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Anzahl der Publikationen: 19
Zeitschriftenartikel
Hopfner, Franziska 
ORCID: https://orcid.org/0000-0001-6524-0281; Tietz, Anja; D'Elia, Yuri; Pattaro, Cristian ORCID: https://orcid.org/0000-0002-4119-0109; Becktepe, Jos S. ORCID: https://orcid.org/0000-0002-3532-3155; Gögele, Martin ORCID: https://orcid.org/0000-0003-4785-4348; Barin, Laura ORCID: https://orcid.org/0000-0001-8139-4686; Pramstaller, Peter P. ORCID: https://orcid.org/0000-0002-9831-8302; Kuhlenbäumer, Gregor ORCID: https://orcid.org/0000-0002-3262-8113 und Melotti, Roberto ORCID: https://orcid.org/0000-0003-4115-317X
(2024):
Archimedes Spiral Ratings: Determinants and Population‐Based Limits of Normal.
In: Movement Disorders Clinical Practice, Bd. 11, Nr. 10: S. 1257-1265
[PDF, 1MB]
ORCID: https://orcid.org/0000-0001-6524-0281; Tietz, Anja; D'Elia, Yuri; Pattaro, Cristian ORCID: https://orcid.org/0000-0002-4119-0109; Becktepe, Jos S. ORCID: https://orcid.org/0000-0002-3532-3155; Gögele, Martin ORCID: https://orcid.org/0000-0003-4785-4348; Barin, Laura ORCID: https://orcid.org/0000-0001-8139-4686; Pramstaller, Peter P. ORCID: https://orcid.org/0000-0002-9831-8302; Kuhlenbäumer, Gregor ORCID: https://orcid.org/0000-0002-3262-8113 und Melotti, Roberto ORCID: https://orcid.org/0000-0003-4115-317X
(2024):
Archimedes Spiral Ratings: Determinants and Population‐Based Limits of Normal.
In: Movement Disorders Clinical Practice, Bd. 11, Nr. 10: S. 1257-1265
[PDF, 1MB]
Jensen, Ida ORCID: https://orcid.org/0009-0006-0270-0029; Heine, Johanne; Ruf, Viktoria C.; Compta, Yaroslau; Porcel, Laura Molina; Troakes, Claire; Vamanu, Albert; Downes, Sophia; Irwin, David; Cohen, Jesse ORCID: https://orcid.org/0000-0003-2554-5181; Lee, Edward B.; Nilsson, Christer; Englund, Elisabet; Nemati, Mojtaba; Katzdobler, Sabrina ORCID: https://orcid.org/0000-0002-3512-5984; Levin, Johannes; Pantelyat, Alex ORCID: https://orcid.org/0000-0002-6427-7485; Seemiller, Joseph; Berger, Stephen; Swieten, John van; Dopper, Elise; Rozenmuller, Annemieke; Kovacs, Gabor G.; Bendahan, Nathaniel ORCID: https://orcid.org/0000-0003-2167-5667; Lang, Anthony E.; Herms, Jochen; Höglinger, Günter ORCID: https://orcid.org/0000-0001-7587-6187 und Hopfner, Franziska ORCID: https://orcid.org/0000-0001-6524-0281
(2024):
Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria.
In: Movement Disorders, Bd. 39, Nr. 9: S. 1514-1522
[PDF, 309kB]
ORCID: https://orcid.org/0009-0006-0270-0029; Heine, Johanne; Ruf, Viktoria C.; Compta, Yaroslau; Porcel, Laura Molina; Troakes, Claire; Vamanu, Albert; Downes, Sophia; Irwin, David; Cohen, Jesse ORCID: https://orcid.org/0000-0003-2554-5181; Lee, Edward B.; Nilsson, Christer; Englund, Elisabet; Nemati, Mojtaba; Katzdobler, Sabrina ORCID: https://orcid.org/0000-0002-3512-5984; Levin, Johannes; Pantelyat, Alex ORCID: https://orcid.org/0000-0002-6427-7485; Seemiller, Joseph; Berger, Stephen; Swieten, John van; Dopper, Elise; Rozenmuller, Annemieke; Kovacs, Gabor G.; Bendahan, Nathaniel ORCID: https://orcid.org/0000-0003-2167-5667; Lang, Anthony E.; Herms, Jochen; Höglinger, Günter ORCID: https://orcid.org/0000-0001-7587-6187 und Hopfner, Franziska ORCID: https://orcid.org/0000-0001-6524-0281
(2024):
Impact of Magnetic Resonance Imaging Markers on the Diagnostic Performance of the International Parkinson and Movement Disorder Society Multiple System Atrophy Criteria.
In: Movement Disorders, Bd. 39, Nr. 9: S. 1514-1522
[PDF, 309kB]
Bernhardt, Alexander Maximilian ORCID: https://orcid.org/0000-0002-2572-5062; Nemati, Mojtaba; Boros, Fanni Annamária; Hopfner, Franziska; Levin, Johannes; Mollenhauer, Brit ORCID: https://orcid.org/0000-0001-8437-3645; Winkler, Jürgen; Zerr, Inga; Zunke, Friederike und Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187
(2024):
α‐Synuclein Seed Amplification Assays from Blood‐Based Extracellular Vesicles in Parkinson's Disease: An Evaluation of the Evidence.
In: Movement Disorders, Bd. 39, Nr. 8: S. 1269-1271
[PDF, 134kB]
ORCID: https://orcid.org/0000-0002-2572-5062; Nemati, Mojtaba; Boros, Fanni Annamária; Hopfner, Franziska; Levin, Johannes; Mollenhauer, Brit ORCID: https://orcid.org/0000-0001-8437-3645; Winkler, Jürgen; Zerr, Inga; Zunke, Friederike und Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187
(2024):
α‐Synuclein Seed Amplification Assays from Blood‐Based Extracellular Vesicles in Parkinson's Disease: An Evaluation of the Evidence.
In: Movement Disorders, Bd. 39, Nr. 8: S. 1269-1271
[PDF, 134kB]
Klietz, Martin; Katzdobler, Sabrina; Levin, Johannes; Wegner, Florian; Hoellerhage, Matthias; Hopfner, Franziska; Krey, Lea; Heine, Johanne; Skripuletz, Thomas und Hoeglinger, Guenter U.
(2022):
HOMER-3 Antibodies Were Not Detected in Two German Cohorts of Patients with Multiple System Atrophy.
In: Movement Disorders, Bd. 37, Nr. 10: S. 2165-2166
[PDF, 119kB]
Hopfner, Franziska; Tietz, Anja K.; Ruf, Viktoria C.; Ross, Owen A.; Koga, Shunsuke; Dickson, Dennis; Aguzzi, Adriano; Attems, Johannes; Beach, Thomas; Beller, Allison; Cheshire, William P.; Deerlin, Vivianna van; Desplats, Paula; Deuschl, Guenther; Duyckaerts, Charles; Ellinghaus, David; Evsyukov, Valentin; Flanagan, Margaret Ellen; Franke, Andre; Frosch, Matthew P.; Gearing, Marla; Gelpi, Ellen; Gerpen, Jay A. van; Ghetti, Bernardino; Glass, Jonathan D.; Grinberg, Lea T.; Halliday, Glenda; Helbig, Ingo; Hollerhage, Matthias; Huitinga, Inge; Irwin, David John; Keene, Dirk C.; Kovacs, Gabor G.; Lee, Edward B.; Levin, Johannes; Marti, Maria J.; Mackenzie, Ian; McKeith, Ian; Mclean, Catriona; Mollenhauer, Brit; Neumann, Manuela; Newell, Kathy L.; Pantelyat, Alex; Pendziwiat, Manuela; Peters, Annette; Porcel, Laura Molina; Rabano, Alberto; Matej, Radoslav; Rajput, Alex; Rajput, Ali; Reimann, Regina; Scott, William K.; Seeley, William; Selvackadunco, Sashika; Simuni, Tanya; Stadelmann, Christine; Svenningsson, Per; Thomas, Alan; Trenkwalder, Claudia; Troakes, Claire; Trojanowski, John Q.; Uitti, Ryan J.; White, Charles L.; Wszolek, Zbigniew K.; Xie, Tao; Ximelis, Teresa; Yebenes, Justo; Mueller, Ulrich; Schellenberg, Gerard D.; Herms, Jochen; Kuhlenbaumer, Gregor und Hoeglinger, Gunter
(2022):
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
In: Movement Disorders, Bd. 37, Nr. 10: S. 2110-2121
[PDF, 2MB]
Liao, Calwing; Castonguay, Charles-Etienne; Heilbron, Karl; Vuokila, Veikko; Medeiros, Miranda; Houle, Gabrielle; Akcimen, Fulya; Ross, Jay P.; Catoire, Helene; Diez-Fairen, Monica; Kang, Jooeun; Mueller, Stefanie H.; Girard, Simon L.; Hopfner, Franziska; Lorenz, Delia; Clark, Lorraine N.; Soto-Beasley, Alexandra I.; Klebe, Stephan; Hallett, Mark; Wszolek, Zbigniew K.; Pendziwiat, Manuela; Lorenzo-Betancor, Oswaldo; Seppi, Klaus; Berg, Daniela; Vilarino-Guell, Carles; Postuma, Ronald B.; Bernard, Genevieve; Dupre, Nicolas; Jankovic, Joseph; Testa, Claudia M.; Ross, Owen A.; Arzberger, Thomas; Chouinard, Sylvain; Louis, Elan D.; Mandich, Paola; Vitale, Carmine; Barone, Paolo; Garcia-Martin, Elena; Alonso-Navarro, Hortensia; Agundez, Jose A. G.; Jimenez-Jimenez, Felix Javier; Pastor, Pau; Rajput, Alex; Deuschl, Gunther; Kuhlenbaumer, Gregor; Meijer, Inge A.; Dion, Patrick A. und Rouleau, Guy A.
(2022):
Association of Essential Tremor With Novel Risk Loci A Genome-Wide Association Study and Meta-analysis.
In: JAMA Neurology, Bd. 79, Nr. 2: S. 185-193
Hopfner, Franziska; Müller, Stefanie H.; Szymczak, Silke; Junge, Olaf; Tittmann, Lukas; May, Sandra; Lohmann, Katja; Grallert, Harald; Lieb, Wolfgang; Strauch, Konstantin und Müller-Nurasyid, Martina
(2020):
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.
In: Movement disorders : official journal of the Movement Disorder Society, Bd. 35, Nr. 7: S. 1245-1248
Hopfner, Franziska; Mueller, Stefanie H.; Szymczak, Silke; Junge, Olaf; Tittmann, Lukas; May, Sandra; Lohmann, Katja; Grallert, Harald; Lieb, Wolfgang; Strauch, Konstantin; Müller-Nurasyi, Martina; Berger, Klaus; Schormair, Barbara; Winkelmann, Juliane; Mollenhauer, Brit; Trenkwalder, Claudia; Maetzler, Walter; Berg, Daniela; Kasten, Meike; Klein, Christine; Höglinger, Günter U.; Gasser, Thomas; Deuschl, Günther; Franke, André; Krawczak, Michael; Dempfle, Astrid und Kuhlenbäumer, Gregor
(2020):
Private variants in PRKN are associated with late-onset Parkinson's disease.
In: Parkinsonism & Related Disorders, Bd. 75: S. 24-26
Sailani, M. Reza; Jahanbani, Fereshteh; Abbott, Charles W.; Lee, Hayan; Zia, Amin; Rego, Shannon; Winkelmann, Juliane; Hopfner, Franziska; Khan, Tahir N.; Katsanis, Nicholas; Mueller, Stefanie H.; Berg, Daniela; Lyman, Katherine M.; Mychajliw, Christian; Deuschl, Guenther; Bernstein, Jonathan A.; Kuhlenbaeumer, Gregor und Snyder, Michael P.
(2020):
Candidate variants inTUBare associated with familial tremor.
In: PLOS Genetics 16(9), e1009010 [PDF, 2MB]
In: PLOS Genetics 16(9), e1009010 [PDF, 2MB]
Hopfner, Franziska; Höglinger, Gunter U.; Kuhlenbaeumer, Gregor; Pottegard, Anton; Wod, Mette; Christensen, Kaare; Tanner, Caroline M. und Deuschl, Gunther
(2020):
beta-adrenoreceptors and the risk of Parkinson's disease.
In: Lancet Neurology, Bd. 19, Nr. 3: S. 247-254
Hopfner, Franziska; Hobert, Markus A.; Maetzler, Corina; Hansen, Clint; Minh Hoang, Pham; Moreau, Caroline; Berg, Daniela; Devos, David und Maetzler, Walter
(8. August 2019):
Mobility Deficits Assessed With Mobile Technology: What Can We Learn From Brain Iron-Altered Animal Models?
In: Frontiers in Neurology, Bd. 10, 833
[PDF, 493kB]
Zeuner, Kirsten L.; Schaeffer, Eva; Hopfner, Franziska; Brueggemann, Norbert und Berg, Daniela
(2019):
Progress of Pharmacological Approaches in Parkinson's Disease.
In: Clinical Pharmacology & Therapeutics, Bd. 105, Nr. 5: S. 1106-1120
Roesler, Thomas W.; Marvian, Amir Tayaranian; Brendel, Matthias; Nykaenen, Niko-Petteri; Hoellerhage, Matthias; Schwarz, Sigrid C.; Hopfner, Franziska; Koeglsperger, Thomas; Respondek, Gesine; Schweyer, Kerstin; Levin, Johannes; Villemagne, Victor L.; Barthel, Henryk; Sabri, Osama; Müller, Ulrich; Meissner, Wassilios G.; Kovacs, Gabor G. und Höglinger, Günter U. ORCID: https://orcid.org/0000-0001-7587-6187
(2019):
Four-repeat tauopathies.
In: Progress in Neurobiology, Bd. 180, UNSP 101644
[PDF, 939kB]
ORCID: https://orcid.org/0000-0001-7587-6187
(2019):
Four-repeat tauopathies.
In: Progress in Neurobiology, Bd. 180, UNSP 101644
[PDF, 939kB]
Hopfner, Franziska; Müller, Stefanie H.; Steppat, Dagmar; Miller, Joanna; Schmidt, Nele; Wandinger, Klaus-Peter; Leypoldt, Frank; Berg, Daniela; Franke, Andre; Lieb, Wolfgang; Tittmann, Lukas; Balzer-Geldsetzer, Monika; Baudrexel, Simon; Dodel, Richard; Hilker-Roggendorf, Rüdiger; Kalbe, Elke; Kassubek, Jan; Klockgether, Thomas; Liepelt-Scarfone, Inga; Mollenhauer, Brit; Neuser, Petra; Reetz, Kathrin; Riedel, Oliver; Schulte, Claudia; Schulz, Jörg B.; Spottke, Annika; Storch, Alexander; Trenkwalder, Claudia; Wittchen, Hans-Ulrich; Witt, Karsten; Wuellner, Ullrich; Deuschl, Gunther und Kuhlenbaeumer, Gregor
(2019):
No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors.
In: Translational Neurodegeneration, Bd. 8, 11
Yilmaz, Rezzak; Hopfner, Franziska; van Eimeren, Thilo und Berg, Daniela
(2019):
Biomarkers of Parkinson's disease: 20years later.
In: Journal of Neural Transmission, Bd. 126, Nr. 7: S. 803-813
Hopfner, Franziska; Wod, Mette; Höglinger, Guenter U.; Blaabjerg, Morten; Roesler, Thomas W.; Kuhlenbaeumer, Gregor; Christensen, Kaare; Deuschl, Guenther und Pottegard, Anton
(2019):
Use of beta 2-adrenoreceptor agonist and antagonist drugs and risk of Parkinson disease.
In: Neurology, Bd. 93, Nr. 2, E135-E142
Respondek, Gesine; Grimm, Max-Joseph; Piot, Ines; Arzberger, Thomas; Compta, Yaroslau; Englund, Elisabet; Ferguson, Leslie W.; Gelpi, Ellen; Roeber, Sigrun; Giese, Armin; Grossman, Murray; Irwin, David J.; Meissner, Wassilios G.; Nilsson, Christer; Pantelyat, Alexander; Rajput, Alex; van Swieten, John C.; Troakes, Claire; Höglinger, Guenter U.; Aiba, Ikuko; Antonini, Angelo; Barone, Paolo; Bhatia, Kailash P.; Boxer, Adam K.; Colosimo, Carlo; Corvol, Jean Christophe; Dickson, Dennis W.; Golbe, Lawrence; Hopfner, Franziska; Josephs, Keith A.; Kassubek, Jan; Kovacs, Gabor G.; Lang, Anthony E.; Levin, Johannes; Litvan, Irene; Hollerhage, Matthias; McFarland, Nikolaus; Morris, Huw R.; Müller, Ulrich; Oertel, Wolfgang H.; Rowe, James B.; Sakakibara, Ruji; Schellenberg, Gerard; Stamelou, Maria; van Eimeren, Thilo; Wenning, Gregor K. und Whitwell, Jennifer L.
(2019):
Validation of the movement disorder society criteria for the diagnosis of 4-repeat tauopathies.
In: Movement Disorders, Bd. 35, Nr. 1: S. 171-176
Müller, Stefanie H.; Girard, Simon L.; Hopfner, Franziska; Merner, Nancy D.; Bourassa, Cynthia V.; Lorenz, Delia; Clark, Lorraine N.; Tittmann, Lukas; Soto-Ortolaza, Alexandra I.; Klebe, Stephan; Hallett, Mark; Schneider, Susanne A.; Hodgkinson, Colin A.; Lieb, Wolfgang; Wszolek, Zbigniew K.; Pendziwiat, Manuela; Lorenzo-Betancor, Oswaldo; Poewe, Werner; Ortega-Cubero, Sara; Seppi, Klaus; Rajput, Alex; Hussl, Anna; Rajput, Ali H.; Berg, Daniela; Dion, Patrick A.; Wurster, Isabel; Shulman, Joshua M.; Srulijes, Karin; Haubenberger, Dietrich; Pastor, Pau; Vilariño-Güell, Carles; Postuma, Ronald B.; Bernard, Geneviève; Ladwig, Karl-Heinz; Dupré, Nicolas; Jankovic, Joseph; Strauch, Konstantin; Panisset, Michel; Winkelmann, Juliane; Testa, Claudia M.; Zeuner, Kirsten E.; Reischl, Eva; Ross, Owen A.; Arzberger, Thomas; Chouinard, Sylvain; Deuschl, Günther; Louis, Elan D.; Kuhlenbäumer, Gregor und Rouleau, Guy A.
(2016):
Genome-wide association study in essential tremor identifies three new loci.
In: Brain, Bd. 139: S. 3163-3169
Hopfner, Franziska; Schormair, Barbara; Knauf, Franziska; Berthele, Achim; Toelle, Thomas R.; Baron, Ralf; Maier, Christoph; Treede, Rolf-Detlef; Binder, Andreas; Sommer, Claudia; Maihoefner, Christian; Kunz, Wolfram; Zimprich, Friedrich; Heemann, Uwe; Pfeufer, Arne; Naebauer, Michael; Kaeaeb, Stefan; Nowak, Barbara; Gieger, Christian; Lichtner, Peter; Trenkwalder, Claudia; Oexle, Konrad und Winkelmann, Juliane
(2011):
Novel SCARB2 mutation in Action Myoclonus-Renal Failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features.
In: BMC Neurology
11:134
[PDF, 731kB]