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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Monti R. Plehm H. Schulz D. Ganten R. Kreutz N. Hübner April, 2004 / Genome Res Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome M. Krzywinski J. Wallis C. Gösele I. Bosdet R. Chiu T. Graves O. Hummel D. Layman C. Mathewson N. Wye B. Zhu D. Albracht J. Asano S. Barber M. Brown-John S. Chan S. Chand A. Cloutier J. Davito C. Fjell T. Gaige D. Ganten N. Girn K. Guggenheimer H. Himmelbauer T. Kreitler S. Leach D. Lee H. Lehrach M. Mayo K. Mead T. Olson P. Pandoh A.L. Prabhu H. Shin S. Taenzer J. Thompson M. Tsai J. Walker G. Yang M. Sekhon L. Hillier H. Zimdahl A. Marziali K. Osoegawa S. Zhao A. Siddiqui P.J. de Jong W. Warren E. Mardis J.D. McPherson R. Wilson N. Hübner S. Jones M. Marra J. Schein August, 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner January 01, 2004 / Folia Biol (Praha) Molecular analysis of the sex hormone-binding globulin gene in the rat hypodactylous mutation (Hd) F. Liska C. Gösele V. Kren N. Hübner D. Krenova January 01, 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal January 01, 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke June, 2006 / Mamm Genome Integrated gene expression profiling and linkage analysis in the rat E. Petretto J. Mangion M. Pravanec N. Hubner T.J. Aitman 2006 Gene chip technology and its application to molecular medicine H. Zimdahl N. Hübner May 22, 2006 / Mol Vis A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family V. Vanita J.R. Singh J.F. Hejtmancik P. Nuernberg H.C. Hennies D. Singh K. Sperling October 11, 2006 / Physiol Genomics Reciprocal congenic lines for a major stroke-QTL on rat chromosome 1 S. Rubattu N. Hubner U. Ganten A. Evangelista R. Stanzione E.D. Angelantonio R. Plehm R. Langanki E. Gianazza L. Sironi G. D'Amati M. Volpe Pagination First page « First Previous page ‹ Previous Page 1 Current page 2 Page 3 Page 4 … Next page Next › Last page Last »
January 01, 2003 / Hum Mol Genet Interaction between blood pressure quantitative trait loci in rats in which trait variation at chromosome 1 is conditional upon a specific allele at chromosome 10 J. Monti R. Plehm H. Schulz D. Ganten R. Kreutz N. Hübner
April, 2004 / Genome Res Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome M. Krzywinski J. Wallis C. Gösele I. Bosdet R. Chiu T. Graves O. Hummel D. Layman C. Mathewson N. Wye B. Zhu D. Albracht J. Asano S. Barber M. Brown-John S. Chan S. Chand A. Cloutier J. Davito C. Fjell T. Gaige D. Ganten N. Girn K. Guggenheimer H. Himmelbauer T. Kreitler S. Leach D. Lee H. Lehrach M. Mayo K. Mead T. Olson P. Pandoh A.L. Prabhu H. Shin S. Taenzer J. Thompson M. Tsai J. Walker G. Yang M. Sekhon L. Hillier H. Zimdahl A. Marziali K. Osoegawa S. Zhao A. Siddiqui P.J. de Jong W. Warren E. Mardis J.D. McPherson R. Wilson N. Hübner S. Jones M. Marra J. Schein
August, 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner
January 01, 2004 / Folia Biol (Praha) Molecular analysis of the sex hormone-binding globulin gene in the rat hypodactylous mutation (Hd) F. Liska C. Gösele V. Kren N. Hübner D. Krenova
January 01, 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal
January 01, 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke
June, 2006 / Mamm Genome Integrated gene expression profiling and linkage analysis in the rat E. Petretto J. Mangion M. Pravanec N. Hubner T.J. Aitman
May 22, 2006 / Mol Vis A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family V. Vanita J.R. Singh J.F. Hejtmancik P. Nuernberg H.C. Hennies D. Singh K. Sperling
October 11, 2006 / Physiol Genomics Reciprocal congenic lines for a major stroke-QTL on rat chromosome 1 S. Rubattu N. Hubner U. Ganten A. Evangelista R. Stanzione E.D. Angelantonio R. Plehm R. Langanki E. Gianazza L. Sironi G. D'Amati M. Volpe