A Potential New Role for Zinc in Age-Related Macular Degeneration through Regulation of Endothelial Fenestration

por Cunningham, Fiona, Cahyadi, Sabrina, Lengyel, Imre
Publicado 2021

Improving the Sequence Ontology terminology for genomic variant annotation

por Cunningham, Fiona, Moore, Barry, Ruiz-Schultz, Nicole, Ritchie, Graham RS, Eilbeck, Karen
Publicado 2015

Application of a modified gaseous exposure system to the in vitro toxicological assessment of tobacco smoke toxicants

por Breheny, Damien, Cunningham, Fiona, Kilford, Joanne, Payne, Rebecca, Dillon, Deborah, Meredith, Clive
Publicado 2014

Global Crises: Gendered Vulnerabilities of Structural Inequality, Environmental Performance, and Modern Slavery

por Cameron, Erinn C., Hemingway, Samantha L., Cunningham, Fiona J., Jacquin, Kristine M.
Publicado 2021

Eradication of early MRSA infection in cystic fibrosis: a novel study design for the STAR-ter trial

por Cunningham, Fiona, Caldwell, Ellen, Mayer-Hamblett, Nicole, Goss, Christopher H., Muhlebach, Marianne S.
Publicado 2022

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

por McLaren, William, Pritchard, Bethan, Rios, Daniel, Chen, Yuan, Flicek, Paul, Cunningham, Fiona
Publicado 2010

Impact of the SARS-CoV-2 pandemic on cystic fibrosis centres and care: survey results from US centres

por Muhlebach, Marianne S., Cunningham, Fiona, LiPuma, John J., Zhou, Juyan J., Saiman, Lisa
Publicado 2021

A database and API for variation, dense genotyping and resequencing data

por Rios, Daniel, McLaren, William M, Chen, Yuan, Birney, Ewan, Stabenau, Arne, Flicek, Paul, Cunningham, Fiona
Publicado 2010

The Ensembl Variant Effect Predictor

por McLaren, William, Gil, Laurent, Hunt, Sarah E., Riat, Harpreet Singh, Ritchie, Graham R. S., Thormann, Anja, Flicek, Paul, Cunningham, Fiona
Publicado 2016

DECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research

por Foreman, Julia, Brent, Simon, Perrett, Daniel, Bevan, Andrew P., Hunt, Sarah E., Cunningham, Fiona, Hurles, Matthew E., Firth, Helen V.
Publicado 2022

A standard variation file format for human genome sequences

por Reese, Martin G, Moore, Barry, Batchelor, Colin, Salas, Fidel, Cunningham, Fiona, Marth, Gabor T, Stein, Lincoln, Flicek, Paul, Yandell, Mark, Eilbeck, Karen
Publicado 2010

The value of primary transcripts to the clinical and non‐clinical genomics community: Survey results and roadmap for improvements

por Morales, Joannella, McMahon, Aoife C., Loveland, Jane, Perry, Emily, Frankish, Adam, Hunt, Sarah, Armean, Irina M., Flicek, Paul, Cunningham, Fiona
Publicado 2021

Ensembl variation resources

por Hunt, Sarah E, McLaren, William, Gil, Laurent, Thormann, Anja, Schuilenburg, Helen, Sheppard, Dan, Parton, Andrew, Armean, Irina M, Trevanion, Stephen J, Flicek, Paul, Cunningham, Fiona
Publicado 2018

Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

por MacArthur, Jacqueline A. L., Morales, Joannella, Tully, Ray E., Astashyn, Alex, Gil, Laurent, Bruford, Elspeth A., Larsson, Pontus, Flicek, Paul, Dalgleish, Raymond, Maglott, Donna R., Cunningham, Fiona
Publicado 2014

Scaling up data curation using deep learning: An application to literature triage in genomic variation resources

por Lee, Kyubum, Famiglietti, Maria Livia, McMahon, Aoife, Wei, Chih-Hsuan, MacArthur, Jacqueline Ann Langdon, Poux, Sylvain, Breuza, Lionel, Bridge, Alan, Cunningham, Fiona, Xenarios, Ioannis, Lu, Zhiyong
Publicado 2018

The European Variation Archive: a FAIR resource of genomic variation for all species

por Cezard, Timothe, Cunningham, Fiona, Hunt, Sarah E, Koylass, Baron, Kumar, Nitin, Saunders, Gary, Shen, April, Silva, Andres F, Tsukanov, Kirill, Venkataraman, Sundararaman, Flicek, Paul, Parkinson, Helen, Keane, Thomas M
Publicado 2021

Ensembl variation resources

por Chen, Yuan, Cunningham, Fiona, Rios, Daniel, McLaren, William M, Smith, James, Pritchard, Bethan, Spudich, Giulietta M, Brent, Simon, Kulesha, Eugene, Marin-Garcia, Pablo, Smedley, Damian, Birney, Ewan, Flicek, Paul
Publicado 2010

Haplosaurus computes protein haplotypes for use in precision drug design

por Spooner, William, McLaren, William, Slidel, Timothy, Finch, Donna K., Butler, Robin, Campbell, Jamie, Eghobamien, Laura, Rider, David, Kiefer, Christine Mione, Robinson, Matthew J., Hardman, Colin, Cunningham, Fiona, Vaughan, Tristan, Flicek, Paul, Huntington, Catherine Chaillan
Publicado 2018

Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor—A tutorial

por Hunt, Sarah E., Moore, Benjamin, Amode, Ridwan M., Armean, Irina M., Lemos, Diana, Mushtaq, Aleena, Parton, Andrew, Schuilenburg, Helen, Szpak, Michał, Thormann, Anja, Perry, Emily, Trevanion, Stephen J., Flicek, Paul, Yates, Andrew D., Cunningham, Fiona
Publicado 2022

The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

por MacArthur, Jacqueline, Bowler, Emily, Cerezo, Maria, Gil, Laurent, Hall, Peggy, Hastings, Emma, Junkins, Heather, McMahon, Aoife, Milano, Annalisa, Morales, Joannella, Pendlington, Zoe May, Welter, Danielle, Burdett, Tony, Hindorff, Lucia, Flicek, Paul, Cunningham, Fiona, Parkinson, Helen
Publicado 2017