Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (2) Bartolomaeus, Theda (1) Blachut, Susanne (1) Chen, Wei Prof. Dr. (3) Dechend, Ralf Priv. Doz. 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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 January 05, 2007 / Am J Med Genet B Neuropsychiatr Genet Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy S. Lorenz A. Heils J.M. Kasper T. Sander January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch March 01, 2007 / Hum Genet Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H. Najmabadi M.M. Motazacker M. Garshasbi K. Kahrizi A. Tzschach W. Chen F. Behjati V. Hadavi S.E. Nieh S.S. Abedini R. Vazifehmand S.G. Firouzabadi P. Jamali M. Falah S.M. Seifati A. Grueters S. Lenzner L.R. Jensen F. Rueschendorf A.W. Kuss H.H. Ropers November 01, 2007 / J Mol Med Dysfunction of dysferlin-deficient hearts K. Wenzel C. Geier F. Qadri N. Huebner H. Schulz B. Erdmann V. Gross D. Bauer R. Dechend R. Dietz K.J. Osterziel S. Spuler C. Oezcelik September 04, 2007 / Genome Biol Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning M.X. Doss S. Chen J. Winkler R. Hippler-Altenburg M. Odenthal C. Wickenhauser S. Balaraman H. Schulz O. Hummel N. Huebner N. Ghosh-Choudhury I. Sotiriadou J. Hescheler A. Sachinidis September 01, 2007 / PLoS Biol Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis C. Soederhaell I. Marenholz T. Kerscher F. Rueschendorf J. Esparza-Gordillo M. Worm C. Gruber G. Mayr M. Albrecht K. Rohde H. Schulz U. Wahn N. Huebner Y.A. Lee November 01, 2007 / J Allergy Clin Immunol A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema F. Schulz I. Marenholz R. Foelster-Holst C. Chen A. Sternjak R. Baumgrass J. Esparza-Gordillo C. Grueber R. Nickel S. Schreiber M. Stoll M. Kurek F. Rueschendorf N. Huebner U. Wahn Y.A. Lee April 01, 2007 / J Neural Transm Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample P. Heiser A. Dempfle S. Friedel K. Konrad A. Hinney H. Kiefl S. Walitza T. Bettecken K. Saar M. Linder A. Warnke B. Herpertz-Dahlmann H. Schaefer H. Remschmidt J. Hebebrand April 01, 2007 / Epilepsy Res Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy A. Hempelmann J. Cobilanschi A. Heils H. Muhle U. Stephani Y. Weber H. Lerche T. 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October 28, 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
January 05, 2007 / Am J Med Genet B Neuropsychiatr Genet Allelic association of a truncation mutation of the KCNMB3 gene with idiopathic generalized epilepsy S. Lorenz A. Heils J.M. Kasper T. Sander
January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch
March 01, 2007 / Hum Genet Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci H. Najmabadi M.M. Motazacker M. Garshasbi K. Kahrizi A. Tzschach W. Chen F. Behjati V. Hadavi S.E. Nieh S.S. Abedini R. Vazifehmand S.G. Firouzabadi P. Jamali M. Falah S.M. Seifati A. Grueters S. Lenzner L.R. Jensen F. Rueschendorf A.W. Kuss H.H. Ropers
November 01, 2007 / J Mol Med Dysfunction of dysferlin-deficient hearts K. Wenzel C. Geier F. Qadri N. Huebner H. Schulz B. Erdmann V. Gross D. Bauer R. Dechend R. Dietz K.J. Osterziel S. Spuler C. Oezcelik
September 04, 2007 / Genome Biol Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning M.X. Doss S. Chen J. Winkler R. Hippler-Altenburg M. Odenthal C. Wickenhauser S. Balaraman H. Schulz O. Hummel N. Huebner N. Ghosh-Choudhury I. Sotiriadou J. Hescheler A. Sachinidis
September 01, 2007 / PLoS Biol Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis C. Soederhaell I. Marenholz T. Kerscher F. Rueschendorf J. Esparza-Gordillo M. Worm C. Gruber G. Mayr M. Albrecht K. Rohde H. Schulz U. Wahn N. Huebner Y.A. Lee
November 01, 2007 / J Allergy Clin Immunol A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema F. Schulz I. Marenholz R. Foelster-Holst C. Chen A. Sternjak R. Baumgrass J. Esparza-Gordillo C. Grueber R. Nickel S. Schreiber M. Stoll M. Kurek F. Rueschendorf N. Huebner U. Wahn Y.A. Lee
April 01, 2007 / J Neural Transm Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample P. Heiser A. Dempfle S. Friedel K. Konrad A. Hinney H. Kiefl S. Walitza T. Bettecken K. Saar M. Linder A. Warnke B. Herpertz-Dahlmann H. Schaefer H. Remschmidt J. Hebebrand
April 01, 2007 / Epilepsy Res Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy A. Hempelmann J. Cobilanschi A. Heils H. Muhle U. Stephani Y. Weber H. Lerche T. Sander