Type 1 diabetes mellitus presenting with diabetic ketoacidosis in a child with Patau syndrome (trisomy 13) and persistent fetal haemoglobin

Por McTaggart, James Suntac, Sivasubramaniam, Sindugaa, Jewell, Rosalyn, Yong, James
Publicado no BMJ Case Rep (2021)

“Distinguishing Clinicopathologic Features of Patients with V600E and V600K BRAF-Mutant Metastatic Melanoma” – Letter

Por Jewell, Rosalyn, Chambers, Philip, Harland, Mark, Laye, Jon, Conway, Caroline, Mitra, Angana, Elliott, Faye, Cook, Martin G., Boon, Andy, Newton-Bishop, Julia
Publicado em 2012

Independent replication of a melanoma subtype gene signature and evaluation of its prognostic value and biological correlates in a population cohort

Por Nsengimana, Jérémie, Laye, Jon, Filia, Anastasia, Walker, Christy, Jewell, Rosalyn, Van den Oord, Joost J, Wolter, Pascal, Patel, Poulam, Sucker, Antje, Schadendorf, Dirk, Jönsson, Göran B, Bishop, D. Timothy, Newton-Bishop, Julia
Publicado no Oncotarget (2015)

Targeting human apurinic/apyrimidinic endonuclease 1 (APE1) in phosphatase and tensin homolog (PTEN) deficient melanoma cells for personalized therapy

Por Abbotts, Rachel, Jewell, Rosalyn, Nsengimana, Jérémie, Maloney, David J, Simeonov, Anton, Seedhouse, Claire, Elliott, Faye, Laye, Jon, Walker, Christy, Jadhav, Ajit, Grabowska, Anna, Ball, Graham, Patel, Poulam M, Newton-Bishop, Julia, Wilson, David M, Madhusudan, Srinivasan
Publicado em 2014

Gene expression profiling of paraffin embedded primary melanoma using the DASL assay identifies increased osteopontin expression as predictive of reduced relapse free survival

Por Conway, Caroline, Mitra, Angana, Jewell, Rosalyn, Randerson-Moor, Juliette, Lobo, Samira, Nsengimana, Jérémie, Edward, Sara, Sanders, D Scott, Cook, Martin, Powell, Barry, Boon, Andy, Elliott, Faye, de Kort, Floor, Knowles, Margaret A., Bishop, D. Timothy, Newton-Bishop, Julia
Publicado em 2009

β-Catenin–mediated immune evasion pathway frequently operates in primary cutaneous melanomas

Por Nsengimana, Jérémie, Laye, Jon, Filia, Anastasia, O’Shea, Sally, Muralidhar, Sathya, Poźniak, Joanna, Droop, Alastair, Chan, May, Walker, Christy, Parkinson, Louise, Gascoyne, Joanne, Mell, Tracey, Polso, Minttu, Jewell, Rosalyn, Randerson-Moor, Juliette, Cook, Graham P., Bishop, D. Timothy, Newton-Bishop, Julia
Publicado no J Clin Invest (2018)

The clinico-pathological and gene expression patterns associated with ulceration of primary melanoma

Por Jewell, Rosalyn, Elliott, Faye, Laye, Jonathan, Nsengimana, Jérémie, Davies, John, Walker, Christy, Conway, Caroline, Mitra, Angana, Harland, Mark, Cook, Martin G., Boon, Andy, Storr, Sarah, Safuan, Sabreena, Martin, Stewart G, Jirström, Karin, Olsson, Håkan, Ingvar, Christian, Lauss, Martin, Bishop, Tim, Jönsson, Göran, Newton-Bishop, Julia
Publicado no Pigment Cell Melanoma Res (2014)

Patterns of expression of DNA repair genes and relapse from melanoma

Por Jewell, Rosalyn, Conway, Caroline, Mitra, Angana, Randerson-Moor, Juliette, Lobo, Samira, Nsengimana, Jérémie, Harland, Mark, Marples, Maria, Edward, Sara, Cook, Martin, Powell, Barry, Boon, Andy, de Kort, Floor, Parker, Katharine A, Cree, Ian A., Barrett, Jennifer H., Knowles, Margaret A., Bishop, D. Timothy, Newton-Bishop, Julia
Publicado em 2010

Inherited variation in the PARP1 gene and survival from melanoma

Por Davies, John R, Jewell, Rosalyn, Affleck, Paul, Anic, Gabriella M, Randerson-Moor, Juliette, Ozola, Aija, Egan, Kathleen M, Elliott, Faye, García-Casado, Zaida, Hansson, Johan, Harland, Mark, Höiom, Veronica, Jian, Guan, Jönsson, Göran, Kumar, Rajiv, Nagore, Eduardo, Wendt, Judith, Olsson, Håkan, Park, Jong Y, Patel, Poulam, Pjanova, Dace, Puig, Susana, Schadendorf, Dirk, Sivaramakrishna Rachakonda, P, Snowden, Helen, Stratigos, Alexander J, Bafaloukos, Dimitrios, Ogbah, Zighereda, Sucker, Antje, Van den Oord, Joost J, Van Doorn, Remco, Walker, Christy, Okamoto, Ichiro, Wolter, Pascal, Barrett, Jennifer H, Timothy Bishop, D, Newton-Bishop, Julia
Publicado em 2014

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Por den Hoed, Joery, de Boer, Elke, Voisin, Norine, Dingemans, Alexander J.M., Guex, Nicolas, Wiel, Laurens, Nellaker, Christoffer, Amudhavalli, Shivarajan M., Banka, Siddharth, Bena, Frederique S., Ben-Zeev, Bruria, Bonagura, Vincent R., Bruel, Ange-Line, Brunet, Theresa, Brunner, Han G., Chew, Hui B., Chrast, Jacqueline, Cimbalistienė, Loreta, Coon, Hilary, Délot, Emmanuèlle C., Démurger, Florence, Denommé-Pichon, Anne-Sophie, Depienne, Christel, Donnai, Dian, Dyment, David A., Elpeleg, Orly, Faivre, Laurence, Gilissen, Christian, Granger, Leslie, Haber, Benjamin, Hachiya, Yasuo, Abedi, Yasmin Hamzavi, Hanebeck, Jennifer, Hehir-Kwa, Jayne Y., Horist, Brooke, Itai, Toshiyuki, Jackson, Adam, Jewell, Rosalyn, Jones, Kelly L., Joss, Shelagh, Kashii, Hirofumi, Kato, Mitsuhiro, Kattentidt-Mouravieva, Anja A., Kok, Fernando, Kotzaeridou, Urania, Krishnamurthy, Vidya, Kučinskas, Vaidutis, Kuechler, Alma, Lavillaureix, Alinoë, Liu, Pengfei, Manwaring, Linda, Matsumoto, Naomichi, Mazel, Benoît, McWalter, Kirsty, Meiner, Vardiella, Mikati, Mohamad A., Miyatake, Satoko, Mizuguchi, Takeshi, Moey, Lip H., Mohammed, Shehla, Mor-Shaked, Hagar, Mountford, Hayley, Newbury-Ecob, Ruth, Odent, Sylvie, Orec, Laura, Osmond, Matthew, Palculict, Timothy B., Parker, Michael, Petersen, Andrea K., Pfundt, Rolph, Preikšaitienė, Eglė, Radtke, Kelly, Ranza, Emmanuelle, Rosenfeld, Jill A., Santiago-Sim, Teresa, Schwager, Caitlin, Sinnema, Margje, Snijders Blok, Lot, Spillmann, Rebecca C., Stegmann, Alexander P.A., Thiffault, Isabelle, Tran, Linh, Vaknin-Dembinsky, Adi, Vedovato-dos-Santos, Juliana H., Schrier Vergano, Samantha A., Vilain, Eric, Vitobello, Antonio, Wagner, Matias, Waheeb, Androu, Willing, Marcia, Zuccarelli, Britton, Kini, Usha, Newbury, Dianne F., Kleefstra, Tjitske, Reymond, Alexandre, Fisher, Simon E., Vissers, Lisenka E.L.M.
Publicado no Am J Hum Genet (2021)