurlock G, Turic D, Hoogendoorn B, Kwon JM, Petersen RC, Tangalos E, Norton J, Morris JC, ... ... Owen MJ, et al. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics. 109: 646-52. PMID 11810277 DOI: 10.1007/S00439-001-0614-1  0.76
2001 Rees MI, Lewis TM, Vafa B, Ferrie C, Corry P, Muntoni F, Jungbluth H, Stephenson JB, Kerr M, Snell RG, Schofield PR, Owen MJ. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Human Genetics. 109: 267-70. PMID 11702206 DOI: 10.1007/S004390100569  0.76
2001 Kirov G, Lowry CA, Stephens M, Oldfield S, O'Donovan MC, Lightman SL, Owen MJ. Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder. Molecular Psychiatry. 6: 671-7. PMID 11673795 DOI: 10.1038/Sj.Mp.4000899  0.76
2001 Maurice D, Pierreux CE, Howell M, Wilentz RE, Owen MJ, Hill CS. Loss of Smad4 function in pancreatic tumors: C-terminal truncation leads to decreased stability Journal of Biological Chemistry. 276: 43175-43181. PMID 11553622 DOI: 10.1074/jbc.M105895200  0.76
2001 Payton A, Holmes J, Barrett JH, Hever T, Fitzpatrick H, Trumper AL, Harrington R, McGuffin P, O'Donovan M, Owen M, Ollier W, Worthington J, Thapar A. Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: A family-based study American Journal of Medical Genetics - Neuropsychiatric Genetics. 105: 464-470. PMID 11449400 DOI: 10.1002/Ajmg.1407  0.76
2001 Bowen T, Williams N, Norton N, Spurlock G, Wittekindt OH, Morris-Rosendahl DJ, Williams H, Brzustowicz L, Hoogendoorn B, Zammit S, Jones G, Sanders RD, Jones LA, McCarthy G, Jones S, ... ... Owen MJ, et al. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation. Molecular Psychiatry. 6: 259-60. PMID 11326292 DOI: 10.1038/Sj.Mp.4000128  0.76
2001 Bray NJ, Owen MJ. Searching for schizophrenia genes. Trends in Molecular Medicine. 7: 169-74. PMID 11286941 DOI: 10.1016/S1471-4914(01)01950-5  0.76
2000 Sham PC, Sterne A, Purcell S, Cherny S, Webster M, Rijsdijk F, Asherson P, Ball D, Craig I, Eley T, Goldberg D, Gray J, Mann A, Owen M, Plomin R. GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Research : the Official Journal of the International Society For Twin Studies. 3: 316-22. PMID 11463153 DOI: 10.1375/136905200320565292  0.76
2000 Bowen T, Ashworth L, Kirov G, Guy CA, Jones IR, McCandless F, Craddock N, O'Donovan MC, Owen MJ. No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder Bipolar Disorders. 2: 328-331. PMID 11252645 DOI: 10.1034/J.1399-5618.2000.020406.X  0.76
2000 Hoogendoorn B, Norton N, Kirov G, Williams N, Hamshere ML, Spurlock G, Austin J, Stephens MK, Buckland PR, Owen MJ, O'Donovan MC. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools Human Genetics. 107: 488-493. PMID 11140947 DOI: 10.1007/S004390000397  0.76
2000 Myers A, Holmans P, Marshall H, Kwon J, Meyer D, Ramic D, Shears S, Booth J, DeVrieze FW, Crook R, Hamshere M, Abraham R, Tunstall N, Rice F, Carty S, ... ... Owen MJ, et al. Susceptibility locus for Alzheimer's disease on chromosome 10. Science (New York, N.Y.). 290: 2304-5. PMID 11125144 DOI: 10.1126/Science.290.5500.2304  0.76
2000 Vincent JB, Yuan QP, Schalling M, Adolfsson R, Helena Azevedo M, Macedo A, Bauer A, DallaTorre C, Medeiros HM, Pato MT, Pato CN, Bowen T, Guy CA, Owen MJ, O'Donovan MC, et al. Long repeat tracts at SCA8 in major psychosis American Journal of Medical Genetics - Neuropsychiatric Genetics. 96: 873-876. PMID 11121201 DOI: 10.1002/1096-8628(20001204)96:6<873::Aid-Ajmg37>3.0.Co;2-9  0.76
2000 Kaptein A, Jansen M, Dilaver G, Kitson J, Dash L, Wang E, Owen MJ, Bodmer JL, Tschopp J, Farrow SN. Studies on the interaction between TWEAK and the death receptor WSL-1/TRAMP (DR3). Febs Letters. 485: 135-41. PMID 11094155 DOI: 10.1016/S0014-5793(00)02219-5  0.76
2000 Austin J, Buckland P, Cardno AG, Williams N, Spurlock G, Hoogendoorn B, Zammit S, Jones G, Sanders R, Jones L, McCarthy G, Jones S, Bray NJ, McGuffin P, Owen MJ, et al. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry. 5: 552-7. PMID 11032391 DOI: 10.1038/Sj.Mp.4000761  0.76
2000 Holmes J, Payton A, Barrett JH, Hever T, Fitzpatrick H, Trumper AL, Harrington R, McGuffin P, Owen M, Ollier W, Worthington J, Thapar A. A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder Molecular Psychiatry. 5: 523-530. PMID 11032386 DOI: 10.1038/Sj.Mp.4000751  0.76
2000 Bray NJ, Williams NM, Bowen T, Cardno AG, Gray M, Jones LA, Murphy KC, Sanders RD, Spurlock G, Odonovan MC, Owen MJ. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics. 10: 83-6. PMID 10994646 DOI: 10.1097/00041444-200010020-00005  0.76
2000 Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, et al. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics. 67: 652-63. PMID 10924404 DOI: 10.1086/303041  0.76
2000 Bowen T, Guy CA, Cardno AG, Vincent JB, Kennedy JL, Jones LA, Gray M, Sanders RD, McCarthy G, Murphy KC, Owen MJ, O'Donovan MC. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics. 10: 33-7. PMID 10909126 DOI: 10.1097/00041444-200010010-00006  0.76
2000 Jönsson EG, Norton N, Gustavsson JP, Oreland L, Owen MJ, Sedvall GC. A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers. Journal of Psychiatric Research. 34: 239-44. PMID 10867119 DOI: 10.1016/S0022-3956(00)00013-3  0.76
2000 Austin J, Hoogendoorn B, Buckland P, Speight G, Cardno A, Bowen T, Williams N, Spurlock G, Sanders R, Jones L, Murphy K, McCarthy G, McGuffin P, Owen MJ, O'Donovan MC. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry. 5: 208-12. PMID 10822351 DOI: 10.1038/Sj.Mp.4000693  0.76
2000 Tunstall N, Owen MJ, Williams J, Rice F, Carty S, Lillystone S, Fraser L, Kehoe P, Neill D, Rudrasingham V, Sham P, Lovestone S. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. The British Journal of Psychiatry : the Journal of Mental Science. 176: 156-9. PMID 10755053 DOI: 10.1192/Bjp.176.2.156  0.44
2000 Hoyne GF, Le Roux I, Corsin-Jimenez M, Tan K, Dunne J, Forsyth LM, Dallman MJ, Owen MJ, Ish-Horowicz D, Lamb JR. Serrate1-induced notch signalling regulates the decision between immunity and tolerance made by peripheral CD4(+) T cells. International Immunology. 12: 177-85. PMID 10653853 DOI: 10.1093/Intimm/12.2.177  0.76
1999 Bowen T, Kirov G, Gill M, Spurlock G, Vallada HP, Murray RM, McGuffin P, Collier DA, Owen MJ, Craddock N. Linkage studies of bipolar disorder with chromosome 18 markers American Journal of Medical Genetics - Neuropsychiatric Genetics. 88: 503-509. PMID 10490707 DOI: 10.1002/(Sici)1096-8628(19991015)88:5<503::Aid-Ajmg13>3.0.Co;2-U  0.76
1999 Guy CA, Bowen T, Jones I, McCandless F, Owen MJ, Craddock N, O'Donovan MC. CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder Neurobiology of Disease. 6: 302-307. PMID 10448057 DOI: 10.1006/Nbdi.1999.0249  0.76
1999 Wavrant-De Vrièze F, Crook R, Holmans P, Kehoe P, Owen MJ, Williams J, Roehl K, Laliiri DK, Shears S, Booth J, Wu W, Goate A, Chartier-Harlin MC, Hardy J, Pérez-Tur J. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters. 269: 67-70. PMID 10430506 DOI: 10.1016/S0304-3940(99)00417-6  0.48
1999 Cardno AG, Bowen T, Guy CA, Jones LA, McCarthy G, Williams NM, Murphy KC, Spurlock G, Gray M, Sanders RD, Craddock N, McGuffin P, Owen MJ, O'Donovan MC. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia Biological Psychiatry. 45: 1592-1596. PMID 10376120 DOI: 10.1016/S0006-3223(99)00033-5  0.76
1999 Rudrasingham V, Wavrant-De Vrièze F, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Rice F, Pérez-Tur J, Frigard B, Morris JC, Carty S, Petersen R, Cottel D, ... ... Owen MJ, et al. Alpha-2 macroglobulin gene and Alzheimer disease. Nature Genetics. 22: 17-9; author reply 2. PMID 10319854 DOI: 10.1038/8726  0.48
1999 Hill L, Craig IW, Asherson P, Ball D, Eley T, Ninomiya T, Fisher PJ, Turic D, McGuffin P, Owen MJ, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Thompson LA, et al. DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. Neuroreport. 10: 843-8. PMID 10208558 DOI: 10.1097/00001756-199903170-00032  0.76
1999 Wavrant-DeVrièze F, Rudrasingham V, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Holmans P, Rice F, Pérez-Tur J, Frigard B, Morris JC, Carty S, Cottel D, ... ... Owen MJ, et al. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters. 262: 137-9. PMID 10203250 DOI: 10.1016/S0304-3940(99)00035-X  0.48
1999 Fisher PJ, Turic D, Williams NM, McGuffin P, Asherson P, Ball D, Craig I, Eley T, Hill L, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Plomin R, Owen MJ. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics. 8: 915-22. PMID 10196382 DOI: 10.1093/Hmg/8.5.915  0.76
1999 Franks E, Guy C, Jacobsen N, Bowen T, Owen MJ, O'Donovan MC, Craddock N. Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder American Journal of Medical Genetics - Neuropsychiatric Genetics. 88: 67-70. PMID 10050970 DOI: 10.1002/(Sici)1096-8628(19990205)88:1<67::Aid-Ajmg12>3.0.Co;2-#  0.76
1999 Guy CA, Bowen T, Williams N, Jones IR, McCandless F, McGuffin P, Owen MJ, Craddock N, O'Donovan MC. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder American Journal of Medical Genetics - Neuropsychiatric Genetics. 88: 57-60. PMID 10050968 DOI: 10.1002/(Sici)1096-8628(19990205)88:1<57::Aid-Ajmg10>3.0.Co;2-6  0.76
1999 Kehoe P, Wavrant-De Vrieze F, Crook R, Wu WS, Holmans P, Fenton I, Spurlock G, Norton N, Williams H, Williams N, Lovestone S, Perez-Tur J, Hutton M, Chartier-Harlin MC, Shears S, ... ... Owen MJ, et al. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics. 8: 237-45. PMID 9931331 DOI: 10.1093/Hmg/8.2.237  0.76
1999 Jacobsen NJO, Williams NM, Owen MJ. CHAPTER 5.4 Finding liability genes for schizophrenia Techniques in the Behavioral and Neural Sciences. 13: 805-819. DOI: 10.1016/S0921-0709(99)80061-3  0.76
1999 Williams NM, Owen MJ. Chapter 2.1.5 DNA pooling in allelic association studies Techniques in the Behavioral and Neural Sciences. 13: 122-131. DOI: 10.1016/S0921-0709(99)80013-3  0.76
1999 Williams NM, Fenton I, Owen MJ. Chapter 1.3 PsycheMap - An online database of psychiatric genetics linkage, association, and genome mapping projects Techniques in the Behavioral and Neural Sciences. 13: 31-39. DOI: 10.1016/S0921-0709(99)80007-8  0.76
1998 Wu WS, Holmans P, Wavrant-DeVrièze F, Shears S, Kehoe P, Crook R, Booth J, Williams N, Pérez-Tur J, Roehl K, Fenton I, Chartier-Harlin MC, Lovestone S, Williams J, Hutton M, ... ... Owen MJ, et al. Genetic studies on chromosome 12 in late-onset Alzheimer disease. Jama. 280: 619-22. PMID 9718053 DOI: 10.1001/Jama.280.7.619  0.48
1998 Bowen T, Guy CA, Craddock N, Cardno AG, Williams NM, Spurlock G, Murphy KC, Jones LA, Gray M, Sanders RD, McCarthy G, Chandy KG, Fantino E, Kalman K, Gutman GA, ... ... Owen MJ, et al. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia Molecular Psychiatry. 3: 266-269. PMID 9672903 DOI: 10.1038/Sj.Mp.4000400  0.76
1998 Williams J, Spurlock G, Holmans P, Mant R, Murphy K, Jones L, Cardno A, Asherson P, Blackwood D, Muir W, Meszaros K, Aschauer H, Mallet J, Laurent C, Pekkarinen P, ... ... Owen MJ, et al. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry. 3: 141-9. PMID 9577838 DOI: 10.1038/Sj.Mp.4000376  0.76
1998 Cardno AG, McCandless F, Bowen T, Guy BCA, Jones LA, Murphy KC, McGuffin P, Owen MJ, Craddock N, O'Donovan MC. Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification Psychiatric Genetics. 8: 29-32. PMID 9564685 DOI: 10.1097/00041444-199800810-00005  0.76
1998 Cardno AG, Murphy KC, Jones LA, Cobb AM, Gray J, McGuffin P, Owen MJ. Polydactyly and psychosis. Five cases of co-occurrence. The British Journal of Psychiatry : the Journal of Mental Science. 172: 184-5. PMID 9519074 DOI: 10.1192/Bjp.172.2.184  0.76
1998 Murphy KC, Jones RG, Griffiths E, Thompson PW, Owen MJ. Chromosome 22qll deletions. An under-recognised cause of idiopathic learning disability British Journal of Psychiatry. 172: 180-183. PMID 9519073 DOI: 10.1192/Bjp.172.2.180  0.76
1998 Spurlock G, Williams J, McGuffin P, Aschauer HN, Lenzinger E, Fuchs K, Sieghart WC, Meszaros K, Fathi N, Laurent C, Mallet J, Macciardi F, Pedrini S, Gill M, Hawi Z, ... ... Owen MJ, et al. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics. 81: 24-8. PMID 9514583 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<24::Aid-Ajmg5>3.0.Co;2-N  0.76
1998 Ball D, Hill L, Eley TC, Chorney MJ, Chorney K, Thompson LA, Detterman DK, Benbow C, Lubinski D, Owen M, McGuffin P, Plomin R. Dopamine markers and general cognitive ability. Neuroreport. 9: 347-9. PMID 9507981 DOI: 10.1097/00001756-199801260-00031  0.76
1998 Bowen T, Norton N, Jacobsen NJ, Guy C, Daniels JK, Sanders RD, Cardno AG, Jones LA, Murphy KC, McGuffin P, Craddock N, O'Donovan MC, Owen MJ. Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry. 3: 67-71. PMID 9491815 DOI: 10.1038/Sj.Mp.4000293  0.76
1998 Arranz MJ, Munro J, Owen MJ, Spurlock G, Sham PC, Zhao J, Kirov G, Collier DA, Kerwin RW. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry. 3: 61-6. PMID 9491814 DOI: 10.1038/Sj.Mp.4000348  0.76
1997 Jönsson EG, Goldman D, Spurlock G, Gustavsson JP, Nielsen DA, Linnoila M, Owen MJ, Sedvall GC. Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience. 247: 297-302. PMID 9477008 DOI: 10.1007/Bf02922258  0.76
1997 Craddock N, McKeon P, Moorhead S, Guy C, Harrison D, Mynett-Johnson L, Claffey E, Feldman E, McGuffin P, Owen MJ, O'Donovan MC. Expanded CAG/CTG repeats in bipolar disorder: No correlation with phenotypic measures of illness severity Biological Psychiatry. 42: 876-881. PMID 9359972 DOI: 10.1016/S0006-3223(96)00516-1  0.76
1997 Rees M, Norton N, Jones I, McCandless F, Scourfield J, Holmans P, Moorhead S, Feldman E, Sadler S, Cole T, Redman K, Farmer A, McGuffin P, Owen MJ, Craddock N. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT) Molecular Psychiatry. 2: 398-402. PMID 9322234 DOI: 10.1038/Sj.Mp.4000256  0.76
1997 Williams NM, Cardno AG, Murphy KC, Jones LA, Asherson P, McGuffin P, Owen MJ. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene Psychiatric Genetics. 7: 83-85. PMID 9285966 DOI: 10.1097/00041444-199722000-00005  0.76
1997 Guy C, Bowen T, Daniels JK, Speight G, McKeon P, Mynett-Johnson L, Claffey E, McGuffin P, Owen MJ, Craddock N, O'Donovan MC. Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. The American Journal of Psychiatry. 154: 1146-7. PMID 9247404 DOI: 10.1176/Ajp.154.8.1146  0.76
1997 Daniels JK, Spurlock G, Williams NM, Cardno AG, Jones LA, Murphy KC, Asherson P, Holmans P, Fenton I, McGuffin P, Owen MJ. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics. 74: 319-23. PMID 9184317 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<319::Aid-Ajmg14>3.0.Co;2-R  0.76
1997 Petrill SA, Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Thompson LA, Detterman DK, Benbow C, Lubinski D, Daniels J, Owen M, McGuffin P. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behavior Genetics. 27: 29-31. PMID 9145541 DOI: 10.1023/A:1025659124405  0.76
1997 Speight G, Guy C, Bowen T, Asherson P, McGuffin P, Craddock N, Owen MJ, O'Donovan MC. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia American Journal of Medical Genetics - Neuropsychiatric Genetics. 74: 204-206. PMID 9129726 DOI: 10.1002/(Sici)1096-8628(19970418)74:2<204::Aid-Ajmg19>3.0.Co;2-M  0.76
1997 Cardno AG, Holmans PA, Harvey I, Williams MB, Owen MJ, McGuffin P. Factor-derived subsyndromes of schizophrenia and familial morbid risks. Schizophrenia Research. 23: 231-8. PMID 9075301 DOI: 10.1016/S0920-9964(96)00093-X  0.76
1996 Jacobsen N, Daniels J, Moorhead S, Harrison D, Feldman E, McGuffin R, Owen MJ, Craddock N. Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1 Psychiatric Genetics. 6: 195-199. PMID 9149325 DOI: 10.1097/00041444-199624000-00005  0.76
1996 Cardno AG, Murphy KC, Jones LA, Guy CA, Asherson P, De Azevedo MHP, Da Cruz Coelho IMO, De Macedo E Santos AJF, Pato CN, Mcguffin P, Owen MJ, O'Donovan MC. Expanded CAG/CTG repeats in schizophrenia: A study of clinical correlates British Journal of Psychiatry. 169: 766-771. PMID 8968636 DOI: 10.1192/Bjp.169.6.766  0.76
1996 O'Donovan MC, Guy C, Craddock N, Bowen T, McKeon P, Macedo A, Maier W, Wildenauer D, Aschauer HN, Sorbi S, Feldman E, Mynett-Johnson L, Claffey E, Nacmias B, Valente J, ... ... Owen MJ, et al. Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder. Psychological Medicine. 26: 1145-53. PMID 8931160 DOI: 10.1017/S0033291700035868  0.76
1996 Kehoe P, Williams J, Holmans P, Liddell M, Lovestone S, Holmes C, Powell J, Neal J, Wilcock G, Owen MJ. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. Neuroreport. 7: 2155-8. PMID 8930979 DOI: 10.1097/00001756-199609020-00019  0.44
1996 Kunugi H, Curtis D, Vallada HP, Nanko S, Powell JF, Murray RM, McGuffin P, Owen MJ, Gill M, Collier DA. A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families. Schizophrenia Research. 22: 61-8. PMID 8908691 DOI: 10.1016/0920-9964(96)00048-5  0.76
1996 Gill M, Vallada H, Collier D, Sham P, Holmans P, Murray R, McGuffin P, Nanko S, Owen M, Antonarakis S, Housman D, Kazazian H, Nestadt G, Pulver AE, Straub RE, et al. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics. 67: 40-5. PMID 8678112 DOI: 10.1002/(Sici)1096-8628(19960216)67:1<40::Aid-Ajmg6>3.0.Co;2-W  0.76
1996 Daniels JK, Williams NM, Williams J, Jones LA, Cardno AG, Murphy KC, Spurlock G, Riley B, Scambler P, Asherson P, McGuffin P, Owen MJ. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. The American Journal of Psychiatry. 153: 268-70. PMID 8561211 DOI: 10.1176/Ajp.153.2.268  0.76
1996 Petrill SA, Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Thompson LA, Detterman DK, Benbow C, Lubinski D, Daniels J, Owen MJ, McGuffin P. DNA markers associated with general and specific cognitive abilities Intelligence. 23: 191-203. DOI: 10.1016/S0160-2896(96)90003-3  0.76
1995 Roberts AG, Whatley SD, Daniels J, Holmans P, Fenton L, Owen MJ, Thompson P, Long C, Elder GH. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23 Human Molecular Genetics. 4: 2387-2390. PMID 8634714 DOI: 10.1093/Hmg/4.12.2387  0.76
1995 Dawson E, Powell JF, Sham P, Shaikh S, Taylor C, Clements A, Asherson P, Sargeant M, Collier D, Nanko S, Whatley S, Murray R, McGuffin P, Owen M, Gill M. Systematic search for major genes in schizophrenia: Methodological issues and results from chromosome 12 American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 424-433. PMID 8546156 DOI: 10.1002/Ajmg.1320600513  0.76
1995 Wotton D, Lake RA, Farr CJ, Owen MJ. The high mobility group transcription factor, SOX4, transactivates the human CD2 enhancer Journal of Biological Chemistry. 270: 7515-7522. PMID 7706298 DOI: 10.1074/Jbc.270.13.7515  0.76
1995 Brändle D, Brduscha-Riem K, Hayday AC, Owen MJ, Hengartner H, Pircher H. T cell development and repertoire of mice expressing a single T cell receptor alpha chain. European Journal of Immunology. 25: 2650-5. PMID 7589140 DOI: 10.1002/Eji.1830250937  0.76
1995 Plomin R, McClearn GE, Smith DL, Skuder P, Vignetti S, Chorney MJ, Chorney K, Kasarda S, Thompson LA, Detterman DK, Petrill SA, Daniels J, Owen MJ, McGuffin P. Allelic associations between 100 DNA markers and high versus low IQ Intelligence. 21: 31-48. DOI: 10.1016/0160-2896(95)90037-3  0.76
1995 Skuder P, Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Kasarda S, Thompson LA, Detterman DK, Petrill SA, Daniels J, Owen MJ, McGuffin P. A polymorphism in mitochondrial DNA associated with IQ? Intelligence. 21: 1-11. DOI: 10.1016/0160-2896(95)90035-7  0.76
1994 Wotton D, Ghysdael J, Wang S, Speck NA, Owen MJ. Cooperative binding of Ets-1 and core binding factor to DNA Molecular and Cellular Biology. 14: 840-850. PMID 8264651 DOI: 10.1128/Mcb.14.1.840  0.76
1994 Wen L, Roberts SJ, Viney JL, Wong FS, Mallick C, Findly RC, Peng Q, Craft JE, Owen MJ, Hayday AC. Immunoglobulin synthesis and generalized autoimmunity in mice congenitally deficient in alpha beta(+) T cells. Nature. 369: 654-8. PMID 8208291 DOI: 10.1038/369654A0  0.76
1994 Seth A, Stern LJ, Ottenhoff TH, Engel I, Owen MJ, Lamb JR, Klausner RD, Wiley DC. Binary and ternary complexes between T-cell receptor, class II MHC and superantigen in vitro. Nature. 369: 324-7. PMID 8183371 DOI: 10.1038/369324A0  0.76
1994 Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, Chorney K, Venditti CP, Kasarda S, Thompson LA, Detterman DK. DNA markers associated with high versus low IQ: the IQ Quantitative Trait Loci (QTL) Project. Behavior Genetics. 24: 107-18. PMID 8024528 DOI: 10.1007/Bf01067815  0.76
1994 Thapar A, Gottesman II, Owen MJ, O'Donovan MC, McGuffin P. The genetics of mental retardation. The British Journal of Psychiatry : the Journal of Mental Science. 164: 747-58. PMID 7952981 DOI: 10.1192/Bjp.164.6.747  0.76
1994 Mullan M, Crawford F. The molecular genetics of Alzheimer's disease. Molecular Neurobiology. 9: 15-22. PMID 7888092 DOI: 10.1007/Bf02816100  1
1994 Daniels JK, Owen MJ, McGuffin P, Thompson L, Detterman DK, Chorney M, Chorney K, Smith D, Skuder P, Vignetti S, McClearn GE, Plomin R. IQ and variation in the number of fragile X CGG repeats: No association in a normal sample Intelligence. 19: 45-50. DOI: 10.1016/0160-2896(94)90052-3  0.76
1993 Viney JL, Prosser HM, Palmer DB, Lipoldová M, Lamb JR, Owen MJ. Analysis of T cell repertoire and function in mice transgenic for the human V beta 3 TCR. International Immunology. 5: 1541-9. PMID 8312224 DOI: 10.1093/Intimm/5.12.1541  0.76
1993 Palmer DB, Viney JL, Ritter MA, Hayday AC, Owen MJ. Expression of the alpha beta T-cell receptor is necessary for the generation of the thymic medulla. Developmental Immunology. 3: 175-9. PMID 8281032 DOI: 10.1155/1993/56290  0.76
1993 Shaikh S, Ball D, Craddock NJ, Castle D, Hunt N, Mant R, Owen MJ, Collier D, Gill M. The dopamine D3 receptor gene: no association with bipolar affective disorder. Journal of Medical Genetics. 30: 308-309. PMID 8098068 DOI: 10.1136/Jmg.30.4.308  0.48
1992 Owen MJ. Will schizophrenia become a graveyard for molecular geneticists? Psychological Medicine. 22: 289-293. PMID 1615098 DOI: 10.1017/S0033291700030221  0.76
1992 Prosser HM, Wotton D, Gegonne A, Ghysdael J, Wang S, Speck NA, Owen MJ. A phorbol ester response element within the human T-cell receptor β-chain enhancer Proceedings of the National Academy of Sciences of the United States of America. 89: 9934-9938. PMID 1409722 DOI: 10.1073/Pnas.89.20.9934  0.76
1991 Mant R, Parfitt E, Hardy J, Owen MJ. Mononucleotide repeat polymorphism in the APP gene Nucleic Acids Research. 19: 4572-4572. PMID 1909436 DOI: 10.1093/Nar/19.16.4572-A  0.48
1991 Owen MJ, Goate AM, Hardy JA. A polymorphic microsatellite repeat sequence on chromosome 21 (D21S80). Nucleic Acids Research. 19: 4574. PMID 1886795 DOI: 10.1093/Nar/19.16.4574  0.76
1991 Mullan MJ, Giuffra L, Hardy JA, Ovenstone I, Haynes AR, James LA, Williamson R, Newton PJ, Owen MJ, Roques P. Clinical and pathologic features of chromosome 21-linked familial Alzheimer's disease. Annals of the New York Academy of Sciences. 640: 177-80. PMID 1776736 DOI: 10.1111/J.1749-6632.1991.Tb00212.X  0.76
1991 Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature. 349: 704-6. PMID 1671712 DOI: 10.1038/349704A0  0.48
1990 Goate AM, Hardy JA, Owen MJ, Haynes A, James L, Farrall M, Mullan MJ, Roques P, Rossor MN. Genetics of Alzheimer's disease. Advances in Neurology. 51: 197-8. PMID 2403711  0.76
1990 St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Owen MJ, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0  0.76
1990 Owen MJ, James LA, Hardy JA, Williamson R, Goate AM. Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21. American Journal of Human Genetics. 46: 316-22. PMID 2301399  0.76
1990 Lake RA, Wotton D, Owen MJ. A 3′ transcriptional enhancer regulates tissue-specific expression of the human CD2 gene Embo Journal. 9: 3129-3136. PMID 2209539 DOI: 10.1002/J.1460-2075.1990.Tb07510.X  0.76
1990 Owen MJ, Mullan MJ. Molecular genetic studies of manic-depression and schizophrenia. Trends in Neurosciences. 13: 29-31. PMID 1688672 DOI: 10.1016/0166-2236(90)90059-J  0.92
1989 Hardy JA, Goate AM, Owen MJ, Mullan MJ, Rossor MN, Pearson RC. Modelling the occurrence and pathology of Alzheimer's disease. Neurobiology of Aging. 10: 429-31; discussion 4. PMID 2812201 DOI: 10.1016/0197-4580(89)90084-5  0.76
1989 John S, Banting GS, Goodfellow PN, Owen MJ. Surface expression of the T cell receptor complex requires charged residues within the α chain transmembrane region European Journal of Immunology. 19: 335-339. PMID 2784768 DOI: 10.1002/EJI.1830190218  0.76
1989 Hardy J, Goate A, Owen MJ, Rossor M. Presenile dementia associated with mosaic trisomy 21 in a patient with a Down syndrome child. The Lancet. 334: 743. PMID 2570989 DOI: 10.1016/S0140-6736(89)90805-2  0.48
1989 Wotton D, Flanagan BF, Owen MJ. Chromatin configuration of the human CD2 gene locus during T-cell development Proceedings of the National Academy of Sciences of the United States of America. 86: 4195-4199. PMID 2567000 DOI: 10.1073/Pnas.86.11.4195  0.76
1989 Goate AM, Haynes AR, Owen MJ, Farrall M, James LA, Lai LY, Mullan MJ, Roques P, Rossor MN, Williamson R. Predisposing locus for Alzheimer's disease on chromosome 21. Lancet. 1: 352-5. PMID 2563508 DOI: 10.1016/S0140-6736(89)91725-X  0.92
1989 Hardy JA, Owen MJ, Goate AM, James LA, Haynes AR, Rossor MN, Roques P, Mullan MJ. Molecular genetics of Alzheimer's disease. Biochemical Society Transactions. 17: 75-6. PMID 2523829 DOI: 10.1042/Bst0170075  0.76
1989 Goate AM, Hardy JA, Owen MJ. The genetic aetiology of alzheimer's disease International Review of Psychiatry. 1: 243-248. DOI: 10.3109/09540268909089418  0.76
1988 Owen MJ. Polymorphic DNA markers and mental disease Psychological Medicine. 18: 529-533. PMID 2903511 DOI: 10.1017/S0033291700008217  0.76
1988 Lang G, Wotton D, Owen MJ, Sewell WA, Brown MH, Mason DY, Crumpton MJ, Kioussis D. The structure of the human CD2 gene and its expression in transgenic mice. The Embo Journal. 7: 1675-82. PMID 2901953 DOI: 10.1002/J.1460-2075.1988.Tb02995.X  0.76
1987 Owen MJ, Crumpton MJ. The role of class I and II antigens in T cell recognition. British Medical Bulletin. 43: 228-40. PMID 3315099 DOI: 10.1093/Oxfordjournals.Bmb.A072173  0.76
1987 Owen MJ, Crumpton MJ, Dunne J, Krissansen G, Lamb J, Sewell W. Structure and expression of genes involved in T lymphocyte recognition and activation. Advances in Experimental Medicine and Biology. 225: 223-31. PMID 2899379 DOI: 10.1007/978-1-4684-5442-0_19  0.76
1987 Sewell WA, Brown MH, Owen MJ, Fink PJ, Kozak CA, Crumpton MJ. The murine homologue of the T lymphocyte CD2 antigen: molecular cloning, chromosome assignment and cell surface expression. European Journal of Immunology. 17: 1015-20. PMID 2440689 DOI: 10.1002/Eji.1830170718  0.76
1986 Sewell WA, Brown MH, Dunne J, Owen MJ, Crumpton MJ. Molecular cloning of the human T-lymphocyte surface CD2 (T11) antigen. Proceedings of the National Academy of Sciences of the United States of America. 83: 8718-22. PMID 3490670 DOI: 10.1073/Pnas.83.22.8718  0.76
1985 Collins MK, Tanigawa G, Kissonerghis AM, Ritter M, Price KM, Tonegawa S, Owen MJ. Regulation of T-cell receptor gene expression in human T-cell development. Proceedings of the National Academy of Sciences of the United States of America. 82: 4503-7. PMID 3874403 DOI: 10.1073/pnas.82.13.4503  0.76
1983 Owen MJ. Synthetic peptides and their impact on immunology Immunology Today. 4: 190-191. DOI: 10.1016/0167-5699(83)90079-8  0.76
1980 Owen MJ, Crumpton MJ. Biochemistry of major human histocompatibility antigens. Immunology Today. 1: 117-22. PMID 25290354 DOI: 10.1016/0167-5699(80)90048-1  0.76
1980 Owen MJ, Knott JC, Crumpton MJ. Labeling of lymphocyte surface antigens by the lipophilic, photoactivatable reagent hexanoyldiiodo-N-(4-azido-2-nitrophenyl)tyramine. Biochemistry. 19: 3092-9. PMID 7397120 DOI: 10.1021/Bi00554A040  0.76
1978 Owen MJ, Auger J, Barber BH, Edwards AJ, Walsh FS, Crumpton MJ. Actin may be present on the lymphocyte surface. Proceedings of the National Academy of Sciences of the United States of America. 75: 4484-8. PMID 309133 DOI: 10.1073/Pnas.75.9.4484  0.76
Show low-probability matches.