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01. September 2013 in Int J Cardiol

Left ventricular non-compaction: prevalence in congenital heart disease

B.E. Stähli
C. Gebhard
P. Biaggi
S. Klaassen
E. Valsangiacomo Buechel
C.H. Attenhofer Jost
R. Jenni
F.C. Tanner
M. Greutmann

01. August 2013 in Am J Med Genet C Semin Med Genet

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7

A.M. Vermeer
K. van Engelen
A.V. Postma
M.J. Baars
I. Christiaans
S. De Haij
S. Klaassen
B.J. Mulder
B. Keavney

11. Juli 2013 in Am J Hum Genet

Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy

A.K. Arndt
S. Schaefer
J.D. Drenckhahn
M.K. Sabeh
E.R. Plovie
A. Caliebe
E. Klopocki
G. Musso
A.A. Werdich
H. Kalwa
M. Heinig
R.F. Padera
K. Wassilew
J. Bluhm
C. Harnack
J. Martitz
P.J. Barton
M. Greutmann
F. Berger
N. Huebner
R. Siebert
H.H. Kramer
S.A. Cook
C.A. Macrae
S. Klaassen

01. März 2013 in Neth Heart J

Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7

K. van Engelen
A.V. Postma
J.B.A. van de Meerakker
J.W. Roos-Hesselink
A.T.J.M. Helderman-van den Enden
H.W. Vliegen
T. Rahman
M.J.H. Baars
J.W. Sels
U. Bauer
T. Pickardt
S.R. Sperling
A.F.M. Moorman
B. Keavney
J. Goodship
S. Klaassen
B.J. Mulder

01. Dezember 2012 in Eur Radiol

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

06. September 2012 in PLoS Genet

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

01. Mai 2012 in Nat Med

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

15. Januar 2012 in Am J Cardiol

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

01. Dezember 2006 in Am J Hum Genet

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

04. Juli 2006 in J Am Coll Cardiol

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