Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: VCL[original query] |
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Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. European heart journal 2005 Apr 26 (8): 794-803. Villard Eric, Duboscq-Bidot Laetitia, Charron Philippe, Benaiche Abdelaziz, Conraads Viviane, Sylvius Nicolas, Komajda Mich |
Variants in the Eppin gene show association with semen quality in Han-Chinese population. Reproductive biomedicine online 2010 Jan 20 (1): 125-31. Ding Xinliang, Zhang Jie, Bian Zenghui, Xia Yankai, Lu Chuncheng, Gu Aihua, Li Yingchun, Song Ling, Wang Shoulin, Wang Xin |
Polymorphisms in FGF12, VCL, CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate. BMC medical genetics 2013 14 53. de Aquino Sibele Nascimento, Messetti Ana Camila, Bagordakis Elizabete, Martelli-Júnior Hercílio, Swerts Mario Sergio Oliveira, Graner Edgard, Coletta Ricardo |
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American journal of human genetics 2014 Mar 94 (3): 349-60. Tragante Vinicius, Barnes Michael R, Ganesh Santhi K, Lanktree Matthew B, Guo Wei, Franceschini Nora, Smith Erin N, Johnson Toby, Holmes Michael V, Padmanabhan Sandosh, Karczewski Konrad J, Almoguera Berta, Barnard John, Baumert Jens, Chang Yen-Pei Christy, Elbers Clara C, Farrall Martin, Fischer Mary E, Gaunt Tom R, Gho Johannes M I H, Gieger Christian, Goel Anuj, Gong Yan, Isaacs Aaron, Kleber Marcus E, Mateo Leach Irene, McDonough Caitrin W, Meijs Matthijs F L, Melander Olle, Nelson Christopher P, Nolte Ilja M, Pankratz Nathan, Price Tom S, Shaffer Jonathan, Shah Sonia, Tomaszewski Maciej, van der Most Peter J, Van Iperen Erik P A, Vonk Judith M, Witkowska Kate, Wong Caroline O L, Zhang Li, Beitelshees Amber L, Berenson Gerald S, Bhatt Deepak L, Brown Morris, Burt Amber, Cooper-DeHoff Rhonda M, Connell John M, Cruickshanks Karen J, Curtis Sean P, Davey-Smith George, Delles Christian, Gansevoort Ron T, Guo Xiuqing, Haiqing Shen, Hastie Claire E, Hofker Marten H, Hovingh G Kees, Kim Daniel S, Kirkland Susan A, Klein Barbara E, Klein Ronald, Li Yun R, Maiwald Steffi, Newton-Cheh Christopher, O'Brien Eoin T, Onland-Moret N Charlotte, Palmas Walter, Parsa Afshin, Penninx Brenda W, Pettinger Mary, Vasan Ramachandran S, Ranchalis Jane E, M Ridker Paul, Rose Lynda M, Sever Peter, Shimbo Daichi, Steele Laura, Stolk Ronald P, Thorand Barbara, Trip Mieke D, van Duijn Cornelia M, Verschuren W Monique, Wijmenga Cisca, Wyatt Sharon, Young J Hunter, Zwinderman Aeilko H, Bezzina Connie R, Boerwinkle Eric, Casas Juan P, Caulfield Mark J, Chakravarti Aravinda, Chasman Daniel I, Davidson Karina W, Doevendans Pieter A, Dominiczak Anna F, FitzGerald Garret A, Gums John G, Fornage Myriam, Hakonarson Hakon, Halder Indrani, Hillege Hans L, Illig Thomas, Jarvik Gail P, Johnson Julie A, Kastelein John J P, Koenig Wolfgang, Kumari Meena, März Winfried, Murray Sarah S, O'Connell Jeffery R, Oldehinkel Albertine J, Pankow James S, Rader Daniel J, Redline Susan, Reilly Muredach P, Schadt Eric E, Kottke-Marchant Kandice, Snieder Harold, Snyder Michael, Stanton Alice V, Tobin Martin D, Uitterlinden André G, van der Harst Pim, van der Schouw Yvonne T, Samani Nilesh J, Watkins Hugh, Johnson Andrew D, Reiner Alex P, Zhu Xiaofeng, de Bakker Paul I W, Levy Daniel, Asselbergs Folkert W, Munroe Patricia B, Keating Brendan |
BALL-SNP: combining genetic and structural information to identify candidate non-synonymous single nucleotide polymorphisms. Genome medicine 2015 7 (1): 65. Mueller Sabine C, Backes Christina, Kalinina Olga V, Meder Benjamin, Stöckel Daniel, Lenhof Hans-Peter, Meese Eckart, Keller Andre |
Sex-specific association of rs4746172 of VCL gene with hypertension in two Han populations from Southern China. Scientific reports 2015 5 15245. Yu Qin, Sun Hong-Peng, Chen Wan-Qun, Chen Xiao-Qiong, Xu Yong, He Yong-Han, Kong Qing-Pe |
Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy. International journal of molecular medicine 2015 Oct . Zhao Yue, Feng Yue, Zhang Yun-Mei, Ding Xiao-Xue, Song Yu-Zhu, Zhang A-Mei, Liu Li, Zhang Hong, Ding Jia-Huan, Xia Xue-Sh |
[Association study between candidate genes involved in cell-cell adhesion and non-syndromic cleft lip with or without cleft palate in Chinese population]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2016 Jun 48 (3): 403-8. Yuan Y, Wang P, Wu-Chou Y H, Ye X Q, Huang S Z, Shi B, Wang K, Wang Z Q, Liu D J, Wang Z F, Wu T, Wang |
Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy. PloS one 2017 8 12 (8): e0182946. Mendes de Almeida Rita, Tavares Joana, Martins Sandra, Carvalho Teresa, Enguita Francisco J, Brito Dulce, Carmo-Fonseca Maria, Lopes Luís Roc |
An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population. Journal of the American Heart Association 2017 Apr 6 (4): . Cheng Jianding, Kyle John W, Lang Di, Wiedmeyer Brandi, Guo Jian, Yin Kun, Huang Lei, Vaidyanathan Ravi, Su Terry, Makielski Jonathan |
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
Targeted next-generation sequencing revealed distinct clinicopathologic and molecular features of VCL-ALK RCC: A unique case from an older patient without clinical evidence of sickle cell trait. Pathology, research and practice 2019 9 215 (11): 152651. Wang Xiao-Tong, Fang Ru, Ye Sheng-Bing, Zhang Ru-Song, Li Rui, Wang Xuan, Ji Rong-Hao, Lu Zhen-Feng, Ma Heng-Hui, Zhou Xiao-Jun, Xia Qiu-Yuan, Rao Q |
Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population. Clinical oral investigations 2020 Jul . Machado Renato Assis, de Oliveira Silva Carolina, Martelli-Junior Hercílio, das Neves Lucimara Teixeira, Coletta Ricardo |
Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation.
Circulation. Genomic and precision medicine 2021 11 14 (6): e003460. Yang Yunju, Bartz Traci M, Brown Michael R, Guo Xiuqing, Zilhão Nuno R, Trompet Stella, Weiss Stefan, Yao Jie, Brody Jennifer A, Defilippi Christopher R, Hoogeveen Ron C, Lin Henry J, Gudnason Vilmundur, Ballantyne Christie M, Dörr Marcus, Jukema J Wouter, Petersmann Astrid, Psaty Bruce M, Rotter Jerome I, Boerwinkle Eric, Fornage Myriam, Jun Goo, Yu Bi |
Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study. Annals of translational medicine 2022 3 10 (3): 129. Shen Cheng, Xu Lei, Sun Xiaoning, Sun Aijun, Ge Jun |
Polymorphisms of acetaldehyde dehydrogenase 2 and alcohol dehydrogenase 1B on the malignant transformation of vocal cord leukoplakia: A Chinese cohort. Molecular carcinogenesis 2022 1 61 (5): 472-480. Han Ping, Li Yixin, Liang Faya, Ye Yuchu, Wang Jingyi, Li Xiaojuan, Ouyang Nengtai, Huang Xiaomi |
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
Human molecular genetics 2022 1 31 (13): 2279-2293. Choquet Hélène, Li Weiyu, Yin Jie, Bradley Rachael, Hoffmann Thomas J, Nandakumar Priyanka, , Mostaedi Rouzbeh, Tian Chao, Ahituv Nadav, Jorgenson Er |
[No Effect of the p.Arg230His Variant Of The VCL Protein on the Course of the Hypertrophic Cardiomyopathy In Russian Family Carrying The p.Gln1233Ter Pathogenic Variant In The MYBPC3 Gene]. Kardiologiia 2023 4 63 (3): 28-35. Filatova E V, Krylova N S, Klass A L, Kovalevskaya E A, Maslova M Yu, Shadrina M I, Poteshkina N G, Slominsky P |
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