Wissenschaftliche Publikationen

28. Oktober 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

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

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

Is there a common genetic basis for all familial cardiomyopathies?

A. Perrot
R. Dietz
K.J. Osterziel

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

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

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

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

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

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