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Items where Subject is Field of Research, Medical and Health Sciences, Clinical Sciences, Medical Genetics (excl. Cancer Genetics)

Journal Article
De Paoli-Iseppi, R and Prentice, L and Marthick, JR and Thomson, R and Holloway, AF and Dickinson, JL and Burgess, J, Multiple endocrine neoplasia type 1: clinical correlates of MEN1 gene methylation, Pathology, 50, (6) pp. 622-628. ISSN 0031-3025 (2018) [Refereed Article] 
Couto, AR and Parreira, B and Thomson, R and Soares, M and Power, DM and Stankovich, J and Armas, JB and Brown, MA, Combined approach for finding susceptibility genes in DISH/chondrocalcinosis families: whole-genome-wide linkage and IBS/IBD studies, Human Genome Variation, 4 Article 17041. ISSN 2054-345X (2017) [Refereed Article]
Blackburn, NB and Marthick, JR and Banks, A and Charlesworth, JC and Marsden, KA and Lowenthal, RM and Blangero, J and Dickinson, JL, Evaluating a CLL susceptibility variant in ITGB2 in families with multiple sub-types of hematological malignancies, Blood, 130, (1) pp. 86-88. ISSN 0006-4971 (2017) [Refereed Article]
Nicol, D and Eckstein, L and Morrison, M and Sherkow, JS and Otlowski, M and Whitton, T and Bubela, T and Burdon, KP and Chalmers, D and Chan, S and Charlesworth, J and Critchley, C and Crossley, M and de Lacey, S and Dickinson, JL and Hewitt, AW and Kamens, J and Kato, K and Kleiderman, E and Kodama, S and Liddicoat, J and Mackey, DA and Newson, AJ and Nielsen, J and Wagner, JK and McWhirter, RE, Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic, Genome Medicine, 9, (1) Article 85. ISSN 1756-994X (2017) [Contribution to Refereed Journal]
Azimi, I and Monteith, GR, Plasma membrane ion channels and epithelial to mesenchymal transition in cancer cells, Endocrine-related cancer, 23, (11) pp. R517-R525. ISSN 1351-0088 (2016) [Refereed Article] 
Davies, G and Armstrong, N and Bis, JC and Blesser, J and Chouraki, V and Giddaluru, S and Hofer, E and Ibrahim-Verbaas, CA and Kirin, M and Lahti, J and van der Lee, SJ and Le Hellard, S and Liu, T and Marioni, RE and Oldmeadow, C and Postmus, I and Smith, AV and Thalamuthu, A and Thomson, R and Vitart, V and Wang, J and Yu, L and Zgaga, L and Zhao, W and Boxall, R and Harris, SE and Hill, WD and Liewald, DC and Luciano, M and Adams, H and Ames, D and Amin, N and Amouyel, P and Assareh, AA and Au, R and Becker, JT and Beiser, A and Berr, C and Bertram, L and Boerwinkle, E and Buckley, BM and Campbell, H and Corley, J and De Jager, PL and Dufouil, C and Eriksson, JG and Espeseth, T and Faul, JD and Ford, I and Gottesman, RF and Griswold, ME and Gudnason, V and Harris, TB and Heiss, G and Hofman, A and Holliday, EG and Huffman, J and Kardia, SLR and Kochan, N and Knopman, DS and Kwok, JB and Lambert, J-C and Lee, T and Li, S-C and Li, G and Loitfelder, M and Lopez, OL and Lundervold, AJ and Lundqvist, A and Mather, KA and Mirza, SS and Nyberg, L and Ostra, BA and Palotie, A and Papenberg, G and Pattie, A and Petrovic, K and Polasek, O and Psaty, BM and Redmond, P and Reppermund, S and Rotter, JI and Schmidt, H and Schuur, M and Schofield, PW and Scott, RJ and Steen, VM and Stott, DJ and van Swieten, JC and Taylor, KD and Trollor, J and Trompet, S and Uitterlinden, AG and Weinstein, G and Widen, E and Windham, BG and Jukema, JW and Wright, MJ and Wright, AF and Yang, Q and Amieva, H and Attia, JR and Bennett, DA and Porteous, H and Raikkonen, K and Reinvang, I and Rudan, I and Sachdev, PS and Schmidt, R and Schofield, PR and Srikanth, V and Starr, JM and Turner, ST and Weir, DR and Wilson, JF and van Dujin, C and Launer, L and Fitzpatrick, AL and Seshadri, S and Mosley Jr, TH and Deary, IJ, Generation Scotland, Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N = 53 949), Molecular Psychiatry, 20, (2) pp. 183-192. ISSN 1359-4184 (2015) [Refereed Article]
Liu, Q and Shin, Y and Kee, JS and Kim, KW and Mohamed Rafei, SR and Perera, AP and Tu, X and Lo, GQ and Ricci, E and Colombel, M and Chiong, E and Thiery, JP and Park, MK, Mach-Zehnder interferometer (MZI) point-of-care system for rapid multiplexed detection of microRNAs in human urine specimens, Biosensors & bioelectronics, 71 pp. 365-372. ISSN 0956-5663 (2015) [Refereed Article] 
Liu, Q and Shin, Y and Kee, JS and Kim, KW and Rafei, SRM and Perera, AP and Tu, X and Lo, G-Q and Ricci, E and Colombel, M and Chiong, E and Thiery, JP and Park, MK, Mach-Zehnder interferometer (MZI) point-of-care system for rapid multiplexed detection of microRNAs in human urine specimens, Biosensors and Bioelectronics, 7 pp. 365-372. ISSN 0956-5663 (2015) [Refereed Article] 
Shin, Y and Perera, AP and Wong, CC and Park, MK, Solid phase nucleic acid extraction technique in a microfluidic chip using a novel non-chaotropic agent: dimethyl adipimidate, Lab on A Chip, 14 pp. 359-368. ISSN 1473-0197 (2014) [Refereed Article] 
Shin, Y and Perera, AP and Wong, CC and Park, MK, Solid phase nucleic acid extraction technique in a microfluidic chip using a novel non-chaotropic agent: dimethyl adipimidate, Lab on A Chip, 14, (2) pp. 359-368. ISSN 1473-0197 (2014) [Refereed Article] 
Sanfilippo, PG and Hewitt, AW and Mountain, JA and Mackey, DA, A geometric morphometric assessment of hand shape and comparison to the 2D:4D digit ratio as a marker of sexual dimorphism, Twin Research and Human Genetics, 16, (2) pp. 590-600. ISSN 1832-4274 (2013) [Refereed Article] 
Shin, Y and Perera, AP and Park, MK, Label-free DNA sensor for detection of bladder cancer biomarkers in urine, Sensors and Actuators - B: Chemical, 178 pp. 200-206. ISSN 0925-4005 (2013) [Refereed Article] 
Shin, Y and Perera, AP and Kee, JS and Song, J and Fang, Q and Lo, G-Q and Kyoung, M, Label-free methylation specific sensor based on silicon microring resonators for detection and quantification of DNA methylation biomarkers in bladder cancer, Sensors and Actuators - B: Chemical, 177 pp. 404-411. ISSN 0925-4005 (2013) [Refereed Article] 
Kim, KW and Shin, Y and Perera, AP and Liu, Q and Kee, JS and Han, K and Yoon, Y-J and Park, MK, Label-free, PCR-free chip-based detection of telomerase activity in bladder cancer cells, Biosensors and Bioelectronics, 45 pp. 152-157. ISSN 0956-5663 (2013) [Refereed Article] 
Bis, JC and Decarli, C and Smith, AV and Van Der Lijn, F and Crivello, F and Fornage, M and Debette, S and Shulman, JM and Schmidt, H and Srikanth, V and Schuur, M and Yu, L and Choi, S-H and Sigurdsson, S and Verhaaren, BFJ and Destefano, AL and Lambert, J-C and Jack, CR and Struchalin, M and Stankovich, J and Ibrahim-Verbaas, CA and Fleischman, D and Zijdenbos, A and Den Heijer, T and Mazoyer, B and Coker, LH and Enzinger, C and Danoy, P and Amin, N and Arfanakis, K and Van Buchem, MA and De Bruijn, RFAG and Beiser, A and Dufouil, C and Huang, J and Cavalieri, M and Thomson, R and Niessen, WJ and Chibnik, LB and Gislason, GK and Hofman, A and Pikula, A and Amouyel, P and Freeman, KB and Phan, TG and Oostra, BA and Stein, JL and Medland, SE and Vasquez, AA and Hibar, DP and Wright, MJ and Franke, B and Martin, NG and Thompson, PM and Nalls, MA and Uitterlinden, AG and Au, R and Elbaz, A and Beare, RJ and Van Swieten, JC and Lopez, OL and Harris, TB and Chouraki, V and Breteler, MMB and De Jager, PL and Becker, JT and Vernooij, MW and Knopman, D and Fazekas, F and Wolf, PA and Van Der Lugt, A and Gudnason, V and Longstreth, WT and Brown, MA and Bennett, DA and Van Duijn, CM and Mosley, TH and Schmidt, R and Tzourio, C and Launer, LJ and Ikram, MA and Seshadri, S, Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, Common variants at 12q14 and 12q24 are associated with hippocampal volume, Nature Genetics, 44, (5) pp. 545-551. ISSN 1061-4036 (2012) [Refereed Article]
Kent Jr, JW and Goring, HHH and Charlesworth, JC and Drigalenko, E and Diego, VP and Curran, JE and Johnson, MP and Dyer, TD and Cole, SA and Jowett, JBM and Mahaney, MC and Comuzzie, AG and Almasy, L and Moses, EK and Blangero, J and Williams-Blangero, S, Genotype age interaction in human transcriptional ageing, Mechanisms of Ageing and Development, 133, (9-10) pp. 581-590. ISSN 0047-6374 (2012) [Refereed Article] 
Ma, GZM and Stankovich, J and Bahlo, M and Booth, DR and Broadley, S and Brown, MA and Browning, BL and Browning, SR and Butzkueven, H and Carroll, WM and Danoy, P and Foote, SJ and Griffiths, L and Heard, RN and Kermode, AG and Lechner-Scott, J and Moscato, P and Perreau, VM and Scott, RJ and Slee, M and Stewart, GJ and Taylor, BV and Wiley, J and Kilpatrick, TJ and Binder, MD and Field, J, Polymorphisms in the Receptor Tyrosine Kinase MERTK Gene Are Associated with Multiple Sclerosis Susceptibility, PL o S One, 6, (2) Article e16964. ISSN 1932-6203 (2011) [Refereed Article]
Riveros, C and Mellor, D and Gandhi, KS and McKay, FC and Cox, MB and Berretta, R and Vaezpour, SY and Inostroza-Ponta, M and Broadley, SA and Heard, RN and Vucic, S and Stewart, GJ and Williams, DW and Scott, RJ and Lechner-Scott, J and Booth, DR and Moscato, P and Bahlo, M and Brown, MA and Browning, BL and Browning, SR and Butzkueven, H and Carroll, WM and Danoy, P and Field, J and Foote, SJ and Griffiths, LR and Kermode, AG and Kilpatrick, TJ and Mason, D and Perreau, VM and Slee, M and Stankovich, J and Taylor, BV and Wiley, J, A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in Multiple Sclerosis , P L o S One, 5, (12) EJ ISSN 1932-6203 (2010) [Refereed Article]
Cox, MB and Cairns, MJ and Gandhi, KS and Carroll, AP and Moscovis, S and Stewart, GJ and Broadley, S and Scott, RJ and Booth, DR and Lechner-Scott, J and Bahlo, M and Butzkueven, H and Brown, MA and Foote, SJ and Griffiths, L and Kilpatrick, TJ and Moscato, P and Perreau, VM and Rubio, JP and Stankovich, J and Taylor, BV and Wiley, J and Heard, RN, MicroRNAs miR-17 and miR-20a Inhibit T Cell Activation Genes and Are Under-Expressed in MS Whole Blood, P L o S One, 5, (8) EJ ISSN 1932-6203 (2010) [Refereed Article]
Gandhi, KS and McKay, FC and Cox, M and Riveros, C and Armstrong, N and Heard, RN and Vucic, S and Williams, DW and Stankovich, J and Brown, M and Danoy, P and Stewart, GJ and Broadley, S and Moscato, P and Lechner-Scott, J and Scott, RJ and Booth, DR and Griffiths, L and Slee, M and Browning, S and Browning, BL and Kilpatrick, T and Rubio, J and Perreau, V and Butzkeuven, H and Tanner, M and Wiley, J and Foote, SJ and Taylor, BVM and Kermode, A and Carroll, B and Bahlo, M, The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis , Human Molecular Genetics, 19, (11) pp. 2134-2143. ISSN 0964-6906 (2010) [Refereed Article]
Hunt, KA and Zhernakova, A and Turner, G and Heap, GAR and Franke, L and Bruinenberg, M and Romanos, J and Dinesen, LC and Ryan, A W and Panesar, D and Gwilliam, R and Takeuchi, F and McLaren, WM and Holmes, GKT and Howdle, PD and Walters, JRF and Sanders, DS and Playford, RJ and Trynka, G and Mulder, CJJ and Mearin, ML and Verbeek, WHM and Trimble, V and Stevens, FM and O'Morain, C and Kennedy, NP and Kelleher, D and Pennington, DJ and Strachan, DP and McArdle, WL and Mein, CA and Wapenaar, MC and Deloukas, P and McGinnis, R and McManus, R and Wijmenga, C and van Heel, DA, Newly identified genetic risk variants for celiac disease related to the immune response, Nature Genetics, 40, (4) pp. 395-402. ISSN 1061-4036 (2008) [Refereed Article] 
van Heel, DA and Franke, L and Hunt, KA and Gwilliam, R and Zhernakova, A and Inouye, M and Wapenaar, MC and Barnardo, MCNM and Bethel, G and Holmes, GKT and Feighery, C and Jewell, D and Kelleher, D and Kumar, P and Travis, S and Walters, JRF and Sanders, DS and Howdle, P and Swift, J and Playford, RJ and McLaren, WM and Mearin, ML and Mulder, C J and McManus, R and McGinnis, R and Cardon, LR and Deloukas, P and Wijmenga, C, A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21, Nature Genetics, 39, (7) pp. 827-829. ISSN 1061-4036 (2007) [Refereed Article] 
Symons, RCA and Turakulov, R and Foote, SJ and Craig, JE and McCartney, PJ and Mackey, DA, No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma, Ophthalmic Genetics, 28, (1) pp. 39-41. ISSN 1381-6810 (2007) [Letter or Note in Journal] 
Thomson, Russell and Quinn, SJ and McKay, JD and Silver, J and Bahlo, M and Fitzgerald, LM and Foote, SJ and Dickinson, JL and Stankovich, J, The advantages of dense marker sets for linkage analysis with very large families, Human Genetics, 121, (3-4) pp. 459-468. ISSN 0340-6717 (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] 
Sakthianandeswaren, A and Elso, CM and Simpson, K and Curtis, JM and Kumar, B and Speed, TP and Handman, E and Foote, SJ, The wound repair response controls outcome to cutaneous leishmaniasis, Proceedings of the National Academy of Sciences of the United States of America, 102, (43) pp. 15551-15556 . ISSN 0027-8424 (2005) [Refereed Article] 
McKay, JD and Thompson, D and Lesueur, F and Stankov, K and Pastore, A and Watfah, C and Strolz, S and Riccabona, G and Moncayo, R and Romeo, G and Goldgar, DE, Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer, Journal of Medical Genetics, 41, (6) pp. 407-412. ISSN 0022-2593 (2004) [Refereed Article] 
Cook, WD and McCaw, BJ and Herring, C and John, DL and Foote, SJ and Nutt, SL and Adams, JM, PU.1 is a suppressor of myeloid leukemia, inactivated in mice by gene deletion and mutation of its DNA binding domain, Blood, 104, (12) pp. 3437-3444. ISSN 0006-4971 (2004) [Refereed Article] 
Baird, PN and Craig, JE and Richardson, AJ and Ring, MA and Sim, P and Stanwix, SP and Foote, SJ and Mackey, DA, Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin, Human genetics, 112, (2) pp. 110-116. ISSN 0340-6717 (2003) [Refereed Article] 
Burdon, KP and Wilkinson, RM and Barbour, JM and Dickinson, JL and Stankovich, J and Mackey, DA and Sale, MM, Investigation of albinism genes in congenital esotropia, Molecular Vision, 9, (83-85 ) pp. 710-714. ISSN 1090-0535 (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, (5) pp. 1120-1130. ISSN 0002-9297 (2003) [Refereed Article] 
Carpinelli, M and Wicks, I and Sims, NA and O'Donnell, K and Hanzinikolas, K and Burt, R and Foote, SJ and Bahlo, M and Alexander, WS and Hilton, DJ, An Ethyl-Nitrosourea-Induced Point Mutation in Phex causes exon skipping, X-linked Hypophosphatemia, and Rickets, American Journal of Pathology, 161, (5) pp. 1925-1933. ISSN 0002-9440 (2002) [Refereed Article] 
Sale, MM and Craig, JE and Charlesworth, JC and Fitzgerald, LM and Hanson, I and Dickinson, JL and Matthews, S and van Heyningen, V and Fingert, J and Mackey, DA, Broad Phenotypic variability in a Single Pedigree With a Novel 1410delC Mutation in the PST Domain of the PAX6 Gene, Human Mutation, 20, (4) pp. 322. ISSN 1098-1004 (2002) [Refereed Article] 
Sale, MM and Fitzgerald, LM and Charlesworth, JC and Bowden, D and Rich, S, Evidence for a Novel Type 1 Diabetes Susceptibility Locus on Chromosome 8, Diabetes, 51, (Supplement 3) pp. S316-S319. ISSN 0012-1797 (2002) [Refereed Article] 
Rubio, J and Bahlo, M and Butzkueven, H and Van der Mei, IAF and Sale, MM and Dickinson, JL and Groom, PS and Johnson, L and Simmons, R and Tait, B and Varney, M and Taylor, BVM and Dwyer, T and Williamson, R and Gough, N and Kilpatrick, T and Speed, T and Foote, SJ, Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis, American Journal of Human Genetics, 70, (5) pp. 1125-1137. ISSN 0002-9297 (2002) [Refereed Article] 
Fullerton, J and Paprocki, P and Foote, SJ and Mackey, DA and Williamson, R and Forrest, S, Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia, Human Genetics, 110, (5) pp. 462-470. ISSN 0340-6717 (2002) [Refereed Article] 
Stankovich, J and Sale, MM and Cooley, HM and Bahlo, M and Reilly, A and Dickinson, JL and Jones, G, Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population, Annals of the Rheumatic Diseases, 61, (12) pp. 1081-1084. ISSN 0003-4967 (2002) [Refereed Article] 
Sale, MM and Fitzgerald, LM and Kagame, K and Erdmann, I and Craig, JE and Dickinson, JL and Copper, R, Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients, Ophthalmic Genetics, 33, (1) pp. 67-69. ISSN 1381-6810 (2002) [Letter or Note in Journal] 
Burt, RA and Marshall, VM and Wagglen, J and Rodda, FR and Senyschen, D and Baldwin, TM and Buckingham, LA and Foote, SJ, Mice that are congenic for the char2 locus are susceptible to malaria, Infection and Immunity, 70, (8) pp. 4750-4753. ISSN 0019-9567 (2002) [Refereed Article] 
Symons, RCA and Daly, MJ and Fridlyand, J and Speed, TP and Cook, WD and Gerondakis, S and Harris, AW and Foote, SJ, Multiple genetic loci modify susceptibility to plasmacytoma-related morbidity in Eu-v-abl transgenic mice, National Academy of Sciences of The United States of America. Proceedings, 99, (17) pp. 11299-11304. ISSN 0027-8424 (2002) [Refereed Article] 
Elso, C and Toohey, B and Reid, GE and Poetter, K and Simpson, RJ and Foote, SJ, Mutation detection using mass spectrometric separation of tiny oligonucleotide fragments, Genome Research, 12, (9) pp. 1428-1433. ISSN 1088-9051 (2002) [Refereed Article] 
Vickers, JC and Craig, JE and Stankovich, J and McCormack, GH and West, AK and Dickinson, JL and McCartney, PJ and Coote, M and Healey, D and Mackey, DA, The apolipoprotein epsilon 4 gene is associated with elevated risk of normal tension glaucoma, Molecular Vision, 8, (40) pp. 389-393. ISSN 1090-0535 (2002) [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, (3) pp. 727-736. ISSN 0002-9297 (2000) [Refereed Article] 
Roberts, AW and Hasegawa, M and Metcalf, D and Foote, SJ, Identification of a genetic locus modulating splenomegaly induced by granulocyte colony-stimulating factor in mice, Leukemia, 14, (4) pp. 657-661. ISSN 0887-6924 (2000) [Refereed Article] 
Symons, RCA and Marshall, VM and Foote, SJ, Improvements in allelic discrimination of microsatellite markers using denaturing polyacrylamide gel electrophoresis, Mammalian Genome, 11, (8) pp. 671-674. ISSN 0938-8990 (2000) [Refereed Article] 
Hasegawa, M and Baldwin, TM and Metcalf, D and Foote, SJ, Progenitor cell mobilization by granulocyte colony-stimulating factor controlled by loci on chromosomes 2 and 11, Blood, 95, (5) pp. 1872-1874. ISSN 0006-4971 (2000) [Refereed Article] 
Hooper, JD and Nicol, DL and Dickinson, JL and Eyre, HJ and Scarman, AL and Normyle, JF and Stuttgen, MA and Douglas, ML and Loveland, KAL and Sutherland, GR and Antalis, TM, Testisin, a New Human Serine Proteinase Expressed by Premeiotic Testicular Germ Cells and Lost in Testicular Germ Cell Tumors, Cancer Research, 59, (13) pp. 3199-3205. ISSN 0008-5472 (1999) [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 - The European consortium on MEN1, Genomics, 37, (3) pp. 354-365. ISSN 0888-7543 (1996) [Refereed Article] 
Bower, S and Nicol, SC and Kirkland, G and Byrne, E, Exercise intolerance in Kearns-Sayre syndrome, Journal of Clinical Neuroscience, 3, (4) pp. 386-389. ISSN 0967-5868 (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. ISSN 0167-6784 (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 Study in Tasmania (GIST), Ophthalmic Genetics, 17, (4) pp. 209-214. ISSN 0167-6784 (1996) [Refereed Article] 
Chapter in Book
Handman, E and Elso, C and Foote, SJ, Genes and susceptibility to leishmaniasis, Advances in Parasitology, Academic Press, JR Baker, R Muller, D Rollinson (ed), London, pp. 1-76. ISBN 0-12-031759-1 (2005) [Research Book Chapter] 
Review
Lin, R and Charlesworth, J and van der Mei, I and Taylor, BV, The genetics of multiple sclerosis, Practical Neurology, 12, (5) pp. 279-288. ISSN 1474-7758 (2012) [Substantial Review]
Rubio, JP and Bahlo, M and Speed, TP and Kilpatrick, TJ and Foote, SJ, The current state of multiple sclerosis genetic research, Annals Academy of Medicine Singapore, 29 pp. 322-30. (2000) [Substantial Review] 
Foote, SJ, Designing new drugs through DNA, Australian Family Physician, 28 pp. 1011-1016. (1999) [Substantial Review] 
Conference Publication
McKercher, C and Venn, A and Sanderson, K and Jose, M and Neil, A, A comparison of the EQ-5D-3L and the AQOL-4D for assessing health-related quality of life in adults with chronic kidney disease, 54th ANZSN ASM 2018, 8-12 September 2018, Sydney (2018) [Conference Extract]
Dickinson, JL and Wheatley, CM and Fitzgerald, L and Brown, M and Craig, JE and Mackey, DA and Sale, MM, Investigation of a possible role for the Norrie Disease gene in Retinopathy of Prematurity, Human Genome Society Conference, Cairns, Australia (2001) [Conference Extract] 
Dickinson, JL and Mackey, DA and Craig, JE and McNaught, AI and Wilkinson, CH and Healey, DL and Rait, JL and Coote, MA and Wong, TL and McCartney, PJ and John, AM and Stone, EM and Sheffield, VC, Predictive DNA testing for glaucoma with the GLC1A gene: experience with a large Australian family, International Human Genome Conference, Brisbane, Australia (1998) [Conference Extract] 
Other Public Output
Dwyer, T, $2.5m for pharmaceutical discovery program, UniTas, University of Tasmania, Tasmania, 136, 23 Feb (1998) [Internal Newsletter] 
Dwyer, T, Environmental and genetic factors associated with the disease multiple sclerosis, 7ZR Radio, Tasmania, 19 Nov (1998) [Media Interview] 
Jones, G, Gene hunt based here, The Examiner, Tasmania, 13 June (1998) [Newspaper Article] 
Dwyer, T, Gene research unit announced, The Advocate, Tasmania, 17 Jan (1998) [Newspaper Article] 
Mackey, DA, Glaucoma testing, The Advocate, Tasmania, 15 Sept (1998) [Newspaper Article] 
Dwyer, T, Honing in, Research News, University of Tasmania, Tasmania, 15, April (1998) [Internal Newsletter] 
Dwyer, T, Menzies Centre wants MS research volunteers for study, The Examiner, Tasmania, 6 Nov (1998) [Newspaper Article] 
Dwyer, T, MS researchers in need of subjects, The Advocate, Tasmania, 5 Nov (1998) [Newspaper Article] 
Dwyer, T, New genetics unit set up, The Mercury, Tasmania, 22 April (1998) [Newspaper Article] 
Mackey, DA, Research coup for state, The Mercury, Tasmania, 17 Jan (1998) [Newspaper Article] 
Jones, G, State lead in arthritis research, The Mercury, Tasmania, 13 June (1998) [Newspaper Article] 
Dwyer, T, State's old families aid university gene study, The Australian, Australia, 26 Jan (1998) [Newspaper Article] 
Mackey, DA, Study based in Tasmania, The Examiner, Tasmania, 5 July (1998) [Newspaper Article] 

This list was generated on Wed Aug 21 16:24:03 2019.