Javier Simón‐Sánchez

Active 2006–2024

Also published as
Javier Simón-Sánchez
52
Papers
19,095
Citations
43
h-index
50
i10-index

Citations

Citations per year for Javier Simón‐Sánchez1990: 1 citations1991: 1 citations1999: 1 citations2001: 1 citations2003: 1 citations2006: 10 citations2007: 33 citations2008: 66 citations2009: 138 citations2010: 173 citations2011: 204 citations2012: 373 citations2013: 336 citations2014: 277 citations2015: 244 citations2016: 259 citations2017: 269 citations2018: 233 citations2019: 687 citations2020: 870 citations2021: 836 citations2022: 684 citations2023: 552 citations2024: 742 citations2025: 332 citations2026: 6 citations1992–1998: no citations, so these years are not shown2000: no citations, so this year is not shown2002: no citations, so this year is not shown2004–2005: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,835 citing papers, 24.1% of this breakdownUnited Kingdom: 1,254 citing papers, 10.7% of this breakdownGermany: 755 citing papers, 6.4% of this breakdownChina: 669 citing papers, 5.7% of this breakdownItaly: 572 citing papers, 4.9% of this breakdownCanada: 494 citing papers, 4.2% of this breakdownAustralia: 424 citing papers, 3.6% of this breakdownNetherlands: 392 citing papers, 3.3% of this breakdownFrance: 387 citing papers, 3.3% of this breakdownSpain: 334 citing papers, 2.8% of this breakdownSweden: 258 citing papers, 2.2% of this breakdownJapan: 253 citing papers, 2.1% of this breakdown
0%24.1%Other 26.7%

Fields

  • Medicine61.3%
  • Biochemistry, Genetics and Molecular Biology27.9%
  • Neuroscience8.4%
  • Immunology and Microbiology0.7%
  • Computer Science0.3%
  • Nursing0.3%
  • Other1.1%

Topics

  • Parkinson's Disease Mechanisms and Treatments12.1%
  • Amyotrophic Lateral Sclerosis Research9.7%
  • Neurogenetic and Muscular Disorders Research4.9%
  • Alzheimer's disease research and treatments4.6%
  • Neurological diseases and metabolism3.9%
  • Genetic Neurodegenerative Diseases3.4%
  • Other61.4%

Coauthors

All papers

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  1. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew B Singleton, Astrid Adarmes‐Gómez, Miquel Aguilar, Akbota Aitkulova, Vadim Akhmetzhanov, Roy N. Alcalay, Ignacio Álvarez, Victoria Álvarez, Sara Bandrés‐Ciga, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Kimberley J. Billingsley, Cornelis Blauwendraat, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, José Brás, Alexis Brice, Kathrin Brockmann, Vivien J. Bubb, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Viorica Chelban, Jordi Clarimón, Carl E Clarke, Yaroslau Compta, Mark Cookson, Jean‐Christophe Corvol, David W. Craig, Fabrice Danjou, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, Raquel Durán, Francisco Escamilla‐Sevilla, Valentina Escott‐Price, Mario Ezquerra, Faraz Faghri, Cici Feliz, Manel Fernández, Rubén Fernández‐Santiago, Steven Finkbeiner, Thomas Foltynie, Ziv Gan‐Or, Ciara García and 170 more - The Lancet Neurology 2019 cited by 2,541

  2. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor - Neuron 2011 cited by 4,469

  3. Genome-wide association study reveals genetic risk underlying Parkinson's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Katrina Gwinn, Marcel van der Brug, Grisel Lopez, Stephen J. Chanock, Arthur Schatzkin, Yikyung Park, Albert R. Hollenbeck, Jianjun Gao, Xuemei Huang, Nick W Wood, Delia Lorenz, Günther Deuschl, Honglei Chen, Olaf Rieß, John Hardy, Andrew Singleton, Thomas Gasser - Nature Genetics 2009 cited by 1,954

  4. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea Calvo, Elisabet Englund, Giuseppe Borghero, Gianluca Floris, Anne M. Remes, Hannu Laaksovirta, Leo McCluskey, John Q. Trojanowski, Vivianna M. Van Deerlin, Gerard D. Schellenberg, Michael A. Nalls, Vivian E. Drory, Chin‐Song Lu, Tu‐Hsueh Yeh, Hiroyuki Ishiura, Yuji Takahashi, Shoji Tsuji, Isabelle Le Ber, Alexis Brice, Carsten Drepper, Nigel Williams, Janine Kirby, Pamela J. Shaw, John Hardy, Pentti J. Tienari, Peter Heutink, Huw R. Morris, Stuart Pickering‐Brown, Bryan J. Traynor - The Lancet Neurology 2012 cited by 1,226

  5. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nigel Williams, Karen Morrison, Carl E Clarke, Kirsten Harvey, Benjamin M. Jacobs, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Susanne A. Schneider, Mark Cookson, Cornelis Blauwendraat, David W. Craig, Kimberley J. Billingsley, Mary B. Makarious, Derek P. Narendra, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hirotaka Iwaki, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, José Brás, Rita Guerreiro, Steven Lubbe, Timothy Troycoco, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Ryan J. Uitti, Owen A. Ross, Francis P. Grenn, Anni Moore, Roy N. Alcalay, Zbigniew K. Wszołek, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Kheireddin Mufti, Jacobus J. van Hilten, Johan Marinus, Astrid D. Adarmes-Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blázquez Estrada, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Ana Cámara, Fátima Carrillo, Mario Carrión‐Claro and 75 more - Nature Communications 2021 cited by 214

  6. Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathrin Brockmann, Janet Brooks, David J. Burn, Elisa Majounie, Gavin Charlesworth, Codrin Lungu, Honglei Chen, Patrick F. Chinnery, Sean Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, Jean‐François Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Jing Dong, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Clare Harris, Jacobus J. van Hilten, Albert Hofman, Albert R. Hollenbeck, Janice L. Holton, Michele Hu, Xuemei Huang, Isabel Wurster, Walter Mätzler, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Jean‐Charles Lambert, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, Delia Lorenz, Codrin Lungu, Alisdair McNeill, Catriona Moorby, Matthew Moore, Huw R. Morris, Karen Morrison, Valentina Escott‐Price, Ese Mudanohwo, Sean S. O’Sullivan, Justin Pearson, Joel S. Perlmutter, Hjörvar Pétursson, Pierre Pollak, Bart Post, Simon Potter, Bernard Ravina, Tamás Révész and 40 more - Brain 2017 cited by 451

  7. Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas Gasser, Peter Heutink, Joshua Shulman, Nicolas Wood, John Hardy, Huw R. Morris, David A. Hinds, Jacob Gratten, Peter M. Visscher, Ziv Gan‐Or, Mike A. Nalls, Andrew Singleton - Movement Disorders 2019 cited by 374

  8. Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas Wood, Patrick A. Lewis, Sebastian R. Schreglmann, Rita Guerreiro, Ruth C. Lovering, Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, Nigel Williams, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Aude Nicolas, Mark Cookson, Sara Bandrés‐Ciga, Cornelis Blauwendraat, David W. Craig, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, Steven Lubbe, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Roy N. Alcalay, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Jacobus J. van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blázquez Estrada, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Jordi Clarimón, Yaroslau Compta and 63 more - JAMA Neurology 2021 cited by 203

  9. Identification of sixteen novel candidate genes for late onset Parkinson’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, Nigel Williams, Karen Morrison, Carl E Clarke, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Mark Cookson, Sara Bandrés‐Ciga, Cornelis Blauwendraat, David W. Craig, Derek P. Narendra, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hirotaka Iwaki, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, José Brás, Rita Guerreiro, Steven Lubbe, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Roy N. Alcalay, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Lynne Krohn, Jacobus J. van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Jordi Clarimón, Yaroslau Compta and 79 more - Molecular Neurodegeneration 2021 cited by 89

  10. Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Patrick A. Lewis, Rita Guerreiro, Ruth C. Lovering, Lea R’Bibo, Mie Rizig, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, N. Williams, Alexis Brice, Fabrice Danjou, Suzanne Lesage, María Martínez, Ayush Giri, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Aude Nicolas, Mark Cookson, Faraz Faghri, Dena Hernández, J. Shulman, Laurie Robak, Steven Lubbe, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Sonja W. Scholz, Xylena Reed, Hampton L. Leonard, Guy A. Rouleau, Lynne Krohan, JJ van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, M. Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, J. Bergareche Yarza, Inmaculada Bernal‐Bernal, M. Blazquez, Magally Bernal, María Teresa Boungiorno, Dolores Buiza‐Rueda, Ana Cámara, María Cárcel, F. Carrillo, Mario Carrión‐Claro, Debora Cerdan, Jordi Clarimón, Yaroslau Compta, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, R. l. Duran, Francisco Escamilla‐Sevilla, Mario Ezquerra, Manel Fernández, Rubén Fernández‐Santiago, C. Garcı́a, Pedro Ruiz, Pilar Gómez‐Garre, Mégane Heredia, Isabel González Aramburu, Ana Gorostidi Pagola and 45 more - npj Parkinson s Disease 2019 cited by 161

  11. 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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dieter Edbauer, Sigrun Roeber, Janine Diehl‐Schmid, Bret M. Evers, Andrew King, Marsel Mesulam, Sandra Weıntraub, Changiz Geula, Kevin F. Bieniek, Leonard Petrucelli, Geoffrey L. Ahern, Eric M. Reiman, Bryan K. Woodruff, Richard J. Caselli, Edward D. Huey, Martin R. Farlow, Jordan Grafman, Simon Mead, Lea T. Grinberg, Salvatore Spina, Murray Grossman, David J. Irwin, Edward B. Lee, EunRan Suh, Julie S. Snowden, David Mann, Nilüfer Ertekin‐Taner, Ryan J. Uitti, Zbigniew K. Wszołek, Keith A. Josephs, Joseph E. Parisi, David S. Knopman, Ronald C. Petersen, John R. Hodges, Olivier Piguet, Ethan G. Geier, Jennifer S. Yokoyama, Robert A. Rissman, Ekaterina Rogaeva, Julia Keith, Lorne Zinman, Maria Carmela Tartaglia, Nigel J. Cairns, Carlos Cruchaga, Bernardino Ghetti, Julia Kofler, Oscar L. López, Thomas G. Beach, Thomas Arzberger, Jochen Herms, Lawrence S. Honig, Jean Paul Vonsattel, Glenda M. Halliday, John B. Kwok, Charles L. White, Marla Gearing, Jonathan D. Glass, Sara Rollinson, Stuart Pickering‐Brown, Jonathan D. Rohrer, John Q. Trojanowski, Vivianna Van Deerlin, Eileen H. Bigio, Claire Troakes, Safa Al‐Sarraj, Yan W. Asmann, Bruce L. Miller, Neill R. Graff‐Radford, Bradley F. Boeve, William W. Seeley and 5 more - Acta Neuropathologica 2019 cited by 128

  12. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

    Authors: , , , , , , , , , , , , , , , , , - The Lancet 2011 cited by 919

  13. Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , John P. Quinn, Kimberley J. Billingsley, Peter Holmans, Kerri J. Kinghorn, Patrick A. Lewis, Valentina Escott‐Price, Nigel Williams, Thomas Foltynie, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Anamika Giri, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Thomas Gasser, Patrizia Rizzu, Manu Sharma, Joshua Shulman, Laurie Robak, Steven Lubbe, Niccolò E. Mencacci, Steven Finkbeiner, Codrin Lungu, Sonja W. Scholz, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohan, Jacobus J. van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, Inmaculada Bernal‐Bernal, Marta Bonilla‐Toribio, Dolores Buiza‐Rueda, Fátima Carrillo, Mario Carrión‐Claro, Pablo Mir, Pilar Gómez‐Garre, Silvia Jesús, Miguel A. Labrador‐Espinosa, Daniel Macías, Laura Vargas‐González, Carlota Méndez‐del‐Barrio, María Teresa Periñán, Cristina Tejera‐Parrado, Mónica Díez-Fairén, Miquel Aguilar, Ignacio Álvarez, María Teresa Boungiorno, María Cárcel, Pau Pástor, Juan Pablo Tartari, Victoria Álvarez, Manuel Menéndez‐González, Marta Blázquez Estrada, Ciara García, Esther Suárez-Sanmartín, Francisco Javier Barrero, Elisabet Mondragón Rezola, Jesús Alberto Bergareche Yarza, Ana Gorostidi Pagola, Adolfo López de Munaín Arregui, Javier Ruiz‐Martínez, Debora Cerdan, J. Duarte, Jordi Clarimón, Oriol Dols‐Icardo and 68 more - npj Parkinson s Disease 2019 cited by 113

  14. C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers

    Authors: , , , , , , , , , , , - Acta Neuropathologica Communications 2016 cited by 81

  15. NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Henry Houlden, Joshua Shulman, Huw R. Morris, Thomas Gasser, Rejko Krüger, Peter Heutink, Manu Sharma, Javier Simón‐Sánchez, Mike A. Nalls, Andrew Singleton, Sonja W. Scholz - Neurobiology of Aging 2017 cited by 158

  16. 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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Manuel A. Friese, Olga Pletnikova, Miren Zulaica, Carmen Lage, Itziar de Rojas, Steffi G. Riedel‐Heller, Ignacio Illán‐Gala, Wei Wei, Bernard Jeune, Adelina Orellana, Florian Then Bergh, Xue Wang, Marc Hulsman, Nina Beker, Niccoló Tesi, Christopher M. Morris, Begoña Indakoetxea, Lyduine E. Collij, Martin Scherer, Estrella Morenas‐Rodríguez, James W. Ironside, Bart N.M. van Berckel, Daniel Alcolea, Heinz Wiendl, Samantha L. Strickland, Pau Pástor, Eloy Rodríguez‐Rodríguez, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Jay A. van Gerpen, Marcel Reinders, Ryan J. Uitti, Lluís Tárraga, Wolfgang Maier, Oriol Dols‐Icardo, Amit Kawalia, Carolina Dalmasso, Merçé Boada, Uwe K. Zettl, Natasja M. van Schoor, Marian Beekman, Mariet Allen, Eliezer Masliah, Adolfo López de Munain, Alexander Pantelyat, Zbigniew K. Wszołek, Owen A. Ross, Dennis W. Dickson, Caroline Graff, David S. Knopman, Rosa Rademakers, Afina W. Lemstra, Yolande A.L. Pijnenburg, Philip Scheltens, Thomas Gasser, Patrick F. Chinnery, Bernhard Hemmer, Martijn Huisman, Juan C. Troncoso, Fermín Moreno, Ellen A. Nøhr, Thorkild I. A. Sørensen, Peter Heutink, Pascual Sánchez‐Juan, Daniëlle Posthuma, Jordi Clarimón, Kaare Christensen, Nilüfer Ertekin‐Taner, Sonja W. Scholz and 5 more - Acta Neuropathologica 2019 cited by 131

  17. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Human Molecular Genetics 2012 cited by 205

  18. A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Aimo Ruokonen, Marjo‐Riitta Järvelin, Jack M. Guralnik, Stefania Bandinelli, Timothy M. Frayling, Andrew Singleton, Luigi Ferrucci - PLoS Genetics 2008 cited by 495

  19. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Sampath Arepalli, Roger A. Barker, Yoav Ben‐Shlomo, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bas Bloem, Zoltán Bochdanovits, Michael von Bonin, José Brás, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Sean Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, Jean‐François Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Jianjun Gao, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Ómar Gústafsson, Clare Harris, Jacobus J. van Hilten, Albert Hofman, Albert R. Hollenbeck, Janice L. Holton, Michele Hu, Xuemei Huang, Heiko Huber, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Helmholtz Zentrum München, Pálmi V. Jónsson, Jean‐Charles Lambert, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Helmholtz Zentrum München, Patricia Limousin, Grisel Lopez, Delia Lorenz, Alisdair McNeill, Catriona Moorby, M. Elyse Moore, Huw R. Morris and 67 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2014 cited by 367

  20. DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

    Authors: , , , , , , , , , , , , , , , - The Lancet Neurology 2008 cited by 228

  21. The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jaime Kulisevsky, Juan Marín‐Lahoz, Javier Pagonabarraga, Berta Pascual‐Sedano, Mario Ezquerra, Anna Maria Novella Càmara, Yaroslau Compta, Manel Fernández, Rubén Fernández‐Santiago, Esteban Muñoz, Eduard Tolosa, Francesc Valldeoriola, Isabel González Aramburu, A Rodríguez, María Sierra, Manuel Menéndez‐González, Marta Blázquez Estrada, Ciara García, Esther Suarez‐San Martin, Pedro Ruiz, Juan Carlos Martínez‐Castrillo, Lydia Vela, Clara Ruz, Francisco Javier Barrero, Francisco Escamilla‐Sevilla, Adolfo Mínguez‐Castellanos, Debora Cerdan, César Tabernero, María José Gómez Heredia, Francisco Pérez Errazquin, Manolo Romero‐Acebal, Cici Feliz, José Luis López-Sendón, Marina Mata, Irene Martínez‐Torres, Jonggeol Jeffrey Kim, Clifton L. Dalgard, Janet Brooks, Sara Sáez-Atiénzar, J. Raphael Gibbs, Rafael Jorda, Juan A. Botía, Luis Bonet‐Ponce, Karen Morrison, Carl E Clarke, Manuela Tan, Huw R. Morris, Connor Edsall, Dena Hernández, Javier Simón‐Sánchez, Mike A. Nalls, Sonja W. Scholz, Adriano Jiménez‐Escrig, J. Duarte, Francisco Vives, Raquel Durán, Janet Hoenicka, Victoria Álvarez, Jon Infante, Marı́a José Martı́, Jordi Clarimón, Adolfo López de Munain, Pau Pástor, Pablo Mir, Andrew Singleton - Movement Disorders 2019 cited by 71

  22. Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christian Rosenmund, Thomas C. Südhof, Nicholas Wood, Dimitri Krainc, Claudio Acuna - Journal of Clinical Investigation 2021 cited by 38

  23. Assessment of the impact of a personalised nutrition intervention in impaired glucose regulation over 26 weeks: a randomised controlled trial

    Authors: , , , , , , , , , , , , , , , , , - Scientific Reports 2024 cited by 19

  24. Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

    Authors: , , , , , , , , , , , , , , , , , , , , , , - PLoS Genetics 2007 cited by 349