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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 0 |
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Polygenic overlap with body-mass index improves prediction of treatment-resistant schizophrenia.
Psychiatry Res. 2023 Jul;325:115217. doi: 10.1016/j.psychres.2023.115217. Epub 2023 Apr 23.
Psychiatry Res. 2023.
PMID: 37146461
Free PMC article.
Converting single nucleotide variants between genome builds: from cautionary tale to solution.
Ormond C, Ryan NM, Corvin A, Heron EA.
Ormond C, et al.
Brief Bioinform. 2021 Sep 2;22(5):bbab069. doi: 10.1093/bib/bbab069.
Brief Bioinform. 2021.
PMID: 33822888
Free PMC article.
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Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction.
Ryan N, Ormond C, Chang YC, Contreras J, Raventos H, Gill M, Heron E, Mathews CA, Corvin A.
Ryan N, et al.
Mol Psychiatry. 2022 Dec;27(12):5020-5027. doi: 10.1038/s41380-022-01771-9. Epub 2022 Oct 12.
Mol Psychiatry. 2022.
PMID: 36224258
Free PMC article.
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Investigating the dark-side of the genome: a barrier to human disease variant discovery?
Ryan NM, Corvin A.
Ryan NM, et al.
Biol Res. 2023 Jul 20;56(1):42. doi: 10.1186/s40659-023-00455-0.
Biol Res. 2023.
PMID: 37468985
Free PMC article.
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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.
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