document.write("<div class='record'>");
document.write("  <div class='authors'>Zanti,\&nbsp;M.*\&nbsp;; O\'Mahony,\&nbsp;D.G.*\&nbsp;; Parsons,\&nbsp;M.T.*\&nbsp;; Li,\&nbsp;H.*\&nbsp;; Dennis,\&nbsp;J.*\&nbsp;; Aittomäkkiki,\&nbsp;K.*\&nbsp;; Andrulis,\&nbsp;I.L.*\&nbsp;; Anton-Culver,\&nbsp;H.*\&nbsp;; Aronson,\&nbsp;K.J.*\&nbsp;; Augustinsson,\&nbsp;A.*\&nbsp;; Becher,\&nbsp;H.*\&nbsp;; Bojesen,\&nbsp;S.E.*\&nbsp;; Bolla,\&nbsp;M.K.*\&nbsp;; Brenner,\&nbsp;H.*\&nbsp;; Brown,\&nbsp;M.A.*\&nbsp;; Buys,\&nbsp;S.S.*\&nbsp;; Canzian,\&nbsp;F.*\&nbsp;; Caputo,\&nbsp;S.M.*\&nbsp;; Castelao,\&nbsp;J.E.*\&nbsp;; Chang-Claude,\&nbsp;J.*\&nbsp;; Czene,\&nbsp;K.*\&nbsp;; Daly,\&nbsp;M.B.*\&nbsp;; De Nicolo,\&nbsp;A.*\&nbsp;; Devilee,\&nbsp;P.*\&nbsp;; Dörk,\&nbsp;T.*\&nbsp;; Dunning,\&nbsp;A.M.*\&nbsp;; Dwek,\&nbsp;M.*\&nbsp;; Eccles,\&nbsp;D.M.*\&nbsp;; Engel,\&nbsp;C.*\&nbsp;; Evans,\&nbsp;D.G.*\&nbsp;; Fasching,\&nbsp;P.A.*\&nbsp;; Gago-Dominguez,\&nbsp;M.*\&nbsp;; Garcia-Closas,\&nbsp;M.*\&nbsp;; García-Sáenz,\&nbsp;J.A.*\&nbsp;; Gentry-Maharaj,\&nbsp;A.*\&nbsp;; Geurts-Giele,\&nbsp;W.R.R.*\&nbsp;; Giles,\&nbsp;G.G.*\&nbsp;; Glendon,\&nbsp;G.*\&nbsp;; Goldberg,\&nbsp;M.S.*\&nbsp;; Garcia,\&nbsp;E.B.G.*\&nbsp;; Gündert,\&nbsp;M.\&nbsp;; Guénel,\&nbsp;P.*\&nbsp;; Hahnen,\&nbsp;E.*\&nbsp;; Haiman,\&nbsp;C.A.*\&nbsp;; Hall,\&nbsp;P.*\&nbsp;; Hamann,\&nbsp;U.*\&nbsp;; Harkness,\&nbsp;E.F.*\&nbsp;; Hogervorst,\&nbsp;F.B.L.*\&nbsp;; Hollestelle,\&nbsp;A.*\&nbsp;; Hoppe,\&nbsp;R.*\&nbsp;; Hopper,\&nbsp;J.L.*\&nbsp;; Houdayer,\&nbsp;C.*\&nbsp;; Houlston,\&nbsp;R.S.*\&nbsp;; Howell,\&nbsp;A.*\&nbsp;; Investigators,\&nbsp;A.*\&nbsp;; Jakimovska,\&nbsp;M.*\&nbsp;; Jakubowska,\&nbsp;A.*\&nbsp;; Jernström,\&nbsp;H.*\&nbsp;; John,\&nbsp;E.M.*\&nbsp;; Kaaks,\&nbsp;R.*\&nbsp;; Kitahara,\&nbsp;C.M.*\&nbsp;; Koutros,\&nbsp;S.*\&nbsp;; Kraft,\&nbsp;P.*\&nbsp;; Kristensen,\&nbsp;V.N.*\&nbsp;; Lacey,\&nbsp;J.V.*\&nbsp;; Lambrechts,\&nbsp;D.*\&nbsp;; Leone,\&nbsp;M.*\&nbsp;; Lindblom,\&nbsp;A.*\&nbsp;; Lush,\&nbsp;M.*\&nbsp;; Mannermaa,\&nbsp;A.*\&nbsp;; Manoochehri,\&nbsp;M.*\&nbsp;; Manoukian,\&nbsp;S.*\&nbsp;; Margolin,\&nbsp;S.*\&nbsp;; Martinez,\&nbsp;M.E.*\&nbsp;; Menon,\&nbsp;U.*\&nbsp;; Milne,\&nbsp;R.L.*\&nbsp;; Monteiro,\&nbsp;A.N.*\&nbsp;; Murphy,\&nbsp;R.A.*\&nbsp;; Neuhausen,\&nbsp;S.L.*\&nbsp;; Nevanlinna,\&nbsp;H.*\&nbsp;; Newman,\&nbsp;W.G.*\&nbsp;; Offit,\&nbsp;K.*\&nbsp;; Park,\&nbsp;S.K.*\&nbsp;; James,\&nbsp;P.*\&nbsp;; Peterlongo,\&nbsp;P.*\&nbsp;; Peto,\&nbsp;J.*\&nbsp;; Plaseska-Karanfilska,\&nbsp;D.*\&nbsp;; Punie,\&nbsp;K.*\&nbsp;; Radice,\&nbsp;P.*\&nbsp;; Rashid,\&nbsp;M.U.*\&nbsp;; Rennert,\&nbsp;G.*\&nbsp;; Romero,\&nbsp;A.*\&nbsp;; Rosenberg,\&nbsp;E.H.*\&nbsp;; Saloustros,\&nbsp;E.*\&nbsp;; Sandler,\&nbsp;D.P.*\&nbsp;; Schmidt,\&nbsp;M.K.*\&nbsp;; Schmutzler,\&nbsp;R.K.*\&nbsp;; Shu,\&nbsp;X.*\&nbsp;; Simard,\&nbsp;J.*\&nbsp;; Southey,\&nbsp;M.C.*\&nbsp;; Stone,\&nbsp;J.*\&nbsp;; Stoppa-Lyonnet,\&nbsp;D.*\&nbsp;; Tamimi,\&nbsp;R.M.*\&nbsp;; Tapper,\&nbsp;W.J.*\&nbsp;; Taylor,\&nbsp;J.A.*\&nbsp;; Teo,\&nbsp;S.H.*\&nbsp;; Teras,\&nbsp;L.R.*\&nbsp;; Terry,\&nbsp;M.B.*\&nbsp;; Thomassen,\&nbsp;M.*\&nbsp;; Troester,\&nbsp;M.A.*\&nbsp;; Vachon,\&nbsp;C.M.*\&nbsp;; Vega,\&nbsp;A.*\&nbsp;; Vreeswijk,\&nbsp;M.P.G.*\&nbsp;; Wang,\&nbsp;Q.*\&nbsp;; Wappenschmidt,\&nbsp;B.*\&nbsp;; Weinberg,\&nbsp;C.R.*\&nbsp;; Wolk,\&nbsp;A.*\&nbsp;; Zheng,\&nbsp;W.*\&nbsp;; Feng,\&nbsp;B.*\&nbsp;; Couch,\&nbsp;F.J.*\&nbsp;; Spurdle,\&nbsp;A.B.*\&nbsp;; Easton,\&nbsp;D.F.*\&nbsp;; Goldgar,\&nbsp;D.E.*\&nbsp;; Michailidou,\&nbsp;K.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=69795&la=de'>A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: Application to \<em\>BRCA1\</em\> and \<em\>BRCA2\</em\>.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 2023:17 (2023)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Scala,\&nbsp;M.*\&nbsp;; Wortmann,\&nbsp;S.B.*\&nbsp;; Kaya,\&nbsp;N.*\&nbsp;; Stellingwerff,\&nbsp;M.D.*\&nbsp;; Pistorio,\&nbsp;A.*\&nbsp;; Glamuzina,\&nbsp;E.*\&nbsp;; van Karnebeek,\&nbsp;C.D.M.*\&nbsp;; Skrypnyk,\&nbsp;C.*\&nbsp;; Iwanicka-Pronicka,\&nbsp;K.*\&nbsp;; Piekutowska-Abramczuk,\&nbsp;D.*\&nbsp;; Ciara,\&nbsp;E.*\&nbsp;; Tort,\&nbsp;F.*\&nbsp;; Sheidley,\&nbsp;B.R.*\&nbsp;; Poduri,\&nbsp;A.*\&nbsp;; Jayakar,\&nbsp;P.*\&nbsp;; Jayakar,\&nbsp;A.*\&nbsp;; Upadia,\&nbsp;J.*\&nbsp;; Walano,\&nbsp;N.*\&nbsp;; Haack,\&nbsp;T.B.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Aldhalaan,\&nbsp;H.M.*\&nbsp;; Karimiani,\&nbsp;E.G.*\&nbsp;; Yildiz,\&nbsp;Y.*\&nbsp;; Ceylan,\&nbsp;A.C.*\&nbsp;; Dameron,\&nbsp;A.*\&nbsp;; Yang,\&nbsp;H.*\&nbsp;; Toosi,\&nbsp;M.B.*\&nbsp;; Ashrafzadeh,\&nbsp;F.*\&nbsp;; Akhondian,\&nbsp;J.*\&nbsp;; Imannezhad,\&nbsp;S.*\&nbsp;; Mirzadeh,\&nbsp;H.S.*\&nbsp;; Maqbool,\&nbsp;S.*\&nbsp;; Farid,\&nbsp;A.*\&nbsp;; Al-Muhaizea,\&nbsp;M.A.*\&nbsp;; Alshwameen,\&nbsp;M.O.*\&nbsp;; Aldowsari,\&nbsp;L.*\&nbsp;; Alsagob,\&nbsp;M.*\&nbsp;; Alyousef,\&nbsp;A.*\&nbsp;; Almass,\&nbsp;R.*\&nbsp;; AlHargan,\&nbsp;A.*\&nbsp;; Alwadei,\&nbsp;A.H.*\&nbsp;; AlRasheed,\&nbsp;M.M.*\&nbsp;; Colak,\&nbsp;D.*\&nbsp;; Alqudairy,\&nbsp;H.*\&nbsp;; Khan,\&nbsp;S.*\&nbsp;; Lines,\&nbsp;M.A.*\&nbsp;; García Cazorla,\&nbsp;M.*\&nbsp;; Ribes,\&nbsp;A.*\&nbsp;; Morava,\&nbsp;E.*\&nbsp;; Bibi,\&nbsp;F.*\&nbsp;; Haider,\&nbsp;S.*\&nbsp;; Ferla,\&nbsp;M.P.*\&nbsp;; Taylor,\&nbsp;J.C.*\&nbsp;; Alsaif,\&nbsp;H.S.*\&nbsp;; Firdous,\&nbsp;A.*\&nbsp;; Hashem,\&nbsp;M.*\&nbsp;; Shashkin,\&nbsp;C.*\&nbsp;; Koneev,\&nbsp;K.*\&nbsp;; Kaiyrzhanov,\&nbsp;R.*\&nbsp;; Efthymiou,\&nbsp;S.*\&nbsp;; Genomics,\&nbsp;Q.S.*\&nbsp;; Schmitt-Mechelke,\&nbsp;T.*\&nbsp;; Ziegler,\&nbsp;A.*\&nbsp;; Issa,\&nbsp;M.Y.*\&nbsp;; Elbendary,\&nbsp;H.M.*\&nbsp;; Striano,\&nbsp;P.*\&nbsp;; Alkuraya,\&nbsp;F.S.*\&nbsp;; Zaki,\&nbsp;M.S.*\&nbsp;; Gleeson,\&nbsp;J.G.*\&nbsp;; Barakat,\&nbsp;T.S.*\&nbsp;; Bierau,\&nbsp;J.*\&nbsp;; van der Knaap,\&nbsp;M.S.*\&nbsp;; Maroofian,\&nbsp;R.*\&nbsp;; Houlden,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=64010&la=de'>Clinico-radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 43, 403-419 (2022)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Smirnov,\&nbsp;D.\&nbsp;; Schlieben,\&nbsp;L.D.\&nbsp;; Peymani,\&nbsp;F.\&nbsp;; Berutti,\&nbsp;R.\&nbsp;; Prokisch,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=65473&la=de'>Guidelines for clinical interpretation of variant pathogenicity using RNA phenotypes.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 43, 1056-1070 (2022)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Itai,\&nbsp;T.*\&nbsp;; Hamanaka,\&nbsp;K.*\&nbsp;; Sasaki,\&nbsp;K.*\&nbsp;; Wagner,\&nbsp;M.\&nbsp;; Kotzaeridou,\&nbsp;U.*\&nbsp;; Brosse,\&nbsp;I.*\&nbsp;; Ries,\&nbsp;M.*\&nbsp;; Kobayashi,\&nbsp;Y.*\&nbsp;; Tohyama,\&nbsp;J.*\&nbsp;; Kato,\&nbsp;M.*\&nbsp;; Ong,\&nbsp;W.P.*\&nbsp;; Chew,\&nbsp;H.B.*\&nbsp;; Rethanavelu,\&nbsp;K.*\&nbsp;; Ranza,\&nbsp;E.*\&nbsp;; Blanc,\&nbsp;X.*\&nbsp;; Uchiyama,\&nbsp;Y.*\&nbsp;; Tsuchida,\&nbsp;N.*\&nbsp;; Fujita,\&nbsp;A.*\&nbsp;; Azuma,\&nbsp;Y.*\&nbsp;; Koshimizu,\&nbsp;E.*\&nbsp;; Mizuguchi,\&nbsp;T.*\&nbsp;; Takata,\&nbsp;A.*\&nbsp;; Miyake,\&nbsp;N.*\&nbsp;; Takahashi,\&nbsp;H.*\&nbsp;; Miyagi,\&nbsp;E.*\&nbsp;; Tsurusaki,\&nbsp;Y.*\&nbsp;; Doi,\&nbsp;H.*\&nbsp;; Taguri,\&nbsp;M.*\&nbsp;; Antonarakis,\&nbsp;S.E.*\&nbsp;; Nakashima,\&nbsp;M.*\&nbsp;; Saitsu,\&nbsp;H.*\&nbsp;; Miyatake,\&nbsp;S.*\&nbsp;; Matsumoto,\&nbsp;N.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60596&la=de'>De novo variants in \<em\>CELF2\</em\>\&nbsp; that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 42, 66-76 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Neuser,\&nbsp;S.*\&nbsp;; Brechmann,\&nbsp;B.*\&nbsp;; Heimer,\&nbsp;G.*\&nbsp;; Brösse,\&nbsp;I.*\&nbsp;; Schubert,\&nbsp;S.*\&nbsp;; O\'Grady,\&nbsp;L.*\&nbsp;; Zech,\&nbsp;M.\&nbsp;; Srivastava,\&nbsp;S.*\&nbsp;; Sweetser,\&nbsp;D.A.*\&nbsp;; Dincer,\&nbsp;Y.*\&nbsp;; Mall,\&nbsp;V.*\&nbsp;; Winkelmann,\&nbsp;J.\&nbsp;; Behrends,\&nbsp;C.*\&nbsp;; Darras,\&nbsp;B.T.*\&nbsp;; Graham,\&nbsp;R.J.*\&nbsp;; Jayakar,\&nbsp;P.*\&nbsp;; Byrne,\&nbsp;B.*\&nbsp;; El Bar-Aluma,\&nbsp;B.*\&nbsp;; Haberman,\&nbsp;Y.*\&nbsp;; Szeinberg,\&nbsp;A.*\&nbsp;; Aldhalaan,\&nbsp;H.M.*\&nbsp;; Hashem,\&nbsp;M.*\&nbsp;; Tenaiji,\&nbsp;A.A.*\&nbsp;; Ismayl,\&nbsp;O.*\&nbsp;; Al Nuaimi,\&nbsp;A.E.*\&nbsp;; Maher,\&nbsp;K.*\&nbsp;; Ibrahim,\&nbsp;S.*\&nbsp;; Khan,\&nbsp;F.*\&nbsp;; Houlden,\&nbsp;H.*\&nbsp;; Ramakumaran,\&nbsp;V.S.*\&nbsp;; Pagnamenta,\&nbsp;A.T.*\&nbsp;; Posey,\&nbsp;J.E.*\&nbsp;; Lupski,\&nbsp;J.R.*\&nbsp;; Tan,\&nbsp;W.H.*\&nbsp;; ElGhazali,\&nbsp;G.*\&nbsp;; Herman,\&nbsp;I.*\&nbsp;; Muñoz,\&nbsp;T.*\&nbsp;; Repetto,\&nbsp;G.M.*\&nbsp;; Seitz,\&nbsp;A.*\&nbsp;; Krumbiegel,\&nbsp;M.*\&nbsp;; Cecilia Poli,\&nbsp;M.*\&nbsp;; Kini,\&nbsp;U.*\&nbsp;; Efthymiou,\&nbsp;S.*\&nbsp;; Meiler,\&nbsp;J.*\&nbsp;; Maroofian,\&nbsp;R.*\&nbsp;; Alkuraya,\&nbsp;F.S.*\&nbsp;; Jamra,\&nbsp;R.A.*\&nbsp;; Popp,\&nbsp;B.*\&nbsp;; Ben-Zeev,\&nbsp;B.*\&nbsp;; Ebrahimi-Fakhari,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61776&la=de'>Clinical, neuroimaging and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 42, 762-776 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Stenton,\&nbsp;S.\&nbsp;; Piekutowska-Abramczuk,\&nbsp;D.*\&nbsp;; Kulterer,\&nbsp;L.\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Claeys,\&nbsp;K.G.*\&nbsp;; Ciara,\&nbsp;E.*\&nbsp;; Eisen,\&nbsp;J.*\&nbsp;; Płoski,\&nbsp;R.*\&nbsp;; Pronicka,\&nbsp;E.*\&nbsp;; Malczyk,\&nbsp;K.*\&nbsp;; Wagner,\&nbsp;M.\&nbsp;; Wortmann,\&nbsp;S.B.\&nbsp;; Prokisch,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60970&la=de'>Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significance.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 42, 310-319 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Torraco,\&nbsp;A.*\&nbsp;; Nasca,\&nbsp;A.*\&nbsp;; Verrigni,\&nbsp;D.*\&nbsp;; Pennisi,\&nbsp;A.*\&nbsp;; Zaki,\&nbsp;M.S.*\&nbsp;; Olivieri,\&nbsp;G.*\&nbsp;; Assouline,\&nbsp;Z.*\&nbsp;; Martinelli,\&nbsp;D.*\&nbsp;; Maroofian,\&nbsp;R.*\&nbsp;; Rizza,\&nbsp;T.*\&nbsp;; Di Nottia,\&nbsp;M.*\&nbsp;; Invernizzi,\&nbsp;F.*\&nbsp;; Lamantea,\&nbsp;E.*\&nbsp;; Longo,\&nbsp;D.*\&nbsp;; Houlden,\&nbsp;H.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Rötig,\&nbsp;A.*\&nbsp;; Dionisi-Vici,\&nbsp;C.*\&nbsp;; Bertini,\&nbsp;E.*\&nbsp;; Ghezzi,\&nbsp;D.*\&nbsp;; Carrozzo,\&nbsp;R.*\&nbsp;; Diodato,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=61540&la=de'>Novel \<em\>NDUFA12\</em\> variants are associated with isolated complex I defect and variable clinical manifestation.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 42, 699-710 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Ascari,\&nbsp;G.*\&nbsp;; Peelman,\&nbsp;F.*\&nbsp;; Farinelli,\&nbsp;P.*\&nbsp;; Rosseel,\&nbsp;T.*\&nbsp;; Lambrechts,\&nbsp;N.*\&nbsp;; Wunderlich,\&nbsp;K.A.*\&nbsp;; Wagner,\&nbsp;M.\&nbsp;; Nikopoulos,\&nbsp;K.*\&nbsp;; Martens,\&nbsp;P.*\&nbsp;; Balikova,\&nbsp;I.*\&nbsp;; Derycke,\&nbsp;L.*\&nbsp;; Holtappels,\&nbsp;G.*\&nbsp;; Krysko,\&nbsp;O.*\&nbsp;; Van Laethem,\&nbsp;T.*\&nbsp;; De Jaegere,\&nbsp;S.*\&nbsp;; Guillemyn,\&nbsp;B.*\&nbsp;; De Rycke,\&nbsp;R.*\&nbsp;; de Bleecker,\&nbsp;J.*\&nbsp;; Creytens,\&nbsp;D.*\&nbsp;; Van Dorpe,\&nbsp;J.*\&nbsp;; Gerris,\&nbsp;J.*\&nbsp;; Bachert,\&nbsp;C.*\&nbsp;; Neuhofer,\&nbsp;C.*\&nbsp;; Walraedt,\&nbsp;S.*\&nbsp;; Bischoff,\&nbsp;A.*\&nbsp;; Pedersen,\&nbsp;L.B.*\&nbsp;; Klopstock,\&nbsp;T.*\&nbsp;; Rivolta,\&nbsp;C.*\&nbsp;; Leroy,\&nbsp;B.P.*\&nbsp;; de Baere,\&nbsp;E.*\&nbsp;; Coppieters,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=58688&la=de'>Functional characterization of the first missense variant in \<em\>CEP78\</em\>, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 41, 998-1011 (2020)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Saoura,\&nbsp;M.*\&nbsp;; Powell,\&nbsp;C.A.*\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Alahmad,\&nbsp;A.*\&nbsp;; Al-Balool,\&nbsp;H.H.*\&nbsp;; Albash,\&nbsp;B.*\&nbsp;; Alfadhel,\&nbsp;M.*\&nbsp;; Alston,\&nbsp;C.L.*\&nbsp;; Bertini,\&nbsp;E.*\&nbsp;; Bonnen,\&nbsp;P.*\&nbsp;; Bratkovic,\&nbsp;D.*\&nbsp;; Carrozzo,\&nbsp;R.*\&nbsp;; Donati,\&nbsp;M.A.*\&nbsp;; Nottia,\&nbsp;M.D.*\&nbsp;; Ghezzi,\&nbsp;D.*\&nbsp;; Goldstein,\&nbsp;A.*\&nbsp;; Haan,\&nbsp;E.*\&nbsp;; Horvath,\&nbsp;R.*\&nbsp;; Hughes,\&nbsp;J.*\&nbsp;; Invernizzi,\&nbsp;F.*\&nbsp;; Lamantea,\&nbsp;E.*\&nbsp;; Lucas,\&nbsp;B.*\&nbsp;; Pinnock,\&nbsp;K.G.*\&nbsp;; Pujantell,\&nbsp;M.*\&nbsp;; Rahman,\&nbsp;S.*\&nbsp;; Rebelo-Guiomar,\&nbsp;P.*\&nbsp;; Santra,\&nbsp;S.*\&nbsp;; Verrigni,\&nbsp;D.*\&nbsp;; McFarland,\&nbsp;R.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Taylor,\&nbsp;R.W.*\&nbsp;; Levinger,\&nbsp;L.*\&nbsp;; Minczuk,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=55976&la=de'>Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3 \'-end processing.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 40, 1731-1748 (2019)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Suleiman,\&nbsp;J.*\&nbsp;; Riedhammer,\&nbsp;K.M.\&nbsp;; Jicinsky,\&nbsp;T.*\&nbsp;; Mundt,\&nbsp;M.*\&nbsp;; Werner,\&nbsp;L.*\&nbsp;; Gusic,\&nbsp;M.\&nbsp;; Burgemeister,\&nbsp;A.L.*\&nbsp;; Alsaif,\&nbsp;H.S.*\&nbsp;; Abdulrahim,\&nbsp;M.*\&nbsp;; Moghrabi,\&nbsp;N.N.*\&nbsp;; Nicolas-Jilwan,\&nbsp;M.*\&nbsp;; AlSayed,\&nbsp;M.*\&nbsp;; Bi,\&nbsp;W.*\&nbsp;; Sampath,\&nbsp;S.*\&nbsp;; Alkuraya,\&nbsp;F.S.*\&nbsp;; El-Hattab,\&nbsp;A.W.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=56343&la=de'>Homozygous loss-of-function variants of \<em\>TASP1\</em\>, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 40, 1985-1992 (2019)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bruni,\&nbsp;F.*\&nbsp;; Meo,\&nbsp;I.D.*\&nbsp;; Bellacchio,\&nbsp;E.*\&nbsp;; Webb,\&nbsp;B.D.*\&nbsp;; McFarland,\&nbsp;R.*\&nbsp;; Chrzanowska-Lightowlers,\&nbsp;Z.M.A.*\&nbsp;; He,\&nbsp;L.*\&nbsp;; Skorupa,\&nbsp;E.*\&nbsp;; Moroni,\&nbsp;I.*\&nbsp;; Ardissone,\&nbsp;A.*\&nbsp;; Walczak,\&nbsp;A.*\&nbsp;; Tyynismaa,\&nbsp;H.*\&nbsp;; Isohanni,\&nbsp;P.*\&nbsp;; Mandel,\&nbsp;H.*\&nbsp;; Prokisch,\&nbsp;H.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Bonnen,\&nbsp;P.E.*\&nbsp;; Enrico,\&nbsp;B.*\&nbsp;; Pronicka,\&nbsp;E.*\&nbsp;; Ghezzi,\&nbsp;D.*\&nbsp;; Taylor,\&nbsp;R.W.*\&nbsp;; Diodato,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52701&la=de'>Clinical, biochemical, and genetic features associated with VARS2-related mitochondrial disease.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 39, 563-578 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>El-Hattab,\&nbsp;A.W.*\&nbsp;; Dai,\&nbsp;H.*\&nbsp;; Almannai,\&nbsp;M.*\&nbsp;; Wang,\&nbsp;J.*\&nbsp;; Faqeih,\&nbsp;E.A.*\&nbsp;; Al Asmari,\&nbsp;A.*\&nbsp;; Saleh,\&nbsp;M.A.M.*\&nbsp;; Elamin,\&nbsp;M.A.O.*\&nbsp;; Alfadhel,\&nbsp;M.*\&nbsp;; Alkuraya,\&nbsp;F.S.*\&nbsp;; Hashem,\&nbsp;M.*\&nbsp;; Aldosary,\&nbsp;M.S.*\&nbsp;; Almass,\&nbsp;R.*\&nbsp;; Almutairi,\&nbsp;F.B.*\&nbsp;; Alsagob,\&nbsp;M.*\&nbsp;; Al-Owain,\&nbsp;M.*\&nbsp;; Al-Sharfa,\&nbsp;S.*\&nbsp;; Al-Hassnan,\&nbsp;Z.N.*\&nbsp;; Rahbeeni,\&nbsp;Z.*\&nbsp;; Al-Muhaizea,\&nbsp;M.A.*\&nbsp;; Makhseed,\&nbsp;N.*\&nbsp;; Foskett,\&nbsp;G.K.*\&nbsp;; Stevenson,\&nbsp;D.A.*\&nbsp;; Gomez-Ospina,\&nbsp;N.*\&nbsp;; Lee,\&nbsp;C.*\&nbsp;; Boles,\&nbsp;R.G.*\&nbsp;; Schrier Vergano,\&nbsp;S.A.*\&nbsp;; Wortmann,\&nbsp;S.B.\&nbsp;; Sperl,\&nbsp;W.*\&nbsp;; Opladen,\&nbsp;T.*\&nbsp;; Hoffmann,\&nbsp;G.F.*\&nbsp;; Hempel,\&nbsp;M.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Alhaddad,\&nbsp;B.\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Chan,\&nbsp;W.*\&nbsp;; Kaya,\&nbsp;N.*\&nbsp;; Wong,\&nbsp;L.J.C.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52274&la=de'>Molecular and clinical spectra of FBXL4 deficiency.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 38, 1649-1659 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kreimer,\&nbsp;A.*\&nbsp;; Zeng,\&nbsp;H.*\&nbsp;; Edwards,\&nbsp;M.D.*\&nbsp;; Guo,\&nbsp;Y.*\&nbsp;; Tian,\&nbsp;K.*\&nbsp;; Shin,\&nbsp;S.*\&nbsp;; Welch,\&nbsp;R.*\&nbsp;; Wainberg,\&nbsp;M.*\&nbsp;; Mohan,\&nbsp;R.*\&nbsp;; Sinnott-Armstrong,\&nbsp;N.A.*\&nbsp;; Li,\&nbsp;Y.*\&nbsp;; Eraslan,\&nbsp;G.\&nbsp;; Amin,\&nbsp;T.B.*\&nbsp;; Goke,\&nbsp;J.*\&nbsp;; Müller,\&nbsp;N.S.\&nbsp;; Kellis,\&nbsp;M.*\&nbsp;; Kundaje,\&nbsp;A.*\&nbsp;; Beer,\&nbsp;M.A.*\&nbsp;; Keles,\&nbsp;S.*\&nbsp;; Gifford,\&nbsp;D.K.*\&nbsp;; Yosef,\&nbsp;N.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=50642&la=de'>Predicting gene expression in massively parallel reporter assays: A comparative study.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 38, 1240-1250 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Wambach,\&nbsp;J.A.*\&nbsp;; Stettner,\&nbsp;G.M.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Writzl,\&nbsp;K.*\&nbsp;; Škofljanec,\&nbsp;A.*\&nbsp;; Maver,\&nbsp;A.*\&nbsp;; Munell,\&nbsp;F.*\&nbsp;; Ossowski,\&nbsp;S.*\&nbsp;; Bosio,\&nbsp;M.*\&nbsp;; Wegner,\&nbsp;D.J.*\&nbsp;; Shinawi,\&nbsp;M.*\&nbsp;; Baldridge,\&nbsp;D.*\&nbsp;; Alhaddad,\&nbsp;B.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Grange,\&nbsp;D.K.*\&nbsp;; Wilichowski,\&nbsp;E.*\&nbsp;; Troxell,\&nbsp;R.*\&nbsp;; Collins,\&nbsp;J.E.*\&nbsp;; Warner,\&nbsp;B.B.*\&nbsp;; Schmidt,\&nbsp;R.E.*\&nbsp;; Pestronk,\&nbsp;A.*\&nbsp;; Cole,\&nbsp;F.S.*\&nbsp;; Steinfeld,\&nbsp;R.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52128&la=de'>Survival among children with \&ldquo;Lethal\&rdquo; congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN).</a></div>");
document.write("  <div class='source'>Hum. Mutat. 38, 1477-1484 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Wortmann,\&nbsp;S.B.\&nbsp;; Timal,\&nbsp;S.*\&nbsp;; Venselaar,\&nbsp;H.*\&nbsp;; Wintjes,\&nbsp;L.T.*\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Feichtinger,\&nbsp;R.G.*\&nbsp;; Onnekink,\&nbsp;C.*\&nbsp;; Mühlmeister,\&nbsp;M.*\&nbsp;; Brandt,\&nbsp;U.*\&nbsp;; Smeitink,\&nbsp;J.A.M.*\&nbsp;; Veltman,\&nbsp;J.A.*\&nbsp;; Sperl,\&nbsp;W.*\&nbsp;; Lefeber,\&nbsp;D.J.*\&nbsp;; Pruijn,\&nbsp;G.J.M.*\&nbsp;; Stojanovic,\&nbsp;V.*\&nbsp;; Freisinger,\&nbsp;P.*\&nbsp;; V Spronsen,\&nbsp;F.*\&nbsp;; Derks,\&nbsp;T.G.*\&nbsp;; Veenstra-Knol,\&nbsp;H.E.*\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Rötig,\&nbsp;A.*\&nbsp;; Tarnopolsky,\&nbsp;M.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Rodenburg,\&nbsp;R.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51893&la=de'>Biallelic variants in \<em\>WARS2 \</em\>encoding mitochondrial tryptophanyl-tRNA synthase in six individuals with mitochondrial encephalopathy.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 38, 1786-1795 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Bögershausen,\&nbsp;N.*\&nbsp;; Gatinois,\&nbsp;V.*\&nbsp;; Riehmer,\&nbsp;V.*\&nbsp;; Kayserili,\&nbsp;H.*\&nbsp;; Becker,\&nbsp;J.*\&nbsp;; Thoenes,\&nbsp;M.*\&nbsp;; Simsek-Kiper,\&nbsp;P.*\&nbsp;; Barat-Houari,\&nbsp;M.*\&nbsp;; Elcioğlu,\&nbsp;N.H.*\&nbsp;; Wieczorek,\&nbsp;D.*\&nbsp;; Tinschert,\&nbsp;S.*\&nbsp;; Sarrabay,\&nbsp;G.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Fabre,\&nbsp;A.*\&nbsp;; Baynam,\&nbsp;G.*\&nbsp;; Sanchez,\&nbsp;E.*\&nbsp;; Nurnberg,\&nbsp;G.*\&nbsp;; Altunoglu,\&nbsp;U.*\&nbsp;; Capri,\&nbsp;Y.*\&nbsp;; Isidor,\&nbsp;B.*\&nbsp;; Lacombe,\&nbsp;D.*\&nbsp;; Corsini,\&nbsp;C.*\&nbsp;; Cormier-Daire,\&nbsp;V.*\&nbsp;; Sanlaville,\&nbsp;D.*\&nbsp;; Giuliano,\&nbsp;F.*\&nbsp;; Sang,\&nbsp;K.L.*\&nbsp;; Kayirangwa,\&nbsp;H.*\&nbsp;; Nürnberg,\&nbsp;P.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Boduroglu,\&nbsp;K.*\&nbsp;; Zoll,\&nbsp;B.*\&nbsp;; Lyonnet,\&nbsp;S.*\&nbsp;; Tzschach,\&nbsp;A.*\&nbsp;; Verloes,\&nbsp;A.*\&nbsp;; Donato,\&nbsp;N.D.*\&nbsp;; Touitou,\&nbsp;I.*\&nbsp;; Netzer,\&nbsp;C.*\&nbsp;; Li,\&nbsp;Y.*\&nbsp;; Geneviève,\&nbsp;D.*\&nbsp;; Yigit,\&nbsp;G.*\&nbsp;; Wollnik,\&nbsp;B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=48929&la=de'>Mutation update for Kabuki syndrome genes \<em\>KMT2D\</em\> and \<em\>KDM6A\</em\> and further delineation of X-linked Kabuki syndrome subtype 2.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 37, 847-864 (2016)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Diodato,\&nbsp;D.*\&nbsp;; Melchionda,\&nbsp;L.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Dallabona,\&nbsp;C.*\&nbsp;; Baruffini,\&nbsp;E.*\&nbsp;; Donnini,\&nbsp;C.*\&nbsp;; Granata,\&nbsp;T.*\&nbsp;; Ragona,\&nbsp;F.*\&nbsp;; Balestri,\&nbsp;P.*\&nbsp;; Margollicci,\&nbsp;M.*\&nbsp;; Lamantea,\&nbsp;E.*\&nbsp;; Nasca,\&nbsp;A.*\&nbsp;; Powell,\&nbsp;C.A.*\&nbsp;; Minczuk,\&nbsp;M.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Lamperti,\&nbsp;C.*\&nbsp;; Zeviani,\&nbsp;M.*\&nbsp;; Ghezzi,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=31535&la=de'>\<em\>VARS2\</em\> and \<em\>TARS2\</em\> mutations in patients with mitochondrial encephalomyopathies.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 35, 983-989 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Baruffini,\&nbsp;E.*\&nbsp;; Dallabona,\&nbsp;C.*\&nbsp;; Invernizzi,\&nbsp;F.*\&nbsp;; Yarham,\&nbsp;J.W.*\&nbsp;; Melchionda,\&nbsp;L.*\&nbsp;; Blakely,\&nbsp;E.L.*\&nbsp;; Lamantea,\&nbsp;E.*\&nbsp;; Donnini,\&nbsp;C.*\&nbsp;; Santra,\&nbsp;S.*\&nbsp;; Vijayaraghavan,\&nbsp;S.*\&nbsp;; Roper,\&nbsp;H.P.*\&nbsp;; Burlina,\&nbsp;A.*\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Walther,\&nbsp;A.\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Taylor,\&nbsp;R.W.*\&nbsp;; Ferrero,\&nbsp;I.*\&nbsp;; Zeviani,\&nbsp;M.*\&nbsp;; Ghezzi,\&nbsp;D.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=27564&la=de'>\<em\>MTO1\</em\> mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 34, 1501-1509 (2013)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Parzefall,\&nbsp;T.*\&nbsp;; Shivatzki,\&nbsp;S.*\&nbsp;; Lenz,\&nbsp;D.R.*\&nbsp;; Rathkolb,\&nbsp;B.\&nbsp;; Ushakov,\&nbsp;K.*\&nbsp;; Karfunkel,\&nbsp;D.*\&nbsp;; Shapira,\&nbsp;Y.*\&nbsp;; Wolf,\&nbsp;M.*\&nbsp;; Mohr,\&nbsp;M.*\&nbsp;; Wolf,\&nbsp;E.*\&nbsp;; Sabrautzki,\&nbsp;S.\&nbsp;; Hrabě de Angelis,\&nbsp;M.\&nbsp;; Frydman,\&nbsp;M.*\&nbsp;; Brownstein,\&nbsp;Z.*\&nbsp;; Avraham,\&nbsp;K.B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=25697&la=de'>Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and mice.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 34, 1102-1110 (2013)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Horn,\&nbsp;D.*\&nbsp;; Kapeller,\&nbsp;J.*\&nbsp;; Rivera-Brugues,\&nbsp;N.\&nbsp;; Moog,\&nbsp;U.*\&nbsp;; Lorenz-Depiereux,\&nbsp;B.\&nbsp;; Eck,\&nbsp;S.H.\&nbsp;; Hempel,\&nbsp;M.*\&nbsp;; Wagenstaller,\&nbsp;J.\&nbsp;; Gawthrope,\&nbsp;A.*\&nbsp;; Monaco,\&nbsp;A.P.*\&nbsp;; Bonin,\&nbsp;M.*\&nbsp;; Riess,\&nbsp;O.*\&nbsp;; Wohlleber,\&nbsp;E.*\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Bezzina,\&nbsp;C.R.*\&nbsp;; Franke,\&nbsp;A.*\&nbsp;; Spranger,\&nbsp;S.*\&nbsp;; Villavicencio-Lorini,\&nbsp;P.*\&nbsp;; Seifert,\&nbsp;W.*\&nbsp;; Rosenfeld,\&nbsp;J.*\&nbsp;; Klopocki,\&nbsp;E.*\&nbsp;; Rappold,\&nbsp;G.A.*\&nbsp;; Strom,\&nbsp;T.M.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=618&la=de'>Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 31, E1851-E1860 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Manke,\&nbsp;T.*\&nbsp;; Heinig,\&nbsp;M.*\&nbsp;; Vingron,\&nbsp;M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44973&la=de'>Quantifying the effect of sequence variation on regulatory interactions.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 31, 477-483 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Molatore,\&nbsp;S.\&nbsp;; Marinoni,\&nbsp;I.\&nbsp;; Lee,\&nbsp;M.S.\&nbsp;; Pulz,\&nbsp;E.\&nbsp;; Ambrosio,\&nbsp;M.R.*\&nbsp;; degli Uberti,\&nbsp;E.C.*\&nbsp;; Zatelli,\&nbsp;M.C.*\&nbsp;; Pellegata,\&nbsp;N.S.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2160&la=de'>A novel germline CDKN1B mutation causing multiple endocrine tumors: Clinical, genetic and functional characterization.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 31, E1825-E1835 (2010)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fritsche,\&nbsp;L.G.*\&nbsp;; Freitag-Wolf,\&nbsp;S.*\&nbsp;; Bettecken,\&nbsp;T.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Keilhauer,\&nbsp;C.N.*\&nbsp;; Krawczak,\&nbsp;M.*\&nbsp;; Weber,\&nbsp;B.H.F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2466&la=de'>Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 30, 1048-1053 (2009)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Collin,\&nbsp;R.W.*\&nbsp;; Kalay,\&nbsp;E.*\&nbsp;; Oostrik,\&nbsp;J.*\&nbsp;; Caylan,\&nbsp;R.*\&nbsp;; Wollnik,\&nbsp;B.*\&nbsp;; Arslan,\&nbsp;S.*\&nbsp;; den Hollander,\&nbsp;A.I.*\&nbsp;; Birinci,\&nbsp;Y.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Toraman,\&nbsp;B.*\&nbsp;; Hoefsloot,\&nbsp;L.H.*\&nbsp;; Cremers,\&nbsp;C.W.*\&nbsp;; Brunner,\&nbsp;H.G.*\&nbsp;; Cremers,\&nbsp;F.P.*\&nbsp;; Karaguzel,\&nbsp;A.*\&nbsp;; Kremer,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=2727&la=de'>Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 28, 718-723 (2007)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fisher,\&nbsp;S.A.*\&nbsp;; Rivera,\&nbsp;A.*\&nbsp;; Fritsche,\&nbsp;L.G.*\&nbsp;; Keilhauer,\&nbsp;C.N.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Rudolph,\&nbsp;G.*\&nbsp;; Weber,\&nbsp;B.H.F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4167&la=de'>Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).</a></div>");
document.write("  <div class='source'>Hum. Mutat. 28, 406-413 (2007)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Schoenborn,\&nbsp;V.*\&nbsp;; Gohlke,\&nbsp;H.\&nbsp;; Heid,\&nbsp;I.M.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Utermann,\&nbsp;G.*\&nbsp;; Kronenberg,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4769&la=de'>Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: To separate the wheat from the chaff.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 28, 1141-1149 (2007)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kalay,\&nbsp;E.*\&nbsp;; Li,\&nbsp;Y.*\&nbsp;; Uzumcu,\&nbsp;A.*\&nbsp;; Uyguner,\&nbsp;O.*\&nbsp;; Collin,\&nbsp;R.W.*\&nbsp;; Caylan,\&nbsp;R.*\&nbsp;; Ulubil-Emiroglu,\&nbsp;M.*\&nbsp;; Kersten,\&nbsp;F.F.*\&nbsp;; Hafiz,\&nbsp;G.*\&nbsp;; van Wijk,\&nbsp;E.*\&nbsp;; Kayserili,\&nbsp;H.*\&nbsp;; Rohmann,\&nbsp;E.*\&nbsp;; Wagenstaller,\&nbsp;J.*\&nbsp;; Hoefsloot,\&nbsp;L.H.*\&nbsp;; Strom,\&nbsp;T.M.*\&nbsp;; Nurnberg,\&nbsp;G.*\&nbsp;; Baserer,\&nbsp;N.*\&nbsp;; den Hollander,\&nbsp;A.I.*\&nbsp;; Cremers,\&nbsp;F.P.*\&nbsp;; Cremers,\&nbsp;C.W.*\&nbsp;; Becker,\&nbsp;C.*\&nbsp;; Brunner,\&nbsp;H.G.*\&nbsp;; Nürnberg,\&nbsp;P.*\&nbsp;; Karaguzel,\&nbsp;A.*\&nbsp;; Basaran,\&nbsp;S.*\&nbsp;; Kubisch,\&nbsp;C.*\&nbsp;; Kremer,\&nbsp;H.*\&nbsp;; Wollnik,\&nbsp;B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4533&la=de'>Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 27, 633-639 (2006)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Jaremko,\&nbsp;M.*\&nbsp;; Justenhoven,\&nbsp;C.*\&nbsp;; Abraham,\&nbsp;B.K.*\&nbsp;; Schroth,\&nbsp;W.*\&nbsp;; Fritz,\&nbsp;P.*\&nbsp;; Brod,\&nbsp;S.*\&nbsp;; Vollmert,\&nbsp;C.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Brauch,\&nbsp;H.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4547&la=de'>MALDI-TOF MS and TaqMan\&reg; assisted SNP genotyping of DNA isolated from formalin-fixed and paraffin-embedded tissues (FFPET).</a></div>");
document.write("  <div class='source'>Hum. Mutat. 25, 232-238 (2005)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Rubie,\&nbsp;C.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Gärtner,\&nbsp;J.*\&nbsp;; Siekiera,\&nbsp;M.*\&nbsp;; Uziel,\&nbsp;G.*\&nbsp;; Kohlmann,\&nbsp;B.*\&nbsp;; Kohlschütter,\&nbsp;A.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Stöber,\&nbsp;G.*\&nbsp;; Bettecken,\&nbsp;T.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22431&la=de'>Sequence diversity of \<em\>KIAA0027/MLC1\</em\>: Are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?</a></div>");
document.write("  <div class='source'>Hum. Mutat. 21, 45-52 (2003)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Calzada-Wack,\&nbsp;J.\&nbsp;; Schnitzbauer,\&nbsp;U.\&nbsp;; Walch,\&nbsp;A.K.*\&nbsp;; Wurster,\&nbsp;K.-H.*\&nbsp;; Kappler,\&nbsp;R.\&nbsp;; Nathrath,\&nbsp;M.\&nbsp;; Hahn,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=9529&la=de'>Analysis of the PTCH Coding Region in Human Rhabdomyosarcoma.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 20, 233-234 (2002)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>von Brederlow,\&nbsp;B.*\&nbsp;; Bolz,\&nbsp;H.*\&nbsp;; Janecke,\&nbsp;A.*\&nbsp;; La O Cabrera,\&nbsp;A.*\&nbsp;; Rudolph,\&nbsp;G.\&nbsp;; Lorenz,\&nbsp;B.*\&nbsp;; Schwinger,\&nbsp;E.*\&nbsp;; Gal,\&nbsp;A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=9528&la=de'>Identification and In Vitro Expression of Novel CDH23 Mutations of Patients with Usher Syndrome Type 1D.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 19, 268-273 (2002)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Werner,\&nbsp;M.\&nbsp;; Sych,\&nbsp;M.*\&nbsp;; Herbon,\&nbsp;N.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; König,\&nbsp;I.R.*\&nbsp;; Wjst,\&nbsp;M.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=22066&la=de'>Large-Scale Determination of SNP Allele Frequencies in DNA Pools Using MALDI-TOF Mass Spectrometry.</a></div>");
document.write("  <div class='source'>Hum. Mutat. 20, 57-64 (2002)</div>");
document.write("</div>");