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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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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-.

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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.