Associated Papers
Biogenic Amine Metabolism and Its Genetic Variations in Autism Spectrum Disorder: A Comprehensive Overview.
Tabolacci C et al.
Biomolecules, 2025
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors.
Akhavanfard S et al.
Nature Communications, 2020
32371905 (PubMed )
Supplement: 41467_2020_16067_MOESM12_ESM.xlsx › Supplementary_Data_9
Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.
Prasad A et al.
Bmc Medical Genetics, 2018
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.
Botros HG et al.
Journal of Pineal Research, 2013
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism.
Wang L et al.
Plos One, 2013
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder.
Etain B et al.
Human Molecular Genetics, 2012
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Chaste P et al.
Journal of Pineal Research, 2011
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability.
Pagan C et al.
Bmc Medical Genetics, 2011
Mutation screening of melatonin-related genes in patients with autism spectrum disorders.
Jonsson L et al.
Bmc Medical Genomics, 2010
Abnormal melatonin synthesis in autism spectrum disorders.
Melke J et al.
Molecular Psychiatry, 2008
Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.
Toma C et al.
Molecular Psychiatry, 2007
The possible interplay of synaptic and clock genes in autism spectrum disorders.
Bourgeron T
Cold Spring Harbor Symposia on Quantitative Biology, 2007
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