Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: VANGL1[original query] |
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Novel mutations in VANGL1 in neural tube defects. Human mutation 2009 Mar . Kibar Z, Bosoi CM, Kooistra M, Salem S, Finnell RH, De Marco P, Merello E, Bassuk AG, Capra V, Gros P |
VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish. Mechanisms of development 2010 1 127 (7-8): 385-92. Reynolds Annie, McDearmid Jonathan R, Lachance Stephanie, De Marco Patrizia, Merello Elisa, Capra Valeria, Gros Philippe, Drapeau Pierre, Kibar Zo |
Expanding the mutational spectrum associated to neural tube defects: literature revision and description of novel VANGL1 mutations. Birth defects research. Part A, Clinical and molecular teratology 2015 Jan 103 (1): 51-61. Merello E, Mascelli S, Raso A, Piatelli G, Consales A, Cama A, Kibar Z, Capra V, Marco Patrizia |
Association between VANGL1 gene polymorphisms and neural tube defects. Neuropediatrics 2014 Aug 45 (4): 234-9. Cai Chunquan, Shi Ouyan, Wang Baiqi, Chang Baoxing, Yang Rui, Wang Yinsong, Wang Fang, Shen Changho |
Genomic Characterization of Esophageal Squamous Cell Carcinoma Reveals Critical Genes Underlying Tumorigenesis and Poor Prognosis. American journal of human genetics 2016 Apr 98 (4): 709-27. Qin Hai-De, Liao Xiao-Yu, Chen Yuan-Bin, Huang Shao-Yi, Xue Wen-Qiong, Li Fang-Fang, Ge Xiao-Song, Liu De-Qing, Cai Qiuyin, Long Jirong, Li Xi-Zhao, Hu Ye-Zhu, Zhang Shao-Dan, Zhang Lan-Jun, Lehrman Benjamin, Scott Alan F, Lin Dongxin, Zeng Yi-Xin, Shugart Yin Yao, Jia Wei-H |
Mutation of the Planar Cell Polarity Gene VANGL1 in Adolescent Idiopathic Scoliosis. Spine 2016 Oct . Andersen Malene Rask, Farooq Muhammad, Koefoed Karen, Kjaer Klaus W, Simony Ane, Christensen Sren Tvorup, Larsen Lars All |
VANGL1 Is Not Associated With the Susceptibility of Adolescent Idiopathic Scoliosis in the Chinese Population. Spine 2017 Nov . Xu Leilei, Sheng Fei, Xia Chao, Feng Zhenhua, Qiu Yong, Zhu Zezha |
Digenic variants of planar cell polarity genes in human neural tube defect patients. Molecular genetics and metabolism 2018 3 124 (1): 94-100. Wang Linlin, Xiao Yanhui, Tian Tian, Jin Lei, Lei Yunping, Finnell Richard H, Ren Aig |
Rare copy number variations of planar cell polarity genes are associated with human neural tube defects. Neurogenetics 2020 May . Tian Tian, Lei Yunping, Chen Yongyan, Guo Yinnan, Jin Lei, Finnell Richard H, Wang Linlin, Ren Aig |
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome. BMC musculoskeletal disorders 2020 Apr 21 (1): 220. Li Ziquan, Zhao Sen, Cai Siyi, Zhang Yuanqiang, Wang Lianlei, Niu Yuchen, Li Xiaoxin, Hu Jianhua, Chen Jingdan, Wang Shengru, Wang Huizi, Liu Gang, Tian Ye, Wu Zhihong, Zhang Terry Jianguo, , Wang Yipeng, Wu N |
Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Journal of the American Society of Nephrology : JASN 2021 Feb . Verbitsky Miguel, Krithivasan Priya, Batourina Ekaterina, Khan Atlas, Graham Sarah E, Marasà Maddalena, Kim Hyunwoo, Lim Tze Y, Weng Patricia L, Sánchez-Rodríguez Elena, Mitrotti Adele, Ahram Dina F, Zanoni Francesca, Fasel David A, Westland Rik, Sampson Matthew G, Zhang Jun Y, Bodria Monica, Kil Byum Hee, Shril Shirlee, Gesualdo Loreto, Torri Fabio, Scolari Francesco, Izzi Claudia, van Wijk Joanna A E, Saraga Marijan, Santoro Domenico, Conti Giovanni, Barton David E, Dobson Mark G, Puri Prem, Furth Susan L, Warady Bradley A, Pisani Isabella, Fiaccadori Enrico, Allegri Landino, Degl'Innocenti Maria Ludovica, Piaggio Giorgio, Alam Shumyle, Gigante Maddalena, Zaza Gianluigi, Esposito Pasquale, Lin Fangming, Simões-E-Silva Ana Cristina, Brodkiewicz Andrzej, Drozdz Dorota, Zachwieja Katarzyna, Miklaszewska Monika, Szczepanska Maria, Adamczyk Piotr, Tkaczyk Marcin, Tomczyk Daria, Sikora Przemyslaw, Mizerska-Wasiak Malgorzata, Krzemien Grazyna, Szmigielska Agnieszka, Zaniew Marcin, Lozanovski Vladimir J, Gucev Zoran, Ionita-Laza Iuliana, Stanaway Ian B, Crosslin David R, Wong Craig S, Hildebrandt Friedhelm, Barasch Jonathan, Kenny Eimear E, Loos Ruth J F, Levy Brynn, Ghiggeri Gian Marco, Hakonarson Hakon, Latos-Biele?ska Anna, Materna-Kiryluk Anna, Darlow John M, Tasic Velibor, Willer Cristen, Kiryluk Krzysztof, Sanna-Cherchi Simone, Mendelsohn Cathy L, Gharavi Ali |
Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect. Molecular genetics & genomic medicine 2022 11 11 (1): e2094. Liu Yan, Dong Liang, Zhi Xiufang, Liu Yang, Zhao Linsheng, Xu Xiaowei, Wang Lu, Zheng Jie, Pu Linjie, Gu Chunyu, Shu Jianbo, Cai Chunqu |
Genome-wide association study stratified by MAPT haplotypes identifies potential novel loci in Parkinson's disease. medRxiv : the preprint server for health sciences 2023 6 . Konstantin Senkevich, Sara Bandres-Ciga, Alejandro Cisterna-García, Eric Yu, Bernabe I Bustos, Lynne Krohn, Steven J Lubbe, Juan A Botía, , Ziv Gan- |
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