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Mencacci, Niccolo E, Reynolds, Regina, Ruiz, Sonia Garcia, Vandrovcova, Jana, Forabosco, Paola, Sanchez-Ferrer, Alvaro, Volpato, Viola, Weale, Michael E, Bhatia, Kailash P, Webber, Caleb et al (show 3 more authors) , Hardy, John, Botia, Juan A and Ryten, Mina (2020) Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders. BRAIN, 143 (9). pp. 2771-2787.

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Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753 et al (show 8 more authors) , Blauwendraat, Cornelis, Gan-Or, Ziv, Gibbs, Raphael ORCID: 0000-0002-6985-0658, Nalls, Mike, Singleton, Andrew, Ryten, Mina, Koks, Sulev ORCID: 0000-0001-6087-6643 and International Parkinson’s Disease Genomics Consortium (IPDGC), (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv.

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Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa ORCID: 0000-0002-9578-018X, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo et al (show 88 more authors) , Botía, Juan, Absil, Julie, Alhusaini, Saud, Alvim, Marina, Auvinen, Pia, Bargallo, Nuria, Bartolini, Emanuele ORCID: 0000-0002-5683-1941, Bender, Benjamin, Bergo, Felipe, Bernardes, Tauana, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris, Blackmon, Karen, Braga, Barbara, Caligiuri, Maria Eugenia ORCID: 0000-0002-2030-5552, Calvo, Anna, Carlson, Chad, Carr, Sarah, Cavalleri, Gianpiero, Cendes, Fernando, Chen, Jian, Chen, Shuai, Cherubini, Andrea, Concha, Luis, David, Philippe, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin, Domin, Martin, Focke, Niels, Foley, Sonya, Franca, Wendy, Gambardella, Antonio ORCID: 0000-0001-7384-3074, Guerrini, Renzo, Hamandi, Khalid, Hibar, Derrek, Isaev, Dmitry ORCID: 0000-0001-9149-0479, Jackson, Graeme, Jahanshad, Neda, Kalviainen, Reetta, Keller, Simon ORCID: 0000-0001-5247-9795, Kochunov, Peter, Kotikalapudi, Raviteja, Kowalczyk, Magdalena ORCID: 0000-0002-5410-0299, Kuzniecky, Ruben, Kwan, Patrick, Labate, Angelo, Langner, Soenke, Lenge, Matteo, Liu, Min, Martin, Pascal, Mascalchi, Mario, Meletti, Stefano ORCID: 0000-0003-0334-539X, Morita, Marcia, O’Brien, Terence, Pariente, Jose, Richardson, Mark, Rodriguez-Cruces, Raul, Rummel, Christian ORCID: 0000-0003-2345-7938, Saavalainen, Taavi, Semmelroch, Mira, Severino, Mariasavina, Striano, Pasquale, Thesen, Thomas, Thomas, Rhys ORCID: 0000-0003-2062-8623, Tondelli, Manuela, Tortora, Domenico, Vaudano, Anna Elisabetta, Vivash, Lucy ORCID: 0000-0002-1182-0907, von Podewils, Felix, Wagner, Jan, Weber, Bernd, Wiest, Roland, Yasuda, Clarissa, Zhang, Guohao, Zhang, Junsong, Leu, Costin ORCID: 0000-0003-0598-3301, Avbersek, Andreja, Thorn, Maria, Whelan, Christopher ORCID: 0000-0003-0308-5583, Thompson, Paul, McDonald, Carrie, Vezzani, Annamaria ORCID: 0000-0003-0573-6175, Sisodiya, Sanjay, ENIGMA-Epilepsy Working Group, and EpiPGX Consortium, (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy. Unknown.