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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 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
in Nat Neurosci

An unconventional role for miRNA: let-7 activates Toll-like receptor 7 and causes neurodegeneration

  • S.M. Lehmann
  • C. Krueger
  • B. Park
  • K. Derkow
  • K. Rosenberger
  • J. Baumgart
  • T. Trimbuch
  • G. Eom
  • M. Hinz
  • D. Kaul
  • P. Habbel
  • R. Kaelin
  • E. Franzoni
  • A. Rybak
  • D. Nguyen
  • R. Veh
  • O. Ninnemann
  • O. Peters
  • R. Nitsch
  • F.L. Heppner
  • D. Golenbock
  • E. Schott
  • H.L. Ploegh
  • F.G. Wulczyn
  • S. Lehnardt
in Dev Biol

The role of Irf6 in tooth epithelial invagination

  • J. Blackburn
  • A. Ohazama
  • K. Kawasaki
  • Y. Otsuka-Tanaka
  • B. Liu
  • K. Honda
  • R.B. Rountree
  • Y. Hu
  • M. Kawasaki
  • W. Birchmeier
  • R. Schmidt-Ullrich
  • A. Kinoshita
  • B.C. Schutte
  • N.L. Hammond
  • M.J. Dixon
  • P.T. Sharpe
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 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
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 Hypertension

Congenic substitution mapping excludes Sa as a candidate gene locus for a blood pressure quantitative trait locus on rat chromosome 1

  • N. Huebner
  • Y.A. Lee
  • K. Lindpaintner
  • D. Ganten
  • R. Kreutz