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/ 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
/ 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
/ J Allergy Clin Immunol

The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma

  • M.H. Dizier
  • P. Margaritte-Jeannin
  • A.M. Madore
  • J. Esparza-Gordillo
  • M.F. Moffatt
  • E. Corda
  • F. Monier
  • M. Guilloud-Bataille
  • A. Franke
  • S. Weidinger
  • I. Annesi-Maesano
  • J. Just
  • I. Pin
  • F. Kauffmann
  • W. Cookson
  • Y.A. Lee
  • C. Laprise
  • M. Lathrop
  • E. Bouzigon
  • F. Demenais
/ 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
/ PLoS Genet

An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity

  • P. Kuehnen
  • M. Mischke
  • S. Wiegand
  • C. Sers
  • B. Horsthemke
  • S. Lau
  • T. Keil
  • Y.A. Lee
  • A. Grueters
  • H. Krude
/ 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
/ 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
/ Mamm Genome

The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4

  • N. Huebner
  • R. Kreutz
  • S. Rubattu
  • Y.A. Lee
  • D. Ganten
  • P.D. Allen
  • K. Lindpaintner

Genetische Analyse des Bluthochdrucks

  • Y.A. Lee
  • N. Huebner
  • D. Ganten