Publications and Further Research Outputs
Peer-Reviewed Publications
Cathal Ormond, Mathieu Cap, Aiden Corvin, Elizabeth A. Heron, Niamh Ryan, Carol Mathews, T26. RARE AND COMMON VARIANT ANALYSIS OF AN OCD PEDIGREE USING WHOLE GENOME SEQUENCING DATA, 99, 2025, pp170 - 171, pp170-171
S.M. Feighan, Katie McArdle, Linda Lisanti, Edna Roche, Cathal Ormonde, Elizabeth A. Heron, Clare Kelly, Ciara J. Molloy, Louise Gallagher, Measuring shifts in attentional bias following satiety: A within-subject eye-tracking study in healthy-weight adults, Physiology & Behavior, 299, 2025, p114993 - 114993, p114993-114993
Cathal Ormond, Niamh Ryan, Juan M. Peralta, Ravindranath Duggirala, Satish Kumar, Elizabeth A. Heron, Joanne E. Curran, David C. Glahn, John Blangero, Aiden Corvin, 58. A RARE, DELETERIOUS COPY NUMBER VARIANT CO-SEGREGATING WITH MAJOR DEPRESSIVE DISORDER IN A MEXICAN-AMERICAN PEDIGREE, 99, 2025, pp84 - 84, pp84-84
Jacqueline Fitzgerald, Ciara J. Molloy, Thomas Dinneen, Niamh Feerick, Matthew L. O"Sullivan, Richard O"Conaill, Maryam Al-Shehhi, Richard B. Reilly, Sally Ann Lynch, Elizabeth A. Heron, Clare Kelly, Sanbing Shen, Louise Gallagher, Evidence of neurocognitive and resting state functional connectivity differences in carriers of NRXN1 deletions, Journal of Neurodevelopmental Disorders, 17, (1), 2025, p62 - 62, p62-62
Niamh Ryan, Cathal Ormond, Juan M. Peralta, Ravindranath Duggirala, Satish Kumar, Elizabeth A. Heron, Joanne E. Curran, David C. Glahn, John Blangero, Aiden Corvin, M33. PRELIMINARY FINDINGS FROM A CNV LINKAGE ANALYSIS OF A MEXICAN AMERICAN PEDIGREE COHORT, 99, 2025, pp125 - 125, pp125-125
Chapter 6 - Genomics of psychiatric disorders in, editor(s)Gregory M. Pastores , Neurogenetics for the Practitioner, 2024, pp79 - 94, [Ryan NM, Ormond C, Brady P, Heron EA , Corvin, A]
Ormond C, Ryan NM, Hedman A, Cannon T, Sullivan P, Gill M, Hultman CM, Heron EA, Johansson, V, and Corvin, A, Whole genome sequencing study of identical twins discordant for psychosis., Translational Psychiatry, 2024
Bates M, Mullen D, Lee E, Costigan D, Heron EA, Kernan N, Barry-OCrowley J, Martin C, Keegan H, Malone, V, Brooks R, Brooks D, Logan, JM, Martini, C, Selemidis S, McFadden J, ORiain C, Spillane CD, Gallagher MF, McCann A, OToole S, OLeary JJ, P53 and TLR4 expression are prognostic markers informing progression free survival of advanced stage high grade serous ovarian cancer, Pathology - Research and Practice, 2024
Ormond C, Ryan NM, Byerley W, Heron EA, Corvin A, Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN, Scientific Reports, 2024
Cathal Ormond, Niamh Ryan, Michal "áp, William Byerley, Aiden Corvin, Elizabeth A. Heron, BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees, Briefings in Bioinformatics, 26, (1), 2024
Dinneen, T.J. and Nà Ghrálaigh, F. and Ormond, C. and Heron, E.A. and Kirov, G. and Lopez, L.M. and Gallagher, L., Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank, npj Genomic Medicine, 9, (1), 2024
Cathal Ormond, Niamh Ryan, William Byerley, Elizabeth A. Heron, Aiden Corvin, PROGRESS UPDATE FROM THE PGC PEDIGREE SEQUENCING WORKING GROUP: RESULTS AND NOVEL METHODOLOGIES, 87, 2024, pp33 - 33, pp33-33
Ormond C., Ryan N.M., Heron E.A., Gill M., Byerley W., Corvin A., Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia, Biological Psychiatry Global Open Science, 3, (4), 2023, p797 - 802, p797-802
Ryan N, Heron EA, Evidence for parent-of-origin effects in autism spectrum disorder: a narrative review, Journal of Applied Genetics, 64, 2023, p303 - 317
Bond L, McTiernan D, Connaughton M, Heron EA, Coogan AN, McGrath J, Sleep problems in children and adolescents in an attention deficit hyperactivity disorder service., Irish journal of psychological medicine, 2023
Murphy G, Naughton A, Durand R, Heron E, McCaughey C, Murphy RT, Pearson I, Long-term Outcomes for Drug-eluting Balloons versus Drug-eluting Stents in the Treatment of Small Vessel Coronary Artery Disease: A Systematic Review and Meta-analysis., Interventional cardiology (London, England), 2023
Heron EA, Valle G, Bernasconi A, Editorial: Identification of phenotypically important genomic variants, Frontiers in Bioinformatics, 2023
Elaine Burke, Elizabeth Heron, Martina Hennessy, Gender bias in academic medicine: a resume study, BMC Medical Education BMC series - open , 23, 2023
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
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]
Schizophrenia genomics in, editor(s)Evangelia Eirini Tsermpini Martin Alda George P. Patrinos , Psychiatric Genomics, Elsevier, 2022, pp17 - 41, [yan, Niamh M and Ormond, Cathal and Brady, Philip and Heron, Elizabeth A and Corvin, Aiden]
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
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
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
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
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
Ormond C, Ryan NM, Corvin A, Heron EA., Converting single nucleotide variants between genome builds: from cautionary tale to solution., Briefings in bioinformatics, 2021
Thekiso TB, McLoughlin DM, Hartnett Y, Casey S, Orji A, Heron EA, Rush G, Kennedy N., Outcome of First-admission Depression Treated in a Specialized Mood Disorders Service., Journal of psychiatric practice, 26, (6), 2020, p461-471
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
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
Dinka Smajlagi", Siobhan Connolly, Håkon Håkonarson, Irwin D. Waldman, Josephine Elia, Elizabeth A. Heron, Jan Haavik, Stefan Johansson, Tetyana Zayats, GENOME-WIDE EXAMINATION OF PARENT-OF-ORIGIN EFFECTS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER, European Neuropsychopharmacology, 29, 2019, pS888 - S889, pS888-S889
Elizabeth C. Corfield, Dinka Smajlagi", Siobhan Connoly, Alexandra Havdahl, Martin Tesli, Håkon Håkonarson, Irwin D. Waldman, Josephine Elia, Elizabeth A. Heron, Ted Reichborn"Kjennerud, Jan Haavik, Stefan Johansson, Tetyana Zayats, S1PARENT-OF-ORIGIN AND MATERNAL EFFECTS IN ATTENTION DEFICIT HYPERACTIVITY DISORDER, 29, 2019, ppS114 - S114, ppS114-S114
Connolly, S. and Anney, R. and Gallagher, L. and Heron, E.A., Evidence of Assortative Mating in Autism Spectrum Disorder, Biological Psychiatry, 86, (4), 2019, p286-293
Sullivan, M.O. and Gallagher, L. and Heron, E.A., Gaining Insights into Aggressive Behaviour in Autism Spectrum Disorder Using Latent Profile Analysis, Journal of Autism and Developmental Disorders, 2019
Connolly, S., Anney, R., Gallagher, L., Heron, E.A., A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3, European Journal of Human Genetics, 25, (2), 2017, p234-239
Merikangas, A.K., Segurado, R., Kelleher, E., Hogan, D., Delaney, C., Gill, M., Gallagher, L., Corvin, A.P., and Heron, E.A., Parental age, birth order and neurodevelopmental disorders, 2016
Falk, M.G., Alston, C.L., McGrory, C.A., (...), Pettitt, A.N., Mengersen, K.L., Recent Bayesian approaches for spatial analysis of 2-D images with application to environmental modelling, Environmental and Ecological Statistics, 2015
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, Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders., Molecular psychiatry, 19, 2014, p872-879
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., The phenotypic manifestations of rare CNVs in schizophrenia., Schizophrenia Research, 158, (1-3), 2014, p255 - 260
Heron, E.A., Cormican, P., Donohoe, G., O'Neill, F.A., Kendler, K.S., Riley, B.P., Gill, M., Corvin, A.P., Morris, D.W., No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset, Schizophrenia Research, 154, (1-3), 2014, p79-82
Connolly, S and Heron, E.A., Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits., Briefings in Bioinformatics, 2014
Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L., The phenotypic manifestations of rare genic CNVs in autism spectrum disorder., Molecular Psychiatry, 2014, p1-7
Thekiso, T.B., Heron, E.A., Masood, B., Murphy, M., McLoughlin, D.M., Kennedy, N., Mauling of the "celtic Tiger": Clinical characteristics and outcome of first-episode depression secondary to the economic recession in Ireland, Journal of Affective Disorders, 151, (2), 2013, p455-460
Jillian P. Casey, Hugh Murphy, Sean Ennis, Sally Ann Lynch, L Bradley, R Mabrouk, Andrew D. Paterson, D. M. McAULEY, Tabib Dabir, Michael E. Dobson, John M. Darlow, Rebecca Darlay, Heather J. Cordell, Andrew Green, P. Puri, David Barton, M McCormack, Elijah Chaila, Deema AL Shawan, Jennifer Conroy, Erin L. Heinzen, David B. Goldstein, N Delanty, Keith W. Caldecott, Gianpiero L. Cavalleri, McConnell, D. FitzPatrick, Nida Shah, C Ryan, D. A. Greene, Denis C. Shields, David Courtney, Sarah D. Atkinson, Edwin H. A. Allen, Jeremy P. Moore, Eleonora Maurizi, Graziella Pellegrini, Graeme C. Black, Franco Mason, Yam G, Wendy McLean, C Moore, Gareth J. McKay, David J. Kavanagh, A Maxwell, Kate O"Neill, Christopher Walsh, Richard Anney, Ning Zhang, Gerard W. O"Keeffe, Thomas A. Moore, Alex Magee, F Stewart, Alison Muir, J McOsker, T Jardine, Alison Wilson, Pascal McKeown, L. D. McKay, Stephen M. Scala, Ingrid Winship, Lennox J. Jeffers, Claire M. Thornton, Patrick J. Morrison, Alister C. Ward, J Turner, Michael F. Byrne, A Harrison, Kristina Pentieva, H McNulty, Anne Parle"McDermott, Carrie MacEwen, Makoto Ozaki, N Cattell, Sean Duffy, A McKnight, Adrian Heagerty, Irene M. Leigh, C Pourreyron, Ildikó Szeverényi, Frances J.D. Smith, Elaine Swan, Lillian M. Smyth, John A. Kilner, S. J. Connolly, Elizabeth A. Heron, Ciara Fahey, Susan Byrne, Róisín McLaughlin, Kevin P. Kenna, Declan Bradley, Michael Gill, Orla Hardiman, Aiden Corvin, Derek W. Morris, L Evenepoel, 16th Meeting of the Irish Society of Human Genetics, Friday 6th September 2013. : Postgraduate Centre, Belfast Health and Social Care Trust., Ulster medical journal/~The Ulster medical journal, 82, (3), 2013, p197 - 204, p197-204
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Gilbert J, Gillberg C, Glessner JT, Green A, Green J, Guter SJ, Heron EA, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Jacob S, Kenny GP, Kim C, Kolevzon A, Kustanovich V, Lajonchere CM, Lamb JA, Law-Smith M, Leboyer M, Le Couteur A, Leventhal BL, Liu XQ, Lombard F, Lord C, Lotspeich L, Lund SC, Magalhaes TR, Mantoulan C, McDougle CJ, Melhem NM, Merikangas A, Minshew NJ, Mirza GK, Munson J, Noakes C, Nygren G, Papanikolaou K, Pagnamenta AT, Parrini B, Paton T, Pickles A, Posey DJ, Poustka F, Ragoussis J, Regan R, Roberts W, Roeder K, Roge B, Rutter ML, Schlitt S, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Sykes N, Tancredi R, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wing K, Wittemeyer K, Wood S, Zurawiecki D, Zwaigenbaum L, Bailey AJ, Battaglia A, Cantor RM, Coon H, Cuccaro ML, Dawson G, Ennis S, Freitag CM, Geschwind DH, Haines JL, Klauck SM, McMahon WM, Maestrini E, Miller J, Monaco AP, Nelson SF, Nurnberger JI, Oliveira G, Parr JR, Pericak-Vance MA, Piven J, Schellenberg GD, Scherer SW, Vicente AM, Wassink TH, Wijsman EM, Betancur C, Buxbaum JD, Cook EH, Gallagher L, Gill M, Hallmayer J, Paterson AD, Sutcliffe JS, Szatmari P, Vieland VJ, Hakonarson H, Devlin B, Individual common variants exert weak effects on the risk for autism spectrum disorderspi., Human molecular genetics, 21, (21), 2012, p4781-92
O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D, Consortium IS, Corvin A, Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility., Molecular Psychiatry, 16, (3), 2011, p286-292
Heron Elizabeth A, O'Dushlane C, Segurado R, Gallagher L, Gill M., Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data., Oxford Journal Mathematics & Physical Sciences Biostatistics, 12, (3), 2011, p445-461
Bridges M, Heron E, O'Dushlaine, Segurado R, The International Schizophrenia Consortium (ISC), Morris DW, Corvin A, Gill M, Pinto C. , Genetic Classification of Populations using Supervised Learning., PLos One, 6, (5), 2011, pe14802
F Stewart, JE Wraith, Karen Tylee, Alan Cooper, Gaetano Rea, Simon McCullough, Susan McNerlan, B. Craig, Patrick J. Morrison, Kevin Meaney, B O"Hici, S. Lynch, David Barton, Lennox J. Jeffers, D Fitzsimons, Eilís McCaughan, Shirley Heggarty, W. H. K. Wright, Peter Hart, Pascal McKeown, Caroline Graham, Elif Da"dan, Derek W. Morris, M Hill, Matthias Rothermundt, F Kästner, Carsten Hohoff, J. Deckert, von Eiff C, Petra Krakowitzky, A. Hargreaves, Edna Rosé, Aiden Corvin, Gary Donohoe, Michael Gill, Patrick O. McKeon, Sulema Rodríguez Roche, E Quinn, Emer Kenny, Paul Cormican, Arthur I. Gates, Nina S. McCarthy, Ciara Vangjeli, Gianpiero L. Cavalleri, Kevin V. Shianna, N Delanty, Eoin O"Brien, Brian J. Harvey, Alanna M. Stanton, Elizabeth A. Heron, William P. Gilks, Praveen Surendran, Denis C. Shields, Stefano Minguzzi, Anne M. Molloy, P. N. Kirke, J Mills, John M. Scott, James Troendle, Faith Pangilinan, L. Brody, Anne Parle"McDermott, Adam Carey, A Hegarty, D. S. Betts, Andrew Beckett, Goldwin Smith, M Humphreys, Tabib Dabir, Sally A. McKee, Alex Magee, F Stewatr, McConnell, Daniel J. Simpson, Leonard Harwood, Grenville Clark, S Alexander, Giuliana Silvestri, Charles C. Willoughby, Deirdre Donnelly, Andrew D. Paterson, Janet Patrick, Peter D. Turnpenny, Eleanor Beattie, L Møller, Jason Hughes, Sandya Tirupathi, Bobbi Herron, E. Healy, Patricia Woods, Diane Beattie, Helen Crawford, Janet L. McDaid, J Turner, Geoffrey Clarke, Tim Morris, Andrew Green, J. R. J. Llewellyn Jones, L Bradley, KA Murtagh, 13th Meeting of the Irish Society of Human Genetics, 79, (3), 2010, pp137 - 145, pp137-145
Nwachukwu I, Crumlish N, Heron EA, Gill M, The Irish Mental Health Act 2001: Impact on involuntary admissions in a community mental health service in Dublin, The Psychiatrist, 34, 2010, p436-440
Heron, E.A., Walsh, C., Bayesian Discrete Latent Spatial Modelling of Crack Initiation in Orthopaedic Hip Replacement Bone Cement, Journal of Applied Statistics, 37, (7), 2010, p1153 - 1171
Pinto, D, Pagnamenta, AT, Klei, L, Anney, R, Merico, D, Regan, R, Conroy, J, Magalhaes, TR, Correia, C, Abrahams, BS, Almeida, J, Bacchelli, E, Bader, GD, Bailey, AJ, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bolte, S, Bolton, PF, Bourgeron, T, Brennan, S, Brian, J, Bryson, SE, Carson, AR, Casallo, G, Casey, J, Chung, BHY, Cochrane, L, Corsello, C, Crawford, EL, Crossett, A, Cytrynbaum, C, Dawson, G, de Jonge, M, Delorme, R, Drmic, I, Duketis, E, Duque, F, Estes, A, Farrar, P, Fernandez, BA, Folstein, SE, Fombonne, E, Freitag, CM, Gilbert, J, Gillberg, C, Glessner, JT, Goldberg, J, Green, A, Green, J, Guter, SJ, Hakonarson, H, Heron, EA, Hill, M, Holt, R, Howe, JL, Hughes, G, Hus, V, Igliozzi, R, Kim, C, Klauck, SM, Kolevzon, A, Korvatska, O, Kustanovich, V, Lajonchere, CM, Lamb, JA, Laskawiec, M, Leboyer, M, Le Couteur, A, Leventhal, BL, Lionel, AC, Liu, XQ, Lord, C, Lotspeich, L, Lund, SC, Maestrini, E, Mahoney, W, Mantoulan, C, Marshall, CR, McConachie, H, McDougle, CJ, McGrath, J, McMahon, WM, Merikangas, A, Migita, O, Minshew, NJ, Mirza, GK, Munson, J, Nelson, SF, Noakes, C, Noor, A, Nygren, G, Oliveira, G, Papanikolaou, K, Parr, JR, Parrini, B, Paton, T, Pickles, A, Pilorge, M, Piven, J, Ponting, CP, Posey, DJ, Poustka, A, Poustka, F, Prasad, A, Ragoussis, J, Renshaw, K, Rickaby, J, Roberts, W, Roeder, K, Roge, B, Rutter, ML, Bierut, LJ, Rice, JP, Salt, J, Sansom, K, Sato, D, Segurado, R, Sequeira, AF, Senman, L, Shah, N, Sheffield, VC, Soorya, L, Sousa, I, Stein, O, Sykes, N, Stoppioni, V, Strawbridge, C, Tancredi, R, Tansey, K, Thiruvahindrapduram, B, Thompson, AP, Thomson, S, Tryfon, A, Tsiantis, J, Van Engeland, H, Vincent, JB, Volkmar, F, Wallace, S, Wang, K, Wang, ZZ, Wassink, TH, Webber, C, Weksberg, R, Wing, K, Wittemeyer, K, Wood, S, Wu, J, Yaspan, BL, Zurawiecki, D, Zwaigenbaum, L, Buxbaum, JD, Cantor, RM, Cook, EH, Coon, H, Cuccaro, ML, Devlin, B, Ennis, S, Gallagher, L, Geschwind, DH, Gill, M, Haines, JL, Hallmayer, J, Miller, J, Monaco, AP, Nurnberger, JI, Paterson, AD, Pericak-Vance, MA, Schellenberg, GD, Szatmari, P, Vicente, AM, Vieland, VJ, Wijsman, EM, Scherer, SW, Sutcliffe, JS, Betancur, C, Functional impact of global rare copy number variation in autism spectrum disorders, NATURE, 466, 2010, p368-372
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu S, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J, A genomewide scan for common alleles affecting risk for autism., Human molecular genetics, 19, (20), 2010, p4072-4082
O'Dushlaine C., Kenny E., Heron E.A., Segurado R., Gill M,, Morris D.W., Corvin A. , The SNP ratio test: pathway analysis of genome-wide association datasets., Bioinformatics, 25, (20), 2009, p2762 - 2763
Elizabeth A. Heron, Cathal Walsh, A Continuous Latent Spatial Model for Crack Initiation in Bone Cement, Journal of the Royal Statistical Society Series C (Applied Statistics), 57, (1), 2008, p25 - 42, p25-42
Tang, S., Heron, E.A., Bayesian inference for a stochastic logistic model with switching points, Ecological Modelling , 219, (1-2), 2008, p153 - 169
Finkenstädt, B., Heron, E.A., Komorowski, M., Edwards, K., Tang, S., Harper, C.V., Davis, J.R., White, M.R., Millar, A.J., Rand, D.A., Reconstruction of transcriptional dynamics from gene reporter data using differential equations, Bioinformatics, 15, (24), 2008, p2901 - 2907
Heron, E.A., Finkenstädt, B. and Rand, D.A. , Bayesian inference for dynamic transcriptional regulation; the Hes1 system as a case study, Bioinformatics, 23, (19), 2007, p2596 - 2603
Non-Peer-Reviewed Publications
C Ormond, N Ryan, E Heron, A Corvin, The Telomere-to-Telomere genome build reduces the proportion of ClinVar variants with mismatching gene annotation information compared to current genome builds, Eur J Hum Genet, 56th European Society of Human Genetics (ESHG) Conference, 2024
Cathal Ormond, Niamh Ryan, William Byerley, Elizabeth Heron, Aiden Corvin, W87. RARE, PATHOGENIC COPY NUMBER VARIANTS CO-SEGREGATE WITH SCHIZOPHRENIA IN PEDIGREE COHORT, European Neuropsychopharmacology, World Congress of Psychiatric Genetics (WCPG), October 10-14, 2023, 2023
Niamh Ryan, Cathal Ormond, Arsalan Arsalan, Elizabeth Heron, Muhammad Ayub, Aiden Corvin, T84. RARE VARIANT ANALYSIS IN A PAIR OF PAKISTANI PEDIGREES WITH A HIGH LOAD OF PSYCHIATRIC ILLNESS, European Neuropsychopharmacology, Abstracts of the World Congress of Psychiatric Genetics (WCPG), October 10-14, 202, 2023
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
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
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
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
Claire Foley, Eleisa Heron, James Walters, Louise Gallagher, Aiden Corvin, SA105 - IDENTIFICATION OF PHENOTYPIC PREDICTORS OF PATHOGENIC COPY NUMBER VARIANTS IN A PSYCHOSIS POPULATION, European Neuropsychopharmacology, XXVth World Congress of Psychiatric Genetics (WCPG), Orlando, Florida, 13 - 17 October 20, 2020
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
Niamh Ryan, Cathal Ormond, Yi-Chieh Chang, Carol A. Mathews, Elizabeth Heron, Michael Gill, Aiden Corvin, M60 GENOMIC ANALYSIS OF A LARGE TOURETTE SYNDROME PEDIGREE, European Neuropsychopharmacology, XXVIIth World Congress of Psychiatric Genetics (WCPG), Los Angeles, California, 2019, 2019
Cathal Ormond, Eliabeth Heron, Niamh Ryan, Viktoria Johansson, Anna Hedman, Christina Hultman, Patrick Sullivan, Michael Gill, Aiden Corvin, M16 IDENTICAL BUT NOT THE SAME - WHOLE GENOME SEQUENCING OF MONOZYGOTIC TWINS DISCORDANT FOR PSYCHIATRIC ILLNESS, European Neuropsychopharmacology, XXVIIth World Congress of Psychiatric Genetics (WCPG), Los Angeles, California, 2019, 2019
Elizabeth Heron, 47th European Mathematical Genetics Meeting (EMGM) 2019, 8-9 April 2019, 2019, Dublin, Ireland, Elizabeth Heron, (5), 83, 225"249
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
Elizabeth Corfield, Dinka Smajlagic, Siobhan Connoly, Alexandra Havdahl, Martin Tesli, Hakon Hakonarson, Irwin Waldman, Josephine Elia, Elizabeth Heron, Ted Reichborn-Kjennerud, Jan Haavik, Stefan Johansson, Tetyana Zayats, SU4 - GENOME-WIDE EXAMINATION OF PARENT-OF-ORIGIN EFFECTS IN CHILDREN WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER, European Neuropsychopharmacology, XXVIIth World Congress of Psychiatric Genetics (WCPG), Los Angeles, California, 2019, 2019
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
C. Foley , E. Heron , L. Gallagher , A. Corvin, P.1.a.028 - Identification of phenotypic predictors of pathogenic copy number variants in a psychosis population, European Neuropsychopharmacology, 30th ECNP Congress, 2017, 2017
S. Connolly, R. Anney, L. Gallagher, E. Heron, Investigation of Assortative Mating in Autism Spectrum Disorders, Human Heredity, 43rd European Mathematical Genetics Meeting (EMGM) 2015, Brest, France, April 16-17, 2015, edited by Emmanuelle Génin, Karen Rouault , 79, 2015, pp28 - 52
Siobhán Connolly, Louise Gallagher, Elizabeth Heron, Investigation of Parent-of-Origin Effects in Autism Spectrum Disorders, 17th Annual Meeting of the Institute of Molecular Medicine, Trinity College Dublin, 2014
Merikangas, A., Heron, E., Anney, R., Corvin, A. and Gallagher, L., Risk factors and clinical correlates of CNVs associated with autism spectrum disorders: evidence for joint contribution of genetic and environmental risk factors, Eur Child Adolesc Psychiatry, 15th International Congress of ESCAP (European Society for Child and Adolescent Psychiatry), Dublin, Ireland, July 6-10, 2013, 2013
AK Merikangas, EA Heron, R Anney, AP Corvin, L Gallagher, Investigating the association between rare copy number variation and developmental anomalies in autism spectrum disorders, Genetic Epidemiology, Nineteenth annual meeting of the International Genetic Epidemiology Society, 34, (8), 2010, pp929 - 929
Research Expertise
Recognition
Memberships
Fellow of the Royal Statistical Society