Search Results - Clemens, Margaret B

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    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk by 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

    Published in Cell
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    Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias by Kaivola, Karri, Ding, Jinhui, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan L., Billingsley, Kimberley, Talkowski, Michael, Dewan, Ramita, Ray, Anindita, Alvarez Jerez, Pilar, Albert, Marilyn S., Resnick, Susan M., Sukumar, Gauthaman, Lott, Nathaniel, Tuck, Meila, Bacikova, Dagmar, Adeleye, Adelani, Black, Sandra E., Gan-Or, Ziv, Rogaeva, Ekaterina, Lesage, Suzanne, Xiromerisiou, Georgia, Calvo, Andrea, Canosa, Antonio, Logroscino, Giancarlo, Clarimon, Jordi, Brett, Francesca, Aarsland, Dag, Al-Sarraj, Safa, Attems, Johannes, McKeith, Ian G., Morris, Christopher M., Morris, Huw R., Pickering-Brown, Stuart, Ryten, Mina, Thomas, Alan J., Troakes, Claire, Albert, Marilyn S., Barrett, Matthew J., Bennett, David A., Dickson, Dennis W., Faber, Kelley, Ferrucci, Luigi, Flanagan, Margaret E., Foroud, Tatiana M., Ghetti, Bernardino, Gibbs, J. Raphael, Goate, Alison, Graff-Radford, Neill R., Kaufmann, Horacio, Kukull, Walter A., Lopez, Grisel, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Renton, Alan E., Ross, Owen A., Serrano, Geidy E., Sidransky, Ellen, Tayebi, Nahid, Torkamani, Ali, Wszolek, Zbigniew K., Broach, James, Drory, Vivian E., Dunckley, Travis L., Gerhard, Glenn, Gibson, Summer B., Heiman-Patterson, Terry D., Jansson, Lilja, Kwan, Justin, Laaksovirta, Hannu, Landers, John E., Landi, Francesco, Le Ber, Isabelle, Lumbroso, Serge, MacGowan, Daniel J.L., Maragakis, Nicholas J., Myllykangas, Liisa, Orrell, Richard W., Pamphlett, Roger, Pulst, Stefan M., Rothstein, Jeffrey D., Shaw, Pamela J., Sidle, Katie C., Simmons, Zachary, Stone, David J., Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Topol, Eric, Ghetti, Bernardino, Landers, John E., Morris, Huw R., Hardy, John A., Moglia, Cristina, Calvo, Andrea, Beach, Thomas G., Ferman, Tanis, Bennett, David A., Traynor, Bryan J.

    Published in Cell genomics
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