Auflistung Universitätsbibliographie nach Autor "Simón-Sánchez, Javier"

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Auflistung Universitätsbibliographie nach Autor "Simón-Sánchez, Javier"

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  • 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
    van der Lee, Sven J.; Conway, Olivia J.; Jansen, Iris; Carrasquillo, Minerva M.; Kleineidam, Luca; van den Akker, Erik; Hernandez, Isabel; van Eijk, Kristel R.; Stringa, Najada; Chen, Jason A.; Zettergren, Anna; Andlauer, Till F. M.; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleo, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E.; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J.; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A.; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illan-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Bergh, Florian Then; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M.; Indakoetxea, Begona; Collij, Lyduine E.; Scherer, Martin; Morenas-Rodriguez, Estrella; Ironside, James W.; van Berckel, Bart N. M.; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L.; Pastor, Pau; Rodriguez Rodriguez, Eloy; Boeve, Bradley F.; Petersen, Ronald C.; Ferman, Tanis J.; van Gerpen, Jay A.; Reinders, Marcel J. T.; Uitti, Ryan J.; Tarraga, Lluis; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Merce; Zettl, Uwe K.; van Schoor, Natasja M.; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; Lopez de Munain, Adolfo; Pantelyat, Alexander; Wszolek, Zbigniew K.; Ross, Owen A.; Dickson, Dennis W.; Graff-Radford, Neill R.; Knopman, David; Rademakers, Rosa; Lemstra, Afina W.; Pijnenburg, Yolande A. L.; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F.; Hemmer, Bernhard; Huisman, Martijn A.; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A.; Sorensen, Thorkild I. A.; Heutink, Peter; Sanchez-Juan, Pascual; Posthuma, Danielle; Clarimon, Jordi; Christensen, Kaare; Ertekin-Taner, Nilufer; Scholz, Sonja W.; Ramirez, Alfredo; Ruiz, Agustin; Slagboom, Eline; van der Flier, Wiesje M.; Holstege, Henne (2019)
  • A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family
    Hanagasi, Hasmet A.; Giri, Anamika; Kartal, Ece; Guven, Gamze; Bilgic, Basar; Hauser, Ann-Kathrin; Emre, Murat; Heutink, Peter; Basak, Nazh; Gasser, Thomas; Simon-Sanchez, Javier; Lohmann, Ebba (2016)
  • Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
    Mencacci, Niccolo E.; Brockmann, Marisa M.; Dai, Jinye; Pajusalu, Sander; Atasu, Burcu; Campos, Joaquin; Pino, Gabriela; Gonzalez-Latapi, Paulina; Patzke, Christopher; Schwake, Michael; Tucci, Arianna; Pittman, Alan; Simon-Sanchez, Javier; Carvill, Gemma L.; Balint, Bettina; Wiethoff, Sarah; Warner, Thomas T.; Papandreou, Apostolos; Soo, Audrey; Rein, Reet; Kadastik-Eerme, Liis; Puusepp, Sanna; Reinson, Karit; Tomberg, Tiiu; Hanagasi, Hasmet; Gasser, Thomas; Bhatia, Kailash P.; Kurian, Manju A.; Lohmann, Ebba; Ounap, Katrin; Rosenmund, Christian; Sudhof, Thomas C.; Wood, Nicholas W.; Krainc, Dimitri; Acuna, Claudio (2021)
  • C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers
    Rizzu, Patrizia; Blauwendraat, Cornelis; Heetveld, Sasja; Lynes, Emily M.; Castillo-Lizardo, Melissa; Dhingra, Ashutosh; Pyz, Elwira; Hobert, Markus; Synofzik, Matthis; Simon-Sanchez, Javier; Francescatto, Margherita; Heutink, Peter (2016)
  • Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe
    Blauwendraat, Cornelis; Francescatto, Margherita; Gibbs, J. Raphael; Jansen, Iris E.; Simon-Sanchez, Javier; Hernandez, Dena G.; Dillman, Allissa A.; Singleton, Andrew B.; Cookson, Mark R.; Rizzu, Patrizia; Heutink, Peter (2016)
  • Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
    Mok, Kin Y.; Sheerin, Una; Simon-Sanchez, Javier; Salaka, Afnan; Chester, Lucy; Escott-Price, Valentina; Mantripragada, Kiran; Doherty, Karen M.; Noyce, Alastair J.; Mencacci, Niccolo E.; Lubbe, Steven J.; Williams-Gray, Caroline H.; Barker, Roger A.; Van Dijk, Karin D.; Berendse, Henk W.; Heutink, Peter; Corvol, Jean-Christophe; Cormier, Florence; Lesage, Suzanne; Brice, Alexis; Brockmann, Kathrin; Schulte, Claudia; Gasser, Thomas; Foltynie, Thomas; Limousin, Patricia; Morrison, Karen E.; Clarke, Carl E.; Sawcer, Stephen; Warner, Tom T.; Lees, Andrew J.; Morris, Huw R.; Nalls, Mike A.; Singleton, Andrew B.; Hardy, John; Abramov, Andrey Y.; Plagnol, Vincent; Williams, Nigel M.; Wood, Nicholas W. (2016)
  • Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
    Jansen, Iris E.; Ye, Hui; Heetveld, Sasja; Lechler, Marie C.; Michels, Helen; Seinstra, Renee I.; Lubbe, Steven J.; Drouet, Valerie; Lesage, Suzanne; Majounie, Elisa; Gibbs, J. Raphael; Nalls, Mike A.; Ryten, Mina; Botia, Juan A.; Vandrovcova, Jana; Simon-Sanchez, Javier; Castillo-Lizardo, Melissa; Rizzu, Patrizia; Blauwendraat, Cornelis; Chouhan, Amit K.; Li, Yarong; Yogi, Puja; Amin, Najaf; van Duijn, Cornelia M.; Morris, Huw R.; Brice, Alexis; Singleton, Andrew B.; David, Della C.; Nollen, Ellen A.; Jain, Shushant; Shulman, Joshua M.; Heutink, Peter (2017)
  • Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
    Pottier, Cyril; Ren, Yingxue; Perkerson, Ralph B., III; Baker, Matt; Jenkins, Gregory D.; van Blitterswijk, Marka; DeJesus-Hernandez, Mariely; van Rooij, Jeroen G. J.; Murray, Melissa E.; Christopher, Elizabeth; McDonnell, Shannon K.; Fogarty, Zachary; Batzler, Anthony; Tian, Shulan; Vicente, Cristina T.; Matchett, Billie; Karydas, Anna M.; Hsiung, Ging-Yuek Robin; Seelaar, Harro; Mol, Merel O.; Finger, Elizabeth C.; Graff, Caroline; Oijerstedt, Linn; Neumann, Manuela; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Prudlo, Johannes; Rizzu, Patrizia; Simon-Sanchez, Javier; Edbauer, Dieter; Roeber, Sigrun; Diehl-Schmid, Janine; Evers, Bret M.; King, Andrew; Mesulam, M. Marsel; Weintraub, Sandra; Geula, Changiz; Bieniek, Kevin F.; Petrucelli, Leonard; Ahern, Geoffrey L.; Reiman, Eric M.; Woodruff, Bryan K.; Caselli, Richard J.; Huey, Edward D.; Farlow, Martin R.; Grafman, Jordan; Mead, Simon; Grinberg, Lea T.; Spina, Salvatore; Grossman, Murray; Irwin, David J.; Lee, Edward B.; Suh, EunRan; Snowden, Julie; Mann, David; Ertekin-Taner, Nilufer; Uitti, Ryan J.; Wszolek, Zbigniew K.; Josephs, Keith A.; Parisi, Joseph E.; Knopman, David S.; Petersen, Ronald C.; Hodges, John R.; Piguet, Olivier; Geier, Ethan G.; Yokoyama, Jennifer S.; Rissman, Robert A.; Rogaeva, Ekaterina; Keith, Julia; Zinman, Lorne; Tartaglia, Maria Carmela; Cairns, Nigel J.; Cruchaga, Carlos; Ghetti, Bernardino; Kofler, Julia; Lopez, Oscar L.; Beach, Thomas G.; Arzberger, Thomas; Herms, Jochen; Honig, Lawrence S.; Vonsattel, Jean Paul; Halliday, Glenda M.; Kwok, John B.; White, Charles L., III; Gearing, Marla; Glass, Jonathan; Rollinson, Sara; Pickering-Brown, Stuart; Rohrer, Jonathan D.; Trojanowski, John Q.; Van Deerlin, Vivianna; Bigio, Eileen H.; Troakes, Claire; Al-Sarraj, Safa; Asmann, Yan; Miller, Bruce L.; Graff-Radford, Neill R.; Boeve, Bradley F.; Seeley, William W.; Mackenzie, Ian R. A. (2019)
  • HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype
    Atasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel-Unaltuna, Nihan; Hauser, Ann-Kathrin; Guven, Gamze; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba (2018)
  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
    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; Bras, Jose; Young, Emily; von Coelln, Rainer; Simon-Sanchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Pihlstrom, 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. (2019)
  • Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population
    Giri, Anamika; Mok, Kin Y.; Jansen, Iris; Sharma, Manu; Tesson, Christelle; Mangone, Graziella; Lesage, Suzanne; Bras, Jose M.; Shulman, Joshua M.; Sheerin, Una-Marie; Diez-Fairen, Monica; Pastor, Pau; Jose Marti, Maria; Ezquerra, Mario; Tolosa, Eduardo; Correia-Guedes, Leonor; Ferreira, Joaquim; Amin, Najaf; van Duijn, Cornelia M.; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Nalls, Michael; Simon-Sanchez, Javier (2017)
  • Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset
    Billingsley, Kimberley J.; Barbosa, Ines A.; Bandres-Ciga, Sara; Quinn, John P.; Bubb, Vivien J.; Deshpande, Charu; Botia, Juan A.; Reynolds, Regina H.; Zhang, David; Simpson, Michael A.; Blauwendraat, Cornelis; Gan-Or, Ziv; Gibbs, J. Raphael; Nalls, Mike A.; Singleton, Andrew; Ryten, Mina; Koks, Sulev; Noyce, A.; Tucci, A.; Middlehurst, B.; Kia, D.; Tan, M.; Houlden, H.; Morris, H. R.; 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, R., I; Escamilla-Sevilla, F.; Ezquerra, M.; Fernandez, M.; Fernandez-Santiago, R.; Garcia, C.; Garcia-Ruiz, P.; Gomez-Garre, P.; Gomez Heredia, M.; Gonzalez-Aramburu, I (2019)
  • Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability
    Reynolds, Regina H.; Botia, Juan; Nalls, Mike A.; Hardy, John; Taliun, Sarah A. Gagliano; Ryten, Mina; Noyce, Alastair J.; Nicolas, Aude; Cookson, Mark R.; Bandres-Ciga, Sara; Gibbs, J. Raphael; Hernandez, Dena G.; Singleton, Andrew B.; Reed, Xylena; Leonard, Hampton; Blauwendraat, Cornelis; Faghri, Faraz; Bras, Jose; Guerreiro, Rita; Tucci, Arianna; Kia, Demis A.; Houlden, Henry; Plun-Favreau, Helene; Mok, Kin Y.; Wood, Nicholas W.; Lovering, Ruth; R'Bibo, Lea; Rizig, Mie; Chelban, Viorica; Trabzuni, Daniah; Tan, Manuela; Morris, Huw R.; Middlehurst, Ben; Quinn, John; Billingsley, Kimberley; Holmans, Peter; Kinghorn, Kerri J.; Lewis, Patrick; Escott-Price, Valentina; Williams, Nigel; Foltynie, Thomas; Brice, Alexis; Danjou, Fabrice; Lesage, Suzanne; Corvol, Jean-Christophe; Martinez, Maria; Giri, Anamika; Schulte, Claudia; Brockmann, Kathrin; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Rizzu, Patrizia; Sharma, Manu; Shulman, Joshua M.; Robak, Laurie; Lubbe, Steven; Mencacci, Niccolo E.; Finkbeiner, Steven; Lungu, Codrin; Scholz, Sonja W.; Gan-Or, Ziv; Rouleau, Guy A.; Krohan, Lynne; van Hilten, Jacobus J.; Marinus, Johan; Adarmes-Gomez, Astrid D.; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fatima; Carrion-Claro, Mario; Mir, Pablo; Gomez-Garre, Pilar; Jesus, Silvia; Labrador-Espinosa, Miguel A.; Macias, Daniel; Vargas-Gonzalez, Laura; Mendez-del-Barrio, Carlota; Perinan-Tocino, Teresa; Tejera-Parrado, Cristina; Diez-Fairen, Monica; Aguilar, Miquel; Alvarez, Ignacio; Teresa Boungiorno, Mara; Carcel, Maria; Pastor, Pau; Pablo Tartari, Juan; Alvarez, Victoria; Menendez Gonzalez, Manuel; Blazquez, Marta; Garcia, Ciara; Suarez-Sanmartin, Esther; Javier Barrero, Francisco; Mondragon Rezola, Elisabet; Bergareche Yarza, Jesus Alberto; Gorostidi Pagola, Ana; de Munain Arregui, Adolfo Lopez; Ruiz-Martinez, Javier; Cerdan, Debora; Duarte, Jacinto (2019)
  • NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
    Blauwendraat, Cornelis; Faghri, Faraz; Pihlstrom, Lasse; Geiger, Joshua T.; Elbaz, Alexis; Lesage, Suzanne; Corvol, Jean-Christophe; May, Patrick; Nicolas, Aude; Abramzon, Yevgeniya; 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, NicholasW.; Houlden, Henry; Shulman, Joshua M.; Morris, Huw R.; Gasser, Thomas; Krueger, Rejko; Heutink, Peter; Sharma, Manu; Simon-Sanchez, Javier; Nalls, Mike A.; Singleton, Andrew B.; Scholz, SonjaW. (2017)
  • No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
    Baradaran-Heravi, Yalda; Dillen, Lubina; Hung Phuoc Nguyen; Van Mossevelde, Sara; Baets, Jonathan; De Jonghe, Peter; Engelborghs, Sebastiaan; De Deyn, Peter P.; Vandenbulcke, Mathieu; Vandenberghe, Rik; Van Damme, Philip; Cras, Patrick; Salmon, Eric; Synofzik, Matthis; Heutink, Peter; Wilke, Carlo; Simon-Sanchez, Javier; Rojas-Garcia, Ricard; Turon-Sans, Janina; Lleo, Alberto; Illan-Gala, Ignacio; Clarimon, Jordi; Borroni, Barbara; Padovani, Alessandro; Pastor, Pau; Diez-Fairen, Monica; Aguilar, Miquel; Gelpi, Ellen; Sanchez-Valle, Raquel; Borrego-Ecija, Sergi; Matej, Radoslav; Parobkova, Eva; Nacmias, Benedetta; Sorbi, Sandro; Bagnoli, Silvia; de Mendonca, Alexandre; Ferreira, Catarina; Fraidakis, Matthew J.; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Almeida, Maria Rosario; Santana, Isabel; Van Broeckhoven, Christine; van der Zee, Julie (2018)
  • Parkinson's disease age at onset genome-wide association study: defining heritability, genetic loci, and α-synuclein mechanisms
    Blauwendraat, Cornelis; Heilbron, Karl; Vallerga, Costanza L.; Bandres-Ciga, Sara; von Coelln, Rainer; Pihlstrom, Lasse; Simon-Sanchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Siitonen, Ari; Iwaki, Hirotaka; Leonard, Hampton; Noyce, Alastair J.; Tan, Manuela; Gibbs, J. Raphael; Hernandez, Dena G.; Scholz, Sonja W.; Jankovic, Joseph; Shulman, Lisa M.; Lesage, Suzanne; Corvol, Jean-Christophe; Brice, Alexis; van Hilten, Jacobus J.; Marinus, Johan; Eerola-Rautio, Johanna; Tienari, Pentti; Majamaa, Kari; Toft, Mathias; Grosset, Donald G.; Gasser, Thomas; Heutink, Peter; Shulman, Joshua M.; Wood, Nicolas; Hardy, John; Morris, Huw R.; Hinds, David A.; Gratten, Jacob; Visscher, Peter M.; Gan-Or, Ziv; Nalls, Mike A.; Singleton, Andrew B. (2019)
  • Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
    Blauwendraat, Cornelis; Wilke, Carlo; Jansen, Iris E.; Schulte, Claudia; Simon-Sanchez, Javier; Metzger, Florian G.; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis (2016)
  • Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
    Kessler, Christoph; Atasu, Burcu; Hanagasi, Hasmet; Simon-Sanchez, Javier; Hauser, Ann-Kathrin; Pak, Meltem; Bilgic, Basar; Erginel-Unaltuna, Nihan; Gurvit, Hakan; Gasser, Thomas; Lohmann, Ebba (2018)
  • SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
    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.; 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; 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 (2019)
  • The Genetic Architecture of Parkinson Disease in Spain : Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
    Bandres-Ciga, Sara; Ahmed, Sarah; Sabir, Marya S.; Blauwendraat, Cornelis; Adarmes-Gomez, Astrid D.; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores; Carrillo, Fatima; Carrion-Claro, Mario; Gomez-Garre, Pilar; Jesus, Silvia; Labrador-Espinosa, Miguel A.; Macias, Daniel; Mendez-del-Barrio, Carlota; Perinan-Tocino, Teresa; Tejera-Parrado, Cristina; Vargas-Gonzalez, Laura; Diez-Fairen, Monica; Alvarez, Ignacio; Pablo Tartari, Juan; Buongiorno, Mariateresa; Aguilar, Miquel; Gorostidi, Ana; Alberto Bergareche, Jesus; Mondragon, Elisabet; Vinagre-Aragon, Ana; Croitoru, Ioana; Ruiz-Martinez, Javier; Dols-Icardo, Oriol; Kulisevsky, Jaime; Marin-Lahoz, Juan; Pagonabarraga, Javier; Pascual-Sedano, Berta; Ezquerra, Mario; Camara, Ana; Compta, Yaroslau; Fernandez, Manel; Fernandez-Santiago, Ruben; Munoz, Esteban; Tolosa, Eduard; Valldeoriola, Francesc; Gonzalez-Aramburu, Isabel; Sanchez Rodriguez, Antonio; Sierra, Maria; Menendez-Gonzalez, Manuel; Blazquez, Marta; Garcia, Ciara; Martin, Esther Suarez-San; Garcia-Ruiz, Pedro; Carlos Martinez-Castrillo, Juan; Vela-Desojo, Lydia; Ruz, Clara; Javier Barrero, Francisco; Escamilla-Sevilla, Francisco; Minguez-Castellanos, Adolfo; Cerdan, Debora; Tabernero, Cesar; Gomez Heredia, Maria Jose; Perez Errazquin, Francisco; Romero-Acebal, Manolo; Feliz, Cici; Luis Lopez-Sendon, Jose; Mata, Marina; Martinez Torres, Irene; Kim, Jonggeol Jeffrey; Dalgard, Clifton L.; Brooks, Janet; Saez-Atienzar, Sara; Raphael Gibbs, J.; Jorda, Rafael; Botia, Juan A.; Bonet-Ponce, Luis; Morrison, Karen E.; Clarke, Carl; Tan, Manuela; Morris, Huw; Edsall, Connor; Hernandez, Dena; Simon-Sanchez, Javier; Nalls, Mike A.; Scholz, Sonja W.; Jimenez-Escrig, Adriano; Duarte, Jacinto; Vives, Francisco; Duran, Raquel; Hoenicka, Janet; Alvarez, Victoria; Infante, Jon; Jose Marti, Maria; Clarimon, Jordi; Lopez de Munain, Adolfo; Pastor, Pau; Mir, Pablo; Singleton, Andrew (2019)