Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 93 Records) |
Query Trace: PITX2[original query] |
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Long-range Pitx2c enhancer-promoter interactions prevent predisposition to atrial fibrillation. Proceedings of the National Academy of Sciences of the United States of America 2019 Oct . Zhang Min, Hill Matthew C, Kadow Zachary A, Suh Ji Ho, Tucker Nathan R, Hall Amelia W, Tran Tien T, Swinton Paul S, Leach John P, Margulies Kenneth B, Ellinor Patrick T, Li Na, Martin James |
Clinical and Genetic Contributors to New-Onset Atrial Fibrillation in Critically Ill Adults. Critical care medicine 2019 10 48 (1): 22-30. Kerchberger V Eric, Huang Yi, Koyama Tatsuki, Shoemaker M Benjamin, Darbar Dawood, Bastarache Julie A, Ware Lorraine B, Shaver Ciara |
Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation. Circulation. Genomic and precision medicine 2020 8 13 (5): 387-395. Weng Lu-Chen, Hall Amelia Weber, Choi Seung Hoan, Jurgens Sean J, Haessler Jeffrey, Bihlmeyer Nathan A, Grarup Niels, Lin Honghuang, Teumer Alexander, Li-Gao Ruifang, Yao Jie, Guo Xiuqing, Brody Jennifer A, Müller-Nurasyid Martina, Schramm Katharina, Verweij Niek, van den Berg Marten E, van Setten Jessica, Isaacs Aaron, Ramírez Julia, Warren Helen R, Padmanabhan Sandosh, Kors Jan A, de Boer Rudolf A, van der Meer Peter, Sinner Moritz F, Waldenberger Melanie, Psaty Bruce M, Taylor Kent D, Völker Uwe, Kanters Jørgen K, Li Man, Alonso Alvaro, Perez Marco V, Vaartjes Ilonca, Bots Michiel L, Huang Paul L, Heckbert Susan R, Lin Henry J, Kornej Jelena, Munroe Patricia B, van Duijn Cornelia M, Asselbergs Folkert W, Stricker Bruno H, van der Harst Pim, Kääb Stefan, Peters Annette, Sotoodehnia Nona, Rotter Jerome I, Mook-Kanamori Dennis O, Dörr Marcus, Felix Stephan B, Linneberg Allan, Hansen Torben, Arking Dan E, Kooperberg Charles, Benjamin Emelia J, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven |
Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.
Circulation. Genomic and precision medicine 2020 08 13 (4): e002680. Baldassari Antoine R, Sitlani Colleen M, Highland Heather M, Arking Dan E, Buyske Steve, Darbar Dawood, Gondalia Rahul, Graff Misa, Guo Xiuqing, Heckbert Susan R, Hindorff Lucia A, Hodonsky Chani J, Ida Chen Yii-Der, Kaplan Robert C, Peters Ulrike, Post Wendy, Reiner Alex P, Rotter Jerome I, Shohet Ralph V, Seyerle Amanda A, Sotoodehnia Nona, Tao Ran, Taylor Kent D, Wojcik Genevieve L, Yao Jie, Kenny Eimear E, Lin Henry J, Soliman Elsayed Z, Whitsel Eric A, North Kari E, Kooperberg Charles, Avery Christy |
Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr . Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H |
Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
Personalized warfarin treatment based on the PITX2 single nucleotide polymorphism rs6843082. International journal of clinical and experimental pathology 2020 13 (11): 2831-2839. Liu Tianhua, Huang Hongman, Liu Xinbing, Yang Yuya, Mei Xiang, Feng Liul |
Predicting atrial fibrillation using a combination of genetic risk score and clinical risk factors. Heart rhythm 2020 Jan . Okubo Yousaku, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Tokuyama Takehito, Motoda Chikaaki, Amioka Michitaka, Hironobe Naoya, Okamura Sho, Ikeuchi Yoshihiro, Miyauchi Syunsuke, Chayama Kazuaki, Kihara Yasu |
The association between polymorphisms in PITX2 and congenital esophageal atresia susceptibility. American journal of translational research 2021 13 (8): 9808-9813. Ke Jiangwei, Tao Junfeng, Chen Ku |
SLC17A3 rs9379800 and Ischemic Stroke Susceptibility at the Northern Region of Malaysia. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2021 Aug 105908. Ching Shu Chai, Wen Lim Jing, Ismail Nor Ismaliza Mohd, Looi Irene, Kooi Cheah Wee, Peng Long Soo, Mui Lee Soon, Tamibmaniam Jayashamani, Muninathan Prema, Hooi Ong Beng, Ali Siti Maisarah Md, Hassan Muhammad Radzi Abu, Mohamad Mohd Saberi, Griffiths Lyn R, Wei Loo Ke |
Atrial fibrillation and left atrial size and function: a Mendelian randomization study. Scientific reports 2021 4 11 (1): 8431. van de Vegte Yordi J, Siland Joylene E, Rienstra Michiel, van der Harst P |
Genetic analysis of patients with primary congenital glaucoma. International ophthalmology 2021 Mar . Ava Sedat, Demirta? At?l?m Arma?an, Karahan Mine, Erdem Seyfettin, Oral Diclehan, Keklikçi U? |
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients. Anatolian journal of cardiology 2021 02 25 (2): 129-138. Ulus Taner, Dural Muhammet, Me?e Pelin, Yetmi? Furkan, Mert Kadir U?ur, Görenek Bülent, Çilingir O?uz, Erzurumluoglu Gökalp Ebru, Arslan Serap, Artan Sevilhan, Aykaç Özlem, Çolak Ertu?rul, Yorgun Hikmet, Canpolat U?ur, Aytemir Kudr |
Genetic insight into sick sinus syndrome.
European heart journal 2021 Feb . Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients. Medicina (Kaunas, Lithuania) 2021 11 57 (11): . Vogel Simon, Rudaka Irina, Rots Dmitrijs, Isakova Jekater?na, Kal?js Oskars, V?ksne Krist?ne, Gail?te Lin |
Variants rs2200733 and rs6843082 Show Different Associations in Asian and Non-Asian Populations With Ischemic Stroke. Frontiers in genetics 2022 13 905560. Wang Dongsen, Hu Xuemei, Yang Xue, Yang Mingfeng, Wu Qingji |
[Interaction between ischemic stroke risk loci identified by genome-wide association studies and sleep habits]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 Jun 54 (3): 412-420. Yang R T, Wang M Y, Li C N, Yu H, Wang X W, Wu J H, Wang S Y, Wang J T, Chen D F, Wu T, Hu Y |
Integrated genomic analysis identifies novel low-frequency cis-regulatory variant rs2279658 associated with VSD risk in Chinese children. Frontiers in cell and developmental biology 2022 12 10 1062403. Jin Lihui, Han Zhenyuan, Jiang Zhongli, Lu Jieru, Wu Yizhuo, Yan Bingqian, Zhang Weibin, Lin Xuedong, Jiang Lvyan, Zhao Pengjun, Sun K |
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome. Experimental eye research 2022 11 226 109307. Zhou Lin, Wang Xiaoli, An Jingqi, Zhang Yao, He Mengxia, Tang |
Genetic insight into sick sinus syndrome.
European heart journal 2021 May 42 (20): 1959-1971. Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Genome-wide analyses identify SCN5A as a susceptibility locus for premature atrial contraction frequency.
iScience 2022 Oct 25 (10): 105210. Thériault Sébastien, Imboden Medea, Biggs Mary L, Austin Thomas R, Aeschbacher Stefanie, Schaffner Emmanuel, Brody Jennifer A, Bartz Traci M, Risch Martin, Grossmann Kirsten, Lin Henry J, Soliman Elsayed Z, Post Wendy S, Risch Lorenz, Krieger Jose E, Pereira Alexandre C, Heckbert Susan R, Sotoodehnia Nona, Probst-Hensch Nicole M, Conen Dav |
Effect of PITX2 genetic variants on the susceptibility to stroke in the Chinese Han population. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2022 1 98 105201. Zhao Weiwei, Hu Xiuxia, Hao Jie, Guo Le, Zhang Wenjie, Liu Jianfeng, Jin Tianbo, Gao Dakuan, Zhi J |
Genome-wide association study-based prediction of atrial fibrillation using artificial intelligence. Open heart 2022 01 9 (1): . Kwon Oh-Seok, Hong Myunghee, Kim Tae-Hoon, Hwang Inseok, Shim Jaemin, Choi Eue-Keun, Lim Hong Euy, Yu Hee Tae, Uhm Jae-Sun, Joung Boyoung, Oh Seil, Lee Moon-Hyoung, Kim Young-Hoon, Pak Hui-N |
Genetic risk factors for postoperative atrial fibrillation-a nationwide genome-wide association study (GWAS). Frontiers in cardiovascular medicine 2023 7 10 1040757. Mathias A Christensen, Alexander Bonde, Martin Silles |
Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype. JACC. Clinical electrophysiology 2023 7 9 (7 Pt 2): 1147-1157. Majd A El-Harasis, Zachary T Yoneda, Giovanni E Davogustto, Diane M Crawford, James L Laws, Bradley Frye, Tarrah Herrmann, Bindiya Patel, Steven A Touchton, Dan M Roden, Travis D Richardson, Pablo Saavedra, Sharon T Shen, Juan C Estrada, Arvindh N Kanagasundram, Jay A Montgomery, Gregory F Michaud, George H Crossley, Christopher R Ellis, M Benjamin Shoemak |
Association of Novel C319T Variant of PITX2 Gene 3'UTR Region With Reproductive Performance in Awassi Sheep. Bioinformatics and biology insights 2023 6 17 11779322231179018. Ahmed H Alkhammas, Tahreer M Al-Thuwaini, Mohammed Baqur S Al-Shuhaib, Neam M Khaza |
Association Between rs2200733 Polymorphism of PITX2 Gene and the Risk of Atrial Fibrillation. Anatolian journal of cardiology 2023 3 27 (3): 160-166. Shen Han Yin, Ahmed Abass Mahamoud, Chao Zhu, Jun Wang, Xiaochen Yu |
Effects of hydroxychloroquine on atrial electrophysiology in in silico wild-type and PITX2 atrial cardiomyocytes. Herz 2023 2 1-9. Song Euij |
Craniofacial and dental features of Axenfeld-Rieger syndrome patients with PITX2 mutations. Orthodontics & craniofacial research 2023 1 . Arte Sirpa, Pöyhönen Minna, Myllymäki Emmi, Ronkainen Elisa, Rice David P, Nieminen Pek |
Genetic Polymorphism on Chromosome 4q25 (rs17570669) May Predict Recurrence After Successful Electrical Cardioversion in Patients with Persistent Atrial Fibrillation. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2024 1 51 (8): 550-556. Taner Ulus, ?lkin Aliyev, Serap Arslan, O?uz Çilingir, Ertu?rul Çol |
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- Page last updated:Apr 22, 2024
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