Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: COL9A1[original query] |
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Identification of a novel common genetic risk factor for lumbar disk disease. JAMA 2001 Apr 285 (14): 1843-9. Paassilta P, Lohiniva J, Göring H H, Perälä M, Räinä S S, Karppinen J, Hakala M, Palm T, Kröger H, Kaitila I, Vanharanta H, Ott J, Ala-Kokko |
Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutations. European journal of human genetics : EJHG 2005 Mar 13 (3): 292-301. Jakkula Eveliina, Mäkitie Outi, Czarny-Ratajczak Malwina, Czarny-Ratacjzak Malwina, Jackson Gail C, Damignani Rita, Susic Miki, Briggs Michael D, Cole William G, Ala-Kokko Lee |
The role of sequence variations within the genes encoding collagen II, IX and XI in non-syndromic, early-onset osteoarthritis. Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2005 Jun 13 (6): 497-507. Jakkula E, Melkoniemi M, Kiviranta I, Lohiniva J, Räinä S S, Perälä M, Warman M L, Ahonen K, Kröger H, Göring H H H, Ala-Kokko |
Evidence for a role of the genomic region of the gene encoding for the alpha1 chain of type IX collagen (COL9A1) in hip osteoarthritis: A population-based study. Arthritis and rheumatism 2005 May 52 (5): 1437-42. Alizadeh B Z, Njajou O T, Bijkerk C, Meulenbelt I, Wildt S C De, Hofman A, Pols H A P, Slagboom P E, Duijn C M V |
[Analysis of association between COL9A1 gene and idiopathic congenital talipes equinovarus]. Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2007 Apr 29 (4): 427-32. Liu Li-Ying, Jin Chun-Lian, Cao Dong-Hua, Zhao Ning, Lin Chang-Kun, Sun Kai-L |
Associations of 25 structural, degradative, and inflammatory candidate genes with lumbar disc desiccation, bulging, and height narrowing. Arthritis and rheumatism 2009 Feb 60 (2): 470-81. Videman Tapio, Saarela Janna, Kaprio Jaakko, Näkki Annu, Levälahti Esko, Gill Kevin, Peltonen Leena, Battié Michele |
[Expression of COL9A1 gene and its polymorphism in children with idiopathic congenital talipes equinovarus]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2011 Jun 13 (6): 478-81. Liu Li-Ying, Jin Chun-Lian, Jiang Li, Lin Chang-K |
Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes. American journal of medical genetics. Part A 2011 Nov 155A (11): 2669-80. Kim Ok-Hwa, Park Hyunwoong, Seong Moon-Woo, Cho Tae-Joon, Nishimura Gen, Superti-Furga Andrea, Unger Sheila, Ikegawa Shiro, Choi In Ho, Song Hae-Ryong, Kim Hyun Woo, Yoo Won Joon, Shim Jong Sup, Chung Chin Youb, Oh Chang-Wug, Jeong Changhoon, Song Kwang Soon, Seo Sang Gyo, Cho Sung Im, Yeo Im Kyung, Kim So Yeon, Park Seungman, Park Sung S |
COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population. PloS one 2015 10 (3): e0120365. Shi Xiaowei, Zhang Feng, Lv Aili, Wen Yan, Guo Xio |
Role of COL9A1 genetic polymorphisms in development of congenital talipes equinovarus in a Chinese population. Genetics and molecular research : GMR 2016 Nov 15 (4): . Zhao X L, Wang Y J, Wu Y L, Han W |
Combined Genetic Biomarkers and Betel Quid Chewing for Identifying High-Risk Group for Oral Cancer Occurrence. Cancer prevention research (Philadelphia, Pa.) 2017 Jun 10 (6): 355-362. Chung Chia-Min, Lee Chien-Hung, Chen Mu-Kuan, Lee Ka-Wo, Lan Cheng-Che E, Kwan Aij-Lie, Tsai Ming-Hsui, Ko Ying-Ch |
Whole-genome sequencing reveals novel genes in ossification of the posterior longitudinal ligament of the thoracic spine in the Chinese population. Journal of orthopaedic surgery and research 2018 Dec 13 (1): 324. Liang Chen, Wang Peng, Liu Xiao, Yang Chenlong, Ma Yunlong, Yong Lei, Zhu Bin, Liu Xiaoguang, Liu Zhongj |
Exome sequencing reveals a novel COL2A1 mutation implicated in multiple epiphyseal dysplasia. American journal of medical genetics. Part A 2019 2 179 (4): 534-541. Dasa Vinod, Eastwood James R B, Podgorski Michal, Park Heewon, Blackstock Christopher, Antoshchenko Tetyana, Rogala Piotr, Bieganski Tadeusz, Jazwinski S Michal, Czarny-Ratajczak Malwi |
Relationship of COL9A1 and SOX9 Genes with Genetic Susceptibility of Postmenopausal Osteoporosis. Calcified tissue international 2019 Nov . Liu Hongliang, Zhao Hongmou, Lin Hua, Li Zhong, Xue Hanzhong, Zhang Yunzhi, Lu J |
Variants in FAT1 and COL9A1 genes in male population with or without substance use to assess the risk factors for oral malignancy. PloS one 2019 14 (1): e0210901. Chung Chia-Min, Hung Chung-Chieh, Lee Chien-Hung, Lee Chi-Pin, Lee Ka-Wo, Chen Mu-Kuan, Yeh Kun-Tu, Ko Ying-Ch |
Gene Environment Interactions Between the COL9A1 Gene and Maternal Drinking of Alcohol Contribute to the Risk of Congenital Talipes Equinovarus. Genetic testing and molecular biomarkers 2020 12 25 (1): 48-54. Zhao Jianwu, Cai Fei, Liu Peng, Wei Jianjiang, Chen Qia |
Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone. Clinica chimica acta; international journal of clinical chemistry 2021 11 524 1-10. He Dongye, Li Yanying, Yang Wanling, Chen Shuxiong, Sun Hailing, Li Ping, Zhang Mei, Ban |
Next-generation sequencing-based mutational analysis of idiopathic short stature and isolated growth hormone deficiency in Korean pediatric patients. Molecular and cellular endocrinology 2021 10 544 111489. Ahn Jungmin, Oh Jiyoung, Suh Junghwan, Song Kyungchul, Kwon Ahreum, Chae Hyun Wook, Oh Jun Suk, Lee Hae In, Lee Myeong Seob, Kim Ho-Seo |
Clinical Characteristics of Short-Stature Patients With Collagen Gene Mutation and the Therapeutic Response to rhGH. Frontiers in endocrinology 2022 3 13 820001. Chen Meiping, Miao Hui, Liang Hanting, Ke Xiaoan, Yang Hongbo, Gong Fengying, Wang Linjie, Duan Lian, Chen Shi, Pan Hui, Zhu Huiju |
Assessment of the COL9A1 Single Nucleotide Polymorphism with Severity of clubfoot in a paediatric population along with their biological mothers. Journal of clinical orthopaedics and trauma 2022 11 35 102064. Raikwar Archana, Singh Ajai, Mahdi Abbas Ali, Yadav Mani |
Mutation survey in Taiwanese patients with Stickler syndrome. Taiwan journal of ophthalmology 2023 1 12 (4): 423-429. Huang Faye, Wang Tzu-Jou, Cho Wan-Hua, Chen Yi-Hao, Wu Pei-Chang, Kuo Hsi-Ku |
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- Page last updated:Jun 03, 2024
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