Dr Desmond Campbell

  • Research Associate (MRC/CSO Social & Public Health Sciences Unit)

Publications

List by: Type | Date

Jump to: 2018 | 2016 | 2015 | 2014 | 2013 | 2012 | 2010 | 2009 | 2008 | 2007 | 2006
Number of items: 31.

2018

Graham, L. A., Aman, A., Campbell, D. D. , Augley, J., Graham, D. , McBride, M. W. , Fraser, N. J., Ferreri, N. R., Dominiczak, A. F. and Padmanabhan, S. (2018) Salt stress in the renal tubules is linked to TAL specific expression of uromodulin and an upregulation of heat shock genes. Physiological Genomics, 50(11), pp. 964-972. (doi:10.1152/physiolgenomics.00057.2018) (PMID:30216136)

Campbell, D. D. , Li, Y. and Sham, P. C. (2018) Multifactorial disease risk calculator: risk prediction for multifactorial disease pedigrees. Genetic Epidemiology, 42(2), pp. 130-133. (doi:10.1002/gepi.22101) (PMID:29178360)

2016

Porsch, R. M. et al. (2016) Sacral agenesis: a pilot whole exome sequencing and copy number study. BMC Medical Genetics, 17(1), 98. (doi:10.1186/s12881-016-0359-2) (PMID:28007035) (PMCID:PMC5178083)

Wong, J. K. L. et al. (2016) Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes. BMC Medical Genomics, 9(1), 75. (doi:10.1186/s12920-016-0236-z) (PMID:27955658) (PMCID:PMC5154011)

Trotta, A. et al. (2016) Interplay between schizophrenia polygenic risk score and childhood adversity in first-presentation psychotic disorder: a pilot study. PLoS ONE, 11(9), e0163319. (doi:10.1371/journal.pone.0163319) (PMID:27648571) (PMCID:PMC5029892)

Li, Y. et al. (2016) Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study. Spine Journal, 16(9), pp. 1079-1089. (doi:10.1016/j.spinee.2016.04.020) (PMID:27157501)

Mak, T. S. H., Kwan, J. S. H., Campbell, D. D. and Sham, P. C. (2016) Local true discovery rate weighted polygenic scores using GWAS summary data. Behavior Genetics, 46(4), pp. 573-582. (doi:10.1007/s10519-015-9770-2) (PMID:26747043)

Zhou, P. et al. (2016) A single nucleotide variant in HNF-1β is associated with maturity-onset diabetes of the young in a large Chinese family. Iranian Journal of Public Health, 45(2), pp. 170-178. (PMID:27114981) (PMCID:PMC4841871)

2015

Toulopoulou, T. et al. (2015) Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry, 20(11), pp. 1386-1396. (doi:10.1038/mp.2014.152) (PMID:25450228)

Toulopoulou, T. et al. (2015) Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry, 20(11), p. 1482. (doi:10.1038/mp.2015.117) (PMID:26283640)

Campbell, D. D. , Porsch, R. M., Cherny, S. S., Capra, V., Merello, E., De Marco, P., Sham, P. C. and Garcia-Barceló, M.-M. (2015) Cost effective assay choice for rare disease study designs. Orphanet Journal of Rare Diseases, 10(1), p. 10. (doi:10.1186/s13023-015-0226-9) (PMID:25648394) (PMCID:PMC4334400)

Yu, D. et al. (2015) Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette’s syndrome and OCD. American Journal of Psychiatry, 172(1), pp. 82-93. (doi:10.1176/appi.ajp.2014.13101306) (PMID:25158072) (PMCID:PMC4282594)

2014

Dickson, H., Cullen, A. E., Reichenberg, A., Hodgins, S., Campbell, D. D. , Morris, R. G. and Laurens, K. R. (2014) Cognitive impairment among children at-risk for schizophrenia. Journal of Psychiatric Research, 50, pp. 92-99. (doi:10.1016/j.jpsychires.2013.12.003) (PMID:24373930)

Iyegbe, C., Campbell, D. , Butler, A., Ajnakina, O. and Sham, P. (2014) The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research. Social Psychiatry and Psychiatric Epidemiology, 49(2), pp. 169-182. (doi:10.1007/s00127-014-0823-2) (PMID:24435092)

Campbell, D. D. (2014) Error in sample size formula. Journal of Human Reproductive Sciences, 7(2), p. 155. (doi:10.4103/0974-1208.138878) (PMCID:PMC4150146)

Campbell, D. D. (2014) Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin, 40(4), pp. 729-736. (doi:10.1093/schbul/sbu069) (PMID:24860087)

2013

Keller, M. C. et al. (2013) Partitioning the heritability of Tourette Syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genetics, 9(10), e1003864. (doi:10.1371/journal.pgen.1003864) (PMID:24204291) (PMCID:PMC3812053)

Scharf, J. M. et al. (2013) Genome-wide association study of Tourette's syndrome. Molecular Psychiatry, 18(6), pp. 721-728. (doi:10.1038/mp.2012.69) (PMID:22889924) (PMCID:PMC3605224)

Zhang, G. et al. (2013) CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. PLoS ONE, 8(3), e59061. (doi:10.1371/journal.pone.0059061) (PMID:23533600) (PMCID:PMC3606459)

2012

Reich, D. et al. (2012) Corrigendum: Reconstructing Native American population history. Nature, 491(7423), p. 288. (doi:10.1038/nature11667)

Reich, D. et al. (2012) Reconstructing Native American population history. Nature, 488(7411), pp. 370-374. (doi:10.1038/nature11258) (PMID:22801491) (PMCID:PMC3615710)

Campbell, D. D. et al. (2012) Amerind ancestry, socioeconomic status and the genetics of type 2 diabetes in a Colombian population. PLoS ONE, 7(4), e33570. (doi:10.1371/journal.pone.0033570) (PMID:22529894) (PMCID:PMC3328483)

Huezo-Diaz, P. et al. (2012) CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP. Journal of Psychopharmacology, 26(3), pp. 398-407. (doi:10.1177/0269881111414451) (PMID:21926427) (PMCID:21926427)

2010

Campbell, D. D. , Sham, P. C., Knight, J., Wickham, H. and Landau, S. (2010) Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates. Genetic Epidemiology, 34(2), pp. 159-170. (doi:10.1002/gepi.20446) (PMID:19771574)

2009

Perroud, N. et al. (2009) Suicidal ideation during treatment of depression with escitalopram and nortriptyline in Genome-Based Therapeutic Drugs for Depression (GENDEP): a clinical trial. BMC Medicine, 7(1), 60. (doi:10.1186/1741-7015-7-60) (PMID:19832967) (PMCID:PMC2768737)

Florez, J. C. et al. (2009) Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes. Diabetologia, 52(8), pp. 1528-1536. (doi:10.1007/s00125-009-1412-x) (PMID:19526211) (PMCID:PMC3113605)

2008

Chen, W. et al. (2008) DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), pp. 1450-1460. (doi:10.1002/ajmg.b.30672) (PMID:18189238)

Zhou, K. et al. (2008) Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological Psychiatry, 64(7), pp. 571-576. (doi:10.1016/j.biopsych.2008.02.024) (PMID:18439570) (PMCID:PMC3589988)

Asherson, P. et al. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13(5), pp. 514-521. (doi:10.1038/sj.mp.4002140) (PMID:18180756)

2007

Campbell, D.D. , Rijsdijk, F.V. and Sham, P.C. (2007) Computation of individual latent variable scores from data with multiple missingness patterns. Behavior Genetics, 37(2), pp. 408-422. (doi:10.1007/s10519-006-9123-2) (PMID:17120140)

2006

Brookes, K. et al. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11(10), pp. 934-953. (doi:10.1038/sj.mp.4001869) (PMID:16894395)

This list was generated on Mon Feb 18 07:13:06 2019 GMT.
Jump to: Articles
Number of items: 31.

Articles

Graham, L. A., Aman, A., Campbell, D. D. , Augley, J., Graham, D. , McBride, M. W. , Fraser, N. J., Ferreri, N. R., Dominiczak, A. F. and Padmanabhan, S. (2018) Salt stress in the renal tubules is linked to TAL specific expression of uromodulin and an upregulation of heat shock genes. Physiological Genomics, 50(11), pp. 964-972. (doi:10.1152/physiolgenomics.00057.2018) (PMID:30216136)

Campbell, D. D. , Li, Y. and Sham, P. C. (2018) Multifactorial disease risk calculator: risk prediction for multifactorial disease pedigrees. Genetic Epidemiology, 42(2), pp. 130-133. (doi:10.1002/gepi.22101) (PMID:29178360)

Porsch, R. M. et al. (2016) Sacral agenesis: a pilot whole exome sequencing and copy number study. BMC Medical Genetics, 17(1), 98. (doi:10.1186/s12881-016-0359-2) (PMID:28007035) (PMCID:PMC5178083)

Wong, J. K. L. et al. (2016) Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes. BMC Medical Genomics, 9(1), 75. (doi:10.1186/s12920-016-0236-z) (PMID:27955658) (PMCID:PMC5154011)

Trotta, A. et al. (2016) Interplay between schizophrenia polygenic risk score and childhood adversity in first-presentation psychotic disorder: a pilot study. PLoS ONE, 11(9), e0163319. (doi:10.1371/journal.pone.0163319) (PMID:27648571) (PMCID:PMC5029892)

Li, Y. et al. (2016) Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study. Spine Journal, 16(9), pp. 1079-1089. (doi:10.1016/j.spinee.2016.04.020) (PMID:27157501)

Mak, T. S. H., Kwan, J. S. H., Campbell, D. D. and Sham, P. C. (2016) Local true discovery rate weighted polygenic scores using GWAS summary data. Behavior Genetics, 46(4), pp. 573-582. (doi:10.1007/s10519-015-9770-2) (PMID:26747043)

Zhou, P. et al. (2016) A single nucleotide variant in HNF-1β is associated with maturity-onset diabetes of the young in a large Chinese family. Iranian Journal of Public Health, 45(2), pp. 170-178. (PMID:27114981) (PMCID:PMC4841871)

Toulopoulou, T. et al. (2015) Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry, 20(11), pp. 1386-1396. (doi:10.1038/mp.2014.152) (PMID:25450228)

Toulopoulou, T. et al. (2015) Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort. Molecular Psychiatry, 20(11), p. 1482. (doi:10.1038/mp.2015.117) (PMID:26283640)

Campbell, D. D. , Porsch, R. M., Cherny, S. S., Capra, V., Merello, E., De Marco, P., Sham, P. C. and Garcia-Barceló, M.-M. (2015) Cost effective assay choice for rare disease study designs. Orphanet Journal of Rare Diseases, 10(1), p. 10. (doi:10.1186/s13023-015-0226-9) (PMID:25648394) (PMCID:PMC4334400)

Yu, D. et al. (2015) Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette’s syndrome and OCD. American Journal of Psychiatry, 172(1), pp. 82-93. (doi:10.1176/appi.ajp.2014.13101306) (PMID:25158072) (PMCID:PMC4282594)

Dickson, H., Cullen, A. E., Reichenberg, A., Hodgins, S., Campbell, D. D. , Morris, R. G. and Laurens, K. R. (2014) Cognitive impairment among children at-risk for schizophrenia. Journal of Psychiatric Research, 50, pp. 92-99. (doi:10.1016/j.jpsychires.2013.12.003) (PMID:24373930)

Iyegbe, C., Campbell, D. , Butler, A., Ajnakina, O. and Sham, P. (2014) The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research. Social Psychiatry and Psychiatric Epidemiology, 49(2), pp. 169-182. (doi:10.1007/s00127-014-0823-2) (PMID:24435092)

Campbell, D. D. (2014) Error in sample size formula. Journal of Human Reproductive Sciences, 7(2), p. 155. (doi:10.4103/0974-1208.138878) (PMCID:PMC4150146)

Campbell, D. D. (2014) Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophrenia Bulletin, 40(4), pp. 729-736. (doi:10.1093/schbul/sbu069) (PMID:24860087)

Keller, M. C. et al. (2013) Partitioning the heritability of Tourette Syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genetics, 9(10), e1003864. (doi:10.1371/journal.pgen.1003864) (PMID:24204291) (PMCID:PMC3812053)

Scharf, J. M. et al. (2013) Genome-wide association study of Tourette's syndrome. Molecular Psychiatry, 18(6), pp. 721-728. (doi:10.1038/mp.2012.69) (PMID:22889924) (PMCID:PMC3605224)

Zhang, G. et al. (2013) CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. PLoS ONE, 8(3), e59061. (doi:10.1371/journal.pone.0059061) (PMID:23533600) (PMCID:PMC3606459)

Reich, D. et al. (2012) Corrigendum: Reconstructing Native American population history. Nature, 491(7423), p. 288. (doi:10.1038/nature11667)

Reich, D. et al. (2012) Reconstructing Native American population history. Nature, 488(7411), pp. 370-374. (doi:10.1038/nature11258) (PMID:22801491) (PMCID:PMC3615710)

Campbell, D. D. et al. (2012) Amerind ancestry, socioeconomic status and the genetics of type 2 diabetes in a Colombian population. PLoS ONE, 7(4), e33570. (doi:10.1371/journal.pone.0033570) (PMID:22529894) (PMCID:PMC3328483)

Huezo-Diaz, P. et al. (2012) CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP. Journal of Psychopharmacology, 26(3), pp. 398-407. (doi:10.1177/0269881111414451) (PMID:21926427) (PMCID:21926427)

Campbell, D. D. , Sham, P. C., Knight, J., Wickham, H. and Landau, S. (2010) Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates. Genetic Epidemiology, 34(2), pp. 159-170. (doi:10.1002/gepi.20446) (PMID:19771574)

Perroud, N. et al. (2009) Suicidal ideation during treatment of depression with escitalopram and nortriptyline in Genome-Based Therapeutic Drugs for Depression (GENDEP): a clinical trial. BMC Medicine, 7(1), 60. (doi:10.1186/1741-7015-7-60) (PMID:19832967) (PMCID:PMC2768737)

Florez, J. C. et al. (2009) Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes. Diabetologia, 52(8), pp. 1528-1536. (doi:10.1007/s00125-009-1412-x) (PMID:19526211) (PMCID:PMC3113605)

Chen, W. et al. (2008) DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(8), pp. 1450-1460. (doi:10.1002/ajmg.b.30672) (PMID:18189238)

Zhou, K. et al. (2008) Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological Psychiatry, 64(7), pp. 571-576. (doi:10.1016/j.biopsych.2008.02.024) (PMID:18439570) (PMCID:PMC3589988)

Asherson, P. et al. (2008) A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13(5), pp. 514-521. (doi:10.1038/sj.mp.4002140) (PMID:18180756)

Campbell, D.D. , Rijsdijk, F.V. and Sham, P.C. (2007) Computation of individual latent variable scores from data with multiple missingness patterns. Behavior Genetics, 37(2), pp. 408-422. (doi:10.1007/s10519-006-9123-2) (PMID:17120140)

Brookes, K. et al. (2006) The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry, 11(10), pp. 934-953. (doi:10.1038/sj.mp.4001869) (PMID:16894395)

This list was generated on Mon Feb 18 07:13:06 2019 GMT.