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Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali 23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit 09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck 01. Dezember 2009 / Circ Cardiovasc Genet Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study E. Fisher N. Stefan K. Saar D. Drogan M.B. Schulze A. Fritsche H.G. Joost H.U. Haering N. Huebner H. Boeing C. Weikert 23. Januar 2009 / PLoS Genet A systematic approach to mapping recessive disease genes in individuals from outbred populations F. Hildebrandt S.F. Heeringa F. Rueschendorf M. Attanasio G. Nuernberg C. Becker D. Seelow N. Huebner G. Chernin C.N. Vlangos W. Zhou J.F. O'Toole B.E. Hoskins M.T. Wolf B.G. Hinkes H. Chaib S. Ashraf S.J. Allen V. Vega-Warner E. Wise H.M. Harville R.H. Lyons J. Washburn J. Macdonald P. Nuernberg E.A. Otto 01. Mai 2009 / Pediatr Allergy Immunol ICOS-gene variants are not associated with atopic disease susceptibility in European children K.C. Beier S. Humberdros H. Witt S. Illi F. Rueschendorf R. Nickel Y.A. Lee S. Lau U. Wahn E. Hamelmann 01. September 2009 / Pediatr Allergy Immunol IL13 variants are associated with total serum IgE and early sensitization to food allergens in children with atopic dermatitis S.E. Zitnik F. Rueschendorf S. Mueller C. Sengler Y.A. Lee R.W. Griffioen P. Meglio U. Wahn H. Witt R. Nickel 01. September 2009 / Basic Res Cardiol Enhancement of the endothelial NO synthase attenuates experimental diastolic heart failure D. Westermann A. Riad U. Richter S. Jaeger K. Savvatis M. Schuchardt N. Bergmann M. Toelle D. Nagorsen M. Gotthardt H.P. Schultheiss C. Tschoepe 01. Februar 2009 / Birth Defects Res A Clin Mol Teratol Genome-wide linkage scan for bladder exstrophy-epispadias complex M. Ludwig F. Rueschendorf K. Saar N. Huebner L. Siekmann S.A. Boyadjiev H. 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28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit
09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck
01. Dezember 2009 / Circ Cardiovasc Genet Association of AHSG gene polymorphisms with fetuin-A plasma levels and cardiovascular diseases in the EPIC-Potsdam study E. Fisher N. Stefan K. Saar D. Drogan M.B. Schulze A. Fritsche H.G. Joost H.U. Haering N. Huebner H. Boeing C. Weikert
23. Januar 2009 / PLoS Genet A systematic approach to mapping recessive disease genes in individuals from outbred populations F. Hildebrandt S.F. Heeringa F. Rueschendorf M. Attanasio G. Nuernberg C. Becker D. Seelow N. Huebner G. Chernin C.N. Vlangos W. Zhou J.F. O'Toole B.E. Hoskins M.T. Wolf B.G. Hinkes H. Chaib S. Ashraf S.J. Allen V. Vega-Warner E. Wise H.M. Harville R.H. Lyons J. Washburn J. Macdonald P. Nuernberg E.A. Otto
01. Mai 2009 / Pediatr Allergy Immunol ICOS-gene variants are not associated with atopic disease susceptibility in European children K.C. Beier S. Humberdros H. Witt S. Illi F. Rueschendorf R. Nickel Y.A. Lee S. Lau U. Wahn E. Hamelmann
01. September 2009 / Pediatr Allergy Immunol IL13 variants are associated with total serum IgE and early sensitization to food allergens in children with atopic dermatitis S.E. Zitnik F. Rueschendorf S. Mueller C. Sengler Y.A. Lee R.W. Griffioen P. Meglio U. Wahn H. Witt R. Nickel
01. September 2009 / Basic Res Cardiol Enhancement of the endothelial NO synthase attenuates experimental diastolic heart failure D. Westermann A. Riad U. Richter S. Jaeger K. Savvatis M. Schuchardt N. Bergmann M. Toelle D. Nagorsen M. Gotthardt H.P. Schultheiss C. Tschoepe
01. Februar 2009 / Birth Defects Res A Clin Mol Teratol Genome-wide linkage scan for bladder exstrophy-epispadias complex M. Ludwig F. Rueschendorf K. Saar N. Huebner L. Siekmann S.A. Boyadjiev H. Reutter