Heron EA - Search Results

1

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. Among authors: heron ea. 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.

2

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.

Kenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW. Kenny EM, et al. Mol Psychiatry. 2014 Aug;19(8):872-9. doi: 10.1038/mp.2013.127. Epub 2013 Oct 15. Mol Psychiatry. 2014. PMID: 24126926

3

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: heron ea. Br J Psychiatry. 2020 May;216(5):275-279. doi: 10.1192/bjp.2019.262. Br J Psychiatry. 2020. PMID: 31964429

4

Converting single nucleotide variants between genome builds: from cautionary tale to solution.

Ormond C, Ryan NM, Corvin A, Heron EA. Ormond C, et al. Among authors: heron ea. Brief Bioinform. 2021 Sep 2;22(5):bbab069. doi: 10.1093/bib/bbab069. Brief Bioinform. 2021. PMID: 33822888 Free PMC article.

5

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.

6

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

Ryan NM, Heron EA. Ryan NM, et al. Among authors: heron ea. 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.

7

The SNP ratio test: pathway analysis of genome-wide association datasets.

O'Dushlaine C, Kenny E, Heron EA, Segurado R, Gill M, Morris DW, Corvin A. O'Dushlaine C, et al. Among authors: heron ea. Bioinformatics. 2009 Oct 15;25(20):2762-3. doi: 10.1093/bioinformatics/btp448. Epub 2009 Jul 20. Bioinformatics. 2009. PMID: 19620097

8

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.

O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D; International Schizophrenia Consortium; Corvin A. O'Dushlaine C, et al. Mol Psychiatry. 2011 Mar;16(3):286-92. doi: 10.1038/mp.2010.7. Epub 2010 Feb 16. Mol Psychiatry. 2011. PMID: 20157312

9

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset.

Heron EA, Cormican P, Donohoe G, O'Neill FA, Kendler KS, Riley BP; Wellcome Trust Case Control Consortium 2; Gill M, Corvin AP, Morris DW. Heron EA, et al. Schizophr Res. 2014 Apr;154(1-3):79-82. doi: 10.1016/j.schres.2014.01.038. Epub 2014 Feb 20. Schizophr Res. 2014. PMID: 24560374 Free PMC article.

10

The phenotypic manifestations of rare CNVs in schizophrenia.

Merikangas AK, Segurado R, Cormican P, Heron EA, Anney RJ, Moore S, Kelleher E, Hargreaves A, Anderson-Schmidt H, Gill M, Gallagher L, Corvin A. Merikangas AK, et al. Among authors: heron ea. Schizophr Res. 2014 Sep;158(1-3):255-60. doi: 10.1016/j.schres.2014.06.016. Epub 2014 Jul 4. Schizophr Res. 2014. PMID: 24999052

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