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Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Foley C, Heron EA, Harold D, Walters J, Owen M, O'Donovan M, Sebat J, Kelleher E, Mooney C, Durand A, Pinto C, Cormican P, Morris D, Donohoe G, Gill M, Gallagher L, Corvin A. Foley C, et al. Among authors: harold d. Br J Psychiatry. 2020 May;216(5):275-279. doi: 10.1192/bjp.2019.262. Br J Psychiatry. 2020. PMID: 31964429
Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia.
Hubbard L, Rees E, Morris DW, Lynham AJ, Richards AL, Pardiñas AF, Legge SE, Harold D, Zammit S, Corvin AC, Gill MG, Hall J, Holmans P, O'Donovan MC, Owen MJ, Donohoe G, Kirov G, Pocklington A, Walters JTR. Hubbard L, et al. Among authors: harold d. Biol Psychiatry. 2021 Jul 1;90(1):28-34. doi: 10.1016/j.biopsych.2020.11.025. Epub 2020 Dec 19. Biol Psychiatry. 2021. PMID: 33678419
Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression.
Whitton L, Cosgrove D, Clarkson C, Harold D, Kendall K, Richards A, Mantripragada K, Owen MJ, O'Donovan MC, Walters J, Hartmann A, Konte B, Rujescu D; WTCCC2; Gill M, Corvin A, Rea S, Donohoe G, Morris DW. Whitton L, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2016 Dec;171(8):1170-1179. doi: 10.1002/ajmg.b.32503. Epub 2016 Oct 20. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27762073
Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory.
Cosgrove D, Mothersill O, Kendall K, Konte B, Harold D, Giegling I, Hartmann A, Richards A, Mantripragada K; Wellcome Trust Case Control Consortium; Owen MJ, O'Donovan MC, Gill M, Rujescu D, Walters J, Corvin A, Morris DW, Donohoe G. Cosgrove D, et al. Among authors: harold d. Neuropsychopharmacology. 2017 Dec;42(13):2612-2622. doi: 10.1038/npp.2017.123. Epub 2017 Jun 13. Neuropsychopharmacology. 2017. PMID: 28607492 Free PMC article.
Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls.
Cosgrove D, Mothersill DO, Whitton L, Harold D, Kelly S, Holleran L, Holland J, Anney R; Wellcome Trust Case Control Consortium; Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, Morris DW, Donohoe G. Cosgrove D, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):369-376. doi: 10.1002/ajmg.b.32620. Epub 2018 Feb 8. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29418072
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Donohoe G, Gill M, Corvin A, Morris DW. Harold D, et al. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. doi: 10.1002/ajmg.b.32716. Epub 2019 Feb 23. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30801977 Free PMC article.
Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls.
Holland JF, Cosgrove D, Whitton L, Harold D, Corvin A, Gill M, Mothersill DO, Morris DW, Donohoe G. Holland JF, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2020 Dec;183(8):445-453. doi: 10.1002/ajmg.b.32820. Epub 2020 Sep 12. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 32918526
97 results