Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Dechend, Ralf Priv. Doz. (1) Herse, Florian PD Dr. (1) Hübner, Norbert Prof. Dr. (10) Hummel, Oliver (3) Lee, Young-Ae Prof. Dr. (3) Marenholz, Ingo Dr. (2) Qadri, Fatimunnisa Dr. (1) Saar, Kathrin Dr. (2) Schlag, Peter M. Prof. Dr. (1) Spuler, Simone Prof. (1) Wenzel, Katrin Dr. (2) (-) Chen, Wei Prof. Dr. (1) 2001 (1) 2002 (1) 2003 (1) 2005 (1) (-) 2007 (2) 2011 (1) 2012 (1) 2013 (1) 2015 (1) 2016 (1) 2019 (1) 2020 (4) 2024 (1) AG Müller/Dechend (ECRC) (8) Cardiac MRI (3) Experimental Ultrahigh-Field MR (1) (-) Genetics and Genomics of Cardiovascular Diseases (2) Hypertension-caused End-Organ Damage (8) Hypertension-Mediated End-Organ Damage (8) Magnetic Resonance (1) Myology (1) Nephrology and Inflammatory Vascular Diseases (5) 2 Results: Active Filter: Chen, Wei Prof. Dr.Genetics and Genomics of Cardiovascular Diseases2007 Sort: Result score Newest to oldest Oldest to newest 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 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
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