Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and KIF11[original query] |
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| Mutation screening of a haplotype block around the insulin degrading enzyme gene and association with Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005 Jul 136B (1): 69-71. Feuk Lars, McCarthy Shane, Andersson Björn, Prince Jonathan A, Brookes Anthony |
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Nature 2007 Feb 445 (7130): 881-5. Sladek Robert, Rocheleau Ghislain, Rung Johan, Dina Christian, Shen Lishuang, Serre David, Boutin Philippe, Vincent Daniel, Belisle Alexandre, Hadjadj Samy, Balkau Beverley, Heude Barbara, Charpentier Guillaume, Hudson Thomas J, Montpetit Alexandre, Pshezhetsky Alexey V, Prentki Marc, Posner Barry I, Balding David J, Meyre David, Polychronakos Constantin, Froguel Philip |
| PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population. PloS one 2009 4 (10): e7643. Hu Cheng, Zhang Rong, Wang Congrong, Wang Jie, Ma Xiaojing, Lu Jingyi, Qin Wen, Hou Xuhong, Wang Chen, Bao Yuqian, Xiang Kunsan, Jia Weipi |
| Association between variants in IDE-KIF11-HHEX and plasma amyloid ß levels. Neurobiology of aging 2012 Jan 33 (1): 199.e13-7. Reitz Christiane, Cheng Rong, Schupf Nicole, Lee Joseph H, Mehta Pankaj D, Rogaeva Ekaterina, St George-Hyslop Peter, Mayeux Richa |
| Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease. Neurobiology of aging 2012 Oct . Bullock JM, Medway C, Cortina-Borja M, Turton JC, Prince JA, Ibrahim-Verbaas CA, Schuur M, Breteler MM, van Duijn CM, Kehoe PG, Barber R, Coto E, Alvarez V, Deloukas P, Hammond N, Combarros O, Mateo I, Warden DR, Lehmann MG, Belbin O, Brown K, Wilcock GK, Heun R, Kölsch H, Smith AD, Lehmann DJ, Morgan K |
| Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis. Scientific reports 2016 6 26564. Li Jia-Kai, Fei Ping, Li Yian, Huang Qiu-Jing, Zhang Qi, Zhang Xiang, Rao Yu-Qing, Li Jing, Zhao Peiqu |
| Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2018 11 59 (13): 5368-5381. Li Jia-Kai, Li Yian, Zhang Xiang, Chen Chun-Li, Rao Yu-Qing, Fei Ping, Zhang Qi, Zhao Peiquan, Li Ji |
| Symmetry of folds in FEVR: A genotype-phenotype correlation study. Experimental eye research 2019 7 186 107720. Wang Zhirong, Chen Chonglin, Sun Limei, Zhang Aiyuan, Liu Chengxi, Huang Li, Ding Xiaoy |
| Novel variants in familial exudative vitreoretinopathy patients with KIF11 mutations and the Genotype-Phenotype correlation. Experimental eye research 2020 7 199 108165. Chen Chonglin, Sun Limei, Li Songshan, Huang Li, Zhang Ting, Wang Zhirong, Yu Bilin, Luo Xiaoling, Ding Xiaoy |
| First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
| Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2020 11 61 (13): 2. Shurygina Maria F, Simonett Joseph M, Parker Maria A, Mitchell Amanda, Grigorian Florin, Lifton Jacob, Nagiel Aaron, Shpak Alexander A, Dadali Elena L, Mishina Irina A, Weleber Richard G, Yang Paul, Pennesi Mark |
| The spectrum of genetic mutations in patients with asymptomatic mild familial exudative vitreoretinopathy. Experimental eye research 2020 1 192 107941. Chen Chonglin, Sun Limei, Li Songshan, Huang Li, Zhang Ting, Wang Zhirong, Yu Bilin, Ding Xiaoy |
| Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11. American journal of ophthalmology 2021 Sep . Yang Junxing, Xiao Xueshan, Li Shiqiang, Mai Guiying, Jia Xiaoyun, Wang Panfeng, Sun Wenmin, Zhang Qingjio |
| Mutation spectrum in a cohort with familial exudative vitreoretinopathy. Molecular genetics & genomic medicine 2022 Jul e2021. Qu Ning, Li Wei, Han Dong-Ming, Gao Jia-Yu, Yang Zheng-Tao, Jiang Li, Liu Tian-Bin, Chen Yan-Xian, Jiang Xiao-Sen, Zhou Liang, Wu Ji-Hong, Huang X |
| Update on the Phenotypic and Genotypic Spectrum of KIF11-Related Retinopathy. Genes 2022 4 13 (4): . Wang You, Zhang Zhaotian, Huang Li, Sun Limei, Li Songshan, Zhang Ting, Ding Xiaoy |
| Rare and Common Variants in KIF15 Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis. American journal of respiratory and critical care medicine 2022 4 206 (1): 56-69. Zhang David, Povysil Gundula, Kobeissy Philippe H, Li Qi, Wang Binhan, Amelotte Mason, Jaouadi Hager, Newton Chad A, Maher Toby M, Molyneaux Philip L, Noth Imre, Martinez Fernando J, Raghu Ganesh, Todd Jamie L, Palmer Scott M, Haefliger Carolina, Platt Adam, Petrovski Slavé, Garcia Joseph A, Goldstein David B, Garcia Christine K |
| Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy. Annals of medicine 2022 11 54 (1): 3286-3298. Mao Jianbo, Chen Yijing, Fang Yuyan, Shao Yirun, Xiang Ziyi, Li Hanxiao, Zhao Shixin, Chen Yiqi, Shen Lij |
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