Publicacións en colaboración con investigadores/as de Norwegian Institute of Public Health (4)

2022

  1. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331

2020

  1. Using methylome data to inform exposome-health association studies: An application to the identification of environmental drivers of child body mass index

    Environment International, Vol. 138

2018

  1. Human Early Life Exposome (HELIX) study: A European population-based exposome cohort

    BMJ Open, Vol. 8, Núm. 9

2014

  1. Euroforgen-NoE collaborative exercise on LRmix to demonstrate standardization of the interpretation of complex DNA profiles

    Forensic Science International: Genetics, Vol. 9, Núm. 1, pp. 47-54