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. (19) Akalin, Altuna Dr. (73) Altmueller, Janine Dr.med. (4) Annibale, Paolo Dr. (1) Arnau Soler, Aleix Dr. (2) Bader, Michael Prof. Dr. (7) Bähring, Sylvia Dr. (8) Bahry, Ella Dr. (1) Barke, Niclas (1) Bartels-Klein, Eireen (1) Bartolomaeus, Theda (2) Berruezo Llacuna, Maria (1) Beule, Dieter Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (4) Blachut, Susanne (6) Blankenstein, Thomas Prof. Dr. (1) Blume, Alexander Dr. (6) Born, Gabriele (1) Borodina, Tatiana Dr. (2) Carvalho, Silvia Filipa (1) Chekulaeva, Marina Dr. (3) Chen, Wei Prof. Dr. (8) Chu, Van Trung Dr. (1) Costanza, Mariantonia Dr. (2) Dartsch, Josephine (1) Daumke, Oliver Prof. Dr. (4) Dechend, Ralf Priv. Doz. 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ScienceChromatin (dys)function in diseaseGenetics and Genomics of Cardiovascular Diseases Sort: Result score Newest to oldest Oldest to newest 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 December 21, 2021 / Circulation Extracellular matrix in heart failure: role of ADAMTS5 in proteoglycan remodeling J. Barallobre-Barreiro T. Radovits M. Fava U. Mayr W.Y. Lin E. Ermolaeva D. Martínez-López E.L. Lindberg E. Duregotti L. Daróczi M. Hasman L.E. Schmidt B. Singh R. Lu F. Baig A.M. Siedlar F. Cuello N. Catibog K. Theofilatos A.M. Shah M.G. Crespo-Leiro N. Doménech N. Hübner B. Merkely M. Mayr 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 January 01, 2004 / Biochem Biophys Res Commun Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats G. Tripodi M. Florio M. Ferrandi R. Modica H. Zimdahl N. Hubner P. Ferrari G. Bianchi January 01, 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner January 01, 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg January 01, 2005 / Nat Genet Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 L.A. Metherell J.P. Chapple S. Cooray A. David C. Becker F. Rueschendorf D. Naville M. Begeot B. Khoo P. Nuernberg A. Huebner M.E. Cheetham A.J.L. Clark January 01, 2005 / Bioinformatics ALOHOMORA: a tool for linkage analysis using 10K SNP array data F. Rueschendorf P. Nuernberg January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
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
December 21, 2021 / Circulation Extracellular matrix in heart failure: role of ADAMTS5 in proteoglycan remodeling J. Barallobre-Barreiro T. Radovits M. Fava U. Mayr W.Y. Lin E. Ermolaeva D. Martínez-López E.L. Lindberg E. Duregotti L. Daróczi M. Hasman L.E. Schmidt B. Singh R. Lu F. Baig A.M. Siedlar F. Cuello N. Catibog K. Theofilatos A.M. Shah M.G. Crespo-Leiro N. Doménech N. Hübner B. Merkely M. Mayr
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
January 01, 2004 / Biochem Biophys Res Commun Effect of Add1 gene transfer on blood pressure in reciprocal congenic strains of Milan rats G. Tripodi M. Florio M. Ferrandi R. Modica H. Zimdahl N. Hubner P. Ferrari G. Bianchi
January 01, 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner
January 01, 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg
January 01, 2005 / Nat Genet Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 L.A. Metherell J.P. Chapple S. Cooray A. David C. Becker F. Rueschendorf D. Naville M. Begeot B. Khoo P. Nuernberg A. Huebner M.E. Cheetham A.J.L. Clark
January 01, 2005 / Bioinformatics ALOHOMORA: a tool for linkage analysis using 10K SNP array data F. Rueschendorf P. Nuernberg
January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst
January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann