@ARTICLE{
author={Vukovic Vladimir R,Hantikainen Essi M,Raftopoulou Athina,Gogele Martin,Rainer Johannes,Domingues Francisco S,Pramstaller Peter P,Garcia-Larsen Vanessa,Pattaro Cristian},
year={2023},
title={Association of dietary proteins with serum creatinine and estimated glomerular filtration rate in a general population sample: the CHRIS study},
journal={JOURNAL OF NEPHROLOGY},
volume={36},
number={1},
pages={103-114},
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={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={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={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={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={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},
}