Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: FYN[original query] |
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Tau phosphorylation pathway genes and cerebrospinal fluid tau levels in Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Oct 159B (7): 874-83. Bekris Lynn M, Millard Steve, Lutz Franziska, Li Gail, Galasko Doug R, Farlow Martin R, Quinn Joseph F, Kaye Jeffrey A, Leverenz James B, Tsuang Debby W, Yu Chang-En, Peskind Elaine |
Multilocus analysis of candidate genes involved in neurogenic inflammation in pediatric asthma and related phenotypes: a case-control study. The Journal of asthma : official journal of the Association for the Care of Asthma 2012 May 49 (4): 329-35. Szczepankiewicz Aleksandra, Sobkowiak Paulina, Rachel Marta, Br?borowicz Anna, Schoneich Natalia, Bruce Kimberley, Kycler Zdzis?awa, Wojsyk-Banaszak Irena, Dmitrzak-W?glarz Moni |
Lack of association of the rs2476601 PTPN22 gene polymorphism with transplanted kidney function. Annals of transplantation : quarterly of the Polish Transplantation Society 0 16 (4): 63-8. Doma?ski Leszek, Bobrek-Lesiakowska Katarzyna, K?oda Karolina, Pawlik Andrzej, Safranow Krzysztof, Kurzawski Mateusz, Wi?niewska Magda, Sulikowski Tadeusz, Ciechanowski Kazimie |
Interaction of polymorphisms in mitotic regulator genes with cigarette smoking and pancreatic cancer risk. Molecular carcinogenesis 2013 Nov 52 Suppl 1 E103-9. Jang Ji-Hyun, Cotterchio Michelle, Borgida Ayelet, Liu Geoffrey, Gallinger Steven, Cleary Sean |
Integrative genomics identifies APOE e4 effectors in Alzheimer's disease. Nature 2013 Aug 500 (7460): 45-50. Rhinn Herve, Fujita Ryousuke, Qiang Liang, Cheng Rong, Lee Joseph H, Abeliovich A |
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 |
Genetic variation of FYN contributes to the molecular mechanisms of coping styles in healthy Chinese-Han participants. Psychiatric genetics 2013 Oct 23 (5): 214-6. Zhao Xiaofeng, Li Jingying, Huang Yinglin, Jin Qiu, Ma Hui, Wang Yuan, Wu Lijuan, Li Jun, Zhu Ga |
FYB gene polymorphisms are associated with susceptibility for systemic lupus erythemathosus (SLE). Human immunology 2013 Aug 74 (8): 1009-14. Addobbati Catarina, Brandão Lucas André Cavalcanti, Guimarães Rafael Lima, Pancotto João Alexandre Trés, Donadi Eduardo Antônio, Crovella Sergio, Segat Ludovica, Sandrin-Garcia Pau |
Integrated enrichment analysis of variants and pathways in genome-wide association studies indicates central role for IL-2 signaling genes in type 1 diabetes, and cytokine signaling genes in Crohn's disease. PLoS genetics 2013 9 (10): e1003770. Carbonetto Peter, Stephens Matth |
Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population. Progress in neuro-psychopharmacology & biological psychiatry 2013 Jul 44 226-32. Li Jun, Liu Jing, Zhao Linnan, Ma Yuanlin, Jia Meixiang, Lu Tianlan, Ruan Yanyan, Li Qizhai, Yue Weihua, Zhang Dai, Wang Lifa |
The association of single nucleotide polymorphism of the Fyn gene with sporadic Alzheimer's disease in the Chinese Han population. Neuroscience letters 2014 Jul 575 80-4. Li Jing, Zhou Hua-Dong, Deng Juan, Zhu Jie, Li Lin, Zhang Meng, Zeng Fan, Wang Yan-Jiang, |
Genome-wide association study of proneness to anger.
PloS one 2014 9 (1): e87257. Mick Eric, McGough James, Deutsch Curtis K, Frazier Jean A, Kennedy David, Goldberg Robert |
A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations. Genetic epidemiology 2014 Dec 38 (8): 661-70. Evangelou Marina, Smyth Deborah J, Fortune Mary D, Burren Oliver S, Walker Neil M, Guo Hui, Onengut-Gumuscu Suna, Chen Wei-Min, Concannon Patrick, Rich Stephen S, Todd John A, Wallace Chr |
Role of the Fyn -93A>G polymorphism (rs706895) in acute rejection after liver transplantation. Human immunology 2015 Sep . Thude Hansjörg, Kramer Kathrin, Peine Sven, Sterneck Martina, Nashan Björn, Koch Marti |
Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population. Autism research : official journal of the International Society for Autism Research 2015 Aug . Shen Yidong, Xun Guanglei, Guo Hui, He Yiqun, Ou Jianjun, Dong Huixi, Xia Kun, Zhao Jingpi |
Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III. Genetics and molecular research : GMR 2015 14 (1): 29-33. Addobbati C J C, de Azevêdo Silva J, Tavares N A C, Araújo J, Guimarães R L, Brandão L, Crovella S, Sandrin-Garcia |
Protein Kinase Activity Decreases with Higher Braak Stages of Alzheimer's Disease Pathology. Journal of Alzheimer's disease : JAD 2015 Oct . Rosenberger Andrea F N, Hilhorst Riet, Coart Elisabeth, García Barrado Leandro, Naji Faris, Rozemuller Annemieke J M, van der Flier Wiesje M, Scheltens Philip, Hoozemans Jeroen J M, van der Vies Saskia |
Integrated molecular analysis of adult T cell leukemia/lymphoma. Nature genetics 2015 Oct . Kataoka Keisuke, Nagata Yasunobu, Kitanaka Akira, Shiraishi Yuichi, Shimamura Teppei, Yasunaga Jun-Ichirou, Totoki Yasushi, Chiba Kenichi, Sato-Otsubo Aiko, Nagae Genta, Ishii Ryohei, Muto Satsuki, Kotani Shinichi, Watatani Yosaku, Takeda June, Sanada Masashi, Tanaka Hiroko, Suzuki Hiromichi, Sato Yusuke, Shiozawa Yusuke, Yoshizato Tetsuichi, Yoshida Kenichi, Makishima Hideki, Iwanaga Masako, Ma Guangyong, Nosaka Kisato, Hishizawa Masakatsu, Itonaga Hidehiro, Imaizumi Yoshitaka, Munakata Wataru, Ogasawara Hideaki, Sato Toshitaka, Sasai Ken, Muramoto Kenzo, Penova Marina, Kawaguchi Takahisa, Nakamura Hiromi, Hama Natsuko, Shide Kotaro, Kubuki Yoko, Hidaka Tomonori, Kameda Takuro, Nakamaki Tsuyoshi, Ishiyama Ken, Miyawaki Shuichi, Yoon Sung-Soo, Tobinai Kensei, Miyazaki Yasushi, Takaori-Kondo Akifumi, Matsuda Fumihiko, Takeuchi Kengo, Nureki Osamu, Aburatani Hiroyuki, Watanabe Toshiki, Shibata Tatsuhiro, Matsuoka Masao, Miyano Satoru, Shimoda Kazuya, Ogawa Seis |
Regulatory region genetic variation is associated with FYN expression in Alzheimer's disease. Neurobiology of aging 2016 Nov 51 43-53. Zahratka Jeffrey A, Shao Yvonne, Shaw McKenzie, Todd Kaitlin, Formica Shane V, Khrestian Maria, Montine Thomas, Leverenz James B, Bekris Lynn |
Genetic alterations and their clinical implications in gastric cancer peritoneal carcinomatosis revealed by whole-exome sequencing of malignant ascites. Oncotarget 2016 Jan . Lim Byungho, Kim Chan, Kim Jeong-Hwan, Kwon Woo Sun, Lee Won Seok, Kim Jeong Min, Park Jun Yong, Kim Hyo Song, Park Kyu Hyun, Kim Tae Soo, Park Jong-Lyul, Chung Hyun Cheol, Rha Sun Young, Kim Seon-You |
Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma. Familial cancer 2018 Aug . Donner Iikki, Katainen Riku, Kaasinen Eevi, Aavikko Mervi, Sipilä Lauri J, Pukkala Eero, Aaltonen Lauri |
Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology. Behavior genetics 2018 3 48 (3): 198-208. Curtis David, Coelewij Leda, Liu Shou-Hwa, Humphrey Jack, Mott Richa |
In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia. Psychiatric genetics 2019 1 29 (2): 44-50. Tsavou Antonia, Curtis Dav |
Characterization of genomic alterations in Chinese colorectal cancer patients. Japanese journal of clinical oncology 2020 Oct . Huang Wei, Li Hui, Shi Xiaoliang, Lin Minglin, Liao Cun, Zhang Shuirong, Shi Weiwei, Zhang Lin, Zhang Xiaolong, Gan Jialia |
In silico development and clinical validation of novel 8 gene signature based on lipid metabolism related genes in colon adenocarcinoma. Pharmacological research 2021 5 169 105644. Jiang Chunhui, Liu Ye, Wen Siyuan, Xu Chunjie, Gu L |
Fyn and Lyn gene polymorphisms impact the risk of thyroid cancer. Molecular genetics and genomics : MGG 2022 Sep . Nisar Asif, Kayani Mahmood Akhtar, Nasir Wajiha, Mehmood Azhar, Ahmed Malik Waqar, Parvez Aamir, Mahjabeen Ishr |
Relationship between RELN signaling pathway genes and language development of autism based on a cluster model. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2022 8 47 (7): 858-864. Shen Yidong, Dong Huixi, Zhao Jingping, Xia Kun, Ou Jianj |
Studies on candidate genes for lithium prophylaxis performed at the Poznan University of Medical Sciences. Psychiatria polska 2023 4 56 (5): 1003-1016. Ewa Ferensztajn-Rochowiak, Monika Dmitrzak-W?glarz, Aleksandra Szczepankiewicz, Maria Skibi?ska, Sebastian Kliwicki, Agnieszka Permoda-Pachuta, Aleksandra Suwalska, Piotr Czerski, Joanna Pawlak, Joanna Haus |
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population.
NPJ Parkinson's disease 2023 2 9 (1): 22. Pan Hongxu, Liu Zhenhua, Ma Jinghong, Li Yuanyuan, Zhao Yuwen, Zhou Xiaoxia, Xiang Yaqin, Wang Yige, Zhou Xun, He Runcheng, Xie Yali, Zhou Qiao, Yuan Kai, Xu Qian, Sun Qiying, Wang Junling, Yan Xinxiang, Zhang Hainan, Wang Chunyu, Lei Lifang, Liu Weiguo, Wang Xuejing, Ding Xuebing, Wang Tao, Xue Zheng, Zhang Zhentao, Chen Ling, Wang Qing, Liu Yonghong, Tang Jiayu, Zhang Xuewei, Peng Shifang, Wang Chaodong, Ding Jianqing, Liu Chunfeng, Wang Lijuan, Chen Haibo, Shen Lu, Jiang Hong, Wu Xinyin, Tan Hongzhuan, Luo Dan, Xiao Shuiyuan, Chen Xiang, Tan Jieqiong, Hu Zhengmao, Chen Chao, Xia Kun, Zhang Zhuohua, Foo Jia Nee, Blauwendraat Cornelis, Nalls Mike A, Singleton Andrew B, Liu Jun, Chan Piu, Zheng Houfeng, Li Jinchen, Guo Jifeng, Yang Jian, Tang Beisha, |
Bioinformatic analysis reveals the clinical value of SASH3 in survival prognosis and immune infiltration of acute myelocytic leukemia (AML). American journal of translational research 2024 1 15 (12): 6858-6866. Yufei Li, Lin Wang, Xueyuan Jia, Yanru Yang, Zhengqi Q |
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- Page last updated:Apr 22, 2024
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