Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 60 Records) |
Query Trace: HDAC9[original query] |
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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, |
Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion. Haematologica 2018 9 104 (1): 128-137. Ohki Kentaro, Kiyokawa Nobutaka, Saito Yuya, Hirabayashi Shinsuke, Nakabayashi Kazuhiko, Ichikawa Hitoshi, Momozawa Yukihide, Okamura Kohji, Yoshimi Ai, Ogata-Kawata Hiroko, Sakamoto Hiromi, Kato Motohiro, Fukushima Keitaro, Hasegawa Daisuke, Fukushima Hiroko, Imai Masako, Kajiwara Ryosuke, Koike Takashi, Komori Isao, Matsui Atsushi, Mori Makiko, Moriwaki Koichi, Noguchi Yasushi, Park Myoung-Ja, Ueda Takahiro, Yamamoto Shohei, Matsuda Koichi, Yoshida Teruhiko, Matsumoto Kenji, Hata Kenichiro, Kubo Michiaki, Matsubara Yoichi, Takahashi Hiroyuki, Fukushima Takashi, Hayashi Yasuhide, Koh Katsuyoshi, Manabe Atsushi, Ohara Akira, |
Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.
Schizophrenia research 2018 11 201 393-399. Nakahara Soichiro, Medland Sarah, Turner Jessica A, Calhoun Vince D, Lim Kelvin O, Mueller Bryon A, Bustillo Juan R, O'Leary Daniel S, Vaidya Jatin G, McEwen Sarah, Voyvodic James, Belger Aysenil, Mathalon Daniel H, Ford Judith M, Guffanti Guia, Macciardi Fabio, Potkin Steven G, van Erp Theo G |
HDAC9 Polymorphism Alters Blood Gene Expression in Patients with Large Vessel Atherosclerotic Stroke. Translational stroke research 2018 4 10 (1): 19-25. Shroff Natasha, Ander Bradley P, Zhan Xinhua, Stamova Boryana, Liu DaZhi, Hull Heather, Hamade Farah R, Dykstra-Aiello Cheryl, Ng Kwan, Sharp Frank R, Jickling Glen |
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 |
HDAC9 Polymorphisms Predict Susceptibility, Severity, and Short-Term Outcome of Large Artery Atherosclerotic Stroke in Chinese Population. Journal of molecular neuroscience : MN 2019 Jan 67 (1): 165-171. Wang Mengmeng, Gu Mengmeng, Li Zibao, Sun Bo, Cheng Xi, Dai Zhengze, Li Shun, Xiao Lulu, Zhao Min, Wang Zhaojun, Lin Ying, Liu Yahong, Xu Jian, Zhang Zhizhong, Liu Xinfe |
Vitamin D-Related Genes, Blood Vitamin D Levels and Colorectal Cancer Risk in Western European Populations. Nutrients 2019 Aug 11 (8): . Fedirko Veronika, Mandle Hannah B, Zhu Wanzhe, Hughes David J, Siddiq Afshan, Ferrari Pietro, Romieu Isabelle, Riboli Elio, Bueno-de-Mesquita Bas, van Duijnhoven Fränzel J B, Siersema Peter D, Tjønneland Anne, Olsen Anja, Perduca Vittorio, Carbonnel Franck, Boutron-Ruault Marie-Christine, Kühn Tilman, Johnson Theron, Krasimira Aleksandrova, Trichopoulou Antonia, Makrythanasis Periklis, Thanos Dimitris, Panico Salvatore, Krogh Vittorio, Sacerdote Carlotta, Skeie Guri, Weiderpass Elisabete, Colorado-Yohar Sandra, Sala Núria, Barricarte Aurelio, Sanchez Maria-Jose, Quirós Ramón, Amiano Pilar, Gylling Björn, Harlid Sophia, Perez-Cornago Aurora, Heath Alicia K, Tsilidis Konstantinos K, Aune Dagfinn, Freisling Heinz, Murphy Neil, Gunter Marc J, Jenab Maz |
Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population. Yonsei medical journal 2019 Jul 60 (7): 651-658. Li Bingyang, Hu Chongyu, Liu Junyu, Liao Xin, Xun Jiayu, Xiao Manqian, Yan Junx |
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
American journal of human genetics 2019 May . Spracklen Cassandra N, Karaderi Tugce, Yaghootkar Hanieh, Schurmann Claudia, Fine Rebecca S, Kutalik Zoltan, Preuss Michael H, Lu Yingchang, Wittemans Laura B L, Adair Linda S, Allison Matthew, Amin Najaf, Auer Paul L, Bartz Traci M, Blüher Matthias, Boehnke Michael, Borja Judith B, Bork-Jensen Jette, Broer Linda, Chasman Daniel I, Chen Yii-Der Ida, Chirstofidou Paraskevi, Demirkan Ayse, van Duijn Cornelia M, Feitosa Mary F, Garcia Melissa E, Graff Mariaelisa, Grallert Harald, Grarup Niels, Guo Xiuqing, Haesser Jeffrey, Hansen Torben, Harris Tamara B, Highland Heather M, Hong Jaeyoung, Ikram M Arfan, Ingelsson Erik, Jackson Rebecca, Jousilahti Pekka, Kähönen Mika, Kizer Jorge R, Kovacs Peter, Kriebel Jennifer, Laakso Markku, Lange Leslie A, Lehtimäki Terho, Li Jin, Li-Gao Ruifang, Lind Lars, Luan Jian'an, Lyytikäinen Leo-Pekka, MacGregor Stuart, Mackey David A, Mahajan Anubha, Mangino Massimo, Männistö Satu, McCarthy Mark I, McKnight Barbara, Medina-Gomez Carolina, Meigs James B, Molnos Sophie, Mook-Kanamori Dennis, Morris Andrew P, de Mutsert Renee, Nalls Mike A, Nedeljkovic Ivana, North Kari E, Pennell Craig E, Pradhan Aruna D, Province Michael A, Raitakari Olli T, Raulerson Chelsea K, Reiner Alex P, Ridker Paul M, Ripatti Samuli, Roberston Neil, Rotter Jerome I, Salomaa Veikko, Sandoval-Zárate America A, Sitlani Colleen M, Spector Tim D, Strauch Konstantin, Stumvoll Michael, Taylor Kent D, Thuesen Betina, Tönjes Anke, Uitterlinden Andre G, Venturini Cristina, Walker Mark, Wang Carol A, Wang Shuai, Wareham Nicholas J, Willems Sara M, Willems van Dijk Ko, Wilson James G, Wu Ying, Yao Jie, Young Kristin L, Langenberg Claudia, Frayling Timothy M, Kilpeläinen Tuomas O, Lindgren Cecilia M, Loos Ruth J F, Mohlke Karen |
Rs10230207 genotype confers changes in HDAC9 and TWIST1, but not FERD3L in lymphoblasts from patients with intracranial aneurysm. Neurogenetics 2019 Mar . Lansdell Theresa A, Fisher Courtney, Simmonds Kent, Reeves Mat J, Woo Daniel, Dorrance Anne M, Demel Stacie |
JAK/STAT-Activating Genomic Alterations Are a Hallmark of T-PLL. Cancers 2019 11 11 (12): . Wahnschaffe Linus, Braun Till, Timonen Sanna, Giri Anil K, Schrader Alexandra, Wagle Prerana, Almusa Henrikki, Johansson Patricia, Bellanger Dorine, López Cristina, Haferlach Claudia, Stern Marc-Henri, Dürig Jan, Siebert Reiner, Mustjoki Satu, Aittokallio Tero, Herling Mar |
[Analysis of genes related to hypothyroidism during pregnancy]. Zhonghua yi xue za zhi 2019 11 99 (42): 3350-3354. Liang L, Mao Y, Zhang J R, Zhang S C, Yang H |
HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype.
Nature genetics 2019 11 51 (11): 1580-1587. Malhotra Rajeev, Mauer Andreas C, Lino Cardenas Christian L, Guo Xiuqing, Yao Jie, Zhang Xiaoling, Wunderer Florian, Smith Albert V, Wong Quenna, Pechlivanis Sonali, Hwang Shih-Jen, Wang Judy, Lu Lingyi, Nicholson Christopher J, Shelton Georgia, Buswell Mary D, Barnes Hanna J, Sigurslid Haakon H, Slocum Charles, Rourke Caitlin O', Rhee David K, Bagchi Aranya, Nigwekar Sagar U, Buys Emmanuel S, Campbell Catherine Y, Harris Tamara, Budoff Matthew, Criqui Michael H, Rotter Jerome I, Johnson Andrew D, Song Ci, Franceschini Nora, Debette Stephanie, Hoffmann Udo, Kälsch Hagen, Nöthen Markus M, Sigurdsson Sigurdur, Freedman Barry I, Bowden Donald W, Jöckel Karl-Heinz, Moebus Susanne, Erbel Raimund, Feitosa Mary F, Gudnason Vilmundur, Thanassoulis George, Zapol Warren M, Lindsay Mark E, Bloch Donald B, Post Wendy S, O'Donnell Christopher |
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 |
Interactive Effects of a Combination of the HDAC3 and HDAC9 Genes with Diabetes Mellitus on the Risk of Ischemic Stroke. Thrombosis and haemostasis 2020 9 121 (3): 396-404. Chiou Hung-Yi, Bai Chyi-Huey, Lien Li-Ming, Hu Chaur-Jong, Jeng Jiann-Shing, Tang Sung-Chun, Lin Huey-Juan, Hsieh Yi-Ch |
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 interaction study reveals age-dependent determinants of responsiveness to inhaled corticosteroids in individuals with asthma.
PloS one 2020 15 (3): e0229241. Dahlin Amber, Sordillo Joanne E, McGeachie Michael, Kelly Rachel S, Tantisira Kelan G, Lutz Sharon M, Lasky-Su Jessica, Wu Ann Ch |
Association of a Multigenetic Pro-Inflammatory Profile with Ischaemic Stroke. Cerebrovascular diseases (Basel, Switzerland) 2020 Mar 1-7. Palm Frederick, Aigner Annette, Pussinen Pirkko Johanna, Urbanek Christian, Buggle Florian, Safer Anton, Becher Heiko, Grau Armin |
HDAC9 rs11984041 polymorphism is associated with diabetic retinopathy in Slovenian patients with type 2 diabetes mellitus. Gene 2021 Jun 796-797 145802. Cilenšek Ines, Lapuh Valentina, Globo?nik Petrovi? Mojca, Petrovi? Dani |
GWAS-linked hot loci predict short-term functional outcome and recurrence of ischemic stroke in Chinese population. American journal of translational research 2021 13 (5): 4521-4534. Zhu Ruixia, Zhao Yating, Tian Dandan, Guo Na, Zhang Chenguang, Liu |
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, |
Potentially functional genetic variants of the notch signaling pathway genes predict survival of Chinese patients with esophageal squamous cell carcinoma. The journal of gene medicine 2022 Jul e3438. Wu Yuanna, Liu Ming, Zhang Ruoxin, Sun Menghong, Wei Qingyi, Zhao Kuaile, Wang Mengy |
Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity.
Nature and science of sleep 2022 14 1075-1087. An Yu-Chin, Tsai Chia-Lin, Liang Chih-Sung, Lin Yu-Kai, Lin Guan-Yu, Tsai Chia-Kuang, Liu Yi, Chen Sy-Jou, Tsai Shih-Hung, Hung Kuo-Sheng, Yang Fu-C |
Genetic and Molecular Characterization Revealed the Prognosis Efficiency of Histone Acetylation in Pan-Digestive Cancers. Journal of oncology 2022 4 2022 3938652. Zhang Tao, Wang Bofang, Gu Baohong, Su Fei, Xiang Lin, Liu Le, Li Xuemei, Wang Xueyan, Gao Lei, Chen H |
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 |
Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm. Clinical research in cardiology : official journal of the German Cardiac Society 2024 4 . Roman Tremmel, Valeria Martínez Pereyra, Incifer Broders, Elke Schaeffeler, Per Hoffmann, Markus M Nöthen, Raffi Bekeredjian, Udo Sechtem, Matthias Schwab, Peter O |
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