Publications:

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NAT2 global landscape: Genetic diversity and acetylation statuses from a systematic review.

Plos One

Gutiérrez-Virgen, Jorge E JE; Piña-Pozas, Maricela M; Hernández-Tobías, Esther A EA; Taja-Chayeb, Lucia L; López-González, Ma de Lourdes ML; Meraz-Ríos, Marco A MA; Gómez, Rocío R

Publication Date: 2023

Variant appearance in text: rs1799929

PubMed Link: 37023111

Variant Present in the following documents:

• Main text
• pone.0283726.s015.xlsx, sheet 1
• pone.0283726.pdf
• pone.0283726.s016.xlsx, sheet 1

View BVdb publication page

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Quantitative and causal analysis for inflammatory genes and the risk of Parkinson's disease.

Frontiers In Immunology

Yi, Minhan M; Li, Jiaxin J; Jian, Shijie S; Li, Binbin B; Huang, Zini Z; Shu, Li L; Zhang, Yuan Y

Publication Date: 2023

Variant appearance in text: rs1799929

PubMed Link: 36926335

Variant Present in the following documents:

• Main text
• fimmu-14-1119315.pdf
• DataSheet_2.pdf

View BVdb publication page

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CYP2C19-rs4986893 confers risk to major depressive disorder and bipolar disorder in the Han Chinese population whereas ABCB1-rs1045642 acts as a protective factor.

Bmc Psychiatry

Zhang, Ting T; Rao, Qingmin Q; Lin, Kangguang K; He, Yongyin Y; Cai, Jintai J; Yang, Mengxin M; Xu, Ying Y; Hou, Le L; Lin, Yulong Y; Liu, Haiying H

Publication Date: 2023-01-25

Variant appearance in text: rs1799929

PubMed Link: 36698099

Variant Present in the following documents:

• Main text
• 12888_2022_Article_4514.pdf

View BVdb publication page

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs1799929

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Genetic susceptibility of bladder cancer in the Lebanese population.

Bmc Medical Genomics

Kourie, Hampig Raphael HR; Succar, Bahaa B; Chouery, Eliane E; Mehawej, Cybel C; Ahmadieh, Nizar N; Zouein, Joseph J; Mardirossian, Avedis A; Jalkh, Nadine N; Sleilaty, Ghassan G; Kattan, Joseph J; Nemr, Elie E

Publication Date: 2022-10-17

Variant appearance in text: NAT2: 481C>T; Leu161=; rs1799929

PubMed Link: 36253817

Variant Present in the following documents:

• 12920_2022_1372_MOESM1_ESM.xlsx, sheet 1
• 12920_2022_1372_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports

Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-10-14

Variant appearance in text: NAT2: L161L

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM12_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
• 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation

Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA

Publication Date: 2022-09-08

Variant appearance in text: NAT2: L161L

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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Influence of N-acetyltransferase 2 (NAT2) genotype/single nucleotide polymorphisms on clearance of isoniazid in tuberculosis patients: a systematic review of population pharmacokinetic models.

European Journal Of Clinical Pharmacology

Thomas, Levin L; Raju, Arun Prasath AP; Chaithra, ; M, Sonal Sekhar SS; Varma, Muralidhar M; Saravu, Kavitha K; Banerjee, Mithu M; Sv, Chidananda Sanju CS; Mallayasamy, Surulivelrajan S; Rao, Mahadev M

Publication Date: 2022-10

Variant appearance in text: NAT2: 481C>T; rs1799929

PubMed Link: 35852584

Variant Present in the following documents:

• Main text
• 228_2022_Article_3362.pdf

View BVdb publication page

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Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing.

Frontiers In Pharmacology

Silgado-Guzmán, Daniel Felipe DF; Angulo-Aguado, Mariana M; Morel, Adrien A; Niño-Orrego, María José MJ; Ruiz-Torres, Daniel-Armando DA; Contreras Bravo, Nora Constanza NC; Restrepo, Carlos Martin CM; Ortega-Recalde, Oscar O; Fonseca-Mendoza, Dora Janeth DJ

Publication Date: 2022

Variant appearance in text: NAT2: 481C>T; Leu161=; rs1799929

PubMed Link: 35846994

Variant Present in the following documents:

• Table1.xlsx, sheet 1

View BVdb publication page

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Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease

Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD

Publication Date: 2022-06-29

Variant appearance in text: NAT2: L161L; rs1799929

PubMed Link: 35768426

Variant Present in the following documents:

• 41531_2022_346_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Single-nucleotide polymorphisms as important risk factors of diabetes among Middle East population.

Human Genomics

Akhlaghipour, Iman I; Bina, Amir Reza AR; Mogharrabi, Mohammad Reza MR; Fanoodi, Ali A; Ebrahimian, Amir Reza AR; Khojasteh Kaffash, Soroush S; Babazadeh Baghan, Atefeh A; Khorashadizadeh, Mohammad Erfan ME; Taghehchian, Negin N; Moghbeli, Meysam M

Publication Date: 2022-04-02

Variant appearance in text: rs1799929

PubMed Link: 35366956

Variant Present in the following documents:

• Main text

View BVdb publication page

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Human Arylamine N-Acetyltransferase 1 (NAT1) Knockout in MDA-MB-231 Breast Cancer Cell Lines Leads to Transcription of NAT2.

Frontiers In Pharmacology

Carlisle, Samantha M SM; Trainor, Patrick J PJ; Doll, Mark A MA; Hein, David W DW

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 35046826

Variant Present in the following documents:

• Main text
• fphar-12-803254.pdf

View BVdb publication page

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Genetic Polymorphisms of Very Important Pharmacogene Variants in the Blang Population from Yunnan Province in China.

Pharmacogenomics And Personalized Medicine

Wang, Yuliang Y; Peng, Linna L; Lu, Hongyan H; Zhang, Zhanhao Z; Xing, Shishi S; Li, Dandan D; He, Chunjuan C; Jin, Tianbo T; Wang, Li L

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34949935

Variant Present in the following documents:

• Main text
• pgpm-14-1647.pdf

View BVdb publication page

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Genetic Polymorphism of Drug Metabolic Gene CYPs, VKORC1, NAT2, DPYD and CHST3 of Five Ethnic Minorities in Heilongjiang Province, Northeast China.

Pharmacogenomics And Personalized Medicine

Zhang, Tingting T; Li, Qiuyan Q; Dong, Bonan B; Liang, Xiao X; Jia, Mansha M; Bai, Jing J; Yu, Jingcui J; Fu, Songbin S

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34876832

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic analysis of pharmacogenomic VIP variants in the Wa population from Yunnan Province of China.

Bmc Genomic Data

Li, Dandan D; Peng, Linna L; Xing, Shishi S; He, Chunjuan C; Jin, Tianbo T

Publication Date: 2021-11-19

Variant appearance in text: rs1799929

PubMed Link: 34798807

Variant Present in the following documents:

• Main text
• 12863_2021_Article_999.pdf

View BVdb publication page

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Analysis of Very Important Pharmacogenomics Variants in the Chinese Lahu Population.

Pharmacogenomics And Personalized Medicine

Cheng, Yujing Y; Li, Qi Q; Yang, Xin X; Ding, Heng H; Chen, Wanlu W; Dai, Run R; Zhang, Chan C

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34629888

Variant Present in the following documents:

• Main text
• pgpm-14-1275.pdf

View BVdb publication page

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Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.

Translational And Clinical Pharmacology

Kim, Byungwook B; Yoon, Deok Yong DY; Lee, SeungHwan S; Jang, In-Jin IJ; Yu, Kyung-Sang KS; Cho, Joo-Youn JY; Oh, Jaeseong J

Publication Date: 2021-09

Variant appearance in text: NAT2: 481C>T; L161L; rs1799929

PubMed Link: 34621706

Variant Present in the following documents:

• tcp-29-135-s001.xls, sheet 1

View BVdb publication page

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Allelic and genotypic frequencies of NAT2, CYP2E1, and AADAC genes in a cohort of Peruvian tuberculosis patients.

Molecular Genetics & Genomic Medicine

Levano, Kelly S KS; Jaramillo-Valverde, Luis L; Tarazona, David D DD; Sanchez, Cesar C; Capristano, Silvia S; Vásquez-Loarte, Tania T; Solari, Lely L; Mendoza-Ticona, Alberto A; Soto, Alonso A; Rojas, Christian C; Zegarra-Chapoñan, Roberto R; Guio, Heinner H

Publication Date: 2021-10

Variant appearance in text: NAT2: 481C>T; L161L; rs1799929

PubMed Link: 34510815

Variant Present in the following documents:

• Main text

View BVdb publication page

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Allelic and genotypic frequencies of NAT2, CYP2E1, and AADAC genes in a cohort of Peruvian tuberculosis patients.

Molecular Genetics & Genomic Medicine

Levano, Kelly S KS; Jaramillo-Valverde, Luis L; Tarazona, David D DD; Sanchez, Cesar C; Capristano, Silvia S; Vásquez-Loarte, Tania T; Solari, Lely L; Mendoza-Ticona, Alberto A; Soto, Alonso A; Rojas, Christian C; Zegarra-Chapoñan, Roberto R; Guio, Heinner H

Publication Date: 2021-10

Variant appearance in text: NAT2: 481C>T; L161L; rs1799929

PubMed Link: 34510815

Variant Present in the following documents:

• Main text

View BVdb publication page

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Identification and epidemiological evaluation of gastric cancer risk factors: based on a field synopsis and meta-analysis in Chinese population.

Aging

Duan, Fujiao F; Song, Chunhua C; Shi, Jiachen J; Wang, Peng P; Ye, Hua H; Dai, Liping L; Zhang, Jianying J; Wang, Kaijuan K

Publication Date: 2021-09-06

Variant appearance in text: rs1799929

PubMed Link: 34491229

Variant Present in the following documents:

• Main text
• aging-13-203484.pdf

View BVdb publication page

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Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population.

Pharmacogenomics And Personalized Medicine

He, Chunjuan C; Peng, Linna L; Xing, Shishi S; Li, Dandan D; Wang, Li L; Jin, Tianbo T

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34429635

Variant Present in the following documents:

• Main text
• pgpm-14-1027.pdf

View BVdb publication page

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Acetylator Status Among Newly Diagnosed and Recurrent Tuberculosis Patients from Kupang, Eastern Part of Indonesia.

Pharmacogenomics And Personalized Medicine

Sahiratmadja, Edhyana E; Rini, Ika Agus IA; Penggoam, Simeon S; Charles, Afandi A; Maskoen, Ani Melani AM; Parwati, Ida I

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34188520

Variant Present in the following documents:

• Main text
• pgpm-14-737.pdf

View BVdb publication page

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NAT2 Gene rs1041983 is Associated with Anti-Tuberculosis Drug Induced Hepatotoxicity Among Pediatric Tuberculosis in Bandung, Indonesia.

The Application Of Clinical Genetics

Headriawan, Achmad A; Pramono, Alvinsyah Adhityo AA; Sukadi, Abdurachman A; Chairulfatah, Alex A; Maskoen, Ani Melani AM; Nataprawira, Heda Melinda HM

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 34113149

Variant Present in the following documents:

• Main text
• tacg-14-297.pdf

View BVdb publication page

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Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse.

International Urogynecology Journal

Allen-Brady, Kristina K; Chua, John W F JWF; Cuffolo, Romana R; Koch, Marianne M; Sorrentino, Felice F; Cartwright, Rufus R

Publication Date: 2021-04-24

Variant appearance in text: rs1799929

PubMed Link: 33893823

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of NAT2 genetic polymorphism with the efficacy of Neurotropin® for the enhancement of aggrecan gene expression in nucleus pulposus cells: a pilot study.

Bmc Medical Genomics

Nakai, Tomoko T; Sakai, Daisuke D; Nakamura, Yoshihiko Y; Horikita, Natsumi N; Matsushita, Erika E; Naiki, Mitsuru M; Watanabe, Masahiko M

Publication Date: 2021-03-11

Variant appearance in text: rs1799929

PubMed Link: 33706752

Variant Present in the following documents:

• 12920_2021_Article_926.pdf

View BVdb publication page

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Gene-environment interactions between air pollution and biotransformation enzymes and risk of birth defects.

Birth Defects Research

Padula, Amy M AM; Yang, Wei W; Schultz, Kathleen K; Lee, Cecilia C; Lurmann, Fred F; Hammond, S Katharine SK; Shaw, Gary M GM

Publication Date: 2021-05-15

Variant appearance in text: rs1799929

PubMed Link: 33569925

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Diversity of Drug-Related Genes in Native Americans of the Brazilian Amazon.

Pharmacogenomics And Personalized Medicine

Fernandes, Marianne Rodrigues MR; Rodrigues, Juliana Carla Gomes JCG; Maroñas, Olalla O; Latorre-Pellicer, Ana A; Cruz, Raquel R; Guerreiro, João Farias JF; Burbano, Rommel Mario Rodriguez RMR; de Assumpção, Paulo Pimentel PP; Ribeiro-Dos-Santos, Andrea A; Dos Santos, Sidney Emanuel Batista SEB; Carracedo, Angel A; Dos Santos, Ney Pereira Carneiro NPC

Publication Date: 2021

Variant appearance in text: rs1799929

PubMed Link: 33519226

Variant Present in the following documents:

• Main text
• pgpm-14-117.pdf

View BVdb publication page

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Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Saudi Journal Of Biological Sciences

Aboul-Soud, Mourad A M MAM; Alzahrani, Alhussain J AJ; Mahmoud, Amer A

Publication Date: 2021-01

Variant appearance in text: NAT2: L161L; rs1799929

PubMed Link: 33424349

Variant Present in the following documents:

• mmc1.xlsx, sheet 1

View BVdb publication page

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: NAT2: 481C>T; L161L; rs1799929

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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Validation of PHASE for deriving N-acetyltransferase 2 haplotypes in the Western Cape mixed ancestry population.

African Journal Of Laboratory Medicine

Swart, Celeste C; Meldau, Surita S; Centner, Chad M CM; Marais, Adrian D AD; Omar, Fierdoz F

Publication Date: 2020

Variant appearance in text: NAT2: 481C>T

PubMed Link: 33392048

Variant Present in the following documents:

• Main text

View BVdb publication page

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Defining eligible patients for allele-selective chemotherapies targeting NAT2 in colorectal cancer.

Scientific Reports

Rendo, Veronica V; Kundu, Snehangshu S; Rameika, Natallia N; Ljungström, Viktor V; Svensson, Richard R; Palin, Kimmo K; Aaltonen, Lauri L; Stoimenov, Ivaylo I; Sjöblom, Tobias T

Publication Date: 2020-12-31

Variant appearance in text: rs1799929

PubMed Link: 33384440

Variant Present in the following documents:

• Main text
• 41598_2020_80288_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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Evaluation of Genetic Polymorphisms of N-acetyltransferase 2 and Relation with Chronic Myeloid Leukemia.

Asian Pacific Journal Of Cancer Prevention : Apjcp

Tebien, Entesar M EM; Khalil, Hiba B HB; Mills, Jeremy J; Elderdery, Abozer Y AY

Publication Date: 2020-12-01

Variant appearance in text: rs1799929

PubMed Link: 33369472

Variant Present in the following documents:

• Main text

View BVdb publication page

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Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations.

Scientific Reports

Al-Mahayri, Zeina N ZN; Patrinos, George P GP; Wattanapokayakit, Sukanya S; Iemwimangsa, Nareenart N; Fukunaga, Koya K; Mushiroda, Taisei T; Chantratita, Wasun W; Ali, Bassam R BR

Publication Date: 2020-12-04

Variant appearance in text: rs1799929

PubMed Link: 33277594

Variant Present in the following documents:

• 41598_2020_78231_MOESM1_ESM.pdf

View BVdb publication page

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Arylamine N-acetyltransferase acetylation polymorphisms: paradigm for pharmacogenomic-guided therapy- a focused review.

Expert Opinion On Drug Metabolism & Toxicology

Hein, David W DW; Millner, Lori M LM

Publication Date: 2021-01

Variant appearance in text: NAT2: L161L; rs1799929

PubMed Link: 33094670

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genotype-Environment Interaction Analysis of NQO1, CYP2E1, and NAT2 Polymorphisms and the Risk of Childhood Acute Lymphoblastic Leukemia: A Report From the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia.

Frontiers In Oncology

Medina-Sanson, Aurora A; Núñez-Enríquez, Juan Carlos JC; Hurtado-Cordova, Eduardo E; Pérez-Saldivar, María Luisa ML; Martínez-García, Anayeli A; Jiménez-Hernández, Elva E; Fernández-López, Juan Carlos JC; Martín-Trejo, Jorge Alfonso JA; Pérez-Lorenzana, Héctor H; Flores-Lujano, Janet J; Amador-Sánchez, Raquel R; Mora-Ríos, Felix Gustavo FG; Peñaloza-González, José Gabriel JG; Duarte-Rodríguez, David Aldebarán DA; Torres-Nava, José Refugio JR; Flores-Bautista, Juan Eduardo JE; Espinosa-Elizondo, Rosa Martha RM; Román-Zepeda, Pedro Francisco PF; Flores-Villegas, Luz Victoria LV; González-Ulivarri, Juana Esther JE; Martínez-Silva, Sofía Irene SI; Espinoza-Anrubio, Gilberto G; Almeida-Hernández, Carolina C; Ramírez-Colorado, Rosario R; Hernández-Mora, Luis L; García-López, Luis Ramiro LR; Cruz-Ojeda, Gabriela Adriana GA; Godoy-Esquivel, Arturo Emilio AE; Contreras-Hernández, Iris I; Medina-Hernández, Abraham A; López-Caballero, María Guadalupe MG; Hernández-Pineda, Norma Angélica NA; Granados-Kraulles, Jorge J; Rodríguez-Vázquez, María Adriana MA; Torres-Valle, Delfino D; Cortés-Reyes, Carlos C; Medrano-López, Francisco F; Pérez-Gómez, Jessica Arleet JA; Martínez-Ríos, Annel A; Aguilar-De Los Santos, Antonio A; Serafin-Díaz, Berenice B; Bekker-Méndez, Vilma Carolina VC; Mata-Rocha, Minerva M; Morales-Castillo, Blanca Angélica BA; Sepúlveda-Robles, Omar Alejandro OA; Ramírez-Bello, Julián J; Rosas-Vargas, Haydeé H; Hidalgo-Miranda, Alfredo A; Mejía-Aranguré, Juan Manuel JM; Jiménez-Morales, Silvia S

Publication Date: 2020

Variant appearance in text: rs1799929

PubMed Link: 33072605

Variant Present in the following documents:

• Main text
• fonc-10-571869.pdf

View BVdb publication page

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Genotype-Guided Hydralazine Therapy.

American Journal Of Nephrology

Collins, Kimberly S KS; Raviele, Anthony L J ALJ; Elchynski, Amanda L AL; Woodcock, Alexander M AM; Zhao, Yang Y; Cooper-DeHoff, Rhonda M RM; Eadon, Michael T MT

Publication Date: 2020

Variant appearance in text: rs1799929

PubMed Link: 32927458

Variant Present in the following documents:

• Main text

View BVdb publication page

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Study on Genotyping Polymorphism and Sequencing of N-Acetyltransferase 2 (NAT2) among Al-Ahsa Population.

Biomed Research International

Zahra, Mohammad Abu MA; Kandeel, Mahmoud M; Aldossary, Sara A SA; Al-Taher, Abdulla A

Publication Date: 2020

Variant appearance in text: NAT2: Leu161Leu; rs1799929

PubMed Link: 32626768

Variant Present in the following documents:

• Main text

View BVdb publication page

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Population Pharmacokinetic and Pharmacogenetic Analysis of Mitotane in Patients with Adrenocortical Carcinoma: Towards Individualized Dosing.

Clinical Pharmacokinetics

Yin, Anyue A; Ettaieb, Madeleine H T MHT; Swen, Jesse J JJ; van Deun, Liselotte L; Kerkhofs, Thomas M A TMA; van der Straaten, Robert J H M RJHM; Corssmit, Eleonora P M EPM; Gelderblom, Hans H; Kerstens, Michiel N MN; Feelders, Richard A RA; Eekhoff, Marelise M; Timmers, Henri J L M HJLM; D'Avolio, Antonio A; Cusato, Jessica J; Guchelaar, Henk-Jan HJ; Haak, Harm R HR; Moes, Dirk Jan A R DJAR

Publication Date: 2021-01

Variant appearance in text: NAT2: 481C>T; L161L; rs1799929

PubMed Link: 32607875

Variant Present in the following documents:

• 40262_2020_913_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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Unexpected Acetylation of Endogenous Aliphatic Amines by Arylamine N-Acetyltransferase NAT2.

Angewandte Chemie (International Ed. In English)

Conway, Louis P LP; Rendo, Veronica V; Correia, Mário S P MSP; Bergdahl, Ingvar A IA; Sjöblom, Tobias T; Globisch, Daniel D

Publication Date: 2020-08-17

Variant appearance in text: rs1799929

PubMed Link: 32497306

Variant Present in the following documents:

• ANIE-59-14342-s001.pdf

View BVdb publication page

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Haplotype-specific PCR for NAT2 diplotyping.

Human Genome Variation

Wichukchinda, Nuanjun N; Pakdee, Jirapa J; Kunhapan, Punna P; Imunchot, Wimala W; Toyo-Oka, Licht L; Tokunaga, Katsushi K; Mahasirimongkol, Surakameth S

Publication Date: 2020

Variant appearance in text: rs1799929

PubMed Link: 32411379

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic polymorphisms of pharmacogenomic VIP variants in the Dai population from Yunnan province.

Molecular Genetics & Genomic Medicine

Cheng, Yujing Y; Dai, Run R; Chen, Wanlu W; Li, Qi Q; Zhang, Chan C; Yang, Tonghua T

Publication Date: 2020-07

Variant appearance in text: rs1799929

PubMed Link: 32347657

Variant Present in the following documents:

• Main text

View BVdb publication page

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Identification of targeted therapy options for gastric adenocarcinoma by comprehensive analysis of genomic data.

Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association

Hescheler, Daniel A DA; Plum, Patrick S PS; Zander, Thomas T; Quaas, Alexander A; Korenkov, Michael M; Gassa, Asmae A; Michel, Maximilian M; Bruns, Christiane J CJ; Alakus, Hakan H

Publication Date: 2020-07

Variant appearance in text: NAT2: L161L

PubMed Link: 32107691

Variant Present in the following documents:

• 10120_2020_1045_MOESM1_ESM.xlsx, sheet 2

View BVdb publication page

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The association between NAT2 acetylator status and adverse drug reactions of sulfasalazine: a systematic review and meta-analysis.

Scientific Reports

Yee, Jeong J; Kim, So Min SM; Han, Ji Min JM; Lee, Nari N; Yoon, Ha Young HY; Gwak, Hye Sun HS

Publication Date: 2020-02-27

Variant appearance in text: rs1799929

PubMed Link: 32107440

Variant Present in the following documents:

• Main text
• 41598_2020_Article_60467.pdf

View BVdb publication page

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NAT2 gene polymorphisms and endometriosis risk: A PRISMA-compliant meta-analysis.

Plos One

Wei, Zhangming Z; Zhang, Mengmeng M; Zhang, Xinyue X; Yi, Mingyu M; Xia, Xiaomeng X; Fang, Xiaoling X

Publication Date: 2019

Variant appearance in text: rs1799929

PubMed Link: 31881062

Variant Present in the following documents:

• Main text

View BVdb publication page

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Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer.

Gut

Montazeri, Zahra Z; Li, Xue X; Nyiraneza, Christine C; Ma, Xiangyu X; Timofeeva, Maria M; Svinti, Victoria V; Meng, Xiangrui X; He, Yazhou Y; Bo, Yacong Y; Morgan, Samuel S; Castellví-Bel, Sergi S; Ruiz-Ponte, Clara C; Fernández-Rozadilla, Ceres C; Carracedo, Ángel Á; Castells, Antoni A; Bishop, Timothy T; Buchanan, Daniel D; Jenkins, Mark A MA; Keku, Temitope O TO; Lindblom, Annika A; van Duijnhoven, Fränzel J B FJB; Wu, Anna A; Farrington, Susan M SM; Dunlop, Malcolm G MG; Campbell, Harry H; Theodoratou, Evropi E; Zheng, Wei W; Little, Julian J

Publication Date: 2020-08

Variant appearance in text: rs1799929

PubMed Link: 31818908

Variant Present in the following documents:

• Main text
• gutjnl-2019-319313supp002.pdf
• gutjnl-2019-319313.pdf
• gutjnl-2019-319313supp003.pdf

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Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports

Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA

Publication Date: 2019-10-09

Variant appearance in text: NAT2: L161L; rs1799929

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1

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Genetic polymorphisms analysis of pharmacogenomic VIP variants in Bai ethnic group from China.

Molecular Genetics & Genomic Medicine

Chen, Wanlu W; Ding, Heng H; Cheng, Yujing Y; Li, Qi Q; Dai, Run R; Yang, Xin X; Zhang, Chan C

Publication Date: 2019-09

Variant appearance in text: rs1799929

PubMed Link: 31361092

Variant Present in the following documents:

• Main text

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A pan-cancer analysis of synonymous mutations.

Nature Communications

Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S

Publication Date: 2019-06-12

Variant appearance in text: NAT2: 481C>T

PubMed Link: 31189880

Variant Present in the following documents:

• 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1

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Targeted ultra-deep sequencing of a South African Bantu-speaking cohort to comprehensively map and characterize common and novel variants in 65 pharmacologically-related genes.

Pharmacogenetics And Genomics

Tshabalala, Sibongile S; Choudhury, Ananyo A; Beeton-Kempen, Natasha N; Martinson, Neil N; Ramsay, Michèle M; Mancama, Dalu D

Publication Date: 2019-09

Variant appearance in text: rs1799929

PubMed Link: 31162291

Variant Present in the following documents:

• pgen-29-167.pdf

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