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Scientific Publications

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/ Am J Hum Genet

Reponse to De Leeuw and Houge

  • A.K. Arndt
  • C.A. Macrae
  • S. Klaassen
/ Nat Genet

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

  • B. Gerull
  • M. Gramlich
  • J. Atherton
  • M. McNabb
  • K. Trombitas
  • S. Sasse-Klaassen
  • J.G. Seidman
  • C. Seidman
  • H. Granzier
  • S. Labeit
  • M. Frenneaux
  • L. Thierfelder
/ FEBS J

Physical mechanisms of chromatin spatial organization

  • A.M. Chiariello
  • S. Bianco
  • A. Esposito
  • L. Fiorillo
  • M. Conte
  • E. Irani
  • F. Musella
  • A. Abraham
  • A. Prisco
  • M. Nicodemi
/ Int J Cardiol

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
/ Front Pediatr

Reduced systolic function and not genetic variants determine outcome in pediatric and adult left ventricular noncompaction cardiomyopathy

  • A. Schultze-Berndt
  • J. Kühnisch
  • C. Herbst
  • F. Seidel
  • N. Al-Wakeel-Marquard
  • J. Dartsch
  • S. Theisen
  • W. Knirsch
  • R. Jenni
  • M. Greutmann
  • E. Oechslin
  • F. Berger
  • S. Klaassen
/ Diabetologia

Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring-the heart as a target for fetal programming in rats

  • T. Schütte
  • S.M. Kedziora
  • N. Haase
  • F. Herse
  • N. Alenina
  • D.N. Müller
  • M. Bader
  • M. Schupp
  • R. Dechend
  • M. Golic
  • K. Kräker
/ Eur J Prev Cardiol

External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy

  • G. Norrish
  • C. Qu
  • E. Field
  • E. Cervi
  • D. Khraiche
  • S. Klaassen
  • T.H. Ojala
  • G. Sinagra
  • H. Yamazawa
  • C. Marrone
  • A. Popoiu
  • F. Centeno
  • S. Schouvey
  • I. Olivotto
  • S.M. Day
  • S. Colan
  • J. Rossano
  • S.G. Wittekind
  • S. Saberi
  • M. Russell
  • A. Helms
  • J. Ingles
  • C. Semsarian
  • P.M. Elliott
  • C.Y. Ho
  • R.Z. Omar
  • J.P. Kaski
/ Nat Commun

Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

  • S. Grosche
  • I. Marenholz
  • J. Esparza-Gordillo
  • A. Arnau-Soler
  • E. Pairo-Castineira
  • F. Rüschendorf
  • T.S. Ahluwalia
  • C. Almqvist
  • A. Arnold
  • H. Baurecht
  • H. Bisgaard
  • K. Bønnelykke
  • S.J. Brown
  • M. Bustamante
  • J.A. Curtin
  • A. Custovic
  • S.C. Dharmage
  • A. Esplugues
  • M. Falchi
  • D. Fernandez-Orth
  • M.A.R. Ferreira
  • A. Franke
  • S. Gerdes
  • C. Gieger
  • H. Hakonarson
  • P.G. Holt
  • G. Homuth
  • N. Hubner
  • P.G. Hysi
  • M.R. Jarvelin
  • R. Karlsson
  • G.H. Koppelman
  • S. Lau
  • M. Lutz
  • P.K.E. Magnusson
  • G.B. Marks
  • M. Müller-Nurasyid
  • M.M. Nöthen
  • L. Paternoster
  • C.E. Pennell
  • A. Peters
  • K. Rawlik
  • C.F. Robertson
  • E. Rodriguez
  • S. Sebert
  • A. Simpson
  • P.M.A. Sleiman
  • M. Standl
  • D. Stölzl
  • K. Strauch
  • A. Szwajda
  • A. Tenesa
  • P.J. Thompson
  • V. Ullemar
  • A. Visconti
  • J.M. Vonk
  • C.A. Wang
  • S. Weidinger
  • M. Wielscher
  • C.L. Sargent
  • C.J. Xu
  • Y.A. Lee
/ Nature

Cell-type specialization is encoded by specific chromatin topologies

  • W. Winick-Ng
  • A. Kukalev
  • I. Harabula
  • L. Zea-Redondo
  • D. Szabó
  • M. Meijer
  • L. Serebreni
  • Y. Zhang
  • S. Bianco
  • A.M. Chiariello
  • I. Irastorza-Azcarate
  • C.J. Thieme
  • T.M. Sparks
  • S. Carvalho
  • L. Fiorillo
  • F. Musella
  • E. Irani
  • E.T. Triglia
  • A.A. Kolodziejczyk
  • A. Abentung
  • G. Apostolova
  • E.J. Paul
  • V. Franke
  • R. Kempfer
  • A. Akalin
  • S.A. Teichmann
  • G. Dechant
  • M.A. Ungless
  • M. Nicodemi
  • L. Welch
  • G. Castelo-Branco
  • A. Pombo
/ PLoS Comput Biol

Multifunctional RNA-binding proteins influence mRNA abundance and translational efficiency of distinct sets of target genes

  • V. Schneider-Lunitz
  • J. Ruiz-Orera
  • N. Hubner
  • S. van Heesch