Keywords: نوع نادر; Genetic variant; Pooled target capture sequencing; Individually indexed target capture sequencing; Rare variant;
مقالات ISI نوع نادر (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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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: نوع نادر; Next-generation sequencing; Polycomb; CNV; Single nucleotide variant; Rare variant; Chromatin remodeling;
Keywords: نوع نادر; Schizophrenia; Sporadic; De novo; ARMS; Kidins220; Rare variant; Neurotrophin; Exome sequencing;
Keywords: نوع نادر; Chemometrics; Genetic epidemiology; Genome-wide association studies; Multivariate data; Multivariate regression technique; Partial least squares; Principal-component regression; Ridge regression; Single-nucleotide polymorphism; Statistical genetics; ASCA;
Keywords: نوع نادر; Runs of homozygosity; GWAS; Schizophrenia; Rare variant; Mutation;
Keywords: نوع نادر; Kidney tumor; Melanotic; Rare variant; Renal mass; Schwannoma;
Keywords: نوع نادر; 60G57; 62G05; 62F15; Bayesian nonparametric inference; Asymptotic credible intervals; Exchangeable random partition; Gibbs-type random probability measure; Index of diversity; Sampling formula; Species sampling problem; Rare variant; Two parameter Poisson
Whole-exome sequencing in a Japanese family with highly aggregated diabetes identifies a candidate susceptibility mutation in ADAMTSL3
Keywords: نوع نادر; Whole-exome sequencing (WES); Rare variant; ADAMTSL3;
Association of Rare Nonsynonymous Variants in PKD1 and PKD2 with Familial Intracranial Aneurysms in a Japanese Population
Keywords: نوع نادر; Intracranial aneurysm; autosomal dominant polycystic kidney disease; PKD1; PKD2; susceptibility gene; rare variant;
A loss-of-function variant in OSBPL1A predisposes to low plasma HDL cholesterol levels and impaired cholesterol efflux capacity
Keywords: نوع نادر; Cholesterol efflux; High-density lipoprotein; Oxysterol-binding protein; OSBPL1A; Rare variant; ABCA1; ATP-binding cassette transporter A-1; ER; Endoplasmic reticulum; GFP; Green fluorescent protein; GST; Glutathione-S-transferase; HDL-C; High-density-lip
Featured ArticleThe role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
Keywords: نوع نادر; Neurodegenerative disease; Alzheimer disease; Frontotemporal lobar degeneration; Amyotrophic lateral sclerosis; Parkinson disease; TREM2; R47H; rs75932628; Rare variant; Genetic association; GWAS; Imputation; Meta-analysis;
A Rare SNP Identified a TCP Transcription Factor Essential for Tendril Development in Cucumber
Keywords: نوع نادر; rare variant; TCP transcription factor; cucumber tendril; homologous organs
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia
Keywords: نوع نادر; Alzheimer's disease; Frontotemporal dementia; TREM2; Genetic association; p.R47H; Rare variant;
Featured ArticleTwo rare AKAP9 variants are associated with Alzheimer's disease in African Americans
Keywords: نوع نادر; Whole-exome sequencing; Late-onset Alzheimer's disease; Rare variant; Genetic association; African American; AKAP9;
Effect of Genome-Wide Genotyping and Reference Panels on Rare Variants Imputation
Keywords: نوع نادر; Genotype imputation; Genome-wide association study; 1000 Genome Project; HapMap; Rare variant; Common disease
Schizophrenia: Maternal inheritance and heteroplasmy of mtDNA mutations
Keywords: نوع نادر; Schizophrenia; mtDNA; Rare variant; Mitochondrial hypothesis;
Allelic and phenotypic spectrum of plasma triglycerides
Keywords: نوع نادر; ABL; abetalipoproteinemia; ANGPTL3; angiopoietin-like 3; ANGPTL4; angiopoietin-like 4; APOA4; apolipoprotein A-IV; APOA5; apolipoprotein A-V; APOB; apolipoprotein B; APOC2; apolipoprotein C-II; APOC3; apolipoprotein C-III; APOE; apolipoprotein E; CAD; cor
Mitochondrial DNA variants in a Japanese population of patients with Alzheimer’s disease
Keywords: نوع نادر; mtDNA; Alzheimer disease; Rare variant; Association study; APOE; Sequencing
Genome-wide approaches to schizophrenia
Keywords: نوع نادر; Genome-wide association; Schizophrenia; Polygenic; CNV; Rare variant; Gene expression; Systems biology