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in FASEB J

Gravity-sensitive signaling drives 3-dimensional formation of multicellular thyroid cancer spheroids

  • J. Grosse
  • M. Wehland
  • J. Pietsch
  • H. Schulz
  • K. Saar
  • N. Huebner
  • C. Eilles
  • J. Bauer
  • K. Abou-El-Ardat
  • S. Baatout
  • X. Ma
  • M. Infanger
  • R. Hemmersbach
  • D. Grimm
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
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
in PLoS Biol

A genetic basis for mechanosensory traits in humans

  • H. Frenzel
  • J. Bohlender
  • K. Pinsker
  • B. Wohlleben
  • J. Tank
  • S.G. Lechner
  • D. Schiska
  • T. Jaijo
  • F. Rueschendorf
  • K. Saar
  • J. Jordan
  • J.M. Millan
  • M. Gross
  • G.R. Lewin
in Nat Methods

Combined RNAi and localization for functionally dissecting long noncoding RNAs

  • D. Chakraborty
  • D. Kappei
  • M. Theis
  • A. Nitzsche
  • L. Ding
  • M. Paszkowski-Rogacz
  • V. Surendranath
  • N. Berger
  • H. Schulz
  • K. Saar
  • N. Hubner
  • F. Buchholz
in FASEB J

Short-term weightlessness produced by parabolic flight maneuvers altered gene expression patterns in human endothelial cells

  • J. Grosse
  • M. Wehland
  • J. Pietsch
  • X. Ma
  • C. Ulbrich
  • H. Schulz
  • K. Saar
  • N. Huebner
  • J. Hauslage
  • R. Hemmersbach
  • M. Braun
  • J. van Loon
  • N. Vagt
  • M. Infanger
  • C. Eilles
  • M. Egli
  • P. Richter
  • T. Baltz
  • R. Einspanier
  • S. Sharbati
  • D. Grimm
in BMC Med Genet

Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis

  • S. Knuppel
  • J. Esparza-Gordillo
  • I. Marenholz
  • H. Holzhutter
  • A. Bauerfeind
  • A. Ruether
  • S. Weidinger
  • Y.A. Lee
  • K. Rohde
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
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