Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Syndrome and AKT1[original query] |
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| Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population. The Journal of clinical psychiatry 2007 Sep 68 (9): 1358-67. Xu Ming-Qing, Xing Qing-He, Zheng Yong-Lan, Li Sheng, Gao Jian-Jun, He Guang, Guo Ting-Wei, Feng Guo-Yin, Xu Feng, He L |
| Lack of association between AKT1 variances versus clinical manifestations and social function in patients with schizophrenia. Journal of psychopharmacology (Oxford, England) 2009 Nov 23 (8): 937-43. Liu Y C, Huang C L, Wu P L, Chang Y C, Huang C H, Lane H |
| Variants of dopamine and serotonin candidate genes as predictors of response to risperidone treatment in first-episode schizophrenia. Pharmacogenomics 2008 Oct 9 (10): 1437-43. Ikeda Masashi, Yamanouchi Yoshio, Kinoshita Yoko, Kitajima Tsuyoshi, Yoshimura Reiji, Hashimoto Shuji, O'Donovan Michael C, Nakamura Jun, Ozaki Norio, Iwata Nak |
| DRD2/AKT1 interaction on D2 c-AMP independent signaling, attentional processing, and response to olanzapine treatment in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2011 Jan 108 (3): 1158-63. Blasi Giuseppe, Napolitano Francesco, Ursini Gianluca, Taurisano Paolo, Romano Raffaella, Caforio Grazia, Fazio Leonardo, Gelao Barbara, Di Giorgio Annabella, Iacovelli Luisa, Sinibaldi Lorenzo, Popolizio Teresa, Usiello Alessandro, Bertolino Alessand |
| AKT1 polymorphisms are associated with risk for metabolic syndrome. Human genetics 2011 Feb 129 (2): 129-39. Devaney Joseph M, Gordish-Dressman Heather, Harmon Brennan T, Bradbury Margaret K, Devaney Stephanie A, Harris Tamara B, Thompson Paul D, Clarkson Priscilla M, Price Thomas B, Angelopoulos Theodore J, Gordon Paul M, Moyna Niall M, Pesca Linda S, VIsich Paul S, Zoeller Robert F, Seip Richard L, Seo Jinwook, Kim Bo Hyoung, Tosi Laura L, Garcia Melissa, Li Rongling, Zmuda Joseph M, Delmonico Matthew J, Lindsay Robert S, Howard Barbara V, Kraus William E, Hoffman Eric |
| A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands. American journal of human genetics 2011 1 88 (1): 42-56. Tan Min-Han, Mester Jessica, Peterson Charissa, Yang Yiran, Chen Jin-Lian, Rybicki Lisa A, Milas Kresimira, Pederson Holly, Remzi Berna, Orloff Mohammed S, Eng Char |
| Germline PIK3CA and AKT1 mutations in Cowden and Cowden-like syndromes. American journal of human genetics 2012 Dec . Orloff MS, He X, Peterson C, Chen F, Chen JL, Mester JL, Eng C |
| A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2013 Sep 169 (3): 277-89. Clayton P, Chatelain P, Tatò L, Yoo H W, Ambler G R, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier |
| Molecular and Clinicopathological Differences by Age at the Diagnosis of Colorectal Cancer. International journal of molecular sciences 2017 Jul 18 (7): . Chang Chu-Cheng, Lin Pei-Ching, Lin Chun-Chi, Lan Yuan-Tzu, Lin Hung-Hsin, Lin Chien-Hsing, Yang Shung-Haur, Liang Wen-Yi, Chen Wei-Shone, Jiang Jeng-Kai, Lin Jen-Kou, Chang Shih-Chi |
| Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos. Gene 2018 Aug . Cid-Soto Miguel A, Martínez-Hernández Angélica, García-Ortíz Humberto, Córdova Emilio J, Barajas-Olmos Francisco, Centeno-Cruz Federico, Contreras-Cubas Cecilia, Mendoza-Caamal Elvia C, Ciceron-Arellano Isabel, Morales-Rivera Monserrat I, Jimenez-Ruiz Juan L, Salas-Martínez Guadalupe, Saldaña-Álvarez Yolanda, Revilla-Monsalve Cristina, Islas-Andrade Sergio, Orozco Lore |
| Clinical and Histologic Overlap and Distinction Among Various Hamartomatous Polyposis Syndromes. Clinical and translational gastroenterology 2019 5 10 (5): 1-9. Gilad Ophir, Rosner Guy, Fliss-Isakov Naomi, Aharon-Kaspi Sivan, Strul Hana, Gluck Nathan, Kariv Revit |
| Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis - A systematic analysis of 204 cases. Scientific reports 2020 Feb 10 (1): 3368. Trautmann Marcel, Rehkämper Jan, Gevensleben Heidrun, Becker Jessica, Wardelmann Eva, Hartmann Wolfgang, Grünewald Inga, Huss Sebasti |
| Association of a genetic variant in AKT1 gene with features of the metabolic syndrome. Genes & diseases 2019 Sep 6 (3): 290-295. Eshaghi Fateme Sadat, Ghazizadeh Hamideh, Kazami-Nooreini Sakine, Timar Ameneh, Esmaeily Habibollah, Mehramiz Mehrane, Avan Amir, Ghayour-Mobarhan Maj |
| Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants. Orphanet journal of rare diseases 2020 Oct 15 (1): 288. Tian Wen, Huang Yingzhao, Sun Liying, Guo Yang, Zhao Sen, Lin Mao, Dong Xiying, Zhong Wenyao, Yin Yuehan, Chen Zefu, Zhang Nan, Zhang Yuanqiang, Wang Lianlei, Lin Jiachen, Yan Zihui, Yang Xinzhuang, Zhao Junhui, Qiu Guixing, Zhang Jianguo, Wu Zhihong, Wu Nan, |
| BRCA1, BRCA2, TP53, PIK3CA, PTEN and AKT1 genes mutations in Burkina Faso breast cancer patients: prevalence, spectrum and novel variant. Molecular genetics and genomics : MGG 2022 6 297 (5): 1257-1268. Ouedraogo Serge Yannick, Zoure Abdou Azaque, Zeye Moutanou Modeste Judes, Kiendrebeogo Touwendpoulimdé Isabelle, Zhou Xi, Sawadogo Alexis Yobi, Simpore Jacques, Chen Hanch |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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