A SNP profiling panel for sample tracking in whole-exome sequencing studies

by Pengelly, Reuben, Gibson, Jane, Andreoletti, Gaia, Collins, Andrew, Mattocks, Christopher J., Ennis, Sarah
Published 2013

Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations

by Pengelly, Reuben, Tapper, William, Gibson, Jane, Knut, Marcin, Tearle, Rick, Collins, Andrew, Ennis, Sarah
Published 2015

Exome analysis of patients with concurrent pediatric inflammatory bowel disease (PIBD) and autoimmune disease

by Andreoletti, Gaia, Ashton, James J., Coelho, Tracy, Willis, C., Haggarty, R., Gibson, Jane, Holloway, John W., Batra, A., Afzal, Nadeem A., Beattie, R. Mark, Ennis, Sarah
Published 2015

Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations

by Tapper, William J., Foulds, Nicola, Cross, Nicholas C. P., Aranaz, Paula, Score, Joannah, Hidalgo-Curtis, Claire, Robinson, David O., Gibson, Jane, Ennis, Sarah, Temple, I. Karen, Collins, Andrew
Published 2014

Whole exome sequencing identifies novel recurrently mutated genes in patients with splenic marginal zone lymphoma

by Parry, Marina, Rose-Zerilli, Matthew J. J., Gibson, Jane, Ennis, Sarah, Walewska, Renata, Forster, Jade, Parker, Helen, Davis, Zadie, Gardiner, Anne, Collins, Andrew, Oscier, David G., Strefford, Jonathan C.
Published 2013

Distinctive genotypes in infants with T-cell acute lymphoblastic leukaemia

by Mansur, Marcela B., van Delft, Frederik W., Colman, Susan M., Furness, Caroline L., Gibson, Jane, Emerenciano, Mariana, Kempski, Helena, Clappier, Emmanuelle, Cave, Hélène, Soulier, Jean, Pombo-, Greaves, Mel, Ford, Anthony M.
Published 2015

Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease

by Rose-Zerilli, Matthew, Gibson, Jane, Wang, Jun, Tapper, Wi, Davis, Zadie, Parker, Helen, Larrayoz, Marta, McCarthy, Helen, Walewska, Renata, Forster, Jade, Gardiner, Anne, Steele, Andrew, Chelala, Claude, Ennis, Sarah, Collins, Andrew, Oakes, Christopher, Oscier, David, Strefford, Jonathan
Published 2016

Genetics and prognostication in splenic marginal zone lymphoma: revelations from deep sequencing

by Parry, Marina, Rose-Zerilli, Matthew J., Ljungstrom, Viktor, Gibson, Jane, Wang, Jun, Walewska, Renata, Parker, Helen, Parker, A, David, Zadie, Gardiner, Anne, McIver-Brown, Neil, Kalpadakis, Christina, Xochelli, Aliki, Anagnostopoulos, Achilles, Fazi, Claudia, Gonzalez de Castro, David, Dearden, Claire, Pratt, Guy, Rosenquist, Richard, Ashton-Key, Margaret, Forconi, Francesco, Collins, Andrew R., Ghia, Paolo, Matutes, Estella, Pangalis, Gerassimos, Stamatopoulos, Kostas, Oscier, David G., Strefford, Jonathan C.
Published 2015

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

by Springelkamp, Henriët, Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J.M, Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D.G, Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M.E, Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Mitchell, Paul, Wang, Jie Jin, Rochtchina, Elena, Attia, John, Scott, Rodney, Holliday, Elizabeth G., Wong, Tien-Yin, Ennis, Sarah, Lotery, Andrew J.
Published 2014