Alexander Zimprich

Alexander Zimprich

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Alexander Zimprich

Alexander Zimprich

Publications by authors named "Alexander Zimprich"

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A rare P2RX7 variant in a Hungarian family with multiple sclerosis.

Mult Scler Relat Disord 2019 01 27;27:340-341. Epub 2018 Oct 27.

Department of Neurology, Medical University of Vienna, Austria. Electronic address:

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http://dx.doi.org/10.1016/j.msard.2018.10.110DOI Listing
January 2019

A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia.

J Neural Transm (Vienna) 2018 12 4;125(12):1877-1883. Epub 2018 Sep 4.

Department of Neurology, Medical University of Vienna, AKH 6A, Währinger Gürtel 18-20, 1097, Vienna, Austria.

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http://dx.doi.org/10.1007/s00702-018-1924-yDOI Listing
December 2018

TPP2 mutation associated with sterile brain inflammation mimicking MS.

Neurol Genet 2018 Dec 13;4(6):e285. Epub 2018 Nov 13.

Department of Neurology (E.M.R., S.P., C.S., F.L., F.Z., A.Z.), Medical University of Vienna, Austria; Institut für Humangenetik (E.G., T.W., T.S.), Helmholtz Zentrum München, Germany; Center for Brain Research (T.Z., H.L.), Medical University of Vienna; Division of Nephrology and Dialysis (C.K.), Department of Internal Medicine III, Medical University of Vienna; Department of Physical Medicine (M.K.), Rehabilitation and Occupational Medicine, Medical University of Vienna, Austria; Lübeck Interdisciplinary Platform for Genome Analytics (C.M.L.), Institutes of Neurogenetics and for Cardiogenetics, University of Lübeck; Department of Neurology and Neuroimaging Center (NIC) (C.M.L.), Focus Program Translational Neuroscience (FTN), University Medical Center of the Johannes Gutenberg University Mainz; Department of Human Genetics (S.H., J.T.E.), Ruhr-University Bochum; Herdecke (J.T.E.), ZBAF, Faculty of Health, University Witten; Department of Neurology (U.K.Z., M.H.), Neuroimmunological Section, University of Rostock; Department of Neurology (A.D.), Department of Clinical Genomics (A.D.), Department of Neuroscience (A.D.), Jeweils Mayo Clinic, Jacksonville, FL; Department of Neurology (S.G.M.), University of Muenster, Germany; Department of Physiology and Biochemistry (M.A., B.M.), School of Medicine, the University of Jordan; The National Center (Institute) for Diabetes (M.E.-K.), Endocrinology and Genetics (NCDEG), Amman, Jordan; Department of Medical Genetics (C.V.-G., A.D.S.), University of British Columbia, Vancouver, Canada; Department of Medical Biochemistry and Microbiology (B.T.), Uppsala University, Sweden; Karl Landsteiner Institute for Neuroimmunological and Neurodegenerative Disorders (W.K.), SMZ-Ost-Donauspital, Vienna, Austria; and Institute for Neuroimmunological and Neurodegenerative Disorders (W.K.), SMZ-Ost-Donauspital, Vienna, Austria.

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http://dx.doi.org/10.1212/NXG.0000000000000285DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244017PMC
December 2018

Reply: No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson's disease.

Brain 2018 03;141(3):e17

Department of Neurodegenerative Diseases, Center of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen and German Centre for Neurodegenerative Diseases, Tübingen, Germany.

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http://dx.doi.org/10.1093/brain/awx380DOI Listing
March 2018

Genome-wide significant association with seven novel multiple sclerosis risk loci.

J Med Genet 2015 Dec 16;52(12):848-55. Epub 2015 Oct 16.

Platform for Genome Analytics, Institutes of Neurogenetics & Integrative and Experimental Genomics, University of Lübeck, Lübeck, Germany Department of Vertebrate Genomics, Max Planck Institute for Molecular Genetics, Berlin, Germany Department of Medicine, School of Public Health, Imperial College London, London, UK.

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http://dx.doi.org/10.1136/jmedgenet-2015-103442DOI Listing
December 2015

A genetic polymorphism of the endogenous opioid dynorphin modulates monetary reward anticipation in the corticostriatal loop.

PLoS One 2014 25;9(2):e89954. Epub 2014 Feb 25.

Social, Cognitive and Affective Neuroscience Unit, Department of Basic Psychological Research and Research Methods, Faculty of Psychology, University of Vienna, Vienna, Austria ; Department of Psychology, University of Gothenburg, Gothenburg, Sweden.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0089954PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934978PMC
January 2015

Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome.

PLoS One 2014 29;9(5):e98092. Epub 2014 May 29.

Neurologische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany; Institut für Humangenetik, Helmholtz Zentrum München, Munich, Germany; Institut für Humangenetik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0098092PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038519PMC
January 2015

VPS35 Parkinson's disease phenotype resembles the sporadic disease.

J Neural Transm (Vienna) 2014 Jul 21;121(7):755-9. Epub 2014 Feb 21.

Department of Neurology, Allgemeines Krankenhaus Linz (AKHL), Krankenhausstr. 9, 4020, Linz, Upper Austria, Austria,

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http://dx.doi.org/10.1007/s00702-014-1179-1DOI Listing
July 2014

Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.

Am J Hum Genet 2014 Jul;95(1):85-95

Neurologische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany; Institut für Humangenetik, Helmholtz Zentrum München, 85764 Munich, Germany; Institut für Humangenetik, Technische Universität München, 81675 Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany; Department of Neurology and Neurosciences, Center for Sleep Sciences and Medicine, Stanford University, Palo Alto, CA 94304, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.06.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085638PMC
July 2014

No evidence for a role of rare CYP27B1 variants in Austrian multiple sclerosis patients.

Mult Scler 2014 Mar 25;20(3):391-2. Epub 2013 Jul 25.

Department of Neurology, Medical University of Vienna, Austria.

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http://dx.doi.org/10.1177/1352458513498130DOI Listing
March 2014

Reply: autosomal recessive epilepsy associated with contactin 2 mutation is different from familial cortical tremor, myoclonus and epilepsy.

Brain 2013 Oct 25;136(Pt 10):e254. Epub 2013 Jun 25.

Department of Clinical Neurology, Medical University of Vienna, 1090 Vienna, Austria.

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http://dx.doi.org/10.1093/brain/awt141DOI Listing
October 2013

The role of SCARB2 as susceptibility factor in Parkinson's disease.

Mov Disord 2013 Apr 13;28(4):538-40. Epub 2013 Feb 13.

Institute of Human Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.

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http://dx.doi.org/10.1002/mds.25349DOI Listing
April 2013

Association of the chromosome 11q13.5 variant with atopic dermatitis in Austrian patients.

Eur J Dermatol 2013 Apr;23(2):142-5

Department of Dermatology, DIAID, Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Waehringer Guertel 18-20 1090 Vienna, Austria.

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http://dx.doi.org/10.1684/ejd.2013.1955DOI Listing
April 2013

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

J Med Genet 2012 Nov;49(11):721-6

Department. of Neurodegenerative diseases, Hertie-Institute for Clinical Brain Research and DZNE- German Center for Neurodegenerative Diseases, Tübingen, Hoppe-Seyler-Str. 3, Tübingen 72076, Germany.

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http://dx.doi.org/10.1136/jmedgenet-2012-101155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488700PMC
November 2012

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease.

Neurogenetics 2012 Aug 16;13(3):281-5. Epub 2012 Jun 16.

Neurologische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, Ismaningerstr 22, 81675 Munich, Germany.

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http://dx.doi.org/10.1007/s10048-012-0334-9DOI Listing
August 2012

Phenocopies in families with essential tremor and restless legs syndrome challenge Mendelian laws. Epigenetics might provide answers.

Parkinsonism Relat Disord 2012 Jul 19;18(6):711-6. Epub 2012 Apr 19.

Department of Clinical Neurology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.1016/j.parkreldis.2012.03.019DOI Listing
July 2012

Lack of association between ABCC2 gene variants and treatment response in epilepsy.

Pharmacogenomics 2012 Jan;13(2):185-90

Department of Clinical Neurology, Medical University of Vienna, Vienna, Austria.

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http://dx.doi.org/10.2217/pgs.11.143DOI Listing
January 2012

Genetics of Parkinson's disease and essential tremor.

Curr Opin Neurol 2011 Aug;24(4):318-23

Department of Neurology, Medizinische Universität Wien, Vienna, Austria.

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http://dx.doi.org/10.1097/WCO.0b013e3283484b87DOI Listing
August 2011

Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease.

Neurobiol Aging 2011 Feb 3;32(2):302-7. Epub 2009 Apr 3.

Department of Neurology, Medical University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria.

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http://dx.doi.org/10.1016/j.neurobiolaging.2009.02.015DOI Listing
February 2011

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.

Muscle Nerve 2009 Mar;39(3):389-91

Department of Neurology, Medical University of Vienna; Währinger Gürtel 18-20, Vienna A-1097, Austria.

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http://dx.doi.org/10.1002/mus.21225DOI Listing
March 2009

Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder.

Psychiatr Genet 2008 Dec;18(6):308-9

Department of Neurology, Medical University of Vienna, Austria.

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http://dx.doi.org/10.1097/YPG.0b013e3283060f6fDOI Listing
December 2008

Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.

Mov Disord 2007 Oct;22(14):2104-9

Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, Center of Neurology, University of Tuebingen, Tuebingen, Germany.

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http://dx.doi.org/10.1002/mds.21692DOI Listing
October 2007

Lack of association between a GABA receptor 1 gene polymorphism and temporal lobe epilepsy.

Epilepsia 2006 Feb;47(2):437-9

Department of Clinical Neurology, Core Unit of Medical Statistics and Informatics, Medical University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria.

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http://dx.doi.org/10.1111/j.1528-1167.2006.00441.xDOI Listing
February 2006

Common variants of LRRK2 are not associated with sporadic Parkinson's disease.

Ann Neurol 2005 Dec;58(6):905-8

Institute of Human Genetics, GSF National Research Center for Environment and Health, Neuherberg, Germany.

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http://dx.doi.org/10.1002/ana.20664DOI Listing
December 2005

Multiple regions of alpha-synuclein are associated with Parkinson's disease.

Ann Neurol 2005 Apr;57(4):535-41

Institute for Human Genetics, GSF-National Research Centre for Environment and Health, Neuherberg, Germany.

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http://dx.doi.org/10.1002/ana.20438DOI Listing
April 2005

PARK11 is not linked with Parkinson's disease in European families.

Eur J Hum Genet 2005 Feb;13(2):193-7

Hertie-Institute for Clinical Brain Research, Department of Neurodegenerative Diseases, University of Tuebingen, Hoppe-Seyler Str. 3, 72076 Tuebingen, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5201317DOI Listing
February 2005

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted.

Eur J Hum Genet 2003 Feb;11(2):138-44

Institute of Human Genetics, GSF National Research Center, D-85764 München-Neuherberg, Germany.

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http://dx.doi.org/10.1038/sj.ejhg.5200938DOI Listing
February 2003

A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy.

Ann Neurol 2002 Feb;51(2):260-3

Department of Neurology, University Hospital of Vienna, Vienna, Austria.

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February 2002

The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3.

Gene 2002 Feb;285(1-2):229-37

Mayo Clinic Jacksonville, Birdsall Building, 4500 San Pablo Road, Jacksonville, FL 32224, USA.

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http://dx.doi.org/10.1016/s0378-1119(02)00402-xDOI Listing
February 2002