5.2(top 5%)
impact factor
317(top 50%)
papers
1.6K(top 50%)
citations
20(top 50%)
h-index
5.5(top 5%)
extended IF
320
all documents
2.7K
doc citations
31(top 50%)
g-index

Top Articles

#TitleJournalYearCitations
1Population genomics of the critically endangered kākāpōCell Genomics2021106
2GA4GH: International policies and standards for data sharing across genomic research and healthcareCell Genomics202194
3Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomesCell Genomics202289
4Global Biobank Meta-analysis Initiative: Powering genetic discovery across human diseaseCell Genomics202285
5Benchmarking challenging small variants with linked and long readsCell Genomics202277
6Functional inference of gene regulation using single-cell multi-omicsCell Genomics202274
7Uncovering novel mutational signatures by de novo extraction with SigProfilerExtractorCell Genomics202274
8PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsCell Genomics202272
9Functional repertoire convergence of distantly related eukaryotic plankton lineages abundant in the sunlit oceanCell Genomics202270
10Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-spaceCell Genomics202259
11Single nucleus multi-omics identifies human cortical cell regulatory genome diversityCell Genomics202258
12Direct detection of RNA modifications and structure using single-molecule nanopore sequencingCell Genomics202255
13Genome-wide spatial expression profiling in formalin-fixed tissuesCell Genomics202145
14Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed programCell Genomics202240
15Molecular analysis of TCGA breast cancer histologic typesCell Genomics202137
16DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouseCell Genomics202237
17Unscrambling cancer genomes via integrated analysis of structural variation and copy numberCell Genomics202234
18Machine learning enables new insights into genetic contributions to liver fat accumulationCell Genomics202134
19Genome-wide risk prediction of common diseases across ancestries in one million peopleCell Genomics202234
20Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilitiesCell Genomics202232
21The Data Use Ontology to streamline responsible access to human biomedical datasetsCell Genomics202131
22Transcriptome-wide Cas13 guide RNA design for model organisms and viral RNA pathogensCell Genomics202130
23The female protective effect against autism spectrum disorderCell Genomics202230
24Meta-analysis fine-mapping is often miscalibrated at single-variant resolutionCell Genomics202230
25Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMedCell Genomics202229
26Regulation of protein abundance in genetically diverse mouse populationsCell Genomics202127
27The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patientsCell Genomics202327
28Association of mitochondrial DNA copy number with cardiometabolic diseasesCell Genomics202126
29Drug screening and genome editing in human pancreatic cancer organoids identifies drug-gene interactions and candidates for off-label therapyCell Genomics202226
30Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer’s disease-specific cis-regulatory elementsCell Genomics202323
31Workshop proceedings: GWAS summary statistics standards and sharingCell Genomics202122
32International federation of genomic medicine databases using GA4GH standardsCell Genomics202122
33Taiwan Biobank: A rich biomedical research database of the Taiwanese populationCell Genomics202221
34Immune disease variants modulate gene expression in regulatory CD4+ T cellsCell Genomics202220
35The HUNT study: A population-based cohort for genetic researchCell Genomics202220
36The human inactive X chromosome modulates expression of the active X chromosomeCell Genomics202320
37Resolution of structural variation in diverse mouse genomes reveals chromatin remodeling due to transposable elementsCell Genomics202320
38SNP-to-gene linking strategies reveal contributions of enhancer-related and candidate master-regulator genes to autoimmune diseaseCell Genomics202219
39Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic EuropeCell Genomics202319
40GA4GH Passport standard for digital identity and access permissionsCell Genomics202118
41The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identificationCell Genomics202118
42Population dynamics and genetic connectivity in recent chimpanzee historyCell Genomics202218
43Sequencing-based genome-wide association studies reporting standardsCell Genomics202117
44Empirical validation of an automated approach to data use oversightCell Genomics202117
45High-throughput characterization of the role of non-B DNA motifs on promoter functionCell Genomics202217
46Incorporating family history of disease improves polygenic risk scores in diverse populationsCell Genomics202217
47Single-cell multiome of the human retina and deep learning nominate causal variants in complex eye diseasesCell Genomics202217
48Expanding the genomic encyclopedia of Actinobacteria with 824 isolate reference genomesCell Genomics202216
49Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversityCell Genomics202216
50GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndromeCell Genomics202115