@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={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={Lohmann Katja,...,Dobricic Valerija S,...,Savic-Pavicevic Dusanka Lj,...,(broj koautora 18)},
year={2017},
title={Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans},
journal={HUMAN MOLECULAR GENETICS},
volume={26},
number={6},
pages={1078-1086},
document_type={Article},
} 

@ARTICLE{
author={Dragasevic-Miskovic Natasa T,Domingo Aloysius,Dobricic Valerija S,Max Christoph,Braenne Ingrid,Petrovic Igor N,Grutz Karen,Pawlack Heike,Tournev Ivailo,Kalaydjieva Luba,Svetel Marina V,Lohmann Katja,Kostic Vladimir S,Westenberger Ana},
year={2016},
title={Seemingly Dominant Inheritance of a Recessive ANO10 Mutation in Romani Families With Cerebellar Ataxia},
journal={MOVEMENT DISORDERS},
volume={31},
number={12},
pages={1929-1931},
document_type={Letter},
} 

@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={Lohmann Katja,Schlicht Felix,Svetel Marina V,...,Kostic Vladimir S,...,(broj koautora 23)},
year={2016},
title={The role of mutations in COL6A3 in isolated dystonia},
journal={JOURNAL OF NEUROLOGY},
volume={263},
number={4},
pages={730-734},
document_type={Article},
} 

@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={Lohmann Katja,...,Kostic Vladimir S,...,Svetel Marina V,...,(broj koautora 40)},
year={2014},
title={Genome-Wide Association Study in Musician's Dystonia: A Risk Variant at the Arylsulfatase G Locus?},
journal={MOVEMENT DISORDERS},
volume={29},
number={7},
pages={921-927},
document_type={Article},
} 

@ARTICLE{
author={Lohmann Katja,...,Kostic Vladimir S,...,(broj koautora 29)},
year={2013},
title={Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene},
journal={ANNALS OF NEUROLOGY},
volume={73},
number={4},
pages={537-545},
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={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={Lohmann Katja,...,Svetel Marina V,...,Kostic Vladimir S,...,(broj koautora 24)},
year={2012},
title={Identification and functional analysis of novel THAP1 mutations},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={20},
number={2},
pages={171-175},
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={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},
}