Associated Papers
Translating IBD Genomics into Clinical Practice.
Singh P et al.
Digestive Diseases and Sciences, 2026
Evaluation of FTO polymorphism in 6-mercaptopurine related intolerance in children with acute lymphoblastic leukemia.
Singh M et al.
Cancer Chemotherapy and Pharmacology, 2023
Identification of genetic variants related to metabolic syndrome by next-generation sequencing.
Lee S et al.
Diabetology & Metabolic Syndrome, 2022
Analysis of coding variants in the human FTO gene from the gnomAD database.
Souza Junior MLF et al.
Plos One, 2022
Comprehensive mutations analyses of FTO (fat mass and obesity-associated gene) and their effects on FTO's substrate binding implicated in obesity.
Kumar R et al.
Frontiers in Nutrition, 2022
35923209 (PubMed )
Supplement: Data_Sheet_1.PDF
Comparison of potential inhibitors and targeting fat mass and obesity-associated protein causing diabesity through docking and molecular dynamics strategies.
Kumar SU et al.
Journal of Cellular Biochemistry, 2021
Variants of Lipid-Related Genes in Adult Japanese Patients with Severe Hypertriglyceridemia.
Matsunaga A et al.
Journal of Atherosclerosis and Thrombosis, 2020
An intronic FTO variant rs16952570 confers protection against thiopurine-induced myelotoxicities in multiethnic Asian IBD patients.
Chen S et al.
The Pharmacogenomics Journal, 2020
Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients.
Park SC et al.
Cells, 2019
NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.
Kakuta Y et al.
Journal of Gastroenterology, 2018
29923122 (PubMed )
Supplement: 535_2018_1486_MOESM1_ESM.pdf
A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD.
Kim HS et al.
Gut, 2017
Genome-Wide Association Studies of Chemotherapeutic Toxicities: Genomics of Inequality.
Mapes B et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2017
NUDT15, FTO, and RUNX1 genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases.
Sato T et al.
Intestinal Research, 2017
Prevalence of loss-of-function FTO mutations in lean and obese individuals.
Meyre D et al.
Diabetes, 2010
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