受强制性开放获取政策约束的文章 - Olaf Riess了解详情
无法在其他位置公开访问的文章：30 篇
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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
A Rauch, D Wieczorek, E Graf, T Wieland, S Endele, T Schwarzmayr, ...
The Lancet 380 (9854), 1674-1682, 2012
强制性开放获取政策： Swiss National Science Foundation
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SCA3: neurological features, pathogenesis and animal models
O Riess, U Rüb, A Pastore, P Bauer, L Schöls
The Cerebellum 7, 125-137, 2008
强制性开放获取政策： German Research Foundation
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Association between genetic variants of IL-1β, IL-6 and TNF-α cytokines and cognitive performance in the elderly general population of the MEMO-study
BT Baune, G Ponath, M Rothermundt, O Riess, H Funke, K Berger
Psychoneuroendocrinology 33 (1), 68-76, 2008
强制性开放获取政策： German Research Foundation
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Age at onset in Huntington’s disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7
S Metzger, M Saukko, H Van Che, L Tong, Y Puder, O Riess, HP Nguyen
Human genetics 128, 453-459, 2010
强制性开放获取政策： British Heart Foundation
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Changes in adult olfactory bulb neurogenesis in mice expressing the A30P mutant form of alpha‐synuclein
F Marxreiter, S Nuber, M Kandasamy, J Klucken, R Aigner, R Burgmayer, ...
European Journal of Neuroscience 29 (5), 879-890, 2009
强制性开放获取政策： German Research Foundation
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The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect
S Gispert, A Kurz, S Waibel, P Bauer, I Liepelt, C Geisen, AD Gitler, ...
Neurobiology of disease 45 (1), 356-361, 2012
强制性开放获取政策： US National Institutes of Health, German Research Foundation
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Generation of a novel rodent model for DYT1 dystonia
K Grundmann, N Glöckle, G Martella, G Sciamanna, TK Hauser, L Yu, ...
Neurobiology of disease 47 (1), 61-74, 2012
强制性开放获取政策： US National Institutes of Health, German Research Foundation
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Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)
P Bauer, E Leshinsky-Silver, L Blumkin, N Schlipf, C Schröder, J Schicks, ...
Neurogenetics 13, 73-76, 2012
强制性开放获取政策： German Research Foundation
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Radiogenomics in head and neck cancer: correlation of radiomic heterogeneity and somatic mutations in TP53, FAT1 and KMT2D
K Zwirner, FJ Hilke, G Demidov, JS Fernandez, S Ossowski, C Gani, ...
Strahlentherapie und Onkologie 195 (9), 771-779, 2019
强制性开放获取政策： German Research Foundation
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Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease
N Abahuni, S Gispert, P Bauer, O Riess, R Krüger, T Becker, G Auburger
Neuroscience letters 414 (2), 126-129, 2007
强制性开放获取政策： German Research Foundation
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Prevalence of THAP1 sequence variants in German patients with primary dystonia
AS Söhn, N Glöckle, AD Doetzer, G Deuschl, U Felbor, HR Topka, ...
Movement disorders 25 (12), 1982-1986, 2010
强制性开放获取政策： German Research Foundation
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Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease
M Sharma, DM Maraganore, JPA Ioannidis, O Riess, JO Aasly, G Annesi, ...
Neurobiology of aging 32 (11), 2108. e1-2108. e5, 2011
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders)
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A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson’s disease patients
C Wahl, S Kautzmann, G Krebiehl, K Strauss, D Woitalla, T Müller, ...
Journal of Neural Transmission 115, 1141-1148, 2008
强制性开放获取政策： German Research Foundation
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The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature
A Traschütz, J van Gaalen, M Oosterloo, M Vreeburg, EJ Kamsteeg, ...
Parkinsonism & related disorders 62, 215-220, 2019
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
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Genetic basis of neurodevelopmental disorders in 103 Jordanian families
T Froukh, O Nafie, SAS Al Hait, L Laugwitz, J Sommerfeld, M Sturm, ...
Clinical Genetics 97 (4), 621-627, 2020
强制性开放获取政策： German Research Foundation
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Systematic data analysis and data mining in CatWalk gait analysis by heat mapping exemplified in rodent models for neurodegenerative diseases
IK Timotius, F Canneva, G Minakaki, S Moceri, AC Plank, N Casadei, ...
Journal of neuroscience methods 326, 108367, 2019
强制性开放获取政策： German Research Foundation, Fundação para a Ciência e a Tecnologia, Portugal …
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Dynamic footprint based locomotion sway assessment in α-synucleinopathic mice using Fast Fourier Transform and Low Pass Filter
IK Timotius, F Canneva, G Minakaki, C Pasluosta, S Moceri, N Casadei, ...
Journal of Neuroscience Methods 296, 1-11, 2018
强制性开放获取政策： German Research Foundation, Fundação para a Ciência e a Tecnologia, Portugal
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Screening of mutations in GNAL in sporadic dystonia patients
C Dufke, M Sturm, C Schroeder, S Moll, T Ott, O Riess, P Bauer, ...
Movement Disorders 29 (9), 1193-1196, 2014
强制性开放获取政策： German Research Foundation
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Bi-allelic truncating mutations in VWA1 cause neuromyopathy
M Deschauer, H Hengel, K Rupprich, M Kreiß, B Schlotter-Weigel, ...
Brain 144 (2), 574-583, 2021
强制性开放获取政策： German Research Foundation, Federal Ministry of Education and Research, Germany
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Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia
M Walter, M Bonin, RS Pullman, EM Valente, M Loi, M Gambarin, ...
Neurobiology of Disease 38 (2), 192-200, 2010
强制性开放获取政策： US National Institutes of Health
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