Search Results - Masellis, A

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    MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study by Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

    Published in Lancet neurology
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    MRI-visible perivascular space volumes, sleep duration and daytime dysfunction in adults with cerebrovascular disease by Ramirez, Joel, Holmes, Melissa F., Berezuk, Courtney, Kwan, Donna, Tan, Brian, Beaton, Derek, Scott, Christopher J.M., Gao, Fuqiang, Yu, Di, Swardfager, Walter, Lawrence-Dewar, Jane, Dowlatshahi, Dar, Saposnik, Gustavo, Murray, Brian J., Symons, Sean, Bartha, Robert, Black, Sandra E., Swartz, Richard H., Strong, Michael, Kleinstiver, Peter, Rashkovan, Natalie, Bronskill, Susan, Finger, Elizabeth, Fischer, Corinne, Freedman, Morris, Kumar, Sanjeev, Pasternak, Stephen, Pollock, Bruce, Rajji, Tarek, Seitz, Dallas, Tang-Wai, David, Tartaglia, Carmela, Varriano, Brenda, Abrahao, Agessandro, Shoesmith, Christen, Lawrence-Dewar, Jane, Kwan, Donna, Tan, Brian, Cornish, Ben, Van Ooteghem, Karen, Faria, Frederico, Montero-Odasso, Manuel, Sarquis-Adamson, Yanina, Black, Alanna, Greenberg, Barry, Hatch, Wendy, Hudson, Chris, Leontieva, Elena, Margolin, Ed, Mandelcorn, Efrem, Brien, Don, Chen, Ying, Coe, Brian, Bonnick, Alisia, Casaubon, Leanne, Dowlatshahi, Dar, Hassan, Ayman, Saposnik, Gustavo, Swartz, Richard H., Breen, David, Grimes, David, Jog, Mandar, Lang, Anthony, Marras, Connie, Masellis, Mario, Steeves, Tom, Bulman, Dennis, Ghani, Mahdi, Hegele, Rob, Robinson, John, Rogaeva, Ekaterina, Farhan, Sali, Nanayakkara, Nuwan, Ramirez, Joel, Scott, Christopher, Symons, Sean, Berezuk, Courtney, Holmes, Melissa, Adamo, Sabrina, Ozzoude, Miracle, Zamyadi, Mojdeh, Arnott, Stephen, Beaton, Derek, Binns, Malcolm, Raamana, Pradeep, Strother, Stephen, Sunderland, Kelly, Theyers, Athena, Uthirakumaran, Abiramy, Zou, Guangyong (GY), Sujanthan, Sujeevini, Munoz, David, Dixon, Roger A., Woulfe, John, Levine, Brian, McLaughlin, Paula, Orange, J.B., Peltsch, Alicia, Roberts, Angela, Troyer, Angela

    Published in Sleep medicine
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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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