Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: CASZ1[original query] |
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Blood pressure and hypertension are associated with 7 loci in the Japanese population. Circulation 2010 Jun 121 (21): 2302-9. Takeuchi Fumihiko, Isono Masato, Katsuya Tomohiro, Yamamoto Ken, Yokota Mitsuhiro, Sugiyama Takao, Nabika Toru, Fujioka Akihiro, Ohnaka Keizo, Asano Hiroyuki, Yamori Yukio, Yamaguchi Shuhei, Kobayashi Shotai, Takayanagi Ryoichi, Ogihara Toshio, Kato Norihi |
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Human molecular genetics 2015 Feb 24 (3): 865-74. Lu Xiangfeng, Wang Laiyuan, Lin Xu, Huang Jianfeng, Charles Gu C, He Meian, Shen Hongbing, He Jiang, Zhu Jingwen, Li Huaixing, Hixson James E, Wu Tangchun, Dai Juncheng, Lu Ling, Shen Chong, Chen Shufeng, He Lin, Mo Zengnan, Hao Yongchen, Mo Xingbo, Yang Xueli, Li Jianxin, Cao Jie, Chen Jichun, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Lu Fanghong, Yao Cailiang, Yu Lin, Xu Lihua, Mu Jianjun, Wu Xianping, Deng Ying, Hu Dongsheng, Zhang Weidong, Ji Xu, Guo Dongshuang, Guo Zhirong, Zhou Zhengyuan, Yang Zili, Wang Renping, Yang Jun, Zhou Xiaoyang, Yan Weili, Sun Ningling, Gao Pingjin, Gu Dongfe |
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
American journal of human genetics 2014 Jul 95 (1): 24-38. Simino Jeannette, Shi Gang, Bis Joshua C, Chasman Daniel I, Ehret Georg B, Gu Xiangjun, Guo Xiuqing, Hwang Shih-Jen, Sijbrands Eric, Smith Albert V, Verwoert Germaine C, Bragg-Gresham Jennifer L, Cadby Gemma, Chen Peng, Cheng Ching-Yu, Corre Tanguy, de Boer Rudolf A, Goel Anuj, Johnson Toby, Khor Chiea-Chuen, , Lluís-Ganella Carla, Luan Jian'an, Lyytikäinen Leo-Pekka, Nolte Ilja M, Sim Xueling, Sõber Siim, van der Most Peter J, Verweij Niek, Zhao Jing Hua, Amin Najaf, Boerwinkle Eric, Bouchard Claude, Dehghan Abbas, Eiriksdottir Gudny, Elosua Roberto, Franco Oscar H, Gieger Christian, Harris Tamara B, Hercberg Serge, Hofman Albert, James Alan L, Johnson Andrew D, Kähönen Mika, Khaw Kay-Tee, Kutalik Zoltan, Larson Martin G, Launer Lenore J, Li Guo, Liu Jianjun, Liu Kiang, Morrison Alanna C, Navis Gerjan, Ong Rick Twee-Hee, Papanicolau George J, Penninx Brenda W, Psaty Bruce M, Raffel Leslie J, Raitakari Olli T, Rice Kenneth, Rivadeneira Fernando, Rose Lynda M, Sanna Serena, Scott Robert A, Siscovick David S, Stolk Ronald P, Uitterlinden Andre G, Vaidya Dhananjay, van der Klauw Melanie M, Vasan Ramachandran S, Vithana Eranga Nishanthie, Völker Uwe, Völzke Henry, Watkins Hugh, Young Terri L, Aung Tin, Bochud Murielle, Farrall Martin, Hartman Catharina A, Laan Maris, Lakatta Edward G, Lehtimäki Terho, Loos Ruth J F, Lucas Gavin, Meneton Pierre, Palmer Lyle J, Rettig Rainer, Snieder Harold, Tai E Shyong, Teo Yik-Ying, van der Harst Pim, Wareham Nicholas J, Wijmenga Cisca, Wong Tien Yin, Fornage Myriam, Gudnason Vilmundur, Levy Daniel, Palmas Walter, Ridker Paul M, Rotter Jerome I, van Duijn Cornelia M, Witteman Jacqueline C M, Chakravarti Aravinda, Rao Dabeeru |
CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy. Clinical chemistry and laboratory medicine 2017 1 55 (9): 1417-1425. Qiu Xing-Biao, Qu Xin-Kai, Li Ruo-Gu, Liu Hua, Xu Ying-Jia, Zhang Min, Shi Hong-Yu, Hou Xu-Min, Liu Xu, Yuan Fang, Sun Yu-Min, Wang Jun, Huang Ri-Tai, Xue Song, Yang Yi-Qi |
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group.
American journal of hypertension 2019 Sep . Irvin Marguerite R, Sitlani Colleen M, Floyd James S, Psaty Bruce M, Bis Joshua C, Wiggins Kerri L, Whitsel Eric A, Sturmer Til, Stewart James, Raffield Laura, Sun Fangui, Liu Ching-Ti, Xu Hanfei, Cupples Adrienne L, Tanner Rikki M, Rossing Peter, Smith Albert, Zilhão Nuno R, Launer Lenore J, Noordam Raymond, Rotter Jerome I, Yao Jie, Li Xiaohui, Guo Xiuqing, Limdi Nita, Sundaresan Aishwarya, Lange Leslie, Correa Adolfo, Stott David J, Ford Ian, Jukema J Wouter, Gudnason Vilmundur, Mook-Kanamori Dennis O, Trompet Stella, Palmas Walter, Warren Helen R, Hellwege Jacklyn N, Giri Ayush, O'donnell Christopher, Hung Adriana M, Edwards Todd L, Ahluwalia Tarunveer S, Arnett Donna K, Avery Christy |
Varicose veins of lower extremities: Insights from the first large-scale genetic study.
PLoS genetics 2019 Apr 15 (4): e1008110. Shadrina Alexandra S, Sharapov Sodbo Z, Shashkova Tatiana I, Tsepilov Yakov |
Variation at ACOT12 and CT62 locus represents susceptibility to psoriasis in Han population. Molecular genetics & genomic medicine 2019 Dec e1098. Xing Jianxiao, Zhao Xincheng, Li Xiaofang, Wang Ying, Li Junqin, Hou Ruixia, Niu Xuping, Yin Guohua, Li Xinhua, Zhang Kaimi |
A variant of the castor zinc finger 1 (CASZ1) gene is differentially associated with the clinical classification of chronic venous disease. Scientific reports 2019 Sep 9 (1): 14011. Jones Gregory T, Marsman Judith, Pardo Luba M, Nijsten Tamar, De Maeseneer Marianne, Phillips Vicky, Lynch-Sutherland Chi, Horsfield Julia, Krysa Jolanda, van Rij Andre |
CASZ1b is a novel transcriptional corepressor of mineralocorticoid receptor. Hypertension research : official journal of the Japanese Society of Hypertension 2020 10 44 (4): 407-416. Yokota Kenichi, Shibata Hirotaka, Kurihara Isao, Kobayashi Sakiko, Murai-Takeda Ayano, Itoh Hiros |
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders. Nature communications 2020 10 11 (1): 4932. Wang Tianyun, Hoekzema Kendra, Vecchio Davide, Wu Huidan, Sulovari Arvis, Coe Bradley P, Gillentine Madelyn A, Wilfert Amy B, Perez-Jurado Luis A, Kvarnung Malin, Sleyp Yoeri, Earl Rachel K, Rosenfeld Jill A, Geisheker Madeleine R, Han Lin, Du Bing, Barnett Chris, Thompson Elizabeth, Shaw Marie, Carroll Renee, Friend Kathryn, Catford Rachael, Palmer Elizabeth E, Zou Xiaobing, Ou Jianjun, Li Honghui, Guo Hui, Gerdts Jennifer, Avola Emanuela, Calabrese Giuseppe, Elia Maurizio, Greco Donatella, Lindstrand Anna, Nordgren Ann, Anderlid Britt-Marie, Vandeweyer Geert, Van Dijck Anke, Van der Aa Nathalie, McKenna Brooke, Hancarova Miroslava, Bendova Sarka, Havlovicova Marketa, Malerba Giovanni, Bernardina Bernardo Dalla, Muglia Pierandrea, van Haeringen Arie, Hoffer Mariette J V, Franke Barbara, Cappuccio Gerarda, Delatycki Martin, Lockhart Paul J, Manning Melanie A, Liu Pengfei, Scheffer Ingrid E, Brunetti-Pierri Nicola, Rommelse Nanda, Amaral David G, Santen Gijs W E, Trabetti Elisabetta, Sedlá?ek Zden?k, Michaelson Jacob J, Pierce Karen, Courchesne Eric, Kooy R Frank, , Nordenskjöld Magnus, Romano Corrado, Peeters Hilde, Bernier Raphael A, Gecz Jozef, Xia Kun, Eichler Evan |
Association of varicose veins with rare protein-truncating variants in PIEZO1 identified by exome sequencing of a large clinical population. Journal of vascular surgery. Venous and lymphatic disorders 2021 Aug . Smelser Diane T, Haley Jeremy S, Ryer Evan J, Elmore James R, Cook Adam M, Carey David |
Association of CASZ1 genetic variants with stroke risk in the Chinese population. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 5 32 (8): 107169. Fan Zhang, Chuanyi Fu, Yidong Deng, Mao Zhang, Hao Peng, Wenan Li, Jian Zhong, Qing Zhou, Li Huang, Shuli Xiao, Jiannong Zh |
Effects of CASZ1, WNT2B and PTPRG SNPs on stroke susceptibility in the Chinese Han population. European journal of clinical investigation 2023 12 e14144. Huan Zhang, Yanting Chang, Yujie Li, Jie Wei, Xiaoya Ma, Wenqian Zhou, Xufeng Zang, Tianbo Jin, Songdi |
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