eCite Digital Repository

Author: Stankovich, J (Dr Jim Stankovich)

Number of items: 114

Journal Article
Bukhari, W and Prain, KM and Waters, P and Woodhall, M and O'Gorman, CM and Clarke, L and Silvestrini, RA and Bundell, CS and Abernethy, D and Bhuta, S and Blum, S and Boggild, M and Boundy, K and Brew, BJ and Brown, M and Brownlee, WJ and Butzkueven, H and Carroll, WM and Chen, C and Coulthard, A and Dale, RC and Das, C and Dear, K and Fabis-Pedrini, MJ and Fulcher, D and Gillis, D and Hawke, S and Heard, R and Henderson, APD and Heshmat, S and Hodgkinson, S and Jimenez-Sanchez, S and Killpatrick, T and King, J and Kneebone, C and Kornberg, AJ and Lechner-Scott, J and Lin, MW and Lynch, C and Macdonell, R and Mason, DF and McCombe, PA and Pender, MP and Pereira, JA and Pollard, JD and Reddel, SW and Shaw, C and Spies, J and Stankovich, J and Sutton, I and Vucic, S and Walsh, M and Wong, RC and Yiu, EM and Barnett, MH and Kermode, AG and Marriott, MP and Parratt, JDE and Slee, M and Taylor, BV and Willoughby, E and Wilson, RJ and Vincent, A and Broadley, SA, Incidence and prevalence of NMOSD in Australia and New Zealand, Journal of Neurology, Neurosurgery and Psychiatry, 88 pp. 632-638. ISSN 0022-3050 (2017) [Refereed Article]
Morley, C and Stankovich, J and Peterson, G and Kinsman, L, Planning for the future: emergency department presentation patterns in Tasmania, Australia, International Emergency Nursing ISSN 1755-599X (2017) [Refereed Article]
Gu, BJ and Field, J and Dutertre, S and Ou, A and Kilpatrick, TJ and Lechner-Scott, J and Scott, R and Lea, R and Taylor, BV and Stankovich, J and Butzkueven, H and Gresle, M and Laws, SM and Petrou, S and Hoffjan, S and Akkad, DA and Graham, CA and Hawkins, S and Glaser, A and Bedri, SK and Hillert, J and Matute, C and Antiguedad, A and Wiley, JS, ANZgene Consortium, A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis, Human Molecular Genetics, 24, (19) pp. 5644-5654. ISSN 0964-6906 (2015) [Refereed Article] 
Inwood, K and Maxwell-Stewart, HJ and Oxley, D and Stankovich, J, Growing Incomes, Growing People In Nineteenth-Century Tasmania, Australian Economic History Review, 55, (2) pp. 187-211. ISSN 0004-8992 (2015) [Refereed Article] 
Maxwell-Stewart, H and Inwood, K and Stankovich, J, Prison and the colonial family, The History of the Family, 20, (2) pp. 231-248. ISSN 1081-602X (2015) [Refereed Article] 
Zochling, J and Newell, F and Charlesworth, JC and Leo, P and Stankovich, J and Cortes, A and Zhou, Y and Stevens, W and Sahhar, J and Roddy, J and Nash, P and Tymms, K and Rischmueller, M and Lester, S and Proudman, S and Brown, MA, An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3, Arthritis Research & Therapy, 16, (5) Article 438. ISSN 1478-6362 (2014) [Refereed Article]
Goris, A and van Setten, J and Diekstra, F and Ripke, S and Patsopoulos, NA and Sawcer, SJ and Barcellos, L and Booth, D and McCauley, JL and Comabella, M and D'Alfonso, SD and Fontaine, B and Hafler, D and Haines, J and Harbo, HF and Hauser, SL and Hawkins, C and Hemmer, B and Hillert, J and Ivinson, A and Kockum, I and Martin, R and Boneschi, FM and Olsson, T and Oturai, A and Pericak-Vance, M and Saarela, J and Spurkland, A and Stewart, G and Zipp, F and van Es, M and Scott, RJ and Lechner-Scott, J and Moscato, P and Heard, RN and Mason, D and Griffiths, L and Broadley, S and Brown, MA and Slee, M and Foote, SJ and Stankovich, J and Taylor, BV and Wiley, J and Bahlo, M and Perreau, V and Field, J and Butzkueven, H and Kilpatrick, TJ and Rubio, J and Marriott, M and Carroll, WM and Kermode, AG and Andersen, PM and Melki, J and Meininger, V and Hardiman, O and Landers, JE and Brown Jr, RH and Shatunov, A and Leigh, N and Al-Chalabi, A and Shaw, CE and Traynor, BJ and Chio, A and Restagno, G and Mora, G and Ophoff, RA and Oksenberg, JR and Van Damme, P and Compston, A and Robberecht, W and Dubois, B and van den Berg, LH and De Jager, PL and Veldink, JH and de Bakker, PI, No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis, Human Molecular Genetics, 23, (7) pp. 1916-1922. ISSN 0964-6906 (2014) [Refereed Article] 
Mechelli, R and Umeton, R and Policano, C and Annibali, V and Coarelli, G and Ricigliano, VAG and Vittori, D and Fornasiero, A and Buscarinu, MC and Romano, S and Salvetti, M and Ristori, G and Sawcer, S and Hellenthal, G and Pirinen, M and Spencer, CCA and Patsopoulos, NA and Moutsianas, L and Dilthey, A and Su, Z and Freeman, C and Hunt, SE and Edkins, S and Gray, E and Booth, DR and Potter, SC and Goris, A and Band, G and Oturai, AB and Strange, A and Saarela, J and Bellenguez, C and Fontaine, B and Gillman, M and Hemmer, B and Gwilliam, R and Zipp, F and Jayakumar, A and Martin, R and Leslie, S and Hawkins, S and Giannoulatou, E and D'alfonso, S and Blackburn, H and Boneschi, FM and Liddle, J and Harbo, HF and Perez, ML and Spurkland, A and Waller, MJ and Mycko, MP and Ricketts, M and Comabella, M and Hammond, N and Kockum, I and McCann, OT and Ban, M and Whittaker, P and Kemppinen, A and Weston, P and Hawkins, C and Widaa, S and Zajicek, J and Dronov, S and Robertson, N and Bumpstead, SJ and Barcellos, LF and Ravindrarajah, R and Abraham, R and Alfredsson, L and Ardlie, K and Aubin, C and Baker, A and Baker, K and Baranzini, SE and Bergamaschi, L and Bergamaschi, R and Bernstein, A and Berthele, A and Boggild, M and Bradfield, JP and Brassat, D and Broadley, SA and Buck, D and Butzkueven, H and Capra, R and Carroll, WM and Cavalla, P and Celius, EG and Cepok, S and Chiavacci, R and Clerget-Darpoux, R and Clysters, K and Comi, G and Cossburn, M and Cournu-Rebeix, I and Cox, MB and Cozen, W and Cree, BAC and Cross, AH and Cusi, D and Daly, MJ and Davis, E and de Bakker, PIW and Debouverie, M and D'hooghe, B and Dixon, K and Dobosi, R and Dubois, B and Ellinghaus, D and Elovaara, I and Esposito, F and Fontenille, C and Foote, S and Franke, A and Galimberti, D and Ghezzi, A and Glessner, J and Gomez, R and Gout, O and Graham, C and Grant, SFA and Guerini, FR and Hakonarson, H and Hall, P and Hamsten, A and Hartung, HP and Heard, RN and Heath, S and Hobart, J and Hoshi, M and Infante-Duarte, C and Ingram, G and Ingram, W and Islam, T and Jagodic, M and Kabesch, M and Kermode, AG and Kilpatrick, TJ and Kim, C and Klopp, N and Koivisto, K and Larsson, M and Lathrop, M and Lechner-Scott, JS and Leone, MA and Leppa, V and Liljedahl, U and Bomfim, IL and Lincoln, RR and Link, J and Liu, J and Lorentzen, AR and Lupoli, S and Macciardi, F and Mack, T and Marriott, M and Martinelli, V and Mason, D and McCauley, JL and Mentch, F and Mero, IL and Mihalova, T and Montalban, X and Mottershead, J and Myhr, KM and Naldi, P and Ollier, W and Page, A and Palotie, A and Pelletier, J and Piccio, L and Pickersgill, T and Piehl, F and Pobywajlo, S and Quach, HL and Ramsay, PP and Reunanen, M and Reynolds, R and Rioux, JD and Rodegher, M and Roesner, S and Rubio, JP and Ruckert, IM and Salvi, E and Santaniello, A and Schaefer, CA and Schreiber, S and Schulze, C and Scott, RJ and Sellebjerg, F and Selmaj, KW and Sexton, D and Shen, L and Simms-Acuna, B and Skidmore, S and Sleiman, PMA and Smestad, C and Sorensen, PS and Sondergaard, HB and Stankovich, J and Strange, RC and Sulonen, AM and Sundqvist, E and Syvanen, AC and Taddeo, F and Taylor, B and Blackwell, JM and Tienari, P and Bramon, E and Tourbah, A and Brown, MA and Tronczynska, E and Casas, JP and Tubridy, N and Corvin, A and Vickery, J and Jankowski, J and Villoslada, P and Markus, HS and Wang, K and Mathew, CG and Wason, J and Palmer, CNA and Wichmann, HE and Plomin, R and Willoughby, E and Rautanen, A and Winkelmann, J and Wittig, M and Trembath, RC and Yaouanq, J and Viswanathan, AC and Zhang, H and Wood, NW and Zuvich, R and Deloukas, P and Langford, C and Duncanson, A and Oksenberg, JR and Pericak-Vance, MA and Haines, JL and Olsson, T and Hillert, J and Ivinson, AJ and De Jager, PL and Peltonen, L and Stewart, GJ and Hafler, DA and Hauser, SL and McVean, G and Donnelly, P and Compston, A, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium, A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis, PLoS One, 8, (5) Article e63300. ISSN 1932-6203 (2013) [Refereed Article]
Lee, SH and Harold, D and Nyholt, DR and Scott, RJ and Lechner-Scott, J and Moscato, P and Booth, DR and Stewart, GJ and Heard, RN and Mason, D and Griffiths, L and Broadley, S and Brown, MA and Slee, M and Foote, SJ and Stankovich, J and Taylor, BV and Wiley, J and Bahlo, M and Perreau, V and Field, J and Butzkueven, H and Kilpatrick, TJ and Rubio, J and Marriott, M and Carroll, WM and Kermode, AG and Anderson, CA and Gordon, SD and Guo, Q and Henders, AK and Lambert, A and Kraft, P and Kennedy, SH and Macgregor, S and Martin, NG and Missmer, SA and Morris, AP and Painter, JN and Roseman, F and Treloar, SA and Wallace, L and Sims, R and Gerrish, A and Chapman, J and Moskvina, V and Abraham, R and Hollingworth, P and Hamshere, M and Pahwa, JS and Dowzell, K and Williams, A and Jones, N and Thomas, C and Stretton, A and Morgan, A and Lovestone, S and Powell, J and Proitsi, P and Lupton, MK and Brayne, C and Rubinsztein, DC and Gill, M and Lawlor, B and Lynch, A and Morgan, K and Brown, K and Passmore, P and Craig, D and McGuinness, B and Todd, S and Holmes, C and Mann, D and Smith, AD and Love, S and Kehoe, PG and Hardy, J and Mead, S and Fox, N and Rossor, M and Collinge, J and Maier, W and Jessen, F and Heun, R and Kolsch, H and Schurmann, B and van den Bussche, H and Heuser, I and Kornhuber, J and Wiltfang, J and Dichgans, M and Frolich, L and Hampel, H and Hull, M and Rujescu, D and Goate, A and Kauwe, JSK and Cruchaga, C and Nowotny, P and Morris, JC and Mayo, K and Livingston, G and Bass, NJ and Gurling, H and McQuillin, A and Gwilliam, R and Deloukas, P and Nothen, MM and Holmans, P and O'Donovan, M and Owen, MJ and Goddard, ME and Zondervan, KT and Williams, J and Montgomery, GW and Wray, NR and Visscher, PM, Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis, Human Molecular Genetics, 22, (4) pp. 832-841. ISSN 0964-6906 (2013) [Refereed Article]
Patsopoulos, NA and Barcellos, LF and Hintzen, RQ and Schaefer, C and van Duijn, CM and Noble, JA and Raj, T and Bernardinelli, L and Booth, D and Comabella, M and Compston, A and D'Alfonso, S and Fontaine, B and Goris, A and Haines, J and Harbo, H and Hauser, S and Hawkins, C and Hemmer, B and Ivinson, A and Lill, C and Martin, R and Martinelli-Boneschi, F and Oturai, A and Palotie, A and Pericak-Vance, M and Saarela, J and Stewart, G and Zipp, F and Scott, RJ and Lechner-Scott, J and Moscato, P and Heard, RN and Mason, D and Griffith, L and Broadley, S and Brown, MA and Slee, M and Foote, SJ and Stankovich, J and Wiley, J and Bahlo, M and Perreau, V and Field, J and Butzkueven, H and Kilpatrick, T and Rubio, J and Marriott, M and Carroll, WM and Kermode, AG and Gourraud, P-A and Stranger, BE and Oksenberg, J and Olsson, T and Taylor, BV and Sawcer, S and Hafler, DA and Carrington, M and De Jager, PL and de Bakker, PIW, Fine-mapping the genetic association of the major histocompatibility complex in Multiple Sclerosis: HLA and non-HLA effects, PLoS Genetics, 9, (11) Article e1003926. ISSN 1553-7404 (2013) [Refereed Article]
Buck, D and Albrecht, E and Aslam, M and Goris, A and Hauenstein, N and Jochim, A and Ban, M and Baranzini, S and Barcellos, L and Beecham, G and Beecham, A and Bernardinelli, L and Booth, D and Steffan, B and Bush, W and Comabella, M and Compston, A and Cotsapas, C and Cree, B and D'Alfonso, S and Daly, M and Damotte, V and Davis, M and de Bakker, P and De Jager, PL and Esposito, F and Fontaine, B and Gourraud, P-A and Green, T and Gulowsen Celius, E and Hadjixenofontos, A and Hafler, D and Haines, J and Harbo, HF and Hauser, S and Hawkins, C and Hillert, J and Hintzen, R and Horakova, D and Ivinson, AJ and Anu, K and Kira, J and Kockum, I and Lincoln, R and Martin, R and Martinelli Boneschi, F and McCauley, JL and Mero, I-L and Oksenberg, J and Olsson, T and Oturai, A and Aarno, P and Patsopoulos, N and Pericak-Vance, M and Rioux, J and Saarela, J and Sawcer, S and Schnetz-Boutaud, N and Finn, S and Soendergaard, H and Sorensen, PS and Spurkland, A and Stankovich, J and Stewart, G and Taylor, B and Ticca, A and West, S and Zipp, F and Cepok, S and Grummel, V and Dubois, B and Berthele, A and Lichtner, P and Gieger, C and Winkelmann, J and Hemmer, B, Wellcome Trust Case Control Consortium, Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis, Annals of Neurology, 73, (1) pp. 86-94. ISSN 0364-5134 (2013) [Refereed Article] 
Lin, R and Charlesworth, J and Stankovich, J and Perreau, VM and Brown, MA and Taylor, BV, ANZgene Consortium, Identity-by-Descent Mapping to Detect Rare Variants Conferring Susceptibility to Multiple Sclerosis, PLoS ONE, 8, (3) Article e56379. ISSN 1932-6203 (2013) [Refereed Article]
O'Gorman, C and Lin, R and Stankovich, J and Broadley, SA, Modelling genetic susceptibility to multiple sclerosis with family data, Neuroepidemiology, 40, (1) pp. 1-12. ISSN 0251-5350 (2013) [Refereed Article]
Baranzini, SE and Khankhanian, P and Patsopoulos, NA and Li, M and Stankovich, J and Cotsapas, C and Sondergaard, HB and Ban, M and Barizzone, N and Bergamaschi, L and Booth, D and Buck, D and Cavalla, P and Celius, EG and Comabella, M and Comi, G and Compston, A and Cournu-Rebeix, I and D'alfonso, S and Damotte, V and Din, L and Dubois, B and Elovaara, I and Esposito, F and Fontaine, B and Franke, A and Goris, A and Gourraud, PA and Graetz, C and Guerini, FR and Guillot-Noel, L and Hafler, D and Hakonarson, H and Hall, P and Hamsten, A and Harbo, HF and Hemmer, B and Hillert, J and Kemppinen, A and Kockum, I and Koivisto, K and Larsson, M and Lathrop, M and Leone, M and Lill, CM and Macciardi, F and Martin, R and Martinelli, V and Martinelli-Boneschi, F and McCauley, JL and Myhr, KM and Naldi, P and Olsson, T and Oturai, A and Pericak-Vance, MA and Perla, F and Reunanen, M and Saarela, J and Saker-Delye, S and Salvetti, M and Sellebjerg, F and Sorensen, PS and Spurkland, A and Stewart, G and Taylor, B and Tienari, P and Winkelmann, J and Zipp, F and Ivinson, AJ and Haines, JL and Sawcer, S and Dejager, P and Hauser, SL and Oksenberg, JR, Wellcome Trust Case Control Consortium 2, Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls, American Journal of Human Genetics: A Record of Research, Review and Bibliographic Material Relating to Heredity in Man, 92, (6) pp. 854-865. ISSN 0002-9297 (2013) [Refereed Article]
Cortes, A and Field, J and Glazov, EA and Hadler, J and Stankovich, J and Brown, MA and Baxter, A and Kermode, AG and Taylor, B and Booth, DR and Mason, D and Stewart, GJ and Butzkueven, H and Charlesworth, J and Wiley, J and Lechner-Scott, J and Field, J and Tajouri, L and Griffiths, L and Slee, M and Brown, MA and Moscato, P and Scott, RJ and Broadley, S and Vucic, S and Kilpatrick, TJ and Carroll, WM, Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes, Human Molecular Genetics, 22, (11) pp. 2283-2292. ISSN 0964-6906 (2013) [Refereed Article] 
Lucas, RM and Ponsonby, AL and Dear, K and Valery, PC and Taylor, B and van der Mei, I and McMichael, AJ and Pender, MP and Chapman, C and Coulthard, A and Kilpatrick, TJ and Stankovich, J and Williams, D and Dwyer, T, Vitamin D status: Multifactorial contribution of environment, genes and other factors in healthy Australian adults across a latitude gradient, Journal of Steroid Biochemistry and Molecular Biology, 136, (13) pp. 300-308. ISSN 0960-0760 (2013) [Refereed Article] 
Wilkins, EJ and Rubio, JP and Kotschet, KE and Cowie, TF and Boon, WC and O'Hely, M and Burfoot, R and Wang, W and Sue, CM and Speed, TP and Stankovich, J and Horne, MK, A DNA resequencing array for genes involved in Parkinson's disease, Parkinsonism and related disorders, 18, (4) pp. 386-390. ISSN 1353-8020 (2012) [Refereed Article] 
Martinelli-Boneschi, F and Esposito, F and Brambilla, P and Lindstrom, E and Lavorgna, G and Stankovich, J and Rodegher, M and Capra, R and Ghezzi, A and Coniglio, G and Colombo, B and Sorosina, M and Martinelli, V and Booth, D and Oturai, AB and Stewart, G and Harbo, HF and Kilpatrick, TJ and Hillert, J and Rubio, JP and Abderrahim, H and Wojcik, J and Comi, G, A genome-wide association study in progressive multiple sclerosis, Multiple Sclerosis, 18, (10) pp. 1384-1394. ISSN 1352-4585 (2012) [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]
Rumbold, AR and Tan, SE and Condon, JR and Taylor-Thomson, D and Nickels, M and Tabrizi, SN and Davy, MLJ and O'Brien, MM and Connors, CM and Zardawi, I and Stankovich, J and Garland, SM, Investigating a cluster of vulvar cancer in young women: a cross-sectional study of genital human papillomavirus prevalence, BMC Infectious Diseases, 12 Article 243. ISSN 1471-2334 (2012) [Refereed Article]
Tegg, EM and Thomson, RJ and Stankovich, JM and Banks, A and Marsden, KA and Lowenthal, RM and Foote, SJ and Dickinson, JL, Anticipation in familial hematologic malignancies, Blood, 117, (4) pp. 1308-1310. ISSN 0006-4971 (2011) [Refereed Article]
Ritchie, ME and Liu, R and Carvalho, BS and Bahlo, M and Booth, DR and Broadley, SA and Brown, MA and Foote, SJ and Griffiths, LR and Kilpatrick, TJ and Lechner-Scott, J and Moscato, P and Perreau, VM and Rubio, JP and Scott, RJ and Stankovich, J and Stewart, GJ and Taylor, BV and Wiley, J and Clarke, G and Cox, MB and Csurhes, PA and Danoy, P and Dickinson, JL and Drysdale, K and Field, J and Greer, JM and Guru, P and Hadler, J and Hoban, E and McMorran, BJ and Jensen, CJ and Johnson, LJ and McCallum, R and Merriman, M and Merriman, T and Polanowski, A and Pryce, K and Tajouri, L and Whittock, L and Wilkins, EJ and Browning, BL and Browning, SR and Perera, D and Butzkueven, H and Carroll, WM and Chapman, C and Kermode, AG and Marriott, M and Mason, D and Heard, RN and Pender, MP and Slee, M and Tubridy, N and Willoughby, E and Irizarry, RA, Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips, BMC Bioinformatics, 12 Article 68. ISSN 1471-2105 (2011) [Refereed Article]
Sawcer, S and Hellenthal, G and Pirinen, M and Spencer, CCA and Patsopoulos, NA and Moutsianas, L and Dilthey, A and Su, Z and Freeman, C and Hunt, SE and Edkins, S and Gray, E and Booth, DR and Potter, SC and Goris, A and Band, G and Oturai, AB and Strange, A and Saarela, J and Bellenguez, C and Fontaine, B and Gillman, M and Hemmer, B and Gwilliam, R and Zipp, F and Jayakumar, A and Martin, R and Leslie, S and Hawkins, S and Giannoulatou, E and D'alfonso, S and Blackburn, H and Boneschi, FM and Liddle, J and Harbo, HF and Perez, ML and Spurkland, A and Waller, MJ and Mycko, MP and Ricketts, M and Comabella, M and Hammond, N and Kockum, I and McCann, OT and Ban, M and Whittaker, P and Kemppinen, A and Weston, P and Hawkins, C and Widaa, S and Zajicek, J and Dronov, S and Robertson, N and Bumpstead, SJ and Barcellos, LF and Ravindrarajah, R and Abraham, R and Alfredsson, L and Ardlie, K and Aubin, C and Baker, A and Baker, K and Baranzini, SE and Bergamaschi, L and Bergamaschi, R and Bernstein, A and Berthele, A and Boggild, M and Bradfield, JP and Brassat, D and Broadley, SA and Buck, D and Butzkueven, H and Capra, R and Carroll, WM and Cavalla, P and Celius, EG and Cepok, S and Chiavacci, R and Clerget-Darpoux, F and Clysters, K and Comi, G and Cossburn, M and Cournu-Rebeix, I and Cox, MB and Cozen, W and Cree, BAC and Cross, AH and Cusi, D and Daly, MJ and Davis, E and de Bakker, PIW and Debouverie, M and D'hooghe, MB and Dixon, K and Dobosi, R and Dubois, B and Ellinghaus, D and Elovaara, I and Esposito, F and Fontenille, C and Foote, SJ and Franke, A and Galimberti, D and Ghezzi, A and Glessner, J and Gomez, R and Gout, O and Graham, C and Grant, SFA and Guerini, FR and Hakonarson, H and Hall, P and Hamsten, A and Hartung, HP and Heard, RN and Heath, S and Hobart, J and Hoshi, M and Infante-Duarte, C and Ingram, G and Ingram, W and Islam, T and Jagodic, M and Kabesch, M and Kermode, AG and Kilpatrick, TJ and Kim, C and Klopp, N and Koivisto, K and Larsson, M and Lathrop, M and Lechner-Scott, JS and Leone, MA and Leppa, V and Liljedahl, U and Bomfim, IL and Lincoln, RR and Link, J and Liu, JJ and Lorentzen, AR and Lupoli, S and Macciardi, F and Mack, T and Marriott, M and Martinelli, V and Mason, D and McCauley, JL and Mentch, F and Mero, IL and Mihalova, T and Montalban, X and Mottershead, J and Myhr, KM and Naldi, P and Ollier, W and Page, A and Palotie, A and Pelletier, J and Piccio, L and Pickersgill, T and Piehl, F and Pobywajlo, S and Quach, HL and Ramsay, PP and Reunanen, M and Reynolds, R and Rioux, J and Rodegher, M and Roesner, S and Rubio, JP and Ruckert, IM and Salvetti, M and Salvi, E and Santaniello, A and Schaefer, CA and Schreiber, S and Schulze, C and Scott, RJ and Sellebjerg, F and Selmaj, KW and Sexton, D and Shen, L and Simms-Acuna, B and Skidmore, S and Sleiman, PMA and Smestad, C and Sorensen, PS and Sondergaard, HB and Stankovich, J and Strange, RC and Sulonen, AM and Sundqvist, E and Syvanen, AC and Taddeo, F and Taylor, B and Blackwell, JM and Tienari, P and Bramon, E and Tourbah, A and Brown, MA and Tronczynska, E and Casas, JP and Tubridy, N and Corvin, A and Vickery, J and Jankowski, J and Villoslada, P and Markus, HS and Wang, K and Mathew, CG and Wason, J and Palmer, CNA and Wichmann, HE and Plomin, R and Willoughby, E and Rautanen, A and Winkelmann, J and Wittig, M and Trembath, RC and Yaouanq, J and Viswanathan, AC and Zhang, HT and Wood, NW and Zuvich, R and Deloukas, P and Langford, C and Duncanson, A and Oksenberg, JR and Pericak-Vance, MA and Haines, JL and Olsson, T and Hillert, J and Ivinson, AJ and De Jager, PL and Peltonen, L and Stewart, GJ and Hafler, DA and Hauser, SL and McVean, G and Donnelly, P and Compston, A and The International Multiple Sclerosis Genetics Consortium & the Wellcome Trust Case Control Consortium , Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis, Nature, 476, (7359) pp. 214-219. ISSN 0028-0836 (2011) [Refereed Article]
Patsopoulos, NA and de Bakker, PI and Esposito, F and Reischl, J and Lehr, S and Bauer, D and Heubach, J and Sandbrink, R and Pohl, C and Edan, G and Kappos, L and Miller, D and Montalban, J and Polman, CH and Freedman, MS and Hartung, HP and Arnason, BG and Comi, G and Cook, S and Filippi, M and Goodin, DS and Jeffery, D and O'Connor, P and Ebers, GC and Langdon, D and Reder, AT and Traboulsee, A and Zipp, F and Schimrigk, S and Hillert, 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 Chapman, C and Foote, SJ and Griffiths, L and Kermode, AG and Kilpatrick, TJ and Lechner-Scott, J and Marriott, M and Mason, D and Moscato, P and Heard, RN and Pender, MP and Perreau, VM and Perera, D and Rubio, JP and Scott, RJ and Slee, M and Stankovich, J and Stewart, GJ and Taylor, BV and Tubridy, N and Willoughby, E and Wiley, J and Matthews, P and Boneschi, FM and Compston, A and Haines, J and Hauser, SL and McCauley, J and Ivinson, A and Oksenberg, JR and Pericak-Vance, M and Sawcer, SJ and De Jager, PL and Hafler, DA, Baya Pharma MS Genetics Working Group, Steering Committees of Studies Evaluating IFNB-1b and a CCR1-Antagonist; ANZgene Consortium; GeneMSA; International Multiple Sclerosis Genetics Consortium, Genome-Wide Meta-Analysis Identifies Novel Multiple Sclerosis Susceptibility Loci, Annals of Neurology, 70, (6) pp. 897-912. ISSN 0364-5134 (2011) [Refereed Article]
Van der Walt, A and Stankovich, J and Bahlo, M and Taylor, BV and Van der Mei, IAF and Foote, SJ and Rubio, JP and Kilpatrick, TJ and Butzkueven, H, Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition , Multiple Sclerosis, 17, (3) pp. 344-352. ISSN 1352-4585 (2011) [Refereed Article]
Wang, JH and Pappas, D and De Jager, P and Pelletier, D and de Bakker, PIW and Kappos, L and Polman, CH and Bahlo, M and Booth, DR and Broadley, SA and Brown, MA and Foote, SJ and Griffiths, LR and Kilpatrick, TJ and Lechner-Scott, J and Moscato, P and Perreau, VM and Rubio, JP and Scott, RJ and Stankovich, J and Stewart, GJ and Taylor, BV and Wiley, J and Danoy, P and Butzkueven, H and Slee, M and Greer, J and Kermode, A and Carroll, W and Chibnik, LB and Hafler, DA and Matthews, PM and Hauser, SL and Baranzini, SE and Oksenberg, JR, Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data, Genome Medicine, 3 Article 3. ISSN 1756-994X (2011) [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]
Field, J and Browning, SR and Johnson, LJ and Danoy, P and Varney, MD and Tait, BD and Gandhi, KS and Charlesworth, JC and Heard, RN and Broadley, SA and Browning, BL and Carroll, WM and Griffiths, LR and Kermode, AG and Lechner-Scott, J and Moscato, P and Perreau, VM and Scott, RJ and Slee, M and Stewart, GJ and Kilpatrick, TJ and Foote, SJ and Bahlo, M and Butzkueven, H and Wiley, J and Booth, DR and Taylor, BV and Brown, MA and Rubio, JP and Stankovich, J, A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis, PLoS ONE, 5, (10) EJ ISSN 1932-6203 (2010) [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]
Xiao, H and Xu, J and Zhou, X and Stankovich, J and Pan, F and Zhang, Z and Xu, S and Lian, L and Ding, C, Associations between the genetic polymorphisms of MTHFR and outcomes of methotrexate treatment in rheumatoid arthritis, Clinical and Experimental Rheumatology, 28, (5) pp. 728-733. ISSN 0392-856X (2010) [Refereed Article]
Jensen, CJ and Stankovich, J and Butzkueven, H and Oldfield, BJ and Rubio, JP, Common variation in the MOG gene influences transcript splicing in humans, Journal of Neuroimmunology, 229, (1-2) pp. 225-231. ISSN 0165-5728 (2010) [Refereed Article]
Tegg, EM and Thomson, RJ and Stankovich, J and Banks, A and Flowers, C and McWhirter, R and Panton, J and Piaszczyk, A and Bahlo, M and Marsden, KA and Lowenthal, RM and Foote, SJ and Dickinson, JL, Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes , British Journal of Haematology, 150, (4) pp. 456-462. ISSN 0007-1048 (2010) [Refereed Article]
Phasukkijwatana, N and Kunhapan, B and Stankovich, J and Chuenkongkaew, WL and Thomson, R and Thornton, T and Bahlo, M and Mushiroda, T and Nakamura, Y and Mahasirimongkol, S and Tun, AW and Srisawat, C and Limwongse, C and Peerapittayamongkol, C and Sura, T and Suthammarak, W and Lertrit, P, Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand , Human Genetics, 128, (1) pp. 39-49. ISSN 0340-6717 (2010) [Refereed Article]
van der Mei, IAF and Ponsonby, AL and Taylor, BV and Stankovich, J and Dickinson, JL and Foote, S and Kemp, A and Dwyer, T, Human Leukocyte Antigen-DR15, Low Infant Sibling Exposure and Multiple Sclerosis: Gene-Environment Interaction, Annals of Neurology, 67, (2) pp. 261-265. ISSN 0364-5134 (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]
Jensen, CJ and Stankovich, J and Van der Walt, A and Bahlo, M and Taylor, BV and van der Mei, IAF and Foote, SJ and Kilpatrick, TJ and Johnson, LJ and Wilkins, E and Field, J and Danoy, P and Brown, MA and Booth, DR and Broadley, SA and Browning, BL and Browning, SR and Carroll, WM and Griffiths, LR 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 Wiley, J and Rubio, JP and Butzkueven, H, Multiple Sclerosis Susceptibility-Associated SNPs Do Not Influence Disease Severity Measures in a Cohort of Australian MS Patients, P L o S One, 5, (4) EJ ISSN 1932-6203 (2010) [Refereed Article]
Bahlo, M and Stankovich, J and Danoy, P and Hickey, PF and Taylor, BV and Browning, SR and Booth, DR and Broadley, SA and Foote, SJ and Griffiths, LR and Kilpatrick, TJ and Lechner-Scott, J and Moscato, P and Perreau, VM and Scott, RJ and Stewart, GJ and Wiley, J and Clarke, G and Cox, MB and Csurhes, PA and Dickinson, JL and Drysdale, K and Field, J and Greer, JM and Guru, P and Hadler, J and Hoban, E and McMorran, BJ and Jensen, CJ and Johnson, LJ and McCallum, R and Merriman, M and Merriman, T and Polanowski, A and Pryce, K and Tajouri, L and Whittock, L and Wilkins, EJ and Browning, BL and Perera, D and Butzkueven, H and Carroll, WM and Chapman, C and Kermode, AG and Marriott, M and Mason, D and Heard, RN and Pender, MP and Slee, M and Tubridy, N and Willoughby, E and Brown, MA and Rubio, JP, Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies, Cancer Epidemiology, Biomarkers and Prevention, 19, (3) pp. 794-798. ISSN 1055-9965 (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]
D'Souza, WJ and Stankovich, J and O'Brien, TJ and Bower, S and Pearce, N and Cook, MJ, The use of computer-assisted-telephone-interviewing to diagnose seizures, epilepsy and Idiopathic Generalized Epilepsy, Epilepsy Research, 91, (1) pp. 20-27. ISSN 0920-1211 (2010) [Refereed Article]
van der Walt, A and Stankovich, J and Bahlo, M and Taylor, BV and van der Mei, IAF and Foote, SJ and Kilpatrick, TJ and Rubio, JP and Butzkueven, H, Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy, Neurology, 73, (13) pp. 1018-1025. ISSN 0028-3878 (2009) [Refereed Article] 
Perera, DI and Stankovich, J and Butzkueven, H and Taylor, BVM and Foote, SJ and Kilpatrick, TJ and Rubio, JP, Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus, Journal of Neuroimmunology, 211, (25) pp. 105-109. ISSN 0165-5728 (2009) [Refereed Article] 
Bahlo, M and Booth, DR and Broadley, SA and Brown, MA and Foote, SJ and Griffiths, LR and Kilpatrick, TJ and Lechner-Scott, J and Moscato, P and Perreau, VM and Rubio, JP and Scott, RJ and Stankovich, J and Stewart, GJ and Taylor, BVM and Wiley, J and Clarke, G and Cox, MB and Csurhes, PA and Danoy, P and Drysdale, KE and Field, J and Greer, JM and Mayura Guru, P and Hadler, J and McMorran, BJ and Jensen, CJ and Johnson, LJ and McCallum, R and Merriman, M and Merriman, T and Pryce, K and Tajouri, L and Wilkins, EJ and Browning, BL and Browning, SR and Perera, DI and Butzkueven, H and Carroll, WM and Chapman, C and Kermode, AG and Marriott, M and Mason, D and Heard, RN and Pender, MP and Slee, M and Tubridy, N and Willoughby, E, Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20, Nature Genetics, 41, (7) pp. 824-830. ISSN 1061-4036 (2009) [Refereed Article] 
Stankovich, J and Butzkueven, H and Marriott, M and Chapman, C and Tubridy, N and Tait, BD and Varney, MD and Taylor, BV and Foote, SJ and Booth, DR and Broadley, S and Greer, JM and Griffiths, LR and Heard, RN and Lechner-Scott, J and Pender, MJ and Scott, RJ and Stewart, GJ and Kilpatrick, TJ and Rubio, JP, HLA-DRB1 associations with disease susceptibility and clinical course in Australians with multiple sclerosis, Tissue Antigens, 74, (1) pp. 17-21. ISSN 0001-2815 (2009) [Refereed Article] 
Fitzgerald, LM and Patterson, B and Thomson, RJ and Polanowski, AM and Quinn, SJ and Brohede, J and Thornton, T and Challis, D and Mackey, DA and Dwyer, T and Foote, SJ and Hannan, GN and Stankovich, J and McKay, JD and Dickinson, JL, Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease, European Journal of Human Genetics, 17 pp. 368-377. ISSN 1018-4813 (2009) [Refereed Article] 
Dickinson, JL and Perera, DI and van der Mei, AF and Ponsonby, AL and Polanowski, AM and Thomson, RJ and Taylor, BV and McKay, JD and Stankovich, J and Dwyer, T, Past environmental sun exposure and risk of multiple sclerosis: a role for the Cdx-2 Vitamin D receptor variant in this interaction , Multiple Sclerosis, 15, (5) pp. 563-570. ISSN 1352-4585 (2009) [Refereed Article] 
Berkovic, SF and Dibbens, LM and Oshlack, A and Silver, JD and Katerelos, M and Vears, DF and Lullmann-Rauch, R and Blanz, J and Zhang, KW and Stankovich, J and Kalnins, RM and Dowling, JP and Andermann, E and Andermann, F and Faldini, E and D'Hooge, R and Vadlamudi, L and Macdonell, RA and Hodgson, BL and Bayly, MA and Savige, J and Mulley, JC and Smyth, GK and Power, DA and Saftig, P and Bahlo, M, Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis, American Journal of Human Genetics, 82, (3) pp. 673-684. ISSN 0002-9297 (2008) [Refereed Article] 
Wray, BN and Stankovich, J and Whittock, LD and Dwyer, T and Ponsonby, AL and Van der Mei, IAF and Taylor, BVM and Dickinson, JL and Foote, SJ and McMorran, BJ, CTLA-4 and multiple sclerosis: The A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population, Journal of Neuroimmunology, 196, (1-2) pp. 139-142. ISSN 0165-5728 (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] 
Dwyer, T and Van der Mei, IAF and Ponsonby, AL and Taylor, BVM and Stankovich, J and McKay, JD and Thomson, Russell and Polanowski, AM and Dickinson, JL, Melanocortin 1 receptor genotype, past environmental sun exposure, and risk of multiple sclerosis, Neurology, 71, (8) pp. 583-589. ISSN 0028-3878 (2008) [Refereed Article] 
Albers, CA and Stankovich, J and Thomson, Russell 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] 
Fitzgerald, LM and Thomson, RJ and Polanowski, AM and Patterson, B and McKay, JD and Stankovich, J and Dickinson, JL, Sequence variants of α-methylacyl-CoA racemase are associated with prostate cancer risk: A replication study in an ethnically homogeneous population, The Prostate, 68, (13) pp. 1373-1379. ISSN 0270-4137 (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 (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] 
Rubio, JP and Bahlo, M and Stankovich, J and Burfoot, RK and Johnson, LJ and Huxtable, S and Butzkueven, H and Lin, L and Taylor, BVM and Speed, TP and Kilpatrick, TJ and Mignot, E and Foote, SJ, Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class 1 region in Tasmanian MS patients, Immunogenetics, 59, (3) pp. 177-186. ISSN 0093-7711 (2007) [Refereed Article] 
Xu, J and Wang, Y and Pan, F and Stankovich, J and Ye, D and Lian, L and Zhang, K and Ding, C, Association of ACE Gene Polymorphism with Genetic Susceptibility to Systemic Lupus Erythematosus in a Chinese Population: A Family-based Association Study, The Journal of Rheumatology, 34, (12) pp. 2408-2411. ISSN 0315-162X (2007) [Refereed Article] 
Chen, C and Scurrah, KJ and Stankovich, J and Garoufalis, P and Dirani, M and Pertile, KK and Richardson, AJ and Mitchell, P and Baird, PN, Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study, Human Genetics, 121, (3-4) pp. 511-520. ISSN 0340-6717 (2007) [Refereed Article] 
Chen, CY and Stankovich, J and Scurrah, KJ and Garoufalis, P and Dirani, M and Pertile, KK and Richardson, AJ and Baird, PN, Linkage Replication of the MYP12 Locus in Common Myopia, Investigative Ophthalmology and Vision Science, 48, (10) pp. 4433-4439. ISSN 0146-0404 (2007) [Refereed Article] 
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] 
Fourlanos, S and Perry, C and Stein, MS and Stankovich, J and Harrison, LC and Colman, PG, A Clinical Screening Tool Identifies Autoimmune Diabetes in Adults, Diabetes Care, 29, (5) pp. 970-975. ISSN 0149-5992 (2006) [Refereed Article] 
Charlesworth, JC and Stankovich, J and Mackey, DA and Craig, JE and Haybittel, M and Westmore, RN and Sale, MM, Confirmation of the Adult-Onset Primary Open Angle Glaucoma Locus GLC1B at 2cen-q13 in an Australian Family, Ophthalmologica, 220, (1) pp. 23-30. ISSN 0030-3755 (2006) [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] 
Zhai, G and Stankovich, J and Cicuttini, F and Ding, C and Jones, G, Familial, structural, and environmental correlates of MRI-defined bone marrow lesions: a sibpair study, Arthritis Research & Therapy, 8, (4) pp. R137. ISSN 1478-6362 (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] 
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, (2-3) pp. 188-199. ISSN 0340-6717 (2005) [Refereed Article] 
Charlesworth, JC and Dyer, TD and Stankovich, J and Blangero, J and Mackey, DA and Craig, JE and Green, CM and Foote, SJ and Baird, PN and Sale, MM, Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree, Investigative Ophthalmology & Visual Science, 46, (10) pp. 3723-3729. ISSN 0146-0404 (2005) [Refereed Article] 
Ding, C and Cicuttini, F and Scott, F and Stankovich, J and Cooley, HM and Jones, G, The genetic contribution and relevance of knee cartilage defects: Case-control and sib-pair studies, Journal of Rheumatology, 32, (10) pp. 1937-42. ISSN 0315-162X (2005) [Refereed Article] 
Zhai, G and Ding, C and Stankovich, J and Cicuttini, F and Jones, G, The genetic contribution to longitudinal changes in knee structural and muscle strength: A Sibpair Study, Arthritis & Rheumatism, 52, (9) pp. 2830-2834. ISSN 0004-3591 (2005) [Refereed Article] 
Dwyer, T and Stankovich, J and Blizzard, CL and Fitzgerald, LM and Dickinson, JL and Reilly, A and Williamson, J and Ashbolt, R and Berwick, M and Sale, MM, Does the Addition of Information on Genotype Improve Prediction of the Risk of Melanoma and Nonmelanoma Skin Cancer beyond That Obtained from Skin Phenotype?, American Journal of Epidemiology, 159, (9) pp. 826-833. ISSN 0002-9262 (2004) [Refereed Article] 
Rubio, JP and Bahlo, M and Tubridy, N and Stankovich, J and Burfoot, R and Butzkueven, H and Chapman, C and Johnson, L and Marriott, M and Mraz, G and Tait, B and Wilkinson, C and Taylor, BV and Speed, TP and Foote, SJ and Kilpatrick, TJ, Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis, Human Genetics, 114, (6) pp. 573-580. ISSN 0340-6717 (2004) [Refereed Article] 
Dwyer, T and Ponsonby, AL and Stankovich, J and Blizzard, CL and Easteal, S, Measuring environmental factors can enhance the search for disease causing genes?, Journal of Epidemiology and Community Health, 58, (7) pp. 613-615. ISSN 0143-005X (2004) [Refereed Article] 
Zhai, G and Stankovich, J and Ding, C and Scott, F and Cicuttini, F and Jones, G, The Genetic Contribution to Muscle Strength, Knee Pain, Cartilage Volume, Bone Size, and Radiographic Osteoarthritis, Arthritis and Rheumatism, 50, (3) pp. 805-810. ISSN 0004-3591 (2004) [Refereed Article] 
Sale, MM and Hazelwood, KF and Zimmett, PZ and Shaw, JE and Stankovich, J and Greenaway, TM and Dwyer, T, Trends in diabetes management practices of patients from an Australian insulin-treated diabetes register, Diabetic Medicine, 21, (2) pp. 165-170. ISSN 0742-3071 (2004) [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] 
Petris, S and Stankovich, J and Chan, DYC and Ottewill, RHH, Modeling the structure of charged binary colloidal dispersions, Langmuir, 19, (4) pp. 1121-1126. ISSN 0743-7463 (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] 
Cooley, HM and Stankovich, J and Jones, G, The association between hormonal and reproductive factors and hand osteoarthritis, Maturitas, 45, (4) pp. 257-265. ISSN 0378-5122 (2003) [Refereed Article] 
Wilkinson, C and van der Straaten, D and Craig, JE and Coote, M and McCartney, PJ and Stankovich, J and Stone, E and Mackey, DA, Tonography demonstrates reduced facility of outflow of aqueous humour in myocilin mutation carriers, Journal of Glaucoma, 12, (3) pp. 237-242. ISSN 1057-0829 (2003) [Refereed Article] 
Jones, G and Cooley, HM and Stankovich, J, A Cross Sectional Study of the Association Between Sex, Smoking, and other Lifestyle Factors and Osteoarthritis of the Hand, Journal of Rheumatology, 29, (8) pp. 1719-1724. ISSN 0315-162X (2002) [Refereed Article] 
Dwyer, T and Blizzard, CL and Ashbolt, R and Plumb, J and Berwick, M and Stankovich, J, Cutaneous Melanin Density of Caucasians Measured by Spectrophotometry and Risk of Malignant Melanoma, Basal Cell Carcinoma, and Squamous Cell Carcinoma of the Skin, American Journal of Epidemiology, 155, (7) pp. 614-621. ISSN 0002-9262 (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] 
Van der Mei, IAF and Blizzard, CL and Stankovich, J and Ponsonby, AL and Dwyer, T, Misclassification due to body hair and seasonal variation on melanin density estimates for skin type using spectrophotometry, Journal of Photochemistry and Photobiology, B: Biology, 68, (1) pp. 45-52. ISSN 1011-1344 (2002) [Refereed Article] 
Dwyer, T and Blizzard, CL and Venn, A and Stankovich, J and Ponsonby, AL and Morley, R, Syndrome X in 8-y-old Australian children: stronger associations with current body fatness than with infant size or growth, International Journal of Obesity, 26, (10) pp. 1301-1309. ISSN 0307-0565 (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] 
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] 
Review
Van der Mei, IAF and Simpson Jr, S and Stankovich, J and Taylor, BV, Individual and Joint Action of Environmental Factors and Risk of MS, Neurologic Clinics , 29, (2) pp. 233-255. (2011) [Substantial Review] 
Simpson Jr, S and Greenhill, K and Van der Mei, I and Stankovich, J and Charlesworth, J and Taylor, BVM, The Varied Mechanisms of Vitamin D in the Onset and Clinical Course of MS: Potential Roles in Modulating Other Etiological Pathways, Current Medical Literature. Neurology, 27, (1) pp. 1-14. (2011) [Substantial Review] 
Dwyer, T and Sale, MM and Stankovich, J and Hazelwood, KF and Mulcahy, N, Using genetic advances to investigate diabetes in Australia, Diabetes, Technology and Therapeutics, 3 pp. 641-646. (2001) [Substantial Review] 
Conference Publication
Khanam, MA and Radford, JC and Castelino, RL and Jose, MD and Kitsos, AR and Stankovich, J and Zaidi, ST and Kinsman, LD and Peterson, GM, Chronic kidney disease (CKD) monitoring in Australian General Practice, 53rd Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), 4-6 September 2017, Darwin, Australia (2017) [Conference Extract]
Radford, J and Castelino, RL and Jose, MD and Kitsos, A and Khanam, M and Stankovich, J and Zaidi, ST and Peterson, GM, Chronic kidney disease in Australian general practice: its prevalence, and associated patient characteristics and comorbidities, 2017 Annual Scientific meeting Australian and New Zealand Society of Nephrology, 4-6 September 2017, Darwin, Australia (2017) [Conference Extract]
Khanam, MA and Radford, JC and Castelino, RL and Jose, MD and Kitsos, AR and Stankovich, J and Zaidi, ST and Kinsman, LD and Peterson, GM, Lipid-lowering therapy among CKD patients in Australian general practice, 53rd Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology (ANZSN), 4-6 September 2017, Darwin, Australia (2017) [Conference Extract]
Morley, C and Stankovich, J and Peterson, GM and Kinsman, LD, Four year trends in emergency department presentations in Tasmania, Emergency Tasmanian Conference 2016, 12-14 August 2016, Prospect Vale, Tasmania (2016) [Conference Extract] 
Hancock, N and Stankovich, J and Robertson, J and Kornaczewski, E and Hughes, S and O'Brien, L and Peterson, GM, An Assessment and Planning Unit reduces length of stay in hospital for General Medical patients (2015) [Conference Extract] 
Griffin, P and Stankovich, J and Leonard, K and Nicholson, H and Kinsman, LD and Butler-Henderson, K and Peterson, GM and Cooke, D and McDonald, A, Prolonged ED access block impacts on patient outcomes in a large regional hospital, 9th Health Services and Policy Research Conference, Melbourne, 2015, 7-9 December, 2015, Melbourne, Australia (2015) [Conference Extract]
Lester, S and Patterson, K and Walker, J and Charlesworth, JC and Stankovich, J and Stevens, W and Sahhar, J and Nash, P and Roddy, J and Hill, C and Nikpour, M and Rischmueller, M and Proudman, S and Brown, M and Zochling, J, Associations between HLA DRB1 Alleles and Autoantibodies in Systemic Sclerosis, Internal Medicine Journal, Vol 44, pp. 2-2. ISSN 1444-0903 (2014) [Conference Extract] 
Charlesworth, J and Stankovich, J and Lewis, P and Byron, J and Stevens, W and Sahhar, J and Roddy, J and Nash, P and Tymms, K and Rischmueller, M and Lester, S and Brown, M and Proudman, S and Zochling, J, An Immunochip Based Interrogation of Scleroderma Susceptibility Variants, Internal Medicine Journal, Vol 42, pp. 2-2. ISSN 1444-0903 (2012) [Conference Extract] 
Charlesworth, J and Stankovich, J and Lewis, P and Byron, J and Stevens, W and Sahhar, J and Proudman, S and Roddy, J and Nash, P and Tymms, K and Brown, M and Zochling, J, An Immunochip-Based Interrogation of Scleroderma Susceptibility Variants, Rheumatology, Vol 51, pp. 15-16. ISSN 1462-0324 (2012) [Conference Extract] 
Lin, R and Perreau, V and Glazov, E and McMorran, B and Bahlo, M and Brown, M and Foote, S and Rubio, J and Charlesworth, J and Thomson, R and Browning, S and Martin, N and Taylor, B and Stankovich, J, Searching for rare variants conferring susceptibility to multiple sclerosis, Multiple Sclerosis Journal; Progress in MS Research Conference, 2011, Melbourne, Australia, pp. 701-702; Vol 18. (2012) [Conference Extract] 
Dickinson, J and Stankovich, J and Thomson, R and Tegg, E and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S, Identification of Susceptibility Genes for Haematological Maligancies, GeneMappers, April, Hobart, Australia (2011) [Conference Extract] 
Charlesworth, JC and Glahn, DC and Curran, JE and Kochunov, P and Stankovich, J and Winkler, A and Carless, M and Johnson, MP and Goering, HHH and Dyer, TD and Moses, EK and Almasy, L and Fox, PT and Olvera, R and Duggirala, R and Taylor, BVM and Blangero, J, Using normal variation in neuroanatomic traits to identify genes and pathways influencing disease: a joint linkage and association analysis of brain lesions, Proceedings of the 8th GeneMappers Conference, 4-6 April 2011, Hotel Grand Chancellor, Hobart, Australia, pp. 56. (2011) [Conference Extract]
Tegg, E and Stankovich, J and Thomson, R and Perera, D and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, JL, Whole genome sequencing of CLL case, GeneMappers, April, Hobart, Australia (2011) [Keynote Presentation] 
Patterson, B and Short, A and Polanowski, AM and Marthick, JR and Thomson, R and Stankovich, J and Dickinson, JL, A role for integrin alpha 2 in familial prostate cancer susceptibility, kConFab: Familial Aspects of Cancer: Research and Practice, August, Kingscliff, Queensland (2010) [Conference Extract] 
Tegg, E and Stankovich, J and Thomson, R and Perera, D and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, J, Familial Haematological malignancies: The Tasmanian experience, Haematology Society of Australia and New Zealand, Australia and New Zealand Society for Blood Transfusion & Australasian Society for Thrombosis and Homeostasis (2010) [Keynote Presentation] 
Tegg, E and Stankovich, J and Thomson, R and Perera, D and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, J, Familial Haematological Malignancies, GeneMappers (2009) [Conference Extract] 
van der Walt, A and Stankovich, J and Bahlo, M and Taylor, BVM and Van der Mei, IAF and Foote, SJ and Kilpatrick, T and Rubio, J and Butzkueven, H, The HLA-DR2 genotype does not affect MS severity, cognition or brain atrophy, Sage Publications Ltd, 9-12 September, Dusseldorf, Germany, pp. Vol 15 (9) p.183. (2009) [Conference Edited] 
Van der Mei, IAF and Ponsonby, AL and Taylor, BVM and Stankovich, J and Dickinson, JL and Foote, SJ and Kemp, A and Dwyer, T, A potentiation of the adverse effect of human leukocyte antigen-DR15 on the risk of multiple sclerosis by low infant sibling exposure: a population based case-control study, Sage Publications Ltd, 17-20 September, Montreal, Canada, pp. Vol 14 (1) S201-S202. (2008) [Conference Edited] 
van der Walt, A and Stankovich, J and Bahlo, M and Taylor, BVM and Van der Mei, IAF and Foote, SJ and Rubio, J and Kilpatrick, T and Butzkueven, H, Apolipoprotein E4 genotype does not influence multiple sclerosis phenotype, severity, cognition or brain atrophy in a large Australian cohort, Sage Publications Ltd, 17-20 September, Montreal, Canada, pp. Vol 14 (1) S204. (2008) [Conference Edited] 
Perera, D and Tegg, E and Stankovich, J and Thomson, R and Silver, J and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, J, Linkage analysis of a large Tasmanian haematological cancer family, GeneMappers (2007) [Conference Extract] 
Tegg, E and Stankovich, J and Thomson, R and Perera, D and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, J, The Tasmanian familial leukaemia and lymphoma research study, Haematology Society of Australia and New Zealand, Australia and New Zealand Society for Blood Transfusion & Australasian Society for Thrombosis and Homeostasis (2007) [Conference Extract] 
Tegg, E and Stankovich, J and Thomson, R and Perera, D and Marsden, K and Lowenthal, R and Flowers, C and Banks, A and Piaszczyk, A and Bahlo, M and Foote, S and Dickinson, J, The Tasmanian familial leukaemia and lymphoma research study, GeneMappers (2007) [Conference Extract] 
Dickinson, J and Thomson, R and Patterson, B and Polanowski, A and Stankovich, J and Fryer, J and Blizzard, L and Dwyer, T, Prostate Cancer Sun Exposure and Genes Modifying Risk, 11th International Congress of Human Genetics, 6-10th August, Brisbane, Australia (2006) [Conference Extract] 
McKay, J and Fitzgerald, L and Stankovich, J and Banks, A and Hazelwood, K and Brohede, J and Hannan, G and Dwyer, T and Dickinson, J, Linkage analysis of a second large prostate cancer family from southern Tasmania, Australia, American Society of Human Genetics Conference, October, Salt Lake City, Utah (2005) [Conference Extract] 
Foote, SJ and Rubio, JP and Bahlo, M and Kilpatrick, TJ and Speed, TP and Stankovich, J and Burfoot, R and Butzkueven, H and Johnson, L and Wilkinson, C and Taylor, BVM and Sale, MM and Van der Mei, IAF and Dickinson, JL and Groom, PS, Multiple Sclerosis: a haplotype association study, Novartis Foundation Symposium, 2005, pp. 31-39. (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 (2005) [Conference Extract] 

This list was generated on Thu Nov 23 07:21:22 2017.