Human Genome Epidemiology Literature Finder
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Records 1 - 21 (of 21 Records) |
| Query Trace: Disease and HDAC9[original query] |
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| Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma. BMC medical genomics 2008 Jun 1 (1): 25. Blons H, Pallier K, Le Corre D, Danel C, Tremblay M, Houdayer C, Fabre-Guillevin E, Riquet M, Dessen P, Laurent-Puig P |
| Confirmed rare copy number variants implicate novel genes in schizophrenia. Biochemical Society transactions 2010 Apr 38 (2): 445-51. Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G |
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, |
| Genome-wide association study of retinopathy in individuals without diabetes.
PloS one 2013 8 (2): e54232. Jensen Richard A, Sim Xueling, Li Xiaohui, Cotch Mary Frances, Ikram M Kamran, Holliday Elizabeth G, Eiriksdottir Gudny, Harris Tamara B, Jonasson Fridbert, Klein Barbara E K, Launer Lenore J, Smith Albert Vernon, Boerwinkle Eric, Cheung Ning, Hewitt Alex W, Liew Gerald, Mitchell Paul, Wang Jie Jin, Attia John, Scott Rodney, Glazer Nicole L, Lumley Thomas, McKnight Barbara, Psaty Bruce M, Taylor Kent, Hofman Albert, de Jong Paulus T V M, Rivadeneira Fernando, Uitterlinden Andre G, Tay Wan-Ting, Teo Yik Ying, Seielstad Mark, Liu Jianjun, Cheng Ching-Yu, Saw Seang-Mei, Aung Tin, Ganesh Santhi K, O'Donnell Christopher J, Nalls Mike A, Wiggins Kerri L, Kuo Jane Z, , , van Duijn Cornelia M, Gudnason Vilmundur, Klein Ronald, Siscovick David S, Rotter Jerome I, Tai E Shong, Vingerling Johannes, Wong Tien |
| Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Stroke; a journal of cerebral circulation 2014 Jan 45 (1): 24-36. Dichgans Martin, Malik Rainer, König Inke R, Rosand Jonathan, Clarke Robert, Gretarsdottir Solveig, Thorleifsson Gudmar, Mitchell Braxton D, Assimes Themistocles L, Levi Christopher, O'Donnell Christopher J, Fornage Myriam, Thorsteinsdottir Unnur, Psaty Bruce M, Hengstenberg Christian, Seshadri Sudha, Erdmann Jeanette, Bis Joshua C, Peters Annette, Boncoraglio Giorgio B, März Winfried, Meschia James F, Kathiresan Sekar, Ikram M Arfan, McPherson Ruth, Stefansson Kari, Sudlow Cathie, Reilly Muredach P, Thompson John R, Sharma Pankaj, Hopewell Jemma C, Chambers John C, Watkins Hugh, Rothwell Peter M, Roberts Robert, Markus Hugh S, Samani Nilesh J, Farrall Martin, Schunkert Heribert, , , , |
| Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7.
Stroke; a journal of cerebral circulation 2014 Nov 45 (11): 3194-9. Foroud Tatiana, Lai Dongbing, Koller Daniel, Van't Hof Femke, Kurki Mitja I, Anderson Craig S, Brown Robert D, Connolly Edward Sander, Eriksson Johan G, Flaherty Matthew, Fornage Myriam, von Und Zu Fraunberg Mikael, Gaál Emília I, Laakso Aki, Hernesniemi Juha, Huston John, Jääskeläinen Juha E, Kiemeney Lambertus A, Kivisaari Riku, Kleindorfer Dawn, Ko Nerissa, Lehto Hanna, Mackey Jason, Meissner Irene, Moomaw Charles J, Mosley Thomas H, Moskala Marek, Niemelä Mika, Palotie Aarno, Pera Joanna, Rinkel Gabriel, Ripke Stephan, Rouleau Guy, Ruigrok Ynte, Sauerbeck Laura, S?owik Agnieszka, Vermeulen Sita H, Woo Daniel, Worrall Bradford B, Broderick Joseph, |
| Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
| Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population.
PloS one 0 10 (10): e0139262. Matsukura Mitsuru, Ozaki Kouichi, Takahashi Atsushi, Onouchi Yoshihiro, Morizono Takashi, Komai Hiroyoshi, Shigematsu Hiroshi, Kudo Toshifumi, Inoue Yoshinori, Kimura Hideo, Hosaka Akihiro, Shigematsu Kunihiro, Miyata Teturo, Watanabe Toshiaki, Tsunoda Tatsuhiko, Kubo Michiaki, Tanaka Toshihi |
| Polymorphism of HDAC9 Gene Is Associated with Increased Risk of Acute Coronary Syndrome in Chinese Han Population. BioMed research international 2016 2016 3746276. Han Zhenhua, Dong Xin, Zhang Chaoying, Wu Yue, Yuan Zuyi, Wang Xinho |
| HDAC9 Variant Rs2107595 Modifies Susceptibility to Coronary Artery Disease and the Severity of Coronary Atherosclerosis in a Chinese Han Population. PloS one 2016 11 (8): e0160449. Wang Xue-Bin, Han Ya-di, Sabina Shrestha, Cui Ning-Hua, Zhang Shuai, Liu Ze-Jin, Li Cong, Zheng Fa |
| 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, , , , |
| Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.
Stroke 2018 Jan 49 (1): 11-18. Duan Lian, Wei Ling, Tian Yanghua, Zhang Zhengshan, Hu Panpan, Wei Qiang, Liu Sugang, Zhang Jun, Wang Yuyang, Li Desheng, Yang Weizhong, Zong Rui, Xian Peng, Han Cong, Bao Xiangyang, Zhao Feng, Feng Jie, Liu Wei, Cao Wuchun, Zhou Guoping, Zhu Chunyan, Yu Fengqiong, Yang Weimin, Meng Yu, Wang Jingye, Chen Xianwen, Wang Yu, Shen Bing, Zhao Bing, Wan Jinghai, Zhang Fengyu, Zhao Gang, Xu Aimin, Zhang Xuejun, Liu Jianjun, Zuo Xianbo, Wang K |
| APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke. Acta neurologica Scandinavica 2018 Jan 137 (1): 133-141. Akinyemi R, Tiwari H K, Arnett D K, Ovbiagele B, Irvin M R, Wahab K, Sarfo F, Srinivasasainagendra V, Adeoye A, Perry R T, Akpalu A, Jenkins C, Arulogun O, Gebregziabher M, Owolabi L, Obiako R, Sanya E, Komolafe M, Fawale M, Adebayo P, Osaigbovo G, Sunmonu T, Olowoyo P, Chukwuonye I, Obiabo Y, Onoja A, Akinyemi J, Ogbole G, Melikam S, Saulson R, Owolabi M, |
| Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.
Alzheimer's research & therapy 2018 Feb 10 (1): 22. Chung Jaeyoon, Zhang Xiaoling, Allen Mariet, Wang Xue, Ma Yiyi, Beecham Gary, Montine Thomas J, Younkin Steven G, Dickson Dennis W, Golde Todd E, Price Nathan D, Ertekin-Taner Nilüfer, Lunetta Kathryn L, Mez Jesse, , Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Schellenberg Gerard, Jun Gyungah R, Farrer Lindsay |
| The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. Journal of thrombosis and thrombolysis 2019 Jan . Bozpolat Adil, Unal Ekrem, Topaloglu Tugba, Taheri Serpil, Bayram Ayse Kacar, Ozcan Alper, Karakukcu Musa, Ozdemir Mehmet Akif, Per Husey |
| Reverse expression pattern of sirtuin-1 and histone deacetylase-9 in coronary artery disease. Archives of physiology and biochemistry 2020 Aug 1-8. Heidari Laleh, Ghaderian Sayyed Mohammad Hossein, Bastami Milad, Hosseini Shadi, Alipour Parsa Saeed, Heidari Sahel, Jafari Hossein, Sohrabifar Nasim, Pirhoushiaran Mary |
| Atherosclerotic Aortic Calcification-Associated Polymorphism in HDAC9 and Associations with Mortality, Cardiovascular Disease, and Kidney Disease. iScience 2020 6 23 (7): 101253. Ärnlöv Johan, Dluzen Douglas F, Nowak Christo |
| Hot Spot TERT Promoter Mutations Are Rare in Sporadic Pancreatic Neuroendocrine Neoplasms and Associated with Telomere Length and Epigenetic Expression Patterns. Cancers 2020 6 12 (6): . Posch Alexandra, Hofer-Zeni Sarah, Klieser Eckhard, Primavesi Florian, Naderlinger Elisabeth, Brandstetter Anita, Filipits Martin, Urbas Romana, Swiercynski Stefan, Jäger Tarkan, Winkelmann Paul, Kiesslich Tobias, Lu Lingeng, Neureiter Daniel, Stättner Stefan, Holzmann Kla |
| Association between rs2107595 HDAC9 gene polymorphism and advanced carotid atherosclerosis in the Slovenian cohort. Lipids in health and disease 2020 Apr 19 (1): 71. Grbi? Emin, Gorki? Nataša, Pleskovi? Aleš, Zorc Marjeta, Ljuca Farid, Gasparini Mladen, Mr?a Božidar, Cilenšek Ines, Manko? Sara, Banach Maciej, Petrovi? Daniel, Fras Zlat |
| Genome-Wide Association Study of Peripheral Artery Disease.
Circulation. Genomic and precision medicine 2021 Oct CIRCGEN119002862. van Zuydam Natalie R, Stiby Alexander, Abdalla Moustafa, Austin Erin, Dahlström Emma H, McLachlan Stela, Vlachopoulou Efthymia, Ahlqvist Emma, Di Liao Chen, Sandholm Niina, Forsblom Carol, Mahajan Anubha, Robertson Neil R, Rayner N William, Lindholm Eero, Sinisalo Juha, Perola Markus, Kallio Milla, Weiss Emily, Price Jackie, Paterson Andrew, Klein Barbara, Salomaa Veikko, Palmer Colin N A, Groop Per-Henrik, Groop Leif, McCarthy Mark I, de Andrade Mariza, Morris Andrew P, Hopewell Jemma C, Colhoun Helen M, Kullo Iftikhar J, |
| Calcification of the abdominal aorta is an under-appreciated cardiovascular disease risk factor in the general population.
Frontiers in cardiovascular medicine 2022 10 9 1003246. Sethi Anurag, Taylor D Leland, Ruby J Graham, Venkataraman Jagadish, Sorokin Elena, Cule Madeleine, Melamud Euge |
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