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Number of items: 10.

Article

Gresle, MM, Jordan, MA, Stankovich, J, Spelman, T, Johnson, LJ, Laverick, L, Hamlett, A, Smith, LD, Jokubaitis, VG, Baker, J, Haartsen, J, Taylor, B, Charlesworth, J ORCID: 0000-0001-6201-3518, Bahlo, M, Speed, TP, Brown, MA, Field, J, Baxter, AG and Butzkueven, H 2020 , 'Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells' , Life Science Alliance, vol. 3, no. 7 , pp. 1-11 , doi: https://doi.org/10.26508/lsa.202000650.

Mitrovi, M, Patsopoulos, NA, Beecham, AH, Dankowski, T, Goris, A, Dubois, B, D'hooghe, MB, Lemmens, R, Van Damme, P, Sondergaard, HB, Sellebjerg, F, Sorensen, PS, Ullum, H, Thorner, LW, Werge, T, Saarela, J, Cournu-Rebeix, I, Damotte, V, Fontaine, B, Guillot-Noel, L, Lathrop, M, Vukusik, S, Gourraud, PA, Andlauer, TFM, Pongratz, V, Buck, D, Gasperi, C, Bayas, A, Heesen, C, Kumpfel, T, Linker, R, Paul, F, Stangel, M, Tackenberg, B, Bergh, FT, Warnke, C, Wiendl, H, Wildemann, B, Zettl, U, Ziemann, U, Tumani, H, Gold, R, Grummel, V, Hemmer, B, Knier, B, Lill, CM, Luessi, F, Dardiotis, E, Agliardi, C, Barizzone, N, Mascia, E, Bernardinelli, L, Comi, G, Cusi, D, Esposito, F, Ferre, L, Comi, C, Galimberti, D, Leone, MA, Sorosina, M, Mescheriakova, J, Hintzen, R, van Duijn, C, Theunissen, CE, Bos, SD, Myhr, K-M, Celius, EG, Lie, BA, Spurkland, A, Comabella, M, Montalban, X, Alfredsson, L, Stridh, P, Hillert, J, Jagodic, M, Piehl, F, Jelcic, I, Martin, R, Sospedra, M, Ban, M, Hawkins, C, Hysi, P, Kalra, S, Karpe, F, Khadake, J, Lachance, G, Neville, M, Santaniello, A, Caillier, SJ, Calabresi, PA, Cree, BAC, Cross, A, Davis, MF, Haines, JL, de Bakker, PIW, Delgado, S, Dembele, M, Edwards, K, Fitzgerald, KC, Hakonarson, H, Konidari, I, Lathi, E, Manrique, CP, Pericak-Vance, MA, Piccio, L, Schaefer, C, McCabe, C, Weiner, H, Goldstein, J, Olsson, T, Hadjigeorgiou, G, Taylor, B, Tajouri, L, Charlesworth, J ORCID: 0000-0001-6201-3518, Booth, DR, Harbo, HF, Ivinson, AJ, Hauser, SL, Compston, A, Stewart, G, Zipp, F, Barcellos, LF, Baranzini, SE, Martinelli-Boneschi, F, D'Alfonso, S, Ziegler, A, Oturai, A, McCauley, JL, Sawcer, SJ, Oksenberg, JR, De Jager, PL, Kockum, I, Hafler, DA and Cotsapas, C 2018 , 'Low-frequency and rare-coding variation contributes to multiple sclerosis risk' , Cell, vol. 175, no. 6 , pp. 1679-1687 , doi: https://doi.org/10.1016/j.cell.2018.09.049.

Mitrovic, M, Patsopoulos, NA, Beecham, AH, Dankowski, T, Goris, A, Dubois, B, D'hooghe, MB, Lemmens, R, Van Damme, P, Sondergaard, HB, Sellebjerg, F, Sorensen, PS, Ullum, H, Thorner, LW, Werge, T, Saarela, J, Cournu-Rebeix, I, Damotte, V, Fontaine, B, Guillot-Noel, L, Lathrop, M, Vukusik, S, Gourraud, P-A, Andlauer, TFM, Pongratz, V, Buck, D, Gasperi, C, Bayas, A, Heesen, C, Kumpfel, T, Linker, R, Paul, F, Stangel, M, Tackenberg, B, Bergh, FT, Warnke, C, Wiendl, H, Wildemann, B, Zettl, U, Ziemann, U, Tumani, H, Gold, R, Grummel, V, Hemmer, B, Knier, B, Lill, CM, Luessi, F, Dardiotis, E, Agliardi, C, Barizzone, N, Mascia, E, Bernardinelli, L, Comi, G, Cusi, D, Esposito, F, Ferre, L, Comi, C, Galimberti, D, Leone, MA, Sorosina, M, Mescheriakova, J, Hintzen, R, van Duijn, C, Theunissen, CE, Bos, SD, Myhr, K-M, Celius, EG, Lie, BA, Spurkland, A, Comabella, M, Montalban, X, Alfredsson, L, Stridh, P, Hillert, J, Jagodic, M, Piehl, F, Jelcic, I, Martin, R, Sospedra, M, Ban, M, Hawkins, C, Hysi, P, Kalra, S, Karpe, F, Khadake, J, Lachance, G, Neville, M, Santaniello, A, Caillier, SJ, Calabresi, PA, Cree, BAC, Cross, A, Davis, MF, Haines, JL, de Bakker, PIW, Delgado, S, Dembele, M, Edwards, K, Fitzgerald, KC, Hakonarson, H, Konidari, I, Lathi, E, Manrique, CP, Pericak-Vance, MA, Piccio, L, Schaefer, C, McCabe, C, Weiner, H, Goldstein, J, Olsson, T, Hadjigeorgiou, G, Taylor, B, Tajouri, L, Charlesworth, J ORCID: 0000-0001-6201-3518, Booth, DR, Harbo, HF, Ivinson, AJ, Hauser, SL, Compston, A, Stewart, G, Zipp, F, Barcellos, LF, Baranzini, SE, Martinelli-Boneschi, F, D'Alfonso, S, Ziegler, A, Oturai, A, McCauley, JL, Sawcer, SJ, Oksenberg, JR, De Jager, PL, Kockum, I, Hafler, DA and Cotsapas, C 2018 , 'Low-frequency and rare-coding variation contributes to multiple sclerosis risk' , Cell, vol. 175, no. 6 , pp. 1679-1687 , doi: https://doi.org/10.1016/j.cell.2018.09.049.

Nicol, D ORCID: 0000-0002-6553-2839, Eckstein, L ORCID: 0000-0002-7161-7521, Morrison, M, Sherkow, JS, Otlowski, M ORCID: 0000-0003-4707-4325, Whitton, T, Bubela, T, Burdon, KP ORCID: 0000-0001-8217-1249, Chalmers, D ORCID: 0000-0002-7925-8818, Chan, S, Charlesworth, J ORCID: 0000-0001-6201-3518, Critchley, C, Crossley, M, de Lacey, S, Dickinson, JL ORCID: 0000-0003-4621-1703, Hewitt, AW ORCID: 0000-0002-5123-5999, Kamens, J, Kato, K, Kleiderman, E, Kodama, S, Liddicoat, J, Mackey, DA, Newson, AJ, Nielsen, J ORCID: 0000-0002-3005-0047, Wagner, JK and McWhirter, RE ORCID: 0000-0002-9409-8074 2017 , 'Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic' , Genome Medicine, vol. 9, no. 1 , pp. 1-4 , doi: https://doi.org/10.1186/s13073-017-0475-4.

Peralta, JM, Blackburn, NB, Porto, A, Blangero, J and Charlesworth, J ORCID: 0000-0001-6201-3518 2018 , 'Genome-wide linkage scan for loci influencing plasma triglyceride levels' , BMC Proceedings, vol. 12, no. Suppl , pp. 1-6 , doi: https://doi.org/10.1186/s12919-018-0137-6.

Pitman, KA ORCID: 0000-0003-3198-9336, Ricci, R, Gasperini, R, Beasley, S ORCID: 0000-0002-8706-5725, Pavez, M, Charlesworth, J ORCID: 0000-0001-6201-3518, Foa, L ORCID: 0000-0003-4131-8341 and Young, KM ORCID: 0000-0002-1686-3463 2019 , 'The voltage-gated calcium channel CaV1.2 promotes adult oligodendrocyte progenitor cell survival in the mouse corpus callosum but not motor cortex' , Glia , pp. 1-17 , doi: https://doi.org/10.1002/glia.23723.

Zhang, Y ORCID: 0000-0003-2969-1960, Zhou, Y ORCID: 0000-0003-1962-2574, van der Mei, IAF ORCID: 0000-0001-9009-7472, Simpson, S ORCID: 0000-0001-6521-3056, Ponsonby, A-L, Lucas, RM, Tettey, P ORCID: 0000-0001-7461-2382, Charlesworth, J ORCID: 0000-0001-6201-3518, Kostner, K and Taylor, BV 2019 , 'Lipid-related genetic polymorphisms significantly modulate the association between lipids and disability progression in multiple sclerosis' , Journal of Neurology, Neurosurgery and Psychiatry , pp. 1-6 , doi: https://doi.org/10.1136/jnnp-2018-319870.

Zhang, Yan ORCID: 0000-0001-9126-4922, Zhou, Y ORCID: 0000-0003-1962-2574, van der Mei, IAF ORCID: 0000-0001-9009-7472, Simpson Jr, S ORCID: 0000-0001-6521-3056, Ponsonby, AL, Lucas, RM, Tettey, P ORCID: 0000-0001-7461-2382, Charlesworth, J ORCID: 0000-0001-6201-3518, Kostner, K and Taylor, BV 2019 , 'Lipid-related genetic polymorphisms significantly modulate the association between lipids and disability progression in multiple sclerosis' , Journal of Neurology, Neurosurgery and Psychiatry , pp. 1-6 , doi: https://doi.org/10.1136/jnnp-2018-319870.

Zhou, Y ORCID: 0000-0003-1962-2574, Cuellar-Partida, G, Simpson Yap, S ORCID: 0000-0001-6521-3056, Lin, X, Claflin, S ORCID: 0000-0001-6545-946X, Burdon, K ORCID: 0000-0001-8217-1249, Charlesworth, J ORCID: 0000-0001-6201-3518 and Taylor, B 2021 , 'Utilising multi-large omics data to elucidate biological mechanisms within multiple sclerosis genetic susceptibility loci' , Multiple Sclerosis Journal , doi: https://doi.org/10.1177/13524585211004422.

Conference or Workshop Item

Werkman, H ORCID: 0000-0001-5603-5024, Magierowski, R ORCID: 0000-0002-7547-8549 and Charlesworth, J ORCID: 0000-0001-6201-3518 2021 , 'An Overview of the Research Data Portal: The University of Tasmania’s first institution-wide digital data repository', paper presented at the eResearch Australasia 2021 Conference, 11-15 October 2021, Virtual Conference, Online (Brisbane, Australia).

This list was generated on Thu Jun 1 02:17:53 2023 AEST.
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