Works by Zimprich, Alexander

Results: 62
    1

    Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease.

    Published in:
    Journal of Parkinson's Disease, 2022, v. 12, n. 1, p. 267, doi. 10.3233/JPD-212851
    By:
    • Domenighetti, Cloé;
    • Sugier, Pierre-Emmanuel;
    • Sreelatha, Ashwin Ashok Kumar;
    • Schulte, Claudia;
    • Grover, Sandeep;
    • Mohamed, Océane;
    • Portugal, Berta;
    • May, Patrick;
    • Bobbili, Dheeraj R.;
    • Radivojkov-Blagojevic, Milena;
    • Lichtner, Peter;
    • Singleton, Andrew B.;
    • Hernandez, Dena G.;
    • Edsall, Connor;
    • Mellick, George D.;
    • Zimprich, Alexander;
    • Pirker, Walter;
    • Rogaeva, Ekaterina;
    • Lang, Anthony E.;
    • Koks, Sulev
    Publication type:
    Article
    2

    Rare variants in LRRK1 and Parkinson's disease.

    Published in:
    Neurogenetics, 2014, v. 15, n. 1, p. 49, doi. 10.1007/s10048-013-0383-8
    By:
    • Schulte, Eva;
    • Ellwanger, Daniel;
    • Dihanich, Sybille;
    • Manzoni, Claudia;
    • Stangl, Katrin;
    • Schormair, Barbara;
    • Graf, Elisabeth;
    • Eck, Sebastian;
    • Mollenhauer, Brit;
    • Haubenberger, Dietrich;
    • Pirker, Walter;
    • Zimprich, Alexander;
    • Brücke, Thomas;
    • Lichtner, Peter;
    • Peters, Annette;
    • Gieger, Christian;
    • Trenkwalder, Claudia;
    • Mewes, Hans-Werner;
    • Meitinger, Thomas;
    • Lewis, Patrick
    Publication type:
    Article
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    PARK11 is not linked with Parkinson's disease in European families.

    Published in:
    European Journal of Human Genetics, 2005, v. 13, n. 2, p. 193, doi. 10.1038/sj.ejhg.5201317
    By:
    • Prestel, Jürgen;
    • Sharma, Manu;
    • Leitner, Petra;
    • Zimprich, Alexander;
    • Vaughan, Jenny R.;
    • Dürr, Alexandra;
    • Bonifati, Vincenzo;
    • De Michele, Giuseppe;
    • Hanagasi, Hasmet A.;
    • Farrer, Matthew;
    • Hofer, Anne;
    • Asmus, Friedrich;
    • Volpe, Giampiero;
    • Meco, Giuseppe;
    • Brice, Alexis;
    • Wood, NicholasW.;
    • Müller-Myhsok, Bertram;
    • Gasser, Thomas
    Publication type:
    Article
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    Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor.

    Published in:
    2009
    By:
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Petursson, Hjorvar;
    • Gustafsson, Omar;
    • Gudjonsdottir, Iris H;
    • Jonsdottir, Gudrun A;
    • Palsson, Stefan T;
    • Jonsson, Thorlakur;
    • Saemundsdottir, Jona;
    • Bjornsdottir, Gyda;
    • Böttcher, Yvonne;
    • Thorlacius, Theodora;
    • Haubenberger, Dietrich;
    • Zimprich, Alexander;
    • Auff, Eduard;
    • Hotzy, Christoph;
    • Testa, Claudia M;
    • Miyatake, Lisa A;
    • Rosen, Ami R;
    • Kristleifsson, Kristleifur
    Publication type:
    Correction Notice
    14

    Variant in the sequence of the LINGO1 gene confers risk of essential tremor.

    Published in:
    Nature Genetics, 2009, v. 41, n. 3, p. 277, doi. 10.1038/ng.299
    By:
    • Stefansson, Hreinn;
    • Steinberg, Stacy;
    • Petursson, Hjorvar;
    • Gustafsson, Omar;
    • Gudjonsdottir, Iris H.;
    • Jonsdottir, Gudrun A.;
    • Palsson, Stefan T.;
    • Jonsson, Thorlakur;
    • Saemundsdottir, Jona;
    • Bjornsdottir1, Gyda;
    • Böttcher, Yvonne;
    • Thorlacius, Theodora;
    • Haubenberger, Dietrich;
    • Zimprich, Alexander;
    • Auff, Eduard;
    • Hotzy, Christoph;
    • Testa, Claudia M.;
    • Miyatake, Lisa A.;
    • Rosen, Ami R.;
    • Kristleifsson, Kristleifur
    Publication type:
    Article
    15

    PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 946, doi. 10.1038/ng.190
    By:
    • Schormair, Barbara;
    • Kemlink, David;
    • Roeske, Darina;
    • Eckstein, Gertrud;
    • Lan Xiong;
    • Lichtner, Peter;
    • Ripke, Stephan;
    • Trenkwalder, Claudia;
    • Zimprich, Alexander;
    • Stiasny-Kolster, Karin;
    • Oertel, Wolfgang;
    • Bachmann, Cornelius G.;
    • Paulus, Walter;
    • Högl, Birgit;
    • Frauscher, Birgit;
    • Gschliesser, Viola;
    • Poewe, Werner;
    • Peglau, Ines;
    • Vodicka, Pavel;
    • Vávrová, Jana
    Publication type:
    Article
    16

    Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

    Published in:
    Nature Genetics, 2007, v. 39, n. 8, p. 1000, doi. 10.1038/ng2099
    By:
    • Winkelmann, Juliane;
    • Schormair, Barbara;
    • Lichtner, Peter;
    • Ripke, Stephan;
    • Lan Xiong;
    • Jalilzadeh, Shapour;
    • Fulda, Stephany;
    • Pütz, Benno;
    • Eckstein, Gertrud;
    • Hauk, Stephanie;
    • Trenkwalder, Claudia;
    • Zimprich, Alexander;
    • Stiasny-Kolster, Karin;
    • Oertel, Wolfgang;
    • Bachmann, Cornelius G.;
    • Paulus, Walter;
    • Peglau, Ines;
    • Eisensehr, Ilonka;
    • Montplaisir, Jacques;
    • Turecki, Gustavo
    Publication type:
    Article
    17

    Mutations in the gene encoding ε-sarcoglycan cause myoclonus?dystonia syndrome.

    Published in:
    Nature Genetics, 2001, v. 29, n. 1, p. 66, doi. 10.1038/ng709
    By:
    • Zimprich, Alexander;
    • Grabowski, Monika;
    • Asmus, Friedrich;
    • Naumann, Markus;
    • Berg, Daniela;
    • Bertram, Markus;
    • Scheidtmann, Karl;
    • Kern, Peter;
    • Winkelmann, Juliane;
    • Müller-Myhsok, Bertram;
    • Riedel, Leonhard;
    • Bauer, Matthias;
    • Müller, Tanja;
    • Castro, Mirna;
    • Meitinger, Thomas;
    • Strom, Tim M.;
    • Gasser, Thomas
    Publication type:
    Article
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    The role of SCARB2 as susceptibility factor in Parkinson's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 4, p. 538, doi. 10.1002/mds.25349
    By:
    • Hopfner, Franziska;
    • Schulte, Eva C.;
    • Mollenhauer, Brit;
    • Bereznai, Benjamin;
    • Knauf, Franziska;
    • Lichtner, Peter;
    • Zimprich, Alexander;
    • Haubenberger, Dietrich;
    • Pirker, Walter;
    • Brücke, Thomas;
    • Peters, Annette;
    • Gieger, Christian;
    • Kuhlenbäumer, Gregor;
    • Trenkwalder, Claudia;
    • Winkelmann, Juliane
    Publication type:
    Article
    20

    Role of LINGO1 polymorphisms in Parkinson's disease.

    Published in:
    Movement Disorders, 2009, v. 24, n. 16, p. 2404, doi. 10.1002/mds.22768
    By:
    • Haubenberger, Dietrich;
    • Hotzy, Christoph;
    • Pirker, Walter;
    • Katzenschlager, Regina;
    • Brücke, Thomas;
    • Zimprich, Fritz;
    • Auff, Eduard;
    • Zimprich, Alexander
    Publication type:
    Article
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    A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.

    Published in:
    2007
    By:
    • Haubenberger, Dietrich;
    • Bonelli, Silvia;
    • Hotzy, Christoph;
    • Leitner, Petra;
    • Lichtner, Peter;
    • Samal, Doris;
    • Katzenschlager, Regina;
    • Djamshidian, Atbin;
    • Brücke, Thomas;
    • Steffelbauer, Michaela;
    • Bancher, Christian;
    • Grossmann, Josef;
    • Ransmayr, Gerhard;
    • Strom, Tim M.;
    • Meitinger, Thomas;
    • Gasser, Thomas;
    • Auff, Eduard;
    • Zimprich, Alexander;
    • Brücke, Thomas
    Publication type:
    journal article
    24

    Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients.

    Published in:
    Movement Disorders, 2005, v. 20, n. 9, p. 1191, doi. 10.1002/mds.20504
    By:
    • Berg, Daniela;
    • Niwar, Marc;
    • Maass, Sylvia;
    • Zimprich, Alexander;
    • Möller, J. Carsten;
    • Wuellner, Ullrich;
    • Schmitz-Hübsch, Tanja;
    • Klein, Christine;
    • Tan, Eng-King;
    • Schöls, Ludger;
    • Marsh, Laura;
    • Dawson, Ted M.;
    • Janetzky, Bernd;
    • Müller, Thomas;
    • Woitalla, Dirk;
    • Kostic, Vladimir;
    • Pramstaller, Peter P.;
    • Oertel, Wolfgang H.;
    • Bauer, Peter;
    • Krueger, Rejko
    Publication type:
    Article
    25

    Blood <i>cis</i>-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome.

    Published in:
    PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098092
    By:
    • Schulte, Eva C.;
    • Schramm, Katharina;
    • Schurmann, Claudia;
    • Lichtner, Peter;
    • Herder, Christian;
    • Roden, Michael;
    • Gieger, Christian;
    • Peters, Annette;
    • Trenkwalder, Claudia;
    • Högl, Birgit;
    • Frauscher, Birgit;
    • Berger, Klaus;
    • Fietze, Ingo;
    • Gross, Nadine;
    • Stiasny-Kolster, Karin;
    • Oertel, Wolfgang;
    • Bachmann, Cornelius G.;
    • Paulus, Walter;
    • Zimprich, Alexander;
    • Völzke, Henry
    Publication type:
    Article
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    Rare Variants in <i>PLXNA4</i> and Parkinson’s Disease.

    Published in:
    PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0079145
    By:
    • Schulte, Eva C.;
    • Stahl, Immanuel;
    • Czamara, Darina;
    • Ellwanger, Daniel C.;
    • Eck, Sebastian;
    • Graf, Elisabeth;
    • Mollenhauer, Brit;
    • Zimprich, Alexander;
    • Lichtner, Peter;
    • Haubenberger, Dietrich;
    • Pirker, Walter;
    • Brücke, Thomas;
    • Bereznai, Benjamin;
    • Molnar, Maria J.;
    • Peters, Annette;
    • Gieger, Christian;
    • Müller-Myhsok, Bertram;
    • Trenkwalder, Claudia;
    • Winkelmann, Juliane
    Publication type:
    Article
    28

    Functional Variant in Complement C3 Gene Promoter and Genetic Susceptibility to Temporal Lobe Epilepsy and Febrile Seizures.

    Published in:
    PLoS ONE, 2010, v. 5, n. 9, p. 1, doi. 10.1371/journal.pone.0012740
    By:
    • Jamali, Sarah;
    • Salzmann, Annick;
    • Perroud, Nader;
    • Ponsole-Lenfant, Magali;
    • Cillario, Jennifer;
    • Roll, Patrice;
    • Roeckel-Trevisiol, Nathalie;
    • Crespel, Ariel;
    • Balzar, Jorg;
    • Schlachter, Kurt;
    • Gruber-Sedlmayr, Ursula;
    • Pataraia, Ekaterina;
    • Baumgartner, Christoph;
    • Zimprich, Alexander;
    • Zimprich, Fritz;
    • Malafosse, Alain;
    • Szepetowski, Pierre
    Publication type:
    Article
    29

    Genetic Structure of Europeans: A View from the North-East.

    Published in:
    PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005472
    By:
    • Nelis, Mari;
    • Esko, Tõnu;
    • Reedik Mägi;
    • Zimprich, Fritz;
    • Zimprich, Alexander;
    • Toncheva, Draga;
    • Karachanak, Sena;
    • Piskáčková, Tereza;
    • Balaščák, Ivan;
    • Peltonen, Leena;
    • Jakkula, Eveliina;
    • Rehnström, Karola;
    • Lathrop, Mark;
    • Heath, Simon;
    • Galan, Pilar;
    • Schreiber, Stefan;
    • Meitinger, Thomas;
    • Pfeufer, Arne;
    • Wichmann, H-Erich;
    • Melegh, Béla
    Publication type:
    Article
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    Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism.

    Published in:
    2020
    By:
    • Borsche, Max;
    • König, Inke R;
    • Delcambre, Sylvie;
    • Petrucci, Simona;
    • Balck, Alexander;
    • Brüggemann, Norbert;
    • Zimprich, Alexander;
    • Wasner, Kobi;
    • Pereira, Sandro L;
    • Avenali, Micol;
    • Deuschle, Christian;
    • Badanjak, Katja;
    • Ghelfi, Jenny;
    • Gasser, Thomas;
    • Kasten, Meike;
    • Rosenstiel, Philip;
    • Lohmann, Katja;
    • Brockmann, Kathrin;
    • Valente, Enza Maria;
    • Youle, Richard J
    Publication type:
    journal article
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    Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease.

    Published in:
    2017
    By:
    • Fitzgerald, Julia C.;
    • Zimprich, Alexander;
    • Carvajal Berrio, Daniel A.;
    • Schindler, Kevin M.;
    • Maurer, Brigitte;
    • Schulte, Claudia;
    • Bus, Christine;
    • Hauser, Anne-Kathrin;
    • Kübler, Manuela;
    • Lewin, Rahel;
    • Reddy Bobbili, Dheeraj;
    • Schwarz, Lisa M.;
    • Vartholomaiou, Evangelia;
    • Brockmann, Kathrin;
    • Wüst, Richard;
    • Madlung, Johannes;
    • Nordheim, Alfred;
    • Riess, Olaf;
    • Martins, L. Miguel;
    • Glaab, Enrico
    Publication type:
    journal article
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    Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1155, doi. 10.1093/brain/awt068
    By:
    • Stogmann, Elisabeth;
    • Reinthaler, Eva;
    • ElTawil, Salwa;
    • El Etribi, Mohammed A.;
    • Hemeda, Mahmoud;
    • El Nahhas, Nevine;
    • Gaber, Ahmed M.;
    • Fouad, Amal;
    • Edris, Sherif;
    • Benet-Pages, Anna;
    • Eck, Sebastian H.;
    • Pataraia, Ekaterina;
    • Mei, Davide;
    • Brice, Alexis;
    • Lesage, Suzanne;
    • Guerrini, Renzo;
    • Zimprich, Friedrich;
    • Strom, Tim M.;
    • Zimprich, Alexander
    Publication type:
    Article
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    Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.

    Published in:
    Annals of Neurology, 2022, v. 92, n. 2, p. 270, doi. 10.1002/ana.26416
    By:
    • Liu, Hui;
    • Dehestani, Mohammad;
    • Blauwendraat, Cornelis;
    • Makarious, Mary B.;
    • Leonard, Hampton;
    • Kim, Jonggeol J.;
    • Schulte, Claudia;
    • Noyce, Alastair;
    • Jacobs, Benjamin M.;
    • Foote, Isabelle;
    • Sharma, Manu;
    • Koks, Sulev;
    • Mellick, George D;
    • Pirker, Walter;
    • Zimprich, Alexander;
    • Lang, Anthony E;
    • Rogaeva, Ekaterina;
    • Taba, Pille;
    • Brice, Alexis;
    • Chartier‐Harlin, Marie‐Christine
    Publication type:
    Article
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    Myoclonus-dystonia syndrome: ε-sarcoglycan mutations and phenotype.

    Published in:
    Annals of Neurology, 2002, v. 52, n. 4, p. 489, doi. 10.1002/ana.10325
    By:
    • Asmus, Friedrich;
    • Zimprich, Alexander;
    • Tezenas Du Montcel, Sophie;
    • Kabus, Christian;
    • Deuschl, Günther;
    • Kupsch, Andreas;
    • Ziemann, Ulf;
    • Castro, Mirna;
    • Kühn, Andrea A.;
    • Strom, Tim M.;
    • Vidailhet, Marie;
    • Bhatia, Kailash P.;
    • Dürr, Alexandra;
    • Wood, Nicholas W.;
    • Brice, Alexis;
    • Gasser, Thomas
    Publication type:
    Article
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    Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.

    Published in:
    2001
    By:
    • Asmus, Friedrich;
    • Zimprich, Alexander;
    • Naumann, Markus;
    • Berg, Daniela;
    • Bertram, Markus;
    • Ceballos-Baumann, Andres;
    • Pruszak-Seel, Roswith;
    • Kabus, Christian;
    • Dichgans, Martin;
    • Fuchs, Sigrid;
    • Müller-Myhsok, Bertram;
    • Gasser, Thomas;
    • Asmus, F;
    • Zimprich, A;
    • Naumann, M;
    • Berg, D;
    • Bertram, M;
    • Ceballos-Baumann, A;
    • Pruszak-Seel, R;
    • Kabus, C
    Publication type:
    journal article
    47

    Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1328, doi. 10.1038/ejhg.2014.300
    By:
    • Schulte, Eva C;
    • Fukumori, Akio;
    • Mollenhauer, Brit;
    • Hor, Hyun;
    • Arzberger, Thomas;
    • Perneczky, Robert;
    • Kurz, Alexander;
    • Diehl-Schmid, Janine;
    • Hüll, Michael;
    • Lichtner, Peter;
    • Eckstein, Gertrud;
    • Zimprich, Alexander;
    • Haubenberger, Dietrich;
    • Pirker, Walter;
    • Brücke, Thomas;
    • Bereznai, Benjamin;
    • Molnar, Maria J;
    • Lorenzo-Betancor, Oswaldo;
    • Pastor, Pau;
    • Peters, Annette
    Publication type:
    Article
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