Associated Papers
Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.
Pagan C et al.
Scientific Reports, 2017
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.
Baetens D et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
27490115 (PubMed )
Supplement: gim2016118x1.zip › Table_S13-S17.xlsx › Table_S13
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Chaste P et al.
Journal of Pineal Research, 2011
Resequencing and association analysis of arylalkylamine N-acetyltransferase (AANAT) gene and its contribution to major depression susceptibility.
Soria V et al.
Journal of Pineal Research, 2010
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