Veröffentlichungen

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

The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface

W. Seifert
Y. Posor
P. Schu
G. Stenbeck
S. Mundlos
S. Klaassen
P. Nürnberg
V. Haucke
U. Kornak
J. Kühnisch

01. August 2016 in Nat Genet

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

A. Sifrim
M.P. Hitz
A. Wilsdon
J. Breckpot
S.H.A. Turki
B. Thienpont
J. McRae
T.W. Fitzgerald
T. Singh
G.J. Swaminathan
E. Prigmore
D. Rajan
H. Abdul-Khaliq
S. Banka
U.M.M. Bauer
J. Bentham
F. Berger
S. Bhattacharya
F. Bu'Lock
N. Canham
I.G. Colgiu
C. Cosgrove
H. Cox
I. Daehnert
A. Daly
J. Danesh
A. Fryer
M. Gewillig
E. Hobson
K. Hoff
T. Homfray
A.K. Kahlert
A. Ketley
H.H. Kramer
K. Lachlan
A.K. Lampe
J.J. Louw
A.K. Manickara
D. Manase
K.P. McCarthy
K. Metcalfe
C. Moore
R. Newbury-Ecob
S.O. Omer
W.H. Ouwehand
S.M. Park
M.J. Parker
T. Pickardt
M.O. Pollard
L. Robert
D.J. Roberts
J. Sambrook
K. Setchfield
B. Stiller
C. Thornborough
O. Toka
H. Watkins
D. Williams
M. Wright
S. Mital
P.E.F. Daubeney
B. Keavney
J. Goodship
R.M. Abu-Sulaiman
S. Klaassen
C.F. Wright
H.V. Firth
J.C. Barrett
K. Devriendt
D.R. FitzPatrick
J.D. Brook
M.E. Hurles

Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies

M. Grothoff
M. Pachowsky
J. Hoffmann
M. Posch
S. Klaassen
L. Lehmkuhl
M. Gutberlet

Rare copy number variants contribute to congenital left-sided heart disease

M.P. Hitz
L.P. Lemieux-Perreault
C. Marshall
Y. Feroz-Zada
R. Davies
S.W. Yang
A.C. Lionel
G. D'Amours
E. Lemyre
R. Cullum
J.L. Bigras
M. Thibeault
P. Chetaille
A. Montpetit
P. Khairy
B. Overduin
S. Klaassen
P. Hoodless
P. Awadalla
J. Hussin
Y. Idaghdour
M. Nemer
A.F. Stewart
C. Boerkoel
S.W. Scherer
A. Richter
M.P. Dube
G. Andelfinger

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

W. Guo
S. Schafer
M.L. Greaser
M.H. Radke
M. Liss
T. Govindarajan
H. Maatz
H. Schulz
S.E. Lincoln
A.M. Parrish
V. Dauksaite
P. Vakeel
S. Klaassen
B. Gerull
L. Thierfelder
V. Regitz-Zagrosek
T.A. Hacker
K.W. Saupe
G.W. Dec
P.T. Ellinor
C.A. MacRae
B. Spallek
R. Fischer
A. Perrot
C. Ozcelik
K. Saar
N. Hubner
M. Gotthardt

Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction

M. Greutmann
M.L. Mah
C.K. Silversides
S. Klaassen
C.H. Attenhofer Jost
R. Jenni
E.N. Oechslin

Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy

A. Heuser
E.R. Plovie
P.T. Ellinor
K.S. Grossmann
J.T. Shin
T. Wichter
C.T. Basson
B.B. Lerman
S. Sasse-Klaassen
L. Thierfelder
C.A. MacRae
B. Gerull

A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26

P.T. Ellinor
S. Sasse-Klaassen
S. Probst
B. Gerull
J.T. Shin
A. Toeppel
A. Heuser
B. Michely
D.M. Yoerger
B.S. Song
B. Pilz
G. Krings
B. Coplin
P.E. Lange
G.W. Dec
H.C. Hennies
L. Thierfelder
C.A. MacRae