document.write("<div class='record'>");
document.write("  <div class='authors'>Hammann,\&nbsp;N.*\&nbsp;; Lenz,\&nbsp;D.*\&nbsp;; Baric,\&nbsp;I.*\&nbsp;; Crushell,\&nbsp;E.*\&nbsp;; Vici,\&nbsp;C.D.*\&nbsp;; Distelmaier,\&nbsp;F.*\&nbsp;; Feillet,\&nbsp;F.*\&nbsp;; Freisinger,\&nbsp;P.*\&nbsp;; Hempel,\&nbsp;M.*\&nbsp;; Khoreva,\&nbsp;A.L.*\&nbsp;; Laass,\&nbsp;M.W.*\&nbsp;; Lacassie,\&nbsp;Y.*\&nbsp;; Lainka,\&nbsp;E.*\&nbsp;; Larson-Nath,\&nbsp;C.*\&nbsp;; Li,\&nbsp;Z.*\&nbsp;; Lipiński,\&nbsp;P.*\&nbsp;; Lurz,\&nbsp;E.*\&nbsp;; Megarbane,\&nbsp;A.*\&nbsp;; Nobre,\&nbsp;S.*\&nbsp;; Olivieri,\&nbsp;G.*\&nbsp;; Peters,\&nbsp;B.*\&nbsp;; Prontera,\&nbsp;P.*\&nbsp;; Schlieben,\&nbsp;L.D.\&nbsp;; Seroogy,\&nbsp;C.M.*\&nbsp;; Sobacchi,\&nbsp;C.*\&nbsp;; Suzuki,\&nbsp;S.C.*\&nbsp;; Tran,\&nbsp;C.L.*\&nbsp;; Vockley,\&nbsp;J.*\&nbsp;; Wang,\&nbsp;J.S.*\&nbsp;; Wagner,\&nbsp;M.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Garbade,\&nbsp;S.F.*\&nbsp;; Kolker,\&nbsp;S.*\&nbsp;; Hoffmann,\&nbsp;G.F.*\&nbsp;; Staufner,\&nbsp;C.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=69817&la=de'>Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 141:108118 (2024)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Morales-Romero,\&nbsp;B.*\&nbsp;; Muñoz-Pujol,\&nbsp;G.*\&nbsp;; Artuch,\&nbsp;R.*\&nbsp;; García-Cazorla,\&nbsp;A.*\&nbsp;; O\'Callaghan,\&nbsp;M.*\&nbsp;; Sykut-Cegielska,\&nbsp;J.*\&nbsp;; Campistol,\&nbsp;J.M.*\&nbsp;; Moreno-Lozano,\&nbsp;P.J.*\&nbsp;; Oud,\&nbsp;M.M.*\&nbsp;; Wevers,\&nbsp;R.A.*\&nbsp;; Lefeber,\&nbsp;D.J.*\&nbsp;; Esteve-Codina,\&nbsp;A.*\&nbsp;; Yépez,\&nbsp;V.A.*\&nbsp;; Gagneur,\&nbsp;J.*\&nbsp;; Wortmann,\&nbsp;S.B.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Ribes,\&nbsp;A.*\&nbsp;; García-Villoria,\&nbsp;J.*\&nbsp;; Tort,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=70846&la=de'>Genome and RNA sequencing were essential to reveal cryptic intronic variants associated to defective ATP6AP1 mRNA processing.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 142:108511 (2024)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>van der Ven,\&nbsp;A.T.*\&nbsp;; Cabrera-Orefice,\&nbsp;A.*\&nbsp;; Wente,\&nbsp;I.*\&nbsp;; Feichtinger,\&nbsp;R.G.*\&nbsp;; Tsiakas,\&nbsp;K.*\&nbsp;; Weiss,\&nbsp;D.*\&nbsp;; Bierhals,\&nbsp;T.*\&nbsp;; Scholle,\&nbsp;L.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Santer,\&nbsp;R.*\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Hempel,\&nbsp;M.*\&nbsp;; Wittig,\&nbsp;I.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=68003&la=de'>Expanding the phenotypic and biochemical spectrum of NDUFAF3-related mitochondrial disease.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 140:107675 (2023)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Friederich,\&nbsp;M.W.*\&nbsp;; Geddes,\&nbsp;G.C.*\&nbsp;; Wortmann,\&nbsp;S.B.*\&nbsp;; Punnoose,\&nbsp;A.*\&nbsp;; Wartchow,\&nbsp;E.*\&nbsp;; Knight,\&nbsp;K.M.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Creadon-Swindell,\&nbsp;G.*\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; van Hove,\&nbsp;J.L.K.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=62305&la=de'>Pathogenic variants in MRPL44 cause infantile cardiomyopathy due to a mitochondrial translation defect.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 133, 362-371 (2021)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Conte,\&nbsp;F.*\&nbsp;; Morava,\&nbsp;E.*\&nbsp;; Bakar,\&nbsp;N.A.*\&nbsp;; Wortmann,\&nbsp;S.B.\&nbsp;; Poerink,\&nbsp;A.J.*\&nbsp;; Grunewald,\&nbsp;S.*\&nbsp;; Crushell,\&nbsp;E.*\&nbsp;; Al-Gazali,\&nbsp;L.*\&nbsp;; de Vries,\&nbsp;M.C.*\&nbsp;; Mørkrid,\&nbsp;L.*\&nbsp;; Hertecant,\&nbsp;J.*\&nbsp;; Brocke Holmefjord,\&nbsp;K.S.*\&nbsp;; Kronn,\&nbsp;D.*\&nbsp;; Feigenbaum,\&nbsp;A.*\&nbsp;; Fingerhut,\&nbsp;R.*\&nbsp;; Wong,\&nbsp;S.Y.*\&nbsp;; van Scherpenzeel,\&nbsp;M.*\&nbsp;; Voermans,\&nbsp;N.C.*\&nbsp;; Lefeber,\&nbsp;D.J.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=60435&la=de'>Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 131, 135-146 (2020)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>O\'Byrne,\&nbsp;J.J.*\&nbsp;; Tarailo-Graovac,\&nbsp;M.*\&nbsp;; Ghani,\&nbsp;A.*\&nbsp;; Champion,\&nbsp;M.*\&nbsp;; Deshpande,\&nbsp;C.*\&nbsp;; Dursun,\&nbsp;A.*\&nbsp;; Ozgul,\&nbsp;R.K.*\&nbsp;; Freisinger,\&nbsp;P.*\&nbsp;; Garber,\&nbsp;I.*\&nbsp;; Haack,\&nbsp;T.B.*\&nbsp;; Horvath,\&nbsp;R.*\&nbsp;; Barić,\&nbsp;I.*\&nbsp;; Husain,\&nbsp;R.A.*\&nbsp;; Kluijtmans,\&nbsp;L.A.J.*\&nbsp;; Kotzaeridou,\&nbsp;U.*\&nbsp;; Morris,\&nbsp;A.A.*\&nbsp;; Ross,\&nbsp;C.J.*\&nbsp;; Santra,\&nbsp;S.*\&nbsp;; Smeitink,\&nbsp;J.*\&nbsp;; Tarnopolsky,\&nbsp;M.*\&nbsp;; Wortmann,\&nbsp;S.B.\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Brunner-Krainz,\&nbsp;M.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Wasserman,\&nbsp;W.W.*\&nbsp;; Wevers,\&nbsp;R.A.*\&nbsp;; Engelke,\&nbsp;U.F.*\&nbsp;; Rodenburg,\&nbsp;R.J.*\&nbsp;; Ting,\&nbsp;T.W.*\&nbsp;; McFarland,\&nbsp;R.*\&nbsp;; Taylor,\&nbsp;R.W.*\&nbsp;; Salvarinova,\&nbsp;R.*\&nbsp;; van Karnebeek,\&nbsp;C.D.M.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=52731&la=de'>The genotypic and phenotypic spectrum of MTO1 deficiency.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 123, 28-42 (2018)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Herebian,\&nbsp;D.*\&nbsp;; Seibt,\&nbsp;A.*\&nbsp;; Smits,\&nbsp;S.H.J.*\&nbsp;; Bünning,\&nbsp;G.*\&nbsp;; Freyer,\&nbsp;C.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Karall,\&nbsp;D.*\&nbsp;; Wredenberg,\&nbsp;A.*\&nbsp;; Wedell,\&nbsp;A.*\&nbsp;; López,\&nbsp;L.C.*\&nbsp;; Mayatepek,\&nbsp;E.*\&nbsp;; Distelmaier,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51208&la=de'>Detection of 6-demethoxyubiquinone in CoQ\<sub\>10 \</sub\>deficiency disorders: Insights into enzyme interactions and identification of potential therapeutics.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 121, 216-223 (2017)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Falk,\&nbsp;M.J.*\&nbsp;; Shen,\&nbsp;L.*\&nbsp;; Gonzalez,\&nbsp;M.*\&nbsp;; Leipzig,\&nbsp;J.*\&nbsp;; Lott,\&nbsp;M.T.*\&nbsp;; Stassen,\&nbsp;A.P.*\&nbsp;; Diroma,\&nbsp;M.A.*\&nbsp;; Navarro-Gomez,\&nbsp;D.*\&nbsp;; Yeske,\&nbsp;P.*\&nbsp;; Bai,\&nbsp;R.*\&nbsp;; Boles,\&nbsp;R.G.*\&nbsp;; Brilhante,\&nbsp;V.*\&nbsp;; Ralph,\&nbsp;D.*\&nbsp;; DaRe,\&nbsp;J.T.*\&nbsp;; Shelton,\&nbsp;R.*\&nbsp;; Terry,\&nbsp;S.F.*\&nbsp;; Zhang,\&nbsp;Z.*\&nbsp;; Copeland,\&nbsp;W.C.*\&nbsp;; van Oven,\&nbsp;M.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Wallace,\&nbsp;D.C.*\&nbsp;; Attimonelli,\&nbsp;M.*\&nbsp;; Krotoski,\&nbsp;D.*\&nbsp;; Zuchner,\&nbsp;S.*\&nbsp;; Gai,\&nbsp;X.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=43030&la=de'>Mitochondrial Disease Sequence Data Resource (MSeqDR): A global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 114, 388-396 (2015)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Banka,\&nbsp;S.*\&nbsp;; de Goede,\&nbsp;C.G.*\&nbsp;; Yue,\&nbsp;W.W.*\&nbsp;; Morris,\&nbsp;A.A.*\&nbsp;; von Bremen,\&nbsp;B.*\&nbsp;; Chandler,\&nbsp;K.E.*\&nbsp;; Feichtinger,\&nbsp;R.G.*\&nbsp;; Hart,\&nbsp;C.*\&nbsp;; Khan,\&nbsp;N.*\&nbsp;; Lunzer,\&nbsp;V.*\&nbsp;; Matakovic,\&nbsp;L.*\&nbsp;; Marquardt,\&nbsp;T.*\&nbsp;; Makowski,\&nbsp;C.C.*\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Debus,\&nbsp;O.*\&nbsp;; Nosaka,\&nbsp;K.*\&nbsp;; Sonwalkar,\&nbsp;H.*\&nbsp;; Zimmermann,\&nbsp;F.A.*\&nbsp;; Sperl,\&nbsp;W.J.*\&nbsp;; Mayr,\&nbsp;J.A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=42825&la=de'>Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: A treatable neurological disorder caused by TPK1 mutations.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 113, 301-306 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Haack,\&nbsp;T.B.\&nbsp;; Gorza,\&nbsp;M.\&nbsp;; Danhauser,\&nbsp;K.\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Haberberger,\&nbsp;B.*\&nbsp;; Wieland,\&nbsp;T.\&nbsp;; Kremer,\&nbsp;L.S.\&nbsp;; Strecker,\&nbsp;V.*\&nbsp;; Graf,\&nbsp;E.\&nbsp;; Memari,\&nbsp;Y.*\&nbsp;; Ahting,\&nbsp;U.*\&nbsp;; Kopajtich,\&nbsp;R.\&nbsp;; Wortmann,\&nbsp;S.B.*\&nbsp;; Rodenburg,\&nbsp;R.J.*\&nbsp;; Kotzaeridou,\&nbsp;U.*\&nbsp;; Hoffmann,\&nbsp;G.F.*\&nbsp;; Sperl,\&nbsp;W.*\&nbsp;; Wittig,\&nbsp;I.*\&nbsp;; Wilichowski,\&nbsp;E.*\&nbsp;; Schottmann,\&nbsp;G.*\&nbsp;; Schuelke,\&nbsp;M.*\&nbsp;; Plecko,\&nbsp;B.*\&nbsp;; Stephani,\&nbsp;U.*\&nbsp;; Strom,\&nbsp;T.M.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Freisinger,\&nbsp;P.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=30734&la=de'>Phenotypic spectrum of eleven patients and five novel\<em\> MTFMT \</em\>mutations identified by exome sequencing and candidate gene screening.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 111, 342-352 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Kraja,\&nbsp;A.T.*\&nbsp;; Chasman,\&nbsp;D.I.*\&nbsp;; North,\&nbsp;K.E.*\&nbsp;; Reiner,\&nbsp;A.P.*\&nbsp;; Yanek,\&nbsp;L.R.*\&nbsp;; Kilpeläinen,\&nbsp;T.O.*\&nbsp;; Smith,\&nbsp;J.A.*\&nbsp;; Dehghan,\&nbsp;A.*\&nbsp;; Dupuis,\&nbsp;J.*\&nbsp;; Johnson,\&nbsp;A.D.*\&nbsp;; Feitosa,\&nbsp;M.F.*\&nbsp;; Tekola-Ayele,\&nbsp;F.*\&nbsp;; Chu,\&nbsp;A.Y.*\&nbsp;; Nolte,\&nbsp;I.M.*\&nbsp;; Dastani,\&nbsp;Z.*\&nbsp;; Morris,\&nbsp;A.*\&nbsp;; Pendergrass,\&nbsp;S.A.*\&nbsp;; Sun,\&nbsp;Y.V.*\&nbsp;; Ritchie,\&nbsp;M.D.*\&nbsp;; Vaez,\&nbsp;A.*\&nbsp;; Lin,\&nbsp;H.*\&nbsp;; Ligthart,\&nbsp;S.*\&nbsp;; Marullo,\&nbsp;L.*\&nbsp;; Rohde,\&nbsp;R.*\&nbsp;; Shao,\&nbsp;Y.*\&nbsp;; Ziegler,\&nbsp;M.A.*\&nbsp;; Im,\&nbsp;H.K.*\&nbsp;; Cross Consortia Pleiotropy (XC-Pleiotropy) (*)\&nbsp;; CHARGE Consortium (*)\&nbsp;; GIANT Consortium (Albrecht,\&nbsp;E. ; Grallert,\&nbsp;H. ; Thorand,\&nbsp;B. ; Gieger,\&nbsp;C. ; Peters,\&nbsp;A. ; Wichmann,\&nbsp;H.-E. ; Illig,\&nbsp;T. ; Müller-Nurasyid,\&nbsp;M. ; Heid,\&nbsp;I.M.)\&nbsp;; Global Lipids Genetics Consortium (*)\&nbsp;; MAGIC Consortium (*)\&nbsp;; Global BPgen Consortium (Eyheramendy,\&nbsp;S. ; Döring,\&nbsp;A. ; Meitinger,\&nbsp;T. ; Pfeufer,\&nbsp;A.)\&nbsp;; ADIPOGen Consortium (*)\&nbsp;; Women\'s Genome Health Study (*)\&nbsp;; Howard University Family Study (*)\&nbsp;; Schnabel,\&nbsp;R.B.*\&nbsp;; Jorgensen,\&nbsp;T.*\&nbsp;; Jorgensen,\&nbsp;M.E.*\&nbsp;; Hansen,\&nbsp;T.*\&nbsp;; Pedersen,\&nbsp;O.*\&nbsp;; Stolk,\&nbsp;R.P.*\&nbsp;; Snieder,\&nbsp;H.*\&nbsp;; Hofman,\&nbsp;A.*\&nbsp;; Uitterlinden,\&nbsp;A.G.*\&nbsp;; Franco,\&nbsp;O.H.*\&nbsp;; Ikram,\&nbsp;M.A.*\&nbsp;; Richards,\&nbsp;J.B.*\&nbsp;; Rotimi,\&nbsp;C.N.*\&nbsp;; Wilson,\&nbsp;J.G.*\&nbsp;; Lange,\&nbsp;L.A.*\&nbsp;; Ganesh,\&nbsp;S.K.*\&nbsp;; Nalls,\&nbsp;M.*\&nbsp;; Rasmussen-Torvik,\&nbsp;L.J.*\&nbsp;; Pankow,\&nbsp;J.S.*\&nbsp;; Coresh,\&nbsp;J.*\&nbsp;; Tang,\&nbsp;W.*\&nbsp;; Kao,\&nbsp;W.H.L.*\&nbsp;; Boerwinkle,\&nbsp;E.*\&nbsp;; Morrison,\&nbsp;A.C.*\&nbsp;; Ridker,\&nbsp;P.M.*\&nbsp;; Becker,\&nbsp;D.M.*\&nbsp;; Rotter,\&nbsp;J.I.*\&nbsp;; Kardia,\&nbsp;S.L.R.*\&nbsp;; Loos,\&nbsp;R.J.F.*\&nbsp;; Larson,\&nbsp;M.G.*\&nbsp;; Hsu,\&nbsp;Y.H.*\&nbsp;; Province,\&nbsp;M.A.*\&nbsp;; Tracy,\&nbsp;R.*\&nbsp;; Voight,\&nbsp;B.F.*\&nbsp;; Vaidya,\&nbsp;D.*\&nbsp;; O\'Donnell,\&nbsp;C.J.*\&nbsp;; Benjamin,\&nbsp;E.J.*\&nbsp;; Alizadeh,\&nbsp;B.Z.*\&nbsp;; Prokopenko,\&nbsp;I.*\&nbsp;; Meigs,\&nbsp;J.B.*\&nbsp;; Borecki,\&nbsp;I.B.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=32402&la=de'>Pleiotropic genes for metabolic syndrome and inflammation.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 112, 317-338 (2014)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Danhauser,\&nbsp;K.\&nbsp;; Iuso,\&nbsp;A.\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Freisinger,\&nbsp;P.*\&nbsp;; Brockmann,\&nbsp;K.*\&nbsp;; Mayr,\&nbsp;J.A.*\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Prokisch,\&nbsp;H.</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6708&la=de'>Cellular rescue-assay aids verification of causative DNA-variants in mitochondrial complex I deficiency.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 103, 161-166 (2011)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>John,\&nbsp;G.\&nbsp;; Hegarty,\&nbsp;J.P.*\&nbsp;; Yu,\&nbsp;W.*\&nbsp;; Berg,\&nbsp;A.*\&nbsp;; Pastor,\&nbsp;D.M.*\&nbsp;; Kelly,\&nbsp;A.A.*\&nbsp;; Wang,\&nbsp;Y.*\&nbsp;; Poritz,\&nbsp;L.S.*\&nbsp;; Schreiber,\&nbsp;S.*\&nbsp;; Koltun,\&nbsp;W.A.*\&nbsp;; Lin,\&nbsp;Z.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6494&la=de'>NKX2-3 variant rs11190140 is associated with IBD and alters binding of NFAT.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 104, 174-179 (2011)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Mayr,\&nbsp;J.A.*\&nbsp;; Bodamer,\&nbsp;O.*\&nbsp;; Haack,\&nbsp;T.B.\&nbsp;; Zimmermann,\&nbsp;F.A.*\&nbsp;; Madignier,\&nbsp;F.\&nbsp;; Prokisch,\&nbsp;H.\&nbsp;; Rauscher,\&nbsp;C.*\&nbsp;; Koch,\&nbsp;J.*\&nbsp;; Sperl,\&nbsp;W.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6750&la=de'>Heterozygous mutation in the X chromosomal \<em\>NDUFA1 \</em\>gene in a girl with complex I deficiency.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 103, 358-361 (2011)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Fisher,\&nbsp;E.*\&nbsp;; Grallert,\&nbsp;H.\&nbsp;; Klapper,\&nbsp;M.*\&nbsp;; Pfäfflin,\&nbsp;A.*\&nbsp;; Schrezenmeir,\&nbsp;J.*\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Boeing,\&nbsp;H.*\&nbsp;; Döring,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=709&la=de'>Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 98, 400-405 (2009)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Böhme,\&nbsp;M.*\&nbsp;; Grallert,\&nbsp;H.\&nbsp;; Fischer,\&nbsp;A.\&nbsp;; Gieger,\&nbsp;C.\&nbsp;; Nitz,\&nbsp;I.*\&nbsp;; Heid,\&nbsp;I.M.\&nbsp;; Kohl,\&nbsp;C.*\&nbsp;; Wichmann,\&nbsp;H.-E.\&nbsp;; Illig,\&nbsp;T.\&nbsp;; Döring,\&nbsp;F.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=85&la=de'>MTTP variants and body mass index, waist circumference and serum cholesterol level: Association analyses in 7582 participants of the KORA study cohort.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 95, 229-232 (2008)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Müller,\&nbsp;T.D.*\&nbsp;; Reichwald,\&nbsp;K.*\&nbsp;; Wermter,\&nbsp;A.K.*\&nbsp;; Brönner,\&nbsp;G.*\&nbsp;; Nguyen,\&nbsp;T.T.*\&nbsp;; Friedel,\&nbsp;S.*\&nbsp;; Koberwitz,\&nbsp;K.\&nbsp;; Engeli,\&nbsp;S.*\&nbsp;; Lichtner,\&nbsp;P.\&nbsp;; Meitinger,\&nbsp;T.\&nbsp;; Schäfer,\&nbsp;H.*\&nbsp;; Hebebrand,\&nbsp;J.*\&nbsp;; Hinney,\&nbsp;A.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4166&la=de'>No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 90, 429-434 (2007)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Tsuchiya,\&nbsp;T.*\&nbsp;; Schwarz,\&nbsp;P.E.*\&nbsp;; Bosque-Plata,\&nbsp;L.D.*\&nbsp;; Geoffrey Hayes,\&nbsp;M.*\&nbsp;; Dina,\&nbsp;C.*\&nbsp;; Froguel,\&nbsp;P.*\&nbsp;; Towers,\&nbsp;G.W.*\&nbsp;; Fischer,\&nbsp;S.*\&nbsp;; Temelkova-Kurktschiev,\&nbsp;T.*\&nbsp;; Rietzsch,\&nbsp;H.*\&nbsp;; Graessler,\&nbsp;J.*\&nbsp;; Vcelák,\&nbsp;J.*\&nbsp;; Palyzová,\&nbsp;D.*\&nbsp;; Selisko,\&nbsp;T.*\&nbsp;; Bendlová,\&nbsp;B.*\&nbsp;; Schulze,\&nbsp;J.*\&nbsp;; Julius,\&nbsp;U.*\&nbsp;; Hanefeld,\&nbsp;M.*\&nbsp;; Weedon,\&nbsp;M.N.*\&nbsp;; Evans,\&nbsp;J.C.*\&nbsp;; Frayling,\&nbsp;T.M.*\&nbsp;; Hattersley,\&nbsp;A.T.*\&nbsp;; Orho-Melander,\&nbsp;M.*\&nbsp;; Groop,\&nbsp;L.*\&nbsp;; Malecki,\&nbsp;M.T.*\&nbsp;; Hansen,\&nbsp;T.*\&nbsp;; Pedersen,\&nbsp;O.*\&nbsp;; Fingerlin,\&nbsp;T.E.*\&nbsp;; Boehnke,\&nbsp;M.*\&nbsp;; Hanis,\&nbsp;C.L.*\&nbsp;; Cox,\&nbsp;N.J.*\&nbsp;; Bell,\&nbsp;G.I.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=44532&la=de'>Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 89, 174-184 (2006)</div>");
document.write("</div>");
document.write("<div class='record'>");
document.write("  <div class='authors'>Gómez-Zaera,\&nbsp;M.*\&nbsp;; Strom,\&nbsp;T.M.*\&nbsp;; Rodriguez,\&nbsp;B.*\&nbsp;; Estivill,\&nbsp;X.*\&nbsp;; Meitinger,\&nbsp;T.*\&nbsp;; Nunes,\&nbsp;V.*</div>");
document.write("  <div class='linked_title'><a href='https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=23579&la=de'>Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.</a></div>");
document.write("  <div class='source'>Mol. Genet. Metab. 72, 72-81 (2001)</div>");
document.write("</div>");