Publications:

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Personalized medicine to implementation science: Thiopurines set for the leap.

Jgh Open : An Open Access Journal Of Gastroenterology And Hepatology

Sharma, Vishal V; Kedia, Saurabh S; Ahuja, Vineet V

Publication Date: 2022-10

Variant appearance in text: FTO: A134T; rs79206939

PubMed Link: 36262539

Variant Present in the following documents:

• Main text
• JGH3-6-651.pdf

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Identification of genetic variants related to metabolic syndrome by next-generation sequencing.

Diabetology & Metabolic Syndrome

Lee, Sanghoo S; Kim, Seol-A SA; Hong, Jeonghoon J; Kim, Yejin Y; Hong, Gayeon G; Baik, SaeYun S; Choi, Kyeonghwan K; Lee, Mi-Kyeong MK; Lee, Kyoung-Ryul KR

Publication Date: 2022-08-23

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 35999587

Variant Present in the following documents:

• Main text
• 13098_2022_Article_893.pdf

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Analysis of coding variants in the human FTO gene from the gnomAD database.

Plos One

Souza Junior, Mauro Lúcio Ferreira MLF; de Sousa, Jaime Viana JV; Guerreiro, João Farias JF

Publication Date: 2022

Variant appearance in text: FTO: Ala134Thr

PubMed Link: 34990463

Variant Present in the following documents:

• Main text
• pone.0248610.pdf

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Analysis of coding variants in the human FTO gene from the gnomAD database.

Plos One

Souza Junior, Mauro Lúcio Ferreira MLF; de Sousa, Jaime Viana JV; Guerreiro, João Farias JF

Publication Date: 2022

Variant appearance in text: FTO: Ala134Thr

PubMed Link: 34990463

Variant Present in the following documents:

• Main text
• pone.0248610.pdf

View BVdb publication page

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Common and Unique Genetic Background between Attention-Deficit/Hyperactivity Disorder and Excessive Body Weight.

Genes

Dmitrzak-Weglarz, Monika M; Paszynska, Elzbieta E; Bilska, Karolina K; Szczesniewska, Paula P; Bryl, Ewa E; Duda, Joanna J; Dutkiewicz, Agata A; Tyszkiewicz-Nwafor, Marta M; Czerski, Piotr P; Hanc, Tomasz T; Slopien, Agnieszka A

Publication Date: 2021-09-13

Variant appearance in text: rs79206939

PubMed Link: 34573389

Variant Present in the following documents:

• Main text
• genes-12-01407.pdf

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Importance of NUDT15 Polymorphisms in Thiopurine Treatments.

Journal Of Personalized Medicine

Tanaka, Yoichi Y; Saito, Yoshiro Y

Publication Date: 2021-08-10

Variant appearance in text: rs79206939

PubMed Link: 34442422

Variant Present in the following documents:

• Main text
• jpm-11-00778.pdf

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Thiopurines in Inflammatory Bowel Disease. How to Optimize Thiopurines in the Biologic Era?

Frontiers In Medicine

Gargallo-Puyuelo, Carla J CJ; Laredo, Viviana V; Gomollón, Fernando F

Publication Date: 2021

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 34336887

Variant Present in the following documents:

• Main text
• fmed-08-681907.pdf

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Variants of Lipid-Related Genes in Adult Japanese Patients with Severe Hypertriglyceridemia.

Journal Of Atherosclerosis And Thrombosis

Matsunaga, Akira A; Nagashima, Mariko M; Yamagishi, Hideko H; Saku, Keijiro K

Publication Date: 2020-12-01

Variant appearance in text: FTO: 400G>A; A134T; rs79206939

PubMed Link: 32115487

Variant Present in the following documents:

• Main text
• jat-27-1264.pdf

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Genetic Studies of Inflammatory Bowel Disease-Focusing on Asian Patients.

Cells

Park, Sung Chul SC; Jeen, Yoon Tae YT

Publication Date: 2019-05-01

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 31052430

Variant Present in the following documents:

• Main text
• cells-08-00404.pdf

View BVdb publication page

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Revisiting the Role of Thiopurines in Inflammatory Bowel Disease Through Pharmacogenomics and Use of Novel Methods for Therapeutic Drug Monitoring.

Frontiers In Pharmacology

Lim, Sheng Zhang SZ; Chua, Eng Wee EW

Publication Date: 2018

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 30349479

Variant Present in the following documents:

• Main text
• fphar-09-01107.pdf

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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.

Journal Of Gastroenterology

Kakuta, Yoichi Y; Kawai, Yosuke Y; Okamoto, Daisuke D; Takagawa, Tetsuya T; Ikeya, Kentaro K; Sakuraba, Hirotake H; Nishida, Atsushi A; Nakagawa, Shoko S; Miura, Miki M; Toyonaga, Takahiko T; Onodera, Kei K; Shinozaki, Masaru M; Ishiguro, Yoh Y; Mizuno, Shinta S; Takahara, Masahiro M; Yanai, Shunichi S; Hokari, Ryota R; Nakagawa, Tomoo T; Araki, Hiroshi H; Motoya, Satoshi S; Naito, Takeo T; Moroi, Rintaro R; Shiga, Hisashi H; Endo, Katsuya K; Kobayashi, Taku T; Naganuma, Makoto M; Hiraoka, Sakiko S; Matsumoto, Takayuki T; Nakamura, Shiro S; Nakase, Hiroshi H; Hisamatsu, Tadakazu T; Sasaki, Makoto M; Hanai, Hiroyuki H; Andoh, Akira A; Nagasaki, Masao M; Kinouchi, Yoshitaka Y; Shimosegawa, Tooru T; Masamune, Atsushi A; Suzuki, Yasuo Y; ,

Publication Date: 2018-09

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 29923122

Variant Present in the following documents:

• 535_2018_1486_MOESM1_ESM.pdf

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NUDT15, FTO, and RUNX1 genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases.

Intestinal Research

Sato, Toshiyuki T; Takagawa, Tetsuya T; Kakuta, Yoichi Y; Nishio, Akihiro A; Kawai, Mikio M; Kamikozuru, Koji K; Yokoyama, Yoko Y; Kita, Yuko Y; Miyazaki, Takako T; Iimuro, Masaki M; Hida, Nobuyuki N; Hori, Kazutoshi K; Ikeuchi, Hiroki H; Nakamura, Shiro S

Publication Date: 2017-07

Variant appearance in text: FTO: Ala134Thr; rs79206939

PubMed Link: 28670229

Variant Present in the following documents:

• Main text
• ir-15-328.pdf

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Genome-Wide Association Studies of Chemotherapeutic Toxicities: Genomics of Inequality.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research

Mapes, Brandon B; El Charif, Omar O; Al-Sawwaf, Shereen S; Dolan, M Eileen ME

Publication Date: 2017-08-01

Variant appearance in text: FTO: A134T; rs79206939

PubMed Link: 28442506

Variant Present in the following documents:

• Main text

View BVdb publication page

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Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing.

Plos One

Yang, Liping L; Cui, Hui H; Yin, Xiaobei X; Dou, Hongliang H; Zhao, Lin L; Chen, Ningning N; Zhang, Jinlu J; Zhang, Huirong H; Li, Genlin G; Ma, Zhizhong Z

Publication Date: 2015

Variant appearance in text: FTO: 400G>A; A134T; rs79206939

PubMed Link: 26496393

Variant Present in the following documents:

• pone.0140684.s004.xlsx, sheet 5

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Prevalence of loss-of-function FTO mutations in lean and obese individuals.

Diabetes

Meyre, David D; Proulx, Karine K; Kawagoe-Takaki, Hiroko H; Vatin, Vincent V; Gutiérrez-Aguilar, Ruth R; Lyon, Debbie D; Ma, Marcella M; Choquet, Helene H; Horber, Fritz F; Van Hul, Wim W; Van Gaal, Luc L; Balkau, Beverley B; Visvikis-Siest, Sophie S; Pattou, François F; Farooqi, I Sadaf IS; Saudek, Vladimir V; O'Rahilly, Stephen S; Froguel, Philippe P; Sedgwick, Barbara B; Yeo, Giles S H GS

Publication Date: 2010-01

Variant appearance in text: FTO: A134T

PubMed Link: 19833892

Variant Present in the following documents:

• Main text
• zdb311.pdf

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