UCD Conway Institute – Prof. Andrew Green

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Prof. Andrew Green
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Professor Andrew Green MB, BCh, BAO, PhD, MRCPI

Book Chapters:

Green A (2005) Chapter 8. Basic genetics in Roberton's textbook of Neonatology. UK, Elsevier Churchill Livingstone.

Peer Reviewed Publications:

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; Hardiman, O; (2006) 'ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis' in NATURE GENETICS , 38, (4) : 411 - 413.

Pirker, M.E., Mohanan, N., Colhoun, E., Barton, D., Green, A., Puri, P. (2006) 'Familial vesicoureteral reflux: influence of sex on prevalence and expression' in JOURNAL OF UROLOGY , 176, (4(2)) : 1776 - 1780.

O¿Connell, S., Butler, K., McMenamin, J., Waldron, M., Green, A.J. (2005) 'Genetic Conditions in the Irish Roma Gypsy Population' in IRISH MEDICAL JOURNAL , 98, (10) .

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' in Human Mutation , 26, (3) : 282 - 284.

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' in EUROPEAN JOURNAL OF HUMAN GENETICS , 13, (4) : 500 - 502.

Daly E., MacDermott E.J., and Green A. (2001) 'Diagnostic review of 66 children with learning disability attending a single centre' in IRISH MEDICAL JOURNAL , 94, (6) : 184 - 185.

McEntagart, M., Carey, A., Breen, C., McQuaid, S., Stallings, R.L., Green, A.J., and King, M.D. (2001) 'Molecular characterisation of a proximal chromosome 18q deletion' in JOURNAL OF MEDICAL GENETICS , 38, (2) : 128 - 129.
Willatt, L.R., Pearson, J., and Green, A.J. (2001) 'Partial trisomy of 2p and neuroblastoma' in AMERICAN JOURNAL OF MEDICAL GENETICS , 102, (3) : 304 - 305.
Willatt, L., Green, A.J., and 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' in JOURNAL OF MEDICAL GENETICS , 38, (10) : 723.
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)' in HUMAN MOLECULAR GENETICS , 6, (9) : 1409 - 1414.
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' in SCIENCE , 277, : 805 - 808.
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' in HUMAN MOLECULAR GENETICS , 6, (13) : 2265 - 2269.
Green, A.J., Smith, M., and Yates, J.R.W (1994) 'Loss of heterozygosity on chromosome 16p in hamartomas from patients with tuberous sclerosis' in NATURE GENETICS , 6, : 193 - 196.
Green, A.J., Johnson, P.H., and Yates, A.R.W. (1994) 'The tuberous sclerosis gene on 9q34 acts as a tumour suppressor' in HUMAN MOLECULAR GENETICS , 3, (10) : 1833 - 1834.
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Other Journals:

A Green (2005) 'Human Biological Material ; Recommendations for collection, use and storage in research' .

Conference Publications:

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,

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,

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,

Murphy, A.M., Lynch, S.A. Green, A.J. (2005) Accuracy of a Clinical Diagnosis of Marfan Syndrome Irish Society for Human Genetics,

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,

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,

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Other Publications:

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