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Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihistrom, Lasse, Guerreiro, Rita, Gibbs, J Raphael, Sabir, Marya, Ahmed, Sarah et al (show 19 more authors) , Ding, Jinhui, Alcalay, Roy N, Hassin-Baer, Sharon, Pittman, Alan M, Brooks, Janet, Edsall, Connor, Hernandez, Dena G, Chung, Sun Ju, Goldwurm, Stefano, Toft, Mathias, Schulte, Claudia, Bras, Jose, Wood, Nicholas W, Brice, Alexis, Morris, Huw R, Scholz, Sonja W, Nalls, Mike A, Singleton, Andrew B and Cookson, Mark R (2018) Frequency of Loss of Function Variants in <i>LRRK2</i> in Parkinson Disease. JAMA NEUROLOGY, 75 (11). pp. 1416-1422.

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Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M, Brady, Stefen, Holton, Janice L, Pittman, Alan M ORCID: 0000-0002-8112-2987, Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David et al (show 20 more authors) , Shieh, Perry B, Needham, Merrilee, Liang, Christina, Zanoteli, Edmar, de Camargo, Leonardo Valente, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J, Dimachkie, Mazen M, Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Singleton, Andrew B, Hanna, Michael G, Houlden, Henry and Muscle Study Group and The International IBM Genetics Consortium, (2016) Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. Neurobiology of aging, 47. 218.e1-218.e9.