Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2) by Furtado, Sarah, Payami, Haydeh, Lockhart, Paul J., Hanson, Melissa, Nutt, John G., Singleton, Andrew A., Singleton, Amanda, Bower, Jamel, Utti, Ryan J., Bird, Thomas D., de la Fuente-Fernandez, Raul, Tsuboi, Yoshio, Klimek, Mary L., Suchowersky, Oksana, Hardy, John, Calne, Donald B., Wszolek, Zbigniew K., Farrer, Matthew, Gwinn-Hardy, Katrina, Stoessl, A. Jon

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Blood and Marrow Transplant Clinical Trials Network Study 1102 heralds a new era in hematopoietic cell transplantation in high‐risk myelodysplastic syndromes: Challenges and opport... by Warlick, Erica D., Ustun, Celalettin, Andreescu, Astrid, Bonagura, Anthony F., Brunner, Andrew, Chandra, Abhinav B., Foran, James M., Juckett, Mark B., Kindwall‐Keller, Tamila L., Klimek, Virginia M., Pease, Daniel F., Steensma, David P., Waldman, Bryce M., Horowitz, Mary M., Burns, Linda J., Khera, Nandita

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Is diet partly responsible for differences in COVID‐19 death rates between and within countries? by Bousquet, Jean, Anto, Josep M., Haahtela, Tari, Cruz, Alvaro A., Aldrey‐Palacios, Oscar, Anto, Josep, Arshad, Hasan, Avolio, Francesca, Azhari, Khuzama, Balotro‐Torres, Christine, Bedbrook, Anna, Bieber, Thomas, Blain, Hubert, Bochenska Marciniak, Malgorzata, Bousquet, Philippe, Braido, Fulvio, Busse, William W., Buters, Jeroen, Caballero‐Fonseca, Fernan, Cano, Antonio, Caraballo, Luis, Caro, Jorge, Chandrasekharan, Ramanathan, Chen, Yuzhi, Chua, Antonio, Chung, Kian Fan, Cingi, Cemal, Coste, André, Custovic, Adnan, Daniilidis, Vasilis, De Guia, Eloisa, Didier, Alain, Djukanovic, Ratko, Dykewicz, Mark, El‐Sayed, Zeinab A., Espinoza, Heidilita, García Cruz, María de la Luz Hortensia, Gayraud, Jacques, Gerth van Wijk, Roy, Iaccarino, Guido, Jiméneracruz Uscanga, Rubén Darío, Johnston, Sebastian, Kardas, Przemyslaw, Kleine‐Tebbe, Jorg, Koffi N'Goran, Bernard, Kompoti, Evangelia, Kopač, Peter, Kraxner, Helga, Kritikos, Vicky, Lalek, Nika, Larenas‐Linnemann, Désiree, Lavrut, Jorge, Le, Lan, Loukidis, Stelios, Madjar, Bojan, Matta Campos, Juan José, Melén, Erik, Merk, Hans, Mogica Martínez, María Dolores, Mohammad, Yousser, Monaco, Alessandro, Montefort, Steve, Mösges, Ralph, Mullol, Joaquim, Nicod, Laurent, Ouoba, Kampadilemba, Palkonen, Susanna, Palmer, Stephen, Panaitescu Bunu, Carmen, Panzner, Petr, Papi, Alberto, Paralchev, Bojidar, Pohl, Wolfgang, Poulsen, Lars, Puy, Robert, Rabe, Klaus, Reider, Norbert, Rodríguez González, Mónica, Ruiz, Mauricio, Sakai, Daiki, Saleh, Wafaa, Sastre‐Dominguez, Joaquin, Serrano, Elie, Shields, Mike, Sutherland, Michael, Sylvestre, Silvia, Takovska, Nadejda, To, Teresa, Todo‐Bom, Ana Maria, Toskala, Elina, Ulmeanu, Ruxandra, Urbancic, Jure, Valovirta, Erkka, Vera‐Munoz, Cécilia, Woo, Kent, Yoshihara, Shigemi, Young, Ian, Zaitoun, Fares, Zidarn, Mihaela, Zubrinich, Celia

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Perceptions of genetic discrimination among people at risk for Huntington’s disease: a cross sectional survey by Bombard, Yvonne, Veenstra, Gerry, Friedman, Jan M, Creighton, Susan, Currie, Lauren, Paulsen, Jane S, Bottorff, Joan L, Hayden, Michael R

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The Educational Needs and Professional Roles of Canadian Physicians and Nurses regarding Genetic Testing and Adult Onset Hereditary Disease by Bottorff, Joan L., Blaine, Sean, Carroll, June C., Esplen, Mary Jane, Evans, Jane, Klimek, Mary Lou Nicolson, Meschino, Wendy, Ritvo, Paul

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Beyond the patient: The broader impact of genetic discrimination among individuals at risk of Huntington disease by Bombard, Yvonne, Palin, JoAnne, Friedman, Jan M., Veenstra, Gerry, Creighton, Susan, Bottorff, Joan L., Hayden, Michael R.

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Mutation Profiling of Therapy-Related Myeloid Neoplasms Using Next-Generation Sequencing Demonstrates Distinct Profiles from De Novo Disease by Shih, Alan H., Rapaport, Franck, Chung, Stephen S., Dolezal, Emily K, Hobson, Sean, Amato, Mary K, Park, Christopher Y., Sekeres, Mikkael A., van den Brink, Marcel R.M., Nimer, Stephen, Levine, Ross L., Maciejewski, Jaroslaw P., Klimek, Virginia M.

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Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study by Li, Jian-Liang, Hayden, Michael R, Warby, Simon C, Durr, Alexandra, Morrison, Patrick J, Nance, Martha, Ross, Christopher A, Margolis, Russell L, Rosenblatt, Adam, Squitieri, Ferdinando, Frati, Luigi, Gómez-Tortosa, Estrella, García, Carmen Ayuso, Suchowersky, Oksana, Klimek, Mary Lou, Trent, Ronald J A, McCusker, Elizabeth, Novelletto, Andrea, Frontali, Marina, Paulsen, Jane S, Jones, Randi, Ashizawa, Tetsuo, Lazzarini, Alice, Wheeler, Vanessa C, Prakash, Ranjana, Xu, Gang, Djoussé, Luc, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, Hakky, Michael, Cupples, L Adrienne, Saint-Hilaire, Marie H, Cha, Jang-Ho J, Hersch, Steven M, Penney, John B, Harrison, Madaline B, Perlman, Susan L, Zanko, Andrea, Abramson, Ruth K, Lechich, Anthony J, Duckett, Ayana, Marder, Karen, Conneally, P Michael, Gusella, James F, MacDonald, Marcy E, Myers, Richard H

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Factors associated with experiences of genetic discrimination among individuals at risk for huntington disease by Bombard, Yvonne, Palin, JoAnne, Friedman, Jan M., Veenstra, Gerry, Creighton, Susan, Paulsen, Jane S., Bottorff, Joan L., Hayden, Michael R.

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