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Items where Author is "Hillert, J"
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Article
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.
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.
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.
Peeters, LM, Parciak, T, Walton, C, Geys, L, Moreau, Y, De Brouwer, E, Raimondi, D, Pirmani, A, Kalincik, T, Edan, G, Simpson-Yap, S ORCID: 0000-0001-6521-3056, De Raedt, L, Dauxais, Y, Gautrais, C, Rodrigues, PR, McKenna, L, Lazovski, N, Hillert, J, Forsberg, L, Spelman, T, McBurney, R, Schmidt, H, Bergmann, A, Braune, S, Stahmann, A, Middleton, R, Salter, A, Bebo, BF, Rojas, JI, van der Walt, A, Butzkueven, H, van der Mei, I ORCID: 0000-0001-9009-7472, Ivanov, R, Hellwig, K, Sciascia do Olival, G, Cohen, JA, Van Hecke, W, Dobson, R, Magyari, M, Brum, DG, Alonso, R, Nicholas, R, Bauer, J, Chertcoff, A, de Seze, J, Louapre, C, Comi, G and Rijke, N 2020
, 'COVID-19 in people with multiple sclerosis: a global data sharing initiative'
, Multiple Sclerosis Journal
, pp. 1-6
, doi: https://doi.org/10.1177/1352458520941485.
ORCID: 0000-0001-6521-3056, De Raedt, L, Dauxais, Y, Gautrais, C, Rodrigues, PR, McKenna, L, Lazovski, N, Hillert, J, Forsberg, L, Spelman, T, McBurney, R, Schmidt, H, Bergmann, A, Braune, S, Stahmann, A, Middleton, R, Salter, A, Bebo, BF, Rojas, JI, van der Walt, A, Butzkueven, H, van der Mei, I ORCID: 0000-0001-9009-7472, Ivanov, R, Hellwig, K, Sciascia do Olival, G, Cohen, JA, Van Hecke, W, Dobson, R, Magyari, M, Brum, DG, Alonso, R, Nicholas, R, Bauer, J, Chertcoff, A, de Seze, J, Louapre, C, Comi, G and Rijke, N 2020
, 'COVID-19 in people with multiple sclerosis: a global data sharing initiative'
, Multiple Sclerosis Journal
, pp. 1-6
, doi: https://doi.org/10.1177/1352458520941485.
Peeters, LM, Parciak, T, Walton, C, Geys, L, Moreau, Y, De Brouwer, E, Raimondi, D, Pirmani, A, Kalincik, T, Edan, G, Simpson-Yap, S ORCID: 0000-0001-6521-3056, De Raedt, L, Dauxais, Y, Gautrais, C, Rodrigues, PR, McKenna, L, Lazovski, N, Hillert, J, Forsberg, L, Spelman, T, McBurney, R, Schmidt, H, Bergmann, A, Braune, S, Stahmann, A, Middleton, R, Salter, A, Bebo, BF, Rojas, JI, van der Walt, A, Butzkueven, H, van der Mei, I ORCID: 0000-0001-9009-7472, Ivanov, R, Hellwig, K, Sciascia do Olival, G, Cohen, JA, Van Hecke, W, Dobson, R, Magyari, M, Brum, DG, Alonso, R, Nicholas, R, Bauer, J, Chertcoff, A, de Seze, J, Louapre, C, Comi, G and Rijke, N 2020
, 'COVID-19 in people with multiple sclerosis: a global data sharing initiative'
, Multiple Sclerosis Journal
, pp. 1-6
, doi: https://doi.org/10.1177/1352458520941485.
ORCID: 0000-0001-6521-3056, De Raedt, L, Dauxais, Y, Gautrais, C, Rodrigues, PR, McKenna, L, Lazovski, N, Hillert, J, Forsberg, L, Spelman, T, McBurney, R, Schmidt, H, Bergmann, A, Braune, S, Stahmann, A, Middleton, R, Salter, A, Bebo, BF, Rojas, JI, van der Walt, A, Butzkueven, H, van der Mei, I ORCID: 0000-0001-9009-7472, Ivanov, R, Hellwig, K, Sciascia do Olival, G, Cohen, JA, Van Hecke, W, Dobson, R, Magyari, M, Brum, DG, Alonso, R, Nicholas, R, Bauer, J, Chertcoff, A, de Seze, J, Louapre, C, Comi, G and Rijke, N 2020
, 'COVID-19 in people with multiple sclerosis: a global data sharing initiative'
, Multiple Sclerosis Journal
, pp. 1-6
, doi: https://doi.org/10.1177/1352458520941485.