上海天昊生物客户发表论文汇总

Mutations in epigenetic regulators are involved in acute lymphoblastic leukemia relapse following allogeneic hematopoietic stem cell transplantation.
Xiao H,et al.
Oncotarget. 2016 Jan 19; 7(3): 2696–2708.
 
 
The complete chloroplast genome sequence of Dioscorea zingiberensis (Dioscoreceae).
Zhou W,et al.
Mitochondrial DNA A DNA MappSeq Anal. 2016 Jul;27(4):2730-1.
 
 
The complete chloroplast genome sequence of medicinal plant Pinellia ternata.
Han L,et al.
Mitochondrial DNA A DNA MappSeq Anal. 2016 Jul;27(4):2921-2.
 
 
Association between WT1 polymorphisms and susceptibility to breast cancer: results from a case-control studyin a southwestern Chinese population.
Qi XW,et al.
Am J Cancer Res. 2015 Feb 15;5(3):1234-50.
 
 
Shared and discrepant susceptibility for carotid artery and aortic arch calcification: A genetic association study.
Zhang Y,et al.
Atherosclerosis. 2015 Aug;241(2):371-5.
 
 
Assessment of functional tag single nucleotide polymorphisms within the DRD2 gene as risk factors for post-traumatic stress disorder in the Han Chinese population.
Duan Z,et al.
J Affect Disord. 2015 Dec 1;188:210-7.
 
 
Association Study of IL-12B Polymorphisms Susceptibility with Ankylosing Spondylitis in Mainland Han Population.
Zhang L,et al.
PLoS One. 2015 Jun 23;10(6):e0130982.
 
 
Analysis of single nucleotide polymorphisms within ADAM12 and risk of knee osteoarthritis in a Chinese Han population.
Wang L,et al.
Biomed Res Int. 2015;2015:518643.
 
 
First Analysis of the Association Between CYP3A4/5, ABCB1 Genetic Polymorphisms and Oxcarbazepine Metabolism and Transport in Chinese Epileptic Patients with Oxcarbazepine Monotherapy and Bitherapy.
Wang P,et al.
J Pharm Pharm Sci. 2015;18(3):256-65.
 
 
Effects of CYP3A4/5 and ABCB1 genetic polymorphisms on carbamazepine metabolism and transport in Chinese patients with epilepsy treated with carbamazepine in monotherapy and bitherapy.
Wang P,et al.
Epilepsy Res. 2015 Nov;117:52-7.
 
 
Association of polymorphisms in the MAFB gene and the risk of coronary artery disease and ischemic stroke: a case-control study.
Yang Q,et al.
Lipids Health Dis. 2015 Jul 25;14:79.
 
 
An ADAM10 promoter polymorphism is a functional variant in severe sepsis patients and confers susceptibility to the development of sepsis.
Cui L,et al.
Crit Care. 2015 Mar 5;19:73.
 
 
Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations.
Jin G,et al.
Am J Hum Genet. 2015 May 7;96(5):832-40.
 
 
Epstein-Barr virus-induced gene 3 (EBI3) polymorphisms and expression are associated with susceptibility to pulmonary tuberculosis.
Zheng R,et al.
Tuberculosis (Edinb). 2015 Jul;95(4):497-504.
 
 
Affection of single-nucleotide polymorphisms in miR-27a, miR-124a, and miR-146a on susceptibility to type 2 diabetes mellitus in Chinese Han people.
Wang TT,et al.
Chin Med J (Engl). 2015 Feb 20;128(4):533-9.
 
 
Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis.
Zhang B,et al.
Int J Mol Sci. 2015 May 26;16(6):11864-72.
 
 
Association between UBE2E2 variant rs7612463 and type 2 diabetes mellitus in a Chinese Han Population.
Kazakova EV,et al.
Acta Biochim Pol. 2015;62(2):241-5.
 
 
Interleukin 12B rs3212227 T > G polymorphism was associated with an increased risk of gastric cardiac adenocarcinoma in a Chinese population.
Yin J,et al.
Dis Esophagus. 2015 Apr;28(3):291-8.
 
 
Association between polymorphisms of interleukin 12 and rheumatoid arthritis associated biomarkers in a Chinese population.
Shen L,et al.
Cytokine. 2015 Dec;76(2):363-7.
 
 
A genome-wide association study of mitochondrial DNA in Chinese men identifies two risk single nucleotide substitutions for idiopathic oligoasthenospermia.
Lu C,et al.
Mitochondrion. 2015 Sep;24:87-92.
 
 
IL1B gene polymorphisms, age and the risk of non-small cell lung cancer in a Chinese population.
Li Y,et al.
Lung Cancer. 2015 Sep;89(3):232-7.
 
 
SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.
Li H,et al.
Genomics. 2015 Aug;106(2):83-7.
 
 
Association of DRD3, COMT, and SLC6A4 Gene Polymorphisms with Type 2 Diabetes in Southern Chinese: A Hospital-Based Case–Control Study.
Xiu L,et al.
Diabetes Technol Ther. 2015 Aug;17(8):580-6.
 
 
Variant TP53BP1 rs560191 G>C is associated with risk of gastric cardia adenocarcinoma in a Chinese Han population.
Zhang S,et al.
Chin J Cancer Res. 2015 Apr;27(2):156-62.
 
 
Association of the VRK2 gene rs3732136 polymorphism with schizophrenia in a Northwest Chinese Han population.
Zhang B,et al.
Genet Mol Res. 2015 Aug 14;14(3):9404-11.
 
 
Genetic Variations of IL17F and IL23A Show Associations with Behçet’s Disease and Vogt-Koyanagi-Harada Syndrome.
Hou S,et al.
Ophthalmology. 2015 Mar;122(3):518-23.
 
 
Up-regulation of long noncoding RNA MALAT1 contributes to proliferation and metastasis in esophageal squamous cell carcinoma.
Hu L,et al.
J Exp Clin Cancer Res. 2015 Jan 22;34:7.
 
 
UAssociation of Tag SNPs and Rare CNVs of the MIR155HG/miR-155 Gene with Epilepsy in the Chinese Han Population.
Tao H,et al.
Biomed Res Int. 2015;2015:837213.
 
 
Interactions between Obesity-Related Copy Number Variants and Dietary Behaviors in Childhood Obesity.
Zhang D,et al.
Nutrients. 2015 Apr 22;7(4):3054-66.
 
 
Association between DEFB103 gene copy number variation and ankylosing spondylitis: a case-control study.
Cai G,et al.
Tissue Antigens. 2015 Sep;86(3):195-8.
 
 
A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Zhang X,et al.
BMC Genomics. 2015 May 8;16:364.
 
 
     
 
Mitochondrial DNA haplogroups and short-term neurological outcomes of ischemic stroke.
Cai B,et al.
SCIENTIFIC REPORTS. 2015 May;5:9864.
 
 
Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes.
Xu F,et al.
Nat Commun. 2015 Nov 26;6:8806.
 
 
Epigenetic deregulated miR-375 contributes to the constitutive activation of JAK2/STAT signaling in myeloproliferative neoplasm.
Yin LH,et al.
Leuk Res. 2015 Apr;39(4):471-8.
 
 
Genomic variations of the mevalonate pathway in porokeratosis.
Zhang Z,et al.
Elife. 2015 Jul 23;4:e06322.
 
 
Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC).
Guo S,et al.
Clin Epigenetics. 2015 Jan 22;7(1):3.
 
 
Correlation of PCSK9 gene polymorphism with cerebral ischemic stroke in Xinjiang Han and Uygur populations
Han D,et al.
Med Sci Monit. 2014 Sep 30;20:1758-67. doi:10.12659/MSM.892091.
 
 
A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss
Du W, et al.
Genomics. 2014 Aug 19. pii: S0888-7543(14)00124-4.
 
 
Genetic variation in BIN1 gene and Alzheimer’s disease risk in Han Chinese individuals
Tan MS, et al.
Neurobiol Aging, 2014, 35(7):1781.e1-8.
 
 
PRPF4 mutations cause autosomal dominant retinitis pigmentosa
Chen X, et al.
Hum Mol Genet, 2014, 23(11):2926-39.
 
 
Clinical relevance of tag single nucleotide polymorphisms within the CAT gene in patients with PTSD in the Chongqing Han population
Duan ZX, et al.
Int J Clin Exp Pathol, 2014, 7(4):1724-32.
 
 
The axis inhibition protein 2 polymorphisms and non-syndromic orofacial clefts susceptibility in a Chinese Han population
Han Y, et al.
J Oral Pathol Med, 2014, 43(7):554-60.
 
 
Gene copy number alterations in the azoospermia-associated AZFc region and their effect on spermatogenic impairment
Lu C, et al.
Mol Hum Reprod, 2014 online.
 
 
Impacts of COX-1 gene polymorphisms on vascular outcomes in atients with ischemic stroke and treated with aspirin
Cao L, et al.
Gene, 2014, 546(2):172-6.
 
 
Pathogenic variants screening in five non-obstructive azoospermiaassociated genes
Lu C, et al.
Mol Hum Reprod, 2014, 20(2):178-83.
 
 
Single nucleotide polymorphisms of the interleukin-33 (IL-33) gene are associated with ankylosing spondylitis in Chinese individuals: a case–control pilot study
Fan D, et al.
Scand J Rheumatol, 2014, 14:1-22.
 
 
Lack of Association Between TESPA1 Gene Polymorphisms (rs1801876, rs2171497, rs4758994, and rs997173) and Ankylosing Spondylitis in a Chinese Population
Liu S, et al.
Inflammation, 2014 online.
 
 
Association between Copy Number Variations HLA-DQA1 and Ankylosing Spondylitis in Chinese Han population
Wang J, et al.
Genes Immun, 2013, 14(8):500-3.
 
 
A1180V of Cardiac Sodium Channel Gene (SCN5A): Is It a Risk Factor for Dilated Cardiomyopathy or Just a Common Variant in Han Chinese?
Shen C, et al.
Dis Markers, 2013, 35(5):531-5.
 
 
ADAM33 polymorphisms are associated with asthma and a distinctive palm dermatoglyphic pattern
Xue W, et al.
Mol Med Rep, 2013, 8(6):1795-800.
 
 
Association between microRNA polymorphisms and humoral immunity to hepatitis B vaccine
Xiong Y, et al.
Hum Vaccin Immunother, 2013, 9(8):1673-8.
 
 
Association of GWAS-linked loci with late-onset Alzheimer’s disease in a northern Han Chinese population
Tan L, et al.
Alzheimers Dement, 2013, 9(5):546-53.
 
 
Haplotype analysis of eight genes of the monoubiquitinated FANCD2–DNA damage–repair pathway in breast cancer patients
Tang LL, et al.
Cancer Epidemiol, 2013, 37(3):311-7.
 
 
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
陈洁君等
风湿病与关节炎,2013,(08):7-10.
 
 
Interleukin 10 rs1800872 T>G Polymorphism was Associated with an Increased Risk of Esophageal Cancer in a Chinese Population
Sun JM, et al.
Asian Pac J Cancer Prev, 2013, 14(6):3443-7.
 
 
Interleukin 17A rs4711998 A>G polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
Yin J, et al.
Dis Esophagus, 2014, 27(1):87-92.
 
 
Interleukin 1B rs16944 G > A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
Zheng L, et al.
"Clin Biochem, 2013, 46(15):1469-73.
 
 
Lack of association between COMT Val158Met polymorphism and late-onset Alzheimer’s disease in Han Chinese
Zhou J, et al.
Neurosci Lett, 2013, 554:162-6.
 
 
NLRP3 polymorphisms are associated with late-onset Alzheimer's disease in Han Chinese
Tan MS, et al.
J Neuroimmunol, 2013, 265(1-2):91-5.
 
 
SIRT2 polymorphism rs10410544 is associated with Alzheimer's disease in a Han Chinese population
Xia M, et al.
J Neurol Sci, 2014, 336(1-2):48-51.
 
 
The relationship between single nucleotide polymorphisms of the NTRK2 gene and sporadic Alzheimer’s disease in the Chinese Han population
Zeng F, et al.
Neurosci Lett, 2013, 550:55-9.
 
 
TMEM106B and APOE polymorphisms interact to confer risk for late-onset Alzheimer’s disease in Han Chinese
Lu RC, et al.
J Neural Transm, 2014, 121(3):283-7.
 
 
Toll-like receptor 9 promoter polymorphism is associated with decreased risk of Alzheimer’s disease in Han Chinese
Wang YL, et al.
J Neuroinflammation, 2013, 10(1):101.
 
 
Association of TOMM40 Polymorphisms with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population
Ma XY, et al.
Neuromolecular Med, 2013, 15(2):279-87.
 
 
Clinical Significance of MYT1L Gene Polymorphisms in Chinese Patients with Gastric Cancer
Zhang Y, et al.
PLoS One, 2013, 8(8):e71979.
 
 
Silencing of DLGAP5 by siRNA Significantly Inhibits the Proliferation and Invasion of Hepatocellular Carcinoma Cells
Liao W, et al.
PLoS One, 2013, 8(12):e80789.
 
 
Detecting Genetic Association of Common Human Facial Morphological Variation Using High Density 3D Image Registration
Peng S, et al.
PLoS Comput Biol, 2013, 9(12):e1003375.
 
 
Genetic variation in Clusterin gene and Alzheimer’s disease risk in Han Chinese
Yu JT, et al.
Neurobiol Aging, 2013, 34(7):1921.e17-23.
 
 
Lack of Association between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and Autism Spectrum Disorder in a Chinese Population
Liu Y, et al.
PLoS One, 2013, 8(2):e56639.
 
 
分子人类学中的单核苷酸突变检测方法的研究进展
胡抗等
生命科学, 2013, 25(1):119-125
 
 
A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese
Yang L, et al.
Hum Mol Genet, 2013, 22(9):1886-94.
 
 
Characterization of large deletions in the F8 gene using multiple competitive amplification and genome walking technique
You GL, et al.
J Thromb Haemost, 2013, 11(6):1103-10.
 
 
Impacts and interactions of PDGFRB, MMP-3, TIMP-2, and RNF213 polymorphisms on the risk of Moyamoya disease in Han Chinese human subjects
Wang X, et al.
Gene, 2013, 526(2):437-42.
 
 
MiR-196a2 rs11614913 T > C polymorphism and risk of esophageal cancer in a Chinese population
Wei J, et al.
Hum Immunol, 2013, 74(9):1199-205.
 
 
Polymorphism rs7214723 in CAMKK1 and lung cancer risk in Chinese population
Zhang YH, et al.
Tumour Biol, 2013, 34(5):3147-52.
 
 
SLC26A4 gene polymorphism and late-onset Alzheimer’s disease in a Han Chinese population from Qingdao, China
Jifang Zhang, et al.
Neural regeneration research,2013,8(8):754-759.
 
 
The -144C/A Polymorphism in the Promoter of HSP90beta Is Associated with Multiple Organ Dysfunction Scores
Zhao Y, et al.
PLoS One, 2013, 8(3):e58646.
 
 
No association of SORT1 gene polymorphism with sporadic Alzheimer’s disease in the Chinese Han population
Zeng F, et al.
Neuroreport, 2013, 24(9):464-8.
 
 
Association and Cumulative Effects of GWAS-Identified Genetic Variants for Nonsyndromic Orofacial Clefts in a Chinese Population
Pan Y, et al.
Environ Mol Mutagen, 2013, 54(4):261-7.
 
 
An Association Study on ADAM10 Promoter Polymorphisms and Atherosclerotic Cerebral Infarction in a Chinese Population
Li Y, et al.
CNS Neurosci Ther, 2013, 19(10):785-94.
 
 
The CRHR1 Gene Contributes to Genetic Susceptibility of Aggressive Behavior Towards Others in Chinese Southwest Han Population
Chen B, et al.
J Mol Neurosci, 2014, 52(4):481-6.
 
 
Evaluation of Five Candidate Genes from GWAS for Association with Oligozoospermia in a Han Chinese Population
Xu M, et al.
PLoS One, 2013, 8(11):e80374.
 
 
Impact of endothelial nitric oxide synthase gene polymorphism on severity of enterovirus 71-infection in Chinese children
Li JA, et al.
Clin Biochem, 2013, 46(18):1842-7.
 
 
The effect of functional MAPKAPK2 copy number variation CNV-30450 on elevating nasopharyngeal carcinoma risk is modulated by EBV infection
Yang L, et al.
Carcinogenesis, 2014, 35(1):46-52.
 
 
Missense variants in CR1 are associated with increased risk of Alzheimer’ disease in Han Chinese
Ma XY, et al.
Neurobiol Aging, 2014, 35(2):443.e17-21.
 
 
Genetic variation in PICALM and Alzheimer’s disease risk in Han Chinese
Jiang T, et al.
Neurobiol Aging, 2014, 35(4):934.e1-3.
 
 
Molecular defects identified by whole exome sequencing in a child with Fanconi anemia
Zheng Z, et al.
Gene, 2013, 530(2):295-300.
 
 
Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy
Zhang Z, et al.
Am J Hum Genet, 2012, 90(1):125-32.
 
 
Combined Erlotinib and Cetuximab overcome the acquired resistance to epidermal growth factor receptors tyrosine kinase inhibitor in non-small-cell lung cancer
Wang M, et al.
J Cancer Res Clin Oncol, 2012, 138(12):2069-77.
 
 
孤独症的临床特征及相关拷贝数变异的研究
张颖等
复旦大学硕士学位论文
 
 
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
林朝文等
中国组织工程研究, 2012, 16(50):9443-9447.
 
 
A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections
Xu X, et al.
BMC Med Genet, 2012, 13:75.
 
 
Absence of gene mutations in KIT-positive carcinoma showing thymus-like elements of the thyroid
Pan Y, et al.
Hum Pathol, 2012, 43(3):350-5.
 
 
BAT3 基因多态性与汉族人群肺癌易感性的相关性 ［BAT3 gene polymorphisms and susceptibility to lung cancer in Han Chinese］
王彬等
现代人类学通讯,6(28):165-173
 
 
Characterisation and validation of a novel panel of the six short tandem repeats for genetic counselling in Chinese haemophilia A pedigrees
Ding QL, et al.
Haemophilia, 2012, 18(4):621-5.
 
 
Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease
Chen X, et al.
J Thromb Haemost, 2012, 10(8):1508-14.
 
 
Physical activity modifies the association between CYBA gene polymorphisms and small artery elasticity in a Chinese population
Zhu Z, et al.
Hypertens Res, 2012, 35(7):739-44.
 
 
Replication of the MTHFD1 L Gene Association with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population
Ma XY, et al.
J Alzheimers Dis, 2012, 29(3):521-5.
 
 
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
 
 
Thirteen Chinese patients with sporadic Paget’s disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis
Gu JM, et al.
J Bone Miner Metab, 2012, 30(5):525-33.
 
 
Clinical Significance of SOD2 and GSTP1 Gene Polymorphisms in Chinese Patients With Gastric Cancer
Xu Z, et al.
Cancer, 2012, 118(22):5489-96.
 
 
A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer
Liu B, et al.
Am J Hum Genet, 2012, 91(2):384-90.
 
 
Association of Fcγ receptor IIB polymorphism with cryptococcal meningitis in HIV-uninfected Chinese patients
Hu XP, et al.
PLoS One, 2012, 7(8):e42439.
 
 
A miRNA Binding Site Single-Nucleotide Polymorphism in the 39-UTR Region of the IL23R Gene Is Associated with Breast Cancer
Wang L, et al.
PLoS One, 2012, 7(12):e49823.
 
 
B-cell Lymphoma 2 rs17757541 C>G Polymorphism was Associated with an Increased Risk of Gastric Cardiac Adenocarcinoma in a Chinese Population
Li Q, et al.
Asian Pac J Cancer Prev, 2013, 14(7):4301-6.
 
 
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
王金花等
解剖学报,2012,43(1):109-113
 
 
SORCS1 and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in a Northern Han Chinese population
Wang HF, et al.
Brain Res, 2012, 1448:111-6.
 
 
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
 
 
Catechol-O-methyltransferase polymorphisms do not play a significant role in pain perception in male Chinese Han population
Xiang X, et al.
Physiol Genomics, 2012, 44(5):318-28.
 
 
HLA-B*58:01 allele is associated with augmented risk for both mild and severe cutaneous adverse reactions induced by allopurinol in Han Chinese
Cao ZH, et al.
Pharmacogenomics, 2012, 13(10):1193-201.
 
 
Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population
Zeng Z, et al.
Clin Rheumatol, 2012, 31(10):1449-54.
 
 
Genetic variations in T-cell activation and effector pathways modulate alloimmune responses after allogeneic hematopoietic stem cell transplantation in patients with hematologic malignancies
Xiao H, et al.
Haematologica, 2012, 97(12):1804-12.
 
 
Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification
Du R, et al.
J Hum Genet, 2012, 57(8):545-51.
 
 
Genetic Association of SLC2A14 Polymorphism with Alzheimer’s Disease in a Han Chinese Population
Wang W, et al.
J Mol Neurosci, 2012, 47(3):481-4.
 
 
Association Analysis of IL-17A and IL-17F Polymorphisms in Chinese Han Women with Breast Cancer
Wang L, et al.
PLoS One, 2012, 7(3):e34400.
 
 
The FCGR2B rs10917661 polymorphism may confer susceptibility to ankylosing spondylitis in Han Chinese: a case-control study
Duan ZH, et al.
Scand J Rheumatol, 2012, 41(3):219-22.
 
 
Genetically elevated levels of circulating triglycerides and brachial-ankle pulse wave velocity in a Chinese population
Yao WM, et al.
"J Hum Hypertens, 2013, 27(4):265-70.
 
 
人类 Y 染色体 36 个新 STR 位点的筛选与鉴定
彭冬铂等
遗传,2012, 34(11):1409-1416
 
 
人类细胞系基因表达中校正因子的选择
孙斯平等
国际遗传学杂志, 2012,35(5):262-267.
 
 
An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer’s disease
Liu QY, et al.
Neurobiol Aging, 2013, 34(5):1519.e13-7.
 
 
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
王金花等
中国组织工程研究与临床康复, 2011,15(33):6252-6256.
 
 
Immunosuppressive cytokine gene polymorphisms and outcome after related and unrelated hematopoietic cell transplantation in Chinese population
Xiao H,et al.
Biol Blood Marrow Transplant, 2011, 17(4):542-9.
 
 
Two novel mutations in the Spastin gene of Chinese patients with hereditary spastic paraplegia
Fei QZ,et al.
Eur J Neurol, 2011, 18(9):1194-6.
 
 
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.
 
 
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.
 
 
Familial Nonsyndromic Patent Ductus Arteriosus Caused by Mutations in TFAP2B
Chen YW,et al.
Pediatr Cardiol, 2011, 32(7):958-65.
 
 
First report of multiple CEBPA mutations contributing to donor origin of leukemia relapse after allogeneic hematopoietic stem cell transplantation
Xiao H,et al.
Blood, 2011, 117(19):5257-60.
 
 
X-linked recessive combined pituitary hormone deficiency is mapped to Xp22.3–Xp11 in a Chinese family
Wang CL,et al.
Genomics, 2011, 98(6):440-4.
 
 
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.
 
 
Rapid method for identification of six common species of mycobacteria based on multiplex SNP analysis
Wang H,et al.
J Clin Microbiol, 2010, 48(1):247-50.
 
 
The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A
Wang XF,et al.
Haemophilia, 2010, 16(4):632-9.
 
 
Relationship between TNFA, TNFB and TNFRII gene polymorphisms and outcome after unrelated hematopoietic cell transplantation in a Chinese population
Xiao HW,et al.
Bone Marrow Transplant, 2011, 46(3):400-7.
 
 
Association of TGF-beta1 gene polymorphisms in exon1 and blood levels with essential hypertension
He F,et al.
Blood Press, 2010, 19(4):225-33.
 
 
Analysis of the association between BTNL2 polymorphism and tuberculosis in Chinese Han population
Lian Y,et al.
Infect Genet Evol, 2010, 10(4):517-21.
 
 
VANGL2 Mutations in Human Cranial Neural-Tube Defects
Lei YP,et al.
N Engl J Med, 2010, 362(23):2232-5.
 
 
K-ras Mutations in the Plasma of Colorecta Cancer Patients
Shen YQ,et al.
LabMedicine, 2010, 41(3):156-158.
 
 
Association between NMDA receptor subunit 2b gene polymorphism and Alzheimer's disease in Chinese Han population in Shanghai
Chen C,et al.
Neurosci Bull, 2010, 26(5):395-400.
 
 
Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families
Gu JM,et al.
Acta Pharmacol Sin, 2009, 30(12):1634-42.
 
 
Association study between C7673T polymorphism in apolipoprotein B gene and cerebral infarction with family history in a Chinese population
Zhang L,et al.
Neurol India, 2009, 57(5):584-8.
 
 
Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family
Ke YH,et al.
Acta Pharmacol Sin, 2009, 30(8):1204-10.
 
 
Haemophilia A in two unrelated females due to F8 gene inversions combined with skewed inactivation of X chromosome
Wang X,et al.
Thromb Haemost, 2009, 101(4):775-8.
 
 
Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia
Yue H, et al.
Bone, 2009, 44(4):547-54.
 
 
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
 
 
MMP2 promoter polymorphism (C-1306T) and risk of recurrence in patients with hepatocellular carcinoma after transplantation
Wu LM, et al.
Clin Genet, 2008, 73(3):273-8.
 
 
Polymorphisms in cytokine genes and their association with acute rejection and recurrence of hepatitis B in Chinese liver transplant recipients
Xie HY, et al.
Arch Med Res, 2008, 39(4):420-8.
 
 
Novel BSCL2 gene mutation E189X in Chinese congenital generalized lipodystrophy child with early onset diabetes mellitus
Jin J, et al.
Eur J Endocrinol, 2007, 157(6):783-7.
 
 
Recipient cytotoxic T lymphocyte antigen-4 +49 G/G genotype is associated with reduced incidence of hepatitis B virus recurrence after liver transplantation among Chinese patients
Jiang Z, et al.
Liver Int, 2007, 27(9):1202-8.
 
 

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