Emilie Serrano

Genetic variations of the melatonin pathway in patients with attention‐deficit and hyperactivity disorders

T. Bourgeron, R. Delorme, C. Gillberg, 2011, Journal of pineal research.

De novo deletion of TBL1XR1 in a child with non‐specific developmental delay supports its implication in intellectual disability

A. Verloes, B. Benzacken, C. Dupont, 2014, American journal of medical genetics. Part A.

Genetic and Functional ascertainment of the Melatonin Pathway in Patients with Attention Deficit and Hyperactivity Disorders

T. Bourgeron, R. Delorme, C. Gillberg, 2018 .

Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population

T. Bourgeron, R. Delorme, C. Gillberg, 2010, PloS one.