Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: FZD4[original query] |
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A 10-gene expression signature of Notch pathway predicts recurrence in ovarian carcinoma. Oncology letters 2015 Sep 10 (3): 1704-1708. Chen Fang, Liu Nai |
Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy. Scientific reports 2015 5 16120. Fei Ping, Zhu Xiong, Jiang Zhilin, Ma Shi, Li Jing, Zhang Qi, Zhou Yu, Xu Yu, Tai Zhengfu, Zhang Lin, Huang Lulin, Yang Zhenglin, Zhao Peiquan, Zhu Xianj |
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 |
Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study.
Oncology letters 2016 Jan 11 (1): 624-632. Qu Li-Shuai, Jin Fei, Guo Yan-Mei, Liu Tao-Tao, Xue Ru-Yi, Huang Xiao-Wu, Xu Min, Chen Tao-Yang, Ni Zheng-Ping, Shen Xi-Zho |
Risk allele of the FZD4 gene for familial exudative vitreoretinopathy. Ophthalmic genetics 2017 11 39 (3): 405-406. Kondo Hiroyuki, Uchio Eiichi, Kusaka Shunji, Higasa Koichi |
Mutation spectrum of NDP, FZD4 and TSPAN12 genes in Indian patients with retinopathy of prematurity. The British journal of ophthalmology 2017 Oct . Rathi Sonika, Jalali Subhadra, Musada Ganeswara Rao, Patnaik Satish, Balakrishnan Divya, Hussain Anjli, Kaur Inderje |
The characteristics of digenic familial exudative vitreoretinopathy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2018 8 256 (11): 2149-2156. Li Yian, Peng Jie, Li Jiakai, Zhang Qi, Li Jing, Zhang Xiang, Fei Ping, She Kaiqin, Zhao Peiqu |
A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk. Cancer research 2018 Sep 78 (18): 5419-5430. Lu Yingchang, Beeghly-Fadiel Alicia, Wu Lang, Guo Xingyi, Li Bingshan, Schildkraut Joellen M, Im Hae Kyung, Chen Yian A, Permuth Jennifer B, Reid Brett M, Teer Jamie K, Moysich Kirsten B, Andrulis Irene L, Anton-Culver Hoda, Arun Banu K, Bandera Elisa V, Barkardottir Rosa B, Barnes Daniel R, Benitez Javier, Bjorge Line, Brenton James, Butzow Ralf, Caldes Trinidad, Caligo Maria A, Campbell Ian, Chang-Claude Jenny, Claes Kathleen B M, Couch Fergus J, Cramer Daniel W, Daly Mary B, deFazio Anna, Dennis Joe, Diez Orland, Domchek Susan M, Dörk Thilo, Easton Douglas F, Eccles Diana M, Fasching Peter A, Fortner Renée T, Fountzilas George, Friedman Eitan, Ganz Patricia A, Garber Judy, Giles Graham G, Godwin Andrew K, Goldgar David E, Goodman Marc T, Greene Mark H, Gronwald Jacek, Hamann Ute, Heitz Florian, Hildebrandt Michelle A T, Høgdall Claus K, Hollestelle Antoinette, Hulick Peter J, Huntsman David G, Imyanitov Evgeny N, Isaacs Claudine, Jakubowska Anna, James Paul, Karlan Beth Y, Kelemen Linda E, Kiemeney Lambertus A, Kjaer Susanne K, Kwong Ava, Le Nhu D, Leslie Goska, Lesueur Fabienne, Levine Douglas A, Mattiello Amalia, May Taymaa, McGuffog Lesley, McNeish Iain A, Merritt Melissa A, Modugno Francesmary, Montagna Marco, Neuhausen Susan L, Nevanlinna Heli, Nielsen Finn C, Nikitina-Zake Liene, Nussbaum Robert L, Offit Kenneth, Olah Edith, Olopade Olufunmilayo I, Olson Sara H, Olsson Håkan, Osorio Ana, Park Sue K, Parsons Michael T, Peeters Petra H M, Pejovic Tanja, Peterlongo Paolo, Phelan Catherine M, Pujana Miquel Angel, Ramus Susan J, Rennert Gad, Risch Harvey, Rodriguez Gustavo C, Rodríguez-Antona Cristina, Romieu Isabelle, Rookus Matti A, Rossing Mary Anne, Rzepecka Iwona K, Sandler Dale P, Schmutzler Rita K, Setiawan Veronica W, Sharma Priyanka, Sieh Weiva, Simard Jacques, Singer Christian F, Song Honglin, Southey Melissa C, Spurdle Amanda B, Sutphen Rebecca, Swerdlow Anthony J, Teixeira Manuel R, Teo Soo H, Thomassen Mads, Tischkowitz Marc, Toland Amanda E, Trichopoulou Antonia, Tung Nadine, Tworoger Shelley S, van Rensburg Elizabeth J, Vanderstichele Adriaan, Vega Ana, Edwards Digna Velez, Webb Penelope M, Weitzel Jeffrey N, Wentzensen Nicolas, White Emily, Wolk Alicja, Wu Anna H, Yannoukakos Drakoulis, Zorn Kristin K, Gayther Simon A, Antoniou Antonis C, Berchuck Andrew, Goode Ellen L, Chenevix-Trench Georgia, Sellers Thomas A, Pharoah Paul D P, Zheng Wei, Long Jiro |
Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q. European journal of human genetics : EJHG 2018 Apr . Potrony Miriam, Puig-Butille Joan Anton, Farnham James M, Giménez-Xavier Pol, Badenas Celia, Tell-Martí Gemma, Aguilera Paula, Carrera Cristina, Malvehy Josep, Teerlink Craig C, Puig Susa |
Genetic association of single nucleotide polymorphisms of FZD4 and BDNF genes with retinopathy of prematurity. Ophthalmic genetics 2018 Feb 1-6. Lasabova Zora, Stanclova Andrea, Grendar Marian, Mikolajcikova Silvia, Calkovska Andrea, Lenhartova Nina, Ziak Peter, Matasova Katarina, Caprnda Martin, Kruzliak Peter, Zibolen Mir |
Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation. Investigative ophthalmology & visual science 2018 12 59 (15): 5726-5734. Chen Chonglin, Liu Chengxi, Wang Zhirong, Sun Limei, Zhao Xiujuan, Li Songshan, Luo Xiaoling, Zhang Aiyuan, Chong Victor, Lu Lin, Ding Xiaoy |
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 |
Next-Generation Sequencing in the Familial Exudative Vitreoretinopathy-Associated Rhegmatogenous Retinal Detachment. Investigative ophthalmology & visual science 2019 6 60 (7): 2659-2666. Chen Chonglin, Wang Zhirong, Sun Limei, Huang Sijian, Li Songshan, Zhang Aiyuan, Luo Xiaoling, Huang Li, Ding Xiaoy |
Detection of FZD4, LRP5 and TSPAN12 Genes Variants in Malay Premature Babies with Retinopathy of Prematurity. Journal of ophthalmic & vision research 0 14 (2): 171-178. Mohd Khair Siti Zulaikha Nashwa, Ismail Abdul Salim, Embong Zunaina, Mohamed Yusoff Abdul Az |
Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families. Clinical & experimental ophthalmology 2019 11 48 (3): 356-365. Xu Huijuan, Zhang Shanshan, Huang Lulin, Zhao Peiquan, Zhang Xiang, Yang Zhenglin, Zhang L |
Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke. CNS neuroscience & therapeutics 2020 9 27 (1): 71-81. Ta Song, Rong Xianfang, Guo Zhen-Ni, Jin Hang, Zhang Peng, Li Fenge, Li Zhihuan, Lin Lilong, Zheng Chenqing, Gu Qingquan, Zhang Yuan, Liu Wenlan, Yang Yi, Chang Junl |
Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR). Ophthalmic genetics 2020 12 42 (2): 200-203. Carrera William, Ng Caleb, Desler Caroline, Jumper J Michael, Agarwal Ani |
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 |
Novel Frizzled-4 Mutation Is Associated With Familial Exudative Vitreoretinopathy Mimicking Persistent Fetal Vasculature. Journal of pediatric ophthalmology and strabismus 2020 1 57 e4-e7. Staropoli Patrick C, Yannuzzi Nicolas A, Patel Nimesh A, Negron Catherin I, Prakhunhungsit Supalert, Berrocal Audina |
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 |
New insights into genetics underlying of plumage color. Animal genetics 2021 12 53 (1): 80-93. Davoodi P, Ehsani A, Vaez Torshizi R, Masoudi A |
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 |
FZD4 in a Large Chinese Population With Familial Exudative Vitreoretinopathy: Molecular Characteristics and Clinical Manifestations. Investigative ophthalmology & visual science 2022 4 63 (4): 7. Lu Jinglin, Huang Li, Sun Limei, Li Songshan, Zhang Zhaotian, Jiang Zhaoxin, Li Jiaqing, Ding Xiaoy |
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 |
Molecular characterization of early breast cancer onset to understand disease phenotypes in African patients. Medical oncology (Northwood, London, England) 2022 11 40 (1): 13. Tonouo Pamela Derliche, Dina Bell Esther, Tiofack Zebaze Arnol Auvaker, Ndounga Eliane, Noa Ananga Sidonie, Atenguena Etienne, Simo Gustave, Njouendou Abdel Jelil, Lueong Smiths |
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 |
Ocular phenotype and genetical analysis in patients with retinopathy of prematurity. BMC ophthalmology 2022 1 22 (1): 22. Tao Tianchang, Meng Xianfen, Xu Ningda, Li Jiarui, Cheng Yong, Chen Yi, Huang Lvzh |
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 2024 1 22 (1): 75. Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zha |
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- Page last updated:Apr 22, 2024
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