Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Disease and ZFHX3[original query] |
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A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.
PLoS genetics 2009 Jan 5 (1): e1000319. Burgner David, Davila Sonia, Breunis Willemijn B, Ng Sarah B, Li Yi, Bonnard Carine, Ling Ling, Wright Victoria J, Thalamuthu Anbupalam, Odam Miranda, Shimizu Chisato, Burns Jane C, Levin Michael, Kuijpers Taco W, Hibberd Martin L, |
| Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population. Human genetics 2011 Mar 129 (3): 239-46. Li Cong, Wang Fan, Yang Yanzong, Fu Fenfen, Xu Chengqi, Shi Lisong, Li Sisi, Xia Yunlong, Wu Gang, Cheng Xiang, Liu Hui, Wang Chuchu, Wang Pengyun, Hao Jianjun, Ke Yuhe, Zhao Yuanyuan, Liu Mugen, Zhang Rongfeng, Gao Lianjun, Yu Bo, Zeng Qiutang, Liao Yuhua, Yang Bo, Tu Xin, Wang Qing |
| 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, |
| Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations. Cerebrovascular diseases (Basel, Switzerland) 2013 36 (3): 181-8. Chou S H-Y, Shulman J M, Keenan B T, Secor E A, Buchman A S, Schneider J, Bennett D A, De Jager P |
| Genetic polymorphisms in ZFHX3 are associated with atrial fibrillation in a Chinese Han population. PloS one 2014 9 (7): e101318. Liu Yaowu, Ni Bixian, Lin Yuan, Chen Xin-guang, Fang Zhen, Zhao Liyan, Hu Zhibin, Zhang Fengxia |
| 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 |
| Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner. BMC genetics 2014 15 (1): 136. Martin Ruairidh I R, Owens W Andrew, Cunnington Michael S, Mayosi Bongani M, Koref Mauro Santibáñez, Keavney Bernard |
| 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 |
| Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation. PLoS genetics 2015 Aug 11 (8): e1005393. Huang Yufeng, Wang Chuchu, Yao Yufeng, Zuo Xiaoyu, Chen Shanshan, Xu Chengqi, Zhang Hongfu, Lu Qiulun, Chang Le, Wang Fan, Wang Pengxia, Zhang Rongfeng, Hu Zhenkun, Song Qixue, Yang Xiaowei, Li Cong, Li Sisi, Zhao Yuanyuan, Yang Qin, Yin Dan, Wang Xiaojing, Si Wenxia, Li Xiuchun, Xiong Xin, Wang Dan, Huang Yuan, Luo Chunyan, Li Jia, Wang Jingjing, Chen Jing, Wang Longfei, Wang Li, Han Meng, Ye Jian, Chen Feifei, Liu Jingqiu, Liu Ying, Wu Gang, Yang Bo, Cheng Xiang, Liao Yuhua, Wu Yanxia, Ke Tie, Chen Qiuyun, Tu Xin, Elston Robert, Rao Shaoqi, Yang Yanzong, Xia Yunlong, Wang Qing |
| 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 2015 8 (5): 7890-7. Sun Shunchang, Zhang Wenwu, Chen Xi, Peng Yunsheng, Chen Qunro |
| The CAA repeat polymorphism in the ZFHX3 gene is associated with risk of coronary heart disease in a Chinese population. The Tohoku journal of experimental medicine 2015 235 (4): 261-6. Sun Shunchang, Zhang Wenwu, Chen Xi, Song Huiw |
| Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
| 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, |
| Epigenome-wide association of myocardial infarction with DNA methylation sites at loci related to cardiovascular disease. Clinical epigenetics 2017 9 54. Nakatochi Masahiro, Ichihara Sahoko, Yamamoto Ken, Naruse Keiko, Yokota Shigeki, Asano Hiroyuki, Matsubara Tatsuaki, Yokota Mitsuhi |
| 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 |
| Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Human molecular genetics 2018 2 27 (9): 1664-1674. Teslovich Tanya M, Kim Daniel Seung, Yin Xianyong, Stancáková Alena, Jackson Anne U, Wielscher Matthias, Naj Adam, Perry John R B, Huyghe Jeroen R, Stringham Heather M, Davis James P, Raulerson Chelsea K, Welch Ryan P, Fuchsberger Christian, Locke Adam E, Sim Xueling, Chines Peter S, Narisu Narisu, Kangas Antti J, Soininen Pasi, , Ala-Korpela Mika, Gudnason Vilmundur, Musani Solomon K, Jarvelin Marjo-Riitta, Schellenberg Gerard D, Speliotes Elizabeth K, Kuusisto Johanna, Collins Francis S, Boehnke Michael, Laakso Markku, Mohlke Karen |
| Integrative molecular characterization of Chinese prostate cancer specimens. Asian journal of andrology 2019 May . Lv Shi-Dong, Wang Hong-Yi, Yu Xin-Pei, Zhai Qi-Liang, Wu Yao-Bin, Wei Qiang, Huang Wen-H |
| Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.
Translational psychiatry 2020 11 10 (1): 403. Hong Shengjun, Prokopenko Dmitry, Dobricic Valerija, Kilpert Fabian, Bos Isabelle, Vos Stephanie J B, Tijms Betty M, Andreasson Ulf, Blennow Kaj, Vandenberghe Rik, Cleynen Isabelle, Gabel Silvy, Schaeverbeke Jolien, Scheltens Philip, Teunissen Charlotte E, Niemantsverdriet Ellis, Engelborghs Sebastiaan, Frisoni Giovanni, Blin Olivier, Richardson Jill C, Bordet Regis, Molinuevo José Luis, Rami Lorena, , Kettunen Petronella, Wallin Anders, Lleó Alberto, Sala Isabel, Popp Julius, Peyratout Gwendoline, Martinez-Lage Pablo, Tainta Mikel, Dobson Richard J B, Legido-Quigley Cristina, Sleegers Kristel, Van Broeckhoven Christine, Ten Kate Mara, Barkhof Frederik, Zetterberg Henrik, Lovestone Simon, Streffer Johannes, Wittig Michael, Franke Andre, Tanzi Rudolph E, Visser Pieter Jelle, Bertram La |
| Circulating tumor DNA as a prognostic marker in high-risk endometrial cancer. Journal of translational medicine 2021 Feb 19 (1): 51. Feng Weiwei, Jia Nan, Jiao Haining, Chen Jun, Chen Yan, Zhang Yueru, Zhu Menghan, Zhu Chongying, Shen Lifei, Long Wenqi |
| 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, |
| 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, |
| Association between cyclin-dependent kinase inhibitor 2B antisense RNA 1 and zinc finger homeobox 3 gene polymorphisms and COVID-19 severity. BMC infectious diseases 2023 8 23 (1): 568. Eman A Badr, Nesreen G Elhelbawy, Alaa Osama Nagy, Amany A Sultan, Shereen S Elnaida |
| Somatic and Germline Variants Affect Prognosis and Susceptibility in Prostate Cancer. Anticancer research 2023 6 43 (7): 2941-2949. Christian Rocca, Giulia Rocca, Pietro Zampieri, Lucio Dell'atti, Nicoletta Bianchi, Carmelo Ippolito, Gianluca Aguia |
| RBM10 Mutation as a Potential Negative Prognostic/Predictive Biomarker to Therapy in Non-Small-Cell Lung Cancer. Clinical lung cancer 2024 8 . Amanda Reyes, Michelle Afkhami, Erminia Massarelli, Jeremy Fricke, Isa Mambetsariev, Xiaochen Li, Giovanny Velasquez, Ravi Salg |
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