Nature Genetics
Nature Genetics is a journal indexed in SJR in Genetics with an H index of 660. Journal with a Single Blind Peer Review review system, and It has a price of 9500 €. It has an SJR impact factor of 16,586 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 16,586.
Nature Genetics focuses its scope in these topics and keywords: human, gene, disease, protein, genetic, genome, cell, association, variation, identifies, ...
Metrics
Scimago and CountryOfPapers database fields
SJR Impact
16,586
H-index
660
Docs (year)
393
Docs 3y
808
Total refs
18156
Cites 3y
16352
Citable 3y
588
Cites/Doc 2y
16.08
Ref/Doc
46.2
Immediate OA
9500 €
Embargoed OA
NPD
Non OA / Submission
0 €
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Researcher reviews
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
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Merlin—rapid analysis of dense genetic maps using sparse gene flow trees
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
An array of problems
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