@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={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={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={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},
}