Fiona Cunningham

Orcid: 0000-0002-7445-2419

According to our database1, Fiona Cunningham authored at least 38 papers between 2003 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of two.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource.
Nucleic Acids Res., January, 2023

Ensembl 2023.
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Nucleic Acids Res., January, 2023

GENCODE: reference annotation for the human and mouse genomes in 2023.
Nucleic Acids Res., January, 2023

2022
Ensembl 2022.
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Nucleic Acids Res., 2022

The European Variation Archive: a FAIR resource of genomic variation for all species.
Nucleic Acids Res., 2022

2021
Ensembl 2021.
Nucleic Acids Res., 2021

GENCODE 2021.
Nucleic Acids Res., 2021

2020
Whole-genome sequencing of patients with rare diseases in a national health system.
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Nat., 2020

Ensembl 2020.
Nucleic Acids Res., 2020

Annotation and curation of human genomic variations: an ELIXIR Implementation Study.
F1000Research, 2020

2019
GENCODE reference annotation for the human and mouse genomes.
Nucleic Acids Res., 2019

Ensembl 2019.
Nucleic Acids Res., 2019

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
Nucleic Acids Res., 2019

2018
Scaling up data curation using deep learning: An application to literature triage in genomic variation resources.
PLoS Comput. Biol., 2018

Ensembl 2018.
Nucleic Acids Res., 2018

Ensembl variation resources.
Database J. Biol. Databases Curation, 2018

2017
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).
Nucleic Acids Res., 2017

Ensembl 2017.
Nucleic Acids Res., 2017

2016
Ensembl 2016.
Nucleic Acids Res., 2016

2015
Ensembl 2015.
Nucleic Acids Res., 2015

Improving the Sequence Ontology terminology for genomic variant annotation.
J. Biomed. Semant., 2015

2014
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants.
Nucleic Acids Res., 2014

Ensembl 2014.
Nucleic Acids Res., 2014

2013
Ensembl 2013.
Nucleic Acids Res., 2013

2012
Ensembl 2012.
Nucleic Acids Res., 2012

Using GVF for Clinical Annotation of Personal Genomes.
Proceedings of the Workshop on Annotation, 2012

2011
Ensembl 2011.
Nucleic Acids Res., 2011

2010
Ensembl's 10th year.
Nucleic Acids Res., 2010

A database and API for variation, dense genotyping and resequencing data.
BMC Bioinform., 2010

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor.
Bioinform., 2010

2009
Ensembl 2009.
Nucleic Acids Res., 2009

2008
Ensembl 2008.
Nucleic Acids Res., 2008

2007
Ensembl 2007.
Nucleic Acids Res., 2007

2006
Ensembl 2006.
Nucleic Acids Res., 2006

2005
Ensembl 2005.
Nucleic Acids Res., 2005

WormBase: a comprehensive data resource for <i>Caenorhabditis</i> biology and genomics.
Nucleic Acids Res., 2005

2004
WormBase: a multi-species resource for nematode biology and genomics.
Nucleic Acids Res., 2004

2003
WormBase: a cross-species database for comparative genomics.
Nucleic Acids Res., 2003


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