Not logged in Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease Watt, Stephen; Vasquez, Louella; Walter, Klaudia; Mann, Alice L.; Kundu, Kousik; Chen, Lu; Sims, Ying; Ecker, Simone; Burden, Frances; Farrow, Samantha; Farr, Ben; Iotchkova, Valentina; Elding, Heather; Mead, Daniel; Tardaguila, Manuel; Ponstingl, Hannes; Richardson, David; Datta, Avik; Flicek, Paul; Clarke, Laura; Downes, Kate; Pastinen, Tomi; Fraser, Peter; Frontini, Mattia; Javierre, Biola-Maria; Spivakov, Mikhail; Soranzo, Nicole Share Save
BioSamples database: an updated sample metadata hub Courtot, Melanie; Cherubin, Luca; Faulconbridge, Adam; Vaughan, Daniel; Green, Matthew; Richardson, David; Harrison, Peter; Whetzel, Patricia L.; Parkinson, Helen; Burdett, Tony Share Save
The BLUEPRINT Data Analysis Portal Maria Fernandez, Jose; de la Torre, Victor; Richardson, David; Royo, Romina; Puiggros, Montserrat; Moncunill, Valenti; Fragkogianni, Stamatina; Clarke, Laura; Flicek, Paul; Rico, Daniel; Torrents, David; de Santa Pau, Enrique Carrillo; Valencia, Alfonso Share Save
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics de Angelis, Martin Hrabe; Nicholson, George; Selloum, Mohammed; White, Jacqueline K.; Morgan, Hugh; Ramirez-Solis, Ramiro; Sorg, Tania; Wells, Sara; Fuchs, Helmut; Fray, Martin; Adams, David J.; Adams, Niels C.; Adler, Thure; Aguilar-Pimentel, Antonio; Ali-Hadji, Dalila; Amann, Gregory; Andre, Philippe; Atkins, Sarah; Auburtin, Aurelie; Ayadi, Abdel; Becker, Julien; Becker, Lore; Bedu, Elodie; Bekeredjian, Raffi; Birling, Marie-Christine; Blake, Andrew; Bottomley, Joanna; Bowl, Michael R.; Brault, Veronique; Busch, Dirk H.; Bussell, James N.; Calzada-Wack, Julia; Cater, Heather; Champy, Marie-France; Charles, Philippe; Chevalier, Claire; Chiani, Francesco; Codner, Gemma F.; Combe, Roy; Cox, Roger; Dalloneau, Emilie; Dierich, Andre; Di Fenza, Armida; Doe, Brendan; Duchon, Arnaud; Eickelberg, Oliver; Esapa, Chris T.; El Fertak, Lahcen; Feigel, Tanja; Emelyanova, Irina; Estabel, Jeanne; Favor, Jack; Flenniken, Ann; Gambadoro, Alessia; Garrett, Lilian; Gates, Hilary; Gerdin, Anna-Karin; Gkoutos, George; Greenaway, Simon; Glasl, Lisa; Goetz, Patrice; Da Cruz, Isabelle Goncalves; Goetz, Alexander; Graw, Jochen; Guimond, Alain; Hans, Wolfgang; Hicks, Geoff; Hoelter, Sabine M.; Hoefler, Heinz; Hancock, John M.; Hoehndorf, Robert; Hough, Tertius; Houghton, Richard; Hurt, Anja; Ivandic, Boris; Jacobs, Hughes; Jacquot, Sylvie; Jones, Nora; Karp, Natasha A.; Katus, Hugo A.; Kitchen, Sharon; Klein-Rodewald, Tanja; Klingenspor, Martin; Klopstock, Thomas; Lalanne, Valerie; Leblanc, Sophie; Lengger, Christoph; le Marchand, Elise; Ludwig, Tonia; Lux, Aline; McKerlie, Colin; Maier, Holger; Mandel, Jean-Louis; Marschall, Susan; Mark, Manuel; Melvin, David G.; Meziane, Hamid; Micklich, Kateryna; Mittelhauser, Christophe; Monassier, Laurent; Moulaert, David; Muller, Stephanie; Naton, Beatrix; Neff, Frauke; Nolan, Patrick M.; Nutter, Lauryl M. J.; Ollert, Markus; Pavlovic, Guillaume; Pellegata, Natalia S.; Peter, Emilie; Petit-Demouliere, Benoit; Pickard, Amanda; Podrini, Christine; Potter, Paul; Pouilly, Laurent; Puk, Oliver; Richardson, David; Rousseau, Stephane; Quintanilla-Fend, Leticia; Quwailid, Mohamed M.; Racz, Ildiko; Rathkolb, Birgit; Riet, Fabrice; Rossant, Janet; Roux, Michel; Rozman, Jan; Ryder, Edward; Salisbury, Jennifer; Santos, Luis; Schaeble, Karl-Heinz; Schiller, Evelyn; Schrewe, Anja; Schulz, Holger; Steinkamp, Ralf; Simon, Michelle; Stewart, Michelle; Stoeger, Claudia; Stoeger, Tobias; Sun, Minxuan; Sunter, David; Teboul, Lydia; Tilly, Isabelle; Tocchini-Valentini, Glauco P.; Tost, Monica; Treise, Irina; Vasseur, Laurent; Velot, Emilie; Vogt-Weisenhorn, Daniela; Wagner, Christelle; Walling, Alison; Wattenhofer-Donze, Marie; Weber, Bruno; Wendling, Olivia; Westerberg, Henrik; Willershaeuser, Monja; Wolf, Eckhard; Wolter, Anne; Wood, Joe; Wurst, Wolfgang; Yildirim, Ali Oender; Zeh, Ramona; Zimmer, Andreas; Zimprich, Annemarie; Holmes, Chris; Steel, Karen P.; Herault, Yann; Gailus-Durner, Valerie; Mallon, Ann-Marie; Brown, Steve D. M. Share Save
Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers Agirre, Xabier; Castellano, Giancarlo; Pascual, Marien; Heath, Simon; Kulis, Marta; Segura, Victor; Bergmann, Anke; Esteve, Anna; Merkel, Angelika; Raineri, Emanuele; Agueda, Lidia; Blanc, Julie; Richardson, David; Clarke, Laura; Datta, Avik; Russinol, Nuria; Queiros, Ana C.; Beekman, Renee; Rodriguez-Madoz, Juan R.; San Jose-Eneriz, Edurne; Fang, Fang; Gutierrez, Norma C.; Garcia-Verdugo, Jose M.; Robson, Michael I.; Schirmer, Eric C.; Guruceaga, Elisabeth; Martens, Joost H. A.; Gut, Marta; Calasanz, Maria J.; Flicek, Paul; Siebert, Reiner; Campo, Elias; San Miguel, Jesus F.; Melnick, Ari; Stunnenberg, Hendrik G.; Gut, Ivo G.; Prosper, Felipe; Martin-Subero, Jose I. Share Save
Communicating with the public: opportunities and rewards for individual ecologists Pace, Michael L.; Hampton, Stephanie E.; Limburg, Karin E.; Bennett, Elena M.; Cook, Elizabeth M.; Davis, Ann E.; Grove, J. Morgan; Kaneshiro, Kenneth Y.; LaDeau, Shannon L.; Likens, Gene E.; McKnight, Diane M.; Richardson, David C.; Strayer, David L. Share Save
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Tarpey, Patrick S.; Raymond, F. Lucy; Nguyen, Lam S.; Rodriguez, Jayson; Hackett, Anna; Vandeleur, Lucianne; Smith, Raffaella; Shoubridge, Cheryl; Edkins, Sarah; Stevens, Claire; O'Meara, Sarah; Tofts, Calli; Barthorpe, Syd; Buck, Gemma; Cole, Jennifer; Halliday, Kelly; Hills, Katy; Jones, David; Mironenko, Tatiana; Perry, Janet; Varian, Jennifer; West, Sofie; Widaa, Sara; Teague, John; Dicks, Ed; Butler, Adam; Menzies, Andrew; Richardson, David; Jenkinson, Andrew; Shepherd, Rebecca; Raine, Keiran; Moon, Jenny; Luo, Yin; Parnau, Josep; Bhat, Shambhu S.; Gardner, Alison; Corbett, Mark; Brooks, Doug; Thomas, Paul; Parkinson-Lawrence, Emma; Porteous, Mary E.; Warner, John P.; Sanderson, Tracy; Pearson, Pauline; Simensen, Richard J.; Skinner, Cindy; Hoganson, George; Superneau, Duane; Wooster, Richard; Bobrow, Martin; Turner, Gillian; Stevenson, Roger E.; Schwartz, Charles E.; Futreal, P. Andrew; Srivastava, Anand K.; Stratton, Michael R.; Gecz, Jozef Share Save
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly Field, Michael; Tarpey, Patrick S.; Smith, Raffaella; Edkins, Sarah; O'Meara, Sarah; Stevens, Claire; Tofts, Calli; Teague, Jon; Butler, Adam; Dicks, Ed; Barthorpe, Syd; Buck, Gemma; Cole, Jennifer; Gray, Kristian; Halliday, Kelly; Hills, Katy; Jenkinson, Andrew; Jones, David; Menzies, Andrew; Mironenko, Tatiana; Perry, Janet; Raine, Keiran; Richardson, David; Shepherd, Rebecca; Small, Alexandra; Varian, Jennifer; West, Sofie; Widaa, Sara; Mallya, Uma; Wooster, Richard; Moon, Jenny; Luo, Ying; Hughes, Helen; Shaw, Marie; Friend, Kathryn L.; Corbett, Mark; Turner, Gillian; Partington, Michael; Mulley, John; Bobrow, Martin; Schwartz, Charles; Stevenson, Roger; Gecz, Jozef; Stratton, Michael R.; Futreal, P. Andrew; Raymond, F. Lucy Share Save
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor Tarpey, Patrick S.; Raymond, F. Lucy; O'Meara, Sarah; Edkins, Sarah; Teague, Jon; Butler, Adam; Dicks, Ed; Stevens, Claire; Tofts, Calli; Avis, Tim; Barthorpe, Syd; Buck, Gemma; Cole, Jennifer; Gray, Kristian; Halliday, Kelly; Harrison, Rachel; Hills, Katy; Jenkinson, Andrew; Jones, David; Menzies, Andrew; Mironenko, Tatiana; Perry, Janet; Raine, Keiran; Richardson, David; Shepherd, Rebecca; Small, Alexandra; Varian, Jennifer; West, Sofie; Widaa, Sara; Mallya, Uma; Moon, Jenny; Luo, Ying; Holder, Susan; Smithson, Sarah F.; Hurst, Jane A.; Clayton-Smith, Jill; Kerr, Bronwyn; Boyle, Jackie; Shaw, Marie; Vandeleur, Lucianne; Rodriguez, Jayson; Slaugh, Rachel; Easton, Douglas F.; Wooster, Richard; Bobrow, Martin; Srivastava, Anand K.; Stevenson, Roger E.; Schwartz, Charles E.; Turner, Gillian; Gecz, Jozef; Futreal, P. Andrew; Stratton, Michael R.; Partington, Michael Share Save
Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation Tarpey, Patrick S.; Stevens, Claire; Teague, Jon; Edkins, Sarah; O'Meara, Sarah; Avis, Tim; Barthorpe, Syd; Buck, Gemma; Butler, Adam; Cole, Jennifer; Dicks, Ed; Gray, Kristian; Halliday, Kelly; Harrison, Rachel; Hills, Katy; Hinton, Jonathon; Jones, David; Menzies, Andrew; Mironenko, Tatiana; Perry, Janet; Raine, Keiran; Richardson, David; Shepherd, Rebecca; Small, Alexandra; Tofts, Calli; Varian, Jennifer; West, Sofie; Widaa, Sara; Yates, Andy; Catford, Rachael; Butler, Julia; Mallya, Uma; Moon, Jenny; Luo, Ying; Dorkins, Huw; Thompson, Deborah; Easton, Douglas F.; Wooster, Richard; Bobrow, Martin; Carpenter, Nancy; Simensen, Richard J.; Schwartz, Charles E.; Stevenson, Roger E.; Turner, Gillian; Partington, Michael; Gecz, Jozef; Stratton, Michael R.; Futreal, P. Andrew; Raymond, F. Lucy Share Save
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set Ikediobi, Ogechi N.; Davies, Helen; Bignell, Graham; Edkins, Sarah; Stevens, Claire; O'Meara, Sarah; Santarius, Thomas; Avis, Tim; Barthorpe, Syd; Brackenbury, Lisa; Buck, Gemma; Butler, Adam; Clements, Jody; Cole, Jennifer; Dicks, Ed; Forbes, Simon; Gray, Kristian; Halliday, Kelly; Harrison, Rachel; Hills, Katy; Hinton, Jonathan; Hunter, Chris; Jenkinson, Andy; Jones, David; Kosmidou, Vivienne; Lugg, Richard; Menzies, Andrew; Mironenko, Tatiana; Parker, Adrian; Perry, Janet; Raine, Keiran; Richardson, David; Shepherd, Rebecca; Small, Alex; Smith, Raffaella; Solomon, Helen; Stephens, Philip; Teague, Jon; Tofts, Calli; Varian, Jennifer; Webb, Tony; West, Sofie; Widaa, Sara; Yates, Andy; Reinhold, William; Weinstein, John N.; Stratton, Michael R.; Futreal, P. Andrew; Wooster, Richard Share Save
A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy Hunter, C; Smith, R; Cahill, DP; Stephens, P; Stevens, C; Teague, J; Greenman, C; Edkins, S; Bignell, G; Davies, H; O'Meara, S; Parker, A; Avis, T; Barthorpe, S; Brackenbury, L; Buck, G; Butler, A; Clements, J; Cole, J; Dicks, E; Forbes, S; Gorton, M; Gray, K; Halliday, K; Harrison, R; Hills, K; Hinton, J; Jenkinson, A; Jones, D; Kosmidou, V; Laman, R; Lugg, R; Menzies, A; Perry, J; Petty, R; Raine, K; Richardson, D; Shepherd, R; Small, A; Solomon, H; Tofts, C; Varian, J; West, S; Widaa, S; Yates, A; Easton, DF; Riggins, G; Roy, JE; Levine, KK; Mueller, W; Batchelor, TT; Louis, DN; Stratton, MR; Futreal, PA; Wooster, R Share Save
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