Journal Articles Nature Medicine Year : 2020

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

Robert Davies
  • Function : Author
Ania Fiksinski
  • Function : Author
Elemi Breetvelt
  • Function : Author
Nigel Williams
  • Function : Author
Stephen Hooper
  • Function : Author
Thomas Monfeuga
  • Function : Author
Anne Bassett
  • Function : Author
Michael Owen
Raquel Gur
  • Function : Author
Bernice Morrow
  • Function : Author
Donna Mcdonald-Mcginn
  • Function : Author
Ann Swillen
  • Function : Author
Eva Chow
  • Function : Author
Marianne van den Bree
Beverly Emanuel
  • Function : Author
Joris Vermeesch
  • Function : Author
Therese van Amelsvoort
  • Function : Author
Celso Arango
  • Function : Author
Marco Armando
  • Function : Author
Linda Campbell
  • Function : Author
Joseph Cubells
  • Function : Author
Stephan Eliez
Sixto Garcia-Minaur
  • Function : Author
Doron Gothelf
  • Function : Author
Wendy Kates
  • Function : Author
Kieran Murphy
  • Function : Author
Clodagh Murphy
  • Function : Author
Declan Murphy
  • Function : Author
Gabriela Repetto
  • Function : Author
Vandana Shashi
  • Function : Author
Tony Simon
  • Function : Author
Damiàn Heine Suñer
  • Function : Author
Stefano Vicari
  • Function : Author
Stephen Scherer
  • Function : Author
Carrie Bearden
Jacob Vorstman
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Dates and versions

hal-03222249 , version 1 (28-09-2023)

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Robert Davies, Ania Fiksinski, Elemi Breetvelt, Nigel Williams, Stephen Hooper, et al.. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature Medicine, 2020, 26 (12), pp.1912-1918. ⟨10.1038/s41591-020-1103-1⟩. ⟨hal-03222249⟩

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