Woman reading in MDC library

Veröffentlichungen

11 Ergebnisse:
Active Filter:
Sortieren:
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 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 J Invest Dermatol

Association screening in the epidermal differentiation complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczema

  • I. Marenholz
  • V.A. Rivera
  • J. Esparza-Gordillo
  • A. Bauerfeind
  • M.A. Lee-Kirsch
  • A. Ciechanowicz
  • M. Kurek
  • T. Piskackova
  • M. Macek
  • Y.A. Lee
in Circ Cardiovasc Genet

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype

  • S. Probst
  • E. Oechslin
  • P. Schuler
  • M. Greutmann
  • P. Boye
  • W. Knirsch
  • F. Berger
  • L. Thierfelder
  • R. Jenni
  • S. Klaassen
in Hum Mol Genet

The eczema risk variant on chromosome 11q13 (rs7927894) in the population-based ALSPAC cohort: a novel susceptibility factor for asthma and hay fever

  • I. Marenholz
  • A. Bauerfeind
  • J. Esparza-Gordillo
  • T. Kerscher
  • R. Granell
  • R. Nickel
  • S. Lau
  • J. Henderson
  • Y.A. Lee
in Circ Cardiovasc Genet

Mutations in the sarcomere protein gene MYH7 in Ebstein's anomaly

  • A.V. Postma
  • K. van Engelen
  • J. van de Meerakker
  • T. Rahman
  • S. Probst
  • M.J. Baars
  • U. Bauer
  • T. Pickardt
  • S.R. Sperling
  • F. Berger
  • A.F. Moorman
  • B.J. Mulder
  • L. Thierfelder
  • B. Keavney
  • J. Goodship
  • S. Klaassen
in Curr Opin Allergy Clin Immunol

Genome-wide approaches to the etiology of eczema

  • J. Esparza-Gordillo
  • I. Marenholz
  • Y.A. Lee