Number of items: 16.
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Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J, Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B, Casey, Bradford, Vitale, Dan et al (show 14 more authors) , Levine, Kristin, Leonard, Hampton, Pantazis, Caroline B, Screven, Laurel A, Hernandez, Dena G, Wegel, Claire E, Solle, Justin, Nalls, Mike A, Blauwendraat, Cornelis, Singleton, Andrew B, Tan, Manuela MX, Iwaki, Hirotaka, Morris, Huw R and Global Parkinson’s Genetics Program (GP2),
(2023)
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
NPJ Parkinson's disease, 9 (1).
p. 131.
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Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa et al (show 23 more authors) , Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A ORCID: 0000-0002-6992-598X, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K ORCID: 0000-0003-2991-6402, Li, Yarong, Yogi, Puja, Amin, Najaf ORCID: 0000-0002-8944-1771, van Duijn, Cornelia M ORCID: 0000-0002-2374-9204, International Parkinson’s Disease Genetics Consortium (IPGDC), , Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C ORCID: 0000-0001-8597-9470, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M and Heutink, Peter
(2017)
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
Genome biology, 18 (1).
22-.
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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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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.
475111-.
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Billingsley, Kimberley J, Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P, Makarious, Mary B, Moore, Anni, Vitale, Daniel, Reed, Xylena et al (show 31 more authors) , Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, UK Brain Expression Consortium UKBEC, Ruth, Chia, Ruth W, Scholz, Sonja J, Traynor, Bryan L, Dalgard, Clifton J, Ehrlich, Debra, Tanaka, Toshiko, Ferrucci, Luigi G, Beach, Thomas E, Serrano, Geidy P, Quinn, John J, Bubb, Vivien ORCID: 0000-0003-2763-7004, Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce-Hoffman, Emma, Brand, Harrison E, Talkowski, Michael, Casey, Bradford, Cookson, Mark R, Markham, Androo A, Nalls, Mike, Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J Raphael B and Singleton, Andrew
(2023)
Genome-Wide Analysis of Structural Variants in Parkinson Disease.
ANNALS OF NEUROLOGY, 93 (5).
pp. 1012-1022.
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Grover, Sandeep, Kumar Sreelatha, Ashwin Ashok, Pihlstrom, Lasse, Domenighetti, Cloe, Schulte, Claudia, Sugier, Pierre-Emmanuel, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Mohamed, Oceane, Portugal, Berta et al (show 73 more authors) , Landoulsi, Zied, May, Patrick, Bobbili, Dheeraj, Edsall, Connor, Bartusch, Felix, Hanussek, Maximilian, Krueger, Jens, Hernandez, Dena G, Blauwendraat, Cornelis, Mellick, George D, Zimprich, Alexander, Pirker, Walter, Tan, Manuela, Rogaeva, Ekaterina, Lang, Anthony, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie, Brockmann, Kathrin, Deutschlaender, Angela B, Hadjigeorgiou, Georges M, Dardiotis, Efthimos, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Burbulla, Lena F, Matsuo, Hirotaka, Kawamura, Yusuke, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Pavelka, Lukas, van de Warrenburg, Bart PC, Bloem, Bastiaan R, Singleton, Andrew B, Aasly, Jan, Toft, Mathias, Guedes, Leonor Correia, Ferreira, Joaquim J, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy L, Ran, Caroline, Belin, Andrea C, Puschmann, Andreas, Hellberg, Clara, Clarke, Carl E, Morrison, Karen E, Krainc, Dimitri, Farrer, Matt J, Kruger, Rejko, Elbaz, Alexis, Gasser, Thomas and Sharma, Manu
(2022)
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium.
NEUROLOGY, 99 (7).
E698-E710.
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Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli et al (show 260 more authors) , Bras, Jose, Young, Emily, von Coelln, Rainer, Simón-Sánchez, Javier, Schulte, Claudia, Sharma, Manu, Krohn, Lynne, Pihlstrøm, Lasse, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G, Scholz, Sonja W, Botia, Juan A, Martinez, Maria, Corvol, Jean-Christophe, Lesage, Suzanne, Jankovic, Joseph, Shulman, Lisa M, Sutherland, Margaret, Tienari, Pentti, Majamaa, Kari, Toft, Mathias, Andreassen, Ole A, Bangale, Tushar, Brice, Alexis, Yang, Jian, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Shulman, Joshua M, Wood, Nicholas W, Hinds, David A, Hardy, John A, Morris, Huw R, Gratten, Jacob, Visscher, Peter M, Graham, Robert R, Singleton, Andrew B, Adarmes-Gómez, Astrid D, Aguilar, Miquel, Aitkulova, Akbota, Akhmetzhanov, Vadim, Alcalay, Roy N, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Barrero, Francisco Javier, Bergareche Yarza, Jesús Alberto, Bernal-Bernal, Inmaculada, Billingsley, Kimberley, Blauwendraat, Cornelis, Blazquez, Marta, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Brice, Alexis, Brockmann, Kathrin, Bubb, Vivien ORCID: 0000-0003-2763-7004, Buiza-Rueda, Dolores, Cámara, Ana, Carrillo, Fátima, Carrión-Claro, Mario, Cerdan, Debora, Chelban, Viorica, Clarimón, Jordi, Clarke, Carl, Compta, Yaroslau, Cookson, Mark R, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla-Sevilla, Francisco, Escott-Price, Valentina, Ezquerra, Mario, Faghri, Faraz, Feliz, Cici, Fernández, Manel, Fernández-Santiago, Rubén, Finkbeiner, Steven, Foltynie, Thomas, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Gasser, Thomas, Gibbs, J Raphael, Gomez Heredia, Maria Jose, Gómez-Garre, Pilar, González, Manuel Menéndez, Gonzalez-Aramburu, Isabel, Guelfi, Sebastian, Guerreiro, Rita, Hardy, John, Hassin-Baer, Sharon, Hernandez, Dena G, Heutink, Peter, Hoenicka, Janet, Holmans, Peter, Houlden, Henry, Infante, Jon, Iwaki, Hirotaka, Jesús, Silvia, Jimenez-Escrig, Adriano, Kaishybayeva, Gulnaz, Kaiyrzhanov, Rauan, Karimova, Altynay, Kia, Demis A, Kinghorn, Kerri J, Koks, Sulev ORCID: 0000-0001-6087-6643, Krohn, Lynne, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A, Leonard, Hampton L, Lesage, Suzanne, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Lungu, Codrin, Macias, Daniel, Majamaa, Kari, Manzoni, Claudia, Marín, Juan, Marinus, Johan, Marti, Maria Jose, Martinez, Maria, Martínez Torres, Irene, Martínez-Castrillo, Juan Carlos, Mata, Marina, Mencacci, Niccolo E, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Mir, Pablo, Mok, Kin Y, Morris, Huw R, Muñoz, Esteban, Nalls, Mike A, Narendra, Derek, Noyce, Alastair J, Ojo, Oluwadamilola O, Okubadejo, Njideka U, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Pihlstrom, Lasse, Plun-Favreau, Helene, Quinn, John ORCID: 0000-0003-3551-7803, R'Bibo, Lea, Reed, Xylena, Rezola, Elisabet Mondragon, Rizig, Mie, Rizzu, Patrizia, Robak, Laurie, Rodriguez, Antonio Sanchez, Rouleau, Guy A, Ruiz-Martínez, Javier, Ruz, Clara, Ryten, Mina, Sadykova, Dinara, Scholz, Sonja W, Schreglmann, Sebastian, Schulte, Claudia, Sharma, Manu, Shashkin, Chingiz, Shulman, Joshua M, Sierra, María, Siitonen, Ari, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Taba, Pille, Tabernero, Cesar, Tan, Manuela X, Tartari, Juan Pablo, Tejera-Parrado, Cristina, Toft, Mathias, Tolosa, Eduard, Trabzuni, Daniah, Valldeoriola, Francesc, van Hilten, Jacobus J, Van Keuren-Jensen, Kendall, Vargas-González, Laura, Vela, Lydia, Vives, Francisco, Williams, Nigel, Wood, Nicholas W, Zharkinbekova, Nazira, Zharmukhanov, Zharkyn, Zholdybayeva, Elena, Zimprich, Alexander, Ylikotila, Pauli, Shulman, Lisa M, von Coelln, Rainer, Reich, Stephen, Savitt, Joseph, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Huber, Karen E, Hicks, Barry, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Noblin, Elizabeth S, Northover, Carrie AM, Pitts, Steven J, Poznik, G David, Sathirapongsasuti, J Fah, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce, Vacic, Vladimir, Wang, Xin, Wilson, Catherine H, Anderson, Tim, Bentley, Steven, Dalrymple-Alford, John, Fowdar, Javed, Gratten, Jacob, Halliday, Glenda, Henders, Anjali K, Hickie, Ian, Kassam, Irfahan, Kennedy, Martin, Kwok, John, Lewis, Simon, Mellick, George, Montgomery, Grant, Pearson, John, Pitcher, Toni, Sidorenko, Julia, Silburn, Peter A, Vallerga, Costanza L, Visscher, Peter M, Wallace, Leanne, Wray, Naomi R, Xue, Angli, Yang, Jian and Zhang, Futao
(2019)
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
The Lancet Neurology, 18 (12).
pp. 1091-1102.
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Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Makarious, Mary B, Bandres-Ciga, Sara, Leonard, Hampton L, Grenn, Francis P, Lake, Julie ORCID: 0000-0002-3441-2455, Krohn, Lynne ORCID: 0000-0001-6554-1666, Tan, Manuela, Kim, Jonggeol J et al (show 28 more authors) , Gibbs, Jesse R, Hernandez, Dena G, Ruskey, Jennifer A, Pihlstrøm, Lasse ORCID: 0000-0002-7635-8645, Toft, Mathias ORCID: 0000-0002-6723-6865, van Hilten, Jacobus J, Marinus, Johan, Schulte, Claudia, Brockmann, Kathrin ORCID: 0000-0002-7515-8596, Sharma, Manu ORCID: 0000-0002-1260-5416, Siitonen, Ari, Majamaa, Kari, Eerola-Rautio, Johanna, Tienari, Pentti J, Grosset, Donald G, Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, Wood, Nick, Hardy, John, Gan-Or, Ziv ORCID: 0000-0003-0332-234X, Heutink, Peter, Gasser, Thomas, Morris, Huw R, Noyce, Alastair J ORCID: 0000-0003-3027-5497, Nalls, Mike A, Singleton, Andrew B and International Parkinson's Disease Genomics Consortium (IPDGC),
(2021)
Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.
Annals of neurology, 90 (1).
pp. 35-42.
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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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Kim, Jonggeol Jeffrey ORCID: 0000-0003-0738-0512, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, 23andMe Research Team, , Iwaki, Hirotaka, Lake, Julie ORCID: 0000-0002-3441-2455, Solsberg, Caroline Warly ORCID: 0000-0001-7049-6281, Leonard, Hampton et al (show 10 more authors) , Makarious, Mary B ORCID: 0000-0002-7978-1051, Tan, Eng-King ORCID: 0000-0003-2977-9743, Singleton, Andrew B, Bandres-Ciga, Sara, Noyce, Alastair J, Global Parkinson’s Genetics Program (GP2), , Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Nalls, Mike A ORCID: 0000-0003-0319-4325, Foo, Jia Nee and Mata, Ignacio
(2024)
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.
Nature genetics, 56 (1).
pp. 27-36.
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Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361, Faghri, Faraz ORCID: 0000-0001-5744-8728, Majounie, Elisa, Koretsky, Mathew J ORCID: 0000-0003-4341-3991, Kim, Jeffrey ORCID: 0000-0003-0738-0512, Levine, Kristin S, Leonard, Hampton ORCID: 0000-0003-2390-8110, Makarious, Mary B ORCID: 0000-0002-7978-1051, Iwaki, Hirotaka ORCID: 0000-0002-8982-7885, Crea, Peter Wild ORCID: 0000-0001-8944-5716 et al (show 24 more authors) , Hernandez, Dena G ORCID: 0000-0002-0188-9927, Arepalli, Sampath, Billingsley, Kimberley ORCID: 0000-0002-8003-4029, Lohmann, Katja ORCID: 0000-0002-5121-1460, Klein, Christine ORCID: 0000-0003-2102-3431, Lubbe, Steven J ORCID: 0000-0002-7103-6671, Jabbari, Edwin ORCID: 0000-0001-6844-882X, Saffie-Awad, Paula ORCID: 0000-0002-8056-365X, Narendra, Derek ORCID: 0000-0002-8696-9108, Reyes-Palomares, Armando ORCID: 0000-0002-0289-6889, Quinn, John P ORCID: 0000-0003-3551-7803, Schulte, Claudia ORCID: 0000-0003-4006-1265, Morris, Huw R ORCID: 0000-0002-5473-3774, Traynor, Bryan J ORCID: 0000-0003-0527-2446, Scholz, Sonja W ORCID: 0000-0002-6623-0429, Houlden, Henry ORCID: 0000-0002-2866-7777, Hardy, John ORCID: 0000-0002-3122-0423, Dumanis, Sonya ORCID: 0000-0002-3345-9497, Riley, Ekemini ORCID: 0000-0001-7040-5191, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Singleton, Andrew ORCID: 0000-0001-5606-700X, Nalls, Mike, Jeff, Janina and Vitale, Dan ORCID: 0000-0002-0637-3671
(2023)
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations.
medRxiv, 4 (11-20).
2023.11.06.23298176-.
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Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya et al (show 31 more authors) , Murphy, Natalie A, Gibbs, J Raphael, Ryten, Mina, Ferrari, Raffaele, Bras, Jose, Guerreiro, Rita, Williams, Julie, Sims, Rebecca, Lubbe, Steven, Hernandez, Dena G, Mok, Kin Y, Robak, Laurie, Campbell, Roy H, Rogaeva, Ekaterina, Traynor, Bryan J, Chia, Ruth, Chung, Sun Ju, Hardy, John A, Brice, Alexis, Wood, Nicholas W, Houlden, Henry, Shulman, Joshua M, Morris, Huw R, Gasser, Thomas, Krüger, Rejko, Heutink, Peter, Sharma, Manu, Simón-Sánchez, Javier, Nalls, Mike A, Singleton, Andrew B and Scholz, Sonja W
(2017)
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.
Neurobiology of Aging, 57.
247.e9-247.e13.
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Grenn, Francis P, Kim, Jonggeol J, Makarious, Mary B, Iwaki, Hirotaka, Illarionova, Anastasia, Brolin, Kajsa, Kluss, Jillian H, Schumacher-Schuh, Artur F, Leonard, Hampton, Faghri, Faraz et al (show 14 more authors) , Billingsley, Kimberley, Krohn, Lynne, Hall, Ashley ORCID: 0000-0003-2962-6384, Diez-Fairen, Monica, Perinan, Maria Teresa, Sandor, Cynthia, Webber, Caleb, Fiske, Brian K, Gibbs, J Raphael, Nalls, Mike A, Singleton, Andrew B, Bandres-Ciga, Sara, Reed, Xylena and Blauwendraat, Cornelis
(2020)
The Parkinson's DiseaseGenome-WideAssociation Study Locus Browser.
MOVEMENT DISORDERS, 35 (11).
pp. 2056-2067.
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Liu, Hui ORCID: 0000-0001-5308-0874, Dehestani, Mohammad, Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Makarious, Mary B, Leonard, Hampton, Kim, Jonggeol J, Schulte, Claudia, Noyce, Alastair ORCID: 0000-0003-3027-5497, Jacobs, Benjamin M, Foote, Isabelle ORCID: 0000-0002-0253-4116 et al (show 6 more authors) , Sharma, Manu ORCID: 0000-0002-1260-5416, International Parkinson's Disease Genomics Consortium; Comprehen, , Nalls, Mike, Singleton, Andrew, Gasser, Thomas and Bandres-Ciga, Sara ORCID: 0000-0003-0056-1361
(2022)
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
Annals of neurology, 92 (2).
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Fernandez-Santiago, Ruben, Martin-Flores, Nuria, Antonelli, Francesca, Cerquera, Catalina, Moreno, Veronica, Bandres-Ciga, Sara, Manduchi, Elisabetta, Tolosa, Eduard, Singleton, Andrew B, Moore, Jason H et al (show 152 more authors) , Noyce, Alastair J, Kaiyrzhanov, Rauan, Middlehurst, Ben, Kia, Demis A, Tan, Manuela, Houlden, Henry, Morris, Huw R, Plun-Favreau, Helene, Holmans, Peter, Hardy, John, Trabzuni, Daniah, Bras, Jose, Quinn, John ORCID: 0000-0003-3551-7803, Mok, Kin Y, Kinghorn, Kerri J, Billingsley, Kimberley, Wood, Nicholas W, Lewis, Patrick, Schreglmann, Sebastian, Guerreiro, Rita, Lovering, Ruth, R'Bibo, Lea, Manzoni, Claudia, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott-Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel, Morrison, Karen E, Clarke, Carl, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Corvol, Jean-Christophe, Martinez, Maria, Schulte, Claudia, Brockmann, Kathrin, Simon-Sanchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Nicolas, Aude, Cookson, Mark R, Bandres-Ciga, Sara, Blauwendraat, Cornelis, Craig, David W, Faghri, Faraz, Gibbs, J Raphael, Hernandez, Dena G, Van Keuren-Jensen, Kendall, Shulman, Joshua M, Iwaki, Hirotaka, Leonard, Hampton L, Nalls, Mike A, Robak, Laurie, Lubbe, Steven, Finkbeiner, Steven, Mencacci, Niccolo E, Lungu, Codrin, Singleton, Andrew B, Scholz, Sonja W, Reed, Xylena, Alcalay, Roy N, Gan-Or, Ziv, Rouleau, Guy A, Krohn, Lynne, van Hilten, Jacobus J, Marinus, Johan, Adarmes-Gomez, Astrid D, Aguilar, Iquel, Alvarez, Ignacio, Alvarez, Victoria, Javier Barrero, Francisco, Bergareche Yarza, Jesus Alberto, Bernal-Bernal, Inmaculada, Blazquez, Marta, Bonilla-Toribio, Marta, Botia, Juan A, Teresa Boungiorno, Maria, Buiza-Rueda, Dolores, Camara, Ana, Carrillo, Fatima, Carrion-Claro, Mario, Cerdan, Debora, Clarimon, Jordi, Compta, Yaroslau, de la Casa, Beatriz, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla-Sevilla, Francisco, Ezquerra, Mario, Feliz, Cici, Fernandez, Manel, Fernandez-Santiago, Ruben, Garcia, Ciara, Garcia-Ruiz, Pedro, Gomez-Garre, Pilar, Gomez Heredia, Maria Jose, Gonzalez-Aramburu, Isabel, Gorostidi Pagola, Ana, Hoenicka, Janet, Infante, Jon, Jesus, Silvia, Jimenez-Escrig, Adriano, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A, Luis Lopez-Sendon, Jose, de Munain Arregui, Adolfo Lopez, Macias, Daniel, Martinez Torres, Irene, Marin, Juan, Jose Marti, Maria, Martinez-Castrillo, Carlos, Mendez-del-Barrio, Carlota, Menendez Gonzalez, Manuel, Mata, Marina, Minguez, Adolfo, Mir, Pablo, Mondragon Rezola, Elisabet, Munoz, Esteban, Pagonabarraga, Javier, Pascual-Sedano, Berta, Pastor, Pau, Perez Errazquin, Francisco, Perinan-Tocino, Teresa, Ruiz-Martinez, Javier, Ruz, Clara, Sanchez Rodriguez, Antonio, Sierra, Maria, Suarez-Sanmartin, Esther, Tabernero, Cesar, Pablo Tartari, Juan, Tejera-Parrado, Cristina, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-Gonzalez, Laura, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Pihlstrom, Lasse, Toft, Mathias, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille, Hassin-Baer, Sharon, Marti, Maria-Josep, Ezquerra, Mario and Malagelada, Cristina
(2019)
<i>SNCA</i> and <i>mTOR</i> Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease.
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van der Lee, Sven J ORCID: 0000-0003-1606-8643, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca ORCID: 0009-0006-3309-6856, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A et al (show 98 more authors) , Zettergren, Anna, Andlauer, Till FM ORCID: 0000-0002-2917-5889, Diez-Fairen, Monica ORCID: 0000-0003-1882-0309, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne ORCID: 0000-0003-0703-2665, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas ORCID: 0000-0003-1573-8908, Moreno-Grau, Sonia, Wagner, Michael ORCID: 0000-0003-2589-6440, Fortea, Juan ORCID: 0000-0002-1340-638X, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A ORCID: 0000-0001-6380-2420, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar ORCID: 0000-0002-2148-381X, Riedel-Heller, Steffi ORCID: 0000-0003-4321-6090, Illán-Gala, Ignacio ORCID: 0000-0002-5418-2052, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo ORCID: 0000-0002-1413-5091, Morris, Christopher M ORCID: 0000-0002-3749-0993, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W ORCID: 0000-0001-5869-2108, van Berckel, Bart NM, Alcolea, Daniel ORCID: 0000-0002-3819-3245, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau ORCID: 0000-0002-7493-8777, Rodríguez Rodríguez, Eloy ORCID: 0000-0001-7742-677X, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer, , EADB (Alzheimer Disease European DNA biobank), , IFGC (International FTD-Genomics Consortium), IPDGC (The Interna, , IPDGC (The International Parkinson Disease Genomics Consortium), , RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementi, , Netherlands Brain Bank (NBB), , Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol ORCID: 0000-0003-2656-8748, Kawalia, Amit, Dalmasso, Maria Carolina ORCID: 0000-0002-4901-9955, Boada, Mercè ORCID: 0000-0003-2617-3009, Zettl, Uwe K, van Schoor, Natasja M ORCID: 0000-0002-0870-0795, Beekman, Marian ORCID: 0000-0003-0585-6206, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander ORCID: 0000-0002-6427-7485, Wszolek, Zbigniew K, Ross, Owen A ORCID: 0000-0003-4813-756X, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W ORCID: 0000-0002-8933-3260, Pijnenburg, Yolande AL ORCID: 0000-0003-2464-1905, Scheltens, Philip ORCID: 0000-0002-1046-6408, Gasser, Thomas ORCID: 0000-0002-1069-1146, Chinnery, Patrick F ORCID: 0000-0002-7065-6617, Hemmer, Bernhard, Huisman, Martijn A ORCID: 0000-0002-9285-6759, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A ORCID: 0000-0001-7039-1105, Sørensen, Thorkild IA, Heutink, Peter ORCID: 0000-0001-5218-1737, Sánchez-Juan, Pascual, Posthuma, Danielle ORCID: 0000-0001-7582-2365, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzhe, , Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W ORCID: 0000-0002-6623-0429, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Ruiz, Agustín ORCID: 0000-0003-2633-2495, Slagboom, Eline, van der Flier, Wiesje M and Holstege, Henne ORCID: 0000-0002-7688-3087
(2019)
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Acta neuropathologica, 138 (2).
pp. 237-250.
This list was generated on Sat Apr 6 12:36:40 2024 BST.