document.write("<div class='record'>");
document.write("  <div class='authors'>Chatzinakos,\&nbsp;C.*\&nbsp;; Lee,\&nbsp;D.*\&nbsp;; Cai,\&nbsp;N.\&nbsp;; Vladimirov,\&nbsp;V.I.*\&nbsp;; Webb,\&nbsp;B.T.*\&nbsp;; Riley,\&nbsp;B.P.*\&nbsp;; Flint,\&nbsp;J.*\&nbsp;; Kendler,\&nbsp;K.S.*\&nbsp;; Ressler,\&nbsp;K.J.*\&nbsp;; Daskalakis,\&nbsp;N.P.*\&nbsp;; Bacanu,\&nbsp;S.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61306&la=en'>Increasing the resolution and precision of psychiatric genome-wide association studies by re-imputing summary statistics using a large, diverse reference panel.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 196, 16-27 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Chatzinakos,\&nbsp;C.*\&nbsp;; Georgiadis,\&nbsp;F.*\&nbsp;; Lee,\&nbsp;D.*\&nbsp;; Cai,\&nbsp;N.\&nbsp;; Vladimirov,\&nbsp;V.I.*\&nbsp;; Docherty,\&nbsp;A.*\&nbsp;; Webb,\&nbsp;B.T.*\&nbsp;; Riley,\&nbsp;B.P.*\&nbsp;; Flint,\&nbsp;J.*\&nbsp;; Kendler,\&nbsp;K.S.*\&nbsp;; Daskalakis,\&nbsp;N.P.*\&nbsp;; Bacanu,\&nbsp;S.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60140&la=en'>TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 183, 454-463 (2020)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kurth,\&nbsp;I.*\&nbsp;; Baumgartner,\&nbsp;M.*\&nbsp;; Schabhüttl,\&nbsp;M.*\&nbsp;; Tomni,\&nbsp;C.*\&nbsp;; Windhager,\&nbsp;R.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Gremel,\&nbsp;K.*\&nbsp;; Auer-Grumbach,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48616&la=en'>Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 171, 875-878 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Mooney,\&nbsp;M.A.*\&nbsp;; McWeeney,\&nbsp;S.K.*\&nbsp;; Faraone,\&nbsp;S.V.*\&nbsp;; Hinney,\&nbsp;A.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; IMAGE2 Consortium*\&nbsp;; German ADHD GWAS Group*\&nbsp;; Nigg,\&nbsp;J.T.*\&nbsp;; Wilmot,\&nbsp;B.*\&nbsp;; EUMODIC Consortium (Wichmann,\&nbsp;H.-E.)</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=49554&la=en'>Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 171, 815-826 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Pappa,\&nbsp;I.*\&nbsp;; St Pourcain,\&nbsp;B.*\&nbsp;; Benke,\&nbsp;K.*\&nbsp;; Cavadino,\&nbsp;A.*\&nbsp;; Hakulinen,\&nbsp;C.*\&nbsp;; Nivard,\&nbsp;M.G.*\&nbsp;; Nolte,\&nbsp;I.M.*\&nbsp;; Tiesler,\&nbsp;C.M.\&nbsp;; Bakermans-Kranenburg,\&nbsp;M.J.*\&nbsp;; Davies,\&nbsp;G.E.*\&nbsp;; Evans,\&nbsp;D.M*\&nbsp;; Geoffroy,\&nbsp;M.C.*\&nbsp;; Grallert,\&nbsp;H.\&nbsp;; Groen-Blokhuis,\&nbsp;M.M.*\&nbsp;; Hudziak,\&nbsp;J.J.*\&nbsp;; Kemp,\&nbsp;J.P.*\&nbsp;; Keltikangas-Järvinen,\&nbsp;L.*\&nbsp;; McMahon,\&nbsp;G.*\&nbsp;; Mileva-Seitz,\&nbsp;V.R.*\&nbsp;; Motazedi,\&nbsp;E.*\&nbsp;; Power,\&nbsp;C.*\&nbsp;; Raitakari,\&nbsp;O.T.*\&nbsp;; Ring,\&nbsp;S.M.*\&nbsp;; Rivadeneira,\&nbsp;F.*\&nbsp;; Rodriguez,\&nbsp;A.*\&nbsp;; Scheet,\&nbsp;P.A.*\&nbsp;; Seppälä,\&nbsp;I.*\&nbsp;; Snieder,\&nbsp;H.*\&nbsp;; Standl,\&nbsp;M.\&nbsp;; Thiering,\&nbsp;E.\&nbsp;; Timpson,\&nbsp;N.J.*\&nbsp;; Veenstra,\&nbsp;R.*\&nbsp;; Velders,\&nbsp;F.P.*\&nbsp;; Whitehouse,\&nbsp;A.J.*\&nbsp;; Smith,\&nbsp;G.D.*\&nbsp;; Heinrich,\&nbsp;J.\&nbsp;; Hyppönen,\&nbsp;E.*\&nbsp;; Lehtimäki,\&nbsp;T.*\&nbsp;; Middeldorp,\&nbsp;C.M.*\&nbsp;; Oldehinkel,\&nbsp;A.J.*\&nbsp;; Pennell,\&nbsp;C.E.*\&nbsp;; Boomsma,\&nbsp;D.I.*\&nbsp;; Tiemeier,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=45347&la=en'>A genome-wide approach to children\&#39;s aggressive behavior: The EAGLE consortium.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 171, 562-572 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Hinney,\&nbsp;A.*\&nbsp;; Albayrak,\&nbsp;Ö.*\&nbsp;; Antel,\&nbsp;J.*\&nbsp;; Volckmar,\&nbsp;A.L.*\&nbsp;; Sims,\&nbsp;R.*\&nbsp;; Chapman,\&nbsp;J.*\&nbsp;; Harold,\&nbsp;D.*\&nbsp;; Gerrish,\&nbsp;A.*\&nbsp;; Heid,\&nbsp;I.M.*\&nbsp;; Winkler,\&nbsp;T.W.*\&nbsp;; Scherag,\&nbsp;A.*\&nbsp;; Wiltfang,\&nbsp;J.*\&nbsp;; Williams,\&nbsp;J.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; GERAD Consortium (*)\&nbsp;; IGAP Consortium (*)\&nbsp;; GIANT Consortium (Albrecht,\&nbsp;E. ; Gieger,\&nbsp;C. ; Grallert,\&nbsp;H. ; Heid,\&nbsp;I.M. ; Illig,\&nbsp;T. ; Müller-Nurasyid,\&nbsp;M. ; Peters,\&nbsp;A. ; Thorand,\&nbsp;B. ; Wichmann,\&nbsp;H.-E.)</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31790&la=en'>Genetic variation at the \<em\>CELF1\</em\> (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer\&#39;s disease and obesity.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 165, 283-293 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Albayrak,\&nbsp;Ö.*\&nbsp;; Pütter,\&nbsp;C.*\&nbsp;; Volckmar,\&nbsp;A.L.*\&nbsp;; Cichon,\&nbsp;S.*\&nbsp;; Hoffmann,\&nbsp;P.*\&nbsp;; Nöthen,\&nbsp;M.M.*\&nbsp;; Jöckel,\&nbsp;K.-H.*\&nbsp;; Schreiber,\&nbsp;S.*\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Faraone,\&nbsp;S.V.*\&nbsp;; Neale,\&nbsp;B.M.*\&nbsp;; Herpertz-Dahlmann,\&nbsp;B.*\&nbsp;; Lehmkuhl,\&nbsp;G.*\&nbsp;; Sinzig,\&nbsp;J.*\&nbsp;; Renner,\&nbsp;T.J.*\&nbsp;; Romanos,\&nbsp;M.*\&nbsp;; Warnke,\&nbsp;A.*\&nbsp;; Lesch,\&nbsp;K.P.*\&nbsp;; Reif,\&nbsp;A.*\&nbsp;; Schimmelmann,\&nbsp;B.G.*\&nbsp;; Scherag,\&nbsp;A.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; Hinney,\&nbsp;A.*\&nbsp;; Psychiatric GWAS Consortium ADHD Subgroup (*)</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25148&la=en'>Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 162, 295-305 (2013)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Byrne,\&nbsp;E.M.*\&nbsp;; Gehrman,\&nbsp;P.R.*\&nbsp;; Medland,\&nbsp;S.E.*\&nbsp;; Nyholt,\&nbsp;D.R.*\&nbsp;; Heath,\&nbsp;A.C.*\&nbsp;; Madden,\&nbsp;P.A.*\&nbsp;; Hickie,\&nbsp;I.B.*\&nbsp;; van Duijn,\&nbsp;C.M.*\&nbsp;; Henders,\&nbsp;A.K.*\&nbsp;; Montgomery,\&nbsp;G.W.*\&nbsp;; Martin,\&nbsp;N.G.*\&nbsp;; Wray,\&nbsp;N.R.*\&nbsp;; Chronogen Consortium (Meitinger,\&nbsp;T. ; Wichmann,\&nbsp;H.-E.)</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=30727&la=en'>A genome-wide association study of sleep habits and insomnia.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 162B, 439-451 (2013)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Hinney,\&nbsp;A.*\&nbsp;; Scherag,\&nbsp;A.*\&nbsp;; Jarick,\&nbsp;I.*\&nbsp;; Albayrak,\&nbsp;Ö.*\&nbsp;; Pütter,\&nbsp;C.*\&nbsp;; Pechlivanis,\&nbsp;S.*\&nbsp;; Dauvermann,\&nbsp;M.R.*\&nbsp;; Beck,\&nbsp;S.*\&nbsp;; Weber,\&nbsp;H.*\&nbsp;; Scherag,\&nbsp;S.*\&nbsp;; Nguyen,\&nbsp;T.T.*\&nbsp;; Volckmar,\&nbsp;A.L.*\&nbsp;; Knoll,\&nbsp;N.*\&nbsp;; Faraone,\&nbsp;S.V.*\&nbsp;; Neale,\&nbsp;B.M.*\&nbsp;; Franke,\&nbsp;B.*\&nbsp;; Cichon,\&nbsp;S.*\&nbsp;; Hoffmann,\&nbsp;P.*\&nbsp;; Nöthen,\&nbsp;M.M.*\&nbsp;; Schreiber,\&nbsp;S.*\&nbsp;; Jöckel,\&nbsp;K.-H.*\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Freitag,\&nbsp;C.*\&nbsp;; Lempp,\&nbsp;T.*\&nbsp;; Meyer,\&nbsp;J.*\&nbsp;; Gilsbach,\&nbsp;S.*\&nbsp;; Herpertz-Dahlmann,\&nbsp;B.*\&nbsp;; Sinzig,\&nbsp;J.*\&nbsp;; Lehmkuhl,\&nbsp;G.*\&nbsp;; Renner,\&nbsp;T.J.*\&nbsp;; Warnke,\&nbsp;A.*\&nbsp;; Romanos,\&nbsp;M.*\&nbsp;; Lesch,\&nbsp;K.P.*\&nbsp;; Reif,\&nbsp;A.*\&nbsp;; Schimmelmann,\&nbsp;B.G.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; Psychiatric GWAS Consortium ADHD Subgroup (*)</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6813&la=en'>Genome-wide association study in German patients with attention deficit/hyperactivity disorder.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 156B, 888-897 (2011)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Mobascher,\&nbsp;A.*\&nbsp;; Rujescu,\&nbsp;D.*\&nbsp;; Mittelstraß,\&nbsp;K.\&nbsp;; Giegling,\&nbsp;I.*\&nbsp;; Lamina,\&nbsp;C.\&nbsp;; Nitz,\&nbsp;B.\&nbsp;; Brenner,\&nbsp;H.*\&nbsp;; Fehr,\&nbsp;C.*\&nbsp;; Breitling,\&nbsp;L.P.*\&nbsp;; Gallinat,\&nbsp;J.*\&nbsp;; Rothenbacher,\&nbsp;D.*\&nbsp;; Raum,\&nbsp;E.*\&nbsp;; Müller,\&nbsp;H.*\&nbsp;; Ruppert,\&nbsp;A.*\&nbsp;; Hartmann,\&nbsp;A.M.*\&nbsp;; Möller,\&nbsp;H.J.*\&nbsp;; Gal,\&nbsp;A.*\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Dahmen,\&nbsp;N.*\&nbsp;; Winterer,\&nbsp;G.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=3236&la=en'>Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 153B, 684-690 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Winterer,\&nbsp;G.*\&nbsp;; Mittelstraß,\&nbsp;K.\&nbsp;; Giegling,\&nbsp;I.*\&nbsp;; Lamina,\&nbsp;C.\&nbsp;; Fehr,\&nbsp;C.*\&nbsp;; Brenner,\&nbsp;H.*\&nbsp;; Breitling,\&nbsp;L.P.*\&nbsp;; Nitz,\&nbsp;B.\&nbsp;; Raum,\&nbsp;E.*\&nbsp;; Müller,\&nbsp;H.*\&nbsp;; Gallinat,\&nbsp;J.*\&nbsp;; Gal,\&nbsp;A.*\&nbsp;; Heim,\&nbsp;K.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Hartmann,\&nbsp;A.M.*\&nbsp;; Möller,\&nbsp;H.J.*\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Dahmen,\&nbsp;N.*\&nbsp;; Rujescu,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5235&la=en'>Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 158B, 1448-1458 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Jamra,\&nbsp;R.A.*\&nbsp;; Klein,\&nbsp;K.*\&nbsp;; Villela,\&nbsp;A.W.*\&nbsp;; Becker,\&nbsp;T.*\&nbsp;; Schulze,\&nbsp;T.G.*\&nbsp;; Schmael,\&nbsp;C.*\&nbsp;; Deschner,\&nbsp;M.*\&nbsp;; Klopp,\&nbsp;N.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Propping,\&nbsp;P.*\&nbsp;; Cichon,\&nbsp;S.*\&nbsp;; Rietschel,\&nbsp;M.*\&nbsp;; Nöthen,\&nbsp;M.M.*\&nbsp;; Schumacher,\&nbsp;J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5095&la=en'>Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 141B, 663-665 (2006)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>de Luca,\&nbsp;A.*\&nbsp;; Conti,\&nbsp;E.*\&nbsp;; Grifone,\&nbsp;N.*\&nbsp;; Amati,\&nbsp;F.*\&nbsp;; Spalletta,\&nbsp;G.*\&nbsp;; Caltagirone,\&nbsp;C.*\&nbsp;; Bonaviri,\&nbsp;G.*\&nbsp;; Pasini,\&nbsp;A.*\&nbsp;; Gennareli,\&nbsp;M.*\&nbsp;; Stafano,\&nbsp;B.*\&nbsp;; Berti,\&nbsp;L.\&nbsp;; Mittler,\&nbsp;G.\&nbsp;; Meisterernst,\&nbsp;M.\&nbsp;; Dallapiccola,\&nbsp;B.*\&nbsp;; Novelli,\&nbsp;G.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22383&la=en'>Association Study Between CAG Trinucleotide Repeats in the PCQAP Gene (PC2 Glutamine/Q- Rich-Associated Protein) and Schizophrenia.</a></div>");
document.write("  <div class='source'>Am. J. Med. Genet. B 116, 32-35 (2003)</div>");
document.write("</div>");