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Format : Academic Journals Subject : age distribution Subject : c-reactive protein Subject : chi-squared test Subject : children Geographic : china Filter by : Subject

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Academic Journal

Correlation between hearing loss and mild cognitive impairment in the elderly population: Mendelian randomization and cross-sectional study.

Authors : Tong Xu; Tao Zong; Jing Liu

Subjects: DIABETES complications; RISK assessment; CROSS-sectional methodCHINA

Source: Frontiers in Aging Neuroscience; 2024, p1-11, 11p

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Academic Journal

Association between mtDNA haplogroups and skeletal fluorosis in Han population residing in drinking water endemic fluorosis area of northern China.

Authors : Ji, Yi; Guo, Ning; Lu, Chunqing

Subjects: RISK assessment; ENVIRONMENTAL health; PHYSICAL diagnosisCHINA

Source: International Journal of Environmental Health Research; May2024, Vol. 34 Issue 5, p2397-2406, 10p

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Academic Journal

Association study of FLT4 and HYDIN single nucleotide polymorphisms with atrial septal defect susceptibility in the Han Chinese population of Southwest China.

Authors : Jin, Ye; Zhao, Miao; Guo, Qiuzhe

Subjects: GENOMICS; RESEARCH funding; CHI-squared testCHINA

Source: Italian Journal of Pediatrics; 4/5/2024, Vol. 50 Issue 1, p1-7, 7p

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Academic Journal

Renal damage and old age: risk factors for thrombosis in patients with ANCA-associated vasculitis.

Authors : Chen, Xin; Zhang, Shuo; You, Ruilian

Subjects: THROMBOSIS risk factors; RISK assessment; VASCULITISCHINA

Source: Thrombosis Journal; 3/20/2024, Vol. 22 Issue 1, p1-10, 10p

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Academic Journal

Gene polymorphisms of molecules of the cGAS-STING signalling pathway are associated with AML in Chinese patients.

Authors : Ma, Yuechan; Wang, Dongmei; Feng, Lei

Subjects: RNA analysis; DNA analysis; LEUKOCYTE countCHINA

Source: Holistic Integrative Oncology; 3/19/2024, Vol. 3 Issue 1, p1-10, 10p

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Academic Journal

Association of vitamin D‐binding protein polymorphisms and serum 25(OH)D concentration varies among Chinese healthy infants of different VDR‐FokI genotypes: A multi‐centre cross‐sectional study.

Authors : Tsang, Hing Wai; Tung, Keith T. S.; Wong, Rosa S.

Subjects: RESEARCH; DNA; SINGLE nucleotide polymorphismsCHINA

Source: Nutrition Bulletin; Mar2024, Vol. 49 Issue 1, p63-72, 10p

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Academic Journal

Causal association of serum biomarkers with oral cavity and oropharyngeal cancer: a mendelian randomization study.

Authors : Liu, Weixing; Liu, Yue; Li, Pei

Subjects: C-reactive protein; TRIGLYCERIDES; SOMATOMEDINCHINA

Source: BMC Oral Health; 12/9/2023, Vol. 23 Issue 1, p1-7, 7p

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Academic Journal

Prediction of asthma using a four-locus gene model including IL13, IL4, FCER1B, and ADRB2 in children of Kazak nationality.

Authors : Bai, Shasha; Lu, Jun; Hua, Li

Subjects: ASTHMA diagnosis; KAZAKHS; SINGLE nucleotide polymorphismsKAZAKHSTAN; CHINA

Source: Italian Journal of Pediatrics; 12/4/2023, Vol. 49 Issue 1, p1-6, 6p

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Academic Journal

PROX1 gene rs340874 single nucleotide polymorphism, body mass index, and early atherosclerosis in Chinese individuals: the CRC study.

Authors : Liu, Xuekui; Yang, Manqing; Liu, Ying

Subjects: BIOMARKERS; CARDIOVASCULAR diseases risk factors; HYPERTENSIONCHINA

Source: International Journal of Diabetes in Developing Countries; Dec2023, Vol. 43 Issue 6, p999-1006, 8p

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Academic Journal

DNMT1 SNPs (rs2114724 and rs2228611) associated with positive symptoms in Chinese patients with schizophrenia.

Authors : Ping, Junjiao; Wan, Jing; Huang, Caiying

Subjects: DNA metabolism; GENETICS of schizophrenia; SCHIZOPHRENIACHINA

Source: Annals of General Psychiatry; 10/13/2023, Vol. 22 Issue 1, p1-10, 10p

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Academic Journal

The PTGS1 (rs1330344) CC Genotype Contributes to Susceptibility to Kawasaki Disease in Southern Chinese Children.

Authors : Zheng, Hao; Fu, Lanyan; Xu, Yufen

Subjects: CORONARY artery injuries; CONFIDENCE intervals; SINGLE nucleotide polymorphismsCHINA

Source: Angiology; Oct2023, Vol. 74 Issue 9, p832-839, 8p

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Academic Journal

Association of LINC-PINT polymorphisms with lumbar disc herniation risk among Chinese Han population: a case control study.

Authors : Wu, Yimin; Bai, Ming; Yu, Yingnan

Subjects: BIOLOGICAL models; C-reactive protein; INTERVERTEBRAL disk displacementCHINA

Source: Journal of Orthopaedic Surgery & Research; 8/8/2023, Vol. 18 Issue 1, p1-10, 10p

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Academic Journal

Association of RNA m7G Modification Gene Polymorphisms with Pediatric Glioma Risk.

Authors : Zhu, Jinhong^1,2 (AUTHOR); Liu, Xiaoping³ (AUTHOR); Chen, Wei¹ (AUTHOR)

Subjects: *CONFIDENCE intervals; *SINGLE nucleotide polymorphisms; *AGE distributionCHINA

Source: BioMed Research International. 1/24/2023, Vol. 2023, p1-10. 10p.

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Academic Journal

SNP rs3803264 polymorphisms in THSD1 and abnormally expressed mRNA are associated with hemorrhagic stroke.

Authors : Changying Chen; Xincheng Gu; Fangyuan Liu

Subjects: HYPERTENSION risk factors; REVERSE transcriptase polymerase chain reaction; KRUSKAL-Wallis TestCHINA

Source: Frontiers in Aging Neuroscience; 5/1/2023, p1-11, 11p

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Academic Journal

Interaction of PTPRD (rs17584499) polymorphism with passive smoking in Chinese women with susceptibility to type 2 diabetes.

Authors : Zeng, Haixia; Pan, Gui; Wu, Juan

Subjects: HDL cholesterol; TRIGLYCERIDES; FASTINGCHINA

Source: International Journal of Diabetes in Developing Countries; Apr2023, Vol. 43 Issue 2, p304-308, 5p

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Academic Journal

Population Pharmacokinetic Modeling Combined With Machine Learning Approach Improved Tacrolimus Trough Concentration Prediction in Chinese Adult Liver Transplant Recipients.

Authors : Li, Zi‐ran; Li, Rui‐dong; Niu, Wan‐jie

Subjects: BIOLOGICAL models; HEMATOCRIT; VORICONAZOLECHINA

Source: Journal of Clinical Pharmacology; Mar2023, Vol. 63 Issue 3, p314-325, 12p

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Academic Journal

Unique genetic variants of lean nonalcoholic fatty liver disease: a retrospective cohort study.

Authors : Li, Jie; Wu, Na; Yang, Yukun

Subjects: BIOMARKERS; CLINICAL pathology; GENETICSCHINA

Source: BMC Endocrine Disorders; 1/11/2023, Vol. 23 Issue 1, p1-10, 10p

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Academic Journal

Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population.

Authors : Shi, Jianrong; Li, Wei; Tao, Ran

Subjects: GENETICS of disease susceptibility; STEROID drugs; SEQUENCE analysisCHINA

Source: Laboratory Medicine; Jan2023, Vol. 54 Issue 1, p35-40, 6p

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Academic Journal

SLC2A9 rs1014290 Polymorphism is Associated with Prediabetes and Type 2 Diabetes.

Authors : Zhang, Xuemei; Hou, Guangsen; Li, Fang

Subjects: ANALYSIS of variance; SINGLE nucleotide polymorphisms; GENETIC polymorphismsCHINA

Source: International Journal of Endocrinology; 12/12/2022, p1-8, 8p

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Academic Journal

Genetic variant in SPAG16 is associated with the susceptibility of ACPA-positive rheumatoid arthritis possibly via regulation of MMP-3.

Authors : Lin, Qingxi; Zhou, Bingxiang; Song, Xiaoxiao

Subjects: STATISTICS; C-reactive protein; GENETICSNORTH America; CHINA

Source: Journal of Orthopaedic Surgery & Research; 11/24/2022, Vol. 17 Issue 1, p1-7, 7p

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Academic Journal

The rs35874116 single nucleotide polymorphism increases sweet intake and the risk of severe early childhood caries: a case–control study.

Authors : Liang, Yan; Yao, Junyu; Qiu, Rongmin

Subjects: GENETIC mutation; SEQUENCE analysis; CONFIDENCE intervalsCHINA

Source: BMC Oral Health; 11/5/2022, Vol. 22 Issue 1, p1-8, 8p

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Academic Journal

5-Amino-4-Imidazolecarboxamide Ribonucleotide Transformylase/IMP Cyclohydrolase Polymorphisms Affect the Susceptibility to Multiple Myeloma.

Authors : Wang, Yu; Ling, Zhian; Hu, Zuojian

Subjects: IMMUNOGLOBULIN analysis; GENETIC mutation; CONFIDENCE intervalsCHINA

Source: Laboratory Medicine; Sep2022, Vol. 53 Issue 5, p465-474, 10p

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Academic Journal

Lack of Association Between HMGB1 Gene Polymorphism and Risk of Henoch-Schonlein Purpura in Childhood.

Authors : Zhaoyang Peng; Qingxia Xue; Wei Li

Subjects: SCHOENLEIN-Henoch purpura; CATHELICIDINS; CONFIDENCE intervalsCHINA

Source: Iranian Journal of Pediatrics; Apr2022, Vol. 32 Issue 2, p1-7, 7p

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Academic Journal

Influences of Vitamin D Levels and Vitamin D-Binding Protein Polymorphisms on Nonalcoholic Fatty Liver Disease Risk in a Chinese Population.

Authors : Wang, Min; Wang, Minxian; Zhang, Ru

Subjects: TRIGLYCERIDES; CONFIDENCE intervals; SINGLE nucleotide polymorphismsCHINA

Source: Annals of Nutrition & Metabolism; 2022, Vol. 78 Issue 2, p61-72, 12p

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Academic Journal

Association of nitric oxide synthase 1 adaptor protein gene polymorphisms with schizophrenia in a Chinese Han population.

Authors : Xueping Yang; Jing Zhou; Zhen Yuan

Subjects: SCHIZOPHRENIA risk factors; GENETICS of schizophrenia; NITRIC-oxide synthasesCHINA

Source: Indian Journal of Psychiatry; Mar/Apr2022, Vol. 64 Issue 2, p130-137, 8p

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Academic Journal

Investigation of the Relationship between CMYC Gene Polymorphisms and Glioma Susceptibility in Chinese Children.

Authors : Lou, Susu; Huang, Xiaokai; Tian, Xiaoqian

Subjects: BIOMARKERS; ACADEMIC medical centers; DNACHINA

Source: Cancer Investigation; Nov 2021, Vol. 39 Issue 10, p819-825, 7p

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Academic Journal

Association Analysis of LEP Signaling Pathway with Type 2 Diabetes Mellitus in Chinese Han Population from South China.

Authors : Yu, Haibing; Xu, Lin; Liu, Hao

Subjects: LEPTIN; SINGLE nucleotide polymorphisms; CASE-control methodCHINA

Source: BioMed Research International; 9/20/2021, p1-13, 13p

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Academic Journal

MYBL2 Gene Polymorphism Is Associated With Acute Lymphoblastic Leukemia Susceptibility in Children.

Authors : Guo, Haixia; Li, Na; Sun, Yaping

Subjects: LYMPHOBLASTIC leukemia; GENETIC polymorphisms; ACUTE leukemiaCHINA

Source: Frontiers in Oncology; 9/8/2021, Vol. 12, p1-9, 9p

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Academic Journal

Identification of sequence polymorphisms in the mitochondrial deoxyribonucleic acid displacement-loop region as risk factors for systemic lupus erythematosus.

Authors : Ruixue Lai; Xiaoyun Zhang; Kuangyuan Qiao

Subjects: DNA; SEQUENCE analysis; CONFIDENCE intervalsCHINA

Source: Archives of Rheumatology; Sep2021, Vol. 36 Issue 3, p375-380, 6p

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Academic Journal

Polymorphisms of 5‐hydroxytryptamine receptor type 3B gene and clinical characteristics for vomiting after breast surgery in chinese han female population.

Authors : Yan, Ting; Su, Jiansheng; Zhou, Linying

Subjects: SURGICAL complication risk factors; VOMITING -- Risk factors; STATISTICSCHINA

Source: Journal of Clinical Pharmacy & Therapeutics; Aug2021, Vol. 46 Issue 4, p936-941, 6p

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Academic Journal

Machine Learning Study of SNPs in Noncoding Regions to Predict Non-small Cell Lung Cancer Susceptibility.

Authors : Huang, Y.^1,2 (AUTHOR); Bao, T.^1,2 (AUTHOR); Zhang, T.^1,2 (AUTHOR)

Subjects: *LUNG cancer; *SINGLE nucleotide polymorphisms; *AGE distributionCHINA

Source: Clinical Oncology. Nov2023, Vol. 35 Issue 11, p701-712. 12p.

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Academic Journal

SNPs at TP63 gene was specifically associated with right‐side cleft lip in Han Chinese population.

Authors : Yin, Bin; Shi, Jia‐Yu; Lin, Yan‐Song

Subjects: SEQUENCE analysis; CONFIDENCE intervals; SINGLE nucleotide polymorphismsCHINA

Source: Oral Diseases; Apr2021, Vol. 27 Issue 3, p559-566, 8p, 4 Charts

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Academic Journal

ALKBH5 Gene Polymorphisms and Hepatoblastoma Susceptibility in Chinese Children.

Authors : Ren, Hui; Zhuo, Zhen-Jian; Duan, Fei

Subjects: GENETIC polymorphisms; CHINESE people; SINGLE nucleotide polymorphismsCHINA

Source: Journal of Oncology; 3/19/2021, p1-6, 6p

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Academic Journal

Association of Leptin Gene Polymorphisms with Rheumatoid Arthritis in a Chinese Population.

Authors : Tao, Sha-Sha; Dan, Yi-Lin; Wu, Guo-Cui

Subjects: ALLELES; CHI-squared test; CONFIDENCE intervalsCHINA

Source: BioMed Research International; 10/6/2020, p1-7, 7p

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Academic Journal

The impacts of gene polymorphisms on methotrexate in Chinese psoriatic patients.

Authors : Chen, M.; Chen, W.; Liu, P.

Subjects: GENETIC polymorphisms; SINGLE nucleotide polymorphisms; FISHER exact testCHINA

Source: Journal of the European Academy of Dermatology & Venereology; Sep2020, Vol. 34 Issue 9, p2059-2065, 7p

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Academic Journal

Interaction between methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and environment with susceptibility to ischemic stroke in Chinese population.

Authors : Zheng, Xing-Zhen; Bian, Xiao-Lin; Sun, Zhe-Hong

Subjects: STROKE risk factors; AGE distribution; ALLELESCHINA

Source: Annals of Indian Academy of Neurology; Jul/Aug2020, Vol. 23 Issue 4, p491-495, 5p

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Academic Journal

Correlations Between the Genetic Variations in the COL1A1, COL5A1, COL12A1, and β-fibrinogen Genes and Anterior Cruciate Ligament Injury in Chinese Patientsa.

Authors : Zhao, Daohong; Zhang, Qi; Lu, Qingnan

Subjects: ALLELES; ANTERIOR cruciate ligament injuries; CHI-squared testCHINA

Source: Journal of Athletic Training (Allen Press); May2020, Vol. 55 Issue 5, p515-521, 7p, 2 Diagrams, 6 Charts

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Academic Journal

Salt-Inducible Kinase 3 Haplotypes Associated with Noise-Induced Hearing Loss in Chinese Workers.

Authors : Yin, Haoyang; Guo, Jiadi; Ding, Enmin

Subjects: HEARING disorders; SINGLE nucleotide polymorphisms; HAPLOTYPESCHINA

Source: Audiology & Neurotology; 2020, Vol. 25 Issue 4, p200-208, 9p, 6 Charts, 1 Graph

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Academic Journal

Association Study of Three Gene Polymorphisms Recently Identified by a Genome-Wide Association Study with Obesity-Related Phenotypes in Chinese Children.

Authors : Song, Qi-Ying; Song, Jie-Yun; Wang, Yang

Subjects: CHILDHOOD obesity; SINGLE nucleotide polymorphisms; OVERWEIGHT childrenCHINA

Source: Obesity Facts: The European Journal of Obesity; Jul2017, Vol. 10 Issue 3, p179-190, 12p

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Academic Journal

Associations of Two Obesity-Related Single-Nucleotide Polymorphisms with Adiponectin in Chinese Children.

Authors : Wu, Lijun; Gao, Liwang; Zhao, Xiaoyuan

Subjects: OBESITY; SINGLE nucleotide polymorphisms; CHILDRENCHINA

Source: International Journal of Endocrinology; 3/15/2017, p1-5, 5p

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Academic Journal

Interferon-Gamma Gene Polymorphism +874 (A/T) in Chinese Children with Henoch-Schönlein Purpura.

Authors : Hui Xu; Wei Li; Haidong Fu

Subjects: INTERFERONS; SINGLE nucleotide polymorphisms; SCHOENLEIN-Henoch purpuraCHINA

Source: Iranian Journal of Allergy, Asthma & Immunology; Jun2014, Vol. 13 Issue 3, p184-189, 6p

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Academic Journal

Common genetic variants associated with lipid profiles in a Chinese pediatric population.

Authors : Shen, Yue; Xi, Bo; Zhao, Xiaoyuan

Subjects: HUMAN genetic variation; BLOOD lipids; LIPOPROTEINSCHINA

Source: Human Genetics; Nov2013, Vol. 132 Issue 11, p1275-1285, 11p

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Academic Journal

Associations between EYA1 single-nucleotide polymorphisms and non-syndromic orofacial clefts in Western Han Chinese.

Authors : Zeng, Ni; Wu, Jun; Zhu, Wen‐Chao

Subjects: CLEFT palate children; SINGLE nucleotide polymorphisms; CRANIOFACIAL abnormalitiesCHINA

Source: Journal of Oral Pathology & Medicine; Oct2013, Vol. 42 Issue 9, p711-715, 5p, 1 Black and White Photograph, 4 Charts

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Academic Journal

Association between brain-derived neurothropic factor variants and asthma in Chinese Han children.

Authors : Yinli, Cao; Jie, Hao; Li, Zhao

Subjects: ASTHMA in children; ASTHMA treatment; SINGLE nucleotide polymorphismsCHINA

Source: Acta Paediatrica; Jun2013, Vol. 102 Issue 6, pe247-e250, 4p

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Academic Journal

A sex-specific effect of the CYP17A1 SNP rs11191548 on blood pressure in Chinese children.

Authors : Wu, L; Xi, B; Zhang, M

Subjects: CYTOCHROME P-450; BLOOD pressure; ENZYMESCHINA

Source: Journal of Human Hypertension; Dec2012, Vol. 26 Issue 12, p731-736, 6p, 5 Charts

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Academic Journal

Study of eight GWAS-identified common variants for association with obesity-related indices in Chinese children at puberty.

Authors : Wang, J; Mei, H; Chen, W

Subjects: OBESITY risk factors; CHILDREN; BODY mass indexCHINA

Source: International Journal of Obesity; Apr2012, Vol. 36 Issue 4, p542-547, 6p

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Academic Journal

Association of LEPR polymorphisms with predisposition and inflammatory response in anti-tuberculosis drug-induced liver injury: A pilot prospective investigation in Western Chinese Han population.

Authors : Zhao, Zhenzhen¹ (AUTHOR); Peng, Wu¹ (AUTHOR); Zhou, Juan¹ (AUTHOR)

Subjects: *SINGLE nucleotide polymorphisms; *LIVER injuries; *LEPTIN receptorsCHINA

Source: Infection, Genetics & Evolution. Nov2019, Vol. 75, pN.PAG-N.PAG. 1p.

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Academic Journal

Association between BDNF gene polymorphisms and attention deficit hyperactivity disorder in school-aged children in Wuhan, China.

Authors : Luo, Liwei¹ (AUTHOR); Jiang, Xueyan¹ (AUTHOR); Cao, Guangan¹ (AUTHOR)

Subjects: *ATTENTION-deficit hyperactivity disorder; *GENETIC polymorphisms; *SINGLE nucleotide polymorphismsWUHAN (China); CHINA

Source: Journal of Affective Disorders. Mar2020, Vol. 264, p304-309. 6p.

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Academic Journal

Association of PPP1R3B polymorphisms with blood lipid and C-reactive protein levels in a Chinese population (PPP1R3B C ).

Authors : Zhang Y; Key Laboratory of Nutrition and Metabolism, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai, China.; Gan W

Subjects: Polymorphism, Single Nucleotide*; C-Reactive Protein/C-Reactive Protein/C-Reactive Protein/*metabolism ; Lipids/Lipids/Lipids/*blood

Source: Journal of diabetes [J Diabetes] 2013 Sep; Vol. 5 (3), pp. 275-81. Date of Electronic Publication: 2013 May 28.Publisher: Blackwell Publishing Asia Country of Publication: Australia NLM ID: 101504326 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Genetic Variant of GPR126 Gene is Functionally Associated With Adolescent Idiopathic Scoliosis in Chinese Population.

Authors : Xiaodong Qin¹; Leilei Xu¹; Chao Xia¹

Subjects: *HUMAN genetic variation; *ADOLESCENT idiopathic scoliosis; *GENE expressionCHINA

Source: Spine (03622436). 10/1/2017, Vol. 42 Issue 19, pE1098-E1103. 6p.

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