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Matthis Synofzik

ResearcherPublications, citations & collaboration network

Matthis Synofzik is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Matthis Synofzik have?

ScholarIQindexed works

Matthis Synofzik has 737 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Matthis Synofzik have?

ScholarIQcitation count

Matthis Synofzik has 22,900 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Matthis Synofzik?

ScholarIQh-index

Matthis Synofzik has an h-index of 76 in OpenAlex.

What is the i10-index of Matthis Synofzik?

ScholarIQi10-index

Matthis Synofzik has an i10-index of 379 in OpenAlex.

What is the ORCID of Matthis Synofzik?

ScholarIQorcid

The ORCID for Matthis Synofzik is on the source record.

What is the OpenAlex record for Matthis Synofzik?

ScholarIQopenalex

The OpenAlex for Matthis Synofzik is on the source record.

What are the most-cited papers on Matthis Synofzik?

ScholarIQmost cited works
Targeted next generation sequencing as a diagnostic tool in epileptic disorders
Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand, Max Schubach, Christian Wilhelm, Isabelle Steiner, Jörg Hansen, Carolina Courage, Sabina Gallati, Sarah Bürki, Susi Strozzi, Barbara Goeggel Simonetti, Sebastian Grunt, Maja Steinlin, Michael Alber, Markus Wolff, Thomas Klopstock, Eva Christina Prott, Rüdiger Lorenz, Christiane Spaich, Sabine Rona, Maya Lakshminarasimhan, Judith F. Kroll, Thomas Dorn, Günter Krämer, Matthis Synofzik, Felicitas Becker, Yvonne Weber, Holger Lerche, Detlef Böhm, Saskia Biskup
Epilepsia. 2012332 CitationsOPEN ACCESS
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina Moore, Jennifer Nicholas, Murray Grossman, Corey T. McMillan, David J. Irwin, Lauren Massimo, Vivianna M Van Deerlin, Jason D. Warren, Nick C. Fox, Martin N. Rossor, Simon Mead, Martina Bocchetta, Bradley F. Boeve, David S. Knopman, Neill R. Graff‐Radford, Leah K. Forsberg, Rosa Rademakers, Zbigniew K. Wszołek, John C. van Swieten, Lize C. Jiskoot, Lieke Meeter, Elise G.P. Dopper, Janne M. Papma, Julie S. Snowden, Jennifer A. Saxon, Matthew Jones, Stuart Pickering‐Brown, Isabelle Le Ber, Agnès Camuzat, Alexis Brice, Paola Caroppo, Roberta Ghidoni, Michela Pievani, Luisa Benussi, Giuliano Binetti, Bradford C. Dickerson, Diane Lucente, Samantha Krivensky, Caroline Graff, Linn Öijerstedt, Marie Fallström, Håkan Thonberg, Nupur Ghoshal, John C. Morris, Barbara Borroni, Alberto Benussi, Alessandro Padovani, Daniela Galimberti, Elio Scarpini, Giorgio Fumagalli, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, Pheth Sengdy, Adam L. Boxer, Howie Rosen, Joanne Taylor, Matthis Synofzik, Carlo Wilke, Patricia Sulzer, John R. Hodges, Glenda M. Halliday, John B. Kwok, Raquel Sánchez‐Valle, Albert Lladó, Sergi Borrego‐Écija, Isabel Santana, Maria Rosário Almeida, Miguel Tábuas‐Pereira, Fermín Moreno, Myriam Barandiarán, Begoña Indakoetxea, Johannes Levin, Adrian Danek, James B. Rowe, Thomas Cope, Markus Otto, Sarah Anderl‐Straub, Alexandre de Mendonça, Carolina Maruta, Mario Masellis, Sandra E. Black, Philippe Couratier, Géraldine Lautrette, Edward D. Huey, Sandro Sorbi, Benedetta Nacmias, Robert Laforce, Marie-Pier L Tremblay, Rik Vandenberghe, Philip Van Damme, Emily Rogalskı, Sandra Weıntraub, Alexander Gerhard, Chiadi U. Onyike, Simon Ducharme, Sokratis G. Papageorgiou, Adeline Su Lyn Ng, Amy Brodtmann, Elizabeth Finger, Rita Guerreiro
The Lancet Neurology. 2019321 CitationsOPEN ACCESS
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
Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALS
Madhurima Chatterjee, Selcuk Özdemir, Christian Fritz, Wiebke Möbius, Luca Kleineidam, Eckhard Mandelkow�, Jacek Biernat, Cem Doğdu, Oliver Peters, Nicoleta Carmen Cosma, Xiao Wang, Luisa‐Sophie Schneider, Josef Priller, Eike Jakob Spruth, Andrea A. Kühn, Patricia Krause, Thomas Klockgether, Ina R. Vogt, Okka Kimmich, Annika Spottke, Daniel C. Hoffmann, Klaus Fließbach, Carolin Miklitz, Cornelia McCormick, Patrick Weydt, Björn Falkenburger, Moritz Brandt, René Guenther, Elisabeth Dinter, Jens Wiltfang, Niels Hansen, Mathias Bähr, Inga Zerr, Agnes Flöel, Peter J. Nestor, Emrah Düzel, Wenzel Glanz, Enise I. Incesoy, Katharina Bürger, Daniel Janowitz, Robert Perneczky, Boris‐Stephan Rauchmann, Franziska Hopfner, Olivia Wagemann, Johannes Levin, Stefan Teipel, Ingo Kilimann, Doreen Göerß, Johannes Prudlo, Thomas Gasser, Kathrin Brockmann, David Mengel, Milan Zimmermann, Matthis Synofzik, Carlo Wilke, Judit Selma‐González, Janina Turón‐Sans, Miguel Santos‐Santos, Daniel Alcolea, Sara Rubio‐Guerra, Juan Fortea, Álvaro Carbayo, Alberto Lleó, Ricardo Rojas‐García, Ignacio Illán‐Gala, Michael Wagner, Ingo Frommann, Sandra Roeske, L Bertram, Michael T. Heneka, Frederic Brosseron, Alfredo Ramı́rez, Matthias Schmid, Rudi Beschorner, Annett Halle, Jochen Herms, Manuela Neumann, Nicolas R. Barthélemy, Randall J. Bateman, Patrizia Rizzu, Peter Heutink, Oriol Dols‐Icardo, Günter U. Höglinger, Andreas Hermann, Anja Schneider
Nature Medicine. 2024194 CitationsOPEN ACCESS

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