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Lüdger Schöls

1995–2025 年に発表

別表記
Ludger Schöls
235
論文数
29,568
被引用数
98
h 指数
222
i10 指数

被引用数

Lüdger Schöls の年別被引用数1940 年: 被引用 1 件1967 年: 被引用 18 件1969 年: 被引用 1 件1982 年: 被引用 1 件1988 年: 被引用 1 件1990 年: 被引用 1 件1994 年: 被引用 2 件1995 年: 被引用 2 件1996 年: 被引用 4 件1997 年: 被引用 22 件1998 年: 被引用 37 件1999 年: 被引用 61 件2000 年: 被引用 100 件2001 年: 被引用 108 件2002 年: 被引用 127 件2003 年: 被引用 178 件2004 年: 被引用 172 件2005 年: 被引用 145 件2006 年: 被引用 166 件2007 年: 被引用 142 件2008 年: 被引用 199 件2009 年: 被引用 218 件2010 年: 被引用 196 件2011 年: 被引用 288 件2012 年: 被引用 205 件2013 年: 被引用 351 件2014 年: 被引用 247 件2015 年: 被引用 274 件2016 年: 被引用 215 件2017 年: 被引用 231 件2018 年: 被引用 255 件2019 年: 被引用 922 件2020 年: 被引用 896 件2021 年: 被引用 942 件2022 年: 被引用 761 件2023 年: 被引用 583 件2024 年: 被引用 1,070 件2025 年: 被引用 400 件2026 年: 被引用 29 件1941〜1966 年は被引用が無いため表示していません1968 年は被引用が無いため表示していません1970〜1981 年は被引用が無いため表示していません1983〜1987 年は被引用が無いため表示していません1989 年は被引用が無いため表示していません1991〜1993 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,653 件、この内訳の 22.7%ドイツ: 引用元論文 1,205 件、この内訳の 10.3%イギリス: 引用元論文 1,046 件、この内訳の 9%イタリア: 引用元論文 682 件、この内訳の 5.8%フランス: 引用元論文 563 件、この内訳の 4.8%カナダ: 引用元論文 460 件、この内訳の 3.9%中国: 引用元論文 440 件、この内訳の 3.8%オランダ: 引用元論文 412 件、この内訳の 3.5%オーストラリア: 引用元論文 385 件、この内訳の 3.3%日本: 引用元論文 359 件、この内訳の 3.1%スペイン: 引用元論文 355 件、この内訳の 3%ベルギー: 引用元論文 249 件、この内訳の 2.1%
0%22.7%その他 24.7%

機関

分野

  • Medicine45.3%
  • Neuroscience33%
  • Biochemistry, Genetics and Molecular Biology19.1%
  • Health Professions0.4%
  • Computer Science0.4%
  • Immunology and Microbiology0.4%
  • その他1.4%

トピック

  • Parkinson's Disease Mechanisms and Treatments11.2%
  • Genetic Neurodegenerative Diseases10.5%
  • Mitochondrial Function and Pathology6.2%
  • Neurological disorders and treatments4.9%
  • Alzheimer's disease research and treatments3.5%
  • Neurological diseases and metabolism3.4%
  • その他60.3%

共著者

全論文

検索で開く
  1. Scale for the assessment and rating of ataxia

    著者: T. Schmitz-Hübsch, Sophie Tézenas du Montcel, L. Baliko, José Berciano, Sylvia Boesch, Chantal Depondt, Paola Giunti, Christoph Globas, Jon Infante, J.-S. Kang, B. Kremer, Caterina Mariotti, Béla Melegh, M. Pandolfo, Maria Rakowicz, Pascale Ribaı̈, Rafał Rola, Lüdger Schöls, Sandra Szymanski, Bart P.C. van de Warrenburg, Alexandra Dürr, Thomas Klockgether - Neurology 2006 被引用: 1,958

  2. Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

    著者: David Pellerin, Matt C. Danzi, Carlo Wilke, M. Renaud, Sarah Fazal, Marie‐Josée Dicaire, Carolin K. Scriba, Catherine Ashton, Christopher Yanick, Danique Beijer, Adriana Rebelo, Clarissa Rocca, Zane Jaunmuktane, Joshua A. Sonnen, Roxanne Larivière, David Genı́s, Laura Molina‐Porcel, Karine Choquet, Rawan Sakalla, Sylvie Provost, Rebecca Robertson, Xavier Allard‐Chamard, Martine Tétreault, Sarah J. Reiling, Sara Nagy, Vikas Nishadham, Meera Purushottam, Seena Vengalil, Mainak Bardhan, Atchayaram Nalini, Zhongbo Chen, Jean Mathieu, Rami Massie, Colin Chalk, Anne‐Louise Lafontaine, François Evoy, Marie‐France Rioux, Jiannis Ragoussis, Kym M. Boycott, Marie‐Pierre Dubé, Antoine Duquette, Henry Houlden, Gianina Ravenscroft, Nigel G. Laing, Phillipa J. Lamont, Mario Saporta, Rebecca Schüle, Lüdger Schöls, Roberta La Piana, Matthis Synofzik, Stephan Züchner, Bernard Brais - New England Journal of Medicine 2022 被引用: 243

  3. AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease

    著者: Rejko Krüger, W. Kuhn, Thomas Müller, Dirk Woitalla, Manuel B. Graeber, Sigfried Kösel, H. Przuntek, Jörg T. Epplen, Lüdger Schöls, Olaf Rieß - Nature Genetics 1998 被引用: 3,885

  4. Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans

    著者: Jack J. Collier, Claire Guissart, Monika Oláhová, Souphatta Sasorith, Florence Piron‐Prunier, Fumi Suomi, David Zhang, Nuria Martinez-Lopez, Nicolas Leboucq, Angela Bahr, Silvia Azzarello‐Burri, Selina Reich, Lüdger Schöls, Tuomo Polvikoski, Pierre Meyer, Lise Larrieu, Andrew M. Schaefer, Hessa S. Alsaif, Suad Alyamani, Stephan Züchner, Inês A. Barbosa, Charu Deshpande, Angela Pyle, Anita Rauch, Matthis Synofzik, Fowzan S. Alkuraya, François Rivier, Mina Ryten, Robert McFarland, Agnés Delahodde, Thomas G. McWilliams, Michel Koenig, Robert W. Taylor - New England Journal of Medicine 2021 被引用: 194

  5. GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response

    著者: Carlo Wilke, David Pellerin, David Mengel, Andreas Traschütz, Matt C. Danzi, Marie‐Josée Dicaire, Manuela Neumann, Holger Lerche, Benjamin Bender, Henry Houlden, RFC1 study group, Jennifer Faber, Richard Roxburgh, José Luiz Pedroso, Paula Camila Alvez, Orlando Graziani Póvoas Barsottini, Chiara Pane, Francesco Saccà, Alessandro Filla, Filippo M. Santorelli, Ivana Ricca, Stephan Züchner, Lüdger Schöls, Bernard Brais, Matthis Synofzik - Brain 2023 被引用: 114

  6. As Frequent as Polyglutamine Spinocerebellar Ataxias: SCA27B in a Large German Autosomal Dominant Ataxia Cohort

    著者: Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik - Movement Disorders 2023 被引用: 65

  7. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

    著者: Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M. de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen, Stephan Ossowski, Peter A.C. ’t Hoen, Antonio Vitobello, Julia M. Schulze‐Hentrich, Olaf Rieß, Han G. Brunner, Anthony J. Brookes, Ana Rath, Gisèle Bonne, Gulcin Gumus, Alain Verloès, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris A. Swertz, Dylan Spalding, Alexander Hoischen, Sergi Beltrán, Holm Graeßner, T. Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Keßler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Lüdger Schöls, Holger Hengel, Peter Heutink, Han G. Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M. de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldız, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, C. Marini Bettolo, Sabine Specht, Jill Clayton‐Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne‐Sophie Denommé‐Pichon, Yannis Duffourd, Émilie Tisserant, Ange‐Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltrán, Marta Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvò, Carles García, Marcos Fernandez-Callejo, Carles Hernandéz-Ferrer, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros‐Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem ほか 123 名 - European Journal of Human Genetics 2021 被引用: 103

  8. Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7

    著者: Udo Rüb, Lüdger Schöls, Henry L. Paulson, Georg Auburger, Pawel Kermer, Joanna C. Jen, Kay Seidel, Horst‐Werner Korf, Thomas Deller - Progress in Neurobiology 2013 被引用: 360

  9. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

    著者: Heike Jacobi, Sophie Tézenas du Montcel, Peter Bauer, Paola Giunti, Arron Cook, Robyn Labrum, Michael Parkinson, Alexandra Dürr, Alexis Brice, Perrine Charles, Cécilia Marelli, Caterina Mariotti, Lorenzo Nanetti, Marta Panzeri, Maria Rakowicz, Anna Sułek, Anna Sobańska, Tanja Schmitz‐Hübsch, Lüdger Schöls, Holger Hengel, László Balikó, Béla Melegh, Alessandro Filla, Antonella Antenora, Jon Infante, José Berciano, Bart P.C. van de Warrenburg, Dagmar Timmann, Sandra Szymanski, Sylvia Boesch, Jun-Suk Kang, Massimo Pandolfo, Jörg B. Schulz, Sonia Molho, Alhassane Diallo, Thomas Klockgether - The Lancet Neurology 2015 被引用: 299

  10. Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

    著者: Maria-Ceù Moreira, Sandra Klur, Masao Watanabe, Andrea H. Németh, Isabelle Le Ber, José-Carlos Moniz, Christine Tranchant, Patrick Aubourg, Meriem Tazir, Lüdger Schöls, Massimo Pandolfo, Jörg B. Schulz, Jean Pouget, Patrick Calvas, Masami Shizuka‐Ikeda, Mikio Shoji, Μakoto Tanaka, Louise Izatt, Christopher E. Shaw, M’zahem Abderrahim, Eimear Dunne, Pascale Bomont, Traki Benhassine, Naïma Bouslam, Giovanni Stévanin, Alexis Brice, Joao C. Guimaraes, Pedro Mendonça, Clara Barbot, Paula Coutinho, Jorge Sequeiros, Alexandra Dürr, Jean‐Marie Warter, Michel Kœnig - Nature Genetics 2004 被引用: 521

  11. Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease

    著者: Andreas Traschütz, Andrea Cortese, Selina Reich, Natalia Dominik, Jennifer Faber, Heike Jacobi, Annette M. Hartmann, Dan Rujescu, Solveig Montaut, Andoni Echaniz‐Laguna, Sevda Erer, Valerie Schütz, Alexander A. Tarnutzer, Marc Sturm, Tobias B. Haack, Nadège Vaucamps-Diedhiou, Hélène Puccio, Lüdger Schöls, Thomas Klockgether, Bart P.C. van de Warrenburg, Martin Paucar, Dagmar Timmann, R.-D Hilgers, José Gazulla, Michael Strupp, Germán Morís, Alessandro Filla, Henry Houlden, Mathieu Anheim, Jon Infante, A. Nazli Basak, Matthis Synofzik, on behalf of the RFC1 Study Group, Banu Özen Barut, Başar Bılgıç, Cavit Boz, Cécile Cauquil, Natalie Deininger, Claudia Dufke, Bülent Elibol, Furkan Erbas, Sibel Ertan, Fatma Genç, Ina Giegling, Yeşim Parman, Salvatore Rossi, Celal Salcin, Meli̇ha Tan, Hilal Taştekin, Christine Tranchant, Günes Uygun, Özge Yağcıoğlu Yassa - Neurology 2021 被引用: 164

  12. IntronicFGF14GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy

    著者: David Pellerin, Carlo Wilke, Andreas Traschütz, Sara Nagy, Riccardo Curró, Marie‐Josée Dicaire, Héctor García‐Moreno, Mathieu Anheim, Thomas Wirth, Jennifer Faber, Dagmar Timmann, Christel Depienne, Dan Rujescu, José Gazulla, Mary M. Reilly, Paola Giunti, Bernard Brais, Henry Houlden, Lüdger Schöls, Michael Strupp, Andrea Cortese, Matthis Synofzik - Journal of Neurology Neurosurgery & Psychiatry 2023 被引用: 45

  13. Neurofilament light levels predict clinical progression and death in multiple system atrophy

    著者: Viorica Chelban, Elham Nikram, Alexandra Pérez‐Soriano, Carlo Wilke, Alexandra Foubert‐Samier, Nirosen Vijiaratnam, Tong Guo, Edwin Jabbari, Simisola Olufodun, Mariel Gonzalez, Konstantin Senkevich, Brice Laurens, Patrice Péran, Olivier Rascol, Anne Pavy‐Le Traon, Emily Todd, Alyssa Costantini, Sondos Alikhwan, Ambreen Tariq, Bai Lin Ng, Esteban Muñoz, Cèlia Painous, Yaroslau Compta, Carme Junqué, Bàrbara Segura, Kristina Zhelcheska, Henny Wellington, Lüdger Schöls, Zane Jaunmuktane, Christopher Kobylecki, Alistair Church, Michele T M Hu, James B. Rowe, P. Nigel Leigh, Luke A. Massey, David J. Burn, Nicola Pavese, Thomas Foltynie, Sofya Pchelina, Nicholas Wood, Amanda Heslegrave, Henrik Zetterberg, Martina Bocchetta, Jonathan D. Rohrer, Marı́a José Martı́, Matthis Synofzik, Huw R. Morris, Wassilios G. Meissner, Henry Houlden - Brain 2022 被引用: 73

  14. Real-life gait assessment in degenerative cerebellar ataxia

    著者: Winfried Ilg, Jens Seemann, Martin A. Giese, Andreas Traschütz, Lüdger Schöls, Dagmar Timmann, Matthis Synofzik - Neurology 2020 被引用: 95

  15. The natural history of spinocerebellar ataxia type 1, 2, 3, and 6

    著者: Heike Jacobi, Peter Bauer, Paola Giunti, Robyn Labrum, M G Sweeney, Perrine Charles, Alexandra Dürr, Cécilia Marelli, Christoph Globas, Christoph Linnemann, Lüdger Schöls, Maria Rakowicz, Rafał Rola, Elżbieta Zdzienicka, T. Schmitz-Hübsch, Roberto Fancellu, Caterina Mariotti, Chiara Tomasello, László Balikó, Béla Melegh, Alessandro Filla, Carlo Rinaldi, Bart P.C. van de Warrenburg, C.C.P. Verstappen, Sandra Szymanski, José Berciano, Jon Infante, Dagmar Timmann, Sylvia Boesch, Sascha Hering, Chantal Depondt, Massimo Pandolfo, J.-S. Kang, Susanne Ratzka, Jörg B. Schulz, Sophie Tézenas du Montcel, Thomas Klockgether - Neurology 2011 被引用: 228

  16. Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study

    著者: Kathrin Reetz, Imis Dogan, R.-D Hilgers, Paola Giunti, Michael Parkinson, Caterina Mariotti, Lorenzo Nanetti, Alexandra Dürr, Claire Ewenczyk, Sylvia Boesch, Wolfgang Nachbauer, Thomas Klopstock, Claudia Stendel, Francisco Javier Rodríguez de Rivera Garrido, Christian Rummey, Lüdger Schöls, Stefanie N. Hayer, Thomas Klockgether, Ilaria Giordano, Claire Didszun, Myriam Rai, Massimo Pandolfo, Jörg B. Schulz, Robyn Labrum, Gilbert Thomas‐Black, Katarina Manso, Nita Solanky, Cinzia Gellera, Alessia Mongelli, Anna Castaldo, Mario Fichera, Francesc Palau, Mar O’Callaghan, Marie Biet, Marie Lorraine Monin, Andreas Eigentler, Elisabetta Indelicato, Matthias Amprosi, Florentine Radelfahr, A. Bischoff, Florian Holtbernd, Nikolina Brčina, Christian Hohenfeld, Georgios Koutsis, Marianthi Breza, Enrico Bertini, Gessica Vasco - The Lancet Neurology 2021 被引用: 97

  17. Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy

    著者: Christiane Kehrer, Saskia Elgün, Christa Raabe, Judith Böhringer, Stefanie Beck‐Wödl, Andrea Bevot, Nadja Kaiser, Lüdger Schöls, Ingeborg Krägeloh‐Mann, Samuel Groeschel - Neurology 2020 被引用: 93

  18. Digital Gait Biomarkers Allow to Capture 1‐Year Longitudinal Change in Spinocerebellar Ataxia Type 3

    著者: Winfried Ilg, Björn Müller, Jennifer Faber, Judith van Gaalen, Holger Hengel, Ina R. Vogt, Guido Hennes, Bart P.C. van de Warrenburg, Thomas Klockgether, Lüdger Schöls, Matthis Synofzik - Movement Disorders 2022 被引用: 56

  19. Altered brain dynamics index levels of arousal in complete locked-in syndrome

    著者: Federico Zilio, Javier Gómez‐Pilar, Ujwal Chaudhary, Stuart Fogel, Tatiana Fomina, Matthis Synofzik, Lüdger Schöls, Shumei Cao, Jun Zhang, Zirui Huang, Niels Birbaumer, Georg Northoff - Communications Biology 2023 被引用: 35

  20. Responsiveness of different rating instruments in spinocerebellar ataxia patients

    著者: T. Schmitz‐Hübsch, R. Fimmers, Maria Rakowicz, Rafał Rola, Elżbieta Zdzienicka, Roberto Fancellu, Caterina Mariotti, Christoph Linnemann, Lüdger Schöls, Dagmar Timmann, Alessandro Filla, Elena Salvatore, Jon Infante, Paola Giunti, Robyn Labrum, B. Kremer, Bart P.C. van de Warrenburg, L. Baliko, Béla Melegh, Chantal Depondt, Jörg B. Schulz, Sophie Tézenas du Montcel, Thomas Klockgether - Neurology 2010 被引用: 190

  21. Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6

    著者: Sophie Tézenas du Montcel, Alexandra Dürr, Maria Rakowicz, Lorenzo Nanetti, Perrine Charles, Anna Sułek, Caterina Mariotti, Rafał Rola, Lüdger Schöls, Peter Bauer, I. Dufaure-Garé, Heike Jacobi, Sylvie Forlani, Tanja Schmitz‐Hübsch, Alessandro Filla, Dagmar Timmann, Bart P. van de Warrenburg, Cecila Marelli, Jun-Suk Kang, Paola Giunti, Arron Cook, László Balikó, Béla Melegh, Sylvia Boesch, Sandra Szymanski, José Berciano, Jon Infante, Katrin Buerk, Marcella Masciullo, Roberto Di Fabio, Chantal Depondt, Susanne Ratka, Giovanni Stévanin, Thomas Klockgether, Alexis Brice, Jean-Louis Golmard - Journal of Medical Genetics 2014 被引用: 123

  22. The Spastic Paraplegia Rating Scale (SPRS)

    著者: Rebecca Schüle, T. Holland-Letz, Sven Klimpe, Jan Kassubek, Thomas Klopstock, Volker Mall, S. Otto, Beate Winner, Lüdger Schöls - Neurology 2006 被引用: 306

  23. Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data

    著者: Kathrin Reetz, Imis Dogan, Ana Sofia Costa, Manuel Dafotakis, Kathrin Fedosov, Paola Giunti, Michael Parkinson, Mary G. Sweeney, Caterina Mariotti, Marta Panzeri, Lorenzo Nanetti, Javier Arpa, Irene Sanz‐Gallego, Alexandra Dürr, Perrine Charles, Sylvia Boesch, Wolfgang Nachbauer, Thomas Klopstock, Ivan Karin, Chantal Depondt, Jennifer Müller vom Hagen, Lüdger Schöls, Ilaria Giordano, Thomas Klockgether, Katrin Bürk, Massimo Pandolfo, Jörg B. Schulz - The Lancet Neurology 2015 被引用: 211

  24. Delineating MT-ATP6 -associated disease

    著者: Claudia Stendel, Christiane Neuhofer, Elisa Floride, Yuqing Shi, Rebecca Ganetzky, Joohyun Park, Peter Freisinger, Cornelia Kornblum, Stephanie Kleinle, Lüdger Schöls, Felix Distelmaier, Georg M. Stettner, Boriana Büchner, Marni J. Falk, Johannes A. Mayr, Matthis Synofzik, Angela Abicht, Tobias B. Haack, Holger Prokisch, Saskia B. Wortmann, Kei Murayama, Fang Fang, Thomas Klopstock, on behalf of the ATP6 Study Group - Neurology Genetics 2020 被引用: 107