Associated Papers
Contrastive sequence signatures between the both sides of a recombination spot reveal an adaptation at PPARD locus from standing variation for pleiotropy since out-of-Africa dispersal.
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Supplement: 12864_2025_11620_MOESM2_ESM.xlsx › TS5
Unpleasant Smell: A Case Report of Trimethylaminuria (Fish Odour Syndrome) in a Child.
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Cureus, 2025
Exploring Trimethylaminuria: Genetics and Molecular Mechanisms, Epidemiology, and Emerging Therapeutic Strategies.
Sidoti A et al.
Biology, 2024
Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.
Zhang T et al.
Peerj, 2024
39465171 (PubMed )
Supplement: peerj-12-18360-s002.7z › drug-metabolizing_enzymes_and_transporter__DMET__microarray › markerlist.xlsx › markerlist.TXT
Adaptive Modelling of Mutated FMO3 Enzyme Could Unveil Unexplored Scenarios Linking Variant Haplotypes to TMAU Phenotypes.
Alibrandi S et al.
Molecules (basel, Switzerland), 2021
Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.
Kim B et al.
Translational and Clinical Pharmacology, 2021
34621706 (PubMed )
Supplement: tcp-29-135-s001.xls › tcp-29-135-s001
Variations in plasma concentrations of tamoxifen metabolites and the effects of genetic polymorphisms on tamoxifen metabolism in Korean patients with breast cancer.
Woo HI et al.
Oncotarget, 2017
First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation.
Scimone C et al.
Journal of Digestive Diseases, 2016
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.
D'Angelo R et al.
Journal of Medical Case Reports, 2014
Trimethylaminuria (fish odor syndrome): genotype characterization among Portuguese patients.
Ferreira F et al.
Gene, 2013
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.
Chalmers RA et al.
Journal of Inherited Metabolic Disease, 2006
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