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researcher

Sean Ennis

Lecturer

School of Medicine
C3.29
Health Sciences Centre
Belfield Dublin 4

Tel: +353 1 716 6685
Email: sean.ennis@ucd.ie

Biography

I am interested in the application of Genomics to genetic diseases. The main focus of my group is to make a meaningful contribution to the field of Human genetics. I am particularly interested in contributing to the progression of gene discovery to diagnostics, and ultimately to the cure or prevention of serious genetic conditions. I have been involved in establishing international collaborative approaches to the study of the genetics of Autism Spectrum Disorder (ASD) and rare genetic diseases.

Professional

         

Conference Contributions

Vaughan, L. and Ennis, S.; The diagnosis of freemartinism in cattle using sex-specific DNA sequences. [Published Abstract], Proc. Thirty Third Winter Scientific Meeting AVTRW, (1996) , Dublin .
ODoherty E., Aherne M., Ennis S., Healy A., Doherty M., Weavers E., Roche J.F. and Sweeney T.; (1999) Prion protein genotype of scrapie-infected sheep in Ireland . [N/A], 5th Agricultural Research Forum, 26th/27th March. Abstract, Irish Journal of Agricultural Research (1999), * , 26-MAR-99 - 27-MAR-99.
   

Education

Year 1994 Institution: University College Dublin
Qualification: PhD Subject:
Year 1981 Institution: Dublin Institute of Technology (DIT), IRL
Qualification: Dip App Bio Scs Subject:
Year 1981 Institution: Dublin Institute of Technology (DIT), IRL
Qualification: Dip Sc Tech Subject:
Year Institution:
Qualification: MICI Subject:
Year Institution:
Qualification: MISAG Subject:
Year 2007 Institution:
Qualification: MICI Subject:
         

Publications

     

Peer Reviewed Journals

Allen NM, Conroy J;Shahwan A;Lynch B;Correa RG;Pena SD;McCreary D;Magalh¿¿es TR;Ennis S;Lynch SA;King MD (2016) 'Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion'. Epilepsia, 57 (1):1-1. [DOI] [Details]
Casey JP, Brennan K;Scheidel N;McGettigan P;Lavin PT;Carter S;Ennis S;Dorkins H;Ghali N;Blacque O;Mc Gee MM;Murphy H;Lynch SA (2016) 'Recessive NEK9 mutation causes a lethal skeletal dysplasia with evidence of cell cycle and ciliary defects'. Human Molecular Genetics, . [DOI] [Details]
Jillian P Casey, Patricia Goggin, Jennifer McDaid, Martin White, Sean Ennis, David R Betts, Jane S Lucas, Basil Elnazir, Sally Ann Lynch (2015) 'A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder'. BMC Medical Genetics, 16 (1):45-45. Available Online Link to full text [Details]
Coleman C, Quinn EM;Ryan AW;Conroy J;Trimble V;Mahmud N;Kennedy N;Corvin AP;Morris DW;Donohoe G;O'Morain C;MacMathuna P;Byrnes V;Kiat C;Trynka G;Wijmenga C;Kelleher D;Ennis S;Anney RJ;McManus R (2015) 'Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci'. European Journal of Human Genetics, . [DOI] [Details]
Morrison MA, Magalhaes TR;Ramke J;Smith SE;Ennis S;Simpson CL;Portas L;Murgia F;Ahn J;Dardenne C;Mayne K;Robinson R;Morgan DJ;Brian G;Lee L;Woo SJ;Zacharaki F;Tsironi EE;Miller JW;Kim IK;Park KH;Bailey-Wilson JE;Farrer LA;Stambolian D;DeAngelis MM (2015) 'Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world'. Frontiers in Genetics, 6 . [DOI] [Details]
Casey; JP, Crushell, E; Thompson, K; Twomey, E; He, L; Ennis, S; Philip, RK; Taylor, RW; King, MD; Lynch, SA. (2015) 'Periventricular calcification, abnormal pterins and dry thickened skin: expanding the clinical spectrum of RMND1 ?'. Journal Of Inherited Metabolic Disease, . [Details]
Allen NM, Conroy J, Shahwan A, Ennis S, Lynch B, Lynch SA, King MD. (2015) 'Chromosomal microarray in unexplained severe early onset epilepsy - A single centre cohort'. European Journal of Paediatric Neurology, . [Details]
Conroy J, Allen NM, Gorman K, Shahwan A, Ennis S, Lynch SA, King MD. (2015) 'NAPB - A Novel SNARE Associated Protein for Early Onset Epileptic Encephalopathy'. Clinical Genetics, . [Details]
Casey, J.P. and McGettigan, P.A. and Healy, F. and Hogg, C. and Reynolds, A. and Kennedy, B.N. and Ennis, S. and Slattery, D. and Lynch, S.A. (2015) 'Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population'. European Journal of Human Genetics, 23 (2):210-217. Available Online [DOI] [Details]
Casey, J; McGettigan, P; Brosnahan, D; Curtis, E; Treacy, E; Ennis, S; Lynch, SA. (2014) 'Atypical Alstrom syndrome with novel ALMS1 mutations precluded by current diagnostic criteria'. European Journal of Medical Genetics, 57 (2-3):55-59. Available Online [DOI] Link to full text [Details]
Seoighe DM, Gadancheva V;Regan R;McDaid J;Brenner C;Ennis S;Betts DR;Eadie PA;Lynch SA (2014) 'A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome'. American Journal of Medical Genetics, Part A, 164A (11):2958-2960. [DOI] [Details]
G¿¿mez-Herreros F, Schuurs-Hoeijmakers JH;McCormack M;Greally MT;Rulten S;Romero-Granados R;Counihan TJ;Chaila E;Conroy J;Ennis S;Delanty N;Cort¿¿s-Ledesma F;de Brouwer AP;Cavalleri GL;El-Khamisy SF;de Vries BB;Caldecott KW (2014) 'TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function'. Nature Genetics, 46 (5):516-521. [DOI] [Details]
Lynn M, Shah N;Conroy J;Ennis S;Morris T;Betts D;O'Sullivan M (2014) 'A Study of Alveolar Rhabdomyosarcoma Copy Number Alterations by Single Nucleotide Polymorphism Analysis'. Diagnostic Molecular Pathology, . [DOI] [Details]
Conroy J, McGettigan PA, McCreary D, Shah N, Collins K, Parry-Fielder B, Moran M, Hanrahan D, Deonna TW, Korff CM, Webb D, Ennis S, Lynch SA, King MD (2014) 'Towards the identification of a genetic basis for Landau-Kleffner syndrome'. Epilepsia, . [Details]
Jillian P Casey, Dubhfeasa Slattery, Paul McGettigan, Claire Hogg, Alison Reynolds, Breandan N Kennedy Sean Ennis Sally Ann Lynch (2014) 'Surprising genetic heterogeneity with known and novel disease genes for primary ciliary dyskinesia in the Irish Traveller population'. European Journal of Human Genetics, . [Details]
Allen NM, Conroy J, Shahwan A, Ennis S, Lynch B, Lynch SA, King MD (2014) 'Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms-A further patient'. American Journal of Medical Genetics Part A, . [Details]
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 (2013) 'Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders'. Molecular Psychiatry, . [DOI] [Details]
Casey, J; McGettigan, P; Healy, F; Hogg, C; Reynolds, A; Kennedy, B; Ennis, S; Slattery, D; Lynch, SA. (2013) 'Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population'. European Journal of Human Genetics, . Available Online [DOI] Link to full text [Details]
Orr, N., Hill, E. W., Gu, J., Govindarajan, P., Conroy, J., van Grevenhof, E. M., Ducro, B. J., van Arendonk, J. A., Knaap, J. H., van Weeren, P. R., Machugh, D. E., Ennis, S., Brama, P. A. (2013) 'Genome-wide association study of osteochondrosis in the tarsocrural joint of Dutch Warmblood horses identifies susceptibility loci on chromosomes 3 and 10'. Animal Genetics, 44 (4):408-12. [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]
Lynn M, Wang Y, Slater J, Shah N, Conroy J, Ennis S, Morris T, Betts DR, Fletcher JA, O'Sullivan MJ (2013) 'High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcoma'. Diagnostic Molecular Pathology, 22 (2):76-84. [DOI] [Details]
Conroy J, McGettigan P, Murphy R, Webb D, Murphy SM, McCoy B, Albertyn C, McCreary D, McDonagh C, Walsh O, Lynch S, Ennis S (2013) 'A novel locus for episodic ataxia:UBR4 the likely candidate'. European Journal of Human Genetics, . [DOI] [Details]
Magalhaes, TR,Casey, JP,Conroy, J,Regan, R,Fitzpatrick, DJ,Shah, N,Sobral, J,Ennis, S (2012) 'HGDP and HapMap Analysis by Ancestry Mapper Reveals Local and Global Population Relationships'. PLoS ONE, 7 . [DOI] [Details]
Casey J, McGettigan P, Lynam-Lennon N, McDermott M, Regan R, Conroy J, Bourke B, O¿ Sullivan J, Crushell E, Lynch SA, Ennis S. (2012) 'Identification of a mutation in LARS as a novel cause of infantile hepatopathy'. Molecular Genetics and Metabolism, 106 (3):351-358. Link to full text [Details]
Casey J, Magalhaes T, Conroy J, Regan R, Shah N, Anney R, Shields D, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan A, Cali P, Correia A, Corsello A, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SA, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter JT, Hakonarson H, Holt R, Hughes G, Hus A, 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 JAS, 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 SH, Haines JL, Hallmayer J, Monaco AP, Nurnberger Jr. JI, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland V, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S. (2012) 'A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder'. Human Genetics, 131 (4):565-579. Link to full text [Details]
Casey J, Nobbs M, McGettigan P, Lynch SA, Ennis S. (2012) 'Recessive mutations in MCM4/PRKDC cause a novel syndrome involving a primary immunodeficiency and a disorder of DNA repair'. Journal of Medical Genetics, 49 (4):242-245. Link to full text [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]
Orr N, Hill EW, Gu J, Govindarajan P, Conroy J, van Grevenhof EM, Ducro BJ, van Arendonk JA, Knaap JH, van Weeren PR, Machugh DE, Ennis S, Brama PA (2012) 'Genome-wide association study of osteochondrosis in the tarsocrural joint of Dutch Warmblood horses identifies susceptibility loci on chromosomes 3 and 10'. Gene, . [DOI] [Details]
Lynch SA, Foulds N, Thuresson AC, Collins AL, Annerén G, Hedberg BO, Delaney CA, Iremonger J, Murray CM, Crolla JA, Costigan C, Lam W, Fitzpatrick DR, Regan R, Ennis S, Sharkey F (2011) 'The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth'. European Journal of Human Genetics, 19 (5):534-539. [DOI] [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, 19 :1082-1089. [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, Ní Chróinín M, Kennedy BN, Lynch SA, 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). Link to full text [Details]
Baker, LB,Conroy, J,Donoghue, V,Mullarkey, M,Shah, N,Murphy, N,Murphy, J,Ennis, S,Lynch, SA; (2011) 'Agenesis of the corpus callosum with midline lipoma associated with an Xp22.31-Xp22.12 deletion'. Journal of Clinical Dysmorphology, 20 :21-25. [DOI] [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]
Abdul Noor, Annabel Whibley, Christian R. Marshall, Peter J. Gianakopoulos, Amelie Piton, Andrew R. Carson, Marija Orlic-Milacic, Anath C. Lionel, Daisuke Sato, Dalila Pinto, Irene Drmic, Carolyn Noakes, Lili Senman, Xiaoyun Zhang, Rong Mo, Julie Gauthier, Jennifer Crosbie, Alistair T. Pagnamenta, Jeffrey Munson, Annette M. Estes, Andreas Fiebig, Andre Franke, Stefan Schreiber, Alexandre F. R. Stewart, Robert Roberts, Ruth McPherson, Stephen J. Guter, Edwin H. Cook, Jr., Geraldine Dawson, Gerard D. Schellenberg, Agatino Battaglia, Elena Maestrini, Autism Genome Project Consortium, Linda Jeng, Terry Hutchison, Evica Rajcan-Separovic, Albert E. Chudley, Suzanne M. E. Lewis, Xudong Liu, Jeanette J. Holden, Bridget Fernandez, Lonnie Zwaigenbaum, Susan E. Bryson, Wendy Roberts, Peter Szatmari, Louise Gallagher, Michael R. Stratton, Jozef Gecz, Angela F. Brady, Charles E. Schwartz, Russell J. Schachar, Anthony P. Monaco, Guy A. Rouleau, Chi-chung Hui, F. Lucy Raymond, Stephen W. Scherer, and John B. Vincent; (2010) 'Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability'. Sci Transl Med, 2 (49):49-68. [Details]
C. T. Correia, A. M. Coutinho, A. F. Sequeira, I. G. Sousa, L. Lourenco Venda, J. P. Almeida, R. L. Abreu, C. Lobo, T. S. Miguel, J. Conroy, L. Cochrane, L. Gallagher, M. Gill, S. Ennis, G. G. Oliveira and A. M. Vicente. ; (2010) 'Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism'. Genes Brain And Behavior, 2010 (9):841-848. [Details]
Orr N, Back W, Gu J, Leegwater P, Govindarajan P, Conroy J, Ducro B, Van Arendonk JAM, MacHugh DE, Ennis S, Hill EW, Brama PAJ ; (2010) 'Genome-wide SNP association-based localization of a dwarfism gene in Friesian dwarf horses'. Animal Genetics, 41 (suppl. 2):2-7. Available Online [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]
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]
Lynch SA; (2010) 'The 12q14 microdeletion syndrome; 6 new cases confirming the role of HMGA2 in growth'. Eurppean Journal of Human Genetics, . [Details]
Correia et al; (2009) 'Increased BDNF levels and association with the NTRK2 gene suggest a disruption of BDNF/TRKB signaling in autism'. Human Molecular Genetics, . [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, 7265 (461):802-808. [Details]
Gallagher L, Conroy J, Cochrane L, Anney RJ, Sutcliffe JS, Carthy P, Dunlop A, Mullarkey M, O'hici B, Green AJ, Ennis S, Gill M, ; (2009) 'Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32'. Journal of Medical Genetics, 150B (4):535-544. [DOI] [Details]
Meisler MH, Russ C, Montgomery KT, Greenway M, Ennis S, Hardiman O, Figlewicz DA, Quenneville NR, Conibear E, Brown RH Jr (2008) 'Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS'. Amyotrophic Lateral Sclerosis, 9 (3):141-148. [DOI] [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]
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]
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]
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]
Greenway MJ, Andersen PM, Russ C, Ennis S, Cashman S, Donaghy C, Patterson V, Swingler R, Kieran D, Prehn J, Morrison KE, Green A, Acharya KR, Brown RH Jr, Hardiman O (2006) 'ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis'. Nature Genetics, 38 (4):411-413. [DOI] [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]
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]
Solari V, Ennis S, Cascio S, Puri P (2004) 'Tumor necrosis factor-alpha gene polymorphism in reflux nephropathy'. Urology, 172 (4 Pt 2):1604-161. [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]
Kelly H, Ennis S, Yonedia A, Bermingham C, Shields D, Molony C, Green AJ, Puri P, Barton DE ; (2004) 'Uroplakin III Is Not a Major Candidate Gene for Primary Vesicoureteral Reflux'. EUROPEAN JOURNAL OF HUMAN GENETICS, 13 :500-502. [Details]
Hunter, A. M., St Clair Gibson, A., Lambert M., Dennis, S., Mullany, H., O'Malley, M.J., Vaughan, C.L., Kay, D., Noakes, T.D.; (2003) 'EMG amplitude in maximal and submaximal exercise is dependent on signal capture rate'. International Journal of Sports Medicine, 24 (2):83-89. [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]
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'. Journal of Pediatric Surgery, 38 (3):497-501. [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]
Rogers, M; Ennis, S; Bailey, DMD; Barrett, T; Kelly, H; Hughes, B; Harrison, RF; Barton, DE; ; (2002) 'Validation of the consensus Y chromosome deletion screening set in the Irish population'. Journal of Medical Genetics, 39 (NA):82-82. [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]
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]
Vaughan L, Schofield W, Ennis S. ; (2001) 'SRY-negative XX sex reversal in a pony: a case report'. Theriogenology, 55 (5):1051-1057. [Details]
O'Doherty E, Aherne M, Ennis S, Weavers E, Roche JF, Sweeney T. ; (2001) 'Prion protein gene polymorphisms in pedigree sheep in Ireland'. Research in Veterinary Science, 70 (1):51-56. [Details]
O'Doherty E, Aherne M, Ennis S, Roche JF and Sweeney T ; (2000) 'A study of PrP (scrapie) genotypes in sheep breeds in Ireland'. IRISH VETERINARY JOURNAL, 54 (106). [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]
O'Doherty, E., Aherne, M., Ennis, S., Weavers, E., Hunter, N., Roche, J.F., Sweeney, T.; (2000) 'Detection of polymorphisms in the prion protein gene in a population of Irish Suffolk sheep'. Veterinary Record, 146 :335-338. [Details]
Ennis, S,Vaughan, L,Gallagher, TF; (1999) 'The diagnosis of freemartinism in cattle using sex-specific DNA sequences'. Research in Veterinary Science, 67 :111-112. [Details]
O'Doherty E, Aherne M, Ennis S, Weavers E, Roche JF and Sweeney T ; (1999) 'Detection of polymorphisms in the ovine prion protein gene in an Irish Suffolk population'. IRISH VETERINARY JOURNAL, 52 (4):190-191. [Details]
ODoherty E., Aherne M., Ennis S., Healy A., Doherty M., Weavers E., Roche J.F. and Sweeney T.; (1999) 'Prion protein genotype of scrapie-infected sheep in Ireland . 5th Agricultural Research Forum, 26th/27th March (Abstract)'. Irish Journal of Agricultural Research, 40 :299. [Details]
Barendse W, Vaiman D, Kemp SJ, Sugimoto Y, Armitage SM, Williams JL, Sun HS, Eggen A, Agaba M, Aleyasin SA, Band M, Bishop MD, Buitkamp J, Byrne K, Collins F, Cooper L, Coppettiers W, Denys B, Drinkwater RD, Easterday K, Elduque C, Ennis S, Erhardt G, Li L (1997) 'A medium-density genetic linkage map of the bovine genome'. Mammalian genome : official journal of the International Mammalian Genome Society, 8 (1):21-28. [Details]
Monteagudo LV, Heriz A, Flavin N, Rogers M, Ennis S, Arruga MV (1996) 'Fluorescent in situ localization of the bovine activin receptor type IIA locus on chromosome 2 (2q2.3-2.4)'. Mammalian genome : official journal of the International Mammalian Genome Society, 7 (11). [Details]
Flavin N, Heriz A, Monteagudo LV, Ennis S, Martin F, Barendse W, Arruga MV, Rogers M. ; (1996) 'Cloning of the bovine activin receptor type II gene (ACVR2) and mapping to chromosome 2 (BTA2) by somatic cell genetic analysis and the genotyping of an associated microsatellite UCD2'. Cell Genetics and Cytogenitics, 75 (1):25-29. [Details]
Flavin, N; Monteagudo, L; Heriz, A; Tejedor, MT; Ennis, S; Rogers, M; Arruga, MV; ; (1996) 'DNA sequence and synteny and linkage mapping of bovine activin receptor type IIA (ActRIIA)'. Cytogenetics and Cell Genetics, 74 (3):231-232. [Details]
Monteagudo, L; Heriz, A; Flavin, N; Ennis, S; Rogers, M; Arruga, MV; ; (1996) 'FISH mapping of activin receptor type IIA (ActRIIA) to bovine chromosome 2q2.2->q2.4'. Cytogenetics and Cell Genetics, 74 (3):237-237. [Details]
Flavin, N; Heriz, A; Monteagudo, LV; Ennis, S; Martin, F; Barendse, W; Arruga, MV; Rogers, M; ; (1996) 'Cloning of the bovine activin receptor type II gene (ACVR2) and mapping to chromosome 2 (BTA2)'. Cytogenetics and Cell Genetics, 75 (1):25-29. [Details]
Rogers M, Flavin N, Ennis S, Condon J, ; (1995) 'UCD001: a bovine cosmid containing a polymorphic dinucleotide repeat maps to chromosome 4'. Animal Genetics, 26 (5):372-373. [Details]
ENNIS, S,GALLAGHER, TF; (1994) 'A PCR-BASED SEX-DETERMINATION ASSAY IN CATTLE BASED ON THE BOVINE AMELOGENIN LOCUS'. Gene, 25 :425-427. [Details]
Gallagher TF, Ennis S, ; (1994) 'A PCR-based sex-determination assay in cattle based on the bovine amelogenin locus'. Animal Genetics, 25 (6):425-427. [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]
O'Doherty E, Aherne M, Ennis S, Hunter N, Weavers E, Roche JF and Sweeney T ; (1999) 'Detection of polymorphisms in the ovine prion protein gene in scrapie infected sheep in Ireland' Irish Journal of Agricultural Research 38 (299A) . [Details]
Monteagudo, L. V., Heriz, A., Flavin, N., Rogers, M., Ennis, S., and Arruga, M. V. ; (1996) 'Fluorescent in situ localization of the bovine activin receptor type IIA locus on chromosome 2 (2q2.3-2.4)' Mammalian Genome 7 :869. [Details]

Conference Publications

T. R. Magalhães , J. Casey , C. Correia , F. Sequeira , M. Espada , S. Ennis , A. M. Vicente and AGP , Autism Genome Project ; (2010) Genome-Wide Association Analysis of Susceptibility Genes in Autism Using with a Gene-Centric Approach 9th Annual International Meeting for Autism Research (IMFAR) [Details]
Autism Genome Project Consortium , AGP Institutions in, North America and Europe,; (2010) Genome-Wide Analysis Identifies Global Rare Variation in Autism 9th Annual International Meeting for Autism Research (IMFAR) [Details]
J. Conroy, J. Casey, N. Shah, R. Regan, M. Morgan, K. Collins, B. Parry-Fielder, S. A. Lynch, M. King, S. Ennis ; (2010) An investigation into the causes of Landau-Kleffner Syndrome ASHG American Society for Human Genetics [Details]
R. Regan, L. Baker, J. Conroy, V. Donoghue, M. Mullarkey, N. Shah, N. Murphy, S. Ennis, S. A. Lynch; (2010) Lipomatous cortical dysplasia with lipoma of the corpus callosum associated with an Xp deletion ASHG American Society for Human Genetics [Details]
Milewski MA, Leahy DT, Conroy J, Ennis S, Mulcahy H, Hyland J, O'Donoghue D, Sheahan K.; (2010) MODERN PATHOLOGY 23: Suppl. 1, 156 Genome-wide DNA methylation profiling of sporadic and familial colorectal cancer [Details]
A. Noor, A. Whibley, C. R. Marshall, AGP. Autism Genome Project Consort., G. A. Rouleau, C. C. Hui, F. L. Raymond, S. W. Scherer, J. B. Vincent; (2010) Disruption at the PTCHD1 locus on Xp22.11 results in autism spectrum disorder and intellectual disability ASHG American Society for Human Genetics [Details]
D. Pinto, S. W. Scherer, Autism Genome Project Consortium (AGP) ; (2010) Functional impact of global rare copy number variation in autism spectrum disorders ASHG American Society for Human Genetics [Details]
J. Buxbaum for the Autism Genome Project Consortium (AGP); (2010) A two-stage genomewide scan for common alleles affecting risk for autism ASHG American Society for Human Genetics [Details]
Milewski MA, Leahy DT, Conroy J, Ennis S, Mulcahy H, Hyland J, O'Donoghue D, Sheahan K.; (2010) LABORATORY INVESTIGATION 90: Suppl. 1, 156 Genome-wide DNA methylation profiling of sporadic and familial colorectal cancer [Details]
J. P. Casey, J. Conroy, R. Regan, N. Shah, E. B. Crushell, S. A. Lynch, S. Ennis; (2010) The use of whole exome sequencing and linkage analysis to identify novel candidate loci for pediatric mitochondrial disorder ASHG American Society for Human Genetics [Details]
A. T. Pagnamenta, D. Pinto, H. Khan, V. J. Vieland, A. S. Le-Couteur, S. W. Scherer, A. P. Monaco, The Autism Genome Project Consortium; (2009) Copy Number Variation Discovery in Autism Spectrum Disorder ASHG American Society for Human Genetics [Details]
R Anney on behalf of the AGP; (2009) THE AUTISM GENOME PROJECT: GENOME-WIDE ASSOCIATION STUDIES IN AUTISM XVII World Congress of Psychiatric Genetics [Details]
): B. L. Yaspan, J. S. Sutcliffe, M. A. Pericak-Vance, J. L. Haines, and the Autism Genome Project; (2009) Pathway analysis of multiple GWAS datasets implicates genes in the extracellular matrix - receptor interaction pathway with autism risk ASHG American Society for Human Genetics [Details]
N. Shah, R. Regan, J. Conroy, T. Magalhaes, J. Casey, R. Anney, A. Green, L. Gallagher, M. Gill, DC. Shields, A. Vicente, S. Ennis; (2009) Parental Origin Bias in de novo CNVs Detected in Autism Probands ASHG American Society for Human Genetics [Details]
J. Casey, T. Magelhaes, J. Conroy, R. Regan, N. Shah, R. Anney, E. Heron, A. Green, L. Gallagher, M. Gill, D. Shields, A. Vicente, S. Ennis, Autism Genome Project ; (2009) Genome-wide homozygous haplotype mapping to identify Autism Spectrum Disorder candidate genes ASHG American Society for Human Genetics [Details]
J. Conroy, AT. Pagnamenta, N. Shah, R. Segurado, J. Casey, R. Regan, T. Magelhaes, K. Tansey, D. Pinto, JB. Cazier, A. Vicente, A. Green, M. Gill, L. Gallagher, AP. Monaco, S. Ennis, Autism Genome Project ; (2009) The Role of the Mitochondria in Autism ASHG American Society for Human Genetics [Details]
S. Ennis on behalf of the Autism Genome Project Consortium (AGP); (2009) The Autism Genome Project: Dissecting the genetic and genomic etiology of autism ASHG American Society for Human Genetics [Details]
. Casey, T. Magelhaes, J. Conroy, R. Regan, N. Shah, R. Anney, E. Heron, A. Green, L. Gallagher, M. Gill, D. Shields, A. Vicente, S. Ennis, Autism Genome Project ; (2009) Genome-wide homozygous haplotype mapping to identify autism spectrum disorder candidate genes 2009 IRCSET Symposium 'Innovation fuelling the Smart Society' [Details]
Richard Anney, On behalf of the Autism Genome Project; (2009) The Autism Genome Project:Genome-wide Association Studies In Autism ISHG Irish Society for Human Genetics [Details]
J. Casey, J. Conroy, R. Regan, N. Shah, T. Magelhaes, A. Green, S A Lynch, S. Ennis,; (2009) The Use of SNP Homozygosity mapping to identify disease genes in Irish Families ISHG Irish Society for Human Genetics [Details]
Naisha Shah, Judith Conroy, Regina Regan, Sean Ennis, Denis C. Shields; (2009) Parental Origin Bias in de novo CNVs Detected in Autism Probands ISHG Irish Society for Human Genetics [Details]
Naisha Shah, Judith Conroy, Regina Regan, Sean Ennis, Denis C. Shields; (2009) Parental Origin Bias in de novo CNVs Detected in Autism Probands Human Variome Project Meeting [Details]
Linda McArdle, Sally Ann Lynch, Sean Ennis, Thomas Morris, David R. Betts; (2009) Tissue Specific Mosaicism of a der(18) in a Developmentally Delayed Boy ISHG Irish Society for Human Genetics [Details]
SA Lynch, M King, J Conroy and S Ennis; (2009) Monozygous Twins discordant for Landau-Kleffner Syndrome ISHG Irish Society for Human Genetics [Details]
R. Regan, S.A. Lynch, C.Costigan, N. Foulds, A. Collins, A.C. Thuresson, G. Annerén , B.O. Hederg , D.R. Fitzpatrick, S.Ennis, F.H. Sharkey6; (2009) The 12q14 microdeletion syndrome, 5 further cases ISHG Irish Society for Human Genetics [Details]
S. Ennis on behalf of the Autism Genome Project Consortium (AGP); (2009) The Autism Genome Project: The Genetics of Autism Spectrum Disorder 9th Annual International Gene Forum 2009 'New Frontiers in Genomics' [Details]
S. Ennis on behalf of the Autism Genome Project Consortium (AGP); (2009) The Autism Genome Project:CNVS in Autism Spectrum Disorder 5th International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism [Details]
R Anney on behalf of the PGC; (2009) COMBINED GWAS OF AUTISM, THE PSYCHIATRIC GWAS CONSORTIUM PGC XVII World Congress of Psychiatric Genetics [Details]
J.S. Sutcliffe, for the Autism Genome Project; (2008) The Autism Genome Project: Dissecting the genetic and genomic etiology of autism ASHG American Society for Human Genetics [Details]
Correia C1,2, Sousa I1, Peixeiro I1, Lourenço L1, Almeida J3, Lontro R3, Galllagher L4,5, Gill M 4,5, Ennis S 6, Oliveira G3, Vicente AM1,2; (2008) The BDNF receptor gene NTRK2 is a susceptibility gene for autism European Society for Human Genetics [Details]
Catarina Correia1,2, Ana Margarida Coutinho, Inês Sousa1, Isabel Peixeiro I1, Lara Lourenço1, Joana Almeida3, Raquel Lontro3, Louise Galllagher4,5, Michael Gill, Sean Ennis4,5, Guiomar Oliveira3, Astrid M. Vicente1,2; (2008) Brain-derived Neurotrophic Factor (BDNF) in autism: plasma levels and analysis of candidate genes BDNF and NTRK2 The XVIth World Congress on Psychiatric Genetics [Details]
G.D. Schellenberg, for the Autism Genome; (2008) Analysis of the EAAT2 glutamate transporter (SLC1A2) locus as an 11p13 positional candidate for autism ASHG American Society for Human Genetics [Details]
VJ Vieland for the AGC and AGP; (2008) New linkage analysis by the Autism Genome Project (AGP) reveals strong evidence of linkage to multiple loci as well as gene-gene interactions ASHG American Society for Human Genetics [Details]
P. Szatmari1, X.-Q. Liu2, J. A.D. Paterson2 and The Autism Genome Project Consortium; (2008) Sex differences in repetitive stereotyped behaviours in autism: implications for genetic liability ASHG American Society for Human Genetics [Details]
O. Stein and the Autism Genome Project; (2008) Data coordinating infrastructure for the Autism Genome Project ASHG American Society for Human Genetics [Details]
L. A. Weiss, D. E. Arking, T. Green, J. F. Gusella, S. L. Santangelo, R. E. Tanzi, P. Sklar, A. Chakravarti, M. J. Daly, Autism Consortium Gene-Finding Group & Autism Genome Project. ; (2008) Genome-wide Association Mapping in Multiplex Autism Families ASHG American Society for Human Genetics [Details]
Thomas Wassink, Kacie Meyer, Val Sheffield, The Autism Genome. ; (2007) A NRXN1 paternal germ-line mutation causing autism in two female siblings 6th Annual International Meeting for Autism Research (IMFAR) [Details]
Schellenberg, Gerard D., Devlin, Bernie, Scherer, Stephen W., The Autism Genome Project (AGP) Consortium. ; (2007) Copy Number Variation and linkage analysis of multiplex autism families 6th Annual International Meeting for Autism Research (IMFAR) [Details]
P Szatmari, X-Q Liu, A Paterson and the Autism Genome Project; (2007) Sex Differences in ASD Phenotypes 6th Annual International Meeting for Autism Research (IMFAR) [Details]
Janine Lamb for the Autism Genome Project; (2007) Autism Genome Project: Genome Screen Linkage and Copy Number Variation analyses Autism Research in the UK - from diagnosis to intervention. The Open University, UK [Details]
Stephen O¿Riordan, Sean Ennis, Andrew Green, Sherly. George, Hilary Hoey, Elaine Hand, Colm Costigan; (2007) Genetics of cystic fibrosis related diabetes and non diabetes Hormone Research [Details]
K. J. Meyer, L. K. Davis, A. L. Librant, D. S. Rudd, E. M. Berg, C. M. Taylor, J. Piven, E. M. Stone, V. C. Sheffield, T. H. Wassink, Autism Genome Project Consortium. ; (2007) A Neurexin 1 deletion implicates a synaptic defect in the pathophysiology of autism ASHG American Society for Human Genetics [Details]
The Autism Genome Project; (2007) Integration of Phenotype, Genotype and Function to Identify Autism Genes The XVth World Congress of Psychiatric Genetics [Details]
Liu X-Q, Paterson AD, Szatmari P. The Autism Genome Project (AGP) Consortium. ; (2007) Genome-wide linkage analysis of ADI-R social and repetitive behaviour domain total scores 6th Annual International Meeting for Autism Research (IMFAR) [Details]
Stephen ORiordan, H. Hoey, S. Ennis, A. Green, E. Hand, S. George, C. Costigan, E. Roche, N. Murphy, G. Canny, P. Greally, D Slattery; (2006) SCREENING FOR DIABETES IN CHILDREN WITH CYSTIC FIBROSIS Proceedings of the Irish Paediatric Association meeting [Details]
B. Devlin for the Autism Genome Project (AGP); (2006) Autism Genome Project: Linkage Analyses ASHG American Society for Human Genetics [Details]
S.W. Scherer for the Autism Genome Project.; (2006) Mining Affymetrix 10KSNPdata from the AutismGenomeProject for copy number variation ASHG American Society for Human Genetics [Details]
Greenway, M., Andersen, P.M., Russ, C., Ennis, S., Cashman, S., Donaghy, C. Victor.; (2005) The genetics of VEGF and Angiogenin European FALS Group Meeting [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]
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]
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]
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]
Stephen Lalor, Louise Gallagher, Geraldine Kearney, Michael Fitzgerald, David E Barton, Andrew J Green, Michael Gill and Sean Ennis. ; (2005) Mutation screening of a break-point candidate gene for autism, UBE2E3, on chromosome 2q31.3 ISHG Irish Society for Human Genetics Annual Scientific Meeting [Details]
Robert J. Goldsmith, Sean Ennis and Sally-Ann Lynch. ; (2005) Analysis of subtelomeric aberrations suspected in unknown causes of mental retardation via Multiplex Ligation-dependent Probe Amplification (MLPA) ISHG Irish Society for Human Genetics Annual Scientific Meeting [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]
Sean Ennis ; (2004) Advances in Molecular Studies in Autism Dublin Molecular Medicine Centre Spring Symposium [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., 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., 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, 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]
S Ennis, K Ryan, P Carthy, A Dunlop, K Dunne, AJ Green; (2004) A locus for Nasal Glioma on chromosome on Chromosome 7p21.1 ASHG Americal Society for Human Genetics Annual Scientific Meeting [Details]
Conroy J, Segurado R, Meally E, Stallings R, Fitzgerald M, Gill M, Ennis S and Gallagher L. ; (2004) Evidence of association for a susceptibility region for Autism on Chromosome 2q The XIIth World Congress on Psychiatric Genetics [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]
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]
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]
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, S Ennis, Geraldine Kearney, Michael Fitzgerald, Raymond Stallings, David E Barton, Michael Gill and Andrew J Green; (2002) Fine Mapping of A Susceptibiltiy Region and Candidate Gene Studies On Chromsome 2q in Autism The Xth World Congress on Psychiatric Genetics, Brussels [Details]
M Rogers, S Ennis, DMD Bailey, T Barrett, H Kelly, B Hughes, RF Harrison, DE Barton; (2002) Validation of the consensus Y chromosome deletion screening set in the Irish population BSHG British Society for Human Genetics [Details]
Sean Ennis, Jane Ng Wanjing, Geraldine Kearney, Michael Fitzgerald, Raymond Stallings, David E Barton, Andrew J Green, Louise Gallagher and Michael Gill. ; (2002) Mapping of a Candidate Region for Autism on Chromosome 2q32 BSHG British Society for Human Genetics [Details]
Mike Alexander, S. Ennis, B.J. Traynor, N. Miller, B. Corr, O. Hardiman, A. Green; (2002) The Role of the APEX gene in Amyotrophic Lateral Sclerosis in the Irish Population BSHG British Society for Human Genetics [Details]
V Solari, S Ennis, A Yoneda, L Wong, ME Höllwarth, A Green, P Puri; (2002) Mutation Analysis of the RET Gene in Total Intestinal Agangllionosis (TIA) with the WAVE DNA Fragment Analysis System American Pediatric Surgical Association 33rd Annual Meeting [Details]
M Rogers, S Ennis, DMD Bailey, T Barrett, H Kelly, B Hughes, RF Harrison, DE Barton; (2002) Validation of the consensus Y chromosome deletion screening set in the Irish population ISHG Irish Society for Human Genetics Annual Scientific Meeting [Details]
Sean Ennis, Jane Ng Wanjing, Geraldine Kearne, Michael Fitzgerald, Raymond Stallings, David E Barton, Andrew J Green, Louise Gallagher and Michael Gill.; (2002) Mapping of a Candidate Region for Autism on Chromosome 2q32 ESHG European Society for Human Genetics [Details]
Mike Alexander, S. Ennis, B.J. Traynor, N. Miller, B. Corr, O. Hardiman, A. Green; (2002) The Role of the APEX gene in Amyotrophic Lateral Sclerosis Clinical Molecular Genetics Society [Details]
Sean Ennis; (2002) Genetics of Autism Genetics Unit, Our Lady’s Hospital for Sick Children The Conway Institute of Biomolecular and Biomedical Research University College Dublin Children’s Research Centre,  Crumlin Research Seminars [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]
MD Alexander, BJ Traynor, S Ennis, N Miller, B Corr, E Frost, A Green, O Hardiman; (2001) The role of the APEX gene in the aetiology of ALS in the Irish population 12th International Symposium on ALS/MND San Fransisco, USA [Details]
S. Ennis; (2001) Genetics of Migraine and Autism Joint meeting of the Irish Institute of Neurology and Neurosurgery and the Institute of Neurosciences, Trinity College [Details]
S. Ennis, M. Ni Chroinin1, P.Tormey, A. J. Green; (2001) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family ASHG Americam society for Human Genetics [Details]
S Ennis, C Bermingham, H Kelly, A Yoneda, S Kelly, D Shields, C Molony, AJ Green, P Puri, DE Barton. ; (2001) Exclusion of the candidate gene Uroplakin III in primary vesicoureteral reflux British Society for Human Genetics [Details]
MD Alexander, S Ennis, BJ Traynor, N Miller, B Corr, O Hardiman, A Green; (2001) The Role of the APEX gene in Amyotrophic Lateral Sclerosis ISHG Irish Society for Human Genetics Annual Meeting [Details]
S Ennis, C Bermingham, H Kelly, A Yoneda, S Kelly, D Shields, C Molony, AJ Green, P Puri, DE Barton; (2001) Exclusion of the candidate gene Uroplakin III in primary vesicoureteral reflux ISHG Irish Society for Human Genetics Annual Meeting [Details]
P Maguire, H O'Shea, S Ennis, A Green. ; (2001) Molecular Genetic Analysis of Tuberous Sclerosis in the Irish Population ISHG Irish Society for Human Genetics Annual Meeting [Details]
S Ennis, M Alexander, P Donlon, E Cassidy, E Tompkins, O Hardiman, V O¿Keane, A Green; (2001) A study of candidate markers in the aetiology of migraine in the Irish population ISHG Irish Society for Human Genetics Annual Meeting [Details]
S Ennis, J Ng Wanjing, G Kearney, M Fitzgerald, R Stallings, DE Barton, AJ Green, L Gallagher and M Gill. ; (2001) Fine Mapping of a Candidate Region for Autism on Chromosome 2q32 ISHG Irish Society for Human Genetics Annual Meeting [Details]
A. J. Green, M. Ni Chroinin1, P.Tormey, S. Ennis, ; (2001) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family ESHG European Society for Human Genetics Annual Meeting [Details]
S. Ennis, Aherne MM, O¿Doherty E, Roche JF and Sweeney T; (2000) Direct haplotyping of Allele 136, 154 and 171 at the Ovine PRNP Locus Transmissible Spongiform Encephalopathies - Problems and Solutions, Faculty of Veterinary Medicine Research Symposium [Details]
M. Ni Chroinin1, P.Tormey, S. Ennis, A. J. Green.; (2000) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family British Society for Human Genetics [Details]
S. O' Leary, S. Ennis, J. Angles, L. Vaughan.and T.Sweeney. ; (2000) Cloning and sequencing of the bovine Nramp1 gene 37th AVTRW Meeting, Irish region [Details]
M. Ni Chroinin1, P.Tormey, S. Ennis, A. J. Green; (2000) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family Proceedings of the Irish society for optamology [Details]
M. Ni Chroinin1, P.Tormey, S. Ennis, A. J. Green. ; (2000) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family ISHG Irish Society for Human Genetics Annual Meeting [Details]
O'Doherty E, Aherne M, Ennis S, Roche JF, Sweeney T ; (1999) Detection of polymorphisms in the ovine prion protein gene in imported sheep breeds in Ireland Prion Protein Symposium Proceedings Tubingen, Germany, [Details]
O¿Doherty E, Aherne MM, Ennis, S, Roche JF and Sweeney T; (1999) Detection of polymorphism in the ovine prion protein gene in imported sheep breeds in England Characterization and Diagnosis of Prion Diseases in Animals and Man, Tubingen, Germany [Details]
Aherne M, O'Doherty E, Ennis S, Roche JF and Sweeney, T ; (1999) PrP genotyping of native sheep breeds in Ireland Prion Protein Symposium Proceedings Tubingen, Germany, [Details]
Ennis S, Aherne M, O'Doherty E, Roche J and Sweeney T ; (1999) Direct haplotyping of Allele 136, 154 and 171 at the Ovine PRNP Locus Prion Protein Symposium Proceedings Tubingen, Germany, [Details]
Aherne MM, O¿Doherty E, Ennis, S, Roche JF and Sweeney T. ; (1999) PrP genotyping of native sheep breeds in Ireland Characterization and Diagnosis of Prion Diseases in Animals and Man, Tubingen, Germany [Details]
Characterization and Diagnosis of Prion Diseases in Animals and Man, Tubingen, Germany ; (1999) Direct haplotyping of Allele 136, 154 and 171 at the Ovine PRNP Locus Characterization and Diagnosis of Prion Diseases in Animals and Man, Tubingen, Germany [Details]
E. O'Doherty, M. Aherne, S. Ennis, J. F. Roche and T. Sweeney; (1999) A Study of PrP (Scrapie) Genotypes in Sheep Breeds in Ireland AVTRW Meeting, Irish region [Details]
E.O'Doherty, M. Aherne, S. Ennis, E. Weavers, J. F. Roche and T. Sweeney. ; (1998) Detection of Polymorphisms in the Ovine Prion Protein Gene in an Irish Suffolk Population 35th AVTRW Meeting, Irish region [Details]
María Victoria Arruga Laviña, L. Monteagudo, A. Heriz, S. Ennis, M. Rogers, N. Flavin.; (1996) Secuencia de DNA y mapa de sintenia y ligamiento del receptor de activina bovina tipo IIA (actriia) Archivos de zootecnia [Details]
N. Flavin, A. Heriz, María Victoria Arruga Laviña, L. Monteagudo, S. Ennis, M. Rogers. ; (1996) Mapeo mediante Fish del receptor de Activina tipo II A (actRIIA) para el cromosoma bovino 2 (2g2.2-2.4) Archivos de zootecnia [Details]
Flavin-N; Monteagudo-L; Heriz-A; Ennis-S; Rogers-M; Arruga-M-V; (1996) DNA sequence and synteny and linkage mapping of bovine activin receptor type IIA (ActRIIA) Archivos de Zootecnia [Details]
Flavin-N; Monteagudo-L; Heriz-A; Ennis-S; Rogers-M; Arruga-M-V; (1996) Fish mapping of activin receptor type IIA (ActRIIA) to bovine chromosome 2 (2q2.2-2.4) Archivos de Zootecnia [Details]
Ennis, S. and Flavin, N. and Rogers, M. ; (1996) Report of the activities of the UCD group in the BovMap project 5th BovMap meeting Tours [Details]
Ennis, S., ; (1996) Development of Genetic and Physical marker maps of the bovine genome a report on the European BovMap project AVTRW Meeting, Irish region [Details]
Vaughan, L. and Ennis, S.; (1996) The diagnosis of freemartinism in cattle using sex specific DNA sequences AVTRW Meeting, Irish region [Details]
W. Barendse, D. Vaiman, S. Kemp, Y. Sugimoto, S. Armitage, J. Williams, S. Sun, A. Eggen, M. Agaba, A. Aleyasin, M. Band, M. Bishop, J. BuitKamp, K. Byrne, F. Collins, L. Cooper, W. Coupettiers, B. Denis, R. Drinkwater, K. Easterday, S. Ennis, G. Erhardt, L. Ferretti, Q. Gao, M. Georges, R. Gurung, B. Harlizius, G. Hawkins, J. Hetzel, T. Hirano, C. Joergensen, M. Kessler, B. Kirkpatrick, B. Konfortov, C. Kuhn, H. Lenstra, H. Leveziel, H. Lewin, B. Leyhe, L. Li, I. Martin Burriel, R. McGraw, R. Miller, D. Moody, S. Moore, S. Nakane, I. Nijman, I. Olsaker, D. Pomp, A. Rando, M.Ron, M. Soller, A. Teale, U. Thieven, B. Urquhart, D. Vage,a. Van De Weghe, S. Varvio, R. Velmalla, J. Vilkki, R. Weikard, C. Woodside, J. Womack, M. Zanotti, P. Zaragoza; (1996) A genetic linkage map of the bovine genome II International Society for Animal Genetics [Details]
Ennis, S. and Flavin, N. and Rogers, M; (1995) Approaches towards integrating the genetic and Physical Bovine maps 4th BovMap meeting Dublin [Details]
Ennis, S. and Flavin, N; (1994) A rapid PCR method for the screening of bovine genomic libraries 3rd BovMap meeting Oslo [Details]
Ennis, S., Roche, J. F., Boland, M.P., and Gallagher, T.F; (1994) Sex determination of Preimplanted bovine embryos AVTRW Meeting, Irish region [Details]
Ennis, S., Roche, J. F. and Gallagher, T.F.; (1994) Cloning of large DNA segments into a bacterial artificial chromosome vector International Society for Animal Genetics Prague, (Invited talk) [Details]
Ennis, S., Roche J. F. and Gallagher, T.F; (1993) Embryo sexing using X-Y homologus Primers at the amelogenin locus International Society for Animal Genetics [Details]
Ennis, S., Roche, J. F., Boland, M.P., and Gallagher, T.F; (1991) exing of bovine embryos using Y chromosome specific sequences 2nd farm animal genome meeting Edinburgh [Details]
Ennis, S. F. and Shirley, I.F; (1986) A new microhaemolytic technique for blood typing International Society for Animal Genetics [Details]
Amorena B., F, Escudero, J. L. Olleta, P. Aljama, S. Ennis, , E . P. Ke11y; (1985) Zarazaga. Grupos Sanguineos en Agrupaciones de la Raza Vacuna Retinta XXI Jornadas Luso-Espanho1as de Genetica [Details]
                       

Abstract

Keohane, C,Bermingham, N,Greene, A,Ennis, S,Casey, J,McGettigan, P,Browne, TJ,O'Brien, O,Dempsey, E (2013) Familial holoprosencephaly-diencephaly hamartoma in Irish siblings. Abstract [Details]
Milewski, M,Leahy, D,Conroy, J,Magalhaes, T,Ennis, S,Maguire, A,Mulcahy, H,Hyland, J,O'Donoghue, D,Sheahan, K (2013) Classification of Colorectal Cancer Based on DNA Methylation Array Analysis. Abstract [Details]
Mccormack, M,O'Connor, GD,Heinzen, E,Shianna, KV,Conroy, J,Ennis, S,Goldstein, D,Delanty, N,Cavalleri, GL (2012) WHOLE EXOME SEQUENCING WITHIN AN IRISH PEDIGREE OF IDIOPATHIC GENERALISED EPILEPSY. 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]
Milewski, MA,Leahy, DT,Conroy, J,Ennis, S,Mulcahy, H,Hyland, J,O'Donoghue, D,Sheahan, K (2010) Genome-Wide DNA Methylation Profiling of Sporadic and Familial Colorectal Cancer. Abstract [Details]
Mc Cabe, S,Doherty, L,McNicholas, WT,Green, AJ,Ennis, S (2003) A further locus for congenital central hypoventilation syndrome (CCHS). Abstract [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. Abstract [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. Abstract [Details]
Rogers, M,Ennis, S,Bailey, DMD,Barrett, T,Kelly, H,Hughes, B,Harrison, RF,Barton, DE (2002) Validation of the consensus Y chromosome deletion screening set in the Irish population. Abstract [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. Abstract [Details]
Ni Chroinin, M,Tormey, P,Ennis, S,Green, AJ (2000) Autosomal recessive colobomatous micro/anophthalmia in a consanguineous Irish traveller family. Abstract [Details]
Flavin, N,Monteagudo, L,Heriz, A,Tejedor, MT,Ennis, S,Rogers, M,Arruga, MV (1996) DNA sequence and synteny and linkage mapping of bovine activin receptor type IIA (ActRIIA). Abstract [Details]
Monteagudo, L,Heriz, A,Flavin, N,Ennis, S,Rogers, M,Arruga, MV (1996) FISH mapping of activin receptor type IIA (ActRIIA) to bovine chromosome 2q2.2->q2.4. Abstract [Details]
                                                               

Research

Research Interests

Dr. Ennis has wide expertise and interests in the application of Genomics to genetic diseases. Among his noted contributions has been his involvement in the establishment of the international bovine Genome Map (BovMap).

More recently he has been involved in the field of human genetics and participates in International collaborative projects on Autism and Motor Neuron Disease (ALS). Recent research findings emanating from these research collaborative groups are among the most exciting in their fields.

He is a co-founder of the Irish Autism Genetics Collaboration (IAGC), which participates in the International Autism Genome Project (AGP) and sits on the Committee of Senior Investigators (CSI) for the AGP.

Prior to leaving office the Minister for Health and Children Mr. Michael Martin awarded 5 million euro to the Irish Autism genetics Collaboration (IAGC) as part of a world wide project, a strong recognition of the IAGC's position in the field. http://www.genetics.ie/news/

 

FUNDING AGENCIES:
Heath Research Board

Research Projects

Sponsor : Enterprise Ireland (EI)
Title : Eur Genome coordinator support
Start Date / End Date : 03-FEB-14 / 04-DEC-14
Sponsor : Irish Research Council for Science Engineering and Technology (IRCSET)
Title : Identification and characterisation of genes and genomic variants involved in Autism Spectrum Disorder.
Start Date / End Date : 01-MAY-08 / 31-JAN-11