PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels von Martin, Antonio Rueda, Williams, Eleanor, Foulger, Rebecca E., Leigh, Sarah, Daugherty, Louise C., Niblock, Olivia, Leong, Ivone U. S., Smith, Katherine R., Gerasimenko, Oleg, Haraldsdottir, Eik, Thomas, Ellen, Scott, Richard H., Baple, Emma, Tucci, Arianna, Brittain, Helen, de Burca, Anna, Ibañez, Kristina, Kasperaviciute, Dalia, Smedley, Damian, Caulfield, Mark, Rendon, Augusto, McDonagh, Ellen M.

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The 100 000 Genomes Project: bringing whole genome sequencing to the NHS von Turnbull, Clare, Scott, Richard H, Thomas, Ellen, Jones, Louise, Murugaesu, Nirupa, Pretty, Freya Boardman, Halai, Dina, Baple, Emma, Craig, Clare, Hamblin, Angela, Henderson, Shirley, Patch, Christine, O’Neill, Amanda, Devereaux, Andrew, Smith, Katherine, Martin, Antonio Rueda, Sosinsky, Alona, McDonagh, Ellen M, Sultana, Razvan, Mueller, Michael, Smedley, Damian, Toms, Adam, Dinh, Lisa, Fowler, Tom, Bale, Mark, Hubbard, Tim, Rendon, Augusto, Hill, Sue, Caulfield, Mark J

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The Distribution of the Anticancer Drug Doxorubicin in Relation to Blood Vessels in Solid Tumors von PRIMEAU, Andrew J, RENDON, Augusto, HEDLEY, David, LILGE, Lothar, TANNOCK, Ian F

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Newborn Screening by Genomic Sequencing: Opportunities and Challenges von Bick, David, Ahmed, Arzoo, Deen, Dasha, Ferlini, Alessandra, Garnier, Nicolas, Kasperaviciute, Dalia, Leblond, Mathilde, Pichini, Amanda, Rendon, Augusto, Satija, Aditi, Tuff-Lacey, Alice, Scott, Richard H

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Comparison of methods for competitive tests of pathway analysis von Evangelou, Marina, Rendon, Augusto, Ouwehand, Willem H, Wernisch, Lorenz, Dudbridge, Frank

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PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources von Perez-Gil, Daniel, Lopez, Francisco J, Dopazo, Joaquin, Marin-Garcia, Pablo, Rendon, Augusto, Medina, Ignacio

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Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans von Rotival, Maxime, Zeller, Tanja, Wild, Philipp S, Maouche, Seraya, Szymczak, Silke, Schillert, Arne, Castagné, Raphaele, Deiseroth, Arne, Proust, Carole, Brocheton, Jessy, Godefroy, Tiphaine, Perret, Claire, Germain, Marine, Eleftheriadis, Medea, Sinning, Christoph R, Schnabel, Renate B, Lubos, Edith, Lackner, Karl J, Rossmann, Heidi, Münzel, Thomas, Rendon, Augusto, Erdmann, Jeanette, Deloukas, Panos, Hengstenberg, Christian, Diemert, Patrick, Montalescot, Gilles, Ouwehand, Willem H, Samani, Nilesh J, Schunkert, Heribert, Tregouet, David-Alexandre, Ziegler, Andreas, Goodall, Alison H, Cambien, François, Tiret, Laurence, Blankenberg, Stefan

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A HaemAtlas: characterizing gene expression in differentiated human blood cells von 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., on behalf of the Bloodomics Consortium

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Transcription factor co-localization patterns affect human cell type-specific gene expression von Wang, Dennis, Rendon, Augusto, Ouwehand, Willem, Wernisch, Lorenz

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Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci von Paul, Dirk S, Albers, Cornelis A, Rendon, Augusto, Voss, Katrin, Stephens, Jonathan, van der Harst, Pim, Chambers, John C, Soranzo, Nicole, Ouwehand, Willem H, Deloukas, Panos

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Canonical Wnt signaling in megakaryocytes regulates proplatelet formation von Macaulay, Iain C., Thon, Jonathan N., Tijssen, Marloes R., Steele, Brian M., MacDonald, Bryan T., Meade, Gerardene, Burns, Philippa, Rendon, Augusto, Salunkhe, Vishal, Murphy, Ronan P., Bennett, Cavan, Watkins, Nicholas A., He, Xi, Fitzgerald, Desmond J., Italiano, Joseph E., Maguire, Patricia B.

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A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site von Nürnberg, Sylvia T., Rendon, Augusto, Smethurst, Peter A., Paul, Dirk S., Voss, Katrin, Thon, Jonathan N., Lloyd-Jones, Heather, Sambrook, Jennifer G., Tijssen, Marloes R., Italiano, Joseph E., Deloukas, Panos, Gottgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H.

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Monocyte gene expression signature of patients with early onset coronary artery disease von Sivapalaratnam, Suthesh, Basart, Hanneke, Watkins, Nicholas A, Maiwald, Stepanie, Rendon, Augusto, Krishnan, Unni, Sondermeijer, Brigitte M, Creemers, Esther E, Pinto-Sietsma, Sara J, Hovingh, Kees, Ouwehand, Willem H, Kastelein, John J P, Goodall, Alison H, Trip, Mieke D

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Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits von Paul, Dirk S, Nisbet, James P, Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R, Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D, Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H, Deloukas, Panos

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Treatment planning using tailored and standard cylindrical light diffusers for photodynamic therapy of the prostate von Rendon, Augusto, Beck, J Christopher, Lilge, Lothar

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Transcription factor and chromatin features predict genes associated with eQTLs von Wang, Dennis, Rendon, Augusto, Wernisch, Lorenz

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Re: Best et al., ‘Unlocking the potential of the UK 100,000 Genomes Project – Lessons learned from analysis of the “Congenital malformations caused by ciliopathies” cohort’... von Brown, Matthew A., Wigley, Christopher, Walker, Susan, Lancaster, Deborah, Rendon, Augusto, Scott, Richard

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Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme von Sosinsky, Alona, Ambrose, John, Cross, William, Turnbull, Clare, Henderson, Shirley, Jones, Louise, Hamblin, Angela, Arumugam, Prabhu, Chan, Georgia, Chubb, Daniel, Noyvert, Boris, Mitchell, Jonathan, Walker, Susan, Bowman, Katy, Pasko, Dorota, Buongermino Pereira, Marianna, Volkova, Nadezda, Rueda-Martin, Antonio, Perez-Gil, Daniel, Lopez, Javier, Pullinger, John, Siddiq, Afshan, Zainy, Tala, Choudhury, Tasnim, Yavorska, Olena, Fowler, Tom, Bentley, David, Kingsley, Clare, Hing, Sandra, Deans, Zandra, Rendon, Augusto, Hill, Sue, Caulfield, Mark, Murugaesu, Nirupa

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Signatures of TOP1 transcription-associated mutagenesis in cancer and germline von Reijns, Martin A. M., Parry, David A., Williams, Thomas C., Nadeu, Ferran, Hindshaw, Rebecca L., Rios Szwed, Diana O., Nicholson, Michael D., Carroll, Paula, Boyle, Shelagh, Royo, Romina, Cornish, Alex J., Xiang, Hang, Ridout, Kate, Schuh, Anna, Aden, Konrad, Palles, Claire, Campo, Elias, Stankovic, Tatjana, Taylor, Martin S., Jackson, Andrew P.

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A call to action to scale up research and clinical genomic data sharing von Stark, Zornitza, Glazer, David, Hofmann, Oliver, Rendon, Augusto, Marshall, Christian R, Ginsburg, Geoffrey S, Lunt, Chris, Allen, Naomi, Effingham, Mark, Hastings Ward, Jillian, Hill, Sue L, Ali, Raghib, Goodhand, Peter, Page, Angela, Rehm, Heidi L, North, Kathryn N, Scott, Richard H

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