Guillain-Barré syndrome following SARS-CoV-2 vaccination in the UK: a prospective surveillance study by Tamborska, Arina A, Singh, Bhagteshwar, Leonhard, Sonja E, Hodel, Eva Maria, Stowe, Julia, Watson-Fargie, Taylor, Fernandes, Peter M, Themistocleous, Andreas C, Roelofs, Jacob, Brennan, Kathryn, Morrice, Caroline, Michael, Benedict D, Jacobs, Bart C, McDonald, Helen, Solomon, Tom, Allen, Christopher M, Amante, Gionathan, Breen, David P, Brennan, Kathryn, Romeiro, Ana Carrilho, Cheng, Shue Jun, Crossingham, Ginette, Evans, Jonathan, Evison, Jon, Fernandes, Peter M, Furby, Julian, Galton, Clare, Gregory, Ralph, Harris, Victoria, Hinze, Stephan, Hogg, Lucy, Holt, James, Isaacs-Itua, Alifa, Knight, Kathryn, McHattie, Andrew, Garrido, Mireia Moragas, Murray, Katy, Ramsamy, Shelby, Ramsay, Scott, Roelofs, Jacob, Samarasekera, Neshika, San, Pyae Phyo, Sawcer, Stephen, Shields, Simon, Tallantyre, Emma, Terry, Robyn, Themistocleous, Andreas C, Tucker, Harry, Tuohy, Orla, Watson-Fargie, Taylor, Whittam, Daniel, Wiblin, Louise, Zeidler, Martin

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Complete MHC haplotype sequencing for common disease gene mapping by Stewart, C Andrew, Horton, Roger, Allcock, Richard J N, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Dunham, Ian, Forbes, Simon, Halls, Karen, Howson, Joanna M M, Humphray, Sean J, Hunt, Sarah, Mungall, Andrew J, Osoegawa, Kazutoyo, Palmer, Sophie, Roberts, Anne N, Rogers, Jane, Sims, Sarah, Wang, Yu, Wilming, Laurens G, Elliott, John F, de Jong, Pieter J, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility by Zuvich, Rebecca L, McCauley, Jacob L, Oksenberg, Jorge R, Sawcer, Stephen J, De Jager, Philip L, Aubin, Cristin, Cross, Anne H, Piccio, Laura, Aggarwal, Neelum T, Evans, Denis, Hafler, David A, Compston, Alastair, Hauser, Stephen L, Pericak-Vance, Margaret A, Haines, Jonathan L

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Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility by Ban, Maria, Elson, Joanna, Walton, Amie, Turnbull, Douglas, Compston, Alastair, Chinnery, Patrick, Sawcer, Stephen

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CIITA variation in the presence of HLA-DRB11501 increases risk for multiple sclerosis by Bronson, Paola G., Caillier, Stacy, Ramsay, Patricia P., McCauley, Jacob L., Zuvich, Rebecca L., De Jager, Philip L., Rioux, John D., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L., Hauser, Stephen L., Oksenberg, Jorge R., Barcellos, Lisa F.

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Evaluation of the established non-MHC multiple sclerosis loci in an Indian population by Pandit, Lekha, Ban, Maria, Sawcer, Stephen, Singhal, Bhim, Nair, Shyam, Radhakrishnan, Kurupath, Shetty, Rajesh, Misri, Z, Hegde, Suresh, Bhat, Irruvathur Gopalakrishna

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Bayes factors in complex genetics by Sawcer, Stephen

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Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history by Traherne, James A, Horton, Roger, Roberts, Anne N, Miretti, Marcos M, Hurles, Matthew E, Stewart, C Andrew, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Palmer, Sophie, Almeida, Jeff, Sims, Sarah, Wilming, Laurens G, Rogers, Jane, de Jong, Pieter J, Carrington, Mary, Elliott, John F, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan

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Experience from two decades of the Cambridge Rapid Access Neurology Clinic by Axinte, Laura T, Fiddes, Barnaby D, Donaghy, Alastair, Whyte, Adam, Allen, Chris, Sawcer, Stephen J, Adam, Robert J, Stacpoole, Sybil RL

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The major cause of multiple sclerosis is environmental: genetics has a minor role - No by Sawcer, Stephen

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Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB115 by Traherne, James A., Barcellos, Lisa F., Sawcer, Stephen J., Compston, Alastair, Ramsay, Patricia P., Hauser, Stephen L., Oksenberg, Jorge R., Trowsdale, John

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Risk in complex genetics: "All models are wrong but some are useful" by Sawcer, Stephen, Wason, James

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Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease by Robinson, Philip C, Leo, Paul J, Pointon, Jennifer J, Harris, Jessica, Cremin, Katie, Bradbury, Linda A, Stebbings, Simon, Harrison, Andrew A, Duncan, Emma L, Evans, David M, Wordsworth, Paul B, Brown, Matthew A

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Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals by Briggs, Farren B.S., Bartlett, Selena E., Goldstein, Benjamin A., Wang, Joanne, McCauley, Jacob L., Zuvich, Rebecca L., De Jager, Philip L., Rioux, John D., Ivinson, Adrian J., Compston, Alastair, Hafler, David A., Hauser, Stephen L., Oksenberg, Jorge R., Sawcer, Stephen J., Pericak-Vance, Margaret A., Haines, Jonathan L., Barcellos, Lisa F.

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No evidence of association of the rare nsSNP rs35667974 in IFIH1 with multiple sclerosis by Bergamaschi, Laura, Ban, Maria, Leone, Maurizio A, Sawcer, Stephen J, D'Alfonso, Sandra

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Neuroanatomical substrates of generalized brain dysfunction in COVID-19 by Newcombe, Virginia F. J., Spindler, Lennart R. B., Das, Tilak, Winzeck, Stefan, Allinson, Kieren, Stamatakis, Emmanuel A., Menon, David K.

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping by Sawcer, Stephen J, Maranian, Mel, Singlehurst, Sara, Yeo, TaiWai, Compston, Alastair, Daly, Mark J, De Jager, Philip L, Gabriel, Stacey, Hafler, David A, Ivinson, Adrian J, Lander, Eric S, Rioux, John D, Walsh, Emily, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Barcellos, Lisa, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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Locus for severity implicates CNS resilience in progression of multiple sclerosis by 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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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis by Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C A, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce A C, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul I W, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica

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Age Related Multiple Sclerosis Severity Score: Disability ranked by age by Manouchehrinia, Ali, Westerlind, Helga, Kingwell, Elaine, Zhu, Feng, Carruthers, Robert, Ramanujam, Ryan, Ban, Maria, Glaser, Anna, Sawcer, Stephen, Tremlett, Helen, Hillert, Jan

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