Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (20) Akalin, Altuna Dr. (1) Albrecht, Jan Philipp (3) Altmueller, Janine Dr.med. (3) Arnau Soler, Aleix Dr. (2) Bader, Michael Prof. Dr. (7) Bähring, Sylvia Dr. (7) Bahry, Ella Dr. (3) Bartels-Klein, Eireen (1) Bartolomaeus, Theda (2) Beule, Dieter Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blachut, Susanne (6) Blankenstein, Thomas Prof. Dr. (1) Born, Gabriele (1) Borodina, Tatiana Dr. (1) Braeuning, Caroline (1) Cano Rincon, Elena Dr. (1) Cerda Jara, Cledi Alicia (1) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (6) Dartsch, Josephine (1) Daumke, Oliver Prof. Dr. (1) Dechend, Ralf Priv. Doz. 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(1) Perrot, Andreas (2) Pilz, Bernhard Dr. (1) Pischon, Tobias Prof. Dr. (4) Pombo, Ana Prof. Dr. (1) Popova, Elena Dr. (3) Popp, Oliver Dr. (5) Preibisch, Stephan Dr. (2) Prigione, Alessandro Prof. Dr. (1) Qadri, Fatimunnisa Dr. (7) Radke, Michael Dr. (3) Rajewsky, Nikolaus Prof. Dr. (5) Richter, Matthias (1) Ruiz Orera, Jorge Dr. (21) Rumberger, Josef Lorenz (1) Saar, Kathrin Dr. (57) Sander, Maike Prof. Dr. (1) Scheidereit, Claus Prof. Dr. (2) Schlag, Peter M. 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Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne October, 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee October, 2006 / Hum Hered SNP-Based analysis of genetic substructure in the German population M. Steffens C. Lamina T. Illig T. Bettecken R. Vogler P. Entz E.K. Suk M.R. Toliat N. Klopp A. Caliebe I.R. Koenig K. Koehler J. Luedemann A.D. Lacava R. Fimmers P. Lichtner A. Ziegler A. Wolf M. Krawczak P. Nuernberg J. Hampe S. Schreiber T. Meitinger H.E. Wichmann K. Roeder T.F. Wienker M.P. Baur November, 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell 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 October, 2006 / Epilepsia Exploration of the genetic architecture of idiopathic generalized epilepsies A. Hempelmann K.P. Taylor A. Heils S. Lorenz J.F. Prud'homme R. Nabbout O. Dulac G. Rudolf F. Zara A. Bianchi R. Robinson R.M. Gardiner A. Covanis D. Lindhout U. Stephani C.E. Elger Y.G. Weber H. Lerche P. Nuernberg K.L. Kron I.E. Scheffer J.C. Mulley S.F. Berkovic T. Sander October 20, 2006 / PLoS Genet Heritability and tissue specificity of expression quantitative trait loci E. Petretto J. Mangion N.J. Dickens S.A. Cook M.K. Kumaran H. Lu J. Fischer H. Maatz V. Kren M. Pravenec N. Hubner T.J. Aitman March, 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 December, 2006 / Neuropsychopharmacology Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar I disorder F.W. Lohoff J.P. Dahl T.N. Ferraro S.E. Arnold J. Gallinat T. Sander W.H. Berrettini November 01, 2006 / Diabetes Dysregulation of the peripheral and adipose tissue endocannabinoid system in human abdominal obesity M. Blueher S. Engeli N. Kloeting J. Berndt M. Fasshauer S. Batkai P. Pacher M.R. Schoen J. Jordan M. 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October, 2006 / Am J Hum Genet Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p M.A. Lee-Kirsch M. Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne
October, 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee
October, 2006 / Hum Hered SNP-Based analysis of genetic substructure in the German population M. Steffens C. Lamina T. Illig T. Bettecken R. Vogler P. Entz E.K. Suk M.R. Toliat N. Klopp A. Caliebe I.R. Koenig K. Koehler J. Luedemann A.D. Lacava R. Fimmers P. Lichtner A. Ziegler A. Wolf M. Krawczak P. Nuernberg J. Hampe S. Schreiber T. Meitinger H.E. Wichmann K. Roeder T.F. Wienker M.P. Baur
November, 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell
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
October, 2006 / Epilepsia Exploration of the genetic architecture of idiopathic generalized epilepsies A. Hempelmann K.P. Taylor A. Heils S. Lorenz J.F. Prud'homme R. Nabbout O. Dulac G. Rudolf F. Zara A. Bianchi R. Robinson R.M. Gardiner A. Covanis D. Lindhout U. Stephani C.E. Elger Y.G. Weber H. Lerche P. Nuernberg K.L. Kron I.E. Scheffer J.C. Mulley S.F. Berkovic T. Sander
October 20, 2006 / PLoS Genet Heritability and tissue specificity of expression quantitative trait loci E. Petretto J. Mangion N.J. Dickens S.A. Cook M.K. Kumaran H. Lu J. Fischer H. Maatz V. Kren M. Pravenec N. Hubner T.J. Aitman
March, 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
December, 2006 / Neuropsychopharmacology Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar I disorder F.W. Lohoff J.P. Dahl T.N. Ferraro S.E. Arnold J. Gallinat T. Sander W.H. Berrettini
November 01, 2006 / Diabetes Dysregulation of the peripheral and adipose tissue endocannabinoid system in human abdominal obesity M. Blueher S. Engeli N. Kloeting J. Berndt M. Fasshauer S. Batkai P. Pacher M.R. Schoen J. Jordan M. Stumvoll