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Items where Author is "Fontaine, B"

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Number of items: 2.

Article

Madireddy, L, Patsopoulos, NA, Cotsapas, C, Bos, SD, Beecham, A, McCauley, J, Kim, K, Jia, X, Santaniello, A, Caillier, SJ, Andlauer, TFM, Barcellos, LF, Berge, T, Bernardinelli, L, Martinelli-Boneschi, F, Booth, DR, Briggs, F, Celius, EG, Comabella, M, Comi, G, Cree, BAC, D'Alfonso, S, Dedham, K, Duquette, P, Efthimios, D, Esposito, F, Fontaine, B, Gasperi, C, Goris, A, Dubois, B, Gourraud, PA, Hadjigeorgiou, G, Haines, J, Hawkins, C, Hemmer, B, Hintzen, R, Horakova, D, Isobe, N, Kalra, S, Kira, Ji, Khalil, M, Kockum, I, Lill, CM, Lincoln, MR, Luessi, F, Martin, R, Oturai, A, Palotie, A, Pericak-Vance, MA, Henry, R, Saarela, J, Ivinson, A, Olsson, T, Taylor, BV, Stewart, GJ, Harbo, HF, Compston, A, Hauser, SL, Hafler, DA, Zipp, F, De Jager, P, Sawcer, S, Oksenberg, JR and Baranzini, SE 2019 , 'A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis' , Nature Communications, vol. 10, no. 1 , pp. 1-12 , doi: 10.1038/s41467-019-09773-y.

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: 10.1016/j.cell.2018.09.049.

This list was generated on Sun Nov 17 02:01:57 2019 AEDT.
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