Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 30 Records) |
| Query Trace: Disease and PITX2[original query] |
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| Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. American journal of human genetics 2002 Feb 70 (2): 448-60. Vincent Andrea L, Billingsley Gail, Buys Yvonne, Levin Alex V, Priston Megan, Trope Graham, Williams-Lyn Donna, Héon Eli |
| Mutational analysis of the PITX2 and NKX2-5 genes in patients with idiopathic atrial fibrillation. International journal of cardiology 2010 Nov 145 (2): 316-7. Boldt Leif-Hendrik, Posch Maximilian G, Perrot Andreas, Polotzki Michael, Rolf Sascha, Parwani Abdul S, Huemer Martin, Wutzler Alexander, Ozcelik Cemil, Haverkamp Wilhe |
| Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years. The Canadian journal of cardiology 0 28 (2): 191-5. Olesen Morten S, Holst Anders G, Jabbari Javad, Nielsen Jonas B, Christophersen Ingrid E, Sajadieh Ahmad, Haunsø Stig, Svendsen Jesper |
| Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations. Stroke; a journal of cerebral circulation 2012 Dec 43 (12): 3161-7. Bevan Steve, Traylor Matthew, Adib-Samii Poneh, Malik Rainer, Paul Nicola L M, Jackson Caroline, Farrall Martin, Rothwell Peter M, Sudlow Cathie, Dichgans Martin, Markus Hugh |
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2012 Nov 11 (11): 951-62. Traylor Matthew, Farrall Martin, Holliday Elizabeth G, Sudlow Cathie, Hopewell Jemma C, Cheng Yu-Ching, Fornage Myriam, Ikram M Arfan, Malik Rainer, Bevan Steve, Thorsteinsdottir Unnur, Nalls Mike A, Longstreth Wt, Wiggins Kerri L, Yadav Sunaina, Parati Eugenio A, Destefano Anita L, Worrall Bradford B, Kittner Steven J, Khan Muhammad Saleem, Reiner Alex P, Helgadottir Anna, Achterberg Sefanja, Fernandez-Cadenas Israel, Abboud Sherine, Schmidt Reinhold, Walters Matthew, Chen Wei-Min, Ringelstein E Bernd, O'Donnell Martin, Ho Weang Kee, Pera Joanna, Lemmens Robin, Norrving Bo, Higgins Peter, Benn Marianne, Sale Michele, Kuhlenbäumer Gregor, Doney Alexander S F, Vicente Astrid M, Delavaran Hossein, Algra Ale, Davies Gail, Oliveira Sofia A, Palmer Colin N A, Deary Ian, Schmidt Helena, Pandolfo Massimo, Montaner Joan, Carty Cara, de Bakker Paul I W, Kostulas Konstantinos, Ferro Jose M, van Zuydam Natalie R, Valdimarsson Einar, Nordestgaard Børge G, Lindgren Arne, Thijs Vincent, Slowik Agnieszka, Saleheen Danish, Paré Guillaume, Berger Klaus, Thorleifsson Gudmar, , Hofman Albert, Mosley Thomas H, Mitchell Braxton D, Furie Karen, Clarke Robert, Levi Christopher, Seshadri Sudha, Gschwendtner Andreas, Boncoraglio Giorgio B, Sharma Pankaj, Bis Joshua C, Gretarsdottir Solveig, Psaty Bruce M, Rothwell Peter M, Rosand Jonathan, Meschia James F, Stefansson Kari, Dichgans Martin, Markus Hugh S, |
| Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy. PloS one 2012 7 (10): e46742. Igo Robert P, Kopplin Laura J, Joseph Peronne, Truitt Barbara, Fondran Jeremy, Bardenstein David, Aldave Anthony J, Croasdale Christopher R, Price Marianne O, Rosenwasser Miriam, Lass Jonathan H, Iyengar Sudha K, |
| 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 2014 May 10 (5): 503-7. Goyal Sandeep K, Wang Li, Upender Raghu, Darbar Dawood, Monahan K |
| Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation. Journal of medical genetics 2015 Jan 52 (1): 28-36. Tsai Chia-Ti, Hsieh Chia-Shan, Chang Sheng-Nan, Chuang Eric Y, Juang Jyh-Ming Jimmy, Lin Lian-Yu, Lai Ling-Ping, Hwang Juey-Jen, Chiang Fu-Tien, Lin Jiunn-L |
| Association of common variations on chromosome 4q25 and left atrial volume in patients with atrial fibrillation. Clinical Medicine Insights. Cardiology 2015 9 39-45. Mints Yuliya, Yarmohammadi Hirad, Khurram Irfan M, Hoyt Hana, Hansford Rozann, Zimmerman Stefan L, Steinberg Steven J, Judge Daniel P, Tomaselli Gordon F, Calkins Hugh, Zipunnikov Vadim, Nazarian Sam |
| Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
| PITX2 loss-of-function mutation contributes to tetralogy of Fallot. Gene 2015 Dec . Sun Yu-Min, Wang Jun, Qiu Xing-Biao, Yuan Fang, Xu Ying-Jia, Li Ruo-Gu, Qu Xin-Kai, Huang Ri-Tai, Xue Song, Yang Yi-Qi |
| Exome array analysis of ischaemic stroke: results from a southern Swedish study. European journal of neurology 2016 12 23 (12): 1722-1728. Söderholm M, Almgren P, Jood K, Stanne T M, Olsson M, Ilinca A, Lorentzen E, Norrving B, Engström G, Melander O, Jern C, Lindgren |
| Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 2016 Mar . Malik Rainer, Traylor Matthew, Pulit Sara L, Bevan Steve, Hopewell Jemma C, Holliday Elizabeth G, Zhao Wei, Abrantes Patricia, Amouyel Philippe, Attia John R, Battey Thomas W K, Berger Klaus, Boncoraglio Giorgio B, Chauhan Ganesh, Cheng Yu-Ching, Chen Wei-Min, Clarke Robert, Cotlarciuc Ioana, Debette Stephanie, Falcone Guido J, Ferro Jose M, Gamble Dale M, Ilinca Andreea, Kittner Steven J, Kourkoulis Christina E, Lemmens Robin, Levi Christopher R, Lichtner Peter, Lindgren Arne, Liu Jingmin, Meschia James F, Mitchell Braxton D, Oliveira Sofia A, Pera Joana, Reiner Alex P, Rothwell Peter M, Sharma Pankaj, Slowik Agnieszka, Sudlow Cathie L M, Tatlisumak Turgut, Thijs Vincent, Vicente Astrid M, Woo Daniel, Seshadri Sudha, Saleheen Danish, Rosand Jonathan, Markus Hugh S, Worrall Bradford B, Dichgans Martin, , , , |
| A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study. Scientific reports 2017 Sep 7 (1): 12175. Hauer Allard J, Pulit Sara L, van den Berg Leonard H, de Bakker Paul I W, Veldink Jan H, Ruigrok Ynte M, |
| Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population. The Canadian journal of cardiology 2016 Nov . Liu Lian, Ebana Yusuke, Nitta Jun-Ichi, Takahashi Yoshihide, Miyazaki Shinsuke, Tanaka Toshihiro, Komura Masatoshi, Isobe Mitsuaki, Furukawa Tetsus |
| Atrial fibrillation associated genetic variation near PITX2 gene increases the risk of preeclampsia. Pregnancy hypertension 2018 Jul 13 214-217. Rani Usha, Praveen Kumar K S, Munisamaiah Munikrishna, Rajesh Deepa, Balakrishna Shara |
| [Rs17042171 at chromosome 4q25 is associated with atrial fibrillation in the Chinese Han population from the central plains]. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2018 Jun 43 (6): 594-603. Wang Xu, Nie Yali, Ning Shuwei, Shi Yong, Zhao Yujie, Niu Siquan, Guo Chengxian, Meng Xiangguang, Yuan Yiqia |
| Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population. Scientific reports 2018 Jun 8 (1): 9284. Saracyn Marek, Kisiel Bart?omiej, Bachta Artur, Franaszczyk Maria, Brodowska-Kania Dorota, ?mudzki Wawrzyniec, Szyma?ski Konrad, Sokalski Antoni, Klatko Wies?aw, Stopi?ski Marek, Grochowski Janusz, Papli?ski Marek, Go?dzik Zdzis?aw, Niemczyk Longin, Bober Barbara, Ko?odziej Maciej, T?ustochowicz Witold, Kami?ski Grzegorz, P?oski Rafa?, Niemczyk Stanis? |
| Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation. Molecular medicine reports 2018 6 18 (2): 1623-1627. Syrimis Andreas, Nicolaou Nayia, Alexandrou Angelos, Papaevripidou Ioannis, Nicolaou Michael, Loukianou Eleni, Sismani Carolina, Malas Stavros, Christophidou-Anastasiadou Violetta, Tanteles George |
| Analysis of clinical and candidate genetic risk factors for postoperative atrial tachycardia after congenital heart surgery in infants. American heart journal 2018 Apr 202 1-4. O'Connor Amy M, Smith Andrew H, Crum Kim, Edwards Todd L, Kannankeril Prince |
| Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Circulation 2018 Nov . Aragam Krishna G, Chaffin Mark, Levinson Rebecca T, McDermott Gregory, Choi Seung-Hoan, Shoemaker M Benjamin, Haas Mary E, Weng Lu-Chen, Lindsay Mark E, Smith J Gustav, Newton-Cheh Christopher, Roden Dan M, London Barry, Wells Quinn S, Ellinor Patrick T, Kathiresan Sekar, Lubitz Steven A, |
| A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation. The American journal of cardiology 2018 12 123 (5): 787-793. Mechakra Asma, Footz Tim, Walter Michael, Aránega Amelia, Hernández-Torres Francisco, Morel Elodie, Millat Gilles, Yang Yi-Qing, Chahine Mohamed, Chevalier Philippe, Christé Georg |
| Novel PITX2 Mutations including a Mutation Causing an Unusual Ophthalmic Phenotype of Axenfeld-Rieger Syndrome. Journal of ophthalmology 2019 7 2019 5642126. Huang Liqin, Meng Yong, Guo Xiangmi |
| 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 |
| Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma. PloS one 2019 1 14 (1): e0211029. Medina-Trillo Cristina, Aroca-Aguilar José-Daniel, Ferre-Fernández Jesús-José, Alexandre-Moreno Susana, Morales Laura, Méndez-Hernández Carmen-Dora, García-Feijoo Julián, Escribano Jul |
| 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 |
| 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, |
| 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 |
| 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, |
| 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 |
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