The Gene Guessing Game

por Dunham, Ian
Publicado 2000

Applications of high-throughput sequencing to chromatin structure and function in mammals

por Dunham, Ian
Publicado 2009

Human genes: Time to follow the roads less traveled?

por Dunham, Ian
Publicado 2018

In silico prediction of novel therapeutic targets using gene–disease association data

por Ferrero, Enrico, Dunham, Ian, Sanseau, Philippe
Publicado 2017

Literature evidence in open targets - a target validation platform

por Kafkas, Şenay, Dunham, Ian, McEntyre, Johanna
Publicado 2017

Future prospects for human genetics and genomics in drug discovery

por Ghoussaini, Maya, Nelson, Matthew R., Dunham, Ian
Publicado 2023

The Characteristics of Human Genes: Analysis of Human Chromosome 22

por Dunham, Ian, Beare, David M., Collins, John E.
Publicado 2003

Functional annotation of non-coding sequence variants

por Ritchie, Graham R. S., Dunham, Ian, Zeggini, Eleftheria, Flicek, Paul
Publicado 2014

Systematic analysis of off-target effects in an RNAi screen reveals microRNAs affecting sensitivity to TRAIL-induced apoptosis

por Sudbery, Ian, Enright, Anton J, Fraser, Andrew G, Dunham, Ian
Publicado 2010

Uncovering new disease indications for G-protein coupled receptors and their endogenous ligands

por Freudenberg, Johannes M, Dunham, Ian, Sanseau, Philippe, Rajpal, Deepak K
Publicado 2018

Ten simple rules for delivering live distance training in bioinformatics across the globe using webinars

por Carvalho-Silva, Denise, Garcia, Leyla, Morgan, Sarah L., Brooksbank, Cath, Dunham, Ian
Publicado 2018

DNA methylation-histone modification relationships across the desmin locus in human primary cells

por Allen, Marianne Lindahl, Koch, Christoph M, Clelland, Gayle K, Dunham, Ian, Antoniou, Michael
Publicado 2009

Evidence That Replication-Associated Mutation Alone Does Not Explain Between-Chromosome Differences In Substitution Rates

por Pink, Catherine J., Swaminathan, Siva K., Dunham, Ian, Rogers, Jane, Ward, Andrew, Hurst, Laurence D.
Publicado 2009

The open targets post-GWAS analysis pipeline

por Peat, Gareth, Jones, William, Nuhn, Michael, Marugán, José Carlos, Newell, William, Dunham, Ian, Zerbino, Daniel
Publicado 2020

Cell-type-specific long-range looping interactions identify distant regulatory elements of the CFTR gene

por Gheldof, Nele, Smith, Emily M., Tabuchi, Tomoko M., Koch, Christoph M., Dunham, Ian, Stamatoyannopoulos, John A., Dekker, Job
Publicado 2010

The human homologue of unc-93 maps to chromosome 6q27 – characterisation and analysis in sporadic epithelial ovarian cancer

por Liu, Ying, Dodds, Phillippa, Emilion, Gracy, Mungall, Andrew J, Dunham, Ian, Beck, Stephan, Wells, R Spencer, Charnock, F Mark L, Ganesan, Trivadi S
Publicado 2002

Where Next for Genetics and Genomics?

por Tyler-Smith, Chris, Yang, Huanming, Landweber, Laura F., Dunham, Ian, Knoppers, Bartha M., Donnelly, Peter, Mardis, Elaine R., Snyder, Michael, McVean, Gil
Publicado 2015

Developing a cluster-based approach for deciphering complexity in individuals with neurodevelopmental differences

por Cuppens, Tania, Kaur, Manpreet, Kumar, Ajay A., Shatto, Julie, Ng, Andy Cheuk-Him, Leclercq, Mickael, Reformat, Marek Z., Droit, Arnaud, Dunham, Ian, Bolduc, François V.
Publicado 2023

Linking rare and common disease: mapping clinical disease-phenotypes to ontologies in therapeutic target validation

por Sarntivijai, Sirarat, Vasant, Drashtti, Jupp, Simon, Saunders, Gary, Bento, A. Patrícia, Gonzalez, Daniel, Betts, Joanna, Hasan, Samiul, Koscielny, Gautier, Dunham, Ian, Parkinson, Helen, Malone, James
Publicado 2016

Sex difference contributes to phenotypic diversity in individuals with neurodevelopmental disorders

por Cuppens, Tania, Shatto, Julie, Mangnier, Loïc, Kumar, Ajay A., Ng, Andy Cheuk-Him, Kaur, Manpreet, Bui, Truong An, Leclercq, Mickael, Droit, Arnaud, Dunham, Ian, Bolduc, Francois V.
Publicado 2023