Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: KIF11[original query] |
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Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies. Diabetes 2007 Dec 56 (12): 3105-11. Grarup Niels, Rose Chrisian S, Andersson Ehm A, Andersen Gitte, Nielsen Arne L, Albrechtsen Anders, Clausen Jesper O, Rasmussen Signe S, Jørgensen Torben, Sandbaek Annelli, Lauritzen Torsten, Schmitz Ole, Hansen Torben, Pedersen Ol |
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 |
Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population. The Journal of clinical endocrinology and metabolism 2008 Jan 93 (1): 310-4. Furukawa Yasushi, Shimada Takeshi, Furuta Hiroto, Matsuno Shohei, Kusuyama Akiko, Doi Asako, Nishi Masahiro, Sasaki Hideyuki, Sanke Tokio, Nanjo Kish |
Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies. Diabetes 2008 Aug 57 (8): 2220-5. Lewis Joshua P, Palmer Nicholette D, Hicks Pamela J, Sale Michele M, Langefeld Carl D, Freedman Barry I, Divers Jasmin, Bowden Donald |
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 |
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
PLoS genetics 2011 Apr 7 (4): e1001363. Sim Xueling, Ong Rick Twee-Hee, Suo Chen, Tay Wan-Ting, Liu Jianjun, Ng Daniel Peng-Keat, Boehnke Michael, Chia Kee-Seng, Wong Tien-Yin, Seielstad Mark, Teo Yik-Ying, Tai E-Shyo |
Genetic variants of IDE-KIF11-HHEX at 10q23.33 associated with type 2 diabetes risk: a fine-mapping study in Chinese population. PloS one 2012 7 (4): e35060. Qian Yun, Lu Feng, Dong Meihua, Lin Yudi, Li Huizhang, Chen Jian, Shen Chong, Jin Guangfu, Hu Zhibin, Shen Hongbi |
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 |
Genetic variants at 10q23.33 are associated with plasma lipid levels in a Chinese population. Journal of biomedical research 2014 Jan 28 (1): 53-8. Liu Sijun, Qian Yun, Lu Feng, Dong Meihua, Lin Yudi, Li Huizhang, Shen Chong, Dai Juncheng, Jiang Yue, Jin Guangfu, Hu Zhibin, Shen Hongbi |
Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy. Genetic testing and molecular biomarkers 2016 May . Zhang Lin, Yang Yeming, Li Shujin, Tai Zhengfu, Huang Lulin, Liu Yuqing, Zhu Xiong, Di Yanan, Qu Chao, Jiang Zhilin, Li Yuanfeng, Zhang Guolin, Kim Ramasamy, Sundaresan Periasamy, Yang Zhenglin, Zhu Xianj |
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 |
CDKAL1 rs7756992 is associated with diabetic retinopathy in a Chinese population with type 2 diabetes. Scientific reports 2017 Aug 7 (1): 8812. Peng Danfeng, Wang Jie, Zhang Rong, Jiang Feng, Tam Claudia H T, Jiang Guozhi, Wang Tao, Chen Miao, Yan Jing, Wang Shiyun, Yan Dandan, He Zhen, Ma Ronald C W, Bao Yuqian, Hu Cheng, Jia Weipi |
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 |
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia. Investigative ophthalmology & visual science 2018 1 59 (1): 338-348. Flitcroft D Ian, Loughman James, Wildsoet Christine F, Williams Cathy, Guggenheim Jeremy A, |
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 |
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing. The Journal of pediatrics 2019 10 215 192-198. Homma Thais Kataoka, Freire Bruna Lucheze, Honjo Kawahira Rachel Sayuri, Dauber Andrew, Funari Mariana Ferreira de Assis, Lerario Antônio Marcondes, Nishi Mirian Yumie, Albuquerque Edoarda Vasco de, Vasques Gabriela de Andrade, Collett-Solberg Paulo Ferrez, Miura Sugayama Sofia Mizuho, Bertola Debora Romeo, Kim Chong Ae, Arnhold Ivo Jorge Prado, Malaquias Alexsandra Christianne, Jorge Alexander Augusto de Li |
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 |
Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2021 12 62 (15): 4. Tao Tianchang, Xu Ningda, Li Jiarui, Li Hongyan, Qu Jinfeng, Yin Hong, Liang Jianhong, Zhao Mingwei, Li Xiaoxin, Huang Lvzh |
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 |
Genotype-phenotype associations in familial exudative vitreoretinopathy: A systematic review and meta-analysis on more than 3200 individuals. PloS one 2022 7 17 (7): e0271326. Wang Xiaona, Chen Jun, Xiong Hui, Yu Xuh |
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 |
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention. Genes 2021 12 13 (1): . Fernàndez-Castillo Noèlia, Cabana-Domínguez Judit, Kappel Djenifer B, Torrico Bàrbara, Weber Heike, Lesch Klaus-Peter, Lao Oscar, Reif Andreas, Cormand B |
Association of HHEX and SLC30A8 Gene Polymorphisms with Gestational Diabetes Mellitus Susceptibility: A Meta-analysis. Biochemical genetics 2023 4 . Wanting Xie, Liuwei Zhang, Jiawei Wang, Yirui Wa |
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- Page last updated:Apr 29, 2024
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