Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation by Manzoni, Claudia, Mamais, Adamantios, Dihanich, Sybille, McGoldrick, Phillip, Devine, Michael J., Zerle, Julia, Kara, Eleanna, Taanman, Jan-Willem, Healy, Daniel G., Marti-Masso, Jose-Felix, Schapira, Anthony H., Plun-Favreau, Helene, Tooze, Sharon, Hardy, John, Bandopadhyay, Rina, Lewis, Patrick A.

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C9orf72 isoforms in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration by Xiao, Shangxi, MacNair, Laura, McLean, Jesse, McGoldrick, Phillip, McKeever, Paul, Soleimani, Serena, Keith, Julia, Zinman, Lorne, Rogaeva, Ekaterina, Robertson, Janice

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Crisis Standard of Care: Management of Infantile Spasms during COVID‐19 by Grinspan, Zachary M., Mytinger, John R., Baumer, Fiona M., Ciliberto, Michael A., Cohen, Bruce H., Dlugos, Dennis J., Harini, Chellamani, Hussain, Shaun A., Joshi, Sucheta M., Keator, Cynthia G., Knupp, Kelly G., McGoldrick, Patricia E., Nickels, Katherine C., Park, Jun T., Pasupuleti, Archana, Patel, Anup D., Pomeroy, Scott L., Shahid, Asim M., Shellhaas, Renee A., Shrey, Daniel W., Singh, Rani K., Wolf, Steven M., Yozawitz, Elissa G., Yuskaitis, Christopher J., Waugh, Jeff L., Pearl, Phillip L.

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Management of Infantile Spasms During the COVID-19 Pandemic by Grinspan, Zachary M., Mytinger, John R., Baumer, Fiona M., Ciliberto, Michael A., Cohen, Bruce H., Dlugos, Dennis J., Harini, Chellamani, Hussain, Shaun A., Joshi, Sucheta M., Keator, Cynthia G., Knupp, Kelly G., McGoldrick, Patricia E., Nickels, Katherine C., Park, Jun T., Pasupuleti, Archana, Patel, Anup D., Shahid, Asim M., Shellhaas, Renee A., Shrey, Daniel W., Singh, Rani K., Wolf, Steven M., Yozawitz, Elissa G., Yuskaitis, Christopher J., Waugh, Jeff L., Pearl, Phillip L.

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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder by Heimer, Gali, Kerätär, Juha M., Riley, Lisa G., Balasubramaniam, Shanti, Eyal, Eran, Pietikäinen, Laura P., Hiltunen, J. Kalervo, Marek-Yagel, Dina, Hamada, Jeffrey, Gregory, Allison, Rogers, Caleb, Hogarth, Penelope, Nance, Martha A., Shalva, Nechama, Veber, Alvit, Tzadok, Michal, Nissenkorn, Andreea, Tonduti, Davide, Renaldo, Florence, Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Annable, Marcus, Blue, Elizabeth Marchani, Buckingham, Kati J., Chin, Jennifer, Chong, Jessica X., Cornejo, Rodolfo, Davis, Colleen P., Frazar, Christopher, He, Zongxiao, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Kolar, Tom, Krauter, Stephanie A., Luksic, Daniel, Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Robertson, Peggy D., Santos-Cortez, Regie, Shankar, Aditi, Slattery, Krystal, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Tackett, Monica, Wang, Gao, Wegener, Marc, Weiss, Jeffrey M., Wernick, Riana I., Wheeler, Marsha M., Yi, Qian, Kraoua, Ichraf, Panteghini, Celeste, Valletta, Lorella, Garavaglia, Barbara, Cowley, Mark J., Gayevskiy, Velimir, Roscioli, Tony, Silberstein, Jonathon M., Hoffmann, Chen, Raas-Rothschild, Annick, Tiranti, Valeria, Anikster, Yair, Christodoulou, John, Kastaniotis, Alexander J., Ben-Zeev, Bruria, Hayflick, Susan J.

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A D2O detector for flux normalization of a pion decay-at-rest neutrino source by Akimov, D., An, P., Awe, C., Barbeau, P.S., Becker, B., Belov, V., Bernardi, I., Blackston, M.A., Bolozdynya, A., Cabrera-Palmer, B., Chernyak, D., Conley, E., Daughhetee, J., Day, E., Detwiler, J., Ding, K., Durand, M.R., Efremenko, Y., Elliott, S.R., Fabris, L., Febbraro, M., Gallo Rosso, A., Galindo-Uribarri, A., Green, M.P., Heath, M.R., Hedges, S., Hoang, D., Hughes, M., Johnson, T., Khromov, A., Konovalov, A., Koros, J., Kozlova, E., Kumpan, A., Li, L., Link, J.M., Liu, J., Mann, K., Markoff, D.M., Mastroberti, J., Mueller, P.E., Newby, J., Parno, D.S., Penttila, S.I., Pershey, D., Rapp, R., Ray, H., Raybern, J., Razuvaeva, O., Reyna, D., Rich, G.C., Ross, J., Rudik, D., Runge, J., Salvat, D.J., Salyapongse, A.M., Scholberg, K., Shakirov, A., Simakov, G., Sinev, G., Snow, W.M., Sosnovstsev, V., Suh, B., Tayloe, R., Tellez-Giron-Flores, K., Tolstukhin, I., Ujah, E., Vanderwerp, J., Varner, R.L., Virtue, C.J., Visser, G., Ward, E.M., Wiseman, C., Wongjirad, T., Yen, Y.-R., Yoo, J., Yu, C.-H., Zettlemoyer, J.

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment by Schrauwen, Isabelle, Chakchouk, Imen, Acharya, Anushree, Liaqat, Khurram, Irfanullah, Nickerson, Deborah A, Bamshad, Michael J, Shah, Khadim, Ahmad, Wasim, Leal, Suzanne M

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