Qi ji Liu

Summary

Affiliation: Shandong University
Country: China

Publications

  1. doi request reprint [Clinical and genetic analysis of a Chinese family affected with X-linked Charcot-Marie-Tooth disease]
    Yapei Feng
    Key Laboratory for Experimental Teratology of Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:659-61. 2013
  2. doi request reprint [Association of two SNPs in 3'UTR of ETS1 gene with systemic lupus erythematosus in a northern Chinese Han population]
    Xiao Fan Guo
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:477-80. 2013
  3. ncbi request reprint Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia
    Yapei Feng
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, PR China
    Singapore Med J 54:251-4. 2013
  4. doi request reprint [Analysis of gene mutation in a family featuring autosomal dominant May-Hegglin anomaly]
    Yapei Feng
    Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:305-8. 2013
  5. pmc Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study
    Ahlem Saadi
    Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong, PR China
    BMC Med Genet 10:71. 2009
  6. pmc A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population
    Qiji Liu
    Department of Medical Genetics and Key Laboratory for Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, Jinan, Shandong 250012, PR China
    BMC Med Genet 10:59. 2009
  7. ncbi request reprint [Characterization of genomic structure and mutation analysis of SMARCA1 gene in a Smith-Fineman-Myers syndrome family]
    Qi ji Liu
    Institute of Medical Genetics, School of Medicine, Shandong University, Jinan 250012, China
    Yi Chuan Xue Bao 31:114-8. 2004
  8. pmc Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population
    Qiurong Fang
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, PR China
    BMC Med Genet 12:133. 2011
  9. ncbi request reprint Association of common polymorphisms in the LRP6 gene with sporadic coronary artery disease in a Chinese population
    Hui Wang
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, China
    Chin Med J (Engl) 125:444-9. 2012
  10. doi request reprint Two single nucleotide polymorphisms in ALOX15 are associated with risk of coronary artery disease in a Chinese Han population
    Kai Zhang
    Chinese Ministry of Education and Chinese Ministry of Public Health, Jinan, Shandong, China
    Heart Vessels 25:368-73. 2010

Collaborators

  • Hui Wang
  • Li Li
  • Long Ma
  • Yao Qin Gong
  • Gui min Gao
  • Min Zhi Chen
  • Jiangxia Li
  • Yu Xia
  • Xiao Li
  • Fu Zhong Xue
  • Ming Chun Wen
  • Aihua Wang
  • Yapei Feng
  • Xin Ke
  • Kai Zhang
  • Xiao Fan Guo
  • Xue Wang
  • Qian Xin
  • Rong Fang Qiu
  • Wen Liu
  • Qiurong Fang
  • Guang hui CHENG
  • Ahlem Saadi
  • Hong yu Zhao
  • Yong chao Liu
  • Zhonglu Liu
  • Kun Kun Wei
  • Wen Na Li
  • Nora Lee
  • Shan Shan
  • Xiaoyan Zhu
  • Shan Qiao
  • Xiaofan Guo
  • Tao Han
  • Meng Zhai
  • Zhao Fu Chi
  • Hai Ling Zhao
  • Guilong Wang
  • Jie Dang
  • Xue Wu Liu
  • Yu Ling Han
  • Li sheng Xu
  • Meng Meng Yang
  • Ming Jie Ding
  • Jin Xiang Wu
  • Jun fei Wang
  • Yue Mei Sun
  • Fang Zheng Dong
  • Li Jun Kang
  • Fen Liu
  • Ning Bo Tang
  • Liang Dong
  • Wen Jian Fei
  • Ji ping Zhao
  • Hailing Zhao
  • Zhi Yong Ma
  • Yuan Yuan Wang
  • Fang Fang Liu
  • Ai ling Dong
  • Huaichen Li
  • Chunhua Wei
  • Ming Hou
  • Pin Wang
  • Dao Xin Ma

Detail Information

Publications20

  1. doi request reprint [Clinical and genetic analysis of a Chinese family affected with X-linked Charcot-Marie-Tooth disease]
    Yapei Feng
    Key Laboratory for Experimental Teratology of Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:659-61. 2013
    ..To study the clinical manifestations and identify causative mutations for a Chinese family affected with X-linked Charcot-Marie-Tooth disease...
  2. doi request reprint [Association of two SNPs in 3'UTR of ETS1 gene with systemic lupus erythematosus in a northern Chinese Han population]
    Xiao Fan Guo
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:477-80. 2013
    ..To assess the association between 2 single nucleotide polymorphisms (SNPs) of ETS1 gene and susceptibility to systemic lupus erythematosus (SLE) in a northern Chinese Han population...
  3. ncbi request reprint Novel deletion of SPAST in a Chinese family with hereditary spastic paraplegia
    Yapei Feng
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, PR China
    Singapore Med J 54:251-4. 2013
    ..Classical genetic studies have identified at least 46 genetic loci responsible for HSP...
  4. doi request reprint [Analysis of gene mutation in a family featuring autosomal dominant May-Hegglin anomaly]
    Yapei Feng
    Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 30:305-8. 2013
    ..To analyze clinical features and mutation in MYH9 gene for a family featuring autosomal dominant May-Hegglin anomaly...
  5. pmc Association study between vitamin D receptor gene polymorphisms and asthma in the Chinese Han population: a case-control study
    Ahlem Saadi
    Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong, PR China
    BMC Med Genet 10:71. 2009
    ..Importantly, variants in the VDR gene have been susceptible in the past to raise the risk of asthma in several populations. These effects of VDR allelic markers remain speculative in the Chinese Han population...
  6. pmc A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population
    Qiji Liu
    Department of Medical Genetics and Key Laboratory for Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, Jinan, Shandong 250012, PR China
    BMC Med Genet 10:59. 2009
    ..In order to determine the role of the SPINK5 in the development of asthma, a case-control study including 669 asthma patients and 711 healthy controls in Han Chinese was conducted...
  7. ncbi request reprint [Characterization of genomic structure and mutation analysis of SMARCA1 gene in a Smith-Fineman-Myers syndrome family]
    Qi ji Liu
    Institute of Medical Genetics, School of Medicine, Shandong University, Jinan 250012, China
    Yi Chuan Xue Bao 31:114-8. 2004
    ..The disease in SFMS family from Shandong is not caused by the mutation within open reading frame of SMARCA1 gene...
  8. pmc Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population
    Qiurong Fang
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, PR China
    BMC Med Genet 12:133. 2011
    ..In this study, we aimed to evaluate the association of polymorphisms in ORMDL3, GSDMB, ZPBP2 and IKZF3 and adult-onset asthma in a Chinese Han population...
  9. ncbi request reprint Association of common polymorphisms in the LRP6 gene with sporadic coronary artery disease in a Chinese population
    Hui Wang
    Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong 250012, China
    Chin Med J (Engl) 125:444-9. 2012
    ..The aim of this study was to determine whether the common variants in LRP6 are associated with sporadic CAD in Chinese...
  10. doi request reprint Two single nucleotide polymorphisms in ALOX15 are associated with risk of coronary artery disease in a Chinese Han population
    Kai Zhang
    Chinese Ministry of Education and Chinese Ministry of Public Health, Jinan, Shandong, China
    Heart Vessels 25:368-73. 2010
    ..136-11.006, P = 0.029). In summary, the present study shows that after adjustment for other confounding CAD factors, rs7217186:T>C and rs2619112:G>A of ALOX15 are associated with increased risk of CAD in this Chinese Han population...
  11. ncbi request reprint [Fine mapping of Smith-Fineman-Myers syndrome and exclusion of GPC3, GPCR2 MST4 and GLUD2 as candidate genes]
    Qi ji Liu
    Institute of Medical Genetics, School of Medicine, Shandong University, Jinan, Shandong, 250012 PR China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 21:198-202. 2004
    ....
  12. ncbi request reprint [Application of homozygosity mapping to the fine mapping of the osteoporosis-pseudoglioma syndrome locus]
    Yao Qin Gong
    Department of Medical Genetics, Medical School of Shandong University, Jinan, PR China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 20:53-5. 2003
    ..To evaluate the role of homozygosity mapping in the fine mapping of the genes responsible for the rare autosomal recessive diseases...
  13. doi request reprint [Association of the ABCG1 gene polymorphism with the susceptibility and severity of coronary atherosclerotic disease]
    Long Ma
    Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27:506-11. 2010
    ..To investigate the association of the ATP-binding cassette sub-family G member 1 (ABCG1) gene polymorphisms with coronary atherosclerotic disease (CAD) in Chinese Han population...
  14. ncbi request reprint [Association study between TNFSF4 and coronary heart disease]
    Min Zhi Chen
    Institute of Medical Genetics, School of Medicine, Shandong University, Jinan 250012, China
    Yi Chuan 33:239-45. 2011
    ..0173)). In principal component score-based logistic regression analysis, the first principal component has statistical significance (P=0.0236). These results indicate that TNFSF4 is a susceptibility gene of CHD in Chinese Han population...
  15. ncbi request reprint [Polymorphic loci and polymorphism analysis of short tandem repeats within XNP gene]
    Qi ji Liu
    Dept of Medical Genetics, Medical School, Shandong University, Jinan 250012, China
    Yi Chuan Xue Bao 29:201-5. 2002
    ..XNPSTR1 and XNPSTR4 localized within 3' end and intron 10, respectively. Two polymorphic short tandem repeats have been identified within XNP gene and will be useful for linkage analysis and gene diagnosis of XNP gene...
  16. doi request reprint Two single nucleotide polymorphisms in TSLP gene are associated with asthma susceptibility in Chinese Han population
    Wen Liu
    Department of Pulmonary Medicine, Qilu Hospital of Shandong University, Jinan, Shandong, China
    Exp Lung Res 38:375-82. 2012
    ..We sought to determine whether single nucleotide polymorphisms (SNPs) in TSLP gene are associated with asthma in Chinese Han population...
  17. doi request reprint [Association of rs2298212 polymorphism in OX40 gene with coronary atherosclerotic disease in Chinese Han population]
    Guang hui CHENG
    Institute of Medical Genetics and Key Laboratory for Experimental Teratology of the Ministry of Education, School of Medicine, Shandong University, Jinan, Shandong, P R China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27:171-5. 2010
    ..To study the association of the OX40 gene rs2298212G/A polymorphism with coronary atherosclerotic disease (CAD) in Chinese Han population...
  18. ncbi request reprint Features of a Chinese family with cerebral cavernous malformation induced by a novel CCM1 gene mutation
    Xue Wang
    Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250012, China
    Chin Med J (Engl) 126:3427-32. 2013
    ..We report a Chinese family with CCMs and intend to explore clinical, pathological, magnetic resonance imaging (MRI) features and pathogenic gene mutation of this family...
  19. ncbi request reprint [N-ras and fms gene mutation in idiopathic thrombocytopenic purpura and myelodysplasia]
    Hong yu Zhao
    Department of Hematology, Qilu Hospital, Shandong University, Jinan 250012, China
    Zhonghua Xue Ye Xue Za Zhi 29:158-60. 2008
    ..To explore the pathogenesis of idiopathic thrombocytopenic purpura (ITP) and improve the differential diagnosis from myelodysplastic syndromes (MDS)...
  20. doi request reprint [Clinical investigation of a family with brachydactyly type A1 and the identification of the disease gene]
    Xin Ke
    Department of Orthopedics, Weihai Economic and Technological Development Zone Hospital of Shandong Province, and Institute of Medical Genetics, Shandong University, Shandong, 264205 PR China
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 26:267-71. 2009
    ..To determine the inheritance mode and pathogenesis of a family with brachydactyly type A1 in Jining, Shandong province via clinical feature and disease gene analysis...