Keywords: مطالعه ارتباط ژنتیکی; Genetic association study; Depression; Depressive symptoms; Hispanics/Latinos;
مقالات ISI مطالعه ارتباط ژنتیکی (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: مطالعه ارتباط ژنتیکی; Obsessive-compulsive disorder; Genetic association study; Oxytocin; OXTR; Age at onset;
Keywords: مطالعه ارتباط ژنتیکی; Dense red blood cells; Sickle cell disease; Genetic association study; GWAS; ATP2B4;
Keywords: مطالعه ارتباط ژنتیکی; Parkinson's disease; Epidemiology; Genetic association study;
Keywords: مطالعه ارتباط ژنتیکی; female infertility; genetic association study; recurrent implantation failure; single nucleotide polymorphism; VEGF;
Keywords: مطالعه ارتباط ژنتیکی; Peripheral arterial disease; Venous thromboembolism; Mitochondrial genome; Genetic association study;
Keywords: مطالعه ارتباط ژنتیکی; electrocardiogram; genetic association study; heart failure; left ventricular hypertrophy; QRS; DHS; deoxyribonuclease hypersensitivity sites; ECG; electrocardiogram; eQTL; expression quantitative trait locus; GWAS; genome-wide association study; LD; link
Keywords: مطالعه ارتباط ژنتیکی; polycystic ovary syndrome; genetic association study; genome-wide association study;
Keywords: مطالعه ارتباط ژنتیکی; Aldehydes; Asthma; Chronic obstructive pulmonary disease; Genetic association study; Longitudinal study
Keywords: مطالعه ارتباط ژنتیکی; Stroke; suicidal ideation; serotonin transporter; serotonin receptor; genetic association study;
Keywords: مطالعه ارتباط ژنتیکی; Parkinson's disease; GWAS; Genetic association study; Single-nucleotide polymorphism;
Keywords: مطالعه ارتباط ژنتیکی; Anorexia nervosa; Obsessive compulsive disorder; Genetic association study; Candidate genes; Glutamate; Serotonin; Neurodevelopment;
Keywords: مطالعه ارتباط ژنتیکی; Breast cancer; Depression; Cytokines; Genetic association study; Interleukins;
Keywords: مطالعه ارتباط ژنتیکی; Leadership role occupancy; Twin design; Genetic association study;
A 35.8 kilobases haplotype spanning ANKK1 and DRD2 is associated with heroin dependence in Han Chinese males
Keywords: مطالعه ارتباط ژنتیکی; ANKK1; Ankyrin repeat and kinase domain containing 1; DRD2; Dopamine receptor D2; SNP(s); Single nucleotide polymorphism(s); HWE; Hardy-Weinberg equilibrium; OR(s); odds ratio(s); CI(s); confidence interval(s); MAF; minor allele frequency; n; number; Bal.
Original ResearchNeuroblastoma survivors are at increased risk for second malignancies: A report from the International Neuroblastoma Risk Group Project
Keywords: مطالعه ارتباط ژنتیکی; Neuroblastoma; Second malignant neoplasms; INRG; Genetic association study;
The mtDNA replication-related genes TFAM and POLG are associated with leprosy in Han Chinese from Southwest China
Keywords: مطالعه ارتباط ژنتیکی; Leprosy; TFAM; POLG; eQTL; Genetic association study;
DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis
Keywords: مطالعه ارتباط ژنتیکی; Linkage analysis; positional cloning; asthma; allergic rhinitis; parent-of-origin effect; DNA methylation; genetic association study; AAR; Asthma and allergic rhinitis comorbidity; AR; Allergic rhinitis; CIT; Causal inference test; CNG; Centre National de
Association analysis of class II cytokine and receptor genes in vitiligo patients
Keywords: مطالعه ارتباط ژنتیکی; Vitiligo; Class II cytokine; Genetic association study; Single-nucleotide polymorphism; Haplotype
MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies
Keywords: مطالعه ارتباط ژنتیکی; Dementia with Lewy bodies; Lewy body disease; Genetic association study; MAPT; tau protein;
Serotonergic genes and depressive disorder in acute coronary syndrome: The Korean depression in ACS (K-DEPACS) study
Keywords: مطالعه ارتباط ژنتیکی; Acute coronary syndrome; Depression; Serotonin transporter; Serotonin receptor; Genetic association study
Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1
Keywords: مطالعه ارتباط ژنتیکی; Genetic association study; Heroin; Multiancestry; Opioid; OPRM1; Prefrontal cortex
No evidence for genetic association between glutamate transporter EAAT2 and Devic's neuromyelitis optica in caucasians and afro-caribbeans
Keywords: مطالعه ارتباط ژنتیکی; Devic's neuromyelitis optica; Excitatory amino acid transporter 2; Glutamate transporter; Glutamate excitotoxicity; Single nucleotide polymorphisms; Genetic association study;
Influence of the BDNF Val66Met polymorphism on coping response to stress in patients with advanced gastric cancer
Keywords: مطالعه ارتباط ژنتیکی; Anxious Preoccupation; BDNF; Cancer; Coping; Genetic association study; Psychosomatics;
Association of rs11190870 near LBX1 with adolescent idiopathic scoliosis in East Asians: a systematic review and meta-analysis
Keywords: مطالعه ارتباط ژنتیکی; Adolescent idiopathic scoliosis; Etiology; Genetic association study; LBX1; Ladybird homeobox 1; rs11190870; Single nucleotide polymorphism
Brain-derived neurotrophic factor (BDNF)-Epigenetic regulation in unipolar and bipolar affective disorder
Keywords: مطالعه ارتباط ژنتیکی; Affective disorders; Depression; Antidepressant therapy; Epigenetics; BDNF methylation; Genetic association study;
A Population-based Assessment of Germline HOXB13 G84E Mutation and Prostate Cancer Risk
Keywords: مطالعه ارتباط ژنتیکی; Genetic association study; HOXB13; Prostate cancer
Credit card borrowing and the monoamine oxidase A (MAOA) gene
Keywords: مطالعه ارتباط ژنتیکی; D14; D91; G02; Credit card borrowing; Present-biased time preferences; MAOA gene; Genetic association study;
A longitudinal study of SLC6A4 DNA promoter methylation and poststroke depression
Keywords: مطالعه ارتباط ژنتیکی; Stroke; Depression; SLC6A4; DNA methylation; Genetic association study;
C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
Keywords: مطالعه ارتباط ژنتیکی; AD; MCI; C9orf72; G4C2 repeat expansion; Genetic association study;
A longitudinal study of BDNF promoter methylation and genotype with poststroke depression
Keywords: مطالعه ارتباط ژنتیکی; Stroke; Depression; BDNF; DNA methylation; Genetic association study;
Mediation analysis reveals a sex-dependent association between ABO gene variants and TG/HDL-C ratio that is suppressed by sE-selectin level
Keywords: مطالعه ارتباط ژنتیکی; ABO gene variants; Suppression effect; Lipid profiles; Inflammatory markers; Genetic association study; TG/HDL-C ratio;
Association of 5HTR1A gene variants with suicidal behavior: Case-control study and updated meta-analysis
Keywords: مطالعه ارتباط ژنتیکی; Suicide; Serotonin receptor; Genetic association study; Meta-analysis; PRISMA; preferred reporting items for systematic reviews and meta-analyses; DSM-IV; diagnostic and statistical manual of mental disorders-IV;
Fine mapping of 11q13.5 identifies regions associated with prostate cancer and prostate cancer death
Keywords: مطالعه ارتباط ژنتیکی; Genetic association study; EMSY; Death; Prostate cancer; Single nucleotide polymorphism;
Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four U.S. populations: The Population Architecture using Genomics and Epidemiology (PAGE) study
Keywords: مطالعه ارتباط ژنتیکی; Ankle brachial index; Carotid artery intima-media thickness; Carotid plaque; Coronary heart disease; Genetic association study; Multiethnic populations; Subclinical atherosclerosis;
Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patients
Keywords: مطالعه ارتباط ژنتیکی; MMP, matrix metalloproteinase; BAV, bicuspid aortic valve; TAA, thoracic aortic aneurysm; TAV, tricuspid aortic valveAortic valve morphology; Thoracic aortic aneurysm; Polymorphisms; Genetic association study
Association of the six transmembrane protein of prostate 2 gene polymorphisms with metabolic syndrome in Han Chinese population
Keywords: مطالعه ارتباط ژنتیکی; Genetic association study; Han Chinese; Metabolic syndrome; STAMP2
A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men
Keywords: مطالعه ارتباط ژنتیکی; Essential hypertension; GOSR2; Single nucleotide polymorphism; Haplotype; Diplotype; Genetic association study
Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: A preliminary study
Keywords: مطالعه ارتباط ژنتیکی; Obsessive-compulsive disorder; Glutamate; Genetic association study; Structural magnetic resonance imaging; Orbital frontal cortex
Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls
Keywords: مطالعه ارتباط ژنتیکی; Borderline personality disorder; NRXN3; Genetic association study; Heroin dependence
The association between cytokine gene polymorphisms and graft rejection in liver transplantation: A systematic review and meta-analysis
Keywords: مطالعه ارتباط ژنتیکی; Cytokine receptor gene; Genetic association study; Graft rejection; Liver transplantation; Meta-analysis
Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis
Keywords: مطالعه ارتباط ژنتیکی; Amyotrophic lateral sclerosis; Genetics; Hemochromatosis; Genetic association study;
Restless legs syndrome in Czech patients with multiple sclerosis: An epidemiological and genetic study
Keywords: مطالعه ارتباط ژنتیکی; Secondary restless legs syndrome; Multiple sclerosis; Genetic association study; Prevalence study
Genetic ancestry and its association with asthma exacerbations among African American subjects with asthma
Keywords: مطالعه ارتباط ژنتیکی; Asthma; continental population groups; African continental ancestry group; genetic association study; health status disparities; minority healthAIM, Ancestry informative marker; ED, Emergency department; ICS, Inhaled corticosteroid; RR, Relative rate; SAP
Serotonergic and BDNF genes and risk of depression after stroke
Keywords: مطالعه ارتباط ژنتیکی; Stroke; Depression; Brain-derived neurotrophic factor; Serotonin transporter; Serotonin receptor; Genetic association study;
Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion
Keywords: مطالعه ارتباط ژنتیکی; endometrium; extracellular matrix; genetic association study; pregnancy; proteolysis
Cholesteryl Ester Transfer Protein (CETP) genotype and cognitive function in persons aged 35 years or older
Keywords: مطالعه ارتباط ژنتیکی; CETP; Cross-sectional analysis; Executive function; Genetic association study; Middle-aged; Systematic review;
Genomic determinants of normal tissue toxicity after radiotherapy for head and neck malignancy: A systematic review
Keywords: مطالعه ارتباط ژنتیکی; Head and neck cancer; Radiotoxicity; Radiotherapy; Toxicity; Genetic polymorphism; Genetic association study; Single nucleotide polymorphism;
Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease
Keywords: مطالعه ارتباط ژنتیکی; CDNF; cerebral dopamine neurotrophic factor; PD; Parkinson disease; SNP; single nucleotide polymorphism; EOPD; early-onset Parkinson disease; GDNF; glial-cell line derived neurotrophic factors; OR; odd ratio; CI; confidence interval; MAF; minor allele fre
Association study: SLC6A18 gene and myocardial infarction
Keywords: مطالعه ارتباط ژنتیکی; Myocardial infarction; SLC6A18; Single nucleotide polymorphism; Haplotype; Genetic association study