The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies von Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.‐A., Alam, A., Roncière, L., Spiegelman, D., Fon, E.A., Trempe, J.‐F., Kalia, L.V., Postuma, R.B., Dupre, N., Rivard, G.‐E., Assouline, S., Amato, D., Gan‐Or, Z.

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Is the endangered Grevy's zebra threatened by hybridization von Cordingley, J.E, Sundaresan, S.R, Fischhoff, I.R, Shapiro, B, Ruskey, J, Rubenstein, D.I

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Sequencing the entire exome of REM sleep behavior and progression to neurodegenerative diseases von Saini, P., Rudakou, U., Yu, E., Ruskey, J., Asayesh, F., Laurent, S., Spiegelman, D., Fahn, S., Waters, C., Monchi, O., Dauvilliers, Y., Dupré, N., Greenbaum, L., Hassin-Baer, S., Espay, A., Rouleau, G., Alcalay, R., Fon, E., Gan-Or, Z.

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Investigation of Autosomal Genetic Sex Differences in Parkinson's disease von Makarious, MB, Bandres-Ciga, S, Grenn, FP, Tan, M, Kim, JJ, Gibbs, JR, Pihlstrøm, L, Toft, M, van Hilten, JJ, Siitonen, A, Majamaa, K, Tienari, PJ, Corvol, J-C, Wood, N, Noyce, AJ, Middlehurst, B, Kia, DA, Houlden, H, Storm, CS, Trabzuni, D, Manzoni, C, Rizig, M, Ryten, M, Escott-Price, V, Foltynie, T, Williams, N, Morrison, KE, Clarke, C, Jacobs, BM, Danjou, F, Simón-Sánchez, J, Rizzu, P, Schneider, SA, Cookson, MR, Craig, DW, Leonard, HL, Lubbe, S, Troycoco, T, Reed, X, Ross, OA, Moore, A, Alcalay, RN, Wszolek, ZK, Mufti, K, Adarmes-Gómez, AD, Alvarez, I, Alvarez, V, Barrero, FJ, Bernal-Bernal, I, Bonilla-Toribio, M, Botía, JA, Boungiorno, MT, Buiza-Rueda, D, Carrillo, F, Carrión-Claro, M, Clarimón, J, Compta, Y, Diez-Fairen, M, Dols-Icardo, O, Duarte, J, Duran, R, Ezquerra, M, Garcia, C, García-Ruiz, P, Gómez-Garre, P, Pagola, AG, Infante, J, Jesús, S, Jimenez-Escrig, A, Labrador-Espinosa, MA, Lopez-Sendon, JL, de Munain Arregui, AL, Martínez-Castrillo, JC, Méndez-Del-Barrio, C, González, MM, Mínguez, A, Mir, P, Rezola, EM, Muñoz, E, Pagonabarraga, J, Periñán-Tocino, T, Ruz, C, Rodriguez, AS, Sierra, M, Suarez-Sanmartin, E, Tabernero, C, Tejera-Parrado, C, Valldeoriola, F, Vela, L, Vives, F, Zimprich, A, Pihlstrom, L, Hassin-Baer, S, Tienari, P, Ojo, OO, Zharkinbekova, N, Akhmetzhanov, V, Kaishybayeva, G, Karimova, A, Khaibullin, T

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Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease von Brown, EE, Blauwendraat, C, Trinh, J, Rizig, M, Nalls, MA, Leveille, E, Ruskey, JA, Jonvik, H, Tan, MMX, Bandres-Ciga, S, Hassin-Baer, S, Brockmann, K, Infante, J, Tolosa, E, Ezquerra, M, Ben Romdhan, S, Benmahdjoub, M, Arezki, M, Mhiri, C, Hardy, J, Singleton, AB, Alcalay, RN, Gasser, T, Grosset, DG, Williams, NM, Pittman, A, Gan-Or, Z, Fernandez-Santiago, R, Brice, A, Lesage, S, Farrer, M, Wood, N, Morris, HR, International Parkinson Disease Genomics Consortium (IPDGC)

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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia von Blauwendraat, C, Reed, X, Krohn, L, Heilbron, K, Bandres-Ciga, S, Tan, M, Gibbs, JR, Hernandez, DG, Kumaran, R, Langston, R, Bonet-Ponce, L, Alcalay, RN, Hassin-Baer, S, Greenbaum, L, Iwaki, H, Leonard, HL, Grenn, FP, Ruskey, JA, Sabir, M, Ahmed, S, Makarious, MB, Pihlstrøm, L, Toft, M, van Hilten, JJ, Marinus, J, Schulte, C, Brockmann, K, Sharma, M, Siitonen, A, Majamaa, K, Eerola-Rautio, J, Tienari, PJ, Team, TAR, Pantelyat, A, Hillis, AE, Dawson, TM, Rosenthal, LS, Albert, MS, Resnick, SM, Ferrucci, L, Morris, CM, Pletnikova, O, Troncoso, J, Grosset, D, Lesage, S, Corvol, J-C, Brice, A, Noyce, AJ, Masliah, E, Wood, N, Hardy, J, Shulman, LM, Jankovic, J, Shulman, JM, Heutink, P, Gasser, T, Cannon, P, Scholz, SW, Morris, H, Cookson, MR, Nalls, MA, Gan-Or, Z, Singleton, AB

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Unusual subclavian artery lacerations resulting from lap-shoulder seatbelt trauma: case reports von RUSKEY, J, LIEBERMAN, M. E, SHAIKH, K. A, TALUCCI, R. C

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Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease von Yu, Eric, Rudakou, Uladzislau, Krohn, Lynne, Mufti, Kheireddin, Ruskey, Jennifer A., Asayesh, Farnaz, Estiar, Mehrdad A., Spiegelman, Dan, Surface, Matthew, Fahn, Stanley, Waters, Cheryl H., Greenbaum, Lior, Espay, Alberto J., Dauvilliers, Yves, Dupré, Nicolas, Rouleau, Guy A., Hassin‐Baer, Sharon, Fon, Edward A., Alcalay, Roy N., Gan‐Or, Ziv

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SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease von Alcalay, Roy N., Mallett, Victoria, Vanderperre, Benoît, Tavassoly, Omid, Dauvilliers, Yves, Wu, Richard Y.J., Ruskey, Jennifer A., Leblond, Claire S., Ambalavanan, Amirthagowri, Laurent, Sandra B., Spiegelman, Dan, Dionne‐Laporte, Alexandre, Liong, Christopher, Levy, Oren A., Fahn, Stanley, Waters, Cheryl, Kuo, Sheng‐Han, Chung, Wendy K., Ford, Blair, Marder, Karen S., Kang, Un Jung, Hassin‐Baer, Sharon, Greenbaum, Lior, Trempe, Jean‐Francois, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Clark, Lorraine N., Langlois, Melanie, Dion, Patrick A., Fon, Edward A., Dupre, Nicolas, Rouleau, Guy A., Gan‐Or, Ziv

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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia von Blauwendraat, Cornelis, Reed, Xylena, Krohn, Lynne, Heilbron, Karl, Bandres-Ciga, Sara, Tan, Manuela, Gibbs, J. Raphael, Hernandez, Dena G., Kumaran, Ravindran, Langston, Rebekah, Bonet-Ponce, Luis, Alcalay, Roy N., Hassin-Baer, Sharon, Greenbaum, Lior, Iwaki, Hirotaka, Leonard, Hampton L., Grenn, Francis P., Ruskey, Jennifer A., Sabir, Marya, Ahmed, Sarah, Makarious, Mary B., Pihlstrom, Lasse, Toft, Mathias, van Hilten, Jacobus J., Marinus, Johan, Schulte, Claudia, Brockmann, Kathrin, Sharma, Manu, Siitonen, Ari, Majamaa, Kari, Eerola-Rautio, Johanna, Tienari, Pentti J., Pantelyat, Alexander, Hillis, Argye E., Dawson, Ted M., Rosenthal, Liana S., Albert, Marilyn S., Resnick, Susan M., Ferrucci, Luigi, Morris, Christopher M., Pletnikova, Olga, Troncoso, Juan, Grosset, Donald, Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, Noyce, Alastair J., Masliah, Eliezer, Wood, Nick, Hardy, John, Shulman, Lisa M., Jankovic, Joseph, Shulman, Joshua M., Heutink, Peter, Gasser, Thomas, Cannon, Paul, Scholz, Sonja W., Morris, Huw, Cookson, Mark R., Nalls, Mike A., Gan-Or, Ziv, Singleton, Andrew B.

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Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies von Krohn, Lynne, Wu, Richard Y. J., Heilbron, Karl, Ruskey, Jennifer A., Laurent, Sandra B., Blauwendraat, Cornelis, Alam, Armaghan, Arnulf, Isabelle, Hu, Michele T. M., Dauvilliers, Yves, Högl, Birgit, Toft, Mathias, Bjørnarå, Kari Anne, Stefani, Ambra, Holzknecht, Evi, Monaca, Christelle Charley, Abril, Beatriz, Plazzi, Giuseppe, Antelmi, Elena, Ferini‐Strambi, Luigi, Young, Peter, Heidbreder, Anna, Cochen De Cock, Valérie, Mollenhauer, Brit, Sixel‐Döring, Friederike, Trenkwalder, Claudia, Sonka, Karel, Kemlink, David, Figorilli, Michela, Puligheddu, Monica, Dijkstra, Femke, Viaene, Mineke, Oertel, Wolfang, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Gagnon, Jean‐François, Nalls, Mike A., Singleton, Andrew B., Desautels, Alex, Montplaisir, Jacques Y., Cannon, Paul, Ross, Owen A., Boeve, Bradley F., Dupré, Nicolas, Fon, Edward A., Postuma, Ronald B., Pihlstrøm, Lasse, Rouleau, Guy A., Gan‐Or, Ziv

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Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease von Saini, Prabhjyot, Rudakou, Uladzislau, Yu, Eric, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Espay, Alberto J., Rouleau, Guy A., Alcalay, Roy N., Fon, Edward A., Postuma, Ronald B., Gan-Or, Ziv

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Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease von Ouled Amar Bencheikh, Bouchra, Senkevich, Konstantin, Rudakou, Uladzislau, Yu, Eric, Mufti, Kheireddin, Ruskey, Jennifer A., Asayesh, Farnaz, Laurent, Sandra B., Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Espay, Alberto J., Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Rouleau, Guy A., Alcalay, Roy N., Fon, Edward A., Gan-Or, Ziv

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Common X‐Chromosome Variants Are Associated with Parkinson Disease Risk von Le Guen, Yann, Napolioni, Valerio, Belloy, Michael E., Yu, Eric, Krohn, Lynne, Ruskey, Jennifer A., Gan‐Or, Ziv, Kennedy, Gabriel, Eger, Sarah J., Greicius, Michael D.

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Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder von Li, Jiao, Ruskey, Jennifer A., Arnulf, Isabelle, Dauvilliers, Yves, Hu, Michele T.M., Högl, Birgit, Leblond, Claire S., Zhou, Sirui, Ambalavanan, Amirthagowri, Ross, Jay P., Bourassa, Cynthia V., Spiegelman, Dan, Laurent, Sandra B, Stefani, Ambra, Charley Monaca, Christelle, Cochen De Cock, Valérie, Boivin, Michel, Ferini‐Strambi, Luigi, Plazzi, Giuseppe, Antelmi, Elena, Young, Peter, Heidbreder, Anna, Labbe, Catherine, Ferman, Tanis J., Dion, Patrick A., Fan, Dongsheng, Desautels, Alex, Gagnon, Jean‐François, Dupré, Nicolas, Fon, Edward A., Montplaisir, Jacques Y., Boeve, Bradley F., Postuma, Ronald B., Rouleau, Guy A., Ross, Owen A., Gan‐Or, Ziv

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Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease von Blauwendraat, Cornelis, Iwaki, Hirotaka, Makarious, Mary B., Grenn, Francis P., Lake, Julie, Krohn, Lynne, Kim, Jonggeol J., Gibbs, Jesse R., Toft, Mathias, Schulte, Claudia, Brockmann, Kathrin, Majamaa, Kari, Grosset, Donald G., Gan‐Or, Ziv, Morris, Huw R., Noyce, Alastair J., Nalls, Mike A., Middlehurst, Ben, Kia, Demis A., Storm, Catherine S., Hardy, John, Mok, Kin Y., Kinghorn, Kerri J., Wood, Nicholas W., Lewis, Patrick, R'Bibo, Lea, Manzoni, Claudia, Rizig, Mie, Guelfi, Sebastian, Chelban, Viorica, Williams, Nigel, Morrison, Karen E., Harvey, Kirsten, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Corvol, Jean‐Christophe, Sharma, Manu, Schneider, Susanne A., Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Billingsley, Kimberley, Makarious, Mary B., Hernandez, Dena G., Shulman, Joshua M., Iwaki, Hirotaka, Leonard, Hampton L., Nalls, Mike A., Troycoco, Timothy, Mencacci, Niccolo E., Scholz, Sonja W., Ross, Owen A., Moore, Anni, Alcalay, Roy N., Gan‐Or, Ziv, Krohn, Lynne, Mufti, Kheireddin, Hilten, Jacobus J., Alvarez, Ignacio, Alvarez, Victoria, Barrero, Francisco Javier, Bernal‐Bernal, Inmaculada, Bonilla‐Toribio, Marta, Boungiorno, María Teresa, Buiza‐Rueda, Dolores, Carrillo, Fátima, Dols‐Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla‐Sevilla, Francisco, Fernández‐Santiago, Rubén, Gómez‐Garre, Pilar, Heredia, Maria Jose Gomez, Pagola, Ana Gorostidi, Hoenicka, Janet, Kulisevsky, Jaime, Munain Arregui, Adolfo López, Macias, Daniel, Torres, Irene Martínez, Marín, Juan, Marti, Maria Jose, Martínez‐Castrillo, Juan Carlos, Mir, Pablo, Rezola, Elisabet Mondragon, Muñoz, Esteban, Pastor, Pau, Errazquin, Francisco Perez, Sierra, María, Suarez‐Sanmartin, Esther, Tabernero, Cesar, Valldeoriola, Francesc, Vela, Lydia, Vives, Francisco, Koks, Sulev, Hassin‐Baer, Sharon, Okubadejo, Njideka U., Ojo, Oluwadamilola O., Kaiyrzhanov, Rauan, Akhmetzhanov, Vadim, Lynch, Timothy L.

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GBA variants in REM sleep behavior disorder: A multicenter study von Krohn, Lynne, Ruskey, Jennifer A., Rudakou, Uladzislau, Leveille, Etienne, Asayesh, Farnaz, Hu, Michele T.M., Arnulf, Isabelle, Dauvilliers, Yves, Högl, Birgit, Stefani, Ambra, Monaca, Christelle Charley, Abril, Beatriz, Plazzi, Giuseppe, Antelmi, Elena, Ferini-Strambi, Luigi, Heidbreder, Anna, Boeve, Bradley F., Espay, Alberto J., De Cock, Valérie Cochen, Mollenhauer, Brit, Sixel-Döring, Friederike, Trenkwalder, Claudia, Sonka, Karel, Kemlink, David, Figorilli, Michela, Puligheddu, Monica, Dijkstra, Femke, Viaene, Mineke, Oertel, Wolfgang, Toffoli, Marco, Gigli, Gian Luigi, Valente, Mariarosaria, Gagnon, Jean-François, Desautels, Alex, Montplaisir, Jacques Y., Postuma, Ronald B., Rouleau, Guy A., Gan-Or, Ziv

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Unusual Subclavian Artery Lacerations Resulting from Lap-Shoulder Seatbelt Trauma: Case Reports von RUSKEY, J., LIEBERMAN, M. E., SHAIKH, K. A., TALUCCI, R. C.

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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects von Krohn, Lynne, Heilbron, Karl, Blauwendraat, Cornelis, Reynolds, Regina H., Yu, Eric, Senkevich, Konstantin, Rudakou, Uladzislau, Estiar, Mehrdad A., Gustavsson, Emil K., Brolin, Kajsa, Ruskey, Jennifer A., Freeman, Kathryn, Asayesh, Farnaz, Chia, Ruth, Arnulf, Isabelle, Hu, Michele T. M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Biscarini, Francesco, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Scholz, Sonja W., Ryten, Mina, Bandres-Ciga, Sara, Noyce, Alastair, Cannon, Paul, Pihlstrøm, Lasse, Nalls, Mike A., Singleton, Andrew B., Rouleau, Guy A., Postuma, Ronald B., Gan-Or, Ziv

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STRAW (STRings for Absorption length in Water): pathfinder for a neutrino telescope in the deep Pacific Ocean von Boehmer, M., Bosma, J., Brussow, D., Farmer, L., Fruck, C., Gernhäuser, R., Gärtner, A., Grant, D., Henningsen, F., Hiller, S., Hoch, M., Holzapfel, K., Jenkyns, R., Khera, Na, Khera, Ni, Krings, K., Kopper, C., Kulin, I., Leismüller, K., Little, J., Macoun, P., Michel, J., Morley, M., Papp, L., Pirenne, B., Qiu, C., Rea, I. C., Resconi, E., Round, A., Ruskey, A., Spannfellner, C., Traxler, M.

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