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/ 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
/ Cell Rep

53BP1 supports immunoglobulin class switch recombination independently of its DNA double-strand break end protection function

  • D. Sundaravinayagam
  • A. Rahjouei
  • M. Andreani
  • D. Tupiņa
  • S. Balasubramanian
  • T. Saha
  • V. Delgado-Benito
  • V. Coralluzzo
  • O. Daumke
  • M. Di Virgilio
/ 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
/ 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
/ 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