Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: AKAP13[original query] |
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Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer. Carcinogenesis 2006 Mar 27 (3): 593-8. Wirtenberger Michael, Tchatchou Sandrine, Hemminki Kari, Klaes Rüdiger, Schmutzler Rita K, Bermejo Justo L, Chen Bowang, Wappenschmidt Barbara, Meindl Alfons, Bartram Claus R, Burwinkel Barba |
The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer. Carcinogenesis 2007 Feb 28 (2): 423-6. Wirtenberger Michael, Schmutzhard Julia, Hemminki Kari, Meindl Alfons, Sutter Christian, Schmutzler Rita K, Wappenschmidt Barbara, Kiechle Marion, Arnold Norbert, Weber Bernhard H F, Niederacher Dieter, Bartram Claus R, Burwinkel Barba |
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
Human molecular genetics 2010 Nov 19 (21): 4304-11. Vitart Veronique, Benci? Goran, Hayward Caroline, Skunca Herman Jelena, Huffman Jennifer, Campbell Susan, Bu?an Kajo, Navarro Pau, Gunjaca Grgo, Marin Josipa, Zgaga Lina, Kolci? Ivana, Polasek Ozren, Kirin Mirna, Hastie Nicholas D, Wilson James F, Rudan Igor, Campbell Harry, Vatavuk Zoran, Fleck Brian, Wright Al |
A regulatory SNP in AKAP13 is associated with blood pressure in Koreans. Journal of human genetics 2011 Mar 56 (3): 205-10. Hong Kyung-Won, Lim Ji-Eun, Oh Bermse |
AKAP13, CACNA1, GRIK4 and GRIA1 genetic variations may be associated with haloperidol efficacy during acute treatment. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2013 Aug 23 (8): 887-94. Drago Antonio, Giegling Ina, Schäfer Martin, Hartmann Annette M, Friedl Marion, Konte Bettina, Möller Hans-Jürgen, De Ronchi Diana, Stassen Hans H, Serretti Alessandro, Rujescu D |
Landscape of the relationship between type 2 diabetes and coronary heart disease through an integrated gene network analysis. Gene 2014 Apr 539 (1): 30-6. Dong Changzheng, Tang Linlin, Liu Zhifang, Bu Shizhong, Liu Qiong, Wang Qinwen, Mai Yifeng, Wang Dao Wen, Duan Shiw |
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities. Journal of neural transmission (Vienna, Austria : 1996) 2017 Nov . Chiocchetti Andreas G, Yousaf Afsheen, Bour Hannah S, Haslinger Denise, Waltes Regina, Duketis Eftichia, Jarczok Tomas, Sachse Michael, Biscaldi Monica, Degenhardt Franziska, Herms Stefan, Cichon Sven, Ackermann Jörg, Koch Ina, Klauck Sabine M, Freitag Christine |
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
The Lancet. Respiratory medicine 2017 Nov 5 (11): 869-880. Allen Richard J, Porte Joanne, Braybrooke Rebecca, Flores Carlos, Fingerlin Tasha E, Oldham Justin M, Guillen-Guio Beatriz, Ma Shwu-Fan, Okamoto Tsukasa, John Alison E, Obeidat Ma'en, Yang Ivana V, Henry Amanda, Hubbard Richard B, Navaratnam Vidya, Saini Gauri, Thompson Norma, Booth Helen L, Hart Simon P, Hill Mike R, Hirani Nik, Maher Toby M, McAnulty Robin J, Millar Ann B, Molyneaux Philip L, Parfrey Helen, Rassl Doris M, Whyte Moira K B, Fahy William A, Marshall Richard P, Oballa Eunice, Bossé Yohan, Nickle David C, Sin Don D, Timens Wim, Shrine Nick, Sayers Ian, Hall Ian P, Noth Imre, Schwartz David A, Tobin Martin D, Wain Louise V, Jenkins R Gis |
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis.
Ophthalmology 2020 May . Meguro Akira, Yamane Takahiro, Takeuchi Masaki, Miyake Masahiro, Fan Qiao, Zhao Wanting, Wang I-Jong, Mizuki Yuki, Yamada Norihiro, Nomura Naoko, Tsujikawa Akitaka, Matsuda Fumihiko, Hosoda Yoshikatsu, Saw Seang-Mei, Cheng Ching-Yu, Tsai Tzu-Hsun, Yoshida Masao, Iijima Yasuhito, Teshigawara Takeshi, Okada Eiichi, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhi |
A deletion mutation within the goat AKAP13 gene is significantly associated with litter size. Animal biotechnology 2021 8 1-7. Zhang Xinwei, Yuan Rongrong, Bai Yangyang, Yang Yuta, Song Xiaoyue, Lan Xianyong, Pan Chuanyi |
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
Evaluation of myopia-associated genes in a Han Chinese population with high myopia. Ophthalmic genetics 2023 5 1-5. Zhenzhen Liu, Guangqi An, Yadan Huo, Youmei Xu, Pengyi Zhou, Kunpeng Xie, Haiyan Zhu, Bo Jin, Liping Du, Xuemin J |
Integrating single-cell analysis and machine learning to create glycosylation-based gene signature for prognostic prediction of uveal melanoma. Frontiers in endocrinology 2023 4 14 1163046. Liu Jianlan, Zhang Pengpeng, Yang Fang, Jiang Keyu, Sun Shiyi, Xia Zhijia, Yao Gang, Tang Ji |
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- Page last updated:Apr 22, 2024
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