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Chen, Zhongbo ORCID: 0000-0001-6668-7202, Zhang, David, Reynolds, Regina H ORCID: 0000-0001-6470-7919, Gustavsson, Emil K ORCID: 0000-0003-0541-7537, García-Ruiz, Sonia, D'Sa, Karishma, Fairbrother-Browne, Aine ORCID: 0000-0002-7196-1410, Vandrovcova, Jana, International Parkinson’s Disease Genomics Consortium (IPDGC), , Hardy, John ORCID: 0000-0002-3122-0423 et al (show 4 more authors) , Houlden, Henry ORCID: 0000-0002-2866-7777, Gagliano Taliun, Sarah A ORCID: 0000-0003-1306-1868, Botía, Juan and Ryten, Mina ORCID: 0000-0001-9520-6957 (2021) Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage. Nature communications, 12 (1). 2076-.

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Billingsley, Kimberley J, Barbosa, Ines A, Bandres-Ciga, Sara, Quinn, John P ORCID: 0000-0003-3551-7803, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Deshpande, Charu, Botia, Juan A, Reynolds, Regina H, Zhang, David, Simpson, Michael A et al (show 136 more authors) , Blauwendraat, Cornelis, Gan-Or, Ziv, Gibbs, J Raphael, Nalls, Mike A, Singleton, Andrew, Ryten, Mina, Koks, Sulev ORCID: 0000-0001-6087-6643, Noyce, A, Tucci, A, Middlehurst, B, Kia, D, Tan, M, Houlden, H, Morris, HR, Plun-Favreau, H, Holmans, P, Hardy, J, Trabzuni, D, Bras, J, Mok, K, Kinghorn, K, Wood, N, Lewis, P, Guerreiro, R, Loverin, R, R'Bibo, L, Rizig, M, Escott-Price, V, Chelban, V, Foltynie, T, Williams, N, Brice, A, Danjou, F, Lesage, S, Martinez, M, Giri, A, Schulte, C, Brockmann, K, Simon-Sanchez, J, Heutink, P, Rizzu, P, Sharma, M, Gasser, T, Nicolas, A, Cookson, M, Faghri, F, Hernandez, D, Shulman, J, Robak, L, Lubbe, S, Finkbeiner, S, Mencacci, N, Lungu, C, Scholz, S, Reed, X, Leonard, H, Rouleau, G, Krohan, L, van Hilten, J, Marinus, J, Adarmes-Gomez, A, Aguilar, M, Alvarez, I, Alvarez, V, Javier Barrero, F, Bergareche Yarza, J, Bernal-Bernal, I, Blazquez, M, Bonilla-Toribio Bernal, M, Boungiorne, M, Buiza-Rueda, Dolores, Camara, A, Carcel, M, Carrillo, F, Carrion-Claro, M, Cerdan, D, Clarimon, J, Compta, Y, Diez-Fairen, M, Dols-Icardo, O, Duarte, J, Duran, RI, Escamilla-Sevilla, F, Ezquerra, M, Fernandez, M, Fernandez-Santiago, R, Garcia, C, Garcia-Ruiz, P, Gomez-Garre, P, Gomez Heredia, M, Gonzalez-Aramburu, I, Gorostidi Pagola, A, Hoenicka, J, Infante, J, Jesus, S, Jimenez-Escrig, A, Kulisevsky, J, Labrador-Espinosa, M, Lopez-Sendon, J, de Munain Arregui, A Lopez, Macias, D, Martinez Torres, I, Marin, J, Jose Marti, M, Martinez-Castrillo, J, Mendez-del-Barrio, C, Menendez Gonzalez, M, Minguez, A, Mir, P, Mondragon Rezola, E, Munoz, E, Pagonabarraga, J, Pastor, P, Perez Errazquin, F, Perinan-Tocino, T, Ruiz-Martinez, J, Ruz, C, Sanchez Rodriguez, A, Sierra, M, Suarez-Sanmartin, E, Tabernero, C, Pablo Tartari, J, Tejera-Parrado, C, Tolosa, E, Valldeoriola, F, Vargas-Gonzalez, L, Vela, L, Vives, F, Zimprich, A, Pihlstrom, L, Taba, P, Majamaa, K, Siitonen, A, Okubadejo, N, Ojo, O and IPDGC, (2019) Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. NPJ PARKINSONS DISEASE, 5 (1). 8-.

Quinn, JP ORCID: 0000-0003-3551-7803, Billingsley, Kimberley, Reynolds, Regina H, Botia, Juan, Nalls, Mike A, Hardy, John, Gagliano Taliun, Sarah A and Ryten, Mina (2019) Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability. npj Parkinson's Disease, 5 (1). 6-.

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Guelfi, Sebastian, D'Sa, Karishma, Botía, Juan A, Vandrovcova, Jana, Reynolds, Regina H, Zhang, David, Trabzuni, Daniah, Collado-Torres, Leonardo, Thomason, Andrew, Quijada Leyton, Pedro et al (show 10 more authors) , Gagliano Taliun, Sarah A, Nalls, Mike A, International Parkinson’s Disease Genomics Consortium (IPDGC), , UK Brain Expression Consortium (UKBEC), , Small, Kerrin S, Smith, Colin, Ramasamy, Adaikalavan, Hardy, John, Weale, Michael E and Ryten, Mina (2020) Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information. Nature communications, 11 (1). 1041-.

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Jabbari, Edwin, Woodside, John, Tan, Manuela MX, Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y, Zhang, David, Reynolds, Regina H, de Silva, Rohan et al (show 13 more authors) , Grimm, Max-Joseph, Respondek, Gesine, Mueller, Ulrich, Al-Sarraj, Safa, Gentleman, Stephen M, Lees, Andrew J ORCID: 0000-0002-2476-4385, Warner, Thomas T, Hardy, John, Revesz, Tamas, Hoeglinger, Guenter U, Holton, Janice L, Ryten, Mina and Morris, Huw R (2018) Variation at the <i>TRIM11</i> locus modifies progressive supranuclear palsy phenotype. ANNALS OF NEUROLOGY, 84 (4). pp. 485-496.

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Altmann, Andre, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa, Tolomeo, Daniele, Reynolds, Regina H, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo et al (show 90 more authors) , Di Sapia, Rossella, Cerovic, Milica, Palma, Eleonora, Ruffolo, Gabriele, Botía, Juan A, Absil, Julie, Alhusaini, Saud, Alvim, Marina KM, Auvinen, Pia, Bargallo, Nuria, Bartolini, Emanuele, Bender, Benjamin, Bergo, Felipe PG, Bernardes, Tauana, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris C, Blackmon, Karen, Braga, Barbara, Caligiuri, Maria Eugenia, Calvo, Anna, Carlson, Chad, Carr, Sarah J, Cavalleri, Gianpiero L, Cendes, Fernando, Chen, Jian, Chen, Shuai, Cherubini, Andrea, Concha, Luis, David, Philippe, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin P, Domin, Martin, Focke, Niels K, Foley, Sonya, Franca, Wendy, Gambardella, Antonio, Guerrini, Renzo, Hamandi, Khalid, Hibar, Derrek P, Isaev, Dmitry, Jackson, Graeme D, Jahanshad, Neda, Kalviainen, Reetta, Keller, Simon S ORCID: 0000-0001-5247-9795, Kochunov, Peter, Kotikalapudi, Raviteja, Kowalczyk, Magdalena A, Kuzniecky, Ruben, Kwan, Patrick, Labate, Angelo, Langner, Soenke, Lenge, Matteo, Liu, Min, Martin, Pascal, Mascalchi, Mario, Meletti, Stefano, Morita‐Sherman, Marcia E, O'Brien, Terence J, Pariente, Jose C, Richardson, Mark P, Rodriguez‐Cruces, Raul, Rummel, Christian, Saavalainen, Taavi, Semmelroch, Mira K, Severino, Mariasavina, Striano, Pasquale, Thesen, Thomas, Thomas, Rhys H, Tondelli, Manuela, Tortora, Domenico, Vaudano, Anna Elisabetta, Vivash, Lucy, Podewils, Felix, Wagner, Jan, Weber, Bernd, Wiest, Roland, Yasuda, Clarissa L, Zhang, Guohao, Zhang, Junsong, Leu, Costin, Avbersek, Andreja, Thom, Maria, Whelan, Christopher D, Thompson, Paul, McDonald, Carrie R, Vezzani, Annamaria and Sisodiya, Sanjay M (2022) A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies. Neuropathology and Applied Neurobiology, 48 (1). e12758-.