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Researchers at UCD

researcher

Andrew Green

Professor of Medical Genetics

School Of Medicine
Our Lady's Hospital
Crumlin
Dublin 12

Tel: 014096902
Email: andrew.green@ucd.ie

Biography

1998 FFPath (RCPI)
1998 FRCPI
1997 Professor of Medical Genetics, UCD
1997 Director of National Centre for Medical Genetics, Our Lady's Hospital, Crumlin, Consultant in Medical Genetics, Our Lady's Hospital, Crumlin
1997 Consultant in Medical Genetics, The Children's Hospital, Temple St.
1995 University Lecturer and Honorary Consultant, Dept. of Medical Genetics, University of Cambridge
1995 PhD (Cantab)
1992 Senior Registrar and Lecturer in Medical Genetics, Addenbrooke's Hospital, Cambridge, and University of Cambridge

Professional

 

Associations

Association: Irish Society for Human genetics, Function/Role: Member
Association: European Society for Human Genetics, Function/Role: Member
Association: British Society for Human Genetics, Function/Role: Member
Association: American Society for Human Genetics, Function/Role: Member
       

Committees

Committee : Irish Council For Bioethics
Committee : UCD research ethics committee
Committee : Genelibrary Ireland - ethics workgroup
Committee : Our Lady's Hospital Crumlin Research ethics committee

Employment

Employer: University of Cambridge
Position: Jeantet Research Fellow and Registrar in Medicine
Employer: Addenbrooke`s NHS Trust and University of Cambridge
Position: Lecturer and Senior Registrar
Employer: Addenbrooke`s NHS Trust and University of Cambrifge
Position: Lecturer and Consultant

Education

Year 1995 Institution: University of Canterbury
Qualification: PhD Subject:
Year 1984 Institution:
Qualification: MB, BCh, BAO Subject:
Year 1986 Institution:
Qualification: MRCPI Subject:
Year 1998 Institution: RCPI
Qualification: FRCPI Subject: Medicine
         

Publications

 

Book Chapters

Green A; (2005) 'Basic genetics' In: Green A; (eds). Roberton's textbook of Neonatology. UK: Elsevier Churchill Livingstone. [Details]
 

Peer Reviewed Journals

Oegema R, Cushion TD;Phelps IG;Chung SK;Dempsey JC;Collins S;Mullins JG;Dudding T;Gill H;Green AJ;Dobyns WB;Ishak GE;Rees MI;Doherty D (2015) 'Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes'. Human Molecular Genetics, 24 (18):5313-5325. [DOI] [Details]
Aloraifi F, McCartan D;McDevitt T;Green AJ;Bracken A;Geraghty J (2015) 'Protein-truncating variants in moderate-risk breast cancer susceptibility genes: A meta-analysis of high-risk case-control screening studies'. Cancer genetics, 208 (9):455-463. [DOI] [Details]
Aloraifi F, Boland MR;Green AJ;Geraghty JG (2015) 'Gene analysis techniques and susceptibility gene discovery in¿¿non-BRCA1/BRCA2 familial breast cancer'. Surgical Oncology, 24 (2):100-109. [DOI] [Details]
Beygo J, Elbracht M;de Groot K;Begemann M;Kanber D;Platzer K;Gillessen-Kaesbach G;Vierzig A;Green A;Heller R;Buiting K;Eggermann T (2015) 'Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32'. European journal of human genetics : EJHG, 23 (2):180-188. [DOI] [Details]
Aloraifi F, McDevitt T;Martiniano R;McGreevy J;McLaughlin R;Egan CM;Cody N;Meany M;Kenny E;Green AJ;Bradley DG;Geraghty JG;Bracken AP (2015) 'Detection of novel germline mutations for breast cancer in non-BRCA1/2 families'. FEBS Journal, 282 (17):3424-3437. [DOI] [Details]
Aloraifi F, Alshehhi M;McDevitt T;Cody N;Meany M;O'Doherty A;Quinn CM;Green AJ;Bracken A;Geraghty JG (2015) 'Phenotypic analysis of familial breast cancer: comparison of BRCAx tumors with BRCA1-, BRCA2-carriers and non-familial breast cancer'. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology, 41 (5):641-646. [DOI] [Details]
O'Shea R, Meany M;Carroll C;Cody N;Healy D;Green A;Lynch SA (2015) 'Predictive Genetic Testing and Alternatives to Face to Face Results Disclosure: A Retrospective Review of Patients Preference for Alternative Modes of BRCA 1 and 2 Results Disclosure in the Republic of Ireland'. Journal of Genetic Counseling, . [DOI] [Details]
Darlow JM, Dobson MG;Darlay R;Molony CM;Hunziker M;Green AJ;Cordell HJ;Puri P;Barton DE (2014) 'A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development'. Molecular genetics & genomic medicine, 2 (1):7-29. [DOI] [Details]
Flanagan, SE,Xie, WJ,Caswell, R,Damhuis, A,Vianey-Saban, C,Akcay, T,Darendeliler, F,Bas, F,Guven, A,Siklar, Z,Ocal, G,Berberoglu, M,Murphy, N,O'Sullivan, M,Green, A,Clayton, PE,Banerjee, I,Clayton, PT,Hussain, K,Weedon, MN,Ellard, S (2013) 'Next-Generation Sequencing Reveals Deep Intronic Cryptic ABCC8 and HADH Splicing Founder Mutations Causing Hyperinsulinism by Pseudoexon Activation'. American Journal of Human Genetics, 92 :131-136. [DOI] [Details]
Farrell MP, Hughes DJ;Drost M;Wallace AJ;Cummins RJ;Fletcher TA;Meany MA;Kay EW;de Wind N;Power DG;Andrews EJ;Green AJ;Gallagher DJ (2013) 'Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity'. Familial Cancer, 12 (4):741-747. [DOI] [Details]
McGorrian C, Constant O;Harper N;O'Donnell C;Codd M;Keelan E;Green A;O'Neill J;Galvin J;Mahon NG (2013) 'Family-based cardiac screening in relatives of victims of sudden arrhythmic death syndrome'. Europace, 15 (7):1050-1058. [DOI] [Details]
Conlon PJ, O'Brien RP, Phelan PJ, Conroy J, O'Kelly P, Green A, Keogan M, O'Neill D, Jennings S, Traynor C, Casey J, McCormack M, Conroy R, Chubb A, Ennis S, Shields DC, Cavalleri GL (2013) 'A genome-wide association study of recipient genotype and medium-term kidney allograft function'. Clinical Transplantation, 27 (3):379-387. [DOI] [Details]
Dobson MG, Darlow JM, Hunziker M, Green AJ, Barton DE, Puri P. (2013) 'Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux'. Kidney International, 84 :327-337. [DOI] [Details]
Palles C, Cazier JB, Howarth KM, Domingo E, Jones AM, Broderick P, Kemp Z, Spain SL, Almeida EG, Salguero I, Sherborne A, Chubb D, Carvajal-Carmona LG, Ma Y, Kaur K, Dobbins S, Barclay E, Gorman M, Martin L, Kovac MB, Humphray S; CORGI Consortium; WGS500 Consortium, Lucassen A, Holmes CC, Bentley D, Donnelly P, Taylor J, Petridis C, Roylance R, Sawyer EJ, Kerr DJ, Clark S, Grimes J, Kearsey SE, Thomas HJ, McVean G, Houlston RS, Tomlinson I. (2013) 'Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas'. Nature Genetics, . [Details]
Jenkinson EM, Clayton-Smith J, Mehta S, Bennett C, Reardon W, Green A, Pearce SH, De Michele G, Conway GS, Cilliers D, Moreton N, Davis JR, Trump D, Newman WG. (2012) 'Perrault syndrome: further evidence for genetic heterogeneity'. Neurology, . [Details]
Dunlop MG, Dobbins SE, Farrington SM, Jones AM, Palles C, Whiffin N, Tenesa A, Spain S, Broderick P, Ooi LY, Domingo E, Smillie C, Henrion M, Frampton M, Martin L, Grimes G, Gorman M, Semple C, Ma YP, Barclay E, Prendergast J, Cazier JB, Olver B, Penegar S, Lubbe S, Chander I, Carvajal-Carmona LG, Ballereau S, Lloyd A, Vijayakrishnan J, Zgaga L, Rudan I, Theodoratou E; The Colorectal Tumour Gene Identification (CORGI) Consortium, Thomas H, Maher E, Evans G, Walker L, Halliday D, Lucassen A, Paterson J, Hodgson S, Homfray T, Side L, Izatt L, Donaldson A, Tomkins S, Morrison P, Brewer C, Henderson A, Davidson R, Murday V, Cook J, Haites N, Bishop T, Sheridan E, Green A, Marks C, Carpenter S, Broughton M, Greenhalge L, Suri M, Starr JM, Deary I, Kirac I, Kovacević D, Aaltonen LA, Renkonen-Sinisalo L, Mecklin JP, Matsuda K, Nakamura Y, Okada Y, Gallinger S, Duggan DJ, Conti D, Newcomb P, Hopper J, Jenkins MA, Schumacher F, Casey G, Easton D, Shah M, Pharoah P, Lindblom A, Liu T; The Swedish Low-Risk Colorectal Cancer Study Group (2012) 'Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk'. Nature Genetics, . [Details]
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, Papanikolaou K, Pagnamenta AT, Parrini B, Paton T, Pickles A, Posey DJ, Poustka F, Ragoussis J, Regan R, Renshaw K, 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 J, 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 Jr, 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 (2012) 'Individual common variants exert weak effects on risk for Autism Spectrum Disorders'. Human Molecular Genetics, . [Details]
Casey J, Kawaguchi R, Morrissey M, Sun H, McGettigan P, Nielsen JE, Conroy J, Regan R, Kenny E, Cormican P, Morris DW, Tormey P, Chróinín MN, Kennedy BN, Lynch S, Green A, Ennis S (2011) 'First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotype'. Human Mutation, 32 (12):1417-1426. [DOI] [Details]
O'Doherty M, Mc Creery K, Green AJ, Tuwir I, Brosnahan D.; (2011) 'Incontinentia pigmenti--ophthalmological observation of a series of cases and review of the literature'. British Journal of Ophthalmology, 95 (1):11-16. [Details]
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI Jr, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S.; (2011) 'A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder'. Human Genetics, . [Details]
Nowakowska BA, de Leeuw N, Ruivenkamp CA, Sikkema-Raddatz B, Crolla JA, Thoelen R, Koopmans M, den Hollander N, van Haeringen A, van der Kevie-Kersemaekers AM, Pfundt R, Mieloo H, van Essen T, de Vries BB, Green A, Reardon W, Fryns JP, Vermeesch JR.; (2011) '] Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies'. European Journal of Human Genetics, . [Details]
Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E; The Autism Genome Project, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L; The AGP Members, Bailey AJ, Fernandez BA, Szatmari P, Scherer SW, Patterson A, Marshall CR, Pinto D, Vincent JB, Fombonne E, Betancur C, Delorme R, Leboyer M, Bourgeron T, Mantoulan C, Roge B, Tauber M, Freitag CM, Poustka F, Duketis E, Klauck SM, Poustka A, Papanikolaou K, Tsiantis J, Gallagher L, Gill M, Anney R, Bolshakova N, Brennan S, Hughes G, McGrath J, Merikangas A, Ennis S, Green A, Casey JP, Conroy JM, Regan R, Shah N, Maestrini E, Bacchelli E, Minopoli F, Stoppioni V, Battaglia A, Igliozzi R, Parrini B, Tancredi R, Oliveira G, Almeida J, Duque F, Vicente A, Correia C, Magalhaes TR, Gillberg C, Nygren G, Jonge MD, Van Engeland H, Vorstman JA, Wittemeyer K, Baird G, Bolton PF, Rutter ML, Green J, Lamb JA, Pickles A, Parr JR, Couteur AL, Berney T, McConachie H, Wallace S, Coutanche M, Foley S, White K, Monaco AP, Holt R, Farrar P, Pagnamenta AT, Mirza GK, Ragoussis J, Sousa I, Sykes N, Wing K, Hallmayer J, Cantor RM, Nelson SF, Geschwind DH, Abrahams BS, Volkmar F, Pericak-Vance MA, Cuccaro ML, Gilbert J, Cook EH, Guter SJ, Jacob S, Nurnberger Jr JI, McDougle CJ, Posey DJ, Lord C, Corsello C, Hus V, Buxbaum JD, Kolevzon A, Soorya L, Parkhomenko E, Leventhal BL, Dawson G, Vieland VJ, Hakonarson H, Glessner JT, Kim C, Wang K, Schellenberg GD, Devlin B, Klei L, Minshew N, Sutcliffe JS, Haines JL, Lund SC, Thomson S, Yaspan BL, Coon H, Miller J, McMahon WM, Munson J, Estes A, Wijsman EM; (2011) 'Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders'. European Journal of Human Genetics, . [Details]
Feenstra I, Hanemaaijer N, Sikkema-Raddatz B, Yntema H, Dijkhuizen T, Lugtenberg D, Verheij J, Green A, Hordijk R, Reardon W, Vries BD, Brunner H, Bongers E, Leeuw ND, van Ravenswaaij-Arts C.; (2011) 'Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis'. European Journal of Human Genetics, . [Details]
Kagami, M,O'Sullivan, MJ,Green, AJ,Watabe, Y,Arisaka, O,Masawa, N,Matsuoka, K,Fukami, M,Matsubara, K,Kato, F,Ferguson-Smith, AC,Ogata, T; (2010) 'The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers'. PLoS Genetics, 6 . [DOI] [Details]
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, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, 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 Z, 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 Jr, Paterson AD, Pericak-Vance MA, Schellenberg GD, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Scherer SW, Sutcliffe JS, Betancur C.; (2010) 'Functional impact of global rare copy number variation in autism spectrum disorders'. Nature, 15 (466):368-372. Link to full text [Details]
van der Klift, HM,Tops, CMJ,Bik, EC,Boogaard, MW,Borgstein, AM,Hansson, KBM,Ausems, MGEM,Garcia, EG,Green, A,Hes, FJ,Izatt, L,van Hest, LP,Alonso, AM,Vriends, AHJT,Wagner, A,van Zelst-Stams, WAG,Vasen, HFA,Morreau, H,Devilee, P,Wijnen, JT; (2010) 'Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients'. Human Mutation, 31 :578-587. [DOI] [Details]
Wormald R, Viani L, Lynch SA, Green AJ; (2010) 'Sensorineural hearing loss in children'. Irish Medical Journal, 103 (2):51-54. [Details]
O'Riordan JM, O'Donoghue D, Green A, Keegan D, Hawkes LA, Payne SJ, Sheahan K, Winter DC; (2010) 'Hereditary mixed polyposis syndrome due to a BMPR1A mutation'. Colorectal Disease, 12 (6):570-573. [Details]
Hoornaert KP, Vereecke I, Dewinter C, Rosenberg T, Beemer FA, Leroy JG, Bendix L, Björck E, Bonduelle M, Boute O, Cormier-Daire V, De Die-Smulders C, Dieux-Coeslier A, Dollfus H, Elting M, Green A, Guerci VI, Hennekam RC, Hilhorts-Hofstee Y, Holder M, Hoyng C, Jones KJ, Josifova D, Kaitila I, Kjaergaard S, Kroes YH, Lagerstedt K, Lees M, Lemerrer M, Magnani C, Marcelis C, Martorell L, Mathieu M, McEntagart M, Mendicino A, Morton J, Orazio G, Paquis V, Reish O, Simola KO, Smithson SF, Temple KI, Van Aken E, Van Bever Y, van den Ende J, Van Hagen JM, Zelante L, Zordania R, De Paepe A, Leroy BP, De Buyzere M, Coucke PJ, Mortier GR; (2010) 'Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients'. European Journal of Human Genetics, 18 (8):872-880. [Details]
Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH Jr, Dawson G, Schellenberg GD, Battaglia A, Maestrini E; Autism Genome Project Consortium, Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB; (2010) 'Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability'. science translational medicine, 2 (49). [Details]
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 SH, 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 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 Jr, 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; (2010) 'A genome-wide scan for common alleles affecting risk for autism'. Human Molecular Genetics, 15 (19-20):4072-4082. Link to full text [Details]
Kagami M, O'Sullivan MJ, Green AJ, Watabe Y, Arisaka O, Masawa N, Matsuoka K, Fukami M, Matsubara K, Kato F, Ferguson-Smith AC, Ogata T; (2010) 'The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers'. PLoS Genetics, 6 (6). [Details]
de Leeuw N, Bulk S, Green A, Jaeckle-Santos L, Baker LA, Zinn AR, Kleefstra T, van der Smagt JJ, Vianne Morgante AM, de Vries BB, van Bokhoven H, de Brouwer AP; (2010) 'UBE2A deficiency syndrome: Mild to severe intellectual disability accompanied by seizures, absent speech, urogenital, and skin anomalies in male patients'. American Journal of Medical Genetics Part A, 52 (12):3084-3090. [Details]
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,; (2010) 'Functional impact of global rare copy number variation in autism spectrum disorders'. Nature, 466 :368-372. [DOI] [Details]
Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A; (2009) 'A genome-wide linkage and association scan reveals novel loci for autism'. Nature, 461 (7265):802-808. [Details]
Darlow, J. M.,Molloy, N. H.,Green, A. J.,Puri, P.,Barton, D. E.; (2009) 'The increased incidence of the RET p.Gly691Ser variant in French-Canadian vesicoureteric reflux patients is not replicated by a larger study in Ireland'. Hum Mutat, 30 (5):E612-7. Available Online [Details]
Becker K, Fitzgerald O, Green AJ, Keogan M, Newbury-Ecob R, Greenhalgh L, Withers S, Hollox EJ, Aldred PM, Armour JA; (2009) 'Constitutional trisomy 8 and Behçet syndrome'. American Journal of Medical Genetics, . [Details]
Canney, A,Sheahan, K,Keegan, D,Tolan, M,Hyland, J,Green, A; (2009) 'Synchronous lung tumours in a patient with metachronous colorectal carcinoma and a germline MSH2 mutation'. J Clin Pathol, 62 :471-473. [DOI] [Details]
Baldridge, D,Schwarze, U,Morello, R,Lennington, J,Bertin, TK,Pace, JM,Pepin, MG,Weis, M,Eyre, DR,Walsh, J,Lambert, D,Green, A,Robinson, H,Michelson, M,Houge, G,Lindman, C,Martin, J,Ward, J,Lemyre, E,Mitchell, JJ,Krakow, D,Rimoin, DL,Cohn, DH,Byers, PH,Lee, B (2008) 'CRTAP and LEPRE1 Mutations in Recessive Osteogenesis Imperfecta'. Human Mutation, 29 :1435-1442. [DOI] [Details]
Murphy, A. M., Sheridan, M., O'Neill, M. B., Green, A., ; (2008) 'The walker-warburg phenotype and genotype among Irish travellers'. Journal of Clinical Dysmorphology, 17 (2):119-120. [Details]
Cody N, Green A, McDevitt T, Lynch SA.; (2008) 'Cascade screening in BRCA1/2 mutation carriers'. Irish Medical Journal, 101 (5):140-142. [Details]
Xiao-Qing Liu1, Andrew D. Paterson1,2, Peter Szatmari3 and The Autism Genome Project Consortium4 Anthony J. Bailey1, Gillian Baird2, Christopher Bartlett3, Agatino Battaglia50, Tom Berney4, Catalina Betancur5, Sven Bölte6, Patrick F. Bolton7, Jessica Brian8, Susan E. Bryson9, Joseph D. Buxbaum10, Rita M. Cantor11, Edwin H. Cook12, Hilary Coon13, Christina Corsello14, Michael L. Cuccaro15, Kenneth L. Davis10, Geraldine Dawson16, Maretha de Jonge17, Bernie Devlin18, Sean Ennis19, Annette Estes16, Eric Fombonne20, Christine M. Freitag21, Louise Gallagher22, Daniel H. Geschwind23, John Gilbert15, Michael Gill22, Christopher Gillberg47, Jeremy Goldberg24, Andrew Green19, Jonathan Green25, Stephen J. Guter12, Jonathan L. Haines26, Joachim Hallmayer27, Vanessa Hus14, Sabine M. Klauck28, Olana ; (2008) 'Genome-wide linkage analyses of quantitative and categorical autism sub-phenotypes'. Biological Psychiatry, 64 (7):561-570. [Details]
Lugtenberg D, Kleefstra T, Oudakker AR, Nillesen WM, Yntema HG, Tzschach A, Raynaud M, Rating D, Journel H, Chelly J, Goizet C, Lacombe D, Pedespan JM, Echenne B, Tariverdian G, O'Rourke D, King MD, Green A, van Kogelenberg M, Van Esch H, Gecz J, Hamel BC, van Bokhoven H, de Brouwer AP.; (2008) 'Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy'. European Journal of Human Genetics, . [Details]
Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, Gallagher L. ; (2008) 'Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32'. American Journal of Medical Genetics, . [Details]
ORiordan S.George S. Ennis S, Green A, Hand E. Costigan C. Murphy N. Roche E.Hoey H; (2008) 'Glycaemic Monitoring, Metabolic Control and Genetic Aspects Of Children and Adolescents with Cystic Fibrosis and Cystic Related Diabetes'. Diabetes Care, . [Details]
Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijmans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ; (2007) 'Mapping autism risk loci using genetic linkage and chromosomal rearrangements'. Nature Genetics, 39 (3):319-328. [Details]
Doherty, LS; Kiely, JL; Deegan, PC; Nolan, G; McCabe, S; Green, AJ; Ennis, S; McNicholas, WT; ; (2007) 'Late-onset central hypoventilation syndrome: a family genetic study'. European Respiratory Journal, 29 (2):312-316. [Details]
Brashear, A, Dobyns, WB, Aguiar, PD, Borg, M, Frijns, CJM, Gollamudi, S, Green, A, Guimaraes, J, Haake, BC, Klein, C, Linazasoro, G, Munchau, A, Raymond, D, Riley, D, Saunders-Pullman, R, Tijssen, MAJ, Webb, D, Zaremba, J, Bressman, SB, Ozelius, LJ, ; (2007) 'The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATPIA3 gene'. Brain, 130 :828-835. [Details]
Kelly, H.,Molony, C. M.,Darlow, J. M.,Pirker, M. E.,Yoneda, A.,Green, A. J.,Puri, P.,Barton, D. E.; (2007) 'A genome-wide scan for genes involved in primary vesicoureteric reflux'. J Med Genet, 44 (11):710-7. [Details]
Cronin S, Greenway MJ, Ennis S, Kieran D, Green A, Prehn JH, Hardiman O.; (2006) 'Elevated serum angiogenin levels in ALS'. Neurology, 67 (10):1833-1836. [Details]
Pirker, M.E., Mohanan, N., Colhoun, E., Barton, D., Green, A., Puri, P.; (2006) 'Familial vesicoureteral reflux: influence of sex on prevalence and expression'. JOURNAL OF UROLOGY, 176 (4(2)):1776-1780. [Details]
Sheahan, K; Fox, EJ; Keegan, D; Leahy, DT; Geraghty, R; Mulcahy, H; Green, A; Hyland, JM; O'Donoghue, DP; ; (2006) 'Molecular screening for HNPCC in an Irish population'. Gut, 55 (NA):85-85. [Details]
Greenway M, Andersen P, Russ C, Ennis S, Cashman S, Donaghy C, Patterson V, Swingler R, Morrison K, Green A, Acharya K R, Brown R H, Hardiman O. ; (2006) 'ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis'. Nature Genetics, 38 (4):411-413. [Details]
Banville, N,Geraghty, R,Fox, E,Leahy, DT,Green, A,Keegan, D,Geoghegan, J,O'Donoghue, D,Hyland, J,Sheahan, K; (2006) 'Medullary carcinoma of the pancreas in a man with hereditary nonpolyposis colorectal cancer due to a mutation of the MSH2 mismatch repair gene'. Human Pathology, 37 (11):1498-1502. [DOI] [Details]
Kelly, H; Ennis, S; Yoneda, A; Bermingham, C; Shields, DC; Molony, C; Green, AJ; Puri, P; Barton, DE; ; (2005) 'Uroplakin III is not a major candidate gene for primary vesicoureteral reflux'. European Journal of Human Genetics, 13 (4):500-502. [Details]
Botzenhart, E.M., Green, A., Ilyina, H., Konig, R., Lowry, R.B., Lo, I.F., Shohat, M., Burke, L., McGaughran, J., Chafai, R., Pierquin, G., Michaelis, R.C., Whiteford, M.L., Simola, K.O., Rosler, B., Kohlhase, J.; (2005) 'SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype'. Human Mutation, 26 (3):282-284. [Details]
O'Connell, S., Butler, K., McMenamin, J., Waldron, M., Green, A.J.; (2005) 'Genetic Conditions in the Irish Roma Gypsy Population'. IRISH MEDICAL JOURNAL, 98 (10). [Details]
Murtagh, A; McTigue, O; Ramsay, L; Hegarty, AM; Green, AJ; Stallings, RL; Corvin, A; ; (2005) 'Interstitial deletion of chromosome 21q and schizophrenia susceptibility'. Schizophrenia Research, 78 (2-3):353-356. [Details]
O'Connell, J; Green, A; Crotty, T; O'Shea, D; McKenna, TJ; ; (2004) 'Li-Fraumeni syndrome with adrenocortical tumors producing estrogens in a young man and testosterone in his 18-month-old daughter'. Endocrinologist, 14 (3):133-137. [Details]
Hurley, ME; White, MJ; Green, AJ; Kelleher, J; ; (2004) 'Antley-Bixler syndrome with radioulnar synostosis'. Pediatric Radiology, 34 (2):148-151. [Details]
Greenway, MJ; Alexander, MD; Ennis, S; Traynor, BJ; Corr, B; Frost, E; Green, A; Hardiman, O; ; (2004) 'A novel candidate region for ALS on chromosome 14q11.2'. Neurology, 63 (10):1936-1938. [Details]
Solari V, Ennis S, Yoneda A, Wong L, Messineo A, Hollwarth ME, Green A, Puri P. ; (2003) 'Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system'. J Pediatr Surg, 38 (3):497-501. [Details]
Daly, PA; Nolan, C; Green, A; Ormiston, W; Cody, N; McDevitt, T; O'hIci, B; Byrne, D; McDermott, E; Carney, DN; O'Higgins, N; Barton, DE; ; (2003) 'Predictive testing for BRCA1 and 2 mutations: a male contribution'. Annals of Oncology, 14 (4):549-553. [Details]
Mc Cabe, S; Doherty, L; McNicholas, WT; Green, AJ; Ennis, S; ; (2003) 'A further locus for congenital central hypoventilation syndrome (CCHS)'. American Journal of Human Genetics, 73 (5):561-561. [Details]
Alexander, MD,Traynor, BJ,Miller, N,Corr, B,Frost, E,McQuaid, S,Brett, FM,Green, A,Hardiman, O; (2002) 'True sporadic ALS associated with a novel SOD-1 mutation'. Annals of Neurology, 52 :680-683. [DOI] [Details]
Gallagher, L; Ennis, S; Kearney, G; Fitzgerald, M; Stallings, R; Barton, D; Green, AJ; Gill, M; ; (2002) 'Fine mapping of a susceptibility region and candidate gene studies on chromosome 2q in autism'. American Journal of Medical Genetics, 114 (7):729-729. [Details]
Ennis, S; Wanjing, JN; Kearney, G; Fitzgerald, M; Stallings, R; Barton, DE; Green, AJ; Gallagher, L; Gill, M; ; (2002) 'Mapping of a candidate region for autism on chromosome 2q32'. Journal of Medical Genetics, 39 (NA):81-81. [Details]
Kelly BD, Becker K, Kermode V, Stallings RL, Murphy RP, Green AJ, Hillery J (2002) 'Dysmorphic features and learning disability in an adult male with pure partial trisomy 17q24-q25 due to a terminal duplication'. American Journal of Medical Genetics, 112 (2):217-220. Available Online [DOI] [Details]
Yoneda, A; Cascio, S; Green, A; Barton, D; Puri, P; ; (2002) 'Angiotensin II type 2 receptor gene is not responsible for familial vesicoureteral reflux'. Urology, 168 (3):1138-1141. [Details]
McDonald, DGM; McMenamin, JB; Farrell, MA; Droogan, O; Green, AJ; ; (2002) 'Familial childhood onset neuropathy and cirrhosis with the 4977bp mitochondrial DNA deletion'. American Journal of Medical Genetics, 111 (2):191-194. [Details]
Wienecke, R; Klemm, E; Karparti, S; Swanson, NA; Green, AJ; DeClue, JE; ; (2002) 'Reduction of expression of tuberin, the tuberous-sclerosis-complex-gene-2 product in tuberous sclerosis complex associated connective tissue nevi and sporadic squamous and basal cell carcinomas'. Journal of Cutaneous Pathology, 29 (5):287-290. [Details]
Ennis, S; Wanjing, JN; Kearney, G; Fitzgerald, M; Stallings, R; Barton, DE; Green, AJ; Gallagher, L; Gill, M; ; (2002) 'Mapping of a candidate region for autism on chromosome 2q32'. European Journal of Human Genetics, 10 (NA):240-240. [Details]
O'hIci, B; Miller, N; McDevitt, T; Cody, N; Daly, PA; Carney, D; McDermott, E; Green, AJ; Barton, DE; ; (2002) 'Analysis of BRCA1 and BRCA2 genes in the Irish poulation using denaturing high performance liquid chromatography (dHPLC)'. British Journal of Cancer, 86 (NA):91-91. [Details]
Ennis, S; Bermingham, C; Kelly, H; Yoneda, A; Kelly, S; Shields, D; Molony, C; Green, AJ; Puri, P; Barton, DE; ; (2001) 'Exclusion of the candidate gene Uroplakin III in primary vesicoureteral reflux'. Journal of Medical Genetics, 38 (NA):67-67. [Details]
Willatt, L.R., Pearson, J., and Green, A.J.; (2001) 'Partial trisomy of 2p and neuroblastoma'. American Journal of Medical Genetics, 102 (3):304-305. [Details]
Daly E., MacDermott E.J., and Green A.; (2001) 'Diagnostic review of 66 children with learning disability attending a single centre'. Irish Medical Journal, 94 (6):184-185. [Details]
McEntagart, M; Carey, A; Breen, C; McQuaid, S; Stallings, RL; Green, AJ; King, MD; ; (2001) 'Molecular characterisation of a proximal chromosome 18q deletion'. Journal of Medical Genetics, 38 (2):128-129. [Details]
Willatt, L; Green, AJ; Trump, D; ; (2001) 'Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: a new variant without phenotypic effect'. Journal of Medical Genetics, 38 (10):723-726. [Details]
McDevitt, T; Miller, N; Ormiston, W; Cody, N; Daly, PA; McDermott, E; Carney, DE; Green, AJ; Barton, DE; AlKindi, S; O'Malley, K; Nolan, C; ; (2000) 'BRCA1 and BRCA2 mutation analysis in Irish breast cancer families'. Journal of Medical Genetics, 37 (NA):35-35. [Details]
Ni Chroinin, M; Tormey, P; Ennis, S; Green, AJ; ; (2000) 'Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family'. Journal of Medical Genetics, 37 (NA):66-66. [Details]
Dunlop, A; MacMahon, P; Green, AJ; Stallings, RL; ; (2000) 'A case of Jacobsen syndrome in a neonate with del(11)(q23.3) and his mother with fra(11)(q23.3)'. Journal of Medical Genetics, 37 (NA):46-46. [Details]
Pittock, SJ; Joyce, C; O'Keane, V; Hugle, B; Hardiman, O; Brett, F; Green, AJ; Barton, DE; King, MD; Webb, DW; ; (2000) 'Rapid-onset dystonia-parkinsonism - A clinical and genetic analysis of a new kindred'. Neurology, 55 (7):991-995. [Details]
Charles, C; Corbally, M; Green, AJ; ; (1999) 'A new autosomal recessive syndrome of midline defects with tibial aplasia and oligodactyly'. Journal of Medical Genetics, 36 (NA):61-61. [Details]
Breen, CJ; Barton, L; Carey, A; Dunlop, A; Glancy, M; Hall, K; Hegarty, AM; Khokhar, MT; Power, M; Ryan, K; Green, AJ; Stallings, RL; ; (1999) 'Applications of comparative genomic hybridisation in constitutional chromosome studies'. Journal of Medical Genetics, 36 (7):511-517. [Details]
Conners, R; Turner, J; Green, AJ; ; (1999) 'A subjective study of genetic counselling differences in 2 Celtic regions'. Journal of Medical Genetics, 36 (NA):74-74. [Details]
Green, AJ, Ali, JBM, Sepp, T, Yates, JRW, ; (1997) 'Mutation detection in the TSC1 gene'. American Journal of Human Genetics, 61 (4):334-334. [Details]
Yates, J.R.W., van Bakel, I., Sepp, T., Payne, S.J., Webb, D.W., Nevin, N., and Green, A.J.; (1997) 'Female germline mosaicism in tuberous sclerosis'. Human Molecular Genetics, 6 (13):2265-2269. [Details]
van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Oweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachataki M, Ravine D, Sampson JR, Reeve MP, Richardson P, Wilmer F, Munro C, Hawkins TL, Sepp T, Ali JB, Ward S, Green AJ, Yates JR, Kwiatkowska J, Henske EP, Short MP, Haines JH, Joszwiak S, and Kwiatkowski DJ; (1997) 'Identification of the Tuberous Sclerosis Gene TSC1 on Chromosome 9q34'. Science, 277 :805-808. [Details]
van Bakel, I., Sepp, T., Yates, J.R.W., and Green, A.J.; (1997) 'Mutations in the TSC2 gene : analysis of the complete coding sequence using the protein truncation test (PTT)'. Human Molecular Genetics, 6 (9):1409-1414. [Details]
Nash, RN; Willatt, LR; Andrews, TA; Green, AJ; ; (1997) 'Recurrent multiple aneuploidies: a family with autosomal recessive failure of mitotic control'. American Journal of Human Genetics, 61 (4):136-136. [Details]
Green, A.J., Smith, M., and Yates, J.R.W; (1994) 'Loss of heterozygosity on chromosome 16p in hamartomas from patients with tuberous sclerosis'. Nature Genetics, 6 :193-196. [Details]
Green, A.J., Johnson, P.H., and Yates, A.R.W.; (1994) 'The tuberous sclerosis gene on 9q34 acts as a tumour suppressor'. Human Molecular Genetics, 3 (10):1833-1834. [Details]
Carmody M, Green A, Kinirons M, O'Meara Y, Donohoe J, Murphy S, ; (1990) 'Familial adult medullary cystic disease with spastic quadriparesis: a new disease association'. Clinical Nephrology, 33 (5):237-240. [Details]
Donohoe J, Green A, O'Meara Y, Sheehan J, Carmody M, Doyle G, ; (1990) 'The use of cyclosporin A in adult nephrotic syndrome: nine cases and literature review'. Irish Journal of Medical Science, 159 (6):178-181. [Details]
Donohoe J, Green A, O'Meara Y, Campbell E, Carmody M, ; (1990) 'Successful treatment with cyclosporin of nephrotic syndrome due to focal segmental glomerulosclerosis recurring in a renal transplant'. Nephrology Dialysis Transplantation, 5 (4):321-322. [Details]
Carmody M, O'Meara Y, Green A, Donohoe J, Hanson J, Murphy DM, McLean P, ; (1989) 'Living related renal transplantation in Ireland: a sixteen year review'. Irish Journal of Medical Science, 158 (8):206-209. [Details]
Donohoe J, O'Meara Y, Green A, Carmody M, Doyle G, ; (1989) 'Systemic vasculitis with renal involvement--a review'. Irish Journal of Medical Science, 158 (12):300-303. [Details]
O'Meara YM, Carmody M, Donohoe J, Green A, Doyle G, Campbell E, Browne O, Walshe JJ. ; (1989) 'Recurrent Glomerulonephritis in Renal Transplants - 14 Years Experience'. Nephrology Dialysis Transplantation, . [Details]

Other Journals

O'Brien RP, Phelan PJ, Conroy J, O'Kelly P, Green A, Keogan M, O'Neill D, Jennings S, Traynor C, Casey J, McCormack M, Conroy R, Chubb A, Ennis S, Shields DC, Cavalleri GL, Conlon PJ (2013) 'A genome-wide association study of recipient genotype and medium-term kidney allograft function' clinical transplantation . [Details]
J. M. Darlow, M. G. Dobson, R. Darlay, C. M. Molony, M. Hunziker, A. J. Green, H. J. Cordell, P. Puri & D. E. Barton (2013) 'A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic' Molecular Genetics and Genomic Medicine . [Details]
Farrell MP, Hughes DJ, Berry IR, Gallagher DJ, Glogowski EA, Payne SJ, Kennedy MJ, Clarke RM, White SA, Muldoon CB, Macdonald F, Rehal P, Crompton D, Roring S, Duke ST, McDevitt T, Barton DE, Hodgson SV, Green AJ, Daly PA (2012) 'Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome' Familial Cancer . [Details]
A Green; (2005) 'Human Biological Material ; Recommendations for collection, use and storage in research' . [Details]

Conference Publications

Higgins M, Crowley A, McDevitt T, Cody N, Meany M, de Baroid C, Adams M, Berkeley E, Nolan C, Clarke R, Farrell M, Daly P, Green A, Barton D; (2009) Spectrum and Incidence of BRCA1 and BRCA2 Mutations in the Republic of Ireland ¿ An Audit British Human Genetics Conference 2009 [Details]
Sheahan, K; Fox, EJ; Keegan, D; Leahy, DT; Geraghty, R; Mulcahy, H; Green, A; Hyland, JM; O'Donoghue, DP; ; (2006) GUT 55: Suppl. 2, A85 Molecular screening for HNPCC in an Irish population [Details]
Gokhale, D., Coyne, F., Healey, C., Green, A., Turner, J., Ryan, C. Mountford R.; (2005) Suspected Paternal Isodisomy of chromosome 5 in a child affected with spinal muscular atrophy British Society of Human Genetics , 12-SEP-05 - 14-SEP-05 [Details]
Roring, S., McQuaid, S., Grehan, D., O'Brien, J., McDermott, M., Barton D. Green, A.; (2005) The Complexity of Hereditary Non-Polyposis Colon Cancer (HNPCC) Diagnosis in the Irish Population Irish Society for Human Genetics , 19-SEP-05 - 19-SEP-05 [Details]
Greenway, M., Russ, C., Ennis, S., Cashman, S., Neng, L., Raman, V., Anderson, P., Green, A. Hardiman, O.; (2005) Segregation of the TAU haplotype in ALS 16th INTERNATIONAL SYMPOSIUM ON ALS/MND , 08-DEC-05 - 10-DEC-05 [Details]
Lalor, S., Gallagher, L., Kearney, G., Fitzgerald, M., Barton, D.E., Green, A.J., Gill, M. Ennis, S.; (2005) Mutation screening of a break-point candidate gene for autism, UBE2E3, on chromosome 2q31.3 Irish Society for Human Genetics , 19-SEP-05 - 19-SEP-05 [Details]
McDevitt, T., O'hIci, B., Cody, N., Adams, M., Miller, N., Ormiston, W., Berkeley, E., Nolan, C., Clarke, R., Daly, P.A., McDermott, E., Carney, D.E., Green, A.J. Barton, D.E.; (2005) Incidence of BRCA1 and BRCA2 Mutations in Irish Breast Cancer Families Irish Society for Human Genetics , 19-SEP-05 - 19-SEP-05 [Details]
Conroy, J., Cochrane, L., Segurado, R., Meally, E., Green, A., Ennis, S., Gill, M. Gallagher, L.; (2005) Further evidence supporting the role of ITGA4 as a candidate gene for Autism Xlllth World Congress of Psychiatic Genetics , 12-OCT-05 - 18-OCT-05 [Details]
Russ, C., Greenway, M., Ennis, S., Green, A., Swingler, R., Hardiman, O. Brown Jr, R.H.,; (2005) Analysis of Vascular endothelial growth factor (VEGF) haplotypes and risk for ALS in North American, Irish and Scottish populations 16th INTERNATIONAL SYMPOSIUM ON ALS/MND , 08-DEC-05 - 10-DEC-05 [Details]
Murphy, A.M., Lynch, S.A. Green, A.J.; (2005) Accuracy of a Clinical Diagnosis of Marfan Syndrome Irish Society for Human Genetics , 19-SEP-05 - 19-SEP-05 [Details]
Conroy J, Cochrane L, Segurado R, Meally E, Green A, Ennis S, Gill M and Gallagher L. ; (2005) Further evidence supporting the role of ITGA4 as a candidate gene for Autism The XIIIth World Congress on Psychiatric Genetics [Details]
Greenway M, Russ C, Ennis S, Traynor B, Green A, Brown RH, Hardiman O. ; (2005) Hypoxia-inducible genes in motor neuron degeneration Biochemical Society [Details]
Greenway M., Ennis S., Alexander M., Green A., Hardiman O. ; (2004) Angiogenesis and ALS: Screening for new mutations in sporadic ALS European Neurological Society [Details]
Greenway M., Ennis S., Alexander M., Green A., Hardiman O; (2004) Identification of a novel candidate region for sporadic amyotrophic lateral sclerosis ESHG European Society for Human Genetics [Details]
Greenway M., Alexander M., Ennis S., Traynor B., Rogers M., O¿Hici B., Lynch C., O¿Toole O., Corr B., Frost E., Green A., Hardiman O. ; (2004) Single nucleotide polymorphisms in Amyotrophic Lateral Sclerosis Proceedings of the Beaumont Hospital Scientific Meeting [Details]
Greenway M., Alexander M., Ennis S., Green A., Hardiman O; (2004) Angiogenesis and ALS: Screening of a novel candidate gene in the Irish ALS Population American Academy of Neurology [Details]
Greenway M, Russ C, Ennis S, Traynor B, Alexander M, Broom W, Corr B, McNally S, Green A, Brown RH, Hardiman O. ; (2004) Molecular genetic analysis of the angiogenin (ANG) gene in two distinct sporadic ALS populations 15th International Symposium on ALS/MND [Details]
Solari, V,Ennis, S,Yoneda, A,Wong, L,Messineo, A,Hollwarth, ME,Green, A,Puri, P (2003) JOURNAL OF PEDIATRIC SURGERY Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system , pp.497-501 [DOI] [Details]
Sarah Mc Cabe, Liam Doherty, Walter T McNicholas , Andrew J Green and Sean Ennis; (2003) A further Locus for Congenital Central Hypoventilation Syndrome (CCHS) BSHG British Society for Human Genetics [Details]
MD Alexander, BJ Traynor, S Ennis, N Miller, B Corr, A Green and O Hardiman; (2003) Association between the D148E APEX polymorphism and a novel candidate gene in the Irish ALS population 14th International Congress on ALS/MND [Details]
Sarah Mc Cabe, Liam Doherty, Walter T McNicholas , Andrew J Green and Sean Ennis. ; (2003) A further Locus for Congenital Central Hypoventilation Syndrome (CCHS) ISHG Irish Society for Human Genetics Annual Scientific Meeting [Details]
Sean Ennis, Louise Gallagher, Geraldine Kearney, Michael Fitzgerald, Raymond Stallings, David E Barton, Andrew J Green, and Michael Gill.; (2002) Mapping of a Candidate Region for Autism on Chromosome 2q32 IMFAR International Meeting for Autism Research [Details]
Louise Gallagher, Sean Ennis, Geraldine Kearney, Michael Fitzgerald, Raymond Stallings, David E Barton, Andrew J Green and Michael Gill.; (2002) Fine Mapping of a susceptibility Region and Candidate gene studies on Chromosome 2q32in Autism ISHG Irish Society for Human Genetics Annual Scientific Meeting [Details]

Published Reports

Lugtenberg D, Kleefstra T, Oudakker AR, Nillesen WM, Yntema HG, Tzschach A, Raynaud M, Rating D, Journel H, Chelly J, Goizet C, Lacombe D, Pedespan JM, Echenne B, Tariverdian G, O'Rourke D, King MD, Green A, van Kogelenberg M, Van Esch H, Gecz J, Hamel BC, van Bokhoven H, de Brouwer AP.; (2008) Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy. . [Details]
           

Reports

Irish Council for Bioethics; (2005) Human Biological Material ; Recommendations for collection, use and storage in research. Reports [Details]
       

Abstract

Aloraifi, F,McDevitt, T,Cody, N,Meanie, M,de Baroid, C,Kelly, R,Bracken, A,Green, A,Geraghty, J (2012) Clinical and Pathological Characteristics of Patients with BRCA1 and BRCA2 Mutation-Negative Familial Breast Cancer in Ireland. Abstract [Details]
Green, A,Casey, J,Kawaguchi, R,Morrissey, M,Sun, H,McGettigan, P,Nielsen, J,Conroy, J,Regan, R,Tormey, P,Chroinin, MN,Kennedy, B,Lynch, SA,Ennis, S (2011) First implication of STRA6 mutations in isolated anophthalmia, microphthalmia and coloboma. Abstract [Details]
Low, E,Mitruskova, B,Riordan, M,Hensey, O,Green, A,Monavari, A,Treacy, E,Murphy, AM (2010) AN UNUSUAL CASE OF RENAL STONES, FAILURE TO THRIVE AND HYPOTONIA IN A MALE INFANT. Abstract [Details]
Sheahan, K,Fox, EJ,Keegan, D,Leahy, DT,Geraghty, R,Mulcahy, H,Green, A,Hyland, JM,O'Donoghue, DP (2006) Molecular screening for HNPCC in an Irish population. Abstract [Details]
                                                             

Letters

Jenkinson, EM,Clayton-Smith, J,Mehta, S,Bennett, C,Reardon, W,Green, A,Pearce, SHS,De Michele, G,Conway, GS,Cilliers, D,Moreton, N,Davis, JRE,Trump, D,Newman, WG (2012) Perrault syndrome: further evidence for genetic heterogeneity. Letters [DOI] [Details]

Research

Research Interests

  • Clinical Genetics
  • Hereditary Breast Cancer
  • Clinical Application of Human Molecular Genetics
  • Genetics of Renal Disease
  • Ethical Issues in Human Genetics

The Department of Medical Genetics, UCD, is based in the National Centre for Medical Genetics, Our Lady's Hospital, Crumlin (http://www.genetics.ie/). There is a wide range of interests covering the applications of molecular genetic technology at both diagnostic and research levels into both single gene and more complex genetic disorders.

The Department has had a long standing collaboration with Dr. Orla Hardiman, consultant neurologist Beaumont hospital, along with the Royal College of Surgeons in Ireland, studying the genetic contribution to amyotrophic lateral sclerosis (ALS), also known as motor neuron disease. The collaboration has been able to take advantage of a well-ascertained database of Irish patients with motor neuron disease, and has recently identified a new genetic locus for ALS on chromosome 14.


The Department has also had a very fruitful collaboration with Prof. Prem Puri, Newman Professor UCD, who has established the world's largest resource of patients with the complex genetic disorder, vesico-ureteric reflux. Genetic studies have been under way on over 700 DNA samples from affected families, and a whole genome scan has identified several very promising leads.


The Department has also had a close links with the Departments of Genetics and psychiatry, Trinity College Dublin, and has collaborated for 2 years in identifying a locus for the genetic component of autism on chromosome 2q. The two groups have formally launched the Irish Autism Genome Collaboration, and are now part of a worldwide consortium identifying the genetic components to autism.



Research Projects

Sponsor : Health Research Board (HRB)
Title : Autism Genome Project
Start Date / End Date : 01-FEB-07 / 30-JUN-11
Sponsor : EU Non Framework
Title : Orpahnet
Start Date / End Date : 01-DEC-03 / 30-NOV-06
Sponsor : Health Research Board (HRB)
Title : Expanding the phenotype of human MELP2 mutations beyond classic rett syndrome
Start Date / End Date : 01-DEC-01 / 30-NOV-02
Sponsor : Health Research Board (HRB)
Title : Transgenomic wave dHPLC/Nucleic Acid Fragment Analysis System
Start Date / End Date : 01-OCT-00 / 14-NOV-00
Sponsor : Health Research Board (HRB)
Title : No Project title to migrate.
Start Date / End Date : 01-AUG-98 / 01-AUG-99
   

Collaborators

 

External Collaborators

Dr. Orla Hardiman
Consultant neurologist Beaumont Hospital, Dublin

Prof. Prem Puri
Newman Professor UCD.