document.write("<div class='record'>");
document.write("  <div class='authors'>Foco,\&nbsp;L.*\&nbsp;; De Bortoli,\&nbsp;M.*\&nbsp;; Del Greco M,\&nbsp;F.*\&nbsp;; Frommelt,\&nbsp;L.S.*\&nbsp;; Volani,\&nbsp;C.*\&nbsp;; Riekschnitz,\&nbsp;D.A.*\&nbsp;; Motta,\&nbsp;B.M.*\&nbsp;; Fuchsberger,\&nbsp;C.*\&nbsp;; Delerue,\&nbsp;T.\&nbsp;; Völker,\&nbsp;U.*\&nbsp;; Huan,\&nbsp;T.*\&nbsp;; Gögele,\&nbsp;M.*\&nbsp;; Winkelmann,\&nbsp;J.\&nbsp;; Dörr,\&nbsp;M.*\&nbsp;; Levy,\&nbsp;D.*\&nbsp;; Waldenberger,\&nbsp;M.\&nbsp;; Teumer,\&nbsp;A.*\&nbsp;; Pramstaller,\&nbsp;P.P.*\&nbsp;; Rossini,\&nbsp;A.*\&nbsp;; Pattaro,\&nbsp;C.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=75264&la=de'>Genomic and molecular evidence that the LncRNA \<em\>DSP-AS1\</em\> modulates desmoplakin expression.</a></div>");
document.write("  <div class='source'>Hum. Genet., DOI: 10.1007/s00439-025-02761-x (2025)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fallerini,\&nbsp;C.*\&nbsp;; Picchiotti,\&nbsp;N.*\&nbsp;; Baldassarri,\&nbsp;M.*\&nbsp;; Zguro,\&nbsp;K.*\&nbsp;; Daga,\&nbsp;S.*\&nbsp;; Fava,\&nbsp;F.*\&nbsp;; Benetti,\&nbsp;E.*\&nbsp;; Amitrano,\&nbsp;S.*\&nbsp;; Bruttini,\&nbsp;M.*\&nbsp;; Palmieri,\&nbsp;M.C.*\&nbsp;; Croci,\&nbsp;S.*\&nbsp;; Lista,\&nbsp;M.*\&nbsp;; Beligni,\&nbsp;G.*\&nbsp;; Valentino,\&nbsp;F.*\&nbsp;; Meloni,\&nbsp;I.*\&nbsp;; Tanfoni,\&nbsp;M.*\&nbsp;; Minnai,\&nbsp;F.*\&nbsp;; Colombo,\&nbsp;F.*\&nbsp;; Cabri,\&nbsp;E.*\&nbsp;; Fratelli,\&nbsp;M.*\&nbsp;; Gabbi,\&nbsp;C.*\&nbsp;; Mantovani,\&nbsp;S.*\&nbsp;; Frullanti,\&nbsp;E.*\&nbsp;; Gori,\&nbsp;M.*\&nbsp;; Crawley,\&nbsp;F.P.*\&nbsp;; Butler-Laporte,\&nbsp;G.*\&nbsp;; Richards,\&nbsp;B.*\&nbsp;; Zeberg,\&nbsp;H.*\&nbsp;; Lipcsey,\&nbsp;M.*\&nbsp;; Hultström,\&nbsp;M.*\&nbsp;; Ludwig,\&nbsp;K.U.*\&nbsp;; Schulte,\&nbsp;E.C.\&nbsp;; Pairo-Castineira,\&nbsp;E.*\&nbsp;; Baillie,\&nbsp;J.K.*\&nbsp;; Schmidt,\&nbsp;A.*\&nbsp;; Frithiof,\&nbsp;R.*\&nbsp;; GEN-COVID Multicenter Study (Protzer,\&nbsp;U.)\&nbsp;; Mari,\&nbsp;F.*\&nbsp;; Renieri,\&nbsp;A.*\&nbsp;; Furini,\&nbsp;S.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=63783&la=de'>Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.</a></div>");
document.write("  <div class='source'>Hum. Genet. 141, 147-173 (2022)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Graw,\&nbsp;J.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55782&la=de'>Mouse models for microphthalmia, anophthalmia and cataracts.</a></div>");
document.write("  <div class='source'>Hum. Genet. 138, 1007-1018 (2019)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Schlicht,\&nbsp;K.*\&nbsp;; Nyczka,\&nbsp;P.*\&nbsp;; Caliebe,\&nbsp;A.*\&nbsp;; Freitag-Wolf,\&nbsp;S.*\&nbsp;; Claringbould,\&nbsp;A.*\&nbsp;; Franke,\&nbsp;L.*\&nbsp;; Võsa,\&nbsp;U.*\&nbsp;; Kardia,\&nbsp;S.L.R.*\&nbsp;; Smith,\&nbsp;J.A.*\&nbsp;; Zhao,\&nbsp;W.*\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Peters,\&nbsp;A.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Strauch,\&nbsp;K.\&nbsp;; Baurecht,\&nbsp;H.*\&nbsp;; Weidinger,\&nbsp;S.*\&nbsp;; Rosenstiel,\&nbsp;P.*\&nbsp;; Hütt,\&nbsp;M.T.*\&nbsp;; Knecht,\&nbsp;C.*\&nbsp;; Szymczak,\&nbsp;S.*\&nbsp;; Krawczak,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55651&la=de'>The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus.</a></div>");
document.write("  <div class='source'>Hum. Genet. 138, 375–388 (2019)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Bertoli-Avella,\&nbsp;A.M.*\&nbsp;; Albrecht,\&nbsp;B.*\&nbsp;; Al Aqeel,\&nbsp;A.I.*\&nbsp;; Alhashem,\&nbsp;A.*\&nbsp;; Al-Sannaa,\&nbsp;N.*\&nbsp;; Bah,\&nbsp;M.*\&nbsp;; Bröhl,\&nbsp;K.*\&nbsp;; Depienne,\&nbsp;C.*\&nbsp;; Dorison,\&nbsp;N.*\&nbsp;; Doummar,\&nbsp;D.*\&nbsp;; Ehmke,\&nbsp;N.*\&nbsp;; Elbendary,\&nbsp;H.M.*\&nbsp;; Gorokhova,\&nbsp;S.*\&nbsp;; Héron,\&nbsp;D.*\&nbsp;; Horn,\&nbsp;D.*\&nbsp;; James,\&nbsp;K.*\&nbsp;; Keren,\&nbsp;B.*\&nbsp;; Kuechler,\&nbsp;A.*\&nbsp;; Ismail,\&nbsp;S.*\&nbsp;; Issa,\&nbsp;M.Y.*\&nbsp;; Marey,\&nbsp;I.*\&nbsp;; Mayer,\&nbsp;M.*\&nbsp;; McEvoy-Venneri,\&nbsp;J.*\&nbsp;; Megarbane,\&nbsp;A.*\&nbsp;; Mignot,\&nbsp;C.*\&nbsp;; Mohamed,\&nbsp;S.*\&nbsp;; Nava,\&nbsp;C.*\&nbsp;; Philip,\&nbsp;N.*\&nbsp;; Ravix,\&nbsp;C.*\&nbsp;; Rolfs,\&nbsp;A.*\&nbsp;; Sadek,\&nbsp;A.A.*\&nbsp;; Segebrecht,\&nbsp;L.*\&nbsp;; Stanley,\&nbsp;V.*\&nbsp;; Trautman,\&nbsp;C.*\&nbsp;; Valence,\&nbsp;S.*\&nbsp;; Villard,\&nbsp;L.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Zaki,\&nbsp;M.S.*\&nbsp;; Gleeson,\&nbsp;J.G.*\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Bauer,\&nbsp;P.*\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54214&la=de'>Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).</a></div>");
document.write("  <div class='source'>Hum. Genet. 137, 753-768 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fritzen,\&nbsp;D.*\&nbsp;; Kuechler,\&nbsp;A.*\&nbsp;; Grimmel,\&nbsp;M.*\&nbsp;; Becker,\&nbsp;J.*\&nbsp;; Peters,\&nbsp;S.*\&nbsp;; Sturm,\&nbsp;M.*\&nbsp;; Hundertmark,\&nbsp;H.*\&nbsp;; Schmidt,\&nbsp;A.*\&nbsp;; Kreiss,\&nbsp;M.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Wieczorek,\&nbsp;D.*\&nbsp;; Haack,\&nbsp;T.B.*\&nbsp;; Beck-Woedl,\&nbsp;S.*\&nbsp;; Cremer,\&nbsp;K.*\&nbsp;; Engels,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53645&la=de'>De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies.</a></div>");
document.write("  <div class='source'>Hum. Genet. 137, 401-411 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Vill,\&nbsp;K.*\&nbsp;; Müller-Felber,\&nbsp;W.*\&nbsp;; Gläser,\&nbsp;D.*\&nbsp;; Kuhn,\&nbsp;M.*\&nbsp;; Teusch,\&nbsp;V.*\&nbsp;; Schreiber,\&nbsp;H.*\&nbsp;; Weis,\&nbsp;J.*\&nbsp;; Klepper,\&nbsp;J.*\&nbsp;; Schirmacher,\&nbsp;A.*\&nbsp;; Blaschek,\&nbsp;A.*\&nbsp;; Wiessner,\&nbsp;M.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Dräger,\&nbsp;B.*\&nbsp;; Hofmeister-Kiltz,\&nbsp;K.*\&nbsp;; Tacke,\&nbsp;M.*\&nbsp;; Gerstl,\&nbsp;L.*\&nbsp;; Young,\&nbsp;P.*\&nbsp;; Horvath,\&nbsp;R.*\&nbsp;; Senderek,\&nbsp;J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=54779&la=de'>SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.</a></div>");
document.write("  <div class='source'>Hum. Genet. 137, 911-919 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Wesdorp,\&nbsp;M.*\&nbsp;; de Koning Gans,\&nbsp;P.A.M.*\&nbsp;; Schraders,\&nbsp;M.*\&nbsp;; Oostrik,\&nbsp;J.*\&nbsp;; Huynen,\&nbsp;M.A.*\&nbsp;; Venselaar,\&nbsp;H.*\&nbsp;; Beynon,\&nbsp;A.J.*\&nbsp;; van Gaalen,\&nbsp;J.*\&nbsp;; Piai,\&nbsp;V.*\&nbsp;; Voermans,\&nbsp;N.*\&nbsp;; van Rossum,\&nbsp;M.M.*\&nbsp;; Hartel,\&nbsp;B.P.*\&nbsp;; Lelieveld,\&nbsp;S.H.*\&nbsp;; Wiel,\&nbsp;L.*\&nbsp;; Verbist,\&nbsp;B.*\&nbsp;; Rotteveel,\&nbsp;L.J.*\&nbsp;; van Dooren,\&nbsp;M.F.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Kunst,\&nbsp;H.P.M.*\&nbsp;; Feenstra,\&nbsp;I.*\&nbsp;; Admiraal,\&nbsp;R.J.C.*\&nbsp;; DOOFNL Consortium*\&nbsp;; Yntema,\&nbsp;H.G.*\&nbsp;; Hoefsloot,\&nbsp;L.H.*\&nbsp;; Pennings,\&nbsp;R.J.E.*\&nbsp;; Kremer,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=53517&la=de'>Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.</a></div>");
document.write("  <div class='source'>Hum. Genet. 137, 389-400 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Pettersson,\&nbsp;M.*\&nbsp;; Albrecht,\&nbsp;B.*\&nbsp;; Bernier,\&nbsp;R.A.*\&nbsp;; Cremer,\&nbsp;K.*\&nbsp;; Eichler,\&nbsp;E.E.*\&nbsp;; Falkenstein,\&nbsp;D.*\&nbsp;; Gerdts,\&nbsp;J.*\&nbsp;; Jansen,\&nbsp;S.*\&nbsp;; Kuechler,\&nbsp;A.*\&nbsp;; Kvarnung,\&nbsp;M.*\&nbsp;; Lindstrand,\&nbsp;A.*\&nbsp;; Nilsson,\&nbsp;D.*\&nbsp;; Nordgren,\&nbsp;A.*\&nbsp;; Pfundt,\&nbsp;R.*\&nbsp;; Spruijt,\&nbsp;L.*\&nbsp;; Surowy,\&nbsp;H.M.*\&nbsp;; de Vries,\&nbsp;B.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Kleefstra,\&nbsp;T.*\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50034&la=de'>Identification of new \<em\>TRIP12\</em\> variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.</a></div>");
document.write("  <div class='source'>Hum. Genet. 136, 179-192 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Caluseriu,\&nbsp;O.*\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Bolduc,\&nbsp;F.V.*\&nbsp;; Noel,\&nbsp;N.C.L.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Surowy,\&nbsp;H.M.*\&nbsp;; Christen,\&nbsp;H.J.*\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50458&la=de'>Heterozygosity for \<em\>ARID2\</em\> loss-of-function mutations in individuals with a Coffin\&ndash;Siris syndrome-like phenotype.</a></div>");
document.write("  <div class='source'>Hum. Genet. 136, 297-305 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Hamdan,\&nbsp;F.F.*\&nbsp;; Altmüller,\&nbsp;J.*\&nbsp;; Beleggia,\&nbsp;F.*\&nbsp;; Elcioğlu,\&nbsp;N.H.*\&nbsp;; Freyer,\&nbsp;C.*\&nbsp;; Gerkes,\&nbsp;E.H.*\&nbsp;; Demirkol,\&nbsp;Y.K.*\&nbsp;; Knupp,\&nbsp;K.G.*\&nbsp;; Kuechler,\&nbsp;A.*\&nbsp;; Li,\&nbsp;Y.*\&nbsp;; Lowenstein,\&nbsp;D.H.*\&nbsp;; Michaud,\&nbsp;J.L.*\&nbsp;; Park,\&nbsp;K.*\&nbsp;; Stegmann,\&nbsp;A.P.A.*\&nbsp;; Veenstra-Knol,\&nbsp;H.E.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Wollnik,\&nbsp;B.*\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Kleefstra,\&nbsp;T.*\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50930&la=de'>Heterozygous \<em\>HNRNPU\</em\> variants cause early onset epilepsy and severe intellectual disability.</a></div>");
document.write("  <div class='source'>Hum. Genet. 136, 821-834 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Hempel,\&nbsp;M.*\&nbsp;; Casar Tena,\&nbsp;T.*\&nbsp;; Diehl,\&nbsp;T.*\&nbsp;; Burczyk,\&nbsp;M.S.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Kubisch,\&nbsp;C.*\&nbsp;; Philipp,\&nbsp;M.*\&nbsp;; Lessel,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50536&la=de'>Compound \<em\>heterozygous GATA5\</em\> mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies.</a></div>");
document.write("  <div class='source'>Hum. Genet. 136, 339-346 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Parenti,\&nbsp;I.*\&nbsp;; Teresa-Rodrigo,\&nbsp;M.E.*\&nbsp;; Pozojevic,\&nbsp;J.*\&nbsp;; Ruiz Gil,\&nbsp;S.*\&nbsp;; Bader,\&nbsp;I.*\&nbsp;; Braunholz,\&nbsp;D.*\&nbsp;; Bramswig,\&nbsp;N.C.*\&nbsp;; Gervasini,\&nbsp;C.*\&nbsp;; Larizza,\&nbsp;L.*\&nbsp;; Pfeiffer,\&nbsp;L.*\&nbsp;; Ozkınay,\&nbsp;F.*\&nbsp;; Ramos,\&nbsp;F.*\&nbsp;; Reiz,\&nbsp;B.*\&nbsp;; Rittinger,\&nbsp;O.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Watrin,\&nbsp;E.*\&nbsp;; Wendt,\&nbsp;K.*\&nbsp;; Wieczorek,\&nbsp;D.*\&nbsp;; Wollnik,\&nbsp;B.*\&nbsp;; Baquero-Montoya,\&nbsp;C.*\&nbsp;; Pié,\&nbsp;J.*\&nbsp;; Deardorff,\&nbsp;M.A.*\&nbsp;; Gillessen-Kaesbach,\&nbsp;G.*\&nbsp;; Kaiser,\&nbsp;F.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50456&la=de'>Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.</a></div>");
document.write("  <div class='source'>Hum. Genet. 136, 307-320 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Brenner,\&nbsp;D.R.*\&nbsp;; Brennan,\&nbsp;P.*\&nbsp;; Boffetta,\&nbsp;P.*\&nbsp;; Amos,\&nbsp;C.I.*\&nbsp;; Spitz,\&nbsp;M.R.*\&nbsp;; Chen,\&nbsp;C.*\&nbsp;; Goodman,\&nbsp;G.*\&nbsp;; Heinrich,\&nbsp;J.\&nbsp;; Bickeböller,\&nbsp;H.*\&nbsp;; Rosenberger,\&nbsp;A.*\&nbsp;; Risch,\&nbsp;A.*\&nbsp;; Muley,\&nbsp;T.*\&nbsp;; McLaughlin,\&nbsp;J.R.*\&nbsp;; Benhamou,\&nbsp;S.*\&nbsp;; Bouchardy,\&nbsp;C.*\&nbsp;; Lewinger,\&nbsp;J.P.*\&nbsp;; Witte,\&nbsp;J.S.*\&nbsp;; Chen,\&nbsp;G.*\&nbsp;; Bull,\&nbsp;S.*\&nbsp;; Hung,\&nbsp;R.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48764&la=de'>Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.</a></div>");
document.write("  <div class='source'>Hum. Genet. 135, 963-963 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Alanay,\&nbsp;Y.*\&nbsp;; Albrecht,\&nbsp;B.*\&nbsp;; Barthelmie,\&nbsp;A.*\&nbsp;; Boduroglu,\&nbsp;K.*\&nbsp;; Braunholz,\&nbsp;D.*\&nbsp;; Caliebe,\&nbsp;A.*\&nbsp;; Chrzanowska,\&nbsp;K.*\&nbsp;; Czeschik,\&nbsp;J.C.*\&nbsp;; Endele,\&nbsp;S.U.*\&nbsp;; Graf,\&nbsp;E.\&nbsp;; Guillén-Navarro,\&nbsp;E.*\&nbsp;; Kiper,\&nbsp;P.O.S.*\&nbsp;; López-González,\&nbsp;V.*\&nbsp;; Parenti,\&nbsp;I.*\&nbsp;; Pozojevic,\&nbsp;J.*\&nbsp;; Ü̈tine,\&nbsp;G.E.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Kaiser,\&nbsp;F.J.*\&nbsp;; Wollnik,\&nbsp;B.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43792&la=de'>Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin\&ndash;Siris and Nicolaides\&ndash;Baraitser syndromes.</a></div>");
document.write("  <div class='source'>Hum. Genet. 134, 553-568 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bramswig,\&nbsp;N.C.*\&nbsp;; Ockeloen,\&nbsp;C.W.*\&nbsp;; Czeschik,\&nbsp;J.C.*\&nbsp;; van Essen,\&nbsp;A.J.*\&nbsp;; Pfundt,\&nbsp;R.*\&nbsp;; Smeitink,\&nbsp;J.*\&nbsp;; Poll-The,\&nbsp;B.T.*\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Wieczorek,\&nbsp;D.*\&nbsp;; Kleefstra,\&nbsp;T.*\&nbsp;; Lüdecke,\&nbsp;H.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=46675&la=de'>\&lsquo;Splitting versus lumping\&rsquo;: Temple\&ndash;Baraitser and Zimmermann\&ndash;Laband syndromes.</a></div>");
document.write("  <div class='source'>Hum. Genet. 134, 1089-1097 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kuechler,\&nbsp;A.*\&nbsp;; Willemsen,\&nbsp;M.H.*\&nbsp;; Albrecht,\&nbsp;B.*\&nbsp;; Bacino,\&nbsp;C.A.*\&nbsp;; Bartholomew,\&nbsp;D.W.*\&nbsp;; van Bokhoven,\&nbsp;H.*\&nbsp;; van den Boogaard,\&nbsp;M.J.*\&nbsp;; Bramswig,\&nbsp;N.*\&nbsp;; Büttner,\&nbsp;C.*\&nbsp;; Cremer,\&nbsp;K.*\&nbsp;; Czeschik,\&nbsp;J.C.*\&nbsp;; Engels,\&nbsp;H.*\&nbsp;; van Gassen,\&nbsp;K.*\&nbsp;; Graf,\&nbsp;E.\&nbsp;; van Haelst,\&nbsp;M.M.*\&nbsp;; He,\&nbsp;W.*\&nbsp;; Hogue,\&nbsp;J.S.*\&nbsp;; Kempers,\&nbsp;M.*\&nbsp;; Koolen,\&nbsp;D.A.*\&nbsp;; Monroe,\&nbsp;G.*\&nbsp;; de Munnik,\&nbsp;S.*\&nbsp;; Pastore,\&nbsp;M.*\&nbsp;; Reis,\&nbsp;A.*\&nbsp;; Reuter,\&nbsp;M.S.*\&nbsp;; Tegay,\&nbsp;D.H.*\&nbsp;; Veltman,\&nbsp;J.A.*\&nbsp;; Visser,\&nbsp;G.*\&nbsp;; van Hasselt,\&nbsp;P.*\&nbsp;; Smeets,\&nbsp;E.E.*\&nbsp;; Vissers,\&nbsp;L.E.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Wissink,\&nbsp;W.*\&nbsp;; Yntema,\&nbsp;H.*\&nbsp;; Zink,\&nbsp;A.M.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Lüdecke,\&nbsp;H.J.*\&nbsp;; Kleefstra,\&nbsp;T.*\&nbsp;; Wieczorek,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32593&la=de'>\<em\>De novo\</em\> mutations in \<em\>beta-catenin (CTNNB1)\</em\> appear to be a frequent cause of intellectual disability: Expanding the mutational and clinical spectrum.</a></div>");
document.write("  <div class='source'>Hum. Genet. 134, 97-109 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Li,\&nbsp;Q.*\&nbsp;; Wojciechowski,\&nbsp;R.*\&nbsp;; Simpson,\&nbsp;C.L.*\&nbsp;; Hysi,\&nbsp;P.G.*\&nbsp;; Verhoeven,\&nbsp;V.J.*\&nbsp;; Ikram,\&nbsp;M.K.*\&nbsp;; Höhn,\&nbsp;R.*\&nbsp;; Vitart,\&nbsp;V.*\&nbsp;; Hewitt,\&nbsp;A.W.*\&nbsp;; Oexle,\&nbsp;K.*\&nbsp;; Mäkelä,\&nbsp;K.M.*\&nbsp;; MacGregor,\&nbsp;S.*\&nbsp;; Pirastu,\&nbsp;M.*\&nbsp;; Fan,\&nbsp;Q.*\&nbsp;; Cheng,\&nbsp;C.Y.*\&nbsp;; St. Pourcain,\&nbsp;B.*\&nbsp;; McMahon,\&nbsp;G.*\&nbsp;; Kemp,\&nbsp;J.P.*\&nbsp;; Northstone,\&nbsp;K.*\&nbsp;; Rahi,\&nbsp;J.S.*\&nbsp;; Cumberland,\&nbsp;P.M.*\&nbsp;; Martin,\&nbsp;N.G.*\&nbsp;; Sanfilippo,\&nbsp;P.G.*\&nbsp;; Lu,\&nbsp;Y.*\&nbsp;; Wang,\&nbsp;Y.X.*\&nbsp;; Hayward,\&nbsp;C.*\&nbsp;; Polasek,\&nbsp;O.*\&nbsp;; Campbell,\&nbsp;H.*\&nbsp;; Bencic,\&nbsp;G.*\&nbsp;; Wright,\&nbsp;A.F.*\&nbsp;; Wedenoja,\&nbsp;J.*\&nbsp;; Zeller,\&nbsp;T.*\&nbsp;; Schillert,\&nbsp;A.*\&nbsp;; Mirshahi,\&nbsp;A.*\&nbsp;; Lackner,\&nbsp;K.J.*\&nbsp;; Yip,\&nbsp;S.P.*\&nbsp;; Yap,\&nbsp;M.K.H.*\&nbsp;; Ried,\&nbsp;J.S.\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Murgia,\&nbsp;F.*\&nbsp;; Wilson,\&nbsp;J.F.*\&nbsp;; Fleck,\&nbsp;B.*\&nbsp;; Yazar,\&nbsp;S.*\&nbsp;; Vingerling,\&nbsp;J.R.*\&nbsp;; Hofman,\&nbsp;A.*\&nbsp;; Uitterlinden,\&nbsp;A.*\&nbsp;; Rivadeneira,\&nbsp;F.*\&nbsp;; Amin,\&nbsp;N.*\&nbsp;; Karssen,\&nbsp;L.C.*\&nbsp;; Oostra,\&nbsp;B.A.*\&nbsp;; Zhou,\&nbsp;X.*\&nbsp;; Teo,\&nbsp;Y.Y.*\&nbsp;; Tai,\&nbsp;E.S.*\&nbsp;; Vithana,\&nbsp;E.*\&nbsp;; Barathi,\&nbsp;V.A.*\&nbsp;; Zheng,\&nbsp;Y.*\&nbsp;; Siantar,\&nbsp;R.G.*\&nbsp;; Neelam,\&nbsp;K.*\&nbsp;; Shin,\&nbsp;Y.K.*\&nbsp;; Lam,\&nbsp;J.S.Y.*\&nbsp;; Yonova-Doing,\&nbsp;E.*\&nbsp;; Venturini,\&nbsp;C.*\&nbsp;; Hosseini,\&nbsp;S.M.*\&nbsp;; Wong,\&nbsp;H.S.*\&nbsp;; Lehtimäki,\&nbsp;T.*\&nbsp;; Kähönen,\&nbsp;M.*\&nbsp;; Raitakari,\&nbsp;O.*\&nbsp;; Timpson,\&nbsp;N.J.*\&nbsp;; Evans,\&nbsp;D.M*\&nbsp;; Khor,\&nbsp;C.C.*\&nbsp;; Aung,\&nbsp;T.*\&nbsp;; Young,\&nbsp;T.L.*\&nbsp;; Mitchell,\&nbsp;P.*\&nbsp;; Klein,\&nbsp;B.*\&nbsp;; van Duijn,\&nbsp;C.M.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Jonas,\&nbsp;J.B.*\&nbsp;; Baird,\&nbsp;P.N.*\&nbsp;; Mackey,\&nbsp;D.A.*\&nbsp;; Wong,\&nbsp;T.Y.*\&nbsp;; Saw,\&nbsp;S.M.*\&nbsp;; Pärssinen,\&nbsp;O.*\&nbsp;; Stambolian,\&nbsp;D.*\&nbsp;; Hammond,\&nbsp;C.J.*\&nbsp;; Klaver,\&nbsp;C.C.*\&nbsp;; Williams,\&nbsp;C.*\&nbsp;; Paterson,\&nbsp;A.D.*\&nbsp;; Bailey-Wilson,\&nbsp;J.E.*\&nbsp;; Guggenheim,\&nbsp;J.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=34362&la=de'>Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: The CREAM consortium.</a></div>");
document.write("  <div class='source'>Hum. Genet. 134, 131-146 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Turpeinen,\&nbsp;H.*\&nbsp;; Seppälä,\&nbsp;I.J.T.*\&nbsp;; Lyytikäinen,\&nbsp;L.-P.*\&nbsp;; Raitoharju,\&nbsp;E.*\&nbsp;; Hutri-Kähönen,\&nbsp;N.*\&nbsp;; Levula,\&nbsp;M.*\&nbsp;; Oksala,\&nbsp;N.K.J.*\&nbsp;; Waldenberger,\&nbsp;M.\&nbsp;; Klopp,\&nbsp;N.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Mononen,\&nbsp;N.*\&nbsp;; Laaksonen,\&nbsp;R.*\&nbsp;; Raitakari,\&nbsp;O.T.*\&nbsp;; Kähönen,\&nbsp;M.*\&nbsp;; Lehtimäki,\&nbsp;T.*\&nbsp;; Pesu,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44095&la=de'>A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure.</a></div>");
document.write("  <div class='source'>Hum. Genet. 134, 627-636 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Ellis,\&nbsp;J.*\&nbsp;; Lange,\&nbsp;E.M.*\&nbsp;; Li,\&nbsp;J.*\&nbsp;; Dupuis,\&nbsp;J.*\&nbsp;; Baumert,\&nbsp;J.J.\&nbsp;; Walston,\&nbsp;J.D.*\&nbsp;; Keating,\&nbsp;B.J.*\&nbsp;; Durda,\&nbsp;P.*\&nbsp;; Fox,\&nbsp;E.R.*\&nbsp;; Palmer,\&nbsp;C.D.*\&nbsp;; Meng,\&nbsp;Y.A.*\&nbsp;; Young,\&nbsp;T.*\&nbsp;; Farlow,\&nbsp;D.N.*\&nbsp;; Schnabel,\&nbsp;R.B.*\&nbsp;; Marzi,\&nbsp;C.\&nbsp;; Larkin,\&nbsp;E.*\&nbsp;; Martin,\&nbsp;L.W.*\&nbsp;; Bis,\&nbsp;J.C.*\&nbsp;; Auer,\&nbsp;P.*\&nbsp;; Ramachandran,\&nbsp;V.S.*\&nbsp;; Gabriel,\&nbsp;S.B.*\&nbsp;; Willis,\&nbsp;M.S.*\&nbsp;; Pankow,\&nbsp;J.S.*\&nbsp;; Papanicolau,\&nbsp;G.J.*\&nbsp;; Rotter,\&nbsp;J.I.*\&nbsp;; Ballantyne,\&nbsp;C.M.*\&nbsp;; Gross,\&nbsp;M.D.*\&nbsp;; Lettre,\&nbsp;G.*\&nbsp;; Wilson,\&nbsp;J.G.*\&nbsp;; Peters,\&nbsp;U.*\&nbsp;; Koenig,\&nbsp;W.*\&nbsp;; Tracy,\&nbsp;R.P.*\&nbsp;; Redline,\&nbsp;S.*\&nbsp;; Reiner,\&nbsp;A.P.*\&nbsp;; Benjamin,\&nbsp;E.J.*\&nbsp;; Lange,\&nbsp;L.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=30926&la=de'>Large multiethnic candidate gene study for C-reactive protein levels: Identification of a novel association at \<em\>CD36\</em\> in African Americans.</a></div>");
document.write("  <div class='source'>Hum. Genet. 133, 985-995 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Brenner,\&nbsp;D.R.*\&nbsp;; Brennan,\&nbsp;P.*\&nbsp;; Boffetta,\&nbsp;P.*\&nbsp;; Amos,\&nbsp;C.I.*\&nbsp;; Spitz,\&nbsp;M.R.*\&nbsp;; Chen,\&nbsp;C.*\&nbsp;; Goodman,\&nbsp;G.*\&nbsp;; Heinrich,\&nbsp;J.\&nbsp;; Bickeböller,\&nbsp;H.*\&nbsp;; Rosenberger,\&nbsp;A.*\&nbsp;; Risch,\&nbsp;A.*\&nbsp;; Muley,\&nbsp;T.*\&nbsp;; McLaughlin,\&nbsp;J.R.*\&nbsp;; Benhamou,\&nbsp;S.*\&nbsp;; Bouchardy,\&nbsp;C.*\&nbsp;; Lewinger,\&nbsp;J.P.*\&nbsp;; Witte,\&nbsp;J.S.*\&nbsp;; Chen,\&nbsp;G.*\&nbsp;; Bull,\&nbsp;S.*\&nbsp;; Hung,\&nbsp;R.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24382&la=de'>Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.</a></div>");
document.write("  <div class='source'>Hum. Genet. 132, 579-589 (2013)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Verhoeven,\&nbsp;V.J.M.*\&nbsp;; Hysi,\&nbsp;P.G.*\&nbsp;; Saw,\&nbsp;S.-M.*\&nbsp;; Vitart,\&nbsp;V.*\&nbsp;; Mirshahi,\&nbsp;A.*\&nbsp;; Guggenheim,\&nbsp;J.A.*\&nbsp;; Cotch,\&nbsp;M.F.*\&nbsp;; Yamashiro,\&nbsp;K.*\&nbsp;; Baird,\&nbsp;P.N.*\&nbsp;; Mackey,\&nbsp;D.A.*\&nbsp;; Wojciechowski,\&nbsp;R.*\&nbsp;; Ikram,\&nbsp;M.K.*\&nbsp;; Hewitt,\&nbsp;A.W.*\&nbsp;; Duggal,\&nbsp;P.*\&nbsp;; Janmahasatian,\&nbsp;S.*\&nbsp;; Khor,\&nbsp;C.-C.*\&nbsp;; Fan,\&nbsp;Q.*\&nbsp;; Zhou,\&nbsp;X.*\&nbsp;; Young,\&nbsp;T.L.*\&nbsp;; Tai,\&nbsp;E.-S.*\&nbsp;; Goh,\&nbsp;L.-K.*\&nbsp;; Li,\&nbsp;Y.-J.*\&nbsp;; Aung,\&nbsp;T.*\&nbsp;; Vithana,\&nbsp;E.*\&nbsp;; Teo,\&nbsp;Y.-Y.*\&nbsp;; Tay,\&nbsp;W.*\&nbsp;; Sim,\&nbsp;X.*\&nbsp;; Rudan,\&nbsp;I.*\&nbsp;; Hayward,\&nbsp;C.*\&nbsp;; Wright,\&nbsp;A.F.*\&nbsp;; Polasek,\&nbsp;O.*\&nbsp;; Campbell,\&nbsp;H.*\&nbsp;; Wilson,\&nbsp;J.F.*\&nbsp;; Fleck,\&nbsp;B.W.*\&nbsp;; Nakata,\&nbsp;I.*\&nbsp;; Yoshimura,\&nbsp;N.*\&nbsp;; Yamada,\&nbsp;R.*\&nbsp;; Matsuda,\&nbsp;F.*\&nbsp;; Ohno-Matsui,\&nbsp;K.*\&nbsp;; Nag,\&nbsp;A.*\&nbsp;; McMahon,\&nbsp;G.*\&nbsp;; St Pourcain,\&nbsp;B.*\&nbsp;; Lu,\&nbsp;Y.*\&nbsp;; Rahi,\&nbsp;J.S.*\&nbsp;; Cumberland,\&nbsp;P.M.*\&nbsp;; Bhattacharya,\&nbsp;S.*\&nbsp;; Simpson,\&nbsp;C.L.*\&nbsp;; Atwood,\&nbsp;L.D.*\&nbsp;; Li,\&nbsp;X.H.*\&nbsp;; Raffel,\&nbsp;L.J.*\&nbsp;; Murgia,\&nbsp;F.*\&nbsp;; Portas,\&nbsp;L.*\&nbsp;; Despriet,\&nbsp;D.D.G.*\&nbsp;; van Koolwijk,\&nbsp;L.M.E.*\&nbsp;; Wolfram,\&nbsp;C.*\&nbsp;; Lackner,\&nbsp;K.J.*\&nbsp;; Tönjes,\&nbsp;A.*\&nbsp;; Mägi,\&nbsp;R.*\&nbsp;; Lehtimäki,\&nbsp;T.*\&nbsp;; Kähönen,\&nbsp;M.*\&nbsp;; Esko,\&nbsp;T.*\&nbsp;; Metspalu,\&nbsp;A.*\&nbsp;; Rantanen,\&nbsp;T.*\&nbsp;; Pärssinen,\&nbsp;O.*\&nbsp;; Klein,\&nbsp;B.E.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Spector,\&nbsp;T.D.*\&nbsp;; Oostra,\&nbsp;B.A.*\&nbsp;; Smith,\&nbsp;A.V.*\&nbsp;; de Jong,\&nbsp;P.T.V.M.*\&nbsp;; Hofman,\&nbsp;A.*\&nbsp;; Amin,\&nbsp;N.*\&nbsp;; Karssen,\&nbsp;L.C.*\&nbsp;; Rivadeneira,\&nbsp;F.*\&nbsp;; Vingerling,\&nbsp;J.R.*\&nbsp;; Eiriksdottir,\&nbsp;G.*\&nbsp;; Gudnason,\&nbsp;V.*\&nbsp;; Döring,\&nbsp;A.\&nbsp;; Bettecken,\&nbsp;T.*\&nbsp;; Uitterlinden,\&nbsp;A.G.*\&nbsp;; Williams,\&nbsp;C.*\&nbsp;; Zeller,\&nbsp;T.*\&nbsp;; Castagné,\&nbsp;R.*\&nbsp;; Oexle,\&nbsp;K.*\&nbsp;; van Duijn,\&nbsp;C.M.*\&nbsp;; Iyengar,\&nbsp;S.K.*\&nbsp;; Mitchell,\&nbsp;P.*\&nbsp;; Wang,\&nbsp;J.J.*\&nbsp;; Höhn,\&nbsp;R.*\&nbsp;; Pfeiffer,\&nbsp;N.*\&nbsp;; Bailey-Wilson,\&nbsp;J.E.*\&nbsp;; Stambolian,\&nbsp;D.*\&nbsp;; Wong,\&nbsp;T.-Y.*\&nbsp;; Hammond,\&nbsp;C.J.*\&nbsp;; Klaver,\&nbsp;C.C.W.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8555&la=de'>Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium.</a></div>");
document.write("  <div class='source'>Hum. Genet. 131, 1467-1480 (2012)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fauth,\&nbsp;C.\&nbsp;; Gribble,\&nbsp;S.M.*\&nbsp;; Porter,\&nbsp;K.M.*\&nbsp;; Codina-Pascual,\&nbsp;M.*\&nbsp;; Ng,\&nbsp;B.L.*\&nbsp;; Kraus,\&nbsp;J.\&nbsp;; Uhrig,\&nbsp;S.*\&nbsp;; Leifheit,\&nbsp;J.*\&nbsp;; Haaf,\&nbsp;T.*\&nbsp;; Fiegler,\&nbsp;H.*\&nbsp;; Carter,\&nbsp;N.P.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5087&la=de'>Micro-array analysis decipher exceptional complex familial chromosomal rearrangement.</a></div>");
document.write("  <div class='source'>Hum. Genet. 119, 145-153 (2006)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Pfuhl,\&nbsp;T.*\&nbsp;; Dürr,\&nbsp;T.*\&nbsp;; Spurk,\&nbsp;A.*\&nbsp;; Schwalbert,\&nbsp;B.*\&nbsp;; Nord,\&nbsp;R.*\&nbsp;; Mysliwietz,\&nbsp;J.\&nbsp;; Kremmer,\&nbsp;E.\&nbsp;; Grässer,\&nbsp;F.A.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=1284&la=de'>Biochemical charcterisation of the proteins encoded by the Di George critical region 6 (DGCR6).</a></div>");
document.write("  <div class='source'>Hum. Genet. 117, 70-80 (2005)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Müller,\&nbsp;S.*\&nbsp;; Hollatz,\&nbsp;M.*\&nbsp;; Wienberg,\&nbsp;J.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=9428&la=de'>Chromosomal phylogeny and evolution of gibbons (Hylobatidae).</a></div>");
document.write("  <div class='source'>Hum. Genet. 113, 493-501 (2003)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bassi,\&nbsp;M.T.*\&nbsp;; Bergen,\&nbsp;A.A.*\&nbsp;; Bitoun,\&nbsp;P.*\&nbsp;; Charles,\&nbsp;S.J.*\&nbsp;; Clementi,\&nbsp;M.*\&nbsp;; Gosselin,\&nbsp;R.*\&nbsp;; Hurst,\&nbsp;J.*\&nbsp;; Lewis,\&nbsp;R.A.*\&nbsp;; Lorenz,\&nbsp;B.*\&nbsp;; Meitinger,\&nbsp;T.*\&nbsp;; Messiaen,\&nbsp;L.*\&nbsp;; Ramesar,\&nbsp;R.S.*\&nbsp;; Ballabio,\&nbsp;A.*\&nbsp;; Schiaffino,\&nbsp;M.V.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23573&la=de'>Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.</a></div>");
document.write("  <div class='source'>Hum. Genet. 108, 51-54 (2001)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Langer,\&nbsp;S.*\&nbsp;; Fauth,\&nbsp;C.*\&nbsp;; Rocchi,\&nbsp;M.*\&nbsp;; Murken,\&nbsp;J.*\&nbsp;; Speicher,\&nbsp;M.R.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23585&la=de'>AcroM fluorescent in situ hybridization analyses of marker chromosomes.</a></div>");
document.write("  <div class='source'>Hum. Genet. 109, 152-158 (2001)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Lohmann,\&nbsp;D.\&nbsp;; Horsthemke,\&nbsp;B.\&nbsp;; Gillessen-Kaesbach,\&nbsp;G.\&nbsp;; Stefani,\&nbsp;F.H.\&nbsp;; Höfler,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=20238&la=de'>Detection of small RB1 Gene Deletions in Retinoblastoma by Multiplex PCR and High- Resolution Gel Electrophoresis.</a></div>");
document.write("  <div class='source'>Hum. Genet. 89, 49-53 (1992)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Cazzola,\&nbsp;M.*\&nbsp;; ASCARI,\&nbsp;E.*\&nbsp;; Barosi,\&nbsp;G.*\&nbsp;; Claudiani,\&nbsp;G.*\&nbsp;; Daccó,\&nbsp;M.*\&nbsp;; Kaltwasser,\&nbsp;J.P.*\&nbsp;; Panaiotopoulos,\&nbsp;N.*\&nbsp;; Schalk,\&nbsp;K.P.*\&nbsp;; Werner,\&nbsp;E.E.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=41748&la=de'>Juvenile idiopathic haemochromatosis: A life-threatening disorder presenting as hypogonadotropic hypogonadism.</a></div>");
document.write("  <div class='source'>Hum. Genet. 65, 149-154 (1983)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Rauscher,\&nbsp;K.H.\&nbsp;; Bauchinger,\&nbsp;M.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=41469&la=de'>Chromosome aberrations induced in patients treated with chemotherapeutic drugs and irradiation for acute lymphatic leukemia.</a></div>");
document.write("  <div class='source'>Hum. Genet. 64, 73-79 (1983)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Wiebel,\&nbsp;F.J.\&nbsp;; Hlavica,\&nbsp;P.\&nbsp;; Grzeschik -,\&nbsp;K.H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=41423&la=de'>Expression of aromatic polycyclic hydrocarbon-induced monooxygenase (aryl hydrocarbon hydroxylase) in man x mouse hybrids is associated with human chromosome 2.</a></div>");
document.write("  <div class='source'>Hum. Genet. 59, 277-280 (1981)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Niese,\&nbsp;D.*\&nbsp;; Grosse-Wilde,\&nbsp;H.\&nbsp;; Dupont,\&nbsp;B.*\&nbsp;; Du Toit,\&nbsp;E.D.*\&nbsp;; Johannsen,\&nbsp;R.*\&nbsp;; Suciu- Foca,\&nbsp;N.M.*\&nbsp;; Stroehmann,\&nbsp;I.*\&nbsp;; Rittner,\&nbsp;C.K.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42530&la=de'>Evidence for subtypic determinants in the HLA-DW3 cluster.</a></div>");
document.write("  <div class='source'>Hum. Genet. 43, 23-30 (1978)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Röhrborn,\&nbsp;G.*\&nbsp;; Sezer,\&nbsp;V.*\&nbsp;; Adler,\&nbsp;I.-D.\&nbsp;; Schmaltz,\&nbsp;A.\&nbsp;; Pawlowitzki,\&nbsp;I.H.*\&nbsp;; Nautsch,\&nbsp;C.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=40952&la=de'>Effects of isoniazid (INH) on the oogenesis of mice.</a></div>");
document.write("  <div class='source'>Hum. Genet. 42, 55-58 (1978)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Rittner,\&nbsp;C.K.*\&nbsp;; Opferkuch,\&nbsp;W.*\&nbsp;; Wellek,\&nbsp;B.*\&nbsp;; Grosse-Wilde,\&nbsp;H.\&nbsp;; Wernet,\&nbsp;P.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=33096&la=de'>Lack of linkage between gene(s) controlling the synthesis of the seventh component of complement and the HLA region on chromosome No. 6 in man.</a></div>");
document.write("  <div class='source'>Hum. Genet. 34, 137-142 (1976)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Rittner,\&nbsp;C.K.*\&nbsp;; Grosse-Wilde,\&nbsp;H.\&nbsp;; Rittner,\&nbsp;B.*\&nbsp;; Netzel,\&nbsp;B.\&nbsp;; Scholz,\&nbsp;S.*\&nbsp;; Lorenz,\&nbsp;H.*\&nbsp;; Albert,\&nbsp;E.D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=41389&la=de'>Linkage group HL-A-MLC-Bf (properdin factor B) - The site of the Bf locus at the immunogenetic linkage group on chromosome 6.</a></div>");
document.write("  <div class='source'>Hum. Genet. 27, 173-183 (1975)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Back,\&nbsp;F.\&nbsp;; Pohl,\&nbsp;W.\&nbsp;; Olbrich,\&nbsp;E.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42095&la=de'>Investigations of defining the arm ratio of the late replicating X-chromosome in man</a></div>");
document.write("  <div class='source'>Hum. Genet. 12, 302-315 (1971)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Lampert,\&nbsp;F.H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=33638&la=de'>Attachment of human chromatin fibers to the nuclear membrane, as seen by electron microscopy.</a></div>");
document.write("  <div class='source'>Hum. Genet. 13, 285-295 (1971)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bauchinger,\&nbsp;M.\&nbsp;; Schmid,\&nbsp;E.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42216&la=de'>Ein Fall mit balancierter (14p+; 15p-)-Translokation.</a></div>");
document.write("  <div class='source'>Hum. Genet. 8, 312-320 (1970)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Murken,\&nbsp;J.D.\&nbsp;; Bauchinger,\&nbsp;M.\&nbsp;; Palitzsch,\&nbsp;D.\&nbsp;; Pfeifer,\&nbsp;H.\&nbsp;; Suschke,\&nbsp;J.\&nbsp;; Haendle,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42524&la=de'>Trisomy D2 in a 21/2 years old girl (47,XX,14+).</a></div>");
document.write("  <div class='source'>Hum. Genet. 10, 254-268 (1970)</div>");
document.write("</div>");