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in Am J Hum Genet

Rare variants in NR2F2 cause congenital heart defects in humans

  • S. Al Turki
  • A.K. Manickaraj
  • C.L. Mercer
  • S.S. Gerety
  • M.P. Hitz
  • S. Lindsay
  • L.C.A. D'Alessandro
  • G.J. Swaminathan
  • J. Bentham
  • A.K. Arndt
  • J. Low
  • J. Breckpot
  • M. Gewillig
  • B. Thienpont
  • H. Abdul-Khaliq
  • C. Harnack
  • K. Hoff
  • H.H. Kramer
  • S. Schubert
  • R. Siebert
  • O. Toka
  • C. Cosgrove
  • H. Watkins
  • A.M. Lucassen
  • I.M. O'Kelly
  • A.P. Salmon
  • F.A. Bu'Lock
  • J. Granados-Riveron
  • K. Setchfield
  • C. Thornborough
  • J.D. Brook
  • B. Mulder
  • S. Klaassen
  • S. Bhattacharya
  • K. Devriendt
  • D.F. Fitzpatrick
  • D.I. Wilson
  • S. Mital
  • M.E. Hurles
in J Allergy Clin Immunol

Novel childhood asthma genes interact with in utero and early-life tobacco smoke exposure

  • S. Scholtens
  • D.S. Postma
  • M.F. Moffatt
  • S. Panasevich
  • R. Granell
  • A.J. Henderson
  • E. Melen
  • F. Nyberg
  • G. Pershagen
  • D. Jarvis
  • A. Ramasamy
  • M. Wjst
  • C. Svanes
  • E. Bouzigon
  • F. Demenais
  • F. Kauffmann
  • V. Siroux
  • E. von Mutius
  • M.J. Ege
  • C. Braun-Fahrlaender
  • J. Genuneit
  • B. Brunekreef
  • H.A. Smit
  • A.H. Wijga
  • M. Kerkhof
  • I. Curjuric
  • M. Imboden
  • G.A. Thun
  • N. Probst-Hensch
  • M.B. Freidin
  • E.I. Bragina
  • I.A. Deev
  • V.P. Puzyrev
  • D. Daley
  • J. Park
  • A. Becker
  • M. Chan-Yeung
  • A.L. Kozyrskyj
  • P. Pare
  • I. Marenholz
  • S. Lau
  • T. Keil
  • Y.A. Lee
  • M. Kabesch
  • C. Wijmenga
  • L. Franke
  • I.M. Nolte
  • J. Vonk
  • A. Kumar
  • M. Farrall
  • W.O.C.M. Cookson
  • D.P. Strachan
  • G.H. Koppelman
  • H.M. Boezen
in PLoS ONE

Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot

  • V. Bansal
  • C. Dorn
  • M. Grunert
  • S. Klaassen
  • R. Hetzer
  • F. Berger
  • S.R. Sperling
in Am J Hum Genet

Reponse to De Leeuw and Houge

  • A.K. Arndt
  • C.A. Macrae
  • S. Klaassen
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