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Items where Subject is Socio-Economic Objective, Health, Clinical Health (Organs, Diseases and Abnormal Conditions), Inherited Diseases (incl. Gene Therapy)

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Journal Article

Tremlett, H and Van der Mei, IAF and Pittas, F and Blizzard, CL and Paley, GA and Dwyer, T and Taylor, BVM and Ponsonby, AL, Adherence to the immunomodulatory drugs for multiple sclerosis: contrasting factors affect stopping drug and missing doses, Pharmacoepidemiology and Drug Safety, 17, (6) pp. 565-576. ISSN 1053-8569 (2008) [Refereed Article]
Arthur, AT and Armati, PJ and Bye, C and Kilpatrick, TJ and Foote, SJ and Butzkueven, H and Taylor, BVM and Tubridy, N and Marriott, M and Chapman, C and Bahlo, M and Speed, TP and Stankovich, J and Heard, RNS and Stewart, GJ and Pollard, JD and Booth, DR, Genes implicated in multiple sclerosis pathogenesis fromconsilience of genotyping and expression profiles in relapse and remission, BMC Medical Genetics, 9, (Mar 19) pp. 17. ISSN 1471-2350 (2008) [Refereed Article]
Murphy, M and Quinn, SJ and Young, J and Parkin, P and Taylor, BVM, Increasing incidence of ALS in Canterbury, New Zealand: A 22-year study, Neurology, 71, (23) pp. 1889-1895. ISSN 0028-3878 (2008) [Refereed Article]
Albers, CA and Stankovich, J and Thomson, RJ and Bahlo, M and Kappen, HJ, Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals, American Journal of Human Genetics, 82, (3) pp. 607-622. ISSN 0002-9297 (2008) [Refereed Article]
Rubio, JP and Stankovich, J and Field, J and Tubridy, N and Marriott, M and Chapman, C and Bahlo, M and Perera, DI and Johnson, LJ and Tait, BD and Varney, MD and Speed, TP and Taylor, BVM and Foote, SJ and Butzkueven, H and Kilpatrick, TJ, Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians, Genes and Immunity, 9, (7) pp. 624-630. ISSN 1466-4879 (2008) [Refereed Article]
Husain, S and Yildirim-Toruner, C and Rubio, JP and Field, J and Kilpatrick, TJ and Foote, SJ and Butzkueven, H and Taylor, BVM and Tubridy, N and Marriott, M and Chapman, C and Bahlo, M and Speed, T and Stankovich, J and Shwalb, M and Cook, S and Devoto, M and Vitale, E, Variants of ST8SIA1 Are Associated with Risk of Developing Multiple Sclerosis, PLoS One, 3, (7) pp. e2653. ISSN 1932-6203 (2008) [Refereed Article]
Burfoot, RK and Jensen, CJ and Field, J and Stankovich, J and Varney, MD and Johnson, LJ and Butzkueven, H and Booth, D and Bahlo, M and Tait, BD and Taylor, BV and Speed, TP and Heard, R and Stewart, GJ and Foote, SJ and Kilpatrick, TJ and Rubio, JP, SNP mapping and candidate gene sequencing in the class 1 region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians, Tissue Antigens, 71, (Oct 30) pp. 42-50. ISSN 0001-2815 (2007) [Refereed Article]
Burfoot, RK and Jensen, CJ and Field, J and Stankovich, J and Varney, MD and Johnson, LJ and Butzkueven, H and Booth, D and Bahlo, M and Tait, BD and Taylor, BVM and Speed, TP and Heard, R and Stewart, GJ and Foote, SJ and Kilpatrick, TJ and Rubio, JP, SNP mapping and candidate gene sequencing in the class Iregion of the HLA complex: searching for multiple sclerosissusceptibility genes in Tasmanians, Tissue Antigens, 71, (1) pp. 42-50. ISSN 0001-2815 (2007) [Refereed Article]
Bahlo, M and Stankovich, J and Speed, TP and Rubio, JP and Burfoot, RK and Foote, SJ, Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data, Human Genetics , 119, (1-2) pp. 38-50. ISSN 0340-6717 (2006) [Refereed Article] 
Lin, E and Pappenfuss, T and Tan, RB and Senyschyn, D and Bahlo, M and Speed, TP and Foote, SJ, Mapping of the Plasmodium chabaudi Resistance Locus Char2, Infection and Immunity, 74, (10) pp. 5814-5819. ISSN 0019-9567 (2006) [Refereed Article] 
Stankovich, J and Cox, CJ and Tan, RB and Montgomery, DS and Huxtable, SJ and Rubio, JP and Ehm, MG and Johnson, L and Butzkueven, H and Kilpatrick, TJ and Speed, TJ and Roses, AD and Bahlo, M and Foote, SJ, On the utility of data from the International HapMap Project for Australian association studies, Human Genetics, 119, (1-2) pp. 220-222. ISSN 0340-6717 (2006) [Refereed Article] 
Hewitt, AW and Fitzgerald, LM and Scotter, LW and Mulhall, LE and McKay, JD and Mackey, DA, Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia, Clinical and Experiemental Opthalmology, 33 pp. 233-239. ISSN 1442-6404 (2005) [Refereed Article] 
Stankovich, J and Bahlo, M and Rubio, JP and Wilkinson, CR and Thomson, RJ and Banks, A and Ring, M and Foote, SJ and Speed, TP, Identifying nineteenth century genealogical links from genotypes, Human Genetics, 117 pp. 188-199. ISSN 0340-6717 (2005) [Refereed Article] 
Stankovich, J and Bahlo, M and Rubio, J and Wilkinson, C and Thomson, R and Banks, A and Ring, M and Foote, S and Speed, T, Identifying nineteenth century genealogical links from genotypes, Human Genetics, 117, (2-3) pp. 188-199. ISSN 0340-6717 (2005) [Refereed Article] 
Monnier, S and Cox, D and Albion, T and Canzian, F, T.I.M.S: TaqMan Information Management System, tools to organize data flow in a genotyping laboratory, BMC Bioinformatics, 6, (246) EJ ISSN 1471-2105 (2005) [Other Refereed Article] 
Oceandy, D and McMorran, BJ and Schreiber, R and Wainwright, B and Kunzelmann, K, GFP-tagged CFTR transgene is functional in the G551D cystic fibrosis mouse colon, Journal of Membrame Biology, 192, (3) pp. 159-167. ISSN 0022-2631 (2003) [Refereed Article] 
Burdon, KP and McKay, JD and Sale, MM and Russell-Eggitt, IM and Mackey, DA and Wirth, MG and Elder, JE and Nicoll, A and Clarke, MP and Fitzgerald, LM and Stankovich, J and Shaw, MA and Sarma, S and Gajovic, S and Gruss, P and Ross, S and Thomas, P and Voss, AK and Thomas, T and Gecz, J and Craig, JE, Mutations in a Novel Gene, NHS, Cause the Pleiotropic Effects of Nance-Horan Syndrome, Including Severe Congenital Cataract, Dental Anomalies, and Mental Retardation, American Journal of Human Genetics, 73 pp. 1120-1130. ISSN 0002-9297 (2003) [Refereed Article] 
Oceandy, D and McMorran, BJ and Smith, S and Schreiber, R and Kunzelmann, K and Alton, E and Hume, D and Wainwright, B, Gene complementation of airway epithelium in the cystic fibrosis mouse is necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities, Human Molecular Genetics, 11, (9) pp. 1059-1067. ISSN 0964-6906 (2002) [Refereed Article] 
Jolly, RD and Brown, SC and Das, A and Walkley, SU, Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease), Neurochemistry International , 40 pp. 565-571. ISSN 0197-0186 (2002) [Refereed Article] 
Lesueur, F and Corbex, M and McKay, JD and Lima, J and Soares, P and Griseri, P and Burgess, J and Ceccheri, I and Landolfi, S and Papotti, M and Amorim, A and Goldgar, D and Romeo, G, Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma, Journal of Medical Genetics, 39, (4) pp. 260-265. ISSN 0022-2593 (2002) [Refereed Article] 
Nishimura, D and Searby, C and Alward, W and Walton, D and Craig, JE and Mackey, DA and Kawase, K and Kanis, A and Patil, S and Stone, E and Sheffield, V, A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Development Defects of the Anterior Chamber of the Eye, Americal Journal of Human Genetics, 68 pp. 364-372. ISSN 0002-9297 (2001) [Refereed Article] 
Jolly, RD and Bayliss, SL and Das, A and Cooke, DG and Brown, SC, ATP synthase activity in ovine ceroid-lipofuscinis (OCL6), European Journal of Padeiatric Neurology, 5 pp. 131-134. ISSN 1090-3798 (2001) [Refereed Article] 
Howell, N and Herrnstadt, C and Mackey, DA, Different patterns of expansion/contraction during the evolution of an mtDNA simple repeat, Molecular Biology and Evolution, 18, (8) pp. 1593-1596. ISSN 0737-4038 (2001) [Letter or Note in Journal] 
Fingert, JH and Clark, AF and Craig, JE and Alward, WLM and Snibson, GR and McLaughlin, M and Tuttle, L and Mackey, DA and Sheffield, VC and Stone, EM, Evaluation of the Myocilin (MYOC) Glaucoma Gene in Monkey and Human Steroid-Induced Ocular Hypertension, Investigative Ophthalmology & Visual Science, 42, (1) pp. 145-152. ISSN 0146-0404 (2001) [Refereed Article] 
McMorran, BJ and Palmer, JS and Lunn, DP and Oceandy, D and Costelloe, EO and Thomas, GR and Hume, DA and Wainwright, BJ, G551D CF mice display an abnormal host response and have impaired clearance of Pseudomonas lung disease, American Journal of Physiology, 281, (3) pp. L740-747. ISSN 0002-9513 (2001) [Refereed Article] 
Dickinson, JL and Sale, MM and Craig, JE and Mackey, DA, Laboratory methods in ophthalmic genetics: obtaining DNA from patients, Ophthalmic Genetics, 22, (1) pp. 49-60. ISSN 1381-6810 (2001) [Professional, Non Refereed Article] 
Dwyer, T and Sale, MM and Stankovich, J, Genetic Epidemiology in Tasmania, Australasian Epidemiologist, 7, (2) pp. 2-4. ISSN 1327-8835 (2000) [Professional, Non Refereed Article] 
Ewen, KR and Bahlo, M and Treloar, SA and Levinson, DF and Morwy, B and Barlow, JW and Foote, SJ, Identification and Analysis of Error Types in High-Throughput Genotyping, American Journal of Human Genetics, 67 pp. 727-736. ISSN 0002-9297 (2000) [Refereed Article] 
Mahony, D and Stringer, BW and Dickinson, JL and Antalis, TM, DNase I hypersensitive sties in the 5' flanking region of the human plasminogen activator inhibitor type 2 (PAI-2) gene are associated with basal and tumor necrosis factor-áá<áimg border=0 src=alpha.gif>-induced transcription in monocytes, European Journal of Biochemistry, 256 pp. 550-559. (1998) [Refereed Article] 
Burgess, JR and Greenaway, TM and Parameswaran, V and Challis, DR and David, R and Shepherd, JJ, Enteropancreatic malignancy associated with multiple endocrine neoplasia Type 1, Cancer, 83, (3) pp. 428-434. (1998) [Refereed Article] 
Burgess, JR and Greenaway, TM and Shepherd, JJ, Expression of the MEN-1 gene in a large kindred with multiple endocrine neoplasia type 1, Journal of Internal Medicine, 1998, (243) pp. 465-470. (1998) [Non Refereed Article] 
Burgess, JR and David, R and Parameswaran, V and Greenaway, TM and Shepherd, JJ, The Outcome of Subtotal Parathyroidectomy for the Treatment of Hyperparathyroidism in Multiple Endocrine Neoplasia Type 1, Arch Surg, 133, (Feb 1998) pp. 126-129. (1998) [Refereed Article] 
Burgess, JR and Duffield, A and Wilkinson, SJ and Ware, R and Greenaway, TM and Percival, J and Hoffman, L, Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid, Journal of Clinical Endocrinology and Metabolism, 82, (2) pp. 345-348. (1997) [Refereed Article] 
Courseaux, A and Grosgeorge, J and Gaudray, P and Pannett, AAJ and Forbes, SA and Williamson, C and Bassett, D and Thakker, RV and Teh, BT and Farnebo, F and Shepherd, JJ and Skogseid, B and Larsson, C and Giraud, S and Zhang, CX and Salandre, J and Calender, A, Definition of the Minimal MEN1 Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13, Genomics, 37, (0570) pp. 354-365. (1996) [Refereed Article] 
Coote, MA and McCartney, PJ and Wilkinson, RM and Mackey, DA, The GIST Score - Ranking Glaucoma for Genetic Studies, Ophthalmic Genetics, 17, (4) pp. 199-208. (1996) [Refereed Article] 
Sack, J and Healey, DL and Degraaf, AP and Wilkinson, RM and Wilkinson, CH and Barbour, JM and Coote, MA and McCartney, PJ and Rait, JL and Cooper, RL and Ring, MA and Mackey, DA, The Problem of Overlapping Glaucoma Families in the Glaucoma Inheritance, Ophthalmic Genetics, 17, (4) pp. 209-214. (1996) [Refereed Article] 

Conference Publication

Hewitt, AW and Poulsen, JP and Kearns, LS and Mackey, DA, A novel twin method for determining the significance of heritability of traits, Abstract, 23-25 November 2005, Mt. Buller, Victoria ISBN --------- (2005) [Conference Extract] 
Mackey, DA and Toh, TY and Liew, SHM and MacKinnon, JR and Hewitt, AW and Poulsen, JL and Spector, TD and Gilbert, CE and Craig, JE and Hammond, CJ, Central corneal thickness is highly heritable: The Twin Eye Studies, Abstract, 23-25 November 2005, Mt. Buller, Victoria ISBN --------- (2005) [Conference Extract] 
Charlesworth, JC and Dyer, TD and Stankovich, J and Blangero, J and Mackey, DA and Craig, JE and Foote, SJ and Baird, PN and Sale, MM, The application of a population based ascertainment correction for the variance components analysis of quantitative traits in a single extended pedigree, Abstract, 23-25 November 2005, Mt. Buller, Victoria ISBN --------- (2005) [Conference Extract] 
Jolly, RD and Brown, SC, ATP synthase activity in ovine ceroid-lipofuscinosis and its response to calcium. , The Sixth International Symposium on Lipofuscin and Ceroid Pigments, 19-22 May 2001, Honululu Hawaii, pp. 1. (2001) [Conference Extract] 
Jolly, RD and Hughes, SM and Jordan, TW and Das, A and Bayliss, SM and Brown, SC, Mitochondrial changes in ovine ceroid-lipofuscinosis (OCL6), International Congress on Neuronal Ceroid Lipofuscinoses Batten Disease, 20-24 September 2000, Oxford UK, pp. 1. (2000) [Conference Extract] 
Heathcote, D and Beamish, MR and Kunde, DA, Tasmanian haemochromatosis study, Proceedings of AIMS 2000, June 2000, Sydney, Australia, pp. 36. (2000) [Conference Extract] 

Thesis

Langbein, AL, An Exploratory Study of Links Between ADHD and a Chromosomal Mutation in a Single Family (2000) [Masters Coursework] 
Fowler, KJ, Functional analysis and genetic mapping of mouse centromere protein genes (2000) [PhD] 

Other Public Output

Williams, R and Heathcote, D, Call to renew genetic screening, Radio National "PM", ABC, Australia, 21 September, 2000 (2000) [Media Interview] 
Sale, MM, Appointment of Director, Genetic Epidemiology Unit, HOFM Radio, Tasmania, 10 March (1999) [Media Interview] 
Sale, MM, Appointment of Director, Genetic Epidemiology Unit, Magic 107 Radio, Tasmania, 10 March (1999) [Media Interview] 
Dwyer, T, Genetic research techniques in Iceland, 7ZR Radio, Tasmania, 17 November (1999) [Media Interview] 
Van der Mei, IAF, Public Forum: Dispelling the myths of MS, 7ZR Radio, Tasmania, 19 May (1999) [Media Interview] 
This list was generated on Mon Nov 23 12:22:50 2009.
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