Veröffentlichungen

29. Juli 2021 in PLoS Genet

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

E. Audain
A. Wilsdon
J. Breckpot
J.M. Izarzugaza
T.W. Fitzgerald
A.K. Kahlert
A. Sifrim
F. Wünnemann
Y. Perez-Riverol
H. Abdul-Khaliq
M. Bak
A.S. Bassett
W.D. Benson
F. Berger
I. Daehnert
K. Devriendt
S. Dittrich
P.E. Daubeney
V. Garg
K. Hackmann
K. Hoff
P. Hofmann
G. Dombrowsky
T. Pickardt
U. Bauer
B.D. Keavney
S. Klaassen
H.H. Kramer
C.R. Marshall
D.M. Milewicz
S. Lemaire
J.S. Coselli
M.E. Mitchell
A. Tomita-Mitchell
S.K. Prakash
K. Stamm
A.F.R. Stewart
C.K. Silversides
R. Siebert
B. Stiller
J.A. Rosenfeld
I. Vater
A.V. Postma
A. Caliebe
J.D. Brook
G. Andelfinger
M.E. Hurles
B. Thienpont
L.A. Larsen
M.P. Hitz

Pathogenic variants associated with dilated cardiomyopathy predict outcome in pediatric myocarditis

F. Seidel
M. Holtgrewe
N. Al-Wakeel-Marquard
B. Opgen-Rhein
J. Dartsch
C. Herbst
D. Beule
T. Pickardt
K. Klingel
D. Messroghli
F. Berger
S. Schubert
J. Kühnisch
S. Klaassen

Diffuse myocardial fibrosis by T1 mapping is associated with heart failure in pediatric primary dilated cardiomyopathy

N. Al-Wakeel-Marquard
F. Seidel
C. Herbst
J. Kühnisch
T. Kuehne
F. Berger
S. Klaassen
D.R. Messroghli

Kardiomyopathie im Neugeborenenalter: Forschungsfortschritte eröffnen neue diagnostische Möglichkeiten [Cardiomyopathy in neonatal age: advances in research open up new diagnostic possibilities]

M. Frenzel
S. Klaassen
K. Klingel
W. Knirsch
O. Kretschmar
J. Kühnisch
A. Oxenius

Familial recurrent myocarditis triggered by exercise in patients with a truncating variant of the desmoplakin gene

W. Poller
J. Haas
K. Klingel
J. Kühnisch
M. Gast
Z. Kaya
F. Escher
E. Kayvanpour
F. Degener
B. Opgen-Rhein
F. Berger
H.C. Mochmann
C. Skurk
B. Heidecker
H.P. Schultheiss
L. Monserrat
B. Meder
U. Landmesser
S. Klaassen

Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3

J. Kühnisch
C. Herbst
N. Al-Wakeel-Marquard
J. Dartsch
M. Holtgrewe
A. Baban
G. Mearini
J. Hardt
K. Kolokotronis
B. Gerull
L. Carrier
D. Beule
S. Schubert
D. Messroghli
F. Degener
F. Berger
S. Klaassen

RIKADA study reveals risk factors in pediatric primary cardiomyopathy

N. Al-Wakeel-Marquard
F. Degener
C. Herbst
J. Kühnisch
J. Dartsch
B. Schmitt
T. Kuehne
D. Messroghli
F. Berger
S. Klaassen

Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype

K. Kolokotronis
J. Kühnisch
E. Klopocki
J. Dartsch
S. Rost
C. Huculak
G. Mearini
S. Störk
L. Carrier
S. Klaassen
B. Gerull