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Lüdger Schöls

ResearcherPublications, citations & collaboration network

Lüdger Schöls is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Lüdger Schöls have?

ScholarIQindexed works

Lüdger Schöls has 1,015 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Lüdger Schöls have?

ScholarIQcitation count

Lüdger Schöls has 37,450 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Lüdger Schöls?

ScholarIQh-index

Lüdger Schöls has an h-index of 99 in OpenAlex.

What is the i10-index of Lüdger Schöls?

ScholarIQi10-index

Lüdger Schöls has an i10-index of 427 in OpenAlex.

What is the ORCID of Lüdger Schöls?

ScholarIQorcid

The ORCID for Lüdger Schöls is on the source record.

What is the OpenAlex record for Lüdger Schöls?

ScholarIQopenalex

The OpenAlex for Lüdger Schöls is on the source record.

What are the most-cited papers on Lüdger Schöls?

ScholarIQmost cited works
Leitlinien für Diagnostik und Therapie in der Neurologie
H. C. Diener, Christian Weimar, Peter Berlit, Günther Deuschl, Christian E. Elger, Ralf Gold, Werner Hacke, Andreas Hufschmidt, Heinrich P. Mattle, Ullrich Meier, W. H. Oertel, Heinz Reichmann, Erich Schmutzhard, Claus‐W. Wallesch, Michael Weller, Hermann Ackermann, Gabriele Arendt, Ralf Baron, Helmuth Steinmetz, Peter-Dirk Berlit, Christian G. Bien, Frank Birklein, Armin Curt, Marcus Deschauer, G. Deuschl, Rolf R. Diehl, Hans‐Christoph Diener, Marianne Dieterich, Karla Eggert, Christian E. Elger, Matthias Endres, Stefanie Förderreuther, Christian Gerloff, Franz X. Glocker, Ralf Gold, Gerhard F. Hamann, Josef G. Heckmann, Michael G. Hennerici, W. Hermann, Stefan Hesse, Dieter Heuß, Wolfgang H. Jost, Eric Jéttler, Reinhard Kaiser, Hans‐Otto Karnath, Oliver Kastrup, Thomas Klockgether, Cornelia Kornblum, Frank Lehmann‐Horn, Heinz Reichmann, Frank Leypoldt, Joachim Liepert, Rainer Lindemuth, Albert C. Ludolph, Matthias Maschke, Arne May, Geert Mayer, Hans‐Michael Meinck, Uta Meyding-Lamadü, Sandra Verena Méller, Kirsten Méller-Vahl, Roland Nau, Gereon Nelles, Wolfgang H. Oertel, Walter Paulus, Hans‐Walter Pfister, Marcus Pohl, Mario Prosiegel, Sebastian Rauer, Heinz Reichmann, E. Bernd Ringelstein, Felix Rosenow, Carsten Saft, Dirk Sander, K. Scheglmann, Uwe Schlegel, Erich Schmutzhard, Christiane Schneider‐Gold, Lüdger Schöls, Paul Walter Schönle, Jörg B. Schulz, Claudia Sommer, Thorsten Steiner, Helmuth Steinmetz, Andreas Straubev, Dominik Straumann, Michael Strupp, Walter Sturm, Hans‐Michael Meinck, Martin Tegenthoff, Eckhard Thiel, Gerhard F. Hamann, Angelika Thöne-Otto, Claudia Trenkwalder, Wolfram Ziegler, Roland Veltkamp, Jens Volkmann, Gunnar Wasner, Jörg R. Weber, Christian Weimar
2012431 Citations
Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study
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. 2015299 Citations
A Pan‐<scp>E</scp>uropean Study of the<i>C9orf72</i>Repeat Associated with<scp>FTLD</scp>: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei‐Hsin Chiang, Marie Westerlund, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni B. Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Michael T. Heneka, Frank Jessen, Radoslav Matěj, Eva Parobková, Gábor G. Kovács, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Patrick Santens, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Marc Cruts, Julie van der Zee, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Stéphanie Philtjens, Kristel Sleegers, Veerle Bäumer, Githa Maes, Ellen Corsmit, Marc Cruts, Marc Cruts, Christine Van Broeckhoven, Tim Van Langenhove, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Stéphanie Philtjens, Jessie Theuns, Kristel Sleegers, Veerle Bäumer, Githa Maes, Marc Cruts, Marc Cruts, Christine Van Broeckhoven, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter P. De Deyn, Patrick Cras, Sebastiaan Engelborghs, Peter P. De Deyn, Mathieu Vandenbulcke, Mathieu Vandenbulcke, Barbara Borroni, Alessandro Padovani
Human Mutation. 2012269 CitationsOPEN ACCESS
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
Mathieu Anheim, B. Monga, Marie‐Céline Fleury, Perrine Charles, Clara Barbot, Mustafa A. Salih, Jean‐Pierre Delaunoy, M. Fritsch, Larissa Arning, Matthis Synofzik, Lüdger Schöls, Jorge Sequeiros, Cyril Goizet, Cécilia Marelli, Isabelle Le Ber, Jeanette Koht, José Gazulla, Jan De Bleecker, Moawia M. Mukhtar, Nathalie Drouot, Lamia Alipacha, Traki Benhassine, M. Chbicheb, A. M’zahem, Abdelmadjid Hamri, B. Chabrol, Jean Pouget, Raymond P. Murphy, Masao Watanabe, Paula Coutinho, Mériem Tazir, Alexandra Dürr, Alexis Brice, Christine Tranchant, M. Koenig
Brain. 2009249 CitationsOPEN ACCESS
Variant in the sequence of the LINGO1 gene confers risk of essential tremor
Hreinn Stefánsson, Stacy Steinberg, Hjörvar Pétursson, Ómar Gústafsson, Iris H Gudjonsdottir, Guðrún A. Jónsdóttir, Stefan Palsson, Thorlákur Jónsson, Jona Saemundsdottir, Gyða Björnsdóttir, Yvonne Böttcher, Theodora Thorlacius, Dietrich Haubenberger, Alexander Zimprich, Eduard Auff, Christoph Hotzy, Claudia Testa, Lisa A Miyatake, Ami Rosen, Kristleifur Kristleifsson, David B. Rye, Friedrich Asmus, Lüdger Schöls, Martin Dichgans, Finnbogi Jakobsson, John Benedikz, Unnur Þorsteinsdóttir, Jeffrey R. Gulcher, Augustine Kong, Kāri Stefánsson
Nature Genetics. 2009226 Citations

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