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Scientific Publications

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/ 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
/ Am J Hypertens

Modulating angiotensin II-induced inflammation by HMG Co-A reductase inhibition

  • R. Dechend
  • A. Fiebler
  • C. Lindschau
  • H. Bischoff
  • D.N. Mueller
  • J.K. Park
  • R. Dietz
  • H. Haller
  • F.C. Luft
/ Nat Genet

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21

  • Y.A. Lee
  • U. Wahn
  • R. Kehrt
  • L. Tarani
  • L. Businco
  • D. Gustafsson
  • F. Andersson
  • A.P. Oranje
  • A. Wolkertstorfer
  • A. von Berg
  • U. Hoffmann
  • W. Kuester
  • T.F. Wienker
  • F. Rueschendorf
  • A. Reis
/ Eur J Heart Fail

Is there a common genetic basis for all familial cardiomyopathies?

  • A. Perrot
  • R. Dietz
  • K.J. Osterziel
/ Am J Med Genet A

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation

  • A. Rauch
  • J. Hoyer
  • S. Guth
  • C. Zweier
  • C. Kraus
  • C. Becker
  • M. Zenker
  • U. Hueffmeier
  • C. Thiel
  • F. Rueschendorf
  • P. Nuernberg
  • A. Reis
  • U. Trautmann
/ Europace

Optimization of cardiac resynchronization guided by Doppler echocardiography: haemodynamic improvement and intraindividual variability with different pacing configurations and atrioventricular delays

  • M. Stockburger
  • S. Fateh-Moghadam
  • A. Nitardy
  • H. Langreck
  • W. Haverkamp
  • R. Dietz
/ J Cardiovasc Magn Reson

Left ventricular outflow tract planimetry by cardiovascular magnetic resonance differentiates obstructive from non-obstructive hypertrophic cardiomyopathy

  • J. Schulz-Menger
  • H. Abdel-Aty
  • A. Busjahn
  • R. Wassmuth
  • B. Pilz
  • R. Dietz
  • M.G. Friedrich
/ J Card Fail

A systematic meta-analysis of the efficacy and heterogeneity of disease management programs in congestive heart failure

  • A. Goehler
  • J.L. Januzzi
  • S.S. Worrell
  • K.J. Osterziel
  • G.S. Gazelle
  • R. Dietz
  • U. Siebert
/ 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
/ 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