Nature Genetics Q1 Unclaimed
Nature Genetics is a journal indexed in SJR in Genetics with an H index of 573. Journal with a Single Blind Peer Review review system, and It has a price of 9500 €. It has an SJR impact factor of 18,861 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 18,861.
Nature Genetics focuses its scope in these topics and keywords: human, gene, disease, protein, association, cell, genome, genetic, variation, identifies, ...
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy: Open Choice
Type of publications:
Publication frecuency: -
9500 €
Inmediate OANPD
Embargoed OA0 €
Non OAMetrics
18,861
SJR Impact factor573
H Index189
Total Docs (Last Year)756
Total Docs (3 years)9059
Total Refs17158
Total Cites (3 years)608
Citable Docs (3 years)23,1
Cites/Doc (2 years)47,93
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Aims and Scope
Best articles by citations
Gene Ontology: tool for the unification of biology
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Principal components analysis corrects for stratification in genome-wide association studies
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
The Genotype-Tissue Expression (GTEx) project
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
Generalized lacZ expression with the ROSA26 Cre reporter strain
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
The Cancer Genome Atlas Pan-Cancer analysis project
A general framework for estimating the relative pathogenicity of human genetic variants
Combinatorial microRNA target predictions
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Common SNPs explain a large proportion of the heritability for human height
Minimum information about a microarray experiment (MIAME)—toward standards for microarray data
A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells
Merlin—rapid analysis of dense genetic maps using sparse gene flow trees
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2
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