Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data

por Lyne, Rachel, Burns, Gavin, Mata, Juan, Penkett, Chris J, Rustici, Gabriella, Chen, Dongrong, Langford, Cordelia, Vetrie, David, Bähler, Jürg
Publicado 2003

Selective nuclear export of specific classes of mRNA from mammalian nuclei is promoted by GANP

por Wickramasinghe, Vihandha O., Andrews, Robert, Ellis, Peter, Langford, Cordelia, Gurdon, John B., Stewart, Murray, Venkitaraman, Ashok R., Laskey, Ronald A.
Publicado 2014

The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss

por Linden Phillips, Luan, Bitner-Glindzicz, Maria, Lench, Nicholas, Steel, Karen P., Langford, Cordelia, Dawson, Sally J., Davis, Adrian, Simpson, Sue, Packer, Claire
Publicado 2013

GENETICS OF GENE EXPRESSION IN PRIMARY IMMUNE CELLS IDENTIFIES CELL-SPECIFIC MASTER REGULATORS AND ROLES OF HLA ALLELES

por Fairfax, Benjamin P, Makino, Seiko, Radhakrishnan, Jayachandran, Plant, Katharine, Leslie, Stephen, Dilthey, Alexander, Ellis, Peter, Langford, Cordelia, Vannberg, Fredrik O, Knight, Julian C
Publicado 2012

Genome-Wide Screening for Genetic Alterations in Esophageal Cancer by aCGH Identifies 11q13 Amplification Oncogenes Associated with Nodal Metastasis

por Ying, Jianming, Shan, Ling, Li, Jisheng, Zhong, Lan, Xue, Liyan, Zhao, Hong, Li, Lili, Langford, Cordelia, Guo, Lei, Qiu, Tian, Lu, Ning, Tao, Qian
Publicado 2012

FRT-seq: Amplification-free, strand-specific, transcriptome sequencing

por Mamanova, Lira, Andrews, Robert M., James, Keith D., Sheridan, Elizabeth M., Ellis, Peter D., Langford, Cordelia F., Ost, Tobias W.B., Collins, John E., Turner, Daniel J.
Publicado 2010

Identification of candidate genes linking systemic inflammation to atherosclerosis; results of a human in vivo LPS infusion study

por Sivapalaratnam, Suthesh, Farrugia, Rosienne, Nieuwdorp, Max, Langford, Cordelia F, van Beem, Rachel T, Maiwald, Stephanie, Zwaginga, Jaap Jan, Gusnanto, Arief, Watkins, Nicholas A, Trip, Mieke D, Ouwehand, Willem H
Publicado 2011

A Novel CpG Island Set Identifies Tissue-Specific Methylation at Developmental Gene Loci

por Illingworth, Robert, Kerr, Alastair, DeSousa, Dina, Jørgensen, Helle, Ellis, Peter, Stalker, Jim, Jackson, David, Clee, Chris, Plumb, Robert, Rogers, Jane, Humphray, Sean, Cox, Tony, Langford, Cordelia, Bird, Adrian
Publicado 2008

Tissue-specific variation in DNA methylation levels along human chromosome 1

por De Bustos, Cecilia, Ramos, Edward, Young, Janet M, Tran, Robert K, Menzel, Uwe, Langford, Cordelia F, Eichler, Evan E, Hsu, Li, Henikoff, Steve, Dumanski, Jan P, Trask, Barbara J
Publicado 2009

Genomic Approaches Uncover Increasing Complexities in the Regulatory Landscape at the Human SCL (TAL1) Locus

por Dhami, Pawandeep, Bruce, Alexander W., Jim, Johanna H., Dillon, Shane C., Hall, Amanda, Cooper, Jonathan L., Bonhoure, Nicolas, Chiang, Kelly, Ellis, Peter D., Langford, Cordelia, Andrews, Robert M., Vetrie, David
Publicado 2010

Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis

por Tomazou, Eleni M, Rakyan, Vardhman K, Lefebvre, Gregory, Andrews, Robert, Ellis, Peter, Jackson, David K, Langford, Cordelia, Francis, Matthew D, Bäckdahl, Liselotte, Miretti, Marcos, Coggill, Penny, Ottaviani, Diego, Sheer, Denise, Murrell, Adele, Beck, Stephan
Publicado 2008

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

por Lewis, Morag A, Quint, Elizabeth, Glazier, Anne M, Fuchs, Helmut, De Angelis, Martin Hrabé, Langford, Cordelia, van Dongen, Stijn, Abreu-Goodger, Cei, Piipari, Matias, Redshaw, Nick, Dalmay, Tamas, Pelayo, Miguel Angel Moreno, Enright, Anton J, Steel, Karen P
Publicado 2009

Complex Exon-Intron Marking by Histone Modifications Is Not Determined Solely by Nucleosome Distribution

por Dhami, Pawandeep, Saffrey, Peter, Bruce, Alexander W., Dillon, Shane C., Chiang, Kelly, Bonhoure, Nicolas, Koch, Christoph M., Bye, Jackie, James, Keith, Foad, Nicola S., Ellis, Peter, Watkins, Nicholas A., Ouwehand, Willem H., Langford, Cordelia, Andrews, Robert M., Dunham, Ian, Vetrie, David
Publicado 2010

5′ isomiR variation is of functional and evolutionary importance

por Tan, Geok Chin, Chan, Elcie, Molnar, Attila, Sarkar, Rupa, Alexieva, Diana, Isa, Ihsan Mad, Robinson, Sophie, Zhang, Shuchen, Ellis, Peter, Langford, Cordelia F., Guillot, Pascale V., Chandrashekran, Anil, Fisk, Nick M., Castellano, Leandro, Meister, Gunter, Winston, Robert M., Cui, Wei, Baulcombe, David, Dibb, Nick J.
Publicado 2014

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

por Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Publicado 2009

A HaemAtlas: characterizing gene expression in differentiated human blood cells

por Watkins, Nicholas A., Gusnanto, Arief, de Bono, Bernard, De, Subhajyoti, Miranda-Saavedra, Diego, Hardie, Debbie L., Angenent, Will G. J., Attwood, Antony P., Ellis, Peter D., Erber, Wendy, Foad, Nicola S., Garner, Stephen F., Isacke, Clare M., Jolley, Jennifer, Koch, Kerstin, Macaulay, Iain C., Morley, Sarah L., Rendon, Augusto, Rice, Kate M., Taylor, Niall, Thijssen-Timmer, Daphne C., Tijssen, Marloes R., van der Schoot, C. Ellen, Wernisch, Lorenz, Winzer, Thilo, Dudbridge, Frank, Buckley, Christopher D., Langford, Cordelia F., Teichmann, Sarah, Göttgens, Berthold, Ouwehand, Willem H.
Publicado 2009

Genomic epidemiology of COVID-19 in care homes in the east of England

por Hamilton, William L, Tonkin-Hill, Gerry, Smith, Emily R, Aggarwal, Dinesh, Houldcroft, Charlotte J, Warne, Ben, Meredith, Luke W, Hosmillo, Myra, Jahun, Aminu S, Curran, Martin D, Parmar, Surendra, Caller, Laura G, Caddy, Sarah L, Khokhar, Fahad A, Yakovleva, Anna, Hall, Grant, Feltwell, Theresa, Pinckert, Malte L, Georgana, Iliana, Chaudhry, Yasmin, Brown, Colin S, Gonçalves, Sonia, Amato, Roberto, Harrison, Ewan M, Brown, Nicholas M, Beale, Mathew A, Spencer Chapman, Michael, Jackson, David K, Johnston, Ian, Alderton, Alex, Sillitoe, John, Langford, Cordelia, Dougan, Gordon, Peacock, Sharon J, Kwiatowski, Dominic P, Goodfellow, Ian G, Torok, M Estee
Publicado 2021

Patterns of within-host genetic diversity in SARS-CoV-2

por Tonkin-Hill, Gerry, Martincorena, Inigo, Amato, Roberto, Lawson, Andrew RJ, Gerstung, Moritz, Johnston, Ian, Jackson, David K, Park, Naomi, Lensing, Stefanie V, Quail, Michael A, Gonçalves, Sónia, Ariani, Cristina, Spencer Chapman, Michael, Hamilton, William L, Meredith, Luke W, Hall, Grant, Jahun, Aminu S, Chaudhry, Yasmin, Hosmillo, Myra, Pinckert, Malte L, Georgana, Iliana, Yakovleva, Anna, Caller, Laura G, Caddy, Sarah L, Feltwell, Theresa, Khokhar, Fahad A, Houldcroft, Charlotte J, Curran, Martin D, Parmar, Surendra, Alderton, Alex, Nelson, Rachel, Harrison, Ewan M, Sillitoe, John, Bentley, Stephen D, Barrett, Jeffrey C, Torok, M Estee, Goodfellow, Ian G, Langford, Cordelia, Kwiatkowski, Dominic
Publicado 2021

High density genetic mapping identifies new susceptibility loci for rheumatoid arthritis

por Eyre, Steve, Bowes, John, Diogo, Dorothée, Lee, Annette, Barton, Anne, Martin, Paul, Zhernakova, Alexandra, Stahl, Eli, Viatte, Sebastien, McAllister, Kate, Amos, Christopher I., Padyukov, Leonid, Toes, Rene E.M., Huizinga, Tom W.J., Wijmenga, Cisca, Trynka, Gosia, Franke, Lude, Westra, Harm-Jan, Alfredsson, Lars, Hu, Xinli, Sandor, Cynthia, de Bakker, Paul I.W., Davila, Sonia, Khor, Chiea Chuen, Heng, Khai Koon, Andrews, Robert, Edkins, Sarah, Hunt, Sarah E, Langford, Cordelia, Symmons, Deborah, Concannon, Pat, Onengut-Gumuscu, Suna, Rich, Stephen S, Deloukas, Panos, Gonzalez-Gay, Miguel A., Rodriguez-Rodriguez, Luis, Ärlsetig, Lisbeth, Martin, Javier, Rantapää-Dahlqvist, Solbritt, Plenge, Robert, Raychaudhuri, Soumya, Klareskog, Lars, Gregersen, Peter K, Worthington, Jane
Publicado 2012

Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21

por Spencer, Chris C.A., Plagnol, Vincent, Strange, Amy, Gardner, Michelle, Paisan-Ruiz, Coro, Band, Gavin, Barker, Roger A., Bellenguez, Celine, Bhatia, Kailash, Blackburn, Hannah, Blackwell, Jennie M., Bramon, Elvira, Brown, Martin A., Brown, Matthew A., Burn, David, Casas, Juan-Pablo, Chinnery, Patrick F., Clarke, Carl E., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Edkins, Sarah, Evans, Jonathan, Freeman, Colin, Gray, Emma, Hardy, John, Hudson, Gavin, Hunt, Sarah, Jankowski, Janusz, Langford, Cordelia, Lees, Andrew J., Markus, Hugh S., Mathew, Christopher G., McCarthy, Mark I., Morrison, Karen E., Palmer, Colin N.A., Pearson, Justin P., Peltonen, Leena, Pirinen, Matti, Plomin, Robert, Potter, Simon, Rautanen, Anna, Sawcer, Stephen J., Su, Zhan, Trembath, Richard C., Viswanathan, Ananth C., Williams, Nigel W., Morris, Huw R., Donnelly, Peter, Wood, Nicholas W.
Publicado 2011