Georg Auburger - Publications

Affiliations: 
Klinik für Neurologie Goethe-Universität Frankfurt am Main, Germany 

155 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Sen NE, Drost J, Gispert S, Torres-Odio S, Damrath E, Klinkenberg M, Hamzeiy H, Akdal G, Güllüoğlu H, Basak AN, Auburger G. Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels. Neurobiology of Disease. PMID 27597528 DOI: 10.1016/j.nbd.2016.09.002  0.6
2016 Halbach MV, Gispert S, Stehning T, Damrath E, Walter M, Auburger G. Atxn2 Knockout and CAG42-Knock-in Cerebellum Shows Similarly Dysregulated Expression in Calcium Homeostasis Pathway. Cerebellum (London, England). PMID 26868665 DOI: 10.1007/s12311-016-0762-4  0.6
2016 Rodríguez-Labrada R, Velázquez-Pérez L, Auburger G, Ziemann U, Canales-Ochoa N, Medrano-Montero J, Vázquez-Mojena Y, González-Zaldivar Y. Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 26846400 DOI: 10.1002/mds.26532  0.6
2015 Brehm N, Rau K, Kurz A, Gispert S, Auburger G. Age-Related Changes of 14-3-3 Isoforms in Midbrain of A53T-SNCA Overexpressing Mice. Journal of Parkinson's Disease. 5: 595-604. PMID 26406140 DOI: 10.3233/JPD-150606  0.6
2015 Schöls L, Reimold M, Seidel K, Globas C, Brockmann K, Karsten Hauser T, Auburger G, Bürk K, den Dunnen W, Reischl G, Korf HW, Brunt ER, Rüb U. No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra. Brain : a Journal of Neurology. 138: 3316-26. PMID 26362908 DOI: 10.1093/brain/awv255  0.6
2015 Halbach MV, Stehning T, Damrath E, Jendrach M, ?en NE, Ba?ak AN, Auburger G. Both ubiquitin ligases FBXW8 and PARK2 are sequestrated into insolubility by ATXN2 PolyQ expansions, but only FBXW8 expression is dysregulated. Plos One. 10: e0121089. PMID 25790475 DOI: 10.1371/journal.pone.0121089  0.6
2015 Dufke C, Hauser AK, Sturm M, Fluhr S, Wächter T, Leube B, Auburger G, Ott T, Bauer P, Gasser T, Grundmann K. Mutations in CIZ1 are not a major cause for dystonia in Germany. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 740-3. PMID 25778706 DOI: 10.1002/mds.26198  0.6
2015 Fittschen M, Lastres-Becker I, Halbach MV, Damrath E, Gispert S, Azizov M, Walter M, Müller S, Auburger G. Genetic ablation of ataxin-2 increases several global translation factors in their transcript abundance but decreases translation rate. Neurogenetics. 16: 181-92. PMID 25721894 DOI: 10.1007/s10048-015-0441-5  0.6
2015 Dominguez-Bautista JA, Klinkenberg M, Brehm N, Subramaniam M, Kern B, Roeper J, Auburger G, Jendrach M. Loss of lysosome-associated membrane protein 3 (LAMP3) enhances cellular vulnerability against proteasomal inhibition. European Journal of Cell Biology. 94: 148-61. PMID 25681212 DOI: 10.1016/j.ejcb.2015.01.003  0.6
2015 Gehrke S, Wu Z, Klinkenberg M, Sun Y, Auburger G, Guo S, Lu B. PINK1 and Parkin control localized translation of respiratory chain component mRNAs on mitochondria outer membrane. Cell Metabolism. 21: 95-108. PMID 25565208 DOI: 10.1016/j.cmet.2014.12.007  0.6
2015 Gispert S, Brehm N, Weil J, Seidel K, Rüb U, Kern B, Walter M, Roeper J, Auburger G. Potentiation of neurotoxicity in double-mutant mice with Pink1 ablation and A53T-SNCA overexpression. Human Molecular Genetics. 24: 1061-76. PMID 25296918 DOI: 10.1093/hmg/ddu520  0.6
2015 Gispert S, Kurz A, Brehm N, Rau K, Walter M, Riess O, Auburger G. Complexin-1 and Foxp1 Expression Changes Are Novel Brain Effects of Alpha-Synuclein Pathology. Molecular Neurobiology. 52: 57-63. PMID 25112678 DOI: 10.1007/s12035-014-8844-0  0.6
2015 Seidel K, Mahlke J, Siswanto S, Krüger R, Heinsen H, Auburger G, Bouzrou M, Grinberg LT, Wicht H, Korf HW, den Dunnen W, Rüb U. The brainstem pathologies of Parkinson's disease and dementia with lewy bodies. Brain Pathology (Zurich, Switzerland). 25: 121-35. PMID 24995389 DOI: 10.1111/bpa.12168  0.6
2014 Brehm N, Bez F, Carlsson T, Kern B, Gispert S, Auburger G, Cenci MA. A Genetic Mouse Model of Parkinson's Disease Shows Involuntary Movements and Increased Postsynaptic Sensitivity to Apomorphine. Molecular Neurobiology. PMID 25307288 DOI: 10.1007/s12035-014-8911-6  0.6
2014 Subramaniam M, Althof D, Gispert S, Schwenk J, Auburger G, Kulik A, Fakler B, Roeper J. Mutant α-synuclein enhances firing frequencies in dopamine substantia nigra neurons by oxidative impairment of A-type potassium channels. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 13586-99. PMID 25297088 DOI: 10.1523/JNEUROSCI.5069-13.2014  0.6
2014 Auburger G, Gispert S, Jendrach M. Mitochondrial acetylation and genetic models of Parkinson's disease. Progress in Molecular Biology and Translational Science. 127: 155-82. PMID 25149217 DOI: 10.1016/B978-0-12-394625-6.00006-4  0.6
2014 Lahut S, Vadasz D, Depboylu C, Ries V, Krenzer M, Stiasny-Kolster K, Basak AN, Oertel WH, Auburger G. The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics. 15: 189-92. PMID 24863655 DOI: 10.1007/s10048-014-0407-z  0.6
2014 Rüb U, Hentschel M, Stratmann K, Brunt E, Heinsen H, Seidel K, Bouzrou M, Auburger G, Paulson H, Vonsattel JP, Lange H, Korf HW, den Dunnen W. Huntington's disease (HD): degeneration of select nuclei, widespread occurrence of neuronal nuclear and axonal inclusions in the brainstem. Brain Pathology (Zurich, Switzerland). 24: 247-60. PMID 24779419 DOI: 10.1111/bpa.12115  0.6
2014 Parganlija D, Klinkenberg M, Domínguez-Bautista J, Hetzel M, Gispert S, Chimi MA, Dröse S, Mai S, Brandt U, Auburger G, Jendrach M. Loss of PINK1 impairs stress-induced autophagy and cell survival. Plos One. 9: e95288. PMID 24751806 DOI: 10.1371/journal.pone.0095288  0.6
2014 Heck MV, Azizov M, Stehning T, Walter M, Kedersha N, Auburger G. Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue. Neurogenetics. 15: 135-44. PMID 24659297 DOI: 10.1007/s10048-014-0397-x  0.6
2014 Heckman MG, Elbaz A, Soto-Ortolaza AI, Serie DJ, Aasly JO, Annesi G, Auburger G, Bacon JA, Boczarska-Jedynak M, Bozi M, Brighina L, Chartier-Harlin MC, Dardiotis E, Destée A, Ferrarese C, et al. Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of Aging. 35: 266.e5-14. PMID 23962496 DOI: 10.1016/j.neurobiolaging.2013.07.013  0.6
2014 Gispert S, Auburger G, Kuruvilla KP, LeDoux MS. Rodent Models of Autosomal Recessive Parkinson Disease Movement Disorders: Genetics and Models: Second Edition. 329-343. DOI: 10.1016/B978-0-12-405195-9.00019-6  0.6
2013 Gispert S, Parganlija D, Klinkenberg M, Dröse S, Wittig I, Mittelbronn M, Grzmil P, Koob S, Hamann A, Walter M, Büchel F, Adler T, Hrabé de Angelis M, Busch DH, Zell A, ... ... Auburger G, et al. Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors. Human Molecular Genetics. 22: 4871-87. PMID 23851121 DOI: 10.1093/hmg/ddt338  0.6
2013 Rüb U, Schöls L, Paulson H, Auburger G, Kermer P, Jen JC, Seidel K, Korf HW, Deller T. Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7. Progress in Neurobiology. 104: 38-66. PMID 23438480 DOI: 10.1016/j.pneurobio.2013.01.001  0.6
2013 Rüb U, Farrag K, Seidel K, Brunt ER, Heinsen H, Bürk K, Melegh B, von Gall C, Auburger G, Bohl J, Korf HW, Hoche F, den Dunnen W. Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2). Neuropathology and Applied Neurobiology. 39: 634-43. PMID 23363055 DOI: 10.1111/nan.12025  0.6
2013 Drost J, Nonis D, Eich F, Leske O, Damrath E, Brunt ER, Lastres-Becker I, Heumann R, Nowock J, Auburger G. Ataxin-2 modulates the levels of Grb2 and SRC but not ras signaling. Journal of Molecular Neuroscience : Mn. 51: 68-81. PMID 23335000 DOI: 10.1007/s12031-012-9949-4  0.6
2013 Almaguer-Mederos LE, Aguilera Rodríguez R, González Zaldivar Y, Almaguer Gotay D, Cuello Almarales D, Laffita Mesa J, Vázquez Mojena Y, Zayas Feria P, Auburger G, Gispert S, Velásquez Pérez L. Estimation of survival in spinocerebellar ataxia type 2 Cuban patients. Clinical Genetics. 83: 293-4. PMID 22758789 DOI: 10.1111/j.1399-0004.2012.01902.x  0.6
2012 Dehorter N, Lozovaya N, Mdzomba BJ, Michel FJ, Lopez C, Tsintsadze V, Tsintsadze T, Klinkenberg M, Gispert S, Auburger G, Hammond C. Subthalamic lesion or levodopa treatment rescues giant GABAergic currents of PINK1-deficient striatum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 18047-53. PMID 23238720 DOI: 10.1523/JNEUROSCI.2474-12.2012  0.6
2012 Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, et al. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics. 49: 721-6. PMID 23125461 DOI: 10.1136/jmedgenet-2012-101155  0.6
2012 Winter P, Kamm C, Biskup S, Köhler A, Leube B, Auburger G, Gasser T, Benecke R, Müller U. DYT7 gene locus for cervical dystonia on chromosome 18p is questionable. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1819-21. PMID 23115116 DOI: 10.1002/mds.25219  0.6
2012 Damrath E, Heck MV, Gispert S, Azizov M, Nowock J, Seifried C, Rüb U, Walter M, Auburger G. ATXN2-CAG42 sequesters PABPC1 into insolubility and induces FBXW8 in cerebellum of old ataxic knock-in mice. Plos Genetics. 8: e1002920. PMID 22956915 DOI: 10.1371/journal.pgen.1002920  0.6
2012 Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, ÖzoÄŸuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, BaÅŸak AN. ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. Plos One. 7: e42956. PMID 22916186 DOI: 10.1371/journal.pone.0042956  0.6
2012 Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, Garraux G, Gispert S, Auburger G, et al. Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology. 79: 659-67. PMID 22786590 DOI: 10.1212/WNL.0b013e318264e353  0.6
2012 Platt NJ, Gispert S, Auburger G, Cragg SJ. Striatal dopamine transmission is subtly modified in human A53Tα-synuclein overexpressing mice. Plos One. 7: e36397. PMID 22570709 DOI: 10.1371/journal.pone.0036397  0.6
2012 Xiao J, Uitti RJ, Zhao Y, Vemula SR, Perlmutter JS, Wszolek ZK, Maraganore DM, Auburger G, Leube B, Lehnhoff K, LeDoux MS. Mutations in CIZ1 cause adult onset primary cervical dystonia. Annals of Neurology. 71: 458-69. PMID 22447717 DOI: 10.1002/ana.23547  0.6
2012 Auburger G, Klinkenberg M, Drost J, Marcus K, Morales-Gordo B, Kunz WS, Brandt U, Broccoli V, Reichmann H, Gispert S, Jendrach M. Primary skin fibroblasts as a model of Parkinson's disease. Molecular Neurobiology. 46: 20-7. PMID 22350618 DOI: 10.1007/s12035-012-8245-1  0.6
2012 Scherzed W, Brunt ER, Heinsen H, de Vos RA, Seidel K, Bürk K, Schöls L, Auburger G, Del Turco D, Deller T, Korf HW, den Dunnen WF, Rüb U. Pathoanatomy of cerebellar degeneration in spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3). Cerebellum (London, England). 11: 749-60. PMID 22198871 DOI: 10.1007/s12311-011-0340-8  0.6
2012 Klinkenberg M, Gispert S, Dominguez-Bautista JA, Braun I, Auburger G, Jendrach M. Restriction of trophic factors and nutrients induces PARKIN expression. Neurogenetics. 13: 9-21. PMID 22028146 DOI: 10.1007/s10048-011-0303-8  0.6
2012 Kurz A, May C, Schmidt O, Müller T, Stephan C, Meyer HE, Gispert S, Auburger G, Marcus K. A53T-alpha-synuclein-overexpression in the mouse nigrostriatal pathway leads to early increase of 14-3-3 epsilon and late increase of GFAP. Journal of Neural Transmission (Vienna, Austria : 1996). 119: 297-312. PMID 21960009 DOI: 10.1007/s00702-011-0717-3  0.6
2012 Gispert S, Kurz A, Waibel S, Bauer P, Liepelt I, Geisen C, Gitler AD, Becker T, Weber M, Berg D, Andersen PM, Krüger R, Riess O, Ludolph AC, Auburger G. The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiology of Disease. 45: 356-61. PMID 21889984 DOI: 10.1016/j.nbd.2011.08.021  0.6
2012 Auburger GW. Spinocerebellar ataxia type 2. Handbook of Clinical Neurology. 103: 423-36. PMID 21827904 DOI: 10.1016/B978-0-444-51892-7.00026-7  0.6
2012 Tozzi A, Costa C, Siliquini S, Tantucci M, Picconi B, Kurz A, Gispert S, Auburger G, Calabresi P. Mechanisms underlying altered striatal synaptic plasticity in old A53T-α synuclein overexpressing mice. Neurobiology of Aging. 33: 1792-9. PMID 21684039 DOI: 10.1016/j.neurobiolaging.2011.05.002  0.6
2011 Yasuno K, BakırcıoÄŸlu M, Low SK, Bilgüvar K, Gaál E, Ruigrok YM, Niemelä M, Hata A, Bijlenga P, Kasuya H, Jääskeläinen JE, Krex D, Auburger G, Simon M, Krischek B, et al. Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk. Proceedings of the National Academy of Sciences of the United States of America. 108: 19707-12. PMID 22106312 DOI: 10.1073/pnas.1117137108  0.6
2011 Weber YG, Kamm C, Suls A, Kempfle J, Kotschet K, Schüle R, Wuttke TV, Maljevic S, Liebrich J, Gasser T, Ludolph AC, Van Paesschen W, Schöls L, De Jonghe P, Auburger G, et al. Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect. Neurology. 77: 959-64. PMID 21832227 DOI: 10.1212/WNL.0b013e31822e0479  0.6
2011 Velázquez-Pérez L, Voss U, Rodríguez-Labrada R, Auburger G, Canales Ochoa N, Sánchez Cruz G, Galicia Polo L, Haro Valencia R, Aguilera Rodríguez R, Medrano Montero J, Laffita Mesa JM, Tuin I. Sleep disorders in spinocerebellar ataxia type 2 patients. Neuro-Degenerative Diseases. 8: 447-54. PMID 21494015 DOI: 10.1159/000324374  0.6
2011 Rodríguez-Labrada R, Velázquez-Pérez L, Seigfried C, Canales-Ochoa N, Auburger G, Medrano-Montero J, Sánchez-Cruz G, Aguilera-Rodríguez R, Laffita-Mesa J, Vázquez-Mojena Y, Verdecia-Ramirez M, Motta M, Quevedo-Batista Y. Saccadic latency is prolonged in Spinocerebellar Ataxia type 2 and correlates with the frontal-executive dysfunctions. Journal of the Neurological Sciences. 306: 103-7. PMID 21481421 DOI: 10.1016/j.jns.2011.03.033  0.6
2011 Lee T, Li YR, Ingre C, Weber M, Grehl T, Gredal O, de Carvalho M, Meyer T, Tysnes OB, Auburger G, Gispert S, Bonini NM, Andersen PM, Gitler AD. Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients. Human Molecular Genetics. 20: 1697-700. PMID 21292779 DOI: 10.1093/hmg/ddr045  0.6
2011 Auburger G, Kurz A. The role of glyoxalases for sugar stress and aging, with relevance for dyskinesia, anxiety, dementia and Parkinson's disease. Aging. 3: 5-9. PMID 21248374  0.6
2011 Hoche F, Balikó L, den Dunnen W, Steinecker K, Bartos L, Sáfrány E, Auburger G, Deller T, Korf HW, Klockgether T, Rüb U, Melegh B. Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stage. Cerebellum (London, England). 10: 245-53. PMID 21128038 DOI: 10.1007/s12311-010-0239-9  0.6
2011 Kurz A, Rabbani N, Walter M, Bonin M, Thornalley P, Auburger G, Gispert S. Alpha-synuclein deficiency leads to increased glyoxalase I expression and glycation stress. Cellular and Molecular Life Sciences : Cmls. 68: 721-33. PMID 20711648 DOI: 10.1007/s00018-010-0483-7  0.6
2010 Elden AC, Kim HJ, Hart MP, Chen-Plotkin AS, Johnson BS, Fang X, Armakola M, Geser F, Greene R, Lu MM, Padmanabhan A, Clay-Falcone D, McCluskey L, Elman L, Juhr D, ... ... Auburger G, et al. Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature. 466: 1069-75. PMID 20740007 DOI: 10.1038/nature09320  0.6
2010 Kurz A, Double KL, Lastres-Becker I, Tozzi A, Tantucci M, Bockhart V, Bonin M, García-Arencibia M, Nuber S, Schlaudraff F, Liss B, Fernández-Ruiz J, Gerlach M, Wüllner U, Lüddens H, ... ... Auburger G, et al. A53T-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice. Plos One. 5: e11464. PMID 20628651 DOI: 10.1371/journal.pone.0011464  0.6
2010 Yasuno K, Bilguvar K, Bijlenga P, Low SK, Krischek B, Auburger G, Simon M, Krex D, Arlier Z, Nayak N, Ruigrok YM, Niemelä M, Tajima A, von und zu Fraunberg M, Dóczi T, et al. Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nature Genetics. 42: 420-5. PMID 20364137 DOI: 10.1038/ng.563  0.6
2010 Mai S, Klinkenberg M, Auburger G, Bereiter-Hahn J, Jendrach M. Decreased expression of Drp1 and Fis1 mediates mitochondrial elongation in senescent cells and enhances resistance to oxidative stress through PINK1. Journal of Cell Science. 123: 917-26. PMID 20179104 DOI: 10.1242/jcs.059246  0.6
2010 Almaguer-Mederos LE, Falcón NS, Almira YR, Zaldivar YG, Almarales DC, Góngora EM, Herrera MP, Batallán KE, Armiñán RR, Manresa MV, Cruz GS, Laffita-Mesa J, Cyuz TM, Chang V, Auburger G, et al. Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis. Clinical Genetics. 78: 169-74. PMID 20095980 DOI: 10.1111/j.1399-0004.2009.01358.x  0.6
2010 Kurz A, Wöhr M, Walter M, Bonin M, Auburger G, Gispert S, Schwarting RK. Alpha-synuclein deficiency affects brain Foxp1 expression and ultrasonic vocalization. Neuroscience. 166: 785-95. PMID 20056137 DOI: 10.1016/j.neuroscience.2009.12.054  0.6
2010 Klinkenberg M, Thurow N, Gispert S, Ricciardi F, Eich F, Prehn JH, Auburger G, Kögel D. Enhanced vulnerability of PARK6 patient skin fibroblasts to apoptosis induced by proteasomal stress. Neuroscience. 166: 422-34. PMID 20045449 DOI: 10.1016/j.neuroscience.2009.12.068  0.6
2009 García-Arencibia M, García C, Kurz A, Rodríguez-Navarro JA, Gispert-Sáchez S, Mena MA, Auburger G, de Yébenes JG, Fernández-Ruiz J. Cannabinoid CB1 receptors are early downregulated followed by a further upregulation in the basal ganglia of mice with deletion of specific park genes. Journal of Neural Transmission. Supplementum. 269-75. PMID 20411785 DOI: 10.1007/978-3-211-92660-4-22  0.6
2009 Jendrach M, Gispert S, Ricciardi F, Klinkenberg M, Schemm R, Auburger G. The mitochondrial kinase PINK1, stress response and Parkinson's disease. Journal of Bioenergetics and Biomembranes. 41: 481-6. PMID 19941155 DOI: 10.1007/s10863-009-9256-0  0.6
2009 Gispert S, Ricciardi F, Kurz A, Azizov M, Hoepken HH, Becker D, Voos W, Leuner K, Müller WE, Kudin AP, Kunz WS, Zimmermann A, Roeper J, Wenzel D, Jendrach M, ... ... Auburger G, et al. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration. Plos One. 4: e5777. PMID 19492057 DOI: 10.1371/journal.pone.0005777  0.6
2009 Cordes J, Larisch R, Henning U, Thünker J, Werner C, Orozco G, Mayoral F, Rivas F, Auburger G, Tosch M, Rietschel M, Gaebel W, Müller HW, Klimke A. Abnormal neuroendocrine response to clomipramine in hereditary affective psychosis. Depression and Anxiety. 26: E111-9. PMID 19288582 DOI: 10.1002/da.20405  0.6
2009 Velázquez-Pérez L, Seifried C, Abele M, Wirjatijasa F, Rodríguez-Labrada R, Santos-Falcón N, Sánchez-Cruz G, Almaguer-Mederos L, Tejeda R, Canales-Ochoa N, Fetter M, Ziemann U, Klockgether T, Medrano-Montero J, Rodríguez-Díaz J, ... ... Auburger G, et al. Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 120: 632-5. PMID 19201647 DOI: 10.1016/j.clinph.2008.12.040  0.6
2009 Fuhrmann N, Alavi MV, Bitoun P, Woernle S, Auburger G, Leo-Kottler B, Yu-Wai-Man P, Chinnery P, Wissinger B. Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy. Journal of Medical Genetics. 46: 136-44. PMID 19181907 DOI: 10.1136/jmg.2008.062570  0.6
2009 van de Loo S, Eich F, Nonis D, Auburger G, Nowock J. Ataxin-2 associates with rough endoplasmic reticulum. Experimental Neurology. 215: 110-8. PMID 18973756 DOI: 10.1016/j.expneurol.2008.09.020  0.6
2008 Nonis D, Schmidt MH, van de Loo S, Eich F, Dikic I, Nowock J, Auburger G. Ataxin-2 associates with the endocytosis complex and affects EGF receptor trafficking. Cellular Signalling. 20: 1725-39. PMID 18602463 DOI: 10.1016/j.cellsig.2008.05.018  0.6
2008 Hoepken HH, Gispert S, Azizov M, Klinkenberg M, Ricciardi F, Kurz A, Morales-Gordo B, Bonin M, Riess O, Gasser T, Kögel D, Steinmetz H, Auburger G. Parkinson patient fibroblasts show increased alpha-synuclein expression. Experimental Neurology. 212: 307-13. PMID 18511044 DOI: 10.1016/j.expneurol.2008.04.004  0.6
2008 Lastres-Becker I, Rüb U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum (London, England). 7: 115-24. PMID 18418684 DOI: 10.1007/s12311-008-0019-y  0.6
2008 Lastres-Becker I, Brodesser S, Lütjohann D, Azizov M, Buchmann J, Hintermann E, Sandhoff K, Schürmann A, Nowock J, Auburger G. Insulin receptor and lipid metabolism pathology in ataxin-2 knock-out mice. Human Molecular Genetics. 17: 1465-81. PMID 18250099 DOI: 10.1093/hmg/ddn035  0.6
2008 Hoche F, Seidel K, Brunt ER, Auburger G, Schöls L, Bürk K, de Vos RA, den Dunnen W, Bechmann I, Egensperger R, Van Broeckhoven C, Gierga K, Deller T, Rüb U. Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7). Neuropathology and Applied Neurobiology. 34: 479-91. PMID 18221259 DOI: 10.1111/j.1365-2990.2007.00933.x  0.6
2008 Tuin I, Voss U, Kessler K, Krakow K, Hilker R, Morales B, Steinmetz H, Auburger G. Sleep quality in a family with hereditary parkinsonism (PARK6). Sleep Medicine. 9: 684-8. PMID 17766179 DOI: 10.1016/j.sleep.2007.07.004  0.6
2007 Exner N, Treske B, Paquet D, Holmström K, Schiesling C, Gispert S, Carballo-Carbajal I, Berg D, Hoepken HH, Gasser T, Krüger R, Winklhofer KF, Vogel F, Reichert AS, Auburger G, et al. Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 12413-8. PMID 17989306 DOI: 10.1523/JNEUROSCI.0719-07.2007  0.6
2007 Abou Jamra R, Fuerst R, Kaneva R, Orozco Diaz G, Rivas F, Mayoral F, Gay E, Sans S, Gonzalez MJ, Gil S, Cabaleiro F, Del Rio F, Perez F, Haro J, Auburger G, et al. The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q. American Journal of Human Genetics. 81: 974-86. PMID 17924339 DOI: 10.1086/521690  0.6
2007 Bruno MK, Lee HY, Auburger GW, Friedman A, Nielsen JE, Lang AE, Bertini E, Van Bogaert P, Averyanov Y, Hallett M, Gwinn-Hardy K, Sorenson B, Pandolfo M, Kwiecinski H, Servidei S, et al. Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia. Neurology. 68: 1782-9. PMID 17515540 DOI: 10.1212/01.wnl.0000262029.91552.e0  0.6
2007 Fernandez-Ruiz J, Velásquez-Perez L, Díaz R, Drucker-Colín R, Pérez-González R, Canales N, Sánchez-Cruz G, Martínez-Góngora E, Medrano Y, Almaguer-Mederos L, Seifried C, Auburger G. Prism adaptation in spinocerebellar ataxia type 2. Neuropsychologia. 45: 2692-8. PMID 17507059 DOI: 10.1016/j.neuropsychologia.2007.04.006  0.6
2007 Abahuni N, Gispert S, Bauer P, Riess O, Krüger R, Becker T, Auburger G. Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease. Neuroscience Letters. 414: 126-9. PMID 17267121 DOI: 10.1016/j.neulet.2006.12.053  0.6
2007 Freund HJ, Barnikol UB, Nolte D, Treuer H, Auburger G, Tass PA, Samii M, Sturm V. Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor-A unusual clinical benefit. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 732-5. PMID 17265523 DOI: 10.1002/mds.21338  0.6
2007 Hoepken HH, Gispert S, Morales B, Wingerter O, Del Turco D, Mülsch A, Nussbaum RL, Müller K, Dröse S, Brandt U, Deller T, Wirth B, Kudin AP, Kunz WS, Auburger G. Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6. Neurobiology of Disease. 25: 401-11. PMID 17141510 DOI: 10.1016/j.nbd.2006.10.007  0.6
2007 Rüb U, Seidel K, Ozerden I, Gierga K, Brunt ER, Schöls L, de Vos RA, den Dunnen W, Schultz C, Auburger G, Deller T. Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy. Brain Research Reviews. 53: 235-49. PMID 17014911 DOI: 10.1016/j.brainresrev.2006.08.003  0.6
2006 Tuin I, Voss U, Kang JS, Kessler K, Rüb U, Nolte D, Lochmüller H, Tinschert S, Claus D, Krakow K, Pflug B, Steinmetz H, Auburger G. Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2). Neurology. 67: 1966-72. PMID 17159102 DOI: 10.1212/01.wnl.0000247054.90322.14  0.6
2006 Rüb U, Brunt ER, Petrasch-Parwez E, Schöls L, Theegarten D, Auburger G, Seidel K, Schultz C, Gierga K, Paulson H, van Broeckhoven C, Deller T, de Vos RA. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7. Neuropathology and Applied Neurobiology. 32: 635-49. PMID 17083478 DOI: 10.1111/j.1365-2990.2006.00772.x  0.6
2006 Gispert-Sanchez S, Auburger G. The role of protein aggregates in neuronal pathology: guilty, innocent, or just trying to help? Journal of Neural Transmission. Supplementum. 111-7. PMID 17017517  0.6
2006 Rüb U, de Vos RA, Brunt ER, Sebestény T, Schöls L, Auburger G, Bohl J, Ghebremedhin E, Gierga K, Seidel K, den Dunnen W, Heinsen H, Paulson H, Deller T. Spinocerebellar ataxia type 3 (SCA3): thalamic neurodegeneration occurs independently from thalamic ataxin-3 immunopositive neuronal intranuclear inclusions. Brain Pathology (Zurich, Switzerland). 16: 218-27. PMID 16911479 DOI: 10.1111/j.1750-3639.2006.00022.x  0.6
2005 Rüb U, Brunt ER, Gierga K, Seidel K, Schultz C, Schöls L, Auburger G, Heinsen H, Ippel PF, Glimmerveen WF, Wittebol-Post D, Arai K, Deller T, de Vos RA. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat. Brain Pathology (Zurich, Switzerland). 15: 287-95. PMID 16389941  0.6
2005 Schumacher J, Kaneva R, Jamra RA, Diaz GO, Ohlraun S, Milanova V, Lee YA, Rivas F, Mayoral F, Fuerst R, Flaquer A, Windemuth C, Gay E, Sanz S, González MJ, ... ... Auburger G, et al. Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24. American Journal of Human Genetics. 77: 1102-11. PMID 16380920 DOI: 10.1086/498619  0.6
2005 Gierga K, Bürk K, Bauer M, Orozco Diaz G, Auburger G, Schultz C, Vuksic M, Schöls L, de Vos RA, Braak H, Deller T, Rüb U. Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2). Acta Neuropathologica. 109: 617-31. PMID 15906049 DOI: 10.1007/s00401-005-1014-8  0.6
2005 Seifried C, Sitzer M, Jen J, Auburger G. [HERNS. A rare, hereditary, multisystemic disease with cerebral microangiopathy]. Der Nervenarzt. 76: 1191-2, 1194-5. PMID 15856153 DOI: 10.1007/s00115-005-1910-0  0.6
2005 Seifried C, Velázquez-Pérez L, Santos-Falcón N, Abele M, Ziemann U, Almaguer LE, Martínez-Góngora E, Sánchez-Cruz G, Canales N, Pérez-González R, Velázquez-Manresa M, Viebahn B, Stuckrad-Barre S, Klockgether T, Fetter M, ... Auburger G, et al. Saccade velocity as a surrogate disease marker in spinocerebellar ataxia type 2. Annals of the New York Academy of Sciences. 1039: 524-7. PMID 15827014 DOI: 10.1196/annals.1325.059  0.6
2005 Kessler KR, Hamscho N, Morales B, Menzel C, Barrero F, Vives F, Gispert S, Auburger G. Dopaminergic function in a family with the PARK6 form of autosomal recessive Parkinson's syndrome. Journal of Neural Transmission (Vienna, Austria : 1996). 112: 1345-53. PMID 15785866 DOI: 10.1007/s00702-005-0281-9  0.6
2005 Rüb U, Gierga K, Brunt ER, de Vos RA, Bauer M, Schöls L, Bürk K, Auburger G, Bohl J, Schultz C, Vuksic M, Burbach GJ, Braak H, Deller T. Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. Journal of Neural Transmission (Vienna, Austria : 1996). 112: 1523-45. PMID 15785863 DOI: 10.1007/s00702-005-0287-3  0.6
2005 Rüb U, Del Turco D, Bürk K, Diaz GO, Auburger G, Mittelbronn M, Gierga K, Ghebremedhin E, Schultz C, Schöls L, Bohl J, Braak H, Deller T. Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2. Neuropathology and Applied Neurobiology. 31: 127-40. PMID 15771706 DOI: 10.1111/j.1365-2990.2004.00617.x  0.6
2005 Hernandez DG, Paisán-Ruíz C, McInerney-Leo A, Jain S, Meyer-Lindenberg A, Evans EW, Berman KF, Johnson J, Auburger G, Schäffer AA, Lopez GJ, Nussbaum RL, Singleton AB. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Annals of Neurology. 57: 453-6. PMID 15732108 DOI: 10.1002/ana.20401  0.6
2005 Gispert S, Trenkwalder C, Mota-Vieira L, Kostic V, Auburger G. Failure to find alpha-synuclein gene dosage changes in 190 patients with familial Parkinson disease. Archives of Neurology. 62: 96-8. PMID 15642855 DOI: 10.1001/archneur.62.1.96  0.6
2005 Cabin DE, Gispert-Sanchez S, Murphy D, Auburger G, Myers RR, Nussbaum RL. Exacerbated synucleinopathy in mice expressing A53T SNCA on a Snca null background. Neurobiology of Aging. 26: 25-35. PMID 15585343 DOI: 10.1016/j.neurobiolaging.2004.02.026  0.6
2004 Abel A, Fonknechten N, Hofer A, Dürr A, Cruaud C, Voit T, Weissenbach J, Brice A, Klimpe S, Auburger G, Hazan J. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Neurogenetics. 5: 239-43. PMID 15517445 DOI: 10.1007/s10048-004-0191-2  0.6
2004 Lee HY, Xu Y, Huang Y, Ahn AH, Auburger GW, Pandolfo M, Kwiecinski H, Grimes DA, Lang AE, Nielsen JE, Averyanov Y, Servidei S, Friedman A, Van Bogaert P, Abramowicz MJ, et al. The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway. Human Molecular Genetics. 13: 3161-70. PMID 15496428 DOI: 10.1093/hmg/ddh330  0.6
2004 Rüb U, Bürk K, Schöls L, Brunt ER, de Vos RA, Diaz GO, Gierga K, Ghebremedhin E, Schultz C, Del Turco D, Mittelbronn M, Auburger G, Deller T, Braak H. Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3. Neurology. 63: 1258-63. PMID 15477548  0.6
2004 Velázquez-Pérez L, Seifried C, Santos-Falcón N, Abele M, Ziemann U, Almaguer LE, Martínez-Góngora E, Sánchez-Cruz G, Canales N, Pérez-González R, Velázquez-Manresa M, Viebahn B, von Stuckrad-Barre S, Fetter M, Klockgether T, ... Auburger G, et al. Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2. Annals of Neurology. 56: 444-7. PMID 15349876 DOI: 10.1002/ana.20220  0.6
2004 Rüb U, Brunt ER, de Vos RA, Del Turco D, Del Tredici K, Gierga K, Schultz C, Ghebremedhin E, Bürk K, Auburger G, Braak H. Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance. Neuropathology and Applied Neurobiology. 30: 402-14. PMID 15305986 DOI: 10.1111/j.1365-2990.2004.00554.x  0.6
2004 Hofer A, Ozkan S, Hermans M, Kubassek N, Sitzer M, Burtscher J, Knopp U, Schoch B, Wanke I, Huebner F, Raabe A, Steinmetz H, Auburger G. Mutations in the lysyl oxidase gene not associated with intracranial aneurysm in central European families. Cerebrovascular Diseases (Basel, Switzerland). 18: 189-93. PMID 15273433 DOI: 10.1159/000079940  0.6
2004 Valente EM, Abou-Sleiman PM, Caputo V, Muqit MM, Harvey K, Gispert S, Ali Z, Del Turco D, Bentivoglio AR, Healy DG, Albanese A, Nussbaum R, González-Maldonado R, Deller T, Salvi S, ... ... Auburger G, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science (New York, N.Y.). 304: 1158-60. PMID 15087508 DOI: 10.1126/science.1096284  0.6
2003 Gispert S, Del Turco D, Garrett L, Chen A, Bernard DJ, Hamm-Clement J, Korf HW, Deller T, Braak H, Auburger G, Nussbaum RL. Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence of aggregate formation. Molecular and Cellular Neurosciences. 24: 419-29. PMID 14572463 DOI: 10.1016/S1044-7431(03)00198-2  0.6
2003 Rüb U, Schultz C, Del Tredici K, Gierga K, Reifenberger G, de Vos RA, Seifried C, Braak H, Auburger G. Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient. Neuropathology and Applied Neurobiology. 29: 418-33. PMID 14507334 DOI: 10.1046/j.1365-2990.2003.00504.x  0.6
2003 Rüb U, Del Turco D, Del Tredici K, de Vos RA, Brunt ER, Reifenberger G, Seifried C, Schultz C, Auburger G, Braak H. Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance. Brain : a Journal of Neurology. 126: 2257-72. PMID 12847080 DOI: 10.1093/brain/awg234  0.6
2003 Hofer A, Hermans M, Kubassek N, Sitzer M, Funke H, Stögbauer F, Ivaskevicius V, Oldenburg J, Burtscher J, Knopp U, Schoch B, Wanke I, Hübner F, Deinsberger W, Meyer B, ... ... Auburger G, et al. Elastin polymorphism haplotype and intracranial aneurysms are not associated in Central Europe. Stroke; a Journal of Cerebral Circulation. 34: 1207-11. PMID 12690215 DOI: 10.1161/01.STR.0000069013.83336.1C  0.6
2002 Kettner M, Willwohl D, Hubbard GB, Rüb U, Dick EJ, Cox AB, Trottier Y, Auburger G, Braak H, Schultz C. Intranuclear aggregation of nonexpanded ataxin-3 in marinesco bodies of the nonhuman primate substantia nigra. Experimental Neurology. 176: 117-21. PMID 12093088 DOI: 10.1006/exnr.2002.7916  0.6
2002 Ha-Hao D, Merle U, Hofmann C, Wesch H, Doll J, Auburger G, Tuma S, Strauss M, Stremmel W. Chances and shortcomins of adenovirus-mediated ATP7B gene transfer in Wilson disease: proof of principle demonstrated in a pilot study with LEC rats. Zeitschrift FüR Gastroenterologie. 40: 209-16. PMID 11961729 DOI: 10.1055/s-2002-25151  0.6
2001 Alexander C, Bernstein SL, Rocchi M, Auburger G. Saturating density of STSs (1/6 kb) in a 1.1 Mb region on 3q28-q29: a valuable resource for cloning of disease genes. European Journal of Human Genetics : Ejhg. 9: 307-10. PMID 11313765 DOI: 10.1038/sj.ejhg.5200630  0.6
2001 Hofele K, Sedelis M, Auburger GW, Morgan S, Huston JP, Schwarting RK. Evidence for a dissociation between MPTP toxicity and tyrosinase activity based on congenic mouse strain susceptibility. Experimental Neurology. 168: 116-22. PMID 11170726 DOI: 10.1006/exnr.2000.7588  0.6
2000 Sedelis M, Hofele K, Auburger GW, Morgan S, Huston JP, Schwarting RK. MPTP susceptibility in the mouse: behavioral, neurochemical, and histological analysis of gender and strain differences. Behavior Genetics. 30: 171-82. PMID 11105391 DOI: 10.1023/A:1001958023096  0.6
2000 Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A, Rodriguez M, Kellner U, Leo-Kottler B, Auburger G, Bhattacharya SS, Wissinger B. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nature Genetics. 26: 211-5. PMID 11017080 DOI: 10.1038/79944  0.6
2000 Sedelis M, Hofele K, Auburger GW, Morgan S, Huston JP, Schwarting RK. Evidence for resistance to MPTP in C57BL/6 x BALB/c F1 hybrids as compared with their progenitor strains. Neuroreport. 11: 1093-6. PMID 10790888  0.6
2000 Nussbaum R, Auburger G. Neurodegeneration in the polyglutamine diseases: Act 1, Scene 1. Nature Neuroscience. 3: 103-4. PMID 10649562 DOI: 10.1038/72042  0.6
1999 Jarman PR, del Grosso N, Valente EM, Leube B, Cassetta E, Bentivoglio AR, Waddy HM, Uitti RJ, Maraganore DM, Albanese A, Frontali M, Auburger G, Bressman SB, Wood NW, Nygaard TG. Primary torsion dystonia: the search for genes is not over. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 395-7. PMID 10449567  0.6
1999 Leube B, Kessler KR, Ferbert A, Ebke M, Schwendemann G, Erbguth F, Benecke R, Auburger G. Phenotypic variability of the DYT1 mutation in German dystonia patients. Acta Neurologica Scandinavica. 99: 248-51. PMID 10225357  0.6
1999 Estrada R, Galarraga J, Orozco G, Nodarse A, Auburger G. Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies. Acta Neuropathologica. 97: 306-10. PMID 10090679 DOI: 10.1007/s004010050989  0.6
1999 Aguiar J, Santurlidis S, Nowok J, Alexander C, Rudnicki D, Gispert S, Schulz W, Auburger G. Identification of the physiological promoter for spinocerebellar ataxia 2 gene reveals a CpG island for promoter activity situated into the exon 1 of this gene and provides data about the origin of the nonmethylated state of these types of islands. Biochemical and Biophysical Research Communications. 254: 315-8. PMID 9918835 DOI: 10.1006/bbrc.1998.9929  0.6
1999 Santos N, Aguiar J, Fernandez J, Vazquez M, Auburger G, Gispert S, Mendoza Y, Garcia J, Velazquez L. Molecular diagnosis of a sample of the Cuban population with spinocerebellar ataxia type 2 Biotecnologia Aplicada. 16: 219-221.  0.6
1999 Aguiar J, Vazquez M, Fernandez J, Mendoza Y, Auburger G. Cloning and sequencing of the 5' region from human spinocerebellar ataxia 2 gene Biotecnologia Aplicada. 16: 165-168.  0.6
1998 Lavedan C, Buchholtz S, Auburger G, Albin RL, Athanassiadou A, Blancato J, Burguera JA, Ferrell RE, Kostic V, Leroy E, Leube B, Mota-Vieira L, Papapetropoulos T, Pericak-Vance MA, Pinkus J, et al. Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 5: 401-2. PMID 10048491  0.6
1998 Duc HH, Hefter H, Stremmel W, Castañeda-Guillot C, Hernández Hernández A, Cox DW, Auburger G. His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype. European Journal of Human Genetics : Ejhg. 6: 616-23. PMID 9887381 DOI: 10.1038/sj.ejhg.5200237  0.6
1998 Becker-Wegerich P, Steuber M, Olbrisch R, Ruzicka T, Auburger G, Hofhaus G. Defects of mitochondrial respiratory chain in multiple symmetric lipomatosis. Archives of Dermatological Research. 290: 652-5. PMID 9879833 DOI: 10.1007/s004030050368  0.6
1998 Leube B, Auburger G. Questionable role of adult-onset focal dystonia among sporadic dystonia patients. Annals of Neurology. 44: 984-5. PMID 9851449 DOI: 10.1002/ana.410440622  0.6
1998 Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, et al. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q. Genome Research. 8: 1216-27. PMID 9847083  0.6
1998 Schmidt T, Landwehrmeyer GB, Schmitt I, Trottier Y, Auburger G, Laccone F, Klockgether T, Völpel M, Epplen JT, Schöls L, Riess O. An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients. Brain Pathology (Zurich, Switzerland). 8: 669-79. PMID 9804376  0.6
1998 Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E, Harta G, Brownstein MJ, Jonnalagada S, Chernova T, Dehejia A, Lavedan C, Gasser T, Steinbach PJ, Wilkinson KD, et al. The ubiquitin pathway in Parkinson's disease. Nature. 395: 451-2. PMID 9774100 DOI: 10.1038/26652  0.6
1998 Auburger G. New genetic concepts and stroke prevention. Cerebrovascular Diseases (Basel, Switzerland). 8: 28-32. PMID 9767196 DOI: 10.1159/000047515  0.6
1998 Orozco G, Rivas F, Gomez MI, Bordallo A, Ortega MV, Requena J, Klimke A, Gaebel W, Larisch R, Müller-Gärtner HW, Auburger G, Propping P, Rietschel M, Nöthen MM. Establishment of an Andalusian family collection for bipolar affective disorder American Journal of Medical Genetics - Neuropsychiatric Genetics. 81: 544-545.  0.6
1997 Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, ... ... Auburger G, et al. SCA2 trinucleotide expansion in German SCA patients. Neurogenetics. 1: 59-64. PMID 10735276  0.6
1997 Leube B, Kessler KR, Goecke T, Auburger G, Benecke R. Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family. Movement Disorders : Official Journal of the Movement Disorder Society. 12: 1000-6. PMID 9399227 DOI: 10.1002/mds.870120625  0.6
1997 Hofele K, Benecke R, Auburger G. Gene locus FPD1 of the dystonic Mount-Reback type of autosomal-dominant paroxysmal choreoathetosis. Neurology. 49: 1252-7. PMID 9371903  0.6
1997 Leube B, Hendgen T, Kessler KR, Knapp M, Benecke R, Auburger G. Evidence for DYT7 being a common cause of cervical dystonia (torticollis) in Central Europe. American Journal of Medical Genetics. 74: 529-32. PMID 9342206 DOI: 10.1002/(SICI)1096-8628(19970919)74:5<529::AID-AJMG15>3.0.CO;2-E  0.6
1997 Alexander C, Stathakis DG, Lin L, Rahman S, Bryant PJ, Auburger G, Chishti AH. Fine scale mapping places DLG1, the gene encoding hDlg, telomeric to the OPA1 candidate region. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 795-6. PMID 9321488 DOI: 10.1007/s003359900578  0.6
1997 Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds. Archives of Neurology. 54: 1073-80. PMID 9311350  0.6
1997 Leube B, Hendgen T, Kessler KR, Knapp M, Benecke R, Auburger G. Sporadic focal dystonia in northwest Germany: molecular basis on chromosome 18p. Annals of Neurology. 42: 111-4. PMID 9225692 DOI: 10.1002/ana.410420117  0.6
1996 Lindblad K, Lunkes A, Maciel P, Stevanin G, Zander C, Klockgether T, Ratzlaff T, Brice A, Rouleau GA, Hudson T, Auburger G, Schalling M. Mutation detection in Machado-Joseph disease using repeat expansion detection. Molecular Medicine (Cambridge, Mass.). 2: 77-85. PMID 8900536  0.6
1996 Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genetics. 14: 269-76. PMID 8896555 DOI: 10.1038/ng1196-269  0.6
1996 Leube B, Rudnicki D, Ratzlaff T, Kessler KR, Benecke R, Auburger G. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution. Human Molecular Genetics. 5: 1673-7. PMID 8894706  0.6
1996 Auburger G, Ratzlaff T, Lunkes A, Nelles HW, Leube B, Binkofski F, Kugel H, Heindel W, Seitz R, Benecke R, Witte OW, Voit T. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197. Genomics. 31: 90-4. PMID 8808284 DOI: 10.1006/geno.1996.0013  0.6
1995 Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity. American Journal of Human Genetics. 56: 183-7. PMID 7825576  0.6
1995 Hernández A, Magariño C, Gispert S, Santos N, Lunkes A, Orozco G, Heredero L, Beckmann J, Auburger G. Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1. Genomics. 25: 433-5. PMID 7789976 DOI: 10.1016/0888-7543(95)80043-L  0.6
1995 Cancel G, Stevanin G, Vernant JC, Durr A, Lepage-Lezin A, Belal S, Ben- Hamida M, Pulst S, Rouleau G, Weissenbach J, LePaslier D, Kucherlapati R, Montgomery K, Fukui K, Auburger G. Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2 [9] American Journal of Human Genetics. 57: 972-975. PMID 7573064  0.6
1995 Lunkes A, Hartung U, Magariño C, Rodríguez M, Palmero A, Rodríguez L, Heredero L, Weissenbach J, Weber J, Auburger G. Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type Kjer. American Journal of Human Genetics. 57: 968-70. PMID 7573062  0.6
1995 Klockgether T, Bürk K, Auburger G, Dichgans J. [Classification and diagnosis of degenerative ataxias]. Der Nervenarzt. 66: 571-81. PMID 7566268  0.6
1994 Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Neurology. 44: 1423-6. PMID 8058142  0.6
1994 Klockgether T, Bürk K, Schulz JB, Dichgans J, Wessel K, Auburger G. Absence of SCA1 mutation in idiopathic cerebellar ataxia. Journal of Neurology, Neurosurgery, and Psychiatry. 57: 1439-40. PMID 7964835 DOI: 10.1136/jnnp.57.11.1439-a  0.6
1994 Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G. Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus. Experimental Neurology. 126: 310-2. PMID 7925830 DOI: 10.1006/exnr.1994.1070  0.6
1993 Gispert S, Nothers C, Orozco G, Auburger G. Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q. Human Heredity. 43: 12-20. PMID 8514320 DOI: 10.1159/000154107  0.6
1993 Auburger G, Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C, Hillermann R, Lunkes A, Khati C, Stevanin G, et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1 Nature Genetics. 4: 295-299. PMID 8358438 DOI: 10.1038/ng0793-295  0.6
1993 Lunkes A, Gispert S, Enczmann J, Auburger G. Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage. Human Genetics. 91: 362-6. PMID 8099059 DOI: 10.1007/BF00217357  0.6
1993 Silveira I, Manaia A, Melki J, Magarino C, Lunkes A, Hernandez A, Gispert S, Burlet P, Rozet JM, Coutinho P, Loureiro JEL, Guimaraes J, Auburger G, Munnich A, Sequeiros J. Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2) Genomics. 17: 556-559. PMID 7902323 DOI: 10.1006/geno.1993.1371  0.6
1990 Orozco Diaz G, Nodarse Fleites A, Cordovés Sagaz R, Auburger G. Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba. Neurology. 40: 1369-75. PMID 2392220  0.6
1990 Auburger G, Diaz GO, Capote RF, Sanchez SG, Perez MP, del Cueto ME, Meneses MG, Farrall M, Williamson R, Chamberlain S. Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population. American Journal of Human Genetics. 46: 1163-77. PMID 1971152  0.6
1988 Reithmann C, Arbogast H, Hallek M, Auburger G, Szinicz L. Studies on the role of central catecholaminergic mechanisms in the antidotal effect of the oxime HI 6 in soman poisoned mice. Archives of Toxicology. 62: 41-4. PMID 3190454 DOI: 10.1007/BF00316255  0.6
1987 Auburger G, Heumann R, Hellweg R, Korsching S, Thoenen H. Developmental changes of nerve growth factor and its mRNA in the rat hippocampus: comparison with choline acetyltransferase. Developmental Biology. 120: 322-8. PMID 2435590 DOI: 10.1016/0012-1606(87)90235-1  0.6
1985 Korsching S, Auburger G, Heumann R, Scott J, Thoenen H. Levels of nerve growth factor and its mRNA in the central nervous system of the rat correlate with cholinergic innervation. The Embo Journal. 4: 1389-93. PMID 2411537  0.6
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