@ARTICLE{
author={Jecmenica-Lukic Milica V,Milovanovic Andona,Mazalica Nina,Westenberger Ana,Tomic-Pesic Aleksandra,Petrovic Igor N,Markovic Vladana V,Kresojevic Nikola D,Klein Christine,Kostic Vladimir S,Dragasevic-Miskovic Natasa T},
year={2025},
title={An Unusual Presentation of a DNMT1 Mutation: Progressive Supranuclear Palsy Look-Alike Disorder},
journal={MOVEMENT DISORDERS CLINICAL PRACTICE},
volume={},
number={},
pages={-},
document_type={Editorial Material; Early Access},
} 

@ARTICLE{
author={Diaw Sokhna Haissatou,Delcambre Sylvie,Much Christoph,Ott Fabian,Kostic Vladimir S,Gajos Agata,Muenchau Alexander,Zittel Simone,Busch Hauke,Gruenewald Anne,Klein Christine,Lohmann Katja},
year={2024},
title={DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery},
journal={NEUROGENETICS},
volume={25},
number={2},
pages={141-147},
document_type={Article},
} 

@ARTICLE{
author={Milovanovic Andona,Dragasevic-Miskovic Natasa T,Thomsen Mirja,Borsche Max,Hinrichs Frauke,Westenberger Ana,Klein Christine,Brueggemann Norbert,Brankovic Marija,Marjanovic Ana,Svetel Marina V,Kostic Vladimir S,Lohmann Katja},
year={2024},
title={<i>RFC1 </i>and <i>FGF14</i> Repeat Expansions in Serbian Patients with Cerebellar Ataxia},
journal={MOVEMENT DISORDERS CLINICAL PRACTICE},
volume={11},
number={6},
pages={626-633},
document_type={Article},
} 

@ARTICLE{
author={Rueda Maria Paulina Castelo,Raftopoulou Athina,Goegele Martin,Borsche Max,Emmert David B,Fuchsberger Christian,Hantikainen Essi M,Vukovic Vladimir R,Klein Christine,Pramstaller Peter P,Pichler Irene,Hicks Andrew A},
year={2021},
title={Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort},
journal={FRONTIERS IN NEUROLOGY},
volume={12},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Baumann Hauke,Ott Fabian,Weber Joachim,Trilck-Winkler Michaela,Munchau Alexander,Zittel Simone,Kostic Vladimir S,Kaiser Frank J,Klein Christine,Busch Hauke,Seibler Philip,Lohmann Katja},
year={2021},
title={Linking Penetrance and Transcription in DYT-THAP1: Insights From a Human iPSC-Derived Cortical Model},
journal={MOVEMENT DISORDERS},
volume={36},
number={6},
pages={1381-1391},
document_type={Article},
} 

@ARTICLE{
author={Baumann Hauke,Trilck-Winkler Michaela,Grosse M,Munchau Alexander,Kostic Vladimir S,Klein Christine,Kaiser Frank J,Seibler Philip,Lohmann Katja},
year={2019},
title={Gene expression analysis in cortical neurons differentiated from 32 induced pluripotent stem cell (iPSC) lines of THAP1 mutation carriers and controls},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={1430-1430},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Baumann H,Trilck M,Jahn M,Muenchau A,Kostic Vladimir S,Klein Christine,Seibler P,Lohmann Katja},
year={2019},
title={Generation and in-depth characterization of 20 induced pluripotent stem cell (iPSC) lines from 10 dystonia patients and healthy carriers of THAP1 mutations},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={27},
number={},
pages={314-314},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kulikovskaja Leonora,Sarajlija Adrijan,Savic-Pavicevic Dusanka Lj,Dobricic Valerija S,Klein Christine,Westenberger Ana},
year={2018},
title={WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype},
journal={NEUROLOGY-GENETICS},
volume={4},
number={2},
pages={-},
document_type={Editorial Material},
} 

@ARTICLE{
author={Dobricic Valerija S,Tomic Aleksandra D,Brankovic Vesna,Kresojevic Nikola D,Jankovic Milena Z,Westenberger Ana,Milic-Rasic Vedrana M,Klein Christine,Novakovic Ivana V,Svetel Marina V,Kostic Vladimir S},
year={2017},
title={GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia},
journal={PARKINSONISM & RELATED DISORDERS},
volume={45},
number={},
pages={81-84},
document_type={Article},
} 

@ARTICLE{
author={Klein Christine,Lang Anthony E,van de Warrenburg Bart P,Sue Carolyn M,Tabrizi Sarah J,Bertram Lars,Mercimek-Mahmutoglu Saadet,Ebrahimi-Fakhari Darius,Warner Thomas T,Durr Alexandra,Assmann Birgit,Kostic Vladimir K,Lohmann Katja,Marras Connie},
year={2016},
title={Reply Letter to Jinnah "Locus Pocus" and Albanese "Complex Dystonia Is Not a Category in the New 2013 Consensus Classification": Necessary Evolution, No Magic!},
journal={MOVEMENT DISORDERS},
volume={31},
number={11},
pages={1760-1762},
document_type={Letter},
} 

@ARTICLE{
author={Marras Connie,Lang Anthony E,van de Warrenburg Bart P,Sue Carolyn M,Tabrizi Sarah J,Bertram Lars,Mercimek-Mahmutoglu Saadet,Ebrahimi-Fakhari Darius,Warner Thomas T,Durr Alexandra,Assmann Birgit,Lohmann Katja,Kostic Vladimir K,Klein Christine},
year={2016},
title={Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force},
journal={MOVEMENT DISORDERS},
volume={31},
number={4},
pages={436-457},
document_type={Review},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir S},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={PARKINSONISM & RELATED DISORDERS},
volume={21},
number={7},
pages={804-807},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Jankovic Milena Z,Petrovic Igor N,Kumar Kishore R,Dragasevic Natasa T,Dobricic Valerija S,Novakovic Ivana V,Svetel Marina V,Klein Christine,Pekmezovic Tatjana D,Kostic Vladimir K},
year={2015},
title={Presenting symptoms of GBA-related Parkinson's disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={22},
number={},
pages={437-437},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Ziegan Julia,Wittstock Matthias,Westenberger Ana,Dobricic Valerija S,Wolters Alexander,Benecke Reiner,Klein Christine,Kamm Christoph},
year={2014},
title={Novel GNAL Mutations in Two German Patients With Sporadic Dystonia},
journal={MOVEMENT DISORDERS},
volume={29},
number={14},
pages={1833-1834},
document_type={Letter},
} 

@ARTICLE{
author={Dobricic Valerija S,Kresojevic Nikola D,Westenberger Ana,Svetel Marina V,Tomic Aleksandra D,Ralic Vesna,Petrovic Igor N,Jecmenica-Lukic Milica V,Lohmann Katja,Novakovic Ivana V,Klein Christine,Kostic Vladimir S},
year={2014},
title={De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient},
journal={MOVEMENT DISORDERS},
volume={29},
number={9},
pages={1190-1193},
document_type={Article},
} 

@ARTICLE{
author={Agosta Federica,Kostic Vladimir S,Davidovic Kristina,Kresojevic Nikola D,Sarro Lidia,Svetel Marina V,Stankovic Iva D,Comi G,Klein Christine,Filippi Massimo},
year={2013},
title={White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations},
journal={MOVEMENT DISORDERS},
volume={28},
number={6},
pages={772-778},
document_type={Article},
} 

@ARTICLE{
author={Kresojevic Nikola D,Mijajlovic Milija D,Peric Stojan Z,Pavlovic Aleksandra M,Svetel Marina V,Jankovic Milena Z,Dobricic Valerija S,Novakovic Ivana V,Lakocevic Milan B,Klein Christine,Kostic Vladimir S},
year={2013},
title={Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations},
journal={PARKINSONISM & RELATED DISORDERS},
volume={19},
number={4},
pages={431-435},
document_type={Article},
} 

@ARTICLE{
author={Kumar Kishore R,Ramirez A,Goebel A,Kresojevic Nikola D,Svetel Marina V,Lohmann Katja,Sue Carolyn M,Rolfs A,Mazzulli JR,Alcalay RN,Krainc D,Klein Christine,Kostic Vladimir S,Gruenewald Alina},
year={2013},
title={Glucocerebrosidase mutations in a Serbian Parkinson's disease population},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={20},
number={2},
pages={402-405},
document_type={Article},
} 

@ARTICLE{
author={Schmitt Ina,Wuellner Ullrich,van Rooyen Jan Pierre,Khazneh Hassan,Becker Julian,Volk Alexander,Kubisch Christian,Becker Tim,Kostic Vladimir S,Klein Christine,Ramirez Alfredo},
year={2012},
title={Variants in the 3 ' UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={20},
number={12},
pages={1265-1269},
document_type={Article},
} 

@ARTICLE{
author={Kumar Kishore R,Weissbach Anne,Heldmann Marcus,Kasten Meike,Tunc Sinem,Sue Carolyn M,Svetel Marina V,Kostic Vladimir S,Segura-Aguilar Juan,Ramirez Alfredo,Simon David K,Vieregge Peter,Muente Thomas F,Hagenah Johann M,Klein Christine,Lohmann Katja},
year={2012},
title={Frequency of the D620N Mutation in VPS35 in Parkinson Disease},
journal={ARCHIVES OF NEUROLOGY},
volume={69},
number={10},
pages={1360-1364},
document_type={Article},
} 

@ARTICLE{
author={Kostic Vladimir S,Jecmenica-Lukic Milica V,Novakovic Ivana V,Dobricic Valerija S,Brajkovic Lela,Krajinovic Maja,Klein Christine,Pavlovic Aleksandra M},
year={2011},
title={Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification},
journal={JOURNAL OF NEUROLOGY},
volume={258},
number={9},
pages={1637-1642},
document_type={Article},
} 

@ARTICLE{
author={Facheris Maurizio F,Hicks Andrew A,Minelli Cosetta,Hagenah Johann M,Kostic Vladimir S,Campbell Susan,Hayward Caroline,Volpato Claudia B,Pattaro Cristian,Vitart Veronique,Wright Alan,Campbell Harry,Klein Christine,Pramstaller Peter P},
year={2011},
title={Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson's Disease},
journal={JOURNAL OF MOLECULAR NEUROSCIENCE},
volume={43},
number={3},
pages={246-250},
document_type={Article},
} 

@ARTICLE{
author={Weissbach Anne,Djarmati Ana,Klein Christine,Dragasevic Natasa T,Zuehlke Christine,Rakovic Aleksandar,Guzvic Miodrag,Butz Elisabeth,Toennies Holger,Siebert Reiner,Petrovic Igor N,Svetel Marina V,Kostic Vladimir S,Lohmann Katja},
year={2010},
title={Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15},
journal={MOVEMENT DISORDERS},
volume={25},
number={11},
pages={1577-1582},
document_type={Article},
} 

@ARTICLE{
author={Svetel Marina V,Ozelius LJ,Buckley Amber,Lohmann Katja,Brajkovic Lela,Klein Christine,Kostic Vladimir S},
year={2010},
title={Rapid-onset dystonia-parkinsonism: case report},
journal={JOURNAL OF NEUROLOGY},
volume={257},
number={3},
pages={472-474},
document_type={Letter},
} 

@ARTICLE{
author={Berisavac Iva I,Svetel Marina V,Djuric Gordana M,Bogosavljevic Visnja,Klein Christine,Illarioshkin SN},
year={2009},
title={Dystonia plus syndromes},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={285},
number={},
pages={S296-S296},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djarmati Ana,Hagenah Johann M,Reetz Kathrin,Winkler Susen,Behrens Maria Isabel,Pawlack Heike,Lohmann Katja,Ramirez Alfredo,Tadic Vera,Brueggemann Norbert,Berg Daniela,Siebner Hartwig R,Lang Anthony E,Pramstaller Peter P,Binkofski Ferdinand,Kostic Vladimir S,Volkmann Jens,Gasser Thomas,Klein Christine},
year={2009},
title={ATP13A2 Variants in Early-Onset Parkinson's Disease Patients and Controls},
journal={MOVEMENT DISORDERS},
volume={24},
number={14},
pages={2104-2111},
document_type={Article},
} 

@ARTICLE{
author={Zschiedrich Katja,Koenig Inke R,Bruggemann Norbert,Kock Norman,Kasten Meike,Leenders Klaus L,Kostic Vladimir S,Vieregge Peter,Ziegler Andreas,Klein Christine,Lohmann Katja},
year={2009},
title={MDR1 variants and risk of Parkinson disease},
journal={JOURNAL OF NEUROLOGY},
volume={256},
number={1},
pages={115-120},
document_type={Article},
} 

@ARTICLE{
author={Rakovic Aleksandar,Stiller Barbara,Djarmati Ana,Flaquer Antonia,Freudenberg Jan,Toliat Mohammad-Reza,Linnebank Michael,Kostic Vladimir S,Lohmann Katja,Paus Sebastian,Nuernberg Peter,Kubisch Christian,Klein Christine,Wuellner Ullrich,Ramirez Alfredo},
year={2009},
title={Genetic Association Study of the P-Type ATPase ATP13A2 in Late-Onset Parkinson's Disease},
journal={MOVEMENT DISORDERS},
volume={24},
number={3},
pages={429-433},
document_type={Article},
} 

@ARTICLE{
author={Cerovac Natasa M,Petrovic Igor N,Klein Christine,Kostic Vladimir S},
year={2007},
title={Delayed-onset dystonia due to perinatal asphyxia: A prospective study},
journal={MOVEMENT DISORDERS},
volume={22},
number={16},
pages={2426-2429},
document_type={Article},
} 

@ARTICLE{
author={Djarmati Ana,Dobricic Valerija S,Kecmanovic Miljana,Marsh P,Jancic-Stefanovic Jasna B,Klein Christine,Djuric Milena Lj,Romac Stanka P},
year={2007},
title={MECP2 mutations in Serbian Rett syndrome patients},
journal={ACTA NEUROLOGICA SCANDINAVICA},
volume={116},
number={6},
pages={413-419},
document_type={Editorial Material},
} 

@ARTICLE{
author={Winkler Susan,Hagenah Johann M,Lincoln S,Heckman M,Haugarvoll K,Lohmann-Hedrich Katja,Kostic Vladimir S,Farrer M,Klein Christine},
year={2007},
title={alpha-Synuclein and Parkinson disease susceptibility},
journal={NEUROLOGY},
volume={69},
number={18},
pages={1745-1750},
document_type={Article},
} 

@ARTICLE{
author={Winkler Susan,Koenig Inke R,Lohmann-Hedrich Katja,Vieregge Peter,Kostic Vladimir S,Klein Christine},
year={2007},
title={Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={15},
number={11},
pages={1163-1168},
document_type={Article},
} 

@ARTICLE{
author={Djarmati Ana,Guzvic Miodrag,Gruenewald Anne,Lang Anthony E,Pramstaller Peter P,Simon David K,Kaindl Angela M,Vieregge Peter,Nygren Anders OH,Beetz Christian,Hedrich Katja,Klein Christine},
year={2007},
title={Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification},
journal={MOVEMENT DISORDERS},
volume={22},
number={12},
pages={1708-1714},
document_type={Article},
} 

@ARTICLE{
author={Kostic Vladimir S,Svetel Marina V,Kabakci Kemal,Ristic Aleksandar J,Petrovic Igor N,Schule B,Kock Norman,Djarmati Ana,Romac Stanka P,Klein Christine},
year={2006},
title={Intrafamilial phenotypic and genetic heterogeneity of dystonia},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={250},
number={1-2},
pages={92-96},
document_type={Article},
} 

@ARTICLE{
author={Stefanova Elka D,Djarmati Ana,Momcilovic Dragana R,Dragasevic Natasa T,Svetel Marina V,Klein Christine,Kostic Vladimir S},
year={2006},
title={Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation},
journal={MOVEMENT DISORDERS},
volume={21},
number={11},
pages={2010-2015},
document_type={Article},
} 

@ARTICLE{
author={Djarmati Ana,Hedrich Katja,Svetel Marina V,Lohnau T,Schwinger E,Romac Stanka P,Pramstaller Peter P,Kostic Vladimir S,Klein Christine},
year={2006},
title={Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?},
journal={MOVEMENT DISORDERS},
volume={21},
number={9},
pages={1526-1530},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Winkler Susan,Hagenah Johann M,Kabakci Kemal,Kasten Meike,Schwinger E,Volkmann Jens,Pramstaller Peter P,Kostic Vladimir S,Vieregge Peter,Klein Christine},
year={2006},
title={Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease},
journal={MOVEMENT DISORDERS},
volume={21},
number={9},
pages={1506-1510},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Hagenah Johann M,Djarmati Ana,Hiller A,Lohnau T,Lasek K,Grunewald RA,Hilker R,Steinlechner S,Boston H,Kock Norman,Schneider-Gold C,Kress W,Siebner Hartwig R,Binkofski Ferdinand,Lencer R,Munchau A,Klein Christine},
year={2006},
title={Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease  Role of a single hit?},
journal={ARCHIVES OF NEUROLOGY},
volume={63},
number={6},
pages={833-838},
document_type={Article},
} 

@ARTICLE{
author={Dragasevic Natasa T,Culjkovic Biljana,Klein Christine,Ristic Aleksandar J,Keckarevic Milica,Topisirovic Ivan,Vukosavic Slobodanka N,Svetel Marina V,Kock Norman,Stefanova Elka D,Romac Stanka P,Kostic Vladimir S},
year={2006},
title={Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients},
journal={MOVEMENT DISORDERS},
volume={21},
number={2},
pages={187-191},
document_type={Article},
} 

@ARTICLE{
author={Berg Daniela,Niwar M,Maass S,Zimprich A,Moller JC,Wuellner U,Schmitz-Hubsch T,Klein Christine,Tan EK,Schols L,Marsh L,Dawson TM,Janetzky B,Muller T,Woitalla D,Kostic Vladimir S,Pramstaller Peter P,Oertel WH,Bauer P,Krueger R,Gasser Thomas,Riess O},
year={2005},
title={Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients},
journal={MOVEMENT DISORDERS},
volume={20},
number={9},
pages={1191-1194},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Pramstaller Peter P,Stubke K,Hiller A,Kabakci Kemal,Purmann S,Kasten Meike,Scaglione C,Schwinger E,Volkmann J,Kostic Vladimir S,Vieregge Peter,Martinelli P,Abbruzzese G,Klein Christine,Zuhlke C},
year={2005},
title={Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?},
journal={MOVEMENT DISORDERS},
volume={20},
number={8},
pages={1060-1062},
document_type={Article},
} 

@ARTICLE{
author={Klein Christine,Djarmati Ana,Hedrich Katja,Schafer N,Scaglione C,Marchese R,Kock Norman,Schule B,Hiller A,Lohnau T,Winkler Susan,Wiegers K,Hering R,Bauer P,Riess O,Abbruzzese G,Martinelli P,Pramstaller Peter P},
year={2005},
title={PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={13},
number={9},
pages={1086-1093},
document_type={Article},
} 

@ARTICLE{
author={Schule B,Kock Norman,Svetel Marina V,Dragasevic Natasa T,Hedrich Katja,Aguiar PD,Liu L,Kabakci Kemal,Garrels J,Meyer EM,Berisavac Ivana I,Schwinger E,Kramer PL,Ozelius LJ,Klein Christine,Kostic Vladimir S},
year={2004},
title={Genetic heterogeneity in ten families with myoclonus-dystonia},
journal={JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY},
volume={75},
number={8},
pages={1181-1185},
document_type={Article},
} 

@ARTICLE{
author={Berisavac Iva I,Klein Christine,Svetel Marina V,Ristic Aleksandar J,Kostic Vladimir S},
year={2004},
title={Myoclonus dystonia (MD) in Serbian population - clinical and genetic analysis},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={11},
number={},
pages={246-247},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kabakci Kemal,Hedrich Katja,Leung JC,Mitterer M,Vieregge Peter,Lencer R,Hagenah Johann M,Garrels J,Witt K,Klostermann F,Svetel Marina V,Friedman J,Kostic Vladimir S,Bressman SB,Breakefield XO,Ozelius LJ,Pramstaller Peter P,Klein Christine},
year={2004},
title={Mutations in DYT1 - Extension of the phenotypic and mutational spectrum},
journal={NEUROLOGY},
volume={62},
number={3},
pages={395-400},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Djarmati Ana,Schafer N,Hering R,Wellenbrock C,Weiss PH,Hilker R,Vieregge Peter,Ozelius LJ,Heutink P,Bonifati V,Schwinger E,Lang Anthony E,Noth J,Bressman SB,Pramstaller Peter P,Riess O,Klein Christine},
year={2004},
title={DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease},
journal={NEUROLOGY},
volume={62},
number={3},
pages={389-394},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Schafer N,Hering R,Hagenah Johann M,Lanthaler AJ,Schwinger E,Kramer PL,Ozelius LJ,Bressman SB,Abbruzzese G,Martinelli P,Kostic Vladimir S,Pramstaller Peter P,Vieregge Peter,Riess O,Klein Christine},
year={2004},
title={The R98Q variation in DJ-1 represents a rare polymorphism},
journal={ANNALS OF NEUROLOGY},
volume={55},
number={1},
pages={145-145},
document_type={Letter},
} 

@ARTICLE{
author={Muller B,Hedrich Katja,Kock Norman,Dragasevic Natasa T,Svetel Marina V,Garrels J,Landt O,Nitschke M,Pramstaller Peter P,Reik W,Schwinger E,Sperner J,Ozelius LJ,Kostic Vladimir S,Klein Christine},
year={2002},
title={Evidence that paternal expression of the epsilon-Sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={71},
number={6},
pages={1303-1311},
document_type={Article},
} 

@ARTICLE{
author={Kock Norman,Muller B,Vieregge Peter,Pramstaller Peter P,Marder K,Abbruzzese G,Martinelli P,Lang Anthony E,Jacobs H,Hagenah Johann M,Harris J,Meija-Santana H,Fahn S,Hedrich Katja,Kann M,Gehlken U,Culjkovic Biljana,Schwinger E,Wszolek ZK,Zuhlke C,Klein Christine},
year={2002},
title={Role of SC42 mutations in early- and late-onset dopa-responsive parkinsonism},
journal={ANNALS OF NEUROLOGY},
volume={52},
number={2},
pages={257-258},
document_type={Letter},
} 

@ARTICLE{
author={Kock Norman,Culjkovic Biljana,Maniak S,Schilling Klaus,Muller B,Zuhlke C,Ozelius L,Klein Christine,Pramstaller Peter P,Kramer PL},
year={2002},
title={Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={71},
number={1},
pages={A205-208},
document_type={Letter},
}