document.write("<div class='record'>");
document.write("  <div class='authors'>Dzinovic,\&nbsp;I.\&nbsp;; Serranová,\&nbsp;T.*\&nbsp;; Prouteau,\&nbsp;C.*\&nbsp;; Colin,\&nbsp;E.*\&nbsp;; Ziegler,\&nbsp;A.*\&nbsp;; Winkelmann,\&nbsp;J.\&nbsp;; Jech,\&nbsp;R.*\&nbsp;; Zech,\&nbsp;M.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61438&la=de'>Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant.</a></div>");
document.write("  <div class='source'>Neurogenetics 22, 137-141 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Dzinovic,\&nbsp;I.\&nbsp;; Serranová,\&nbsp;T.*\&nbsp;; Prouteau,\&nbsp;C.*\&nbsp;; Colin,\&nbsp;E.*\&nbsp;; Ziegler,\&nbsp;A.*\&nbsp;; Winkelmann,\&nbsp;J.\&nbsp;; Jech,\&nbsp;R.*\&nbsp;; Zech,\&nbsp;M.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63725&la=de'>Correction to: Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant.</a></div>");
document.write("  <div class='source'>Neurogenetics, DOI: 10.1007/s10048-021-00641-w (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Amprosi,\&nbsp;M.*\&nbsp;; Zech,\&nbsp;M.\&nbsp;; Steiger,\&nbsp;R.*\&nbsp;; Nachbauer,\&nbsp;W.*\&nbsp;; Eigentler,\&nbsp;A.*\&nbsp;; Gizewski,\&nbsp;E.R.*\&nbsp;; Guger,\&nbsp;M.*\&nbsp;; Indelicato,\&nbsp;E.*\&nbsp;; Boesch,\&nbsp;S.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=59973&la=de'>Familial writer\'s cramp: A clinical clue for inherited coenzyme Q\<sub\>10\</sub\> deficiency.</a></div>");
document.write("  <div class='source'>Neurogenetics 22, 81–86 (2020)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Spiegler,\&nbsp;S.*\&nbsp;; Rath,\&nbsp;M.*\&nbsp;; Hoffjan,\&nbsp;S.*\&nbsp;; Dammann,\&nbsp;P.*\&nbsp;; Sure,\&nbsp;U.*\&nbsp;; Pagenstecher,\&nbsp;A.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Felbor,\&nbsp;U.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52500&la=de'>First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencing.</a></div>");
document.write("  <div class='source'>Neurogenetics 19, 55–59 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Carecchio,\&nbsp;M.*\&nbsp;; Picillo,\&nbsp;M.*\&nbsp;; Valletta,\&nbsp;L.*\&nbsp;; Elia,\&nbsp;A.E.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Cozzolino,\&nbsp;A.*\&nbsp;; Vitale,\&nbsp;A.*\&nbsp;; Garavaglia,\&nbsp;B.*\&nbsp;; Iuso,\&nbsp;A.\&nbsp;; Bagella,\&nbsp;C.F.*\&nbsp;; Pappatà,\&nbsp;S.*\&nbsp;; Barone,\&nbsp;P.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Romito,\&nbsp;L.*\&nbsp;; Tiranti,\&nbsp;V.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51541&la=de'>Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: A de novo PSEN-1 mutation.</a></div>");
document.write("  <div class='source'>Neurogenetics 18, 175-178 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Glasgow,\&nbsp;R.I.C.*\&nbsp;; Thompson,\&nbsp;K.*\&nbsp;; Barbosa,\&nbsp;I.A.*\&nbsp;; He,\&nbsp;L.*\&nbsp;; Alston,\&nbsp;C.L.*\&nbsp;; Deshpande,\&nbsp;C.*\&nbsp;; Simpson,\&nbsp;M.A.*\&nbsp;; Morris,\&nbsp;A.A.M.*\&nbsp;; Neu,\&nbsp;A.*\&nbsp;; Löbel,\&nbsp;U.*\&nbsp;; Hall,\&nbsp;J.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Haack,\&nbsp;T.B.*\&nbsp;; Hempel,\&nbsp;M.*\&nbsp;; McFarland,\&nbsp;R.*\&nbsp;; Taylor,\&nbsp;R.W.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52264&la=de'>Novel \<em\>GFM2 \</em\>variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits.</a></div>");
document.write("  <div class='source'>Neurogenetics 18, 1-9 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Zech,\&nbsp;M.\&nbsp;; Jech,\&nbsp;R.*\&nbsp;; Wagner,\&nbsp;M.\&nbsp;; Mantel,\&nbsp;T.*\&nbsp;; Boesch,\&nbsp;S.*\&nbsp;; Nocker,\&nbsp;M.*\&nbsp;; Jochim,\&nbsp;A.*\&nbsp;; Berutti,\&nbsp;R.\&nbsp;; Havránková,\&nbsp;P.*\&nbsp;; Fečíková,\&nbsp;A.*\&nbsp;; Kemlink,\&nbsp;D.*\&nbsp;; Roth,\&nbsp;J.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Poewe,\&nbsp;W.*\&nbsp;; Růžička,\&nbsp;E.*\&nbsp;; Haslinger,\&nbsp;B.*\&nbsp;; Winkelmann,\&nbsp;J.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51768&la=de'>Molecular diversity of combined and complex dystonia: Insights from diagnostic exome sequencing.</a></div>");
document.write("  <div class='source'>Neurogenetics 18, 195–205 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Baertling,\&nbsp;F.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Rodenburg,\&nbsp;R.J.*\&nbsp;; Schaper,\&nbsp;J.*\&nbsp;; Seibt,\&nbsp;A.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Mayatepek,\&nbsp;E.*\&nbsp;; Hadzik,\&nbsp;B.*\&nbsp;; Selcan,\&nbsp;G.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Distelmaier,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44015&la=de'>\<em\>MRPS22\</em\> mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities.</a></div>");
document.write("  <div class='source'>Neurogenetics 16, 237-240 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Distelmaier,\&nbsp;F.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Catarino,\&nbsp;C.B.*\&nbsp;; Gallenmüller,\&nbsp;C.*\&nbsp;; Rodenburg,\&nbsp;R.J.T.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Baertling,\&nbsp;F.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Mayatepek,\&nbsp;E.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Klopstock,\&nbsp;T.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44083&la=de'>\<em\>MRPL44\</em\> mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy.</a></div>");
document.write("  <div class='source'>Neurogenetics 16, 319-323 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Schulte,\&nbsp;E.C.\&nbsp;; Ellwanger,\&nbsp;D.C.*\&nbsp;; Dihanich,\&nbsp;S.*\&nbsp;; Manzoni,\&nbsp;C.*\&nbsp;; Stangl,\&nbsp;K.*\&nbsp;; Schormair,\&nbsp;B.\&nbsp;; Graf,\&nbsp;E.\&nbsp;; Eck,\&nbsp;S.\&nbsp;; Mollenhauer,\&nbsp;B.*\&nbsp;; Haubenberger,\&nbsp;D.*\&nbsp;; Pirker,\&nbsp;W.*\&nbsp;; *\&nbsp;; Brücke,\&nbsp;T.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Peters,\&nbsp;A.\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Trenkwalder,\&nbsp;C.*\&nbsp;; Mewes,\&nbsp;H.-W.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Lewis,\&nbsp;P.A.*\&nbsp;; Klünemann,\&nbsp;H.H.*\&nbsp;; Winkelmann,\&nbsp;J.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=28394&la=de'>Rare variants in \<em\>LRRK1\</em\> and Parkinson\&#39;s disease.</a></div>");
document.write("  <div class='source'>Neurogenetics 15, 49-57 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Schmied,\&nbsp;M.C.*\&nbsp;; Zehetmayer,\&nbsp;S.*\&nbsp;; Reindl,\&nbsp;M.*\&nbsp;; Ehling,\&nbsp;R.*\&nbsp;; Bajer-Kornek,\&nbsp;B.*\&nbsp;; Leutmezer,\&nbsp;F.*\&nbsp;; Zebenholzer,\&nbsp;K.*\&nbsp;; Hotzy,\&nbsp;C.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Huber,\&nbsp;K.*\&nbsp;; Khalil,\&nbsp;M.*\&nbsp;; Fuchs,\&nbsp;S.*\&nbsp;; Schmidt,\&nbsp;H.*\&nbsp;; Auff,\&nbsp;E.*\&nbsp;; Kristoferitsch,\&nbsp;W.*\&nbsp;; Fazekas,\&nbsp;F.*\&nbsp;; Berger,\&nbsp;T.*\&nbsp;; Vass,\&nbsp;K.*\&nbsp;; *</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8018&la=de'>Replication study of Multiple Sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.</a></div>");
document.write("  <div class='source'>Neurogenetics 13, 181-187 (2012)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Schulte,\&nbsp;E.C.\&nbsp;; Mollenhauer,\&nbsp;B.*\&nbsp;; *\&nbsp;; Bereznai,\&nbsp;B.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Haubenberger,\&nbsp;D.*\&nbsp;; Pirker,\&nbsp;W.*\&nbsp;; Brücke,\&nbsp;T.*\&nbsp;; Molnar,\&nbsp;M.J.*\&nbsp;; Peters,\&nbsp;A.\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Trenkwalder,\&nbsp;C.*\&nbsp;; Winkelmann,\&nbsp;J.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8573&la=de'>Variants in \<em\>eukaryotic translation initiation factor 4G1\</em\> in sporadic Parkinson\&#39;s disease.</a></div>");
document.write("  <div class='source'>Neurogenetics 13, 281-285 (2012)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Soehn,\&nbsp;A.S.*\&nbsp;; Franck,\&nbsp;T.*\&nbsp;; Biskup,\&nbsp;S.*\&nbsp;; Giaime,\&nbsp;E.*\&nbsp;; Melle,C.*\&nbsp;; Rott,\&nbsp;R.*\&nbsp;; Cebo,\&nbsp;D.*\&nbsp;; Kalbacher,\&nbsp;H.*\&nbsp;; Ott,\&nbsp;E.*\&nbsp;; Pahnke,\&nbsp;J.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Kruger,\&nbsp;R.*\&nbsp;; Gasser,\&nbsp;T.*\&nbsp;; Berg,\&nbsp;D.*\&nbsp;; von Eggeling,\&nbsp;F.*\&nbsp;; Engelender,\&nbsp;S.*\&nbsp;; da Costa,\&nbsp;C.A.*\&nbsp;; Riess,\&nbsp;O.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1601&la=de'>Periphilin is a novel interactor of synphilin-1, a protein implicated in Parkinson\&#39;s disease.</a></div>");
document.write("  <div class='source'>Neurogenetics 11, 203-215 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Stogmann,\&nbsp;E.*\&nbsp;; El Tawil,\&nbsp;S.*\&nbsp;; Wagenstaller,\&nbsp;J.\&nbsp;; Gaber,\&nbsp;A.*\&nbsp;; Edris,\&nbsp;S.*\&nbsp;; Abdelhady,\&nbsp;A.*\&nbsp;; Assem-Hilger,\&nbsp;E.*\&nbsp;; Leutmezer,\&nbsp;F.*\&nbsp;; Bonelli,\&nbsp;S.*\&nbsp;; Baumgartner,\&nbsp;C.*\&nbsp;; Zimprich,\&nbsp;F.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Zimpel,\&nbsp;A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3528&la=de'>A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.</a></div>");
document.write("  <div class='source'>Neurogenetics 10, 73-77 (2009)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kemlink,\&nbsp;D.\&nbsp;; Plazzi,\&nbsp;G.*\&nbsp;; Vetrugno,\&nbsp;R.*\&nbsp;; Provini,\&nbsp;F.*\&nbsp;; Polo,\&nbsp;O.*\&nbsp;; Stiasny-Kolster,\&nbsp;K.*\&nbsp;; Oertel,\&nbsp;W.*\&nbsp;; Nevsimalova,\&nbsp;S.*\&nbsp;; Sonka,\&nbsp;K.*\&nbsp;; Högl,\&nbsp;B.*\&nbsp;; Frauscher,\&nbsp;B.*\&nbsp;; Hadjigeorgiou,\&nbsp;G.M.*\&nbsp;; Pramstaller,\&nbsp;P.P.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Müller-Myhsok,\&nbsp;B.*\&nbsp;; Winkelmann,\&nbsp;J.\&nbsp;; Montagna,\&nbsp;P.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=383&la=de'>Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13.</a></div>");
document.write("  <div class='source'>Neurogenetics 9, 75-82 (2008)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Stogmann,\&nbsp;E.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Baumgartner,\&nbsp;C.*\&nbsp;; Schmied,\&nbsp;M.*\&nbsp;; Hotzy,\&nbsp;C.*\&nbsp;; Asmus,\&nbsp;F.*\&nbsp;; Leutmezer,\&nbsp;F.*\&nbsp;; Bonelli,\&nbsp;S.*\&nbsp;; Assem-Hilger,\&nbsp;E.\&nbsp;; Vass,\&nbsp;K.*\&nbsp;; Hatala,\&nbsp;K.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Zimprich,\&nbsp;F.*\&nbsp;; *</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3226&la=de'>Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.</a></div>");
document.write("  <div class='source'>Neurogenetics 7, 265-268 (2006)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Asmus,\&nbsp;F.*\&nbsp;; Schoenian,\&nbsp;S.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Münz,\&nbsp;M.*\&nbsp;; Mayer,\&nbsp;P.*\&nbsp;; Müller-Myhsok,\&nbsp;B.*\&nbsp;; *\&nbsp;; Remschmidt,\&nbsp;H.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; Bandmann,\&nbsp;O.*\&nbsp;; Gasser,\&nbsp;T.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23508&la=de'>Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome.</a></div>");
document.write("  <div class='source'>Neurogenetics 6, 55-56 (2005)</div>");
document.write("</div>");