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  1. 1
    Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy

    Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy Autor Monica Gagliardi, Radha Procopio, Grazia Annesi, Jolanda Buonocore, Mariagrazia Talarico, Aldo Quattrone, Andrea Quattrone

    Vydáno 2025
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  2. 2
    Homozygous c.649dupC mutation in <i>PRRT2</i> worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences

    Homozygous c.649dupC mutation in <i>PRRT2</i> worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences Autor Angelo Labate, Patrizia Tarantino, Maurizio Viri, Laura Mumoli, Monica Gagliardi, Antonino Romeo, Federico Zara, Grazia Annesi, Antonio Gambardella

    Vydáno 2012
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  3. 3
    Divergent effects of the <scp>T</scp>1174S <scp><i>SCN1A</i></scp> mutation associated with seizures and hemiplegic migraine

    Divergent effects of the <scp>T</scp>1174S <scp><i>SCN1A</i></scp> mutation associated with seizures and hemiplegic migraine Autor Sandrine Cestèle, Angelo Labate, Raffaella Rusconi, Patrizia Tarantino, Laura Mumoli, Silvana Franceschetti, Grazia Annesi, Massimo Mantegazza, Antonio Gambardella

    Vydáno 2013
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  4. 4
    Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1 Na<sup>+</sup>Channel Mutant

    Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Na<sub>v</sub>1.1 Na<sup>+</sup>Channel Mutant Autor Raffaella Rusconi, Paolo Scalmani, Rita Restano‐Cassulini, Giulia Giunti, Antonio Gambardella, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Massimo Mantegazza

    Vydáno 2007
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  5. 5
    Identification of an Na <sub>v</sub> 1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures

    Identification of an Na <sub>v</sub> 1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures Autor Massimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, Emanuele Schiavon, Ferdinanda Annesi, Rita Restano‐Cassulini, Angelo Labate, Sara Carrideo, R. Chifari, Maria Paola Canevini, R. Canger, Silvana Franceschetti, Grazia Annesi, Enzo Wanke, Aldo Quattrone

    Vydáno 2005
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  6. 6
    Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson’s disease – a multicenter study

    Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson’s disease – a multicenter study Autor Malin von Otter, Petra Bergström, Aldo Quattrone, Elvira Valeria De Marco, Grazia Annesi, Peter Söderkvist, Stephanie Bezzina Wettinger, Marek Droździk, Monika Białecka, Hans Nissbrandt, Christine Klein, Michael Nilsson, Ola Hammarsten, Staffan Nilsson, Henrik Zetterberg

    Vydáno 2014
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  7. 7
    Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease

    Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease Autor Silvana Franceschetti, Antonio Gambardella, Laura Canafoglia, Pasquale Striano, Hannes Lohi, Elena Di Gennaro, Leonarda Ianzano, Pierangelo Veggiotti, Vito Sofia, Roberto Biondi, Salvatore Striano, Cinzia Gellera, Grazia Annesi, Francesca Madia, Donatella Civitelli, Francesca E. Rocca, Aldo Quattrone, G. Avanzini, Berge A. Minassian, Federico Zara

    Vydáno 2006
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  8. 8
    Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

    Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study Autor Alexis Elbaz, Lorene M. Nelson, Haydeh Payami, John P. A. Ioannidis, Brian Fiske, Grazia Annesi, Andrea Carmine Belin, Stewart A. Factor, Carlo Ferrarese, Georgios M. Hadjigeorgiou, Donald S. Higgins, Hideshi Kawakami, Rejko Krüger, Karen Marder, Richard Mayeux, George D. Mellick, John G. Nutt, Beate Ritz, Ali Samii, Caroline M. Tanner, Christine Van Broeckhoven, Stephen K. Van Den Eeden, Karin Wirdefeldt, Cyrus P. Zabetian, Marie Dehem, Jennifer S. Montimurro, Audrey Southwick, R Myers, Thomas A Trikalinos

    Vydáno 2006
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  9. 9
    A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

    A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Autor Rejko Krüger, Manu Sharma, Olaf Rieß, Thomas Gasser, Christine Van Broeckhoven, Jessie Theuns, Jan Aasly, Grazia Annesi, Anna Rita Bentivoglio, Alexis Brice, Ana Djarmati, Alexis Elbaz, Matthew J. Farrer, Carlo Ferrarese, J. Mark Gibson, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P. A. Ioannidis, Barbara Jasińska‐Myga, Christine Klein, Jean‐Charles Lambert, Suzanne Lesage, Juei-Jueng Lin, Timothy Lynch, George D. Mellick, Francesa de Nigris, Grzegorz Opala, Alessandro Prigione, Aldo Quattrone, Owen A. Ross, Wataru Satake, Peter A. Silburn, Eng King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Demetrius M. Maraganore

    Vydáno 2009
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  10. 10
    Independent and joint effects of the <i>MAPT</i> and <i>SNCA</i> genes in Parkinson disease

    Independent and joint effects of the <i>MAPT</i> and <i>SNCA</i> genes in Parkinson disease Autor Alexis Elbaz, Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto‐Ortolaza, Frédéric Moisan, Jan Aasly, Grazia Annesi, Maria Bozi, Laura Brighina, Marie‐Christine Chartier‐Harlin, A. Destée, Carlo Ferrarese, Alessandro Ferraris, Jonathan Gibson, Suzana Gispert, Georgios M. Hadjigeorgiou, Barbara Jasińska‐Myga, Christine Klein, Rejko Krüger, Jean‐Charles Lambert, Katja Lohmann, Simone van de Loo, Marie‐Anne Loriot, Timothy Lynch, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Leonidas Stefanis, Ryan J. Uitti, Enza Maria Valente, Carles Vilariño‐Güell, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer

    Vydáno 2010
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  11. 11
    Global investigation and meta-analysis of the <i>C9orf72</i> (G <sub>4</sub> C <sub>2</sub> ) <sub>n</sub> repeat in Parkinson disease

    Global investigation and meta-analysis of the <i>C9orf72</i> (G <sub>4</sub> C <sub>2</sub> ) <sub>n</sub> repeat in Parkinson disease Autor Jessie Theuns, Aline Verstraeten, Kristel Sleegers, Eline Wauters, Ilse Gijselinck, Stefanie Smolders, David Crosiers, Ellen Corsmit, Ellen Elinck, Manu Sharma, Rejko Krüger, Suzanne Lesage, Alexis Brice, Sun Ju Chung, Mi‐Jung Kim, Young Jin Kim, Owen A. Ross, Zbigniew K. Wszołek, Ekaterina Rogaeva, Zhengrui Xi, Anthony E. Lang, Christine Klein, Anne Weißbach, George D. Mellick, Peter A. Silburn, Georgios M. Hadjigeorgiou, Efthimios Dardiotis, Nobutaka Hattori, Kotaro Ogaki, Eng‐King Tan, Yi Zhao, Jan Aasly, Enza Maria Valente, Simona Petrucci, Grazia Annesi, Aldo Quattrone, Carlo Ferrarese, Laura Brighina, Angela Deutschländer, Andreas Puschmann, Christer Nilsson, Gaëtan Garraux, Mark S. LeDoux, Ronald F. Pfeiffer, Magdalena Boczarska‐Jedynak, Grzegorz Opala, Demetrius M. Maraganore, Sebastiaan Engelborghs, Peter Paul De Deyn, Patrick Cras, Marc Cruts, Christine Van Broeckhoven

    Vydáno 2014
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  12. 12
    A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies Autor Michael A. Nalls, Raquel Durán, Grisel Lopez, Marzena Kurzawa‐Akanbi, Ian G. McKeith, Patrick F. Chinnery, Christopher M. Morris, Jessie Theuns, David Crosiers, Patrick Cras, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, David M. A. Mann, Julie S. Snowden, Stuart Pickering‐Brown, Nicola Halliwell, Yvonne S. Davidson, Linda Gibbons, Jenny Harris, Una-Marie Sheerin, José Brás, John Hardy, Lorraine N. Clark, Karen Marder, Lawrence S. Honig, Daniela Berg, Walter Maetzler, Kathrin Brockmann, Thomas Gasser, Fabiana Novellino, Aldo Quattrone, Grazia Annesi, Elvira Valeria De Marco, Ekaterina Rogaeva, Mario Masellis, Sandra E. Black, Juan M. Bilbao, Tatiana Foroud, Bernardino Ghetti, William C. Nichols, Nathan Pankratz, Glenda M. Halliday, Suzanne Lesage, Stephan Klebe, Alexandra Dürr, Charles Duyckaerts, Alexis Brice, Benoit I. Giasson, John Q. Trojanowski, Howard I. Hurtig, Nahid Tayebi, Claudia Landazabal, Melanie A. Knight, Margaux F. Keller, Andrew Singleton, Tyra G. Wolfsberg, Ellen Sidransky

    Vydáno 2013
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  13. 13
    A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

    A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants Autor Manu Sharma, John P. A. Ioannidis, Jan Aasly, Grazia Annesi, Alexis Brice, Lars Bertram, Maria Bozi, Maria Barcikowska, David Crosiers, Carl E Clarke, Maurizio Facheris, Matthew J. Farrer, Gaëtan Garraux, Suzana Gispert, Georg Auburger, Carles Vilariño‐Güell, Georgios M. Hadjigeorgiou, Andrew A. Hicks, Nobutaka Hattori, Beom S. Jeon, Zygmunt Jamrozik, Anna Krygowska‐Wajs, Suzanne Lesage, Christina M. Lill, Juei‐Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E. Lang, Cécile Libioulle, Miho Murata, Vincent Mok, Barbara Jasińska‐Myga, George D. Mellick, Karen Morrison, Thomas Meitnger, Alexander Zimprich, Grzegorz Opala, Peter P. Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne Stockton, Wataru Satake, Peter A. Silburn, Tim M. Strom, Jessie Theuns, Eng King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J. Uitti, Christine Van Broeckhoven, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Harumi Yomono, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius M. Maraganore, Rejko Krüger

    Vydáno 2012
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  14. 14
    Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease Autor E. Sidransky, Mike A. Nalls, Jan Aasly, J. Aharon‐Peretz, Grazia Annesi, Egberto Reis Barbosa, Anat Bar‐Shira, Daniela Berg, José Brás, Alexis Brice, Chien‐Ming Chen, Lorraine N. Clark, Christel Condroyer, Elvira Valeria De Marco, Alexandra Dürr, Michael J. Eblan, S Fahn, Matthew J. Farrer, Hon‐Chung Fung, Ziv Gan‐Or, Thomas Gasser, Ruth Gershoni‐Baruch, Nir Giladi, Alida Griffith, Tanya Gurevich, Cristina Januário, Peter Kropp, Anthony E. Lang, Guey‐Jen Lee‐Chen, Suzanne Lesage, K. Marder, Ignácio F. Mata, Anat Mirelman, Jun Mitsui, Ikuko Mizuta, Giuseppe Nicoletti, Catarina R. Oliveira, Ruth Ottman, Avi Orr‐Urtreger, Lygia da Veiga Pereira, Aldo Quattrone, Ekaterina Rogaeva, A. Rolfs, Hanna Rosenbaum, Roberto Rozenberg, Ali Samii, T. Samaddar, Claudia Schulte, Manu Sharma, Andrew Singleton, Mariana Spitz, Eng‐King Tan, N. Tayebi, Tatsushi Toda, A. R. Troiano, Shoji Tsuji, Matthias Wittstock, Tyra G. Wolfsberg, Yih‐Ru Wu, Cyrus P. Zabetian, Yirui Zhao, Shira G. Ziegler

    Vydáno 2009
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  15. 15
    Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

    Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study Autor Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman, Jan Aasly, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien, Maria Bozi, Alexis Brice, Laura Brighina, Christine Van Broeckhoven, Jonathan Carr, Marie‐Christine Chartier‐Harlin, Efthimios Dardiotis, Dennis W. Dickson, Nancy N. Diehl, Alexis Elbaz, Carlo Ferrarese, Alessandro Ferraris, Brian Fiske, J. Mark Gibson, Rachel A. Gibson, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P. A. Ioannidis, Barbara Jasińska‐Myga, Beom S. Jeon, Yun Joong Kim, Christine Klein, Rejko Krüger, Elli Kyratzi, Suzanne Lesage, Chin‐Hsien Lin, Timothy Lynch, Demetrius M. Maraganore, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Sung Sup Park, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Young H. Sohn, Leonidas Stefanis, Vera Tadić, Jessie Theuns, Hiroyuki Tomiyama, Ryan J. Uitti, Enza Maria Valente, Simone van de Loo, Demetrios K. Vassilatis, Carles Vilariño‐Güell, Linda R. White, Karin Wirdefeldt, Zbigniew K. Wszołek, Ruey‐Meei Wu, Matthew J. Farrer

    Vydáno 2011
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  16. 16
    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease

    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease Autor Cloé Domenighetti, Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed, Berta Portugal, Patrick May, Dheeraj Reddy Bobbili, Milena Radivojkov‐Blagojevic, Peter Lichtner, Andrew Singleton, Dena G. Hernandez, Connor Edsall, George D. Mellick, Alexander Zimprich, Walter Pirker, Ekaterina Rogaeva, Anthony E. Lang, Sulev Kõks, Pille Taba, Suzanne Lesage, Alexis Brice, Jean‐Christophe Corvol, Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimos Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Stefano Duga, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Hirotaka Matsuo, Yusuke Kawamura, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Pierre Kolber, Bart P. van de Warrenburg, Bastiaan R. Bloem, Jan Aasly, Mathias Toft, Lasse Pihlstrøm, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Clara Hellberg, Carl E Clarke, Karen Morrison, Manuela Tan, Dimitri Krainc, Lena F. Burbulla, Matthew J. Farrer, Rejko Krüger, Thomas Gasser, Manu Sharma, Alexis Elbaz

    Vydáno 2021
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  17. 17
    Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study

    Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study Autor Cloé Domenighetti, Pierre‐Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Océane Mohamed, Berta Portugal, Patrick May, Dheeraj Reddy Bobbili, Milena Radivojkov‐Blagojevic, Peter Lichtner, Andrew B. Singleton, Dena G. Hernandez, Connor Edsall, George D. Mellick, Alexander Zimprich, Walter Pirker, Ekaterina Rogaeva, Anthony E. Lang, Sulev Kõks, Pille Taba, Suzanne Lesage, Alexis Brice, Jean‐Christophe Corvol, Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimos Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Stefano Duga, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Hirotaka Matsuo, Yusuke Kawamura, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Pierre Kolber, Bart P.C. van de Warrenburg, Bastiaan R. Bloem, Jan Aasly, Mathias Toft, Lasse Pihlstrøm, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Clara Hellberg, Carl E Clarke, Karen Morrison, Manuela Tan, Dimitri Krainc, Lena F. Burbulla, Matthew J. Farrer, Rejko Krüger, Thomas Gasser, Manu Sharma, Alexis Elbaz

    Vydáno 2022
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  18. 18
    Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease

    Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Autor Sandeep Grover, Ashwin Ashok Kumar Sreelatha, Lasse Pihlstrøm, Cloé Domenighetti, Claudia Schulte, Pierre‐Emmanuel Sugier, Milena Radivojkov‐Blagojevic, Peter Lichtner, Océane Mohamed, Berta Portugal, Zied Landoulsi, Patrick May, Dheeraj Reddy Bobbili, Connor Edsall, Felix Bartusch, Maximilian Hanussek, Jens Krüger, Dena G. Hernandez, Cornelis Blauwendraat, George D. Mellick, Alexander Zimprich, Walter Pirker, Manuela Tan, Ekaterina Rogaeva, Anthony E. Lang, Sulev Kõks, Pille Taba, Suzanne Lesage, Alexis Brice, Jean‐Christophe Corvol, Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimos Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Lena F. Burbulla, Hirotaka Matsuo, Yusuke Kawamura, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Lukas Pavelka, Bart P.C. van de Warrenburg, Bastiaan R. Bloem, Andrew Singleton, Jan Aasly, Mathias Toft, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Clara Hellberg, Carl E Clarke, Karen Morrison, Dimitri Krainc, Matthew J. Farrer, Rejko Krüger, Alexis Elbaz, Thomas Gasser, Manu Sharma

    Vydáno 2022
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  19. 19
    Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project

    Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Projec... Autor Eva‐Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad‐Annuar, Bashayer Al‐Mubarak, Roy N. Alcalay, Victoria Álvarez, Ignacio Amorín, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A. Barker, Melinda Barkhuizen, A. Nazlı Başak, Vincenzo Bonifati, Agnita J.W. Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimón, Mario Cornejo‐Olivas, Leonor Correia Guedes, Jean‐Christophe Corvol, David Crosiers, Joana Damásio, Parimal Das, Patrícia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim J. Ferreira, Emilia Gatto, Gençer Genç, Nir Giladi, Pilar Gómez‐Garre, Haşmet Hanağası, Nobutaka Hattori, Fayçal Hentati, Dorota Hoffman‐Zacharska, С. Н. Иллариошкин, Joseph Jankovic, Silvia Jesús, Valtteri Kaasinen, Anneke J.A. Kievit, Péter Klivényi, Vladimir Kostić, Dariusz Koziorowski, Andrea A. Kühn, Anthony E. Lang, Shen‐Yang Lim, Chin‐Hsien Lin, Katja Lohmann, Vladana Marković, Mika H. Martikainen, George D. Mellick, Marcelo Merello, Łukasz Milanowski, Pablo Mir, Özgür Öztop Çakmak, Márcia Mattos Gonçalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther Sammler, Maria Skaalum Petersen, Matěj Škorvánek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vítor Tumas, Enza Maria Valente, Bart P.C. van de Warrenburg, Caroline H. Williams‐Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein

    Vydáno 2023
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  20. 20
    Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

    Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers Autor Pierre‐Emmanuel Sugier, Elise A. Lucotte, Cloé Domenighetti, Matthew H. Law, Mark M. Iles, Kevin M. Brown, Christopher I. Amos, James McKay, Rayjean J. Hung, Mojgan Karimi, Delphine Bacq‐Daian, Anne Boland, Robert Olaso, Jean‐François Deleuze, Fabienne Lesueur, Evgenia Ostroumova, Ausrele Kesminiene, Florent de Vathaire, Pascal Guénel, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, Sandeep Grover, Patrick May, Dheeraj Reddy Bobbili, Milena Radivojkov‐Blagojevic, Peter Lichtner, Andrew Singleton, Dena G. Hernandez, Connor Edsall, George D. Mellick, Alexander Zimprich, Walter Pirker, Ekaterina Rogaeva, Anthony E. Lang, Sulev Kõks, Pille Taba, Suzanne Lesage, Alexis Brice, Jean‐Christophe Corvol, Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimios Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Hirotaka Matsuo, Akiyoshi Nakayama, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Pierre Kolber, Bart P.C. van de Warrenburg, Bastiaan R. Bloem, Jan Aasly, Mathias Toft, Lasse Pihlstrøm, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Emil Ygland, Carl E Clarke, Karen Morrison, Manuela Tan, Dimitri Krainc, Lena F. Burbulla, Matthew J. Farrer, Rejko Krüger, Thomas Gasser, Manu Sharma, Thérèse Truong, Alexis Elbaz

    Vydáno 2023
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