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Article
Graves, JS, Barcellos, LF, Simpson Jr, S 
ORCID: 0000-0001-6521-3056, Belman, A, Lin, R, Taylor, BV, Ponsonby, AL, Dwyer, T, Krupp, L, Waubant, E and van der Mei, IAF ORCID: 0000-0001-9009-7472 2018
, 'The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults'
, Multiple Sclerosis and Related Disorders, vol. 19
, pp. 161-165
, doi: https://doi.org/10.1016/j.msard.2017.10.008.
ORCID: 0000-0001-6521-3056, Belman, A, Lin, R, Taylor, BV, Ponsonby, AL, Dwyer, T, Krupp, L, Waubant, E and van der Mei, IAF ORCID: 0000-0001-9009-7472 2018
, 'The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults'
, Multiple Sclerosis and Related Disorders, vol. 19
, pp. 161-165
, doi: https://doi.org/10.1016/j.msard.2017.10.008.
Graves, JS, Barcellos, LF, Simpson, S ORCID: 0000-0001-6521-3056, Belman, A, Lin, R, Taylor, BV, Ponsonby, A-L, Dwyer, T, Krupp, L, Waubant, E and van der Mei, IAF ORCID: 0000-0001-9009-7472 2018
, 'The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults'
, Multiple Sclerosis and Related Disorders, vol. 19
, pp. 161-165
, doi: https://doi.org/10.1016/j.msard.2017.10.008.
ORCID: 0000-0001-6521-3056, Belman, A, Lin, R, Taylor, BV, Ponsonby, A-L, Dwyer, T, Krupp, L, Waubant, E and van der Mei, IAF ORCID: 0000-0001-9009-7472 2018
, 'The multiple sclerosis risk allele within the AHI1 gene is associated with relapses in children and adults'
, Multiple Sclerosis and Related Disorders, vol. 19
, pp. 161-165
, doi: https://doi.org/10.1016/j.msard.2017.10.008.
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: https://doi.org/10.1038/s41467-019-09773-y.
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
, pp. 1-12
, doi: https://doi.org/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: 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.
Sharp, GC, Salas, LA, Monnereau, C, Allard, C, Yousefi, P, Everson, TM, Bohlin, J, Xu, Z, Huang, R-C, Reese, SE, Xu, C-J, Baiz, N, Hoyo, C, Agha, G, Roy, R, Holloway, JW, Ghantous, A, Merid, SK, Bakulski, KM, Kupers, LK, Zhang, H, Richmond, RC, Page, CM, Duijts, L, Lie, RT, Melton, PE ORCID: 0000-0003-4026-2964, Vonk, JM, Nohr, EA, Williams-DeVane, C, Huen, K, Rifas-Shiman, SL, Ruiz-Arenas, C, Gonseth, S, Rezwan, FI, Herceg, Z, Ekstrom, S, Croen, L, Falahi, F, Perron, P, Karagas, MR, Quraishi, BM, Suderman, M, Magnus, MC, Jaddoe, VWV, Taylor, JA, Anderson, D, Zhao, S, Smit, HA, Josey, MJ, Bradman, A, Baccarelli, AA, Bustamante, M, Haberg, SE, Pershagen, G, Hertz-Picciotto, I, Newschaffer, C, Corpeleijn, E, Bouchard, L, Lawlor, DA, Maguire, RL, Barcellos, LF, Smith, GD, Eskenazi, B, Karmaus, W, Marsit, CJ, Hivert, M-F, Snieder, H, Fallin, MD, Melen, E, Munthe-Kaas, MC, Arshad, H, Wiemels, JL, Annesi-Maesano, I, Vrijheid, M, Oken, E, Holland, N, Murphy, SK, Sorensen, TIA, Koppelman, GH, Newnham, JP, Wilcox, AJ, Nystad, W, London, SJ, Felix, JF and Relton, CL 2017
, 'Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: Findings from the pregnancy and childhood epigenetics (PACE) consortium'
, Human Molecular Genetics, vol. 26, no. 20
, pp. 4067-4085
, doi: https://doi.org/10.1093/hmg/ddx290.
ORCID: 0000-0003-4026-2964, Vonk, JM, Nohr, EA, Williams-DeVane, C, Huen, K, Rifas-Shiman, SL, Ruiz-Arenas, C, Gonseth, S, Rezwan, FI, Herceg, Z, Ekstrom, S, Croen, L, Falahi, F, Perron, P, Karagas, MR, Quraishi, BM, Suderman, M, Magnus, MC, Jaddoe, VWV, Taylor, JA, Anderson, D, Zhao, S, Smit, HA, Josey, MJ, Bradman, A, Baccarelli, AA, Bustamante, M, Haberg, SE, Pershagen, G, Hertz-Picciotto, I, Newschaffer, C, Corpeleijn, E, Bouchard, L, Lawlor, DA, Maguire, RL, Barcellos, LF, Smith, GD, Eskenazi, B, Karmaus, W, Marsit, CJ, Hivert, M-F, Snieder, H, Fallin, MD, Melen, E, Munthe-Kaas, MC, Arshad, H, Wiemels, JL, Annesi-Maesano, I, Vrijheid, M, Oken, E, Holland, N, Murphy, SK, Sorensen, TIA, Koppelman, GH, Newnham, JP, Wilcox, AJ, Nystad, W, London, SJ, Felix, JF and Relton, CL 2017
, 'Maternal BMI at the start of pregnancy and offspring epigenome-wide DNA methylation: Findings from the pregnancy and childhood epigenetics (PACE) consortium'
, Human Molecular Genetics, vol. 26, no. 20
, pp. 4067-4085
, doi: https://doi.org/10.1093/hmg/ddx290.
Zhou, Y ORCID: 0000-0003-1962-2574, Graves, JS, Simpson Jr, S ORCID: 0000-0001-6521-3056, Charlesworth, JC ORCID: 0000-0001-6201-3518, van der Mei, I ORCID: 0000-0001-9009-7472, Waubant, E, Barcellos, LF, Belman, A, Krupp, L, Lucas, R, Ponsonby, AL and Taylor, BV 2017
, 'Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis'
, Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 10
, pp. 864-868
, doi: https://doi.org/10.1136/jnnp-2017-315971.
ORCID: 0000-0003-1962-2574, Graves, JS, Simpson Jr, S ORCID: 0000-0001-6521-3056, Charlesworth, JC ORCID: 0000-0001-6201-3518, van der Mei, I ORCID: 0000-0001-9009-7472, Waubant, E, Barcellos, LF, Belman, A, Krupp, L, Lucas, R, Ponsonby, AL and Taylor, BV 2017
, 'Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis'
, Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 10
, pp. 864-868
, doi: https://doi.org/10.1136/jnnp-2017-315971.
Zhou, Y ORCID: 0000-0003-1962-2574, Graves, JS, Simpson, S ORCID: 0000-0001-6521-3056, Charlesworth, JC ORCID: 0000-0001-6201-3518, van der Mei, I ORCID: 0000-0001-9009-7472, Waubant, E, Barcellos, LF, Belman, A, Krupp, L, Lucas, R, Ponsonby, A-L and Taylor, BV 2017
, 'Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis'
, Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 10
, pp. 864-868
, doi: https://doi.org/10.1136/jnnp-2017-315971.
ORCID: 0000-0003-1962-2574, Graves, JS, Simpson, S ORCID: 0000-0001-6521-3056, Charlesworth, JC ORCID: 0000-0001-6201-3518, van der Mei, I ORCID: 0000-0001-9009-7472, Waubant, E, Barcellos, LF, Belman, A, Krupp, L, Lucas, R, Ponsonby, A-L and Taylor, BV 2017
, 'Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis'
, Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 10
, pp. 864-868
, doi: https://doi.org/10.1136/jnnp-2017-315971.