@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={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={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={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={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={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,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={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},
}