Associated Papers
Exploring Mitochondrial DNA Copy Number in Italian Children with ADHD: Implications for Neurobiological Mechanisms.
Citrigno L et al.
Diseases (basel, Switzerland), 2025
Impact of CYP2D6, MAOA, and UGT2B7 genetic variants on recurrence of Plasmodium Vivax in the Brazilian Amazon.
da Silva GS et al.
Scientific Reports, 2025
Aggressiveness in Italian Children with ADHD: MAOA Gene Polymorphism Involvement.
Neri L et al.
Diseases (basel, Switzerland), 2024
An increase in urinary primaquine and a reduction in urinary primaquine-5,6-orthoquinone in the Thai population with CYP2D6 reduced enzyme function.
Pookmanee W et al.
Heliyon, 2024
The MAOA rs979605 Genetic Polymorphism Is Differentially Associated with Clinical Improvement Following Antidepressant Treatment between Male and Female Depressed Patients.
Chappell K et al.
International Journal of Molecular Sciences, 2022
Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
Prakash A et al.
Scientific Reports, 2021
33986442 (PubMed )
Supplement: 41598_2021_89798_MOESM3_ESM.xlsx › Table_S1
Effects of MAO-A and CYP450 on primaquine metabolism in healthy volunteers.
Ariffin NM et al.
Parasitology Research, 2019
Mutation Screening of 1,237 Cancer Genes across Six Model Cell Lines of Basal-Like Breast Cancer.
Olsson E et al.
Plos One, 2015
26670335 (PubMed )
Supplement: pone.0144528.s005.xlsx › TableS3
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s007.pdf
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