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 em 2010

Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression

Por Almlöf, Jonas Carlsson, Lundmark, Per, Lundmark, Anders, Ge, Bing, Maouche, Seraya, Göring, Harald H. H., Liljedahl, Ulrika, Enström, Camilla, Brocheton, Jessy, Proust, Carole, Godefroy, Tiphaine, Sambrook, Jennifer G., Jolley, Jennifer, Crisp-Hihn, Abigail, Foad, Nicola, Lloyd-Jones, Heather, Stephens, Jonathan, Gwilliam, Rhian, Rice, Catherine M., Hengstenberg, Christian, Samani, Nilesh J., Erdmann, Jeanette, Schunkert, Heribert, Pastinen, Tomi, Deloukas, Panos, Goodall, Alison H., Ouwehand, Willem H., Cambien, François, Syvänen, Ann-Christine
Publicado em 2012

Mutations in tropomyosin 4 underlie a rare form of human macrothrombocytopenia

Por Pleines, Irina, Woods, Joanne, Chappaz, Stephane, Kew, Verity, Foad, Nicola, Ballester-Beltrán, José, Aurbach, Katja, Lincetto, Chiara, Lane, Rachael M., Schevzov, Galina, Alexander, Warren S., Hilton, Douglas J., Astle, William J., Downes, Kate, Nurden, Paquita, Westbury, Sarah K., Mumford, Andrew D., Obaji, Samya G., Collins, Peter W., Delerue, Fabien, Ittner, Lars M., Bryce, Nicole S., Holliday, Mira, Lucas, Christine A., Hardeman, Edna C., Ouwehand, Willem H., Gunning, Peter W., Turro, Ernest, Tijssen, Marloes R., Kile, Benjamin T.
Publicado no J Clin Invest (2017)

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 em 2009

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

Por Westbury, Sarah K, Turro, Ernest, Greene, Daniel, Lentaigne, Claire, Kelly, Anne M, Bariana, Tadbir K, Simeoni, Ilenia, Pillois, Xavier, Attwood, Antony, Austin, Steve, Jansen, Sjoert BG, Bakchoul, Tamam, Crisp-Hihn, Abi, Erber, Wendy N, Favier, Rémi, Foad, Nicola, Gattens, Michael, Jolley, Jennifer D, Liesner, Ri, Meacham, Stuart, Millar, Carolyn M, Nurden, Alan T, Peerlinck, Kathelijne, Perry, David J, Poudel, Pawan, Schulman, Sol, Schulze, Harald, Stephens, Jonathan C, Furie, Bruce, Robinson, Peter N, van Geet, Chris, Rendon, Augusto, Gomez, Keith, Laffan, Michael A, Lambert, Michele P, Nurden, Paquita, Ouwehand, Willem H, Richardson, Sylvia, Mumford, Andrew D, Freson, Kathleen
Publicado no Genome Med (2015)

Transcriptional diversity during lineage commitment of human blood progenitors

Por Chen, Lu, Kostadima, Myrto, Martens, Joost H.A., Canu, Giovanni, Garcia, Sara P., Turro, Ernest, Downes, Kate, Macaulay, Iain C., Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert B.G., Astle, William J., Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C., Consortium, BRIDGE, Choudry, Fizzah A., Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N., Jansen, Joop H., Favier, Rémi, Fenech, Matthew E., Foad, Nicola, Freson, Kathleen, van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M., Kerstens, Hindrik H.D., Kooner, Jaspal S., Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A., Richardson, David, Sammut, Stephen J., Slodkowicz, Greg, Tamuri, Asif U., Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J., Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H., Stunnenberg, Hendrik G., Frontini, Mattia, Rendon, Augusto
Publicado no Science (2014)

FTO genotype is associated with phenotypic variability of body mass index

Por Yang, Jian, Loos, Ruth J. F., Powell, Joseph E., Medland, Sarah E., Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Mägi, Reedik, Waite, Lindsay, Smith, Albert Vernon, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, Tõnu, Fischer, Krista, Zhao, Jing Hua, Demirkan, Ayşe, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an, Heard-Costa, Nancy L., White, Charles, Jackson, Anne U., Preuss, Michael, Ziegler, Andreas, Eriksson, Joel, Kutalik, Zoltán, Frau, Francesca, Nolte, Ilja M., Van Vliet-Ostaptchouk, Jana V., Hottenga, Jouke-Jan, Jacobs, Kevin B., Verweij, Niek, Goel, Anuj, Medina-Gomez, Carolina, Estrada, Karol, Bragg-Gresham, Jennifer Lynn, Sanna, Serena, Sidore, Carlo, Tyrer, Jonathan, Teumer, Alexander, Prokopenko, Inga, Mangino, Massimo, Lindgren, Cecilia M., Assimes, Themistocles L., Shuldiner, Alan R., Hui, Jennie, Beilby, John P., McArdle, Wendy L., Hall, Per, Haritunians, Talin, Zgaga, Lina, Kolcic, Ivana, Polasek, Ozren, Zemunik, Tatijana, Oostra, Ben A., Junttila, M. Juhani, Grönberg, Henrik, Schreiber, Stefan, Peters, Annette, Hicks, Andrew A., Stephens, Jonathan, Foad, Nicola S., Laitinen, Jaana, Pouta, Anneli, Kaakinen, Marika, Willemsen, Gonneke, Vink, Jacqueline M., Wild, Sarah H., Navis, Gerjan, Asselbergs, Folkert W., Homuth, Georg, John, Ulrich, Iribarren, Carlos, Harris, Tamara, Launer, Lenore, Gudnason, Vilmundur, O’Connell, Jeffrey R., Boerwinkle, Eric, Cadby, Gemma, Palmer, Lyle J., James, Alan L., Musk, Arthur W., Ingelsson, Erik, Psaty, Bruce M., Beckmann, Jacques S., Waeber, Gerard, Vollenweider, Peter, Hayward, Caroline, Wright, Alan F., Rudan, Igor, Groop, Leif C., Metspalu, Andres, Khaw, Kay Tee, van Duijn, Cornelia M., Borecki, Ingrid B., Province, Michael A., Wareham, Nicholas J., Tardif, Jean-Claude, Huikuri, Heikki V., Cupples, L. Adrienne, Atwood, Larry D., Fox, Caroline S., Boehnke, Michael, Collins, Francis S., Mohlke, Karen L., Erdmann, Jeanette, Schunkert, Heribert, Hengstenberg, Christian, Stark, Klaus, Lorentzon, Mattias, Ohlsson, Claes, Cusi, Daniele, Staessen, Jan A., Van der Klauw, Melanie M., Pramstaller, Peter P., Kathiresan, Sekar, Jolley, Jennifer D., Ripatti, Samuli, Jarvelin, Marjo-Riitta, de Geus, Eco J. C., Boomsma, Dorret I., Penninx, Brenda, Wilson, James F., Campbell, Harry, Chanock, Stephen J., van der Harst, Pim, Hamsten, Anders, Watkins, Hugh, Hofman, Albert, Witteman, Jacqueline C., Zillikens, M. Carola, Uitterlinden, André G., Rivadeneira, Fernando, Zillikens, M. Carola, Kiemeney, Lambertus A., Vermeulen, Sita H., Abecasis, Goncalo R., Schlessinger, David, Schipf, Sabine, Stumvoll, Michael, Tönjes, Anke, Spector, Tim D., North, Kari E., Lettre, Guillaume, McCarthy, Mark I., Berndt, Sonja I., Heath, Andrew C., Madden, Pamela A. F., Nyholt, Dale R., Montgomery, Grant W., Martin, Nicholas G., McKnight, Barbara, Strachan, David P., Hill, William G., Snieder, Harold, Ridker, Paul M., Thorsteinsdottir, Unnur, Stefansson, Kari, Frayling, Timothy M., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M.
Publicado em 2012