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Neurobiol Aging, 2014, 35(7):1781.e1-8. |
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PRPF4 mutations cause autosomal dominant retinitis pigmentosa |
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A1180V of Cardiac Sodium Channel Gene (SCN5A): Is It a Risk Factor for Dilated Cardiomyopathy or Just a Common Variant in Han Chinese? |
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HLA-DQA1基因拷贝数目多态性与中国汉族人群类风湿关节炎易感性的研究 |
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Interleukin 10 rs1800872 T>G Polymorphism was Associated with an Increased Risk of Esophageal Cancer in a Chinese Population |
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Asian Pac J Cancer Prev, 2013, 14(6):3443-7. |
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Interleukin 17A rs4711998 A>G polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population |
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Interleukin 1B rs16944 G > A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population |
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Lack of association between COMT Val158Met polymorphism and late-onset Alzheimer’s disease in Han Chinese |
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NLRP3 polymorphisms are associated with late-onset Alzheimer's disease in Han Chinese |
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J Neuroimmunol, 2013, 265(1-2):91-5. |
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SIRT2 polymorphism rs10410544 is associated with Alzheimer's disease in a Han Chinese population |
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J Neurol Sci, 2014, 336(1-2):48-51. |
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The relationship between single nucleotide polymorphisms of the NTRK2 gene and sporadic Alzheimer’s disease in the Chinese Han population |
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TMEM106B and APOE polymorphisms interact to confer risk for late-onset Alzheimer’s disease in Han Chinese |
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J Neural Transm, 2014, 121(3):283-7. |
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Toll-like receptor 9 promoter polymorphism is associated with decreased risk of Alzheimer’s disease in Han Chinese |
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J Neuroinflammation, 2013, 10(1):101. |
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Association of TOMM40 Polymorphisms with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population |
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Neuromolecular Med, 2013, 15(2):279-87. |
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Clinical Significance of MYT1L Gene Polymorphisms in Chinese Patients with Gastric Cancer |
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Silencing of DLGAP5 by siRNA Significantly Inhibits the Proliferation and Invasion of Hepatocellular Carcinoma Cells |
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Detecting Genetic Association of Common Human Facial Morphological Variation Using High Density 3D Image Registration |
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A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese |
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Hum Mol Genet, 2013, 22(9):1886-94. |
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Characterization of large deletions in the F8 gene using multiple competitive amplification and genome walking technique |
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Impacts and interactions of PDGFRB, MMP-3, TIMP-2, and RNF213 polymorphisms on the risk of Moyamoya disease in Han Chinese human subjects |
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Polymorphism rs7214723 in CAMKK1 and lung cancer risk in Chinese population |
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SLC26A4 gene polymorphism and late-onset Alzheimer’s disease in a Han Chinese population from Qingdao, China |
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The -144C/A Polymorphism in the Promoter of HSP90beta Is Associated with Multiple Organ Dysfunction Scores |
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Association and Cumulative Effects of GWAS-Identified Genetic Variants for Nonsyndromic Orofacial Clefts in a Chinese Population |
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Environ Mol Mutagen, 2013, 54(4):261-7. |
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An Association Study on ADAM10 Promoter Polymorphisms and Atherosclerotic Cerebral Infarction in a Chinese Population |
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The CRHR1 Gene Contributes to Genetic Susceptibility of Aggressive Behavior Towards Others in Chinese Southwest Han Population |
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Evaluation of Five Candidate Genes from GWAS for Association with Oligozoospermia in a Han Chinese Population |
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Impact of endothelial nitric oxide synthase gene polymorphism on severity of enterovirus 71-infection in Chinese children |
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The effect of functional MAPKAPK2 copy number variation CNV-30450 on elevating nasopharyngeal carcinoma risk is modulated by EBV infection |
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Missense variants in CR1 are associated with increased risk of Alzheimer’ disease in Han Chinese |
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Combined Erlotinib and Cetuximab overcome the acquired resistance to epidermal growth factor receptors tyrosine kinase inhibitor in non-small-cell lung cancer |
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J Cancer Res Clin Oncol, 2012, 138(12):2069-77. |
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孤独症的临床特征及相关拷贝数变异的研究 |
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广西壮族女性碱性成纤维生长因子基因单核苷酸多态性与骨质疏松 |
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A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections |
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Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees |
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Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease |
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J Thromb Haemost, 2012, 10(8):1508-14. |
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Physical activity modifies the association between CYBA gene polymorphisms and small artery elasticity in a Chinese population |
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Hypertens Res, 2012, 35(7):739-44. |
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Replication of the MTHFD1 L Gene Association with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population |
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J Alzheimers Dis, 2012, 29(3):521-5. |
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染色体15q11.2和15q13.3区域的微缺失与中国儿童失神癫痫的相关性 |
张平平等 |
实用儿科临床杂志,2012,27(7):522-525 |
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Thirteen Chinese patients with sporadic Paget’s disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis |
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J Bone Miner Metab, 2012, 30(5):525-33. |
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Clinical Significance of SOD2 and GSTP1 Gene Polymorphisms in Chinese Patients With Gastric Cancer |
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A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer |
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Am J Hum Genet, 2012, 91(2):384-90. |
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Association of Fcγ receptor IIB polymorphism with cryptococcal meningitis in HIV-uninfected Chinese patients |
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PLoS One, 2012, 7(8):e42439. |
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A miRNA Binding Site Single-Nucleotide Polymorphism in the 39-UTR Region of the IL23R Gene Is Associated with Breast Cancer |
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PLoS One, 2012, 7(12):e49823. |
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B-cell Lymphoma 2 rs17757541 C>G Polymorphism was Associated with an Increased Risk of Gastric Cardiac Adenocarcinoma in a Chinese Population |
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Asian Pac J Cancer Prev, 2013, 14(7):4301-6. |
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广西百色地区壮族妇女脂联素基因单核苷酸多态性与骨密度的关系 |
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解剖学报,2012,43(1):109-113 |
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FTO基因单核苷酸多态性与中国汉族儿童/青少年肥胖的关联性研究 |
许玉洋等 |
浙江大学硕士学位论文 |
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Catechol-O-methyltransferase polymorphisms do not play a significant role in pain perception in male Chinese Han population |
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Physiol Genomics, 2012, 44(5):318-28. |
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Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population |
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Clin Rheumatol, 2012, 31(10):1449-54. |
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Genetic variations in T-cell activation and effector pathways modulate alloimmune responses after allogeneic hematopoietic stem cell transplantation in patients with hematologic malignancies |
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Haematologica, 2012, 97(12):1804-12. |
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Association Analysis of IL-17A and IL-17F Polymorphisms in Chinese Han Women with Breast Cancer |
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The FCGR2B rs10917661 polymorphism may confer susceptibility to ankylosing spondylitis in Han Chinese: a case-control study |
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Scand J Rheumatol, 2012, 41(3):219-22. |
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人类 Y 染色体 36 个新 STR 位点的筛选与鉴定 |
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遗传,2012, 34(11):1409-1416 |
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人类细胞系基因表达中校正因子的选择 |
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国际遗传学杂志, 2012,35(5):262-267. |
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广西百色地区壮族男性人群骨密度与脂联素基因单核苷酸多态性的关系 |
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Immunosuppressive cytokine gene polymorphisms and outcome after related and unrelated hematopoietic cell transplantation in Chinese population |
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Biol Blood Marrow Transplant, 2011, 17(4):542-9. |
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Two novel mutations in the Spastin gene of Chinese patients with hereditary spastic paraplegia |
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Eur J Neurol, 2011, 18(9):1194-6. |
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人染色体 8p11(CHRNB3-CHRNA6)区域基因多态性与中国汉族人群肺癌易感性的相关性 |
张晓博等 |
遗传, 2011,33(8):886-894. |
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新疆维吾尔族健康人中 Tim-3基因结构分析 |
王燕等 |
山东大学学报, 2011,49(2):88-92. |
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非小细胞肺癌中EGFR和K-ras基因突变与蛋白表达相关性的研究 |
栾焕玲等 |
中国癌症杂志, 2010, 20(7):486-491. |
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The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A |
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Haemophilia, 2010, 16(4):632-9. |
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VANGL2 Mutations in Human Cranial Neural-Tube Defects |
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N Engl J Med, 2010, 362(23):2232-5. |
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Association study between C7673T polymorphism in apolipoprotein B gene and cerebral infarction with family history in a Chinese population |
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Neurol India, 2009, 57(5):584-8. |
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Haemophilia A in two unrelated females due to F8 gene inversions combined with skewed inactivation of X chromosome |
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Thromb Haemost, 2009, 101(4):775-8. |
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载脂蛋白B基因C7673T多态与有家族聚集现象脑出血的关系 |
张乐等 |
中华医学遗传学杂志, 2008,25(2):145-149 |
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