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Dr. Elizabeth Heron

Assistant Professor (Psychiatry)
TRINITY CENTRE, S J H


  Bayesian Inference   Bioinformatics   Biostatistical methods   Genetics   MATHEMATICAL MODELLING   Statistics
Details Date From Date To
Fellow of the Royal Statistical Society 2005 Present
Chapter 2 Schizophrenia genomics in, editor(s)Evangelia Eirini Tsermpini, Martin Alda, and George P. Patrinos , Psychiatric Genomics, 2022, [Ryan NM, Ormond C, Brady P, Heron EA, Corvin A], Book Chapter, PUBLISHED  DOI
McGrath J, Cawley B, McTiernan D, Marques L, Goncerz E, Heron EA, Madden J, Bond L, Quinn C, Mulholland K, Dowling B , Service user satisfaction with care in a specialist service for young people with attention deficit hyperactivity disorder., Irish Journal of Psychological Medicine, 2022, Journal Article, PUBLISHED  DOI
Lombard, Nolan & Heron, A Scoping Review of the Use of Rasch Analysis Methodology to strengthen Self-Report Occupational Therapy Mental Health Measures, Occupational Therapy in Mental Heath, 2022, Journal Article, PUBLISHED  DOI
Lombard Kim, Nolan Clodagh & Heron Elizabeth A., Refining the psychometirc properties of the Trinity Student Occupational Performance Profile - A self-report measure of occupational difficulties within the student role, British Journal of Occupational Therapy, 2022, p1 - 10, Journal Article, PUBLISHED  DOI
Ryan N, Ormond C, Chang YC, Contreras J, Raventos H, Gill M, Heron E, Mathews CA, & Corvin A, Identity-by-descent analysis of a large Tourette's syndrome pedigree from Costa Rica implicates genes involved in neuronal development and signal transduction, Molecular Psychiatry, 2022, Journal Article, PUBLISHED
O'Toole SA, Huang Y, Norris L, Power Foley M, Shireen R, McDonald S, Kamran W, Ibrahim N, Ward M, Thompson C, Murphy C, D'Arcy T, Farah N, Heron E, O'Leary JJ, Abu Saadeh F, Gleeson N., HE4 and CA125 as preoperative risk stratifiers for lymph node metastasis in endometrioid carcinoma of the endometrium: A retrospective study in a cohort with histological proof of lymph node status., Gynecologic oncology, 2021, Journal Article, PUBLISHED  DOI
Forde E, Leech M, Robert C, Heron E, Marignol L, Influence of Inter-Observer Delineation Variability on Radiomic Features of the Parotid Gland, Physica Medica, (82), 2021, p240 - 248, Journal Article, PUBLISHED  DOI
Ormond C, Ryan NM, Corvin A, Heron EA., Converting single nucleotide variants between genome builds: from cautionary tale to solution., Briefings in bioinformatics, 2021, Journal Article, PUBLISHED  DOI
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., Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study., The British journal of psychiatry : the journal of mental science, 216, (5), 2020, p275-279 , Journal Article, PUBLISHED  TARA - Full Text  DOI
Kelleher E, McNamara P, Dunne J, Fitzmaurice B, Heron EA, Whitty P, Walsh R, Mooney C, Hogan D, Conlon N, Gill M, Vincent A, Doherty CP, Corvin A., Prevalence of N-Methyl-d-Aspartate Receptor antibody (NMDAR-Ab) encephalitis in patients with first episode psychosis and treatment resistant schizophrenia on clozapine, a population based study., Schizophrenia research, 222, 2020, p455-461 , Journal Article, PUBLISHED  DOI
  

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C Ormond, NM Ryan, W Byerley, A Corvin, EA Heron, A Bayesian framework to model co-segregation in pedigrees using next-generation sequencing data, HUMAN HEREDITY, 50th European Mathematical Genetics Meeting, Cambridge, April 21-22, 2022, 87, Karger, 2022, pp17 - 17, Oral Presentation, PUBLISHED
C Ormond, N Ryan, W Byerley, A Corvin, E Heron, T16. A Bayesian framework to model pedigree-based causality using next-generation sequencing data, European Neuropsychopharmacology , Abstracts of the World Congress of Psychiatric Genetics, September 13-17, 63, 2022, ppe176 - e177, Poster, PUBLISHED
Cathal Ormond Niamh M. Ryan William Byerley Elizabeth A Heron Michael Gill Aiden Corvin , TU74. A CO-SEGREGATION ANALYSIS OF ULTRA-RARE VARIANTS IN FAMILIES MULTIPLY AFFECTED BY SCHIZOPHRENIA USING WHOLE GENOME SEQUENCING, European Neuropsychopharmacology, 2021, Poster, PUBLISHED
Niamh M. Ryan Cathal Ormond Kazima Bulaeva Elizabeth A Heron Michael Gill Aiden Corvin , TH75. SEQUENCING STUDY OF A CONSANGUINEOUS PEDIGREE WITH A HIGH LOAD OF SCHIZOPHRENIA, European Neuropsychopharmacology, 2021, Poster, PUBLISHED
C Ormond, A Corvin, E Heron, A Comparison of Two Software Tools for Disease-Gene Prioritization for Family-Based Sequencing Studies, Human Heredity, 84, Karger, 2020, pp218 - 218, Poster, PUBLISHED
D Smajlagic, S Connolly, H Hakonarson, I Waldman, J Elia, E Heron, J Haavik, S Johansson, T Zayats,, SU4 - GENOME-WIDE EXAMINATION OF PARENT-OF-ORIGIN EFFECTS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER, European Neuropsychopharmacology, 29, 2019, ppS888 - S889, Poster, PUBLISHED
N Ryan, L Gallagher, E Heron, SA22INVESTIGATING PARENT-OF-ORIGIN EFFECTS IN AUTISM SPECTRUM DISORDER USING NEXT GENERATION SEQUENCING DATA, European Neuropsychopharmacology , XXVIth World Congress of Psychiatric Genetics (WCPG) , Glasgow, Scotland, 11 - 15 October 2018, 2019, ppS1199 - S1200, Poster, PUBLISHED
Ryan, Niamh & Ormond, Cathal & Arsalan, Arsalan & Byerley, William & Ayub, Muhammad & Matthews, Carol & Heron, Elizabeth & Gill, Michael & Corvin, Aiden. , S97DETECTION OF RARE INHERITED CNVS ASSOCIATED WITH PSYCHIATRIC ILLNESS FROM FAMILY WHOLE GENOME SEQUENCING DATA., European Neuropsychopharmacology., 2019, Poster, PUBLISHED
Corfield, Elizabeth & Smajlagic, Dinka & Connoly, Siobhan & Havdahl, Alexandra & Tesli, Martin & Waldman, Irwin & Elia, Josephine & Heron, Elizabeth & Reichborn-Kjennerud, Ted & Haavik, Jan & Johansson, Stefan & Zayats, Tetyana. , S1PARENT-OF-ORIGIN AND MATERNAL EFFECTS IN ATTENTION DEFICIT HYPERACTIVITY DISORDER. , European Neuropsychopharmacology, , 2019, Poster, PUBLISHED
Niamh Ryan, Louise Gallagher, Elizabeth Heron, Investigating Parent-of-Origin Effects in Autism Spectrum Disorders Using Next Generation Sequencing Data, European Neuropsychopharmacology, World Congress of Psychiatric Genetics, Glasgow, Scotland, 11-15 October 2018, 2018, Poster, PUBLISHED

  

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