Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and meta-analysis and CDKN2B[original query] |
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Genome-wide association study identifies five susceptibility loci for glioma.
Nature genetics 2009 Aug 41 (8): 899-904. Shete Sanjay, Hosking Fay J, Robertson Lindsay B, Dobbins Sara E, Sanson Marc, Malmer Beatrice, Simon Matthias, Marie Yannick, Boisselier Blandine, Delattre Jean-Yves, Hoang-Xuan Khe, El Hallani Soufiane, Idbaih Ahmed, Zelenika Diana, Andersson Ulrika, Henriksson Roger, Bergenheim A Tommy, Feychting Maria, Lönn Stefan, Ahlbom Anders, Schramm Johannes, Linnebank Michael, Hemminki Kari, Kumar Rajiv, Hepworth Sarah J, Price Amy, Armstrong Georgina, Liu Yanhong, Gu Xiangjun, Yu Robert, Lau Ching, Schoemaker Minouk, Muir Kenneth, Swerdlow Anthony, Lathrop Mark, Bondy Melissa, Houlston Richard |
| Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.
Circulation. Cardiovascular genetics 2011 Dec . Murabito JM, White CC, Kavousi M, Sun YY, Feitosa MF, Nambi V, Lamina C, Schillert A, Coassin S, Bis JC, Broer L, Crawford DC, Franceschini N, Frikke-Schmidt R, Haun M, Holewijn S, Huffman JE, Hwang SJ, Kiechl S, Kollerits B, Montasser ME, Nolte IM, Rudock ME, Senft A, Teumer A, van der Harst P, Vitart V, Waite LL, Wood AR, Wassel CL, Absher DM, Allison MA, Amin N, Arnold A, Asselbergs FW, Aulchenko Y, Bandinelli S, Barbalic M, Boban M, Brown-Gentry K, Couper DJ, Criqui MH, Dehghan A, den Heijer M, Dieplinger B, Ding J, Dörr M, Espinola-Klein C, Felix SB, Ferrucci L, Folsom AR, Fraedrich G, Gibson Q, Goodloe R, Gunjaca G, Haltmayer M, Heiss G, Hofman A, Kieback A, Kiemeney LA, Kolcic I, Kullo IJ, Kritchevsky SB, Lackner KJ, Li X, Lieb W, Lohman K, Meisinger C, Melzer D, Mohler ER, Mudnic I, Mueller T, Navis G, Oberhollenzer F, Olin JW, O'Connell J, O'Donnell CJ, Palmas W, Penninx BW, Petersmann A, Polasek O, Psaty BM, Rantner B, Rice K, Rivadeneira F, Rotter JI, Seldenrijk A, Stadler M, Summerer M, Tanaka T, Tybjærg-Hansen A, Uitterlinden AG, van Gilst WH, Vermeulen SH, Wild SH, Wild PS, Willeit J, Zeller T, Zemunik T, Zgaga L, Assimes TL, Blankenberg S, Boerwinkle E, Campbell H, Cooke JP, de Graaf J, Herrington D, Kardia SL, Mitchell BD, Murray A, Münzel T, Newman A, Oostra BA, Rudan I, Shuldiner AR, Snieder H, van Duijn CM, Völker U, Wright AF, Wichmann HE, Wilson JF, Witteman JC, Liu Y, Hayward C, Borecki IB, Ziegler A, North KE, Cupples LA, Kronenberg F |
| Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Human molecular genetics 2012 Nov 21 (22): 4980-95. Timofeeva Maria N, Hung Rayjean J, Rafnar Thorunn, Christiani David C, Field John K, Bickeböller Heike, Risch Angela, McKay James D, Wang Yufei, Dai Juncheng, Gaborieau Valerie, McLaughlin John, Brenner Darren, Narod Steven A, Caporaso Neil E, Albanes Demetrius, Thun Michael, Eisen Timothy, Wichmann H-Erich, Rosenberger Albert, Han Younghun, Chen Wei, Zhu Dakai, Spitz Margaret, Wu Xifeng, Pande Mala, Zhao Yang, Zaridze David, Szeszenia-Dabrowska Neonilia, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Mates Dana, Bencko Vladimir, Foretova Lenka, Janout Vladimir, Krokan Hans E, Gabrielsen Maiken Elvestad, Skorpen Frank, Vatten Lars, Njølstad Inger, Chen Chu, Goodman Gary, Lathrop Mark, Benhamou Simone, Vooder Tõnu, Välk Kristjan, Nelis Mari, Metspalu Andres, Raji Olaide, Chen Ying, Gosney John, Liloglou Triantafillos, Muley Thomas, Dienemann Hendrik, Thorleifsson Gudmar, Shen Hongbing, Stefansson Kari, Brennan Paul, Amos Christopher I, Houlston Richard, Landi Maria Teresa, |
| Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nature genetics 2012 Aug 44 (8): 890-4. Lu Xiangfeng, Wang Laiyuan, Chen Shufeng, He Lin, Yang Xueli, Shi Yongyong, Cheng Jing, Zhang Liang, Gu C Charles, Huang Jianfeng, Wu Tangchun, Ma Yitong, Li Jianxin, Cao Jie, Chen Jichun, Ge Dongliang, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Zhou Xiaoyang, Chen Lanying, Liu Donghua, Chen Jingping, Duan Xiufang, Hao Yongchen, Wang Ligui, Lu Fanghong, Liu Zhendong, Yao Cailiang, Shen Chong, Pu Xiaodong, Yu Lin, Fang Xianghua, Xu Lihua, Mu Jianjun, Wu Xianping, Zheng Runping, Wu Naqiong, Zhao Qi, Li Yun, Liu Xiaoli, Wang Mengqin, Yu Dahai, Hu Dongsheng, Ji Xu, Guo Dongshuang, Sun Dongling, Wang Qianqian, Yang Ying, Liu Fangchao, Mao Qunxia, Liang Xiaohua, Ji Jingfeng, Chen Panpan, Mo Xingbo, Li Dianjiang, Chai Guoping, Tang Yida, Li Xiangdong, Du Zhenhan, Liu Xuehui, Dou Chenlong, Yang Zili, Meng Qingjie, Wang Dong, Wang Renping, Yang Jun, Schunkert Heribert, Samani Nilesh J, Kathiresan Sekar, Reilly Muredach P, Erdmann Jeanette, , Peng Xiaozhong, Wu Xigui, Liu Depei, Yang Yuejin, Chen Runsheng, Qiang Boqin, Gu Dongfe |
| Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls. Molecular biology reports 2013 Jan 40 (1): 337-43. Guo Jin, Li Wei, Wu Zhenqiang, Cheng Xiaoru, Wang Yang, Chen T |
| Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human reproduction update 0 20 (5): 702-16. Rahmioglu Nilufer, Nyholt Dale R, Morris Andrew P, Missmer Stacey A, Montgomery Grant W, Zondervan Krina |
| Independent Replication and Meta-Analysis for Endometriosis Risk Loci. Twin research and human genetics : the official journal of the International Society for Twin Studies 2015 Oct 18 (5): 518-25. Sapkota Yadav, Fassbender Amelie, Bowdler Lisa, Fung Jenny N, Peterse Daniëlle, O Dorien, Montgomery Grant W, Nyholt Dale R, D'Hooghe Thomas |
| Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2017 Feb 15 (1): 53-58. Zhao Jikuang, Wu Xizheng, Nie Sheng, Gao Xiang, Sun Jie, Li Keqin, Zhang Tiefeng, Huang |
| Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7. PloS one 2017 12 (12): e0186678. Shiga Yukihiro, Nishiguchi Koji M, Kawai Yosuke, Kojima Kaname, Sato Kota, Fujita Kosuke, Takahashi Mai, Omodaka Kazuko, Araie Makoto, Kashiwagi Kenji, Aihara Makoto, Iwata Takeshi, Mabuchi Fumihiko, Takamoto Mitsuko, Ozaki Mineo, Kawase Kazuhide, Fuse Nobuo, Yamamoto Masayuki, Yasuda Jun, Nagasaki Masao, Nakazawa Toru, |
| Associations Between Common Polymorphisms of CDKN2B-AS and Susceptibility to ASCVD. Angiology 2020 Jul 3319720941387. Huang Yupeng, Jin Hongyan, Yang Guoka |
| CDKN2B-AS1 gene rs4977574 A/G polymorphism and coronary heart disease: A meta-analysis of 40,979 subjects. Journal of cellular and molecular medicine 2021 Aug . Li Yan-Yan, Wang Hui, Zhang Yang-Ya |
| 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, |
| Genetic association between CDKN2B/CDKN2B-AS1 gene polymorphisms with primary glaucoma in a North Indian cohort: an original study and an updated meta-analysis. BMC medical genomics 2021 Jan 14 (1): 1. Thakur Nanamika, Kupani Manu, Mannan Rashim, Pruthi Archna, Mehrotra Sanja |
| Associated genetic variants and potential pathogenic mechanisms of brain arteriovenous malformation. Journal of neurointerventional surgery 2022 4 . Liu Junyu, Li Yifeng, Zhang Hao, Luo Chun, Yuan Dun, Jiang Weixi, Yan Junx |
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