Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: NEDD9[original query] |
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Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Human molecular genetics 2008 Mar 17 (5): 759-67. Li Yonghong, Grupe Andrew, Rowland Charles, Holmans Peter, Segurado Ricardo, Abraham Richard, Jones Lesley, Catanese Joseph, Ross David, Mayo Kevin, Martinez Maribel, Hollingworth Paul, Goate Alison, Cairns Nigel J, Racette Brad A, Perlmutter Joel S, O'Donovan Michael C, Morris John C, Brayne Carol, Rubinsztein David C, Lovestone Simon, Thal Leon J, Owen Michael J, Williams Jul |
Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease. Human molecular genetics 2008 Sep 17 (18): 2863-7. Chapuis Julien, Moisan Frédéric, Mellick Georges, Elbaz Alexis, Silburn Peter, Pasquier Florence, Hannequin Didier, Lendon Corinne, Campion Dominique, Amouyel Philippe, Lambert Jean-Charl |
Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease. Neuroscience letters 2010 Jun 477 (3): 121-3. Tedde Andrea, Bagnoli Silvia, Piaceri Irene, Lucenteforte Ersilia, Bessi Valentina, Bracco Laura, Mugelli Alessandro, Sorbi Sandro, Nacmias Benedet |
Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's disease : JAD 2010 20 (4): 1181-8. Laumet Geoffroy, Chouraki Vincent, Grenier-Boley Benjamin, Legry Vanessa, Heath Simon, Zelenika Diana, Fievet Nathalie, Hannequin Didier, Delepine Marc, Pasquier Florence, Hanon Olivier, Brice Alexis, Epelbaum Jacques, Berr Claudine, Dartigues Jean-Francois, Tzourio Christophe, Campion Dominique, Lathrop Mark, Bertram Lars, Amouyel Philippe, Lambert Jean-Charl |
NEDD9 is genetically associated with Alzheimer's disease in a Han Chinese population. Brain research 2011 Jan 1369 230-4. Xing Yao-Yao, Yu Jin-Tai, Yan Wen-Jing, Chen Wei, Zhong Xiao-Ling, Jiang Hong, Wang Ping, Tan L |
NEDD9 gene polymorphism influences the risk of Alzheimer disease and cognitive function in Chinese older persons. Alzheimer disease and associated disorders 0 26 (1): 88-90. Fu Yan, He Fang, Tang Nelson Leung Sang, Tam Cindy Woon Chi, Lui Victor Wing Cheong, Chiu Helen Fung Kum, Lam Linda Chiu |
Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. PloS one 2011 6 (1): e14562. Li Yan, Fu Li, Wong Alissa Michelle Go, Fan Yan-Hui, Li Miao-Xin, Bei Jin-Xin, Jia Wei-Hua, Zeng Yi-Xin, Chan Danny, Cheung Kenneth M C, Sham Pak, Chua Daniel, Guan Xin-Yuan, Song You-Qia |
NEDD9 rs760678 polymorphism and the risk of Alzheimer's disease: a meta-analysis. Neuroscience letters 2012 Oct 527 (2): 121-5. Wang Yucheng, Bi Liqing, Wang Hui, Li Yanyan, Di Qun, Xu Wei, Qian Y |
Genome-wide association study of primary open angle glaucoma risk and quantitative traits. Molecular vision 2012 18 1083-92. Gibson Jane, Griffiths Helen, De Salvo Gabriella, Cole Mick, Jacob Aby, Macleod Alex, Yang Yit, Menon Geeta, Cree Angela, Ennis Sarah, Lotery Andr |
Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.
Ophthalmic genetics 0 34 (1-2): 35-42. Lin Hui-Ju, Huang Yu-Chuen, Lin Jane-Ming, Liao Wen-Ling, Wu Jer-Yuarn, Chen Chien-Hsiun, Chou Yi-Chun, Chen Liuh-An, Lin Chao-Jen, Tsai Fuu-J |
Gene-based testing of interactions in association studies of quantitative traits. PLoS genetics 2013 9 (2): e1003321. Ma Li, Clark Andrew G, Keinan Al |
Consortium-based genome-wide meta-analysis for childhood dental caries traits.
Human molecular genetics 2018 Jun . Haworth Simon, Shungin Dmitry, van der Tas Justin T, Vucic Strahinja, Medina-Gomez Carolina, Yakimov Victor, Feenstra Bjarke, Shaffer John R, Lee Myoung Keun, Standl Marie, Thiering Elisabeth, Wang Carol, Bønnelykke Klaus, Waage Johannes, Jessen Leon Eyrich, Nørrisgaard Pia Elisabeth, Joro Raimo, Seppälä Ilkka, Raitakari Olli, Dudding Tom, Grgic Olja, Ongkosuwito Edwin, Vierola Anu, Eloranta Aino-Maija, West Nicola X, Thomas Steven J, McNeil Daniel W, Levy Steven M, Slayton Rebecca, Nohr Ellen A, Lehtimäki Terho, Lakka Timo, Bisgaard Hans, Pennell Craig, Kühnisch Jan, Marazita Mary L, Melbye Mads, Geller Frank, Rivadeneira Fernando, Wolvius Eppo B, Franks Paul W, Johansson Ingegerd, Timpson Nicholas |
Loss of LKB1 Protein Expression Correlates with Increased Risk of Recurrence and Death in Patients with Resected, Stage II or III Colon Cancer. Cancer research and treatment 2019 Mar . Sfakianaki Maria, Papadaki Chara, Tzardi Maria, Trypaki Maria, Alam Sardar, Lagoudaki Eleni D, Messaritakis Ippokratis, Zoras Odysseas, Mavroudis Dimitris, Georgoulias Vassilis, Souglakos Jo |
Whole-genome sequencing identifies potential candidate genes for reproductive traits in pigs. Genomics 2019 Jan . Li Xinjian, Ye Jianwei, Han Xuelei, Qiao Ruimin, Li Xiuling, Lv Gang, Wang Kej |
PKM2 Expression as Biomarker for Resistance to Oxaliplatin-Based Chemotherapy in Colorectal Cancer. Cancers 2020 7 12 (8): . Sfakianaki Maria, Papadaki Chara, Tzardi Maria, Trypaki Maria, Manolakou Stavroula, Messaritakis Ippokratis, Saridaki Zenia, Athanasakis Elias, Mavroudis Dimitrios, Tsiaoussis John, Gouvas Nikolaos, Souglakos Jo |
How Cancer Risk SNPs May Contribute to Prostate Cancer Disparities. Cancer research 2021 Jul 81 (14): 3764-3765. Mavura Mnaya Y, Huang Franklin |
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients. Clinical neurology and neurosurgery 2021 Jan 202 106487. Albuz Burcu, Ozdemir Ozturk, Silan Fat |
Genome-wide association studies identified loci associated with both feed conversion ratio and residual feed intake in Yorkshire pigs. Genome 2022 5 65 (7): 405-412. Wang Kai, Wang Shujie, Ji Xiang, Chen Dong, Shen Qi, Yu Yang, Xiao Weihang, Wu Pingxian, Yuan Jun, Gu Yiren, Tang Guoqi |
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- Page last updated:Mar 25, 2024
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