GREVE: Genomic Recurrent Event ViEwer to assist the identification of patterns across individual cancer samples

by Cazier, Jean-Baptiste, Holmes, Chris C., Broxholme, John
Published 2012

A Novel Test for Gene-Ancestry Interactions in Genome-Wide Association Data

by Davies, Joanna L., Cazier, Jean-Baptiste, Dunlop, Malcolm G., Houlston, Richard S., Tomlinson, Ian P., Holmes, Chris C.
Published 2012

Choice of transcripts and software has a large effect on variant annotation

by McCarthy, Davis J, Humburg, Peter, Kanapin, Alexander, Rivas, Manuel A, Gaulton, Kyle, Cazier, Jean-Baptiste, Donnelly, Peter
Published 2014

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population

by Villanueva, Pia, Newbury, Dianne F, Jara, Lilian, De Barbieri, Zulema, Mirza, Ghazala, Palomino, Hernán M, Fernández, María Angélica, Cazier, Jean-Baptiste, Monaco, Anthony P, Palomino, Hernán
Published 2011

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

by Holt, Richard, Sykes, Nuala H, Conceição, Inês C, Cazier, Jean-Baptiste, Anney, Richard JL, Oliveira, Guiomar, Gallagher, Louise, Vicente, Astrid, Monaco, Anthony P, Pagnamenta, Alistair T
Published 2012

Nutrigenomics of High Fat Diet Induced Obesity in Mice Suggests Relationships between Susceptibility to Fatty Liver Disease and the Proteasome

by Waller-Evans, Helen, Hue, Christophe, Fearnside, Jane, Rothwell, Alice R., Lockstone, Helen E., Caldérari, Sophie, Wilder, Steven P., Cazier, Jean-Baptiste, Scott, James, Gauguier, Dominique
Published 2013

Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

by Styrkarsdottir, Unnur, Cazier, Jean-Baptiste, Kong, Augustine, Rolfsson, Ottar, Larsen, Helene, Bjarnadottir, Emma, Johannsdottir, Vala D, Sigurdardottir, Margret S, Bagger, Yu, Christiansen, Claus, Reynisdottir, Inga, Grant, Struan F. A, Jonasson, Kristjan, Frigge, Michael L, Gulcher, Jeffrey R, Sigurdsson, Gunnar, Stefansson, Kari
Published 2003

Analysis of colorectal cancers in British Bangladeshi identifies early onset, frequent mucinous histotype and a high prevalence of RBFOX1 deletion

by Sengupta, Neel, Yau, Christopher, Sakthianandeswaren, Anuratha, Mouradov, Dmitri, Gibbs, Peter, Suraweera, Nirosha, Cazier, Jean-Baptiste, Polanco-Echeverry, Guadalupe, Ghosh, Anil, Thaha, Mohamed, Ahmed, Shafi, Feakins, Roger, Propper, David, Dorudi, Sina, Sieber, Oliver, Silver, Andrew, Lai, Cecilia
Published 2013

Transcriptome Profiling in Rat Inbred Strains and Experimental Cross Reveals Discrepant Genetic Architecture of Genome-Wide Gene Expression

by Kaisaki, Pamela J., Otto, Georg W., Argoud, Karène, Collins, Stephan C., Wallis, Robert H., Wilder, Steven P., Yau, Anthony C. Y., Hue, Christophe, Calderari, Sophie, Bihoreau, Marie-Thérèse, Cazier, Jean-Baptiste, Mott, Richard, Gauguier, Dominique
Published 2016

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

by van Schouwenburg, Pauline A., Davenport, Emma E., Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C., Lockstone, Helen E., Cazier, Jean-Baptiste, Chapel, Helen M., Knight, Julian C., Patel, Smita Y.
Published 2015

Large Scale Association Analysis Identifies Three Susceptibility Loci for Coronary Artery Disease

by Saade, Stephanie, Cazier, Jean-Baptiste, Ghassibe-Sabbagh, Michella, Youhanna, Sonia, Badro, Danielle A., Kamatani, Yoichiro, Hager, Jörg, Yeretzian, Joumana S., El-Khazen, Georges, Haber, Marc, Salloum, Angelique K., Douaihy, Bouchra, Othman, Raed, Shasha, Nabil, Kabbani, Samer, Bayeh, Hamid El, Chammas, Elie, Farrall, Martin, Gauguier, Dominique, Platt, Daniel E., Zalloua, Pierre A.
Published 2011

Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis

by Hager, Jörg, Kamatani, Yoichiro, Cazier, Jean-Baptiste, Youhanna, Sonia, Ghassibe-Sabbagh, Michella, Platt, Daniel E., Abchee, Antoine B., Romanos, Jihane, Khazen, Georges, Othman, Raed, Badro, Danielle A., Haber, Marc, Salloum, Angelique K., Douaihy, Bouchra, Shasha, Nabil, Kabbani, Samer, Sbeite, Hana, Chammas, Elie, el Bayeh, Hamid, Rousseau, Francis, Zelenika, Diana, Gut, Ivo, Lathrop, Mark, Farrall, Martin, Gauguier, Dominique, Zalloua, Pierre A.
Published 2012

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

by Vernes, Sonja C., Oliver, Peter L., Spiteri, Elizabeth, Lockstone, Helen E., Puliyadi, Rathi, Taylor, Jennifer M., Ho, Joses, Mombereau, Cedric, Brewer, Ariel, Lowy, Ernesto, Nicod, Jérôme, Groszer, Matthias, Baban, Dilair, Sahgal, Natasha, Cazier, Jean-Baptiste, Ragoussis, Jiannis, Davies, Kay E., Geschwind, Daniel H., Fisher, Simon E.
Published 2011

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12

by Fernandez-Rozadilla, Ceres, Cazier, Jean-Baptiste, Tomlinson, Ian P, Carvajal-Carmona, Luis G, Palles, Claire, Lamas, María J, Baiget, Montserrat, López-Fernández, Luis A, Brea-Fernández, Alejandro, Abulí, Anna, Bujanda, Luis, Clofent, Juan, Gonzalez, Dolors, Xicola, Rosa, Andreu, Montserrat, Bessa, Xavier, Jover, Rodrigo, Llor, Xavier, Moreno, Víctor, Castells, Antoni, Carracedo, Ángel, Castellvi-Bel, Sergi, Ruiz-Ponte, Clara
Published 2013

Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series

by Dumas, Marc-Emmanuel, Domange, Céline, Calderari, Sophie, Martínez, Andrea Rodríguez, Ayala, Rafael, Wilder, Steven P., Suárez-Zamorano, Nicolas, Collins, Stephan C., Wallis, Robert H., Gu, Quan, Wang, Yulan, Hue, Christophe, Otto, Georg W., Argoud, Karène, Navratil, Vincent, Mitchell, Steve C., Lindon, John C., Holmes, Elaine, Cazier, Jean-Baptiste, Nicholson, Jeremy K., Gauguier, Dominique
Published 2016

Differential clonal evolution in oesophageal cancers in response to neo-adjuvant chemotherapy

by Findlay, John M., Castro-Giner, Francesc, Makino, Seiko, Rayner, Emily, Kartsonaki, Christiana, Cross, William, Kovac, Michal, Ulahannan, Danny, Palles, Claire, Gillies, Richard S., MacGregor, Thomas P., Church, David, Maynard, Nicholas D., Buffa, Francesca, Cazier, Jean-Baptiste, Graham, Trevor A., Wang, Lai-Mun, Sharma, Ricky A., Middleton, Mark, Tomlinson, Ian
Published 2016

Correction: Exome Sequencing in an Admixed Isolated Population IndicatesNFXL1 Variants Confer a Risk for Specific Language Impairment

by Villanueva, Pía, Nudel, Ron, Hoischen, Alexander, Fernández, María Angélica, Simpson, Nuala H., Gilissen, Christian, Reader, Rose H., Jara, Lillian, Magdalena Echeverry, María, Francks, Clyde, Baird, Gillian, Conti-Ramsden, Gina, O’Hare, Anne, Bolton, Patrick F., Hennessy, Elizabeth R., Palomino, Hernán, Carvajal-Carmona, Luis, Veltman, Joris A., Cazier, Jean-Baptiste, Barbieri, Zulema De, Fisher, Simon E., Newbury, Dianne F.
Published 2015

Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

by Villanueva, Pía, Nudel, Ron, Hoischen, Alexander, Fernández, María Angélica, Simpson, Nuala H., Gilissen, Christian, Reader, Rose H., Jara, Lillian, Echeverry, Maria Magdalena, Francks, Clyde, Baird, Gillian, Conti-Ramsden, Gina, O’Hare, Anne, Bolton, Patrick F., Hennessy, Elizabeth R., Palomino, Hernán, Carvajal-Carmona, Luis, Veltman, Joris A., Cazier, Jean-Baptiste, De Barbieri, Zulema, Fisher, Simon E., Newbury, Dianne F.
Published 2015

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

by Spain, Sarah L., Carvajal-Carmona, Luis G., Howarth, Kimberley M., Jones, Angela M., Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm, Houlston, Richard S., Tomlinson, Ian P.M.
Published 2012

Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development

by Lise, Stefano, Clarkson, Yvonne, Perkins, Emma, Kwasniewska, Alexandra, Sadighi Akha, Elham, Parolin Schnekenberg, Ricardo, Suminaite, Daumante, Hope, Jilly, Baker, Ian, Gregory, Lorna, Green, Angie, Allan, Chris, Lamble, Sarah, Jayawant, Sandeep, Quaghebeur, Gerardine, Cader, M. Zameel, Hughes, Sarah, Armstrong, Richard J. E., Kanapin, Alexander, Rimmer, Andrew, Lunter, Gerton, Mathieson, Iain, Cazier, Jean-Baptiste, Buck, David, Taylor, Jenny C., Bentley, David, McVean, Gilean, Donnelly, Peter, Knight, Samantha J. L., Jackson, Mandy, Ragoussis, Jiannis, Németh, Andrea H.
Published 2012