Assessing the Protective Quality of Wax Coatings on Bronze Sculptures Using Hydrogel Patches in Impedance Measurements by England, Alice H, Hosbein, Kathryn N, Price, Capri A, Wylder, Morgan K, Miller, Kenna S, Clare, Tami Lasseter

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A mixed‐methods approach to improve the measurement of alcohol‐induced blackouts: ABOM‐2 by Boness, Cassandra L., Gatten, Natalie, Treece, Mc Kenna, Miller, Mary Beth

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Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS by Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.

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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene by Kenna, Kevin P., Chia, Ruth, Dominov, Janice A., Nalls, Mike A., van Vugt, Joke J.F.A., Simone, Isabella, Caredda, Carla, Milia, Antonio, Floris, Gianluca, Caponnetto, Claudia, Mandich, Paola, Mora, Gabriele, Sideri, Riccardo, Penco, Silvana, Mandrioli, Jessica, Trojsi, Francesca, Ticca, Anna, Ortu, Enzo, Pugliatti, Maura, Benigni, Michele, Brunetti, Maura, Marrali, Giuseppe, Riva, Nilo, Conforti, Francesca L., Messina, Sonia, D’Alfonso, Sandra, Baloh, Robert H., Penny, Michelle, Moreno, Cristiane de Araujo Martins, Chung, Wendy K., Cirulli, Elizabeth T., Harris, Tim, Krueger, Brian J., Lasseigne, Brittany N., McKenna-Yasek, Diane, Myers, Richard M., Pulst, Stefan M., Raphael, Alya R., Rouleau, Guy A., Sapp, Peter C., Waite, Lindsay L., Wang, Quanli, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Hornstein, Eran, Patsopoulos, Nikolaos A., Kaye, Julia, Wyman, Stacia, LeNail, Alexander, Baxi, Emily, LeNail, Alex, Benatar, Michael, Hussain, Sumaira, Swenson, Andrea, Jackson, Carlayne, So, Yuen, Wuu, Joanne, Silani, Vincenzo, Fogh, Isabella, Cereda, Cristina, Ceroni, Mauro, Mazzini, Letizia, Maderna, Luca, Sorarù, Gianni, Bernard, Emilien, Laaksovirta, Hannu, McKenna-Yasek, Diane, Asress, Seneshaw, Al-Sarraj, Safa, Scholz, Sonja W., MacGowan, Daniel J.L., Kirby, Janine, Pioro, Erik P., Pamphlett, Roger, Dunckley, Travis L., Troncoso, Juan C., Moisse, Matthieu, Drory, Vivian E., Turner, Martin R., Blair, Ian P., de Carvalho, Mamede, Hide, Winston, Glass, Jonathan, Mill, Jonathan, Newhouse, Stephen, Pulit, Sara, Robberecht, Wim, Shaw, Pamela, van den Berg, Leonard, Williams, Kelly L., Zatz, Mayana, Rothstein, Jeffrey D., Simmons, Zachary, Van Damme, Philip, Sabatelli, Mario, Trojanowski, John Q., Brown, Robert H., Veldink, Jan H., Tienari, Pentti

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ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function by de Majo, Martina, Topp, Simon D., Smith, Bradley N., Nishimura, Agnes L., Chen, Han-Jou, Gkazi, Athina Soragia, Miller, Jack, Wong, Chun Hao, Vance, Caroline, Baas, Frank, ten Asbroek, Anneloor L.M.A., Kenna, Kevin P., Ticozzi, Nicola, Redondo, Alberto Garcia, Esteban-Pérez, Jesús, Tiloca, Cinzia, Verde, Federico, Duga, Stefano, Morrison, Karen E., Shaw, Pamela J., Kirby, Janine, Turner, Martin R., Talbot, Kevin, Hardiman, Orla, Glass, Jonathan D., de Belleroche, Jacqueline, Gellera, Cinzia, Ratti, Antonia, Al-Chalabi, Ammar, Brown, Robert H., Silani, Vincenzo, Landers, John E., Shaw, Christopher E.

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways by Cirulli, Elizabeth T., Lasseigne, Brittany N., Petrovski, Slavé, Sapp, Peter C., Dion, Patrick A., Leblond, Claire S., Couthouis, Julien, Lu, Yi-Fan, Wang, Quanli, Krueger, Brian J., Ren, Zhong, Keebler, Jonathan, Han, Yujun, Levy, Shawn E., Boone, Braden E., Wimbish, Jack R., Waite, Lindsay L., Jones, Angela L., Carulli, John P., Day-Williams, Aaron G., Staropoli, John F., Xin, Winnie W., Chesi, Alessandra, Raphael, Alya R., McKenna-Yasek, Diane, Cady, Janet, de Jong, J. M. B. Vianney, Kenna, Kevin P., Smith, Bradley N., Topp, Simon, Miller, Jack, Gkazi, Athina, Al-Chalabi, Ammar, van den Berg, Leonard H., Veldink, Jan, Silani, Vincenzo, Ticozzi, Nicola, Shaw, Christopher E., Baloh, Robert H., Appel, Stanley, Simpson, Ericka, Lagier-Tourenne, Clotilde, Pulst, Stefan M., Gibson, Summer, Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Grossman, Murray, Shneider, Neil A., Chung, Wendy K., Ravits, John M., Glass, Jonathan D., Sims, Katherine B., Van Deerlin, Vivianna M., Maniatis, Tom, Hayes, Sebastian D., Ordureau, Alban, Swarup, Sharan, Landers, John, Baas, Frank, Allen, Andrew S., Bedlack, Richard S., Harper, J. Wade, Gitler, Aaron D., Rouleau, Guy A., Brown, Robert, Harms, Matthew B., Cooper, Gregory M., Harris, Tim, Myers, Richard M., Goldstein, David B.

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis by Smith, Bradley N, Topp, Simon D, Fallini, Claudia, Shibata, Hideki, Chen, Han-Jou, Troakes, Claire, King, Andrew, Ticozzi, Nicola, Kenna, Kevin P, Soragia-Gkazi, Athina, Miller, Jack W, Sato, Akane, Dias, Diana Marques, Jeon, Maryangel, Vance, Caroline, Wong, Chun Hao, de Majo, Martina, Kattuah, Wejdan, Mitchell, Jacqueline C, Scotter, Emma L, Parkin, Nicholas W, Sapp, Peter C, Nolan, Matthew, Nestor, Peter J, Simpson, Michael, Weale, Michael, Lek, Monkel, Baas, Frank, Vianney de Jong, J M, Ten Asbroek, Anneloor L M A, Redondo, Alberto Garcia, Esteban-Pérez, Jesús, Tiloca, Cinzia, Verde, Federico, Duga, Stefano, Leigh, Nigel, Pall, Hardev, Morrison, Karen E, Al-Chalabi, Ammar, Shaw, Pamela J, Kirby, Janine, Turner, Martin R, Talbot, Kevin, Hardiman, Orla, Glass, Jonathan D, De Belleroche, Jacqueline, Maki, Masatoshi, Moss, Stephen E, Miller, Christopher, Gellera, Cinzia, Ratti, Antonia, Al-Sarraj, Safa, Brown, Jr, Robert H, Silani, Vincenzo, Landers, John E, Shaw, Christopher E

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Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis by Dewan, Ramita, Keagle, Pamela, Bacikova, Dagmar, Soltis, Anthony R., Kost, Jason, Colombrita, Claudia, Lewis, Elizabeth A., Pensato, Viviana, Castellotti, Barbara, McLaughlin, Russell L., Comi, Giacomo P., Ceroni, Mauro, Gagliardi, Stella, van Blitterswijk, Marka, Corrado, Lucia, Sorarù, Gianni, Williams, Kelly L., Morrison, Karen E., Veldink, Jan H., Brown, Robert H., Ambrose, John C., Brittain, H., Elgar, Greg, Halai, Dina, Holman, James E., Jackson, Rob, Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Riesgo-Ferreiro, Pablo, Rogers, Tim, Watters, Sarah A., Arepalli, Sampath, Chiò, Adriano, Dunckley, Travis L., Faghri, Faraz, Feldman, Eva, Floeter, Mary Kay, Gerhard, Glenn, Jansson, Lilja, Kirby, Janine, Mora, Gabriele, Nalls, Mike A., Pulst, Stefan M., Ravits, John M., Renton, Alan E., Robberecht, Wim, Robey, Ian, Dols-Icardo, Oriol, Illán-Gala, Ignacio, Lleó, Alberto, Khoshnood, Behzad, Sorbi, Sandro, Pastor, Pau, Bigio, Eileen H., Black, Sandra E., Brunetti, Maura, Canosa, Antonio, Gan-Or, Ziv, Goate, Alison, Hupalo, Daniel, Infante, Jon, Kaufmann, Horacio, Kim, Ronald C., Krüger, Rejko, Logroscino, Giancarlo, Love, Seth, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Reynolds, Regina H., Scherzer, Clemens R., Serrano, Geidy E., Xiromerisiou, Georgia, Phatnani, Hemali, Kwan, Justin, Broach, James R., Arcila-Londono, Ximena, Malaspina, Andrea, Thompson, Leslie M., Dardiotis, Efthimios, Chandran, Siddharthan, Butovsky, Oleg, Dubnau, Joshua, Harms, Matt, Poss, Mary, Phillips-Cremins, Jennifer, Altschuler, Steven, Hu, Michele T.M., Leigh, P. Nigel, Massey, Luke A., Pavese, Nicola, Vaughan, Jenny, Rowe, James B., Ghidoni, Roberta, Ryten, Mina, Tanaka, Toshiko, Ferrucci, Luigi, Vonsattel, Jean Paul, Landers, John E.

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Innate αβ T Cells Mediate Antitumor Immunity by Orchestrating Immunogenic Macrophage Programming by Hundeyin, Mautin, Kurz, Emma, Mishra, Ankita, Rossi, Juan Andres Kochen, Liudahl, Shannon M, Leis, Kenna R, Mehrotra, Harshita, Kim, Mirhee, Torres, Luisana E, Ogunsakin, Adesola, Link, Jason, Sears, Rosalie C, Sivagnanam, Shamilene, Goecks, Jeremy, Islam, K M Sadeq, Dolgalev, Igor, Savadkar, Shivraj, Wang, Wei, Aykut, Berk, Leinwand, Joshua, Diskin, Brian, Adam, Salma, Israr, Muhammad, Gelas, Maeliss, Lish, Justin, Chin, Kathryn, Farooq, Mohammad Saad, Wadowski, Benjamin, Wu, Jingjing, Shah, Suhagi, Adeegbe, Dennis O, Pushalkar, Smruti, Vasudevaraja, Varshini, Saxena, Deepak, Wong, Kwok-Kin, Coussens, Lisa M, Miller, George

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Psychometrics of the Drinker Inventory of Consequences (DrInC) by Forcehimes, Alyssa A, Tonigan, J. Scott, Miller, William R, Kenna, George A, Baer, John S

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Abstract LB-104: Clinical actionability and clinical trial matching for GENIE patient genotypes using My Cancer Genome, Personalized Cancer Therapy, and OncoKB by Micheel, Christine M., Chakravarty, Debayani, Gao, Jiaojiong, Maurer, Ian, Miller, Clinton, Shaw, Kenna R., Levy, Mia A., Schultz, Nikolaus

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Innate αβ T cells Mediate Anti-tumor Immunity by Orchestrating Immunogenic Macrophage Programming by Hundeyin, Mautin, Kurz, Emma, Mishra, Ankita, Kochen Rossi, Juan Andres, Liudahl, Shannon M., Leis, Kenna R., Mehrotra, Harshita, Kim, Mirhee, Torres, Luisana E., Ogunsakin, Adesola, Link, Jason, Sears, Rosalie C., Sivagnanam, Shamilene, Goecks, Jeremy, Islam, KM Sadeq, Dolgalev, Igor, Savadkar, Shivraj, Wang, Wei, Aykut, Berk, Leinwand, Joshua, Diskin, Brian, Adam, Salma, Israr, Muhammad, Gelas, Maeliss, Lish, Justin, Chin, Kathryn, Farooq, Mohammad Saad, Wadowski, Benjamin, Wu, Jingjing, Shah, Suhagi, Adeegbe, Dennis O., Pushalkar, Smruti, Vasudevaraja, Varshini, Saxena, Deepak, Wong, Kwok-Kin, Coussens, Lisa M., Miller, George

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Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss by Dai, Pu, Stewart, Andrew K, Chebib, Fouad, Hsu, Ann, Rozenfeld, Julia, Huang, Deliang, Kang, Dongyang, Lip, Va, Fang, Hong, Shao, Hong, Liu, Xin, Yu, Fei, Yuan, Huijun, Kenna, Margaret, Miller, David T, Shen, Yiping, Yang, Weiyan, Zelikovic, Israel, Platt, Orah S, Han, Dongyi, Alper, Seth L, Wu, Bai-Lin

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Bicortical Screw Fixation of Distal Fibula Fractures With a Lateral Plate: An Anatomic and Biomechanical Study of a New Technique by Milner, Brenton F., MD, Mercer, Deana, MD, Firoozbakhsh, Keikhosrow, PhD, Larsen, Kenna, MD, DeCoster, Thomas A., MD, Miller, Richard A., MD

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Open-Set Recognition in the Age of Vision-Language Models by Miller, Dimity, Sünderhauf, Niko, Kenna, Alex, Mason, Keita

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The diagnosis of esophagitis by Ballem, C. Miller, Fletcher, H. W., Mc Kenna, Richard D.

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