H. Olivié

The medical care of children with autism.

H. Olivié, 2012, European journal of pediatrics.

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

G. Cooper, P. Fergelot, K. Devriendt, 2020, European Journal of Human Genetics.

STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability

Golder N Wilson, I. Simonic, Soo-Mi Park, 2017, Journal of Medical Genetics.

Clinical practice

H. Olivié, 2011, European Journal of Pediatrics.

The clinical relevance of intragenic NRXN1 deletions

H. Peeters, L. Gallagher, T. de Ravel, 2017, Journal of Medical Genetics.