36.3(top 1%)
Impact Factor
39.1(top 1%)
extended IF
645(top 1%)
H-Index
16.7K
authors
7.1K
papers
2M
citations
14.3K
citing journals
387.9K
citing authors

Most Cited Articles of Nature Genetics

TitleYearCitations
Gene ontology: tool for the unification of biology. The Gene Ontology Consortium200025.6K
A framework for variation discovery and genotyping using next-generation DNA sequencing data20117.3K
Principal components analysis corrects for stratification in genome-wide association studies20067.1K
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes20035.8K
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase19954.7K
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals20034.6K
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results19954.6K
Generalized lacZ expression with the ROSA26 Cre reporter strain19994.3K
The Genotype-Tissue Expression (GTEx) project20134.2K
The Cancer Genome Atlas Pan-Cancer analysis project20133.9K
Combinatorial microRNA target predictions20053.8K
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 219993.8K
A general framework for estimating the relative pathogenicity of human genetic variants20143.6K
Minimum information about a microarray experiment (MIAME)-toward standards for microarray data20013.3K
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease19983.3K
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis19963.2K
Common SNPs explain a large proportion of the heritability for human height20102.9K
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells20002.9K
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees20022.9K
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease20132.7K
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness20062.6K
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP320012.5K
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing20082.5K
Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome20072.4K
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers19972.4K