Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: PIK3C3[original query] |
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Identification of PIK3C3 promoter variant associated with bipolar disorder and schizophrenia. Biological psychiatry 2004 May 55 (10): 981-8. Stopkova Pavla, Saito Takuya, Papolos Demitri F, Vevera Jan, Paclt Ivo, Zukov Ilja, Bersson Yonina B, Margolis Benjamin A, Strous Rael D, Lachman Herbert |
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2007 Dec 104 (50): 19942-7. Lencz Todd, Lambert Christophe, DeRosse Pamela, Burdick Katherine E, Morgan T Vance, Kane John M, Kucherlapati Raju, Malhotra Anil |
Replication of a genome-wide case-control study of esophageal squamous cell carcinoma. International journal of cancer. Journal international du cancer 2008 Oct 123 (7): 1610-5. Ng David, Hu Nan, Hu Ying, Wang Chaoyu, Giffen Carol, Tang Ze-Zhong, Han Xiao-You, Yang Howard H, Lee Maxwell P, Goldstein Alisa M, Taylor Philip |
Investigation of variants in the promoter region of PIK3C3 in schizophrenia. Neuroscience letters 2008 May 437 (1): 42-4. Tang Ruqi, Zhao Xinzhi, Fang Chao, Tang Wei, Huang Ke, Wang Lei, Li Huafang, Feng Guoyin, Zhu Shaomin, Liu Huijun, He Lin, Shi Yongyo |
No evidence for excess runs of homozygosity in bipolar disorder. Psychiatric genetics 2009 Aug 19 (4): 165-70. Vine Anna E, McQuillin Andrew, Bass Nicholas J, Pereira Ana, Kandaswamy Radhika, Robinson Michele, Lawrence Jacob, Anjorin Adebayo, Sklar Pamela, Gurling Hugh M D, Curtis Dav |
Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. Journal of biomedicine & biotechnology 2010 2010 826434. Kariuki Silvia N, Franek Beverly S, Mikolaitis Rachel A, Utset Tammy O, Jolly Meenakshi, Skol Andrew D, Niewold Timothy |
Genetic association of the Phosphoinositide-3 kinase in schizophrenia and bipolar disorder and interaction with a BDNF gene polymorphism. Brain and behavior 2011 Nov 1 (2): 119-24. Carrard Anthony, Salzmann Annick, Perroud Nader, Gafner Jérémie, Malafosse Alain, Karege Félici |
Clinical significance of de novo and inherited copy-number variation. Human mutation 2013 Dec 34 (12): 1679-87. Vulto-van Silfhout Anneke T, Hehir-Kwa Jayne Y, van Bon Bregje W M, Schuurs-Hoeijmakers Janneke H M, Meader Stephen, Hellebrekers Claudia J M, Thoonen Ilse J M, de Brouwer Arjan P M, Brunner Han G, Webber Caleb, Pfundt Rolph, de Leeuw Nicole, de Vries Bert B |
Associations of novel variants in PIK3C3, INSR and MAP3K4 of the ATM pathway genes with pancreatic cancer risk. American journal of cancer research 2020 10 (7): 2128-2144. Zhao Ling-Ling, Liu Hong-Liang, Luo Sheng, Walsh Kyle M, Li Wei, Wei Qing |
mTOR pathway gene mutations predict response to immune checkpoint inhibitors in multiple cancers. Journal of translational medicine 2022 6 20 (1): 247. Cheng Lei, Wang Yanan, Qiu Lixin, Chang Yuanyuan, Lu Haijiao, Liu Chenchen, Zhang Bo, Zhou Yan, Bai Hao, Xiong Liwen, Zhong Hua, Nie Wei, Han Baoh |
Novel variants in genes related to vesicle-mediated-transport modify Parkinson's disease risk. Molecular genetics and metabolism 2023 5 139 (2): 107608. Orly Goldstein, Mali Gana-Weisz, Sandro Banfi, Vincenzo Nigro, Anat Bar-Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Roy N Alcalay, Avi Orr-Urtreg |
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- Page last updated:Apr 22, 2024
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