Title | Citations | PageRank | Year |
---|---|---|---|
Ensembl 2019. | 2 | 0.38 | 2019 |
Gencode Reference Annotation For The Human And Mouse Genomes | 9 | 0.61 | 2019 |
Ensembl variation resources. | 0 | 0.34 | 2018 |
Ensembl 2017. | 0 | 0.34 | 2017 |
The New Nhgri-Ebi Catalog Of Published Genome-Wide Association Studies (Gwas Catalog) | 46 | 2.51 | 2017 |
Ensembl 2016. | 34 | 1.89 | 2016 |
Ensembl 2015. | 77 | 3.44 | 2015 |
Improving the Sequence Ontology terminology for genomic variant annotation | 1 | 0.41 | 2015 |
Locus Reference Genomic: Reference Sequences For The Reporting Of Clinically Relevant Sequence Variants | 8 | 1.86 | 2014 |
Ensembl 2014. | 72 | 5.79 | 2014 |
Using GVF for Clinical Annotation of Personal Genomes. | 0 | 0.34 | 2012 |
Ensembl'S 10th Year | 52 | 6.01 | 2010 |
A database and API for variation, dense genotyping and resequencing data. | 17 | 2.53 | 2010 |
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor | 84 | 8.65 | 2010 |
Ensembl 2008. | 163 | 27.63 | 2008 |
Ensembl 2005. | 114 | 18.34 | 2007 |
Ensembl 2006. | 131 | 29.58 | 2006 |