Transcriptomic profiling facilitates classification of response to influenza challenge

por Davenport, Emma E., Antrobus, Richard D., Lillie, Patrick J., Gilbert, Sarah, Knight, Julian C.
Publicado 2014

Mechanistic study of the effect of Endothelin SNPs in microvascular angina – Protocol of the PRIZE Endothelin Sub-Study

por Abraham, George R., Morrow, Andrew J., Oliveira, Joana, Weir-McCall, Jonathan R., Davenport, Emma E., Berry, Colin, Davenport, Anthony P., Hoole, Stephen P.
Publicado 2022

IMPACT: Genomic Annotation of Cell-State-Specific Regulatory Elements Inferred from the Epigenome of Bound Transcription Factors

por Amariuta, Tiffany, Luo, Yang, Gazal, Steven, Davenport, Emma E., van de Geijn, Bryce, Ishigaki, Kazuyoshi, Westra, Harm-Jan, Teslovich, Nikola, Okada, Yukinori, Yamamoto, Kazuhiko, Price, Alkes L., Raychaudhuri, Soumya
Publicado 2019

Epstein-Barr virus reactivation in sepsis due to community-acquired pneumonia is associated with increased morbidity and an immunosuppressed host transcriptomic endotype

por Goh, Cyndi, Burnham, Katie L., Ansari, M. Azim, de Cesare, Mariateresa, Golubchik, Tanya, Hutton, Paula, Overend, Lauren E., Davenport, Emma E., Hinds, Charles J., Bowden, Rory, Knight, Julian C.
Publicado 2020

Genomic landscape of the individual host response and outcomes in sepsis: a prospective cohort study

por Davenport, Emma E, Burnham, Katie L, Radhakrishnan, Jayachandran, Humburg, Peter, Hutton, Paula, Mills, Tara C, Rautanen, Anna, Gordon, Anthony C, Garrard, Christopher, Hill, Adrian V S, Hinds, Charles J, Knight, Julian C
Publicado 2016

Inducible apelin receptor knockdown reduces differentiation efficiency and contractility of hESC-derived cardiomyocytes

por Macrae, Robyn G C, Colzani, Maria T, Williams, Thomas L, Bayraktar, Semih, Kuc, Rhoda E, Pullinger, Anna L, Bernard, William G, Robinson, Emma L, Davenport, Emma E, Maguire, Janet J, Sinha, Sanjay, Davenport, Anthony P
Publicado 2022

Genetically personalised organ-specific metabolic models in health and disease

por Foguet, Carles, Xu, Yu, Ritchie, Scott C., Lambert, Samuel A., Persyn, Elodie, Nath, Artika P., Davenport, Emma E., Roberts, David J., Paul, Dirk S., Di Angelantonio, Emanuele, Danesh, John, Butterworth, Adam S., Yau, Christopher, Inouye, Michael
Publicado 2022

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

por van Schouwenburg, Pauline A., Davenport, Emma E., Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C., Lockstone, Helen E., Cazier, Jean-Baptiste, Chapel, Helen M., Knight, Julian C., Patel, Smita Y.
Publicado 2015

Discovering in vivo cytokine-eQTL interactions from a lupus clinical trial

por Davenport, Emma E., Amariuta, Tiffany, Gutierrez-Arcelus, Maria, Slowikowski, Kamil, Westra, Harm-Jan, Luo, Yang, Shen, Ciyue, Rao, Deepak A., Zhang, Ying, Pearson, Stephen, von Schack, David, Beebe, Jean S., Bing, Nan, John, Sally, Vincent, Michael S., Zhang, Baohong, Raychaudhuri, Soumya
Publicado 2018

An immune dysfunction score for stratification of patients with acute infection based on whole blood gene expression

por Cano-Gamez, Eddie, Burnham, Katie L, Goh, Cyndi, Allcock, Alice, Malick, Zunaira H., Overend, Lauren, Kwok, Andrew, Smith, David A., Peters-Sengers, Hessel, Antcliffe, David, McKechnie, Stuart, Scicluna, Brendon P., van der Poll, Tom, Gordon, Anthony C., Hinds, Charles J., Davenport, Emma E., Knight, Julian C.
Publicado 2022

Transcriptional reprogramming from innate immune functions to a pro-thrombotic signature by monocytes in COVID-19

por Maher, Allison K., Burnham, Katie L., Jones, Emma M., Tan, Michelle M. H., Saputil, Rocel C., Baillon, Laury, Selck, Claudia, Giang, Nicolas, Argüello, Rafael, Pillay, Clio, Thorley, Emma, Short, Charlotte-Eve, Quinlan, Rachael, Barclay, Wendy S., Cooper, Nichola, Taylor, Graham P., Davenport, Emma E., Dominguez-Villar, Margarita
Publicado 2022

BurkHostGEN: a study protocol for evaluating variations in the Burkholderia pseudomallei and host genomes associated with melioidosis infection

por Angchagun, Kesorn, Boonklang, Phumrapee, Chomkatekaew, Chalita, Pakdeerat, Sukritpong, Wongsuwan, Gumphol, Amornchai, Premjit, Wuthiekanun, Vanaporn, Panapipat, Salwaluk, Ngernseng, Thatsanun, Waithira, Naomi, Walton, Steve, Limmathurotsakul, Direk, Surawong, Anoree, Siriboon, Suwatthiya, Chamnan, Parinya, Chantratita, Narisara, Dunachie, Susie, Corander, Jukka, Davenport, Emma E., Knight, Julian, Parkhill, Julian, Peacock, Sharon J., Thomson, Nicholas R., Day, Nicholas P.J., Chewapreecha, Claire
Publicado 2023

A community approach to mortality prediction in sepsis via gene expression analysis

por Sweeney, Timothy E., Perumal, Thanneer M., Henao, Ricardo, Nichols, Marshall, Howrylak, Judith A., Choi, Augustine M., Bermejo-Martin, Jesús F., Almansa, Raquel, Tamayo, Eduardo, Davenport, Emma E., Burnham, Katie L., Hinds, Charles J., Knight, Julian C., Woods, Christopher W., Kingsmore, Stephen F., Ginsburg, Geoffrey S., Wong, Hector R., Parnell, Grant P., Tang, Benjamin, Moldawer, Lyle L., Moore, Frederick E., Omberg, Larsson, Khatri, Purvesh, Tsalik, Ephraim L., Mangravite, Lara M., Langley, Raymond J.
Publicado 2018

Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study

por Rautanen, Anna, Mills, Tara C, Gordon, Anthony C, Hutton, Paula, Steffens, Michael, Nuamah, Rosamond, Chiche, Jean-Daniel, Parks, Tom, Chapman, Stephen J, Davenport, Emma E, Elliott, Katherine S, Bion, Julian, Lichtner, Peter, Meitinger, Thomas, Wienker, Thomas F, Caulfield, Mark J, Mein, Charles, Bloos, Frank, Bobek, Ilona, Cotogni, Paolo, Sramek, Vladimir, Sarapuu, Silver, Kobilay, Makbule, Ranieri, V Marco, Rello, Jordi, Sirgo, Gonzalo, Weiss, Yoram G, Russwurm, Stefan, Schneider, E Marion, Reinhart, Konrad, Holloway, Paul A H, Knight, Julian C, Garrard, Chris S, Russell, James A, Walley, Keith R, Stüber, Frank, Hill, Adrian V S, Hinds, Charles J
Publicado 2015

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

por Taylor, Jenny C, Martin, Hilary C, Lise, Stefano, Broxholme, John, Cazier, Jean-Baptiste, Rimmer, Andy, Kanapin, Alexander, Lunter, Gerton, Fiddy, Simon, Allan, Chris, Aricescu, A. Radu, Attar, Moustafa, Babbs, Christian, Becq, Jennifer, Beeson, David, Bento, Celeste, Bignell, Patricia, Blair, Edward, Buckle, Veronica J, Bull, Katherine, Cais, Ondrej, Cario, Holger, Chapel, Helen, Copley, Richard R, Cornall, Richard, Craft, Jude, Dahan, Karin, Davenport, Emma E, Dendrou, Calliope, Devuyst, Olivier, Fenwick, Aimée L, Flint, Jonathan, Fugger, Lars, Gilbert, Rodney D, Goriely, Anne, Green, Angie, Greger, Ingo H., Grocock, Russell, Gruszczyk, Anja V, Hastings, Robert, Hatton, Edouard, Higgs, Doug, Hill, Adrian, Holmes, Chris, Howard, Malcolm, Hughes, Linda, Humburg, Peter, Johnson, David, Karpe, Fredrik, Kingsbury, Zoya, Kini, Usha, Knight, Julian C, Krohn, Jonathan, Lamble, Sarah, Langman, Craig, Lonie, Lorne, Luck, Joshua, McCarthy, Davis, McGowan, Simon J, McMullin, Mary Frances, Miller, Kerry A, Murray, Lisa, Németh, Andrea H, Nesbit, M Andrew, Nutt, David, Ormondroyd, Elizabeth, Oturai, Annette Bang, Pagnamenta, Alistair, Patel, Smita Y, Percy, Melanie, Petousi, Nayia, Piazza, Paolo, Piret, Sian E, Polanco-Echeverry, Guadalupe, Popitsch, Niko, Powrie, Fiona, Pugh, Chris, Quek, Lynn, Robbins, Peter A, Robson, Kathryn, Russo, Alexandra, Sahgal, Natasha, van Schouwenburg, Pauline A, Schuh, Anna, Silverman, Earl, Simmons, Alison, Sørensen, Per Soelberg, Sweeney, Elizabeth, Taylor, John, Thakker, Rajesh V, Tomlinson, Ian, Trebes, Amy, Twigg, Stephen RF, Uhlig, Holm H, Vyas, Paresh, Vyse, Tim, Wall, Steven A, Watkins, Hugh, Whyte, Michael P, Witty, Lorna, Wright, Ben, Yau, Chris, Buck, David, Humphray, Sean, Ratcliffe, Peter J, Bell, John I, Wilkie, Andrew OM, Bentley, David, Donnelly, Peter, McVean, Gilean
Publicado 2015