ZFHX3 c.-49-35067A>T

Variant ID: 16-73029160-T-A

NM_006885.3(ZFHX3):c.-49-35067A>T

This variant was identified in 66 publications

View GRCh38 version.




Publications:


Integrated analysis of circRNA-associated ceRNA network in ischemic stroke.

Frontiers In Genetics
Fan, Rongli R; Hu, Die D; Wang, Maiqiu M; Zheng, Huilin H; Zhou, Yifeng Y; Zhang, Lei L
Publication Date: 2023

Variant appearance in text: rs7193343
PubMed Link: 37323662
Variant Present in the following documents:
  • Main text
  • fgene-14-1153518.pdf
View BVdb publication page



Predicting atrial fibrillation after ischemic stroke: clinical, genetics and electrocardiogram modelling.

Cerebrovascular Diseases Extra
Poh, Mervyn Qi Wei MQW; Tham, Carol Huilian CH; Chee, Jeremiah David Ming Siang JDMS; Saffari, Seyed Ehsan SE; Tan, Kenny Wee Kian KWK; Tan, Li Wei LW; Ng, Ebonne Yulin EY; Yeo, Celestia Pei Xuan CPX; Seet, Christopher Ying Hao CYH; Xie, Joanne Peiting JP; Lai, Jonathan Yexian JY; Singh, Rajinder R; Tan, Eng-King EK; Tu, Tian Ming TM
Publication Date: 2022-12-15

Variant appearance in text: rs7193343
PubMed Link: 36521445
Variant Present in the following documents:
  • Main text
  • cee-0013-0009.pdf
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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: rs7193343
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.

Journal Of The American Heart Association
Shi, Mengyao M; Kelly, Tanika N TN; Zhu, Zhengbao Z; Li, Changwei C; Shen, Chong C; Sun, Yingxian Y; Wang, Aili A; Shan, Guangliang G; Bu, Xiaoqing X; Guo, Daoxia D; Zhao, Jingbo J; Xu, Tan T; Peng, Hao H; Xu, Tian T; Zhong, Chongke C; Sun, Xiao X; Chen, Jing J; Zhang, Yonghong Y; He, Jiang J
Publication Date: 2022-10-04

Variant appearance in text: rs7193343
PubMed Link: 36193932
Variant Present in the following documents:
  • JAH3-11-e025245.pdf
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Ischemic Stroke Genetics: What Is New and How to Apply It in Clinical Practice?

Genes
Ekkert, Aleksandra A; Šliachtenko, Aleksandra A; Grigaitė, Julija J; Burnytė, Birutė B; Utkus, Algirdas A; Jatužis, Dalius D
Publication Date: 2021-12-24

Variant appearance in text: rs7193343
PubMed Link: 35052389
Variant Present in the following documents:
  • Main text
  • genes-13-00048.pdf
View BVdb publication page



Ischemic Stroke Genetics: What Is New and How to Apply It in Clinical Practice?

Genes
Ekkert, Aleksandra A; Šliachtenko, Aleksandra A; Grigaitė, Julija J; Burnytė, Birutė B; Utkus, Algirdas A; Jatužis, Dalius D
Publication Date: 2021-12-24

Variant appearance in text: rs7193343
PubMed Link: 35052389
Variant Present in the following documents:
  • Main text
  • genes-13-00048.pdf
View BVdb publication page



Association between ZFHX3 and PRRX1 Polymorphisms and Atrial Fibrillation Susceptibility from Meta-Analysis.

International Journal Of Hypertension
Wu, Liting L; Chu, Min M; Zhuang, Wenfang W
Publication Date: 2021

Variant appearance in text: rs7193343
PubMed Link: 34950514
Variant Present in the following documents:
  • Main text
  • ijhy2021-9423576.pdf
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Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis.

Medicine
Wei, Yue Y; Wang, Lingjie L; Lin, Changjian C; Xie, Yun Y; Bao, Yangyang Y; Luo, Qingzhi Q; Zhang, Ning N
Publication Date: 2021-12-10

Variant appearance in text: rs7193343
PubMed Link: 34889223
Variant Present in the following documents:
  • Main text
View BVdb publication page



Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa).

International Journal Of Molecular Sciences
Rubio-Alarcón, Marcos M; Cámara-Checa, Anabel A; Dago, María M; Crespo-García, Teresa T; Nieto-Marín, Paloma P; Marín, María M; Merino, José Luis JL; Toquero, Jorge J; Salguero-Bodes, Rafael R; Tamargo, Juan J; Cebrián, Jorge J; Delpón, Eva E; Caballero, Ricardo R
Publication Date: 2021-12-02

Variant appearance in text: rs7193343
PubMed Link: 34884836
Variant Present in the following documents:
  • Main text
  • ijms-22-13031.pdf
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Zfhx3 Transcription Factor Represses the Expression of SCN5A Gene and Decreases Sodium Current Density (INa).

International Journal Of Molecular Sciences
Rubio-Alarcón, Marcos M; Cámara-Checa, Anabel A; Dago, María M; Crespo-García, Teresa T; Nieto-Marín, Paloma P; Marín, María M; Merino, José Luis JL; Toquero, Jorge J; Salguero-Bodes, Rafael R; Tamargo, Juan J; Cebrián, Jorge J; Delpón, Eva E; Caballero, Ricardo R
Publication Date: 2021-12-02

Variant appearance in text: rs7193343
PubMed Link: 34884836
Variant Present in the following documents:
  • Main text
  • ijms-22-13031.pdf
View BVdb publication page



Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs7193343
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
View BVdb publication page



Genetics of atrial fibrillation-practical applications for clinical management: if not now, when and how?

Cardiovascular Research
Kany, Shinwan S; Reissmann, Bruno B; Metzner, Andreas A; Kirchhof, Paulus P; Darbar, Dawood D; Schnabel, Renate B RB
Publication Date: 2021-06-16

Variant appearance in text: rs7193343
PubMed Link: 33982075
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of methylation changes associated with positive and negative growth deviance in Gambian infants using a targeted methyl sequencing approach of genomic DNA.

Faseb Bioadvances
Quilter, Claire R CR; Harvey, Kerry M KM; Bauer, Julien J; Skinner, Benjamin M BM; Gomez, Maria M; Shrivastava, Manu M; Doel, Andrew M AM; Drammeh, Saikou S; Dunger, David B DB; Moore, Sophie E SE; Ong, Ken K KK; Prentice, Andrew M AM; Bernstein, Robin M RM; Sargent, Carole A CA; Affara, Nabeel A NA
Publication Date: 2021-04

Variant appearance in text: rs7193343
PubMed Link: 33842847
Variant Present in the following documents:
  • FBA2-3-205-s004.xlsx, sheet 4
View BVdb publication page



The Effects of Single Nucleotide Polymorphisms in Korean Patients with Early-onset Atrial Fibrillation after Catheter Ablation.

Journal Of Korean Medical Science
Park, Yae Min YM; Roh, Seung Young SY; Lee, Dae In DI; Shim, Jaemin J; Choi, Jong Il JI; Park, Sang Weon SW; Kim, Young Hoon YH
Publication Date: 2020-12-21

Variant appearance in text: rs7193343
PubMed Link: 33350184
Variant Present in the following documents:
  • Main text
  • jkms-35-e411.pdf
View BVdb publication page



Clinical and Genetic Contributors to New-Onset Atrial Fibrillation in Critically Ill Adults.

Critical Care Medicine
Kerchberger, V Eric VE; Huang, Yi Y; Koyama, Tatsuki T; Shoemaker, M Benjamin MB; Darbar, Dawood D; Bastarache, Julie A JA; Ware, Lorraine B LB; Shaver, Ciara M CM
Publication Date: 2020-01

Variant appearance in text: rs7193343
PubMed Link: 31599812
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between gene variants and the recurrence of atrial fibrillation: An updated meta-analysis.

Medicine
Jiang, Tao T; Wang, Ya-Nan YN; Qu, Qiang Q; Qi, Ting-Ting TT; Chen, Yun-Dai YD; Qu, Jian J
Publication Date: 2019-06

Variant appearance in text: rs7193343
PubMed Link: 31169720
Variant Present in the following documents:
  • Main text
View BVdb publication page



Is population structure in the genetic biobank era irrelevant, a challenge, or an opportunity?

Human Genetics
Lawson, Daniel John DJ; Davies, Neil Martin NM; Haworth, Simon S; Ashraf, Bilal B; Howe, Laurence L; Crawford, Andrew A; Hemani, Gibran G; Davey Smith, George G; Timpson, Nicholas John NJ
Publication Date: 2020-01

Variant appearance in text: rs7193343
PubMed Link: 31030318
Variant Present in the following documents:
  • 439_2019_Article_2014.pdf
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Can Genetic Risk Scoring Predict Atrial Fibrillation Ablation Outcomes?

Korean Circulation Journal
Lin, Chin Yu CY; Hu, Yu Feng YF; Lin, Yenn Jiang YJ; Chen, Shih Ann SA
Publication Date: 2019-04

Variant appearance in text: rs7193343
PubMed Link: 30808086
Variant Present in the following documents:
  • Main text
  • kcj-49-350.pdf
View BVdb publication page



New Insight to the Pathogenetic Mechanism of Kawasaki Disease (KD): the Relationship between Clinical Diversity and Genetic Heterogeneity.

Korean Circulation Journal
Yoo, Byung Won BW
Publication Date: 2019-01

Variant appearance in text: rs7193343
PubMed Link: 30468043
Variant Present in the following documents:
  • Main text
  • kcj-49-109.pdf
View BVdb publication page



Genetics of Atrial Fibrillation.

Journal Of The American Heart Association
Feghaly, Julien J; Zakka, Patrick P; London, Barry B; MacRae, Calum A CA; Refaat, Marwan M MM
Publication Date: 2018-10-16

Variant appearance in text: rs7193343
PubMed Link: 30371258
Variant Present in the following documents:
  • Main text
  • JAH3-7-e009884.pdf
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A Chromosome 4q25 Variant is Associated with Atrial Fibrillation Recurrence After Catheter Ablation: A Systematic Review and Meta-Analysis.

Journal Of Atrial Fibrillation
Rattanawong, Pattara P; Chenbhanich, Jirat J; Vutthikraivit, Wasawat W; Chongsathidkiet, Pakawat P
Publication Date: 2018-04

Variant appearance in text: rs7193343
PubMed Link: 29988284
Variant Present in the following documents:
  • Main text
View BVdb publication page



Monogenic, Polygenic, and MicroRNA Markers for Ischemic Stroke.

Molecular Neurobiology
Chen, Wu W; Sinha, Bharati B; Li, Yi Y; Benowitz, Larry L; Chen, Qinhua Q; Zhang, Zhenghong Z; Patel, Nirav J NJ; Aziz-Sultan, Ali M AM; Chiocca, Antonio E AE; Wang, Xin X
Publication Date: 2019-02

Variant appearance in text: rs7193343
PubMed Link: 29948938
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.

Plos One
Chalazan, Brandon B; Mol, Denise D; Sridhar, Arvind A; Alzahrani, Zain Z; Darbar, Sara D SD; Ornelas-Loredo, Aylin A; Farooqui, Abdullah A; Argos, Maria M; Daviglus, Martha L ML; Konda, Sreenivas S; Rehman, Jalees J; Darbar, Dawood D
Publication Date: 2018

Variant appearance in text: rs7193343
PubMed Link: 29624624
Variant Present in the following documents:
  • Main text
  • pone.0194480.pdf
View BVdb publication page



Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.

Scientific Reports
Wang, Pengxia P; Qin, Weixi W; Wang, Pengyun P; Huang, Yufeng Y; Liu, Ying Y; Zhang, Rongfeng R; Li, Sisi S; Yang, Qin Q; Wang, Xiaojing X; Chen, Feifei F; Liu, Jingqiu J; Yang, Bo B; Cheng, Xiang X; Liao, Yuhua Y; Wu, Yanxia Y; Ke, Tie T; Tu, Xin X; Ren, Xiang X; Yang, Yanzong Y; Xia, Yunlong Y; Luo, Xiaoping X; Liu, Mugen M; Li, He H; Liu, Jingyu J; Xiao, Yi Y; Chen, Qiuyun Q; Xu, Chengqi C; Wang, Qing K QK
Publication Date: 2018-02-19

Variant appearance in text: rs7193343
PubMed Link: 29459676
Variant Present in the following documents:
  • Main text
View BVdb publication page



Population-Wide Genetic Risk Prediction of Complex Diseases: A Pilot Feasibility Study in Macau Population for Precision Public Healthcare Planning.

Scientific Reports
Tsui, Nancy B Y NBY; Cheng, Gregory G; Chung, Teresa T; Lam, Christopher W K CWK; Yee, Anita A; Chung, Peter K C PKC; Kwan, Tsz-Ki TK; Ko, Elaine E; He, Daihai D; Wong, Wing-Tak WT; Lau, Johnson Y N JYN; Lau, Lok Ting LT; Fok, Manson M
Publication Date: 2018-01-30

Variant appearance in text: rs7193343
PubMed Link: 29382849
Variant Present in the following documents:
  • 41598_2017_19017_MOESM1_ESM.pdf
View BVdb publication page



Association study between ZFHX3 gene polymorphisms and obesity in Korean population.

Journal Of Exercise Rehabilitation
Yang, Seung-Ae SA
Publication Date: 2017-08

Variant appearance in text: rs7193343
PubMed Link: 29114518
Variant Present in the following documents:
  • Main text
  • jer-13-4-491.pdf
View BVdb publication page



Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities.

Journal Of The Neurological Sciences
Owolabi, Mayowa M; Peprah, Emmanuel E; Xu, Huichun H; Akinyemi, Rufus R; Tiwari, Hemant K HK; Irvin, Marguerite R MR; Wahab, Kolawole Wasiu KW; Arnett, Donna K DK; Ovbiagele, Bruce B
Publication Date: 2017-11-15

Variant appearance in text: rs7193343
PubMed Link: 29111012
Variant Present in the following documents:
  • Main text
View BVdb publication page



A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study.

Scientific Reports
Hauer, Allard J AJ; Pulit, Sara L SL; van den Berg, Leonard H LH; de Bakker, Paul I W PIW; Veldink, Jan H JH; Ruigrok, Ynte M YM; ,
Publication Date: 2017-09-22

Variant appearance in text: rs7193343
PubMed Link: 28939865
Variant Present in the following documents:
  • Main text
  • 41598_2017_7404_MOESM1_ESM.pdf
  • 41598_2017_Article_7404.pdf
View BVdb publication page



Bioinformatics analysis of gene expression profiling for identification of potential key genes among ischemic stroke.

Medicine
Zhai, Kaihua K; Kong, Xiangli X; Liu, Boyu B; Lou, Jiyu J
Publication Date: 2017-08

Variant appearance in text: rs7193343
PubMed Link: 28834871
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic heterogeneity of atrial fibrillation susceptibility loci across racial or ethnic groups.

European Heart Journal
Huang, Henry H; Darbar, Dawood D
Publication Date: 2017-09-07

Variant appearance in text: rs7193343
PubMed Link: 28637342
Variant Present in the following documents:
  • Main text
View BVdb publication page



Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease.

Clinical Epigenetics
Nakatochi, Masahiro M; Ichihara, Sahoko S; Yamamoto, Ken K; Naruse, Keiko K; Yokota, Shigeki S; Asano, Hiroyuki H; Matsubara, Tatsuaki T; Yokota, Mitsuhiro M
Publication Date: 2017

Variant appearance in text: rs7193343
PubMed Link: 28515798
Variant Present in the following documents:
  • Main text
  • 13148_2017_Article_353.pdf
View BVdb publication page



Association of atrial fibrillation susceptibility genes, atrial fibrillation phenotypes and response to catheter ablation: a gene-based analysis of GWAS data.

Journal Of Translational Medicine
Husser, Daniela D; Büttner, Petra P; Ueberham, Laura L; Dinov, Borislav B; Sommer, Philipp P; Arya, Arash A; Hindricks, Gerhard G; Bollmann, Andreas A
Publication Date: 2017-04-05

Variant appearance in text: rs7193343
PubMed Link: 28381281
Variant Present in the following documents:
  • Main text
  • 12967_2017_Article_1170.pdf
View BVdb publication page



Association of Single Nucleotide Polymorphisms with Atrial Fibrillation and the Outcome after Catheter Ablation.

Acta Cardiologica Sinica
Hu, Yu-Feng YF; Wang, Hsueh-Hsiao HH; Yeh, Hung-I HI; Lee, Kun-Tai KT; Lin, Yenn-Jiang YJ; Chang, Shih-Lin SL; Lo, Li-Wei LW; Tuan, Ta-Chuan TC; Li, Cheng-Hung CH; Chao, Tze-Fan TF; Chung, Fa-Po FP; Liao, Jo-Nan JN; Tang, Paul Wei Hua PW; Tsai, Wei-Chung WC; Chiou, Chuen-Wang CW; Chen, Shih-Ann SA
Publication Date: 2016-09

Variant appearance in text: rs7193343
PubMed Link: 27713600
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genotype influence in responses to therapy for atrial fibrillation.

Expert Review Of Cardiovascular Therapy
Huang, Henry H; Darbar, Dawood D
Publication Date: 2016-10

Variant appearance in text: rs7193343
PubMed Link: 27409154
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomics of Atrial Fibrillation.

Current Cardiology Reports
Gutierrez, Alejandra A; Chung, Mina K MK
Publication Date: 2016-06

Variant appearance in text: rs7193343
PubMed Link: 27139902
Variant Present in the following documents:
  • Main text
View BVdb publication page



The 4q25, 1q21, and 16q22 polymorphisms and recurrence of atrial fibrillation after pulmonary vein isolation.

Archives Of Medical Science : Ams
Kiliszek, Marek M; Kozluk, Edward E; Franaszczyk, Maria M; Lodzinski, Piotr P; Piatkowska, Agnieszka A; Ploski, Rafal R; Opolski, Grzegorz G
Publication Date: 2016-02-01

Variant appearance in text: rs7193343
PubMed Link: 26925117
Variant Present in the following documents:
  • Main text
  • AMS-12-24393.pdf
View BVdb publication page



Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.

The Lancet. Neurology
, ; ,
Publication Date: 2016-02

Variant appearance in text: rs7193343
PubMed Link: 26708676
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene-guided therapy for catheter-ablation of atrial fibrillation: are we there yet?

Journal Of Interventional Cardiac Electrophysiology : An International Journal Of Arrhythmias And Pacing
Huang, Henry H; Darbar, Dawood D
Publication Date: 2016-01

Variant appearance in text: rs7193343
PubMed Link: 26660272
Variant Present in the following documents:
  • Main text
View BVdb publication page



Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success.

Journal Of The American Heart Association
Choi, Eue-Keun EK; Park, Jae Hyung JH; Lee, Ji-Young JY; Nam, Chung Mo CM; Hwang, Min Ki MK; Uhm, Jae-Sun JS; Joung, Boyoung B; Ko, Young-Guk YG; Lee, Moon-Hyoung MH; Lubitz, Steven A SA; Ellinor, Patrick T PT; Pak, Hui-Nam HN
Publication Date: 2015-08-13

Variant appearance in text: rs7193343
PubMed Link: 26272656
Variant Present in the following documents:
  • Main text
View BVdb publication page



Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.

Plos Genetics
Huang, Yufeng Y; Wang, Chuchu C; Yao, Yufeng Y; Zuo, Xiaoyu X; Chen, Shanshan S; Xu, Chengqi C; Zhang, Hongfu H; Lu, Qiulun Q; Chang, Le L; Wang, Fan F; Wang, Pengxia P; Zhang, Rongfeng R; Hu, Zhenkun Z; Song, Qixue Q; Yang, Xiaowei X; Li, Cong C; Li, Sisi S; Zhao, Yuanyuan Y; Yang, Qin Q; Yin, Dan D; Wang, Xiaojing X; Si, Wenxia W; Li, Xiuchun X; Xiong, Xin X; Wang, Dan D; Huang, Yuan Y; Luo, Chunyan C; Li, Jia J; Wang, Jingjing J; Chen, Jing J; Wang, Longfei L; Wang, Li L; Han, Meng M; Ye, Jian J; Chen, Feifei F; Liu, Jingqiu J; Liu, Ying Y; Wu, Gang G; Yang, Bo B; Cheng, Xiang X; Liao, Yuhua Y; Wu, Yanxia Y; Ke, Tie T; Chen, Qiuyun Q; Tu, Xin X; Elston, Robert R; Rao, Shaoqi S; Yang, Yanzong Y; Xia, Yunlong Y; Wang, Qing K QK
Publication Date: 2015-08

Variant appearance in text: rs7193343
PubMed Link: 26267381
Variant Present in the following documents:
  • Main text
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A complex insertion/deletion polymorphism in the compositionally biased region of the ZFHX3 gene in patients with coronary heart disease in a Chinese population.

International Journal Of Clinical And Experimental Medicine
Sun, Shunchang S; Zhang, Wenwu W; Chen, Xi X; Peng, Yunsheng Y; Chen, Qunrong Q
Publication Date: 2015

Variant appearance in text: rs7193343
PubMed Link: 26221345
Variant Present in the following documents:
  • Main text
View BVdb publication page



Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons.

Bmc Cardiovascular Disorders
Zhai, ChuanNan C; Cong, HongLiang H; Liu, YuJie Y; Zhang, Ying Y; Liu, XianFeng X; Zhang, Hao H; Ren, ZhiJing Z
Publication Date: 2015-06-26

Variant appearance in text: rs7193343
PubMed Link: 26112950
Variant Present in the following documents:
  • Main text
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Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.

Journal Of The American Heart Association
Chen, Shanshan S; Wang, Chuchu C; Wang, Xiaojing X; Xu, Chengqi C; Wu, Manman M; Wang, Pengxia P; Tu, Xin X; Wang, Qing K QK
Publication Date: 2015-05-07

Variant appearance in text: rs7193343
PubMed Link: 25953654
Variant Present in the following documents:
  • Main text
View BVdb publication page



The role of transcription factors in atrial fibrillation.

Journal Of Thoracic Disease
Zhou, Mengchen M; Liao, Yuhua Y; Tu, Xin X
Publication Date: 2015-02

Variant appearance in text: rs7193343
PubMed Link: 25713730
Variant Present in the following documents:
  • Main text
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Common genetic variants and response to atrial fibrillation ablation.

Circulation. Arrhythmia And Electrophysiology
Shoemaker, M Benjamin MB; Bollmann, Andreas A; Lubitz, Steven A SA; Ueberham, Laura L; Saini, Harsimran H; Montgomery, Jay J; Edwards, Todd T; Yoneda, Zachary Z; Sinner, Moritz F MF; Arya, Arash A; Sommer, Philipp P; Delaney, Jessica J; Goyal, Sandeep K SK; Saavedra, Pablo P; Kanagasundram, Arvindh A; Whalen, S Patrick SP; Roden, Dan M DM; Hindricks, Gerhard G; Ellis, Christopher R CR; Ellinor, Patrick T PT; Darbar, Dawood D; Husser, Daniela D
Publication Date: 2015-04

Variant appearance in text: rs7193343
PubMed Link: 25684755
Variant Present in the following documents:
  • Main text
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The reduction of vascular disease risk mutations contributes to longevity in the Chinese population.

Meta Gene
He, Yong-Han YH; Lu, Xiang X; Bi, Ming-Xin MX; Yang, Li-Qin LQ; Xu, Liang-You LY; Kong, Qing-Peng QP
Publication Date: 2014-12

Variant appearance in text: rs7193343
PubMed Link: 25606459
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic and clinical risk prediction model for postoperative atrial fibrillation.

Circulation. Arrhythmia And Electrophysiology
Kolek, Matthew J MJ; Muehlschlegel, J Daniel JD; Bush, William S WS; Parvez, Babar B; Murray, Katherine T KT; Stein, C Michael CM; Shoemaker, M Benjamin MB; Blair, Marcia A MA; Kor, Kaylen C KC; Roden, Dan M DM; Donahue, Brian S BS; Fox, Amanda A AA; Shernan, Stanton K SK; Collard, Charles D CD; Body, Simon C SC; Darbar, Dawood D
Publication Date: 2015-02

Variant appearance in text: rs7193343
PubMed Link: 25567478
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of ischemic stroke in young adults.

Circulation. Cardiovascular Genetics
Cheng, Yu-Ching YC; Cole, John W JW; Kittner, Steven J SJ; Mitchell, Braxton D BD
Publication Date: 2014-06

Variant appearance in text: rs7193343
PubMed Link: 24951665
Variant Present in the following documents:
  • Main text
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A contemporary review on the genetic basis of atrial fibrillation.

Methodist Debakey Cardiovascular Journal
Roberts, Jason D JD; Gollob, Michael H MH
Publication Date: 2014

Variant appearance in text: rs7193343
PubMed Link: 24932358
Variant Present in the following documents:
  • Main text
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Severity of obstructive sleep apnea influences the effect of genotype on response to anti-arrhythmic drug therapy for atrial fibrillation.

Journal Of Clinical Sleep Medicine : Jcsm : Official Publication Of The American Academy Of Sleep Medicine
Goyal, Sandeep K SK; Wang, Li L; Upender, Raghu R; Darbar, Dawood D; Monahan, Ken K
Publication Date: 2014-05-15

Variant appearance in text: rs7193343
PubMed Link: 24910551
Variant Present in the following documents:
  • Main text
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Association between NINJ2 gene polymorphisms and ischemic stroke: a family-based case-control study.

Journal Of Thrombosis And Thrombolysis
Zhu, Yanping Y; Liu, Kuo K; Tang, Xun X; Wang, Jinwei J; Yu, Zhiping Z; Wu, Yiqun Y; Chen, Dafang D; Wang, Xueyin X; Fang, Kai K; Li, Na N; Huang, Shaoping S; Hu, Yonghua Y
Publication Date: 2014-11

Variant appearance in text: rs7193343
PubMed Link: 24664524
Variant Present in the following documents:
  • Main text
  • 11239_2014_Article_1065.pdf
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Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations.

Cerebrovascular Diseases (Basel, Switzerland)
Chou, S H-Y SH; Shulman, J M JM; Keenan, B T BT; Secor, E A EA; Buchman, A S AS; Schneider, J J; Bennett, D A DA; De Jager, P L PL
Publication Date: 2013

Variant appearance in text: rs7193343
PubMed Link: 24135527
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Genetic mechanisms of atrial fibrillation: impact on response to treatment.

Nature Reviews. Cardiology
Darbar, Dawood D; Roden, Dan M DM
Publication Date: 2013-06

Variant appearance in text: rs7193343
PubMed Link: 23591267
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Novel genetic markers improve measures of atrial fibrillation risk prediction.

European Heart Journal
Everett, Brendan M BM; Cook, Nancy R NR; Conen, David D; Chasman, Daniel I DI; Ridker, Paul M PM; Albert, Christine M CM
Publication Date: 2013-08

Variant appearance in text: rs7193343
PubMed Link: 23444395
Variant Present in the following documents:
  • Main text
  • supp_eht033_eht033supp.pdf
  • eht033.pdf
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Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion.

Heart Rhythm
Parvez, Babar B; Shoemaker, M Benjamin MB; Muhammad, Raafia R; Richardson, Rachael R; Jiang, Lan L; Blair, Marcia A MA; Roden, Dan M DM; Darbar, Dawood D
Publication Date: 2013-06

Variant appearance in text: rs7193343
PubMed Link: 23428961
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Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.

Journal Of The American College Of Cardiology
Parvez, Babar B; Vaglio, Joseph J; Rowan, Shane S; Muhammad, Raafia R; Kucera, Gayle G; Stubblefield, Tanya T; Carter, Shannon S; Roden, Dan D; Darbar, Dawood D
Publication Date: 2012-08-07

Variant appearance in text: rs7193343
PubMed Link: 22726630
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Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.

Journal Of Internal Medicine
Smith, J G JG; Almgren, P P; Engström, G G; Hedblad, B B; Platonov, P G PG; Newton-Cheh, C C; Melander, O O
Publication Date: 2012-12

Variant appearance in text: rs7193343
PubMed Link: 22690879
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Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.

Plos One
Delaney, Jessica T JT; Jeff, Janina M JM; Brown, Nancy J NJ; Pretorius, Mias M; Okafor, Henry E HE; Darbar, Dawood D; Roden, Dan M DM; Crawford, Dana C DC
Publication Date: 2012

Variant appearance in text: rs7193343
PubMed Link: 22384221
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Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.

Nature Genetics
, ; , ; Bellenguez, Céline C; Bevan, Steve S; Gschwendtner, Andreas A; Spencer, Chris C A CC; Burgess, Annette I AI; Pirinen, Matti M; Jackson, Caroline A CA; Traylor, Matthew M; Strange, Amy A; Su, Zhan Z; Band, Gavin G; Syme, Paul D PD; Malik, Rainer R; Pera, Joanna J; Norrving, Bo B; Lemmens, Robin R; Freeman, Colin C; Schanz, Renata R; James, Tom T; Poole, Deborah D; Murphy, Lee L; Segal, Helen H; Cortellini, Lynelle L; Cheng, Yu-Ching YC; Woo, Daniel D; Nalls, Michael A MA; Müller-Myhsok, Bertram B; Meisinger, Christa C; Seedorf, Udo U; Ross-Adams, Helen H; Boonen, Steven S; Wloch-Kopec, Dorota D; Valant, Valerie V; Slark, Julia J; Furie, Karen K; Delavaran, Hossein H; Langford, Cordelia C; Deloukas, Panos P; Edkins, Sarah S; Hunt, Sarah S; Gray, Emma E; Dronov, Serge S; Peltonen, Leena L; Gretarsdottir, Solveig S; Thorleifsson, Gudmar G; Thorsteinsdottir, Unnur U; Stefansson, Kari K; Boncoraglio, Giorgio B GB; Parati, Eugenio A EA; Attia, John J; Holliday, Elizabeth E; Levi, Chris C; Franzosi, Maria-Grazia MG; Goel, Anuj A; Helgadottir, Anna A; Blackwell, Jenefer M JM; Bramon, Elvira E; Brown, Matthew A MA; Casas, Juan P JP; Corvin, Aiden A; Duncanson, Audrey A; Jankowski, Janusz J; Mathew, Christopher G CG; Palmer, Colin N A CN; Plomin, Robert R; Rautanen, Anna A; Sawcer, Stephen J SJ; Trembath, Richard C RC; Viswanathan, Ananth C AC; Wood, Nicholas W NW; Worrall, Bradford B BB; Kittner, Steven J SJ; Mitchell, Braxton D BD; Kissela, Brett B; Meschia, James F JF; Thijs, Vincent V; Lindgren, Arne A; Macleod, Mary Joan MJ; Slowik, Agnieszka A; Walters, Matthew M; Rosand, Jonathan J; Sharma, Pankaj P; Farrall, Martin M; Sudlow, Cathie L M CL; Rothwell, Peter M PM; Dichgans, Martin M; Donnelly, Peter P; Markus, Hugh S HS
Publication Date: 2012-02-05

Variant appearance in text: rs7193343
PubMed Link: 22306652
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Blood biomarkers in cardioembolic stroke.

Current Cardiology Reviews
García-Berrocoso, Teresa T; Fernández-Cadenas, Israel I; Delgado, Pilar P; Rosell, Anna A; Montaner, Joan J
Publication Date: 2010-08

Variant appearance in text: rs7193343
PubMed Link: 21804778
Variant Present in the following documents:
  • Main text
  • CCR-6-194.pdf
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Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population.

Plos One
Kiliszek, Marek M; Franaszczyk, Maria M; Kozluk, Edward E; Lodzinski, Piotr P; Piatkowska, Agnieszka A; Broda, Grażyna G; Ploski, Rafal R; Opolski, Grzegorz G
Publication Date: 2011

Variant appearance in text: rs7193343
PubMed Link: 21760908
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Genetic susceptibility to ischemic stroke.

Nature Reviews. Neurology
Meschia, James F JF; Worrall, Bradford B BB; Rich, Stephen S SS
Publication Date: 2011-05-31

Variant appearance in text: rs7193343
PubMed Link: 21629240
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Genome-wide association studies of atrial fibrillation: past, present, and future.

Cardiovascular Research
Sinner, Moritz F MF; Ellinor, Patrick T PT; Meitinger, Thomas T; Benjamin, Emelia J EJ; Kääb, Stefan S
Publication Date: 2011-03-01

Variant appearance in text: rs7193343
PubMed Link: 21245058
Variant Present in the following documents:
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