The killer immunoglobulin-like receptor KIR3DL1 in combination with HLA-Bw4 is protective against multiple sclerosis in African Americans von Hollenbach, J A, Pando, M J, Caillier, S J, Gourraud, P-A, Oksenberg, J R

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Genotype-Phenotype Correlations in Multiple Sclerosis: "HLA" Genes Influence Disease Severity Inferred by [superscript 1]HMR Spectroscopy and MRI Measures von Okuda, D. T, Srinivasan, R, Oksenberg, J. R, Goodin, D. S, Baranzini, S. E, Beheshtian, A, Waubant, E, Zamvil, S. S, Leppert, D, Qualley, P, Lincoln, R, Gomez, R, Caillier, S, George, M, Wang, J, Nelson, S. J, Cree, B. A. C, Hauser, S. L, Pelletier, D

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Multiple sclerosis susceptibility alleles in African Americans von Johnson, B A, Wang, J, Taylor, E M, Caillier, S J, Herbert, J, Khan, O A, Cross, A H, De Jager, P L, Gourraud, P-A F, Cree, B C A, Hauser, S L, Oksenberg, J R

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Copy number variation in pediatric multiple sclerosis von McElroy, JP, Krupp, LB, Johnson, BA, McCauley, JL, Qi, Z, Caillier, SJ, Gourraud, PA, Yu, J, Nathanson, L, Belman, AL, Hauser, SL, Waubant, E, Hedges, DJ, Oksenberg, JR

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SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients von McElroy, J P, Isobe, N, Gourraud, P A, Caillier, S J, Matsushita, T, Kohriyama, T, Miyamoto, K, Nakatsuji, Y, Miki, T, Hauser, S L, Oksenberg, J R, Kira, J

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Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans von Brassat, D, Motsinger, A A, Caillier, S J, Erlich, H A, Walker, K, Steiner, L L, Cree, B A C, Barcellos, L F, Pericak-Vance, M A, Schmidt, S, Gregory, S, Hauser, S L, Haines, J L, Oksenberg, J R, Ritchie, M D

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High-resolution MHC sequencing reveals local genetic architecture of multiple sclerosis in a trans-ethnic cohort von Wade, K.J., Kizer, K., Suseno, R., Boquett, J.A., Caillier, S., Oksenberg, J., Norman, P.J., Augusto, D., Hollenbach, J.A.

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Genotype–Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measures von Okuda, D. T., Srinivasan, R., Oksenberg, J. R., Goodin, D. S., Baranzini, S. E., Beheshtian, A., Waubant, E., Zamvil, S. S., Leppert, D., Qualley, P., Lincoln, R., Gomez, R., Caillier, S., George, M., Wang, J., Nelson, S. J., Cree, B. A. C., Hauser, S. L., Pelletier, D.

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Pharmacogenomic analysis of interferon receptor polymorphisms in multiple sclerosis von Sriram, U, Barcellos, L F, Villoslada, P, Rio, J, Baranzini, S E, Caillier, S, Stillman, A, Hauser, S L, Montalban, X, Oksenberg, J R

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KIR2DL1001/HLA-C2 is associated with risk for multiple sclerosis von Williams, J.C., Kichula, K., Kline, N., Kizer, K., Suseno, R., Boquett, J.A., Wade, K.J., Caillier, S., Oksenberg, J., Augusto, D., Norman, P.J., Hollenbach, J.A.

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Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis von Barcellos, L F, Ramsay, P P, Caillier, S J, Sawcer, S, Haines, J, Schmidt, S, Pericak-Vance, M, Compston, D A S, Gabatto, P, Hauser, S L, Oksenberg, J R

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Locus for severity implicates CNS resilience in progression of multiple sclerosis von Harroud, Adil, Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., Engelenburg, Hendrik J., Beecham, Ashley H., Alfredsson, Lars, Alikhani, Katayoun, Amezcua, Lilyana, Andlauer, Till F. M., Ban, Maria, Barcellos, Lisa F., Barizzone, Nadia, Berge, Tone, Berthele, Achim, Bittner, Stefan, Bos, Steffan D., Briggs, Farren B. S., Caillier, Stacy J., Calabresi, Peter A., Caputo, Domenico, Carmona-Burgos, David X., Cavalla, Paola, Celius, Elisabeth G., Cerono, Gabriel, Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., D’Alfonso, Sandra, Dardiotis, Efthimios, De Jager, Philip L., Delgado, Silvia R., Dubois, Bénédicte, Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Filippi, Massimo, Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Hamann, Jörg, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Khalil, Michael, Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Malhotra, Sunny, Manouchehrinia, Ali, Manrique, Clara P., Martinelli-Boneschi, Filippo, Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Olsson, Tomas, Oturai, Annette, Pääkkönen, Kimmo, Parnell, Grant P., Patsopoulos, Nikolaos A., Pericak-Vance, Margaret A., Piehl, Fredrik, Rubio, Justin P., Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Silva, Claudia, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vasileiou, Elena S., Vecchio, Domizia, Voortman, Margarete M., Weiner, Howard L., Wever, Dennis

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Osteopontin polymorphisms and disease course in multiple sclerosis von Caillier, S, Barcellos, L F, Baranzini, S E, Swerdlin, A, Lincoln, R R, Steinman, L, Martin, E, Haines, J L, Pericak-Vance, M, Hauser, S L, Oksenberg, J R

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Ovarian aging is associated with gray matter volume and disability in women with MS von Graves, Jennifer S, Henry, Roland G, Cree, Bruce A.C, Lambert-Messerlian, Geralyn, Greenblatt, Ruth M, Waubant, Emmanuelle, Cedars, Marcelle I, Zhu, Alyssa, Bacchetti, Peter, Hauser, Stephen L, Oksenberg, Jorge R

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Gut microbiome of multiple sclerosis patients and paired household healthy controls reveal associations with disease risk and course von Zhou, Xiaoyuan, Baumann, Ryan, Gao, Xiaohui, Mendoza, Myra, Singh, Sneha, Katz Sand, Ilana, Xia, Zongqi, Cox, Laura M., Chitnis, Tanuja, Yoon, Hongsup, Moles, Laura, Caillier, Stacy J., Santaniello, Adam, Ackermann, Gail, Harroud, Adil, Lincoln, Robin, Gomez, Refujia, González Peña, Antonio, Digga, Elise, Hakim, Daniel Joseph, Vazquez-Baeza, Yoshiki, Soman, Karthik, Warto, Shannon, Humphrey, Greg, Farez, Mauricio, Gerdes, Lisa Ann, Oksenberg, Jorge R., Zamvil, Scott S., Chandran, Siddharthan, Connick, Peter, Otaegui, David, Castillo-Triviño, Tamara, Hauser, Stephen L., Gelfand, Jeffrey M., Weiner, Howard L., Hohlfeld, Reinhard, Wekerle, Hartmut, Graves, Jennifer, Bar-Or, Amit, Cree, Bruce A.C., Correale, Jorge, Knight, Rob, Baranzini, Sergio E.

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Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS von Gianfrancesco, Milena A, Stridh, Pernilla, Rhead, Brooke, Shao, Xiaorong, Xu, Edison, Graves, Jennifer S, Chitnis, Tanuja, Waldman, Amy, Lotze, Timothy, Schreiner, Teri, Belman, Anita, Greenberg, Benjamin, Weinstock-Guttman, Bianca, Aaen, Gregory, Tillema, Jan M, Hart, Janace, Caillier, Stacy, Ness, Jayne, Harris, Yolanda, Rubin, Jennifer, Candee, Meghan, Krupp, Lauren, Gorman, Mark, Benson, Leslie, Rodriguez, Moses, Mar, Soe, Kahn, Ilana, Rose, John, Roalstad, Shelly, Casper, T Charles, Shen, Ling, Quach, Hong, Quach, Diana, Hillert, Jan, Bäärnhielm, Maria, Hedstrom, Anna, Olsson, Tomas, Kockum, Ingrid, Alfredsson, Lars, Metayer, Catherine, Schaefer, Catherine, Barcellos, Lisa F, Waubant, Emmanuelle

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Neurofilament Light Chain Elevation and Disability Progression in Multiple Sclerosis von Abdelhak, Ahmed, Benkert, Pascal, Schaedelin, Sabine, Boscardin, W. John, Cordano, Christian, Oechtering, Johanna, Ananth, Kirtana, Granziera, Cristina, Melie-Garcia, Lester, Montes, Shivany Condor, Beaudry-Richard, Alexandra, Achtnichts, Lutz, Oertel, Frederike C, Lalive, Patrice H, Leppert, David, Müller, Stefanie, Henry, Roland G, Pot, Caroline, Matthias, Amandine, Salmen, Anke, Oksenberg, Jorge R, Disanto, Giulio, Zecca, Chiara, D’Souza, Marcus, Du Pasquier, Renaud, Bridel, Claire, Gobbi, Claudio, Kappos, Ludwig, Hauser, Stephen L, Cree, Bruce A. C, Kuhle, Jens, Green, Ari J

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Specific hypomethylation programs underpin B cell activation in early multiple sclerosis von Ma, Qin, Caillier, Stacy J., Muzic, Shaun, Wilson, Michael R., Henry, Roland G., Cree, Bruce A. C., Hauser, Stephen L., Didonna, Alessandro, Oksenberg, Jorge R.

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Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans von Shams, Hengameh, Shao, Xiaorong, Santaniello, Adam, Kirkish, Gina, Harroud, Adil, Ma, Qin, Isobe, Noriko, Schaefer, Catherine A, McCauley, Jacob L, Cree, Bruce A C, Didonna, Alessandro, Baranzini, Sergio E, Patsopoulos, Nikolaos A, Hauser, Stephen L, Barcellos, Lisa F, Henry, Roland G, Oksenberg, Jorge R

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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

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