Qi ji Liu

Summary

Affiliation: Shandong University
Country: China

Publications

  1. ncbi 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
  2. ncbi [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
  3. ncbi 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
  4. ncbi 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
  5. ncbi 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
  6. ncbi 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
  7. ncbi [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
  8. ncbi [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
  9. ncbi [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
  10. ncbi [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

Collaborators

  • Yao Qin Gong
  • Hui Wang
  • Li Li
  • Min Zhi Chen
  • Gui min Gao
  • Aihua Wang
  • Fu Zhong Xue
  • Kai Zhang
  • Guang hui CHENG
  • Long Ma
  • Wen Liu
  • Qiurong Fang
  • Ahlem Saadi
  • Xin Ke
  • Hong yu Zhao
  • Fen Liu
  • Li sheng Xu
  • Ming Chun Wen
  • Fang Zheng Dong
  • Ning Bo Tang
  • Jin Xiang Wu
  • Wen Jian Fei
  • Yu Ling Han
  • Meng Meng Yang
  • Ming Jie Ding
  • Jun fei Wang
  • Rong Fang Qiu
  • Li Jun Kang
  • Liang Dong
  • Ji ping Zhao
  • Yue Mei Sun
  • Hailing Zhao
  • Yuan Yuan Wang
  • Zhi Yong Ma
  • Fang Fang Liu
  • Chunhua Wei
  • Huaichen Li
  • Ai ling Dong
  • Xiao Fang Li
  • Pin Wang
  • Dao Xin Ma
  • Ming Hou

Detail Information

Publications14

  1. ncbi 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...
  2. ncbi [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...
  3. ncbi 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...
  4. ncbi 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...
  5. ncbi 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...
  6. ncbi 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...
  7. ncbi [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...
  8. ncbi [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...
  9. ncbi [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...
  10. ncbi [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...
  11. ncbi 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...
  12. ncbi [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)...
  13. ncbi [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...
  14. ncbi [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
    ..CONCLUSION: GPCR2 GPC3, MST4 and GLUD2 were excluded as pathogenic genes for SFMS. The refined SFMS locus will assist in the identification and characterization of other candidate genes for SFMS...