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How has Burkhard Gess's publication output changed over time?
ScholarIQpublication output · 2011–2022
Output grew0% over the shown period — from 1 works in 2011 to 1 in 2022.
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20112013201420172018201920212022
What are the most-cited papers on Burkhard Gess?
ScholarIQmost cited works
Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update
Angela Dispenzieri, Teresa Coelho, Isabel Conceição, Márcia Waddington‐Cruz, Jonas Wixner, Arnt V. Kristen, Claudio Rapezzi, Violaine Planté‐Bordeneuve, Juan González‐Moreno, Mathew S. Maurer, Martha Grogan, Doug Chapman, Leslie Amass, the THAOS investigators, Pablo García Pavía, Ivaylo Tarnev, José González‐Costello, Maria Alejandra Gonzalez Duarte Briseno, Hartmut Schmidt, Brian Drachman, Fábio Barroso, Taro Yamashita, Olivier Lairez, Yoshiki Sekijima, Giuseppe Vita, Eun‐Seok Jeon, Mazen Hanna, David Slosky, Marco Luigetti, Samantha LoRusso, Francisco Muñoz Beamud, David Adams, H. Moelgaard, Rayomand Press, Calogero Lino Cirami, Hans Nienhuis, Josep Maria Campistol Plana, Jocelyn Inamo, Daniel Jacoby, Michele Emdin, Dianna Quan, Scott L. Hummel, Ronald Witteles, Amir Dori, Sanjiv J. Shah, Daniel J. Lenihan, Olga Azevedo, Srinivas Murali, Saša Živković, Soon-Chai Low, José Nativi-Nicolau, Nowell M. Fine, José Tallaj, Carsten Tschöepe, Roberto Fernández‐Torrón, Michael Polydefkis, Giampaolo Merlini, Sorina Bădeliță, Stephen S. Gottlieb, James M. Tauras, Edileide Barros Correia, Hector Ventura, Burkhard Gess, Felix Darstein, Jeeyoung Oh, Tessa Marburger, Johan Van Cleemput, Valeria Salutto, Yeşim Parman, Chi‐Chao Chao, Nitasha Sarswat, Christopher R. Mueller, D. Eric Steidley, Jeffrey Ralph, Alberta L. Warner, William Cotts, James E. Hoffman, Marcelo Rugiero, Sonoko Misawa, J.L. Muñoz Blanco, Lucía Galán Dávila, Menachem Sadeh, Jin Luo, Theodoros Kyriakides, Annabel Wang, Horacio Kaufmann, Saša Živković
Orphanet Journal of Rare Diseases. 202291 CitationsOPEN ACCESS
Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies
Maike F. Dohrn, Nicola Glöckle, Lejla Mulahasanovic, Corina Heller, Julia Mohr, Christine Bauer, Erik Riesch, Andrea C. Becker, Florian Battke, Konstanze Hörtnagel, Thorsten Hornemann, Saranya Suriyanarayanan, Markus Blankenburg, Jörg B. Schulz, Kristl G. Claeys, Burkhard Gess, István Katona, A. Ferbert, Debora Vittore, Alexander Grimm, Stefan Wolking, Lüdger Schöls, Holger Lerche, Georg Christoph Korenke, Dirk Fischer, Bertold Schrank, Urania Kotzaeridou, Gerhard Kurlemann, Bianca Dräger, Anja Schirmacher, Peter Young, Beate Schlotter‐Weigel, Saskia Biskup
S135837084. 201780 Citations
Caveolin-1–mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotype
Camila C. Portugal, Renato Socodato, Teresa Canedo, Cátia M. Silva, Tânia Martins, Vivian S. M. Coreixas, Erick Correia Loiola, Burkhard Gess, Dominik Röhr, Ana Raquel Santiago, Peter Young, Richard D. Minshall, Roberto Paes‐de‐Carvalho, António Francisco Ambrósio, João B. Relvas
S155937366. 201779 CitationsOPEN ACCESS
Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population
Burkhard Gess, Anja Schirmacher, Matthias Boentert, Peter Young
S50004817. 201375 Citations
Prognostic factors in ALS: a comparison between Germany and China
Johannes Dorst, Lu Chen, Angela Rosenbohm, Jens Dreyhaupt, Annemarie Hübers, Joachim Schuster, Jochen H. Weishaupt, Jan Kassubek, Burkhard Gess, Thomas Meyer, Ute Weyen, Andreas Hermann, Jürgen Winkler, Torsten Grehl, Tim Hagenacker, Paul Lingor, Jan Christoph Koch, Anne D. Sperfeld, Susanne Petri, Julian Großkreutz, Moritz Metelmann, Joachim Wolf, Andrea Sylvia Winkler, Thomas Klopstock, Matthias Boentert, Siw Johannesen, Alexander Storch, Bertold Schrank, Daniel Zeller, Xiaolu Liu, Lu Tang, Dongsheng Fan, Albert C. Ludolph
Journal of Neurology. 201971 Citations
Related on ScholarIQ
Evangelisches Krankenhaus Bielefeld
Institution
Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update
Paper
Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies
Paper
Caveolin-1–mediated internalization of the vitamin C transporter SVCT2 in microglia triggers an inflammatory phenotype
Paper
Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population
Paper
Prognostic factors in ALS: a comparison between Germany and China
Paper