Ryan N - Search Results

1

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.

2

Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disorders.

Bach S, Ryan NM, Guasoni P, Corvin AP, El-Nemr RA, Khan D, Sanfeliu A, Tropea D. Bach S, et al. Sci Rep. 2020 Dec 17;10(1):22255. doi: 10.1038/s41598-020-79268-0. Sci Rep. 2020. PMID: 33335218 Free PMC article.

3

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.

4

Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review.

Ryan NM, Heron EA. Ryan NM, et al. J Appl Genet. 2023 May;64(2):303-317. doi: 10.1007/s13353-022-00742-8. Epub 2023 Jan 30. J Appl Genet. 2023. PMID: 36710277 Free PMC article. Review.

5

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.

6

Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia.

Ormond C, Ryan NM, Heron EA, Gill M, Byerley W, Corvin A. Ormond C, et al. Biol Psychiatry Glob Open Sci. 2023 Feb 16;3(4):797-802. doi: 10.1016/j.bpsgos.2023.02.002. eCollection 2023 Oct. Biol Psychiatry Glob Open Sci. 2023. PMID: 37881554 Free PMC article.

7

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders.

Ryan NM, Lihm J, Kramer M, McCarthy S, Morris SW, Arnau-Soler A, Davies G, Duff B, Ghiban E, Hayward C, Deary IJ, Blackwood DHR, Lawrie SM, McIntosh AM, Evans KL, Porteous DJ, McCombie WR, Thomson PA. Ryan NM, et al. Mol Psychiatry. 2018 Dec;23(12):2254-2265. doi: 10.1038/s41380-018-0087-4. Epub 2018 Jun 7. Mol Psychiatry. 2018. PMID: 29880880 Free PMC article.

8

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

Howard DM, Hall LS, Hafferty JD, Zeng Y, Adams MJ, Clarke TK, Porteous DJ, Nagy R, Hayward C, Smith BH, Murray AD, Ryan NM, Evans KL, Haley CS, Deary IJ, Thomson PA, McIntosh AM. Howard DM, et al. Transl Psychiatry. 2017 Nov 30;7(11):1263. doi: 10.1038/s41398-017-0010-9. Transl Psychiatry. 2017. PMID: 29187746 Free PMC article.

9

SuRFing the genomics wave: an R package for prioritising SNPs by functionality.

Ryan NM, Morris SW, Porteous DJ, Taylor MS, Evans KL. Ryan NM, et al. Genome Med. 2014 Oct 14;6(10):79. doi: 10.1186/s13073-014-0079-1. eCollection 2014. Genome Med. 2014. PMID: 25400697 Free PMC article.

10

Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disorders.

Walker RM, Sussmann JE, Whalley HC, Ryan NM, Porteous DJ, McIntosh AM, Evans KL. Walker RM, et al. Bipolar Disord. 2016 Aug;18(5):410-22. doi: 10.1111/bdi.12415. Epub 2016 Jul 21. Bipolar Disord. 2016. PMID: 27440233 Free PMC article.

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