Nature Genetics

ISSN: 1061-4036

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Nature Genetics Q1 Unclaimed

Nature Publishing Group United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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 3000 €. 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: gene, human, disease, protein, cell, genetic, association, genome, identifies, variation, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Scopus WOS
Categories: Genetics (Q1)
Price

3000 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

Nature Genetics

18,861

SJR Impact factor

573

H Index

189

Total Docs (Last Year)

756

Total Docs (3 years)

9059

Total Refs

17158

Total Cites (3 years)

608

Citable Docs (3 years)

23,10

Cites/Doc (2 years)

47,93

Ref/Doc

Aims and Scope


gene, human, disease, protein, cell, genetic, association, genome, identifies, variation, sequencing, loci, type, study, kidney, expression, chromosome, encoding, evolution, mutations,



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Principal components analysis corrects for stratification in genome-wide association studies

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The Genotype-Tissue Expression (GTEx) project

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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Generalized lacZ expression with the ROSA26 Cre reporter strain

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The Cancer Genome Atlas Pan-Cancer analysis project

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A general framework for estimating the relative pathogenicity of human genetic variants

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

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Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells

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Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

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A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

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Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing

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The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

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Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome

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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

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Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2

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