Publications:

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DNA methylation profile in the whole blood of acute coronary syndrome patients with aspirin resistance.

Journal Of Clinical Laboratory Analysis

Yu, Qinglin Q; Yang, Jin J; Wang, Jiang J; Yu, Ruoyan R; Li, Jiyi J; Cheng, Ji J; Hu, Yingchu Y; Li, Zhenwei Z; Zheng, Nan N; Zhang, Zhaoxia Z; Li, Xiaojing X; Wang, Yong Y; Du, Weiping W; Zhu, Keqi K; Chen, Xiaomin X; Su, Jia J

Publication Date: 2022-12-22

Variant appearance in text: rs3842788

PubMed Link: 36550638

Variant Present in the following documents:

• JCLA-37-e24821.pdf

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Mechanism of Improving Aspirin Resistance: Blood-Activating Herbs Combined With Aspirin in Treating Atherosclerotic Cardiovascular Diseases.

Frontiers In Pharmacology

Zhao, Yixi Y; Yang, Shengjie S; Wu, Min M

Publication Date: 2021

Variant appearance in text: rs3842788

PubMed Link: 34975490

Variant Present in the following documents:

• Main text
• fphar-12-794417.pdf

View BVdb publication page

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Genetic Variants in PTGS1 and NOS3 Genes Increase the Risk of Upper Gastrointestinal Bleeding: A Case-Control Study.

Frontiers In Pharmacology

Forgerini, Marcela M; Urbano, Gustavo G; de Nadai, Tales Rubens TR; Batah, Sabrina Setembre SS; Fabro, Alexandre Todorovic AT; Mastroianni, Patrícia de Carvalho PC

Publication Date: 2021

Variant appearance in text: rs3842788

PubMed Link: 34290607

Variant Present in the following documents:

• Main text
• fphar-12-671835.pdf

View BVdb publication page

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Influence of Polymorphisms Involved in Platelet Activation and Inflammatory Response on Aspirin-Related Upper Gastrointestinal Bleeding: A Case-Control Study.

Frontiers In Pharmacology

Mallah, Narmeen N; Zapata-Cachafeiro, Maruxa M; Aguirre, Carmelo C; Ibarra-García, Eguzkiñe E; Palacios-Zabalza, Itziar I; Macías-García, Fernando F; Domínguez-Muñoz, J Enrique JE; Piñeiro-Lamas, María M; Ibáñez, Luisa L; Vidal, Xavier X; Vendrell, Lourdes L; Martin-Arias, Luis L; Sáinz-Gil, María M; Velasco-González, Verónica V; Figueiras, Adolfo A

Publication Date: 2020

Variant appearance in text: rs3842788

PubMed Link: 32655394

Variant Present in the following documents:

• Main text
• fphar-11-00860.pdf

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: PTGS1: 123G>A; Q41Q; rs3842788

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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Interaction between COX-1 and COX-2 increases susceptibility to ischemic stroke in a Chinese population.

Bmc Neurology

Zhao, Lei L; Fang, Jinghuan J; Zhou, Muke M; Zhou, Jie J; Yu, Lihua L; Chen, Ning N; He, Li L

Publication Date: 2019-11-17

Variant appearance in text: rs3842788

PubMed Link: 31735164

Variant Present in the following documents:

• Main text
• 12883_2019_Article_1505.pdf

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Introducing the first whole genomes of nationals from the United Arab Emirates.

Scientific Reports

AlSafar, Habiba S HS; Al-Ali, Mariam M; Elbait, Gihan Daw GD; Al-Maini, Mustafa H MH; Ruta, Dymitr D; Peramo, Braulio B; Henschel, Andreas A; Tay, Guan K GK

Publication Date: 2019-10-11

Variant appearance in text: rs3842788

PubMed Link: 31604968

Variant Present in the following documents:

• 41598_2019_50876_MOESM2_ESM.xlsx, sheet 2

View BVdb publication page

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Next-Generation Sequencing of PTGS Genes Reveals an Increased Frequency of Non-synonymous Variants Among Patients With NSAID-Induced Liver Injury.

Frontiers In Genetics

Lucena, María Isabel MI; García-Martín, Elena E; Daly, Ann K AK; Blanca, Miguel M; Andrade, Raúl J RJ; Agúndez, José A G JAG

Publication Date: 2019

Variant appearance in text: rs3842788

PubMed Link: 30873208

Variant Present in the following documents:

• Main text
• fgene-10-00134.pdf

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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease

Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D

Publication Date: 2019-02-27

Variant appearance in text: PTGS1: 123G>A; Gln41Gln; rs3842788

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1

View BVdb publication page

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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal

Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL

Publication Date: 2019-04

Variant appearance in text: rs3842788

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases

Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ

Publication Date: 2017-05-23

Variant appearance in text: PTGS1: Q41Q; rs3842788

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

View BVdb publication page

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rs5911 and rs3842788 Genetic Polymorphism, Blood Stasis Syndrome, and Plasma TXB2 and hs-CRP Levels Are Associated with Aspirin Resistance in Chinese Chronic Stable Angina Patients.

Evidence-Based Complementary And Alternative Medicine : Ecam

Xue, Mei M; Yang, Xuesong X; Yang, Lin L; Kou, Na N; Miao, Yu Y; Wang, Mingming M; Ren, Junhua J; Zhao, Quanli Q

Publication Date: 2017

Variant appearance in text: rs3842788

PubMed Link: 28465708

Variant Present in the following documents:

• Main text
• ECAM2017-9037094.pdf

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The IL-1B Genetic Polymorphism Is Associated with Aspirin-Induced PepticUlcers in a Korean Ethnic Group.

Gut And Liver

Cho, Jae Hee JH; Choi, Ja Sung JS; Chun, Song Wook SW; Lee, Sangheun S; Han, Ki Jun KJ; Kim, Hee Man HM

Publication Date: 2016-05-23

Variant appearance in text: rs3842788

PubMed Link: 26601827

Variant Present in the following documents:

• Main text
• gnl-10-362.pdf

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The Effect of Xuefuzhuyu Oral Liquid on Aspirin Resistance and Its Association with rs5911, rs5787, and rs3842788 Gene Polymorphisms.

Evidence-Based Complementary And Alternative Medicine : Ecam

Xue, Mei M; Yang, Lin L; Kou, Na N; Miao, Yu Y; Wang, Mingming M; Zhao, Quanli Q; Ren, Junhua J; Zhang, Shaoyan S; Shi, Dazhuo D; Chen, Keji K

Publication Date: 2015

Variant appearance in text: rs3842788

PubMed Link: 26495016

Variant Present in the following documents:

• Main text

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Genetic Variants in Cyclooxygenase-2 Contribute to Post-treatment Pain among Endodontic Patients.

Journal Of Endodontics

Applebaum, Elizabeth E; Nackley, Andrea G AG; Bair, Eric E; Maixner, William W; Khan, Asma A AA

Publication Date: 2015-08

Variant appearance in text: rs3842788

PubMed Link: 26081267

Variant Present in the following documents:

• Main text

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Identification of common genetic variants controlling transcript isoform variation in human whole blood.

Nature Genetics

Zhang, Xiaoling X; Joehanes, Roby R; Chen, Brian H BH; Huan, Tianxiao T; Ying, Saixia S; Munson, Peter J PJ; Johnson, Andrew D AD; Levy, Daniel D; O'Donnell, Christopher J CJ

Publication Date: 2015-04

Variant appearance in text: rs3842788

PubMed Link: 25685889

Variant Present in the following documents:

• Main text

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Effect of common single nucleotide polymorphisms in COX-1 gene on related metabolic activity in diabetic patients treated with acetylsalicylic acid.

Archives Of Medical Science : Ams

Postula, Marek M; Janicki, Piotr K PK; Rosiak, Marek M; Kaplon-Cieslicka, Agnieszka A; Kondracka, Agnieszka A; Trzepla, Ewa E; Filipiak, Krzysztof J KJ; Kosior, Dariusz A DA; Czlonkowski, Andrzej A; Opolski, Grzegorz G

Publication Date: 2014-12-22

Variant appearance in text: rs3842788

PubMed Link: 25624859

Variant Present in the following documents:

• Main text
• AMS-10-20887.pdf

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Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.

Human Genetics

Liu, Xin X; Wang, Guoying G; Hong, Xiumei X; Tsai, Hui-Ju HJ; Liu, Rong R; Zhang, Shanchun S; Wang, Hongjian H; Pearson, Colleen C; Ortiz, Katherin K; Wang, Deli D; Hirsch, Emmet E; Zuckerman, Barry B; Wang, Xiaobin X

Publication Date: 2012-03

Variant appearance in text: rs3842788

PubMed Link: 21847588

Variant Present in the following documents:

• Main text

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Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.

Bmc Cancer

Küry, Sébastien S; Buecher, Bruno B; Robiou-du-Pont, Sébastien S; Scoul, Catherine C; Colman, Hélène H; Le Neel, Tanguy T; Le Houérou, Claire C; Faroux, Roger R; Ollivry, Jean J; Lafraise, Bernard B; Chupin, Louis-Dominique LD; Sébille, Véronique V; Bézieau, Stéphane S

Publication Date: 2008-11-07

Variant appearance in text: PTGS1: 123G>A; Gln41Gln; rs3842788

PubMed Link: 18992148

Variant Present in the following documents:

• Main text
• 1471-2407-8-326.pdf
• 1471-2407-8-326-S3.xls, sheet 1

View BVdb publication page

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Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1).

Pharmacogenetics And Genomics

Lee, Craig R CR; Bottone, Frank G FG; Krahn, Joseph M JM; Li, Leping L; Mohrenweiser, Harvey W HW; Cook, Molly E ME; Petrovich, Robert M RM; Bell, Douglas A DA; Eling, Thomas E TE; Zeldin, Darryl C DC

Publication Date: 2007-02

Variant appearance in text: PTGS1: Q41Q; rs3842788

PubMed Link: 17301694

Variant Present in the following documents:

• Main text

View BVdb publication page

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