Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: PIK3R3[original query] |
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Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer. Cancer research 2010 Mar 70 (6): 2389-96. Koutros Stella, Schumacher Fredrick R, Hayes Richard B, Ma Jing, Huang Wen-Yi, Albanes Demetrius, Canzian Federico, Chanock Stephen J, Crawford E David, Diver W Ryan, Feigelson Heather Spencer, Giovanucci Edward, Haiman Christopher A, Henderson Brian E, Hunter David J, Kaaks Rudolf, Kolonel Laurence N, Kraft Peter, Le Marchand Loïc, Riboli Elio, Siddiq Afshan, Stampfer Mier J, Stram Daniel O, Thomas Gilles, Travis Ruth C, Thun Michael J, Yeager Meredith, Berndt Sonja |
Genetic variants in epidermal growth factor receptor pathway genes and risk of esophageal squamous cell carcinoma and gastric cancer in a Chinese population. PloS one 2013 8 (7): e68999. Li Wen-Qing, Hu Nan, Wang Zhaoming, Yu Kai, Su Hua, Wang Lemin, Wang Chaoyu, Chanock Stephen J, Burdett Laurie, Ding Ti, Qiao You-Lin, Fan Jin-Hu, Wang Yuan, Xu Yi, Giffen Carol, Xiong Xiaoqin, Murphy Gwen, Tucker Margaret A, Dawsey Sanford M, Freedman Neal D, Abnet Christian C, Goldstein Alisa M, Taylor Philip |
Whole genomes redefine the mutational landscape of pancreatic cancer. Nature 2015 Feb 518 (7540): 495-501. Waddell Nicola, Pajic Marina, Patch Ann-Marie, Chang David K, Kassahn Karin S, Bailey Peter, Johns Amber L, Miller David, Nones Katia, Quek Kelly, Quinn Michael C J, Robertson Alan J, Fadlullah Muhammad Z H, Bruxner Tim J C, Christ Angelika N, Harliwong Ivon, Idrisoglu Senel, Manning Suzanne, Nourse Craig, Nourbakhsh Ehsan, Wani Shivangi, Wilson Peter J, Markham Emma, Cloonan Nicole, Anderson Matthew J, Fink J Lynn, Holmes Oliver, Kazakoff Stephen H, Leonard Conrad, Newell Felicity, Poudel Barsha, Song Sarah, Taylor Darrin, Waddell Nick, Wood Scott, Xu Qinying, Wu Jianmin, Pinese Mark, Cowley Mark J, Lee Hong C, Jones Marc D, Nagrial Adnan M, Humphris Jeremy, Chantrill Lorraine A, Chin Venessa, Steinmann Angela M, Mawson Amanda, Humphrey Emily S, Colvin Emily K, Chou Angela, Scarlett Christopher J, Pinho Andreia V, Giry-Laterriere Marc, Rooman Ilse, Samra Jaswinder S, Kench James G, Pettitt Jessica A, Merrett Neil D, Toon Christopher, Epari Krishna, Nguyen Nam Q, Barbour Andrew, Zeps Nikolajs, Jamieson Nigel B, Graham Janet S, Niclou Simone P, Bjerkvig Rolf, Grützmann Robert, Aust Daniela, Hruban Ralph H, Maitra Anirban, Iacobuzio-Donahue Christine A, Wolfgang Christopher L, Morgan Richard A, Lawlor Rita T, Corbo Vincenzo, Bassi Claudio, Falconi Massimo, Zamboni Giuseppe, Tortora Giampaolo, Tempero Margaret A, , Gill Anthony J, Eshleman James R, Pilarsky Christian, Scarpa Aldo, Musgrove Elizabeth A, Pearson John V, Biankin Andrew V, Grimmond Sean |
Rare copy number variants implicated in posterior urethral valves. American journal of medical genetics. Part A 2015 Dec . Boghossian Nansi S, Sicko Robert J, Kay Denise M, Rigler Shannon L, Caggana Michele, Tsai Michael Y, Yeung Edwina H, Pankratz Nathan, Cole Benjamin R, Druschel Charlotte M, Romitti Paul A, Browne Marilyn L, Fan Ruzong, Liu Aiyi, Brody Lawrence C, Mills James |
Atlas of human diseases influenced by genetic variants with extreme allele frequency differences. Human genetics 2016 Oct . Sulovari Arvis, Chen Yolanda H, Hudziak James J, Li Daw |
Screening for susceptibility genes in hereditary non-polyposis colorectal cancer. Oncology letters 2018 Jun 15 (6): 9413-9419. Yu Li, Yin Bo, Qu Kaiying, Li Jingjing, Jin Qiao, Liu Ling, Liu Chunlan, Zhu Yuxing, Wang Qi, Peng Xiaowei, Zhou Jianda, Cao Peiguo, Cao |
Genetic variants in PI3K/Akt/mTOR pathway genes contribute to gastric cancer risk. Gene 2018 May . Ge Yuqiu, Liu Hanting, Qiu Xiaonan, Ma Gaoxiang, Wang Haixiao, Du Mulong, Wang Meilin, Zhao Qinghong, Tao Guoquan, Chu Haiyan, Zhang Zhengdo |
Study on the association between PI3K/AKT/mTOR signaling pathway gene polymorphism and susceptibility to gastric cancer. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 0 22 (6): 1488-1493. Qi Lei, Sun Kewen, Zhuang Yun, Yang Jing, Chen Jianpi |
Screening of Graves' disease susceptibility genes by whole exome sequencing in a three-generation family. BMC medical genomics 2021 Feb 14 (1): 46. Hu Zhuoqing, Li Wei, Li Miaosheng, Wei Hao, Hu Zhihui, Chen Yanting, Luo Ai, Li Wang |
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance. Frontiers in endocrinology 2021 1 11 582516. Li Lele, Gao Fenqi, Fan Lijun, Su Chang, Liang Xuejun, Gong ChunX |
PIK3R3 missense and NOTCH2 synonymous single nucleotide polymorphisms are associated with liver cancer. Digestive diseases (Basel, Switzerland) 2022 12 . Wang Baofeng, Min Weili, Zhang Wenjie, Liu Qiufang, Guo Xufeng, Zhan Jianshui, Lei Ming, Zan Ying, Ma Qingyong, Ma Hongbi |
PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry. Research and practice in thrombosis and haemostasis 2023 8 7 (4): 100175. Kate Burley, Lucy Fitzgibbon, David van Heel, , Dragana Vuckovic, Andrew D Mumford, |
Rare-variant association analysis reveals known and new age-related hearing loss genes. European journal of human genetics : EJHG 2023 2 . Cornejo-Sanchez Diana M, Li Guangyou, Fabiha Tabassum, Wang Ran, Acharya Anushree, Everard Jenna L, Kadlubowska Magda K, Huang Yin, Schrauwen Isabelle, Wang Gao T, DeWan Andrew T, Leal Suzanne |
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- Page last updated:Apr 22, 2024
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