Fiona Cunningham
Molecular Biology · 2004–2022
A researcher in the Science corpus: 32 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 576 citations into it
Whom Fiona Cunningham trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Martin Kircher
- Xiaoming Liu
- Jason Ernst
- Xueqiu Jian
- Prateek Kumar
- Ivan A. Adzhubei
- Hashem A. Shihab
- Benedict Paten
- B. Reva
- Zemin Ning
Who trusts Fiona Cunningham overall
Papers from Fiona Cunningham's perspective
Ordered by how strongly the researchers Fiona Cunningham trusts endorse each paper. Same corpus, a different order for every researcher.
- dbSNP: the NCBI database of genetic variation
- Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs. (Genome Research)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- Basic local alignment search tool.
- GENCODE: producing a reference annotation for ENCODE (Genome Biology)
- Ensembl’s 10th year (Nucleic Acids Res.)
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- The Human Gene Mutation Database: 2008 update
- A method and server for predicting damaging missense mutations
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Ensembl’s 10th year (2009) — 318 citations
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor — 1,610 citations
- The Ensembl Variant Effect Predictor (2016) — 7,148 citations
- Ensembl 2007 (2006) — 531 citations
- Ensembl 2011 (2010) — 480 citations
- Ensembl 2012 (2011) — 647 citations
- Ensembl 2009 (2008) — 549 citations
- Ensembl 2015 (2014) — 825 citations
- Ensembl 2014 (2013) — 908 citations
- Ensembl 2008 (2007) — 353 citations
- A joint NCBI and EMBL-EBI transcript set for clinical genomics and research (2022) — 465 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- Ensembl 2022 (2021) — 465 citations
- GENCODE reference annotation for the human and mouse genomes (2018) — 2,759 citations
- Ensembl 2020 (2019) — 1,385 citations
- Ensembl 2016 (2015) — 1,132 citations
- Ensembl variation resources (2010) — 307 citations
- Ensembl 2013 (2012) — 685 citations
- Ensembl 2018 (2017) — 2,474 citations