Keywords: انواع نادر; Addiction; Exome; Rare variants; Tobacco; Nicotine; Alcohol; PRS; Pathway analysis;
مقالات ISI انواع نادر (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: انواع نادر; Exome sequencing; Rare variants; Lung cancer; Susceptibility loci;
Keywords: انواع نادر; DNA variant; genetics; genome-wide association; inflammasome; inflammation; inflammatory bowel disease; innate immunity; interleukin; missing heritability; mutation; NOD-like receptor (NLR); nucleotide oligomerization domain (NOD) protein; periodontal dis
Keywords: انواع نادر; TAAR1; Psychiatry; Exome sequencing; Rare variants; SNPs; Association;
Keywords: انواع نادر; Genetics; RLS; GWAS; Rare variants; PLM;
Keywords: انواع نادر; Parkinson's disease; Common risk loci; Rare variants; Whole exome sequencing; Variant aggregation test;
Keywords: انواع نادر; Genetics; Genome-wide association study; Alzheimer's disease; High-throughput technologies; Rare variants; Epidemiology of neurodegenerative disorders;
Keywords: انواع نادر; AAC; amino acid coding; AF; atrial fibrillation; BMI; body mass index; ECG; electrocardiogram; ESP; Exome Sequencing Project; GWAS; genome-wide association study; IQR; interquartile range; LVEDD; left ventricular end-diastolic diameter; LVEF; left ventric
Keywords: انواع نادر; Genome-wide association study; Rare variants; Pooled association tests; Variable-threshold approach;
Keywords: انواع نادر; Hirschsprung disease; Rare variants; GWAS; Next generation sequencing; Systems biology; Functional assays;
Genetic Determinants of IgA Nephropathy: Eastern Perspective
Keywords: انواع نادر; IgA nephropathy (IgAN); genome-wide association study (GWAS); common variants; rare variants; copy number variants (CNV);
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
Keywords: انواع نادر; Frontotemporal dementia; Sortilin; Granulin; Rare variants; Genetic association;
Influence of low frequency PSEN1 variants on familial Alzheimer's disease risk in Brazil
Keywords: انواع نادر; Alzheimer's disease; PSEN1; Rare variants; Mutational screening;
Novel PDE10A transcript diversity in the human striatum: Insights into gene complexity, conservation and regulation
Keywords: انواع نادر; SNP; single nucleotide polymorphism; cAMP; cyclic adenosine monophosphate; cGMP; cyclic guanosine monophosphate; MSN; medium spiny neurons; HC; healthy control; BD; bipolar disorder; RLM-RACE; RNA ligase mediated rapid amplification of cDNA ends; IRB; ins
Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels
Keywords: انواع نادر; CETP; HDL-C; Genetic association; Rare variants; Sequencing
More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk
Keywords: انواع نادر; TREM2; Rare variants; LOAD;
Immune deficiencies, infection, and systemic immune disordersRare variants at 16p11.2 are associated with common variable immunodeficiency
Keywords: انواع نادر; Immunodeficiency; immunogenetics; genome-wide association study; ITGAM; rare variants; CR3; Complement receptor 3; CVID; Common variable immunodeficiency; DC; Dendritic cell; FUS; Fused-in-sarcoma; GWAS; Genome-wide association study; IIBDGC; Internationa
Using volcano plots and regularized-chi statistics in genetic association studies
Keywords: انواع نادر; Volcano plot; Regularized-chi; Genetic association analysis; Rare variants; SNPs; Type-2 diabetes
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
Keywords: انواع نادر; TREM2; Alzheimer's disease; Frontotemporal dementia; Rare variants; Meta-analysis; IgV-set domain;
Low frequency genetic variants in the μ-opioid receptor (OPRM1) affect risk for addiction to heroin and cocaine
Keywords: انواع نادر; OPRM1; Addiction; Cocaine; Heroin; Rare variants; Genetics;
A Population-Specific Uncommon Variant in GRIN3A Associated with Schizophrenia
Keywords: انواع نادر; Bipolar disorder; CFB; DNMT1; FAAH; GRIN3A; MYO18B; NR3A; rare variants;
Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population
Keywords: انواع نادر; Parkinson disease; Glucocerebrosidase; Gaucher disease; Rare variants; Common complex disease;
Schizophrenia as a neuronal synaptic disorder related to multiple rare genetic mutations
Keywords: انواع نادر; Association and functional studies; GAP-43; NRGN; Rare variants; Schizophrenia; SYP
Genetic and functional analyses of the gene encoding synaptophysin in schizophrenia
Keywords: انواع نادر; Synaptophysin; SYP; Schizophrenia; Rare variants; Association and functional study;
Genetic and functional analysis of the gene encoding neurogranin in schizophrenia
Keywords: انواع نادر; NRGN; Schizophrenia; Rare variants; Association and functional study;
Genetic and functional analysis of the gene encoding GAP-43 in schizophrenia
Keywords: انواع نادر; GAP-43; Schizophrenia; Rare variants; Association and functional study;
MAGI1 Copy Number Variation in Bipolar Affective Disorder and Schizophrenia
Keywords: انواع نادر; Bipolar affective disorder; copy number variation; MAGI1; MAGI2; rare variants; schizophrenia;
Rare variants in the lipoprotein lipase (LPL) gene are common in hypertriglyceridemia but rare in Type III hyperlipidemia
Keywords: انواع نادر; Hypertriglyceridemia; Rare variants; Lipoprotein lipase; Type III hyperlipidemia;
Resequencing the Apolipoprotein A5 (APOA5) gene in patients with various forms of hypertriglyceridemia
Keywords: انواع نادر; APOA5; Resequencing; Rare variants; Hypertriglyceridemia; Type III Hyperlipidemia;
Schizophrénie, génétique et cognition
Keywords: انواع نادر; Endophénotype; COMT; Common disease common variant; Variants rares; Endophenotype; COMT; Common disease common variant; Rare variants;
Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia
Keywords: انواع نادر; Resequencing; Copy number variations; Rare variants; Chorea-acanthocytosis; McLeod syndrome
Rare Nonsynonymous Variants in Alpha-4 Nicotinic Acetylcholine Receptor Gene Protect Against Nicotine Dependence
Keywords: انواع نادر; CHRNA4; deep sequencing; imaging genetics; nicotine dependence; nonsynonymous; rare variants;
A novel application of pattern recognition for accurate SNP and indel discovery from high-throughput data: Targeted resequencing of the glucocorticoid receptor co-chaperone FKBP5 in a Caucasian population
Keywords: انواع نادر; Pattern recognition; Next-generation sequencing analysis; Indels; Rare variants; FKBP5; HLA;
Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients
Keywords: انواع نادر; CNVs (copy number variants); Psychiatric disorders; MLPA; Rare variants; CNS (central nervous system) candidate genes
Application of genetic/genomic approaches to allergic disorders
Keywords: انواع نادر; Gene; allergy; database; browser; genome; common variants; rare variants; HapMap; imputation; AD; Atopic dermatitis; AIM; Ancestry-informative markers; CNV; Copy number variation; CNVR; Copy number variation region; FLG; Filaggrin; GO; Gene Ontology; GWAS
The Genetics of Autism: Key Issues, Recent Findings, and Clinical Implications
Keywords: انواع نادر; Autism genetics; Rare variants; Copy number variation; Association;
Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility
Keywords: انواع نادر; Rare variants; private alleles; asthma; IL4; IgE; African Americans; MAF; Minor allele frequency; SNP; Single nucleotide polymorphism;
Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study
Keywords: انواع نادر; SQSTM1/p62; Alzheimer's disease; Rare variants; Meta-analysis; European early-onset dementia consortium;
Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry
Keywords: انواع نادر; Rare variants; CTLA-4; Type 1 diabetes; Genetic association; Pooled DNA;