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in Clin Genet

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
in J Am Heart Assoc

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
in Hum Mutat

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
in J Am Coll Cardiol

Left ventricular noncompaction: phenotype in an integrated model of cardiomyopathy?

  • E. Oechslin
  • S. Klaassen
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
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
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
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
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
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