Glioblastoma adaptation traced through decline of an IDH1 clonal driver and macro-evolution of a double-minute chromosome
Favero, F., McGranahan, N., Salm, M., Birkbak, N.J., Sanborn, J.Z., Benz, S.C., Becq, J., Peden, J.F., Kingsbury, Z., Grocok, R.J., Humphray, S., Bentley, D., Spencer-Dene, B., Gutteridge, A., Brada, M., Roger, S., Dietrich, P.-Y., Forshew, T., Gerlinger, M., Rowan, A., Stamp, G., Eklund, A.C., Szallasi, Z., Swanton, C.
Published in Annals of oncology (01.05.2015)
Published in Annals of oncology (01.05.2015)
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Repeat‐associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58
Saunders, Nigel J., Jeffries, Alex C., Peden, John F., Hood, Derek W., Tettelin, Herve, Rappuoli, Rino, Moxon, E. Richard
Published in Molecular microbiology (01.07.2000)
Published in Molecular microbiology (01.07.2000)
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Simple sequence repeats in the Helicobacter pylori genome
Saunders, Nigel J., Peden, John F., Hood, Derek W., Moxon, E. Richard
Published in Molecular microbiology (01.03.1998)
Published in Molecular microbiology (01.03.1998)
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Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16
DANIELS, Rachael J, PEDEN, John F, HIGGS, Douglas R, LLOYD, Christine, HORSLEY, Sharon W, CLARK, Kevin, TUFARELLI, Cristina, KEARNEY, Lyndal, BUCKLE, Veronica J, DOGGETT, Norman A, FLINT, Jonathan
Published in Human molecular genetics (15.02.2001)
Published in Human molecular genetics (15.02.2001)
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Codon usage: mutational bias, translational selection, or both?
Sharp, P M, Stenico, M, Peden, J F, Lloyd, A T
Published in Biochemical Society transactions (01.11.1993)
Published in Biochemical Society transactions (01.11.1993)
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Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects
Horsley, S W, Daniels, R J, Anguita, E, Raynham, H A, Peden, J F, Villegas, A, Vickers, M A, Green, S, Waye, J S, Chui, D H, Ayyub, H, MacCarthy, A B, Buckle, V J, Gibbons, R J, Kearney, L, Higgs, D R
Published in European journal of human genetics : EJHG (01.03.2001)
Published in European journal of human genetics : EJHG (01.03.2001)
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SNP cherry picker: maximizing the chance of finding an association with a disease SNP
Harris, Mark, Martin, Jeremy M. R., Peden, John F., Rawlings, Christopher J.
Published in Bioinformatics (01.11.2003)
Published in Bioinformatics (01.11.2003)
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Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
Clarke, Robert, Peden, John F, Hopewell, Jemma C, Kyriakou, Theodosios, Goel, Anuj, Heath, Simon C, Parish, Sarah, Barlera, Simona, Franzosi, Maria Grazia, Rust, Stephan, Bennett, Derrick, Silveira, Angela, Malarstig, Anders, Green, Fiona R, Lathrop, Mark, Gigante, Bruna, Leander, Karin, de Faire, Ulf, Seedorf, Udo, Hamsten, Anders, Collins, Rory, Watkins, Hugh, Farrall, Martin
Published in The New England journal of medicine (24.12.2009)
Published in The New England journal of medicine (24.12.2009)
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A Large-Scale, Consortium-Based Genomewide Association Study of Asthma
Moffatt, Miriam F, Gut, Ivo G, Demenais, Florence, Strachan, David P, Bouzigon, Emmanuelle, Heath, Simon, von Mutius, Erika, Farrall, Martin, Lathrop, Mark, Cookson, William O.C.M
Published in The New England journal of medicine (23.09.2010)
Published in The New England journal of medicine (23.09.2010)
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A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Peden, John F., Hopewell, Jemma C., Saleheen, Danish, Chambers, John C., Hager, Jorg, Collins, Rory, Danesh, John, Elliott, Paul, Farrall, Martin, Stirrups, Kathy, Zhang, Weihua, Hamsten, Anders, Parish, Sarah, Lathrop, Mark, Watkins, Hugh, Clarke, Robert, Deloukas, Panos, Kooner, Jaspal S., Goel, Anuj, Ongen, Halit, Strawbridge, Rona J., Heath, Simon, Mälarstig, Anders, Helgadottir, Anna, Öhrvik, John, Murtaza, Muhammed, Potter, Simon, Hunt, Sarah E., Delepine, Marc, Jalilzadeh, Shapour, Axelsson, Tomas, Syvänen, Ann-Christine, Gwilliam, Rhian, Bumpstead, Suzannah, Gray, Emma, Edkins, Sarah, Folkersen, Lasse, Kyriakou, Theodosios, Franco-Cereceda, Anders, Gabrielsen, Anders, Seedorf, Udo, Eriksson, Per, Offer, Alison, Bowman, Louise, Sleight, Peter, Armitage, Jane, Peto, Richard, Abecasis, Goncalo, Ahmed, Nabeel, Caulfield, Mark, Donnelly, Peter, Froguel, Philippe, Kooner, Angad S., McCarthy, Mark I., Samani, Nilesh J., Scott, James, Sehmi, Joban, Silveira, Angela, Hellenius, Mai-Lis, van't Hooft, Ferdinand M., Olsson, Gunnar, Rust, Stephan, Assmann, Gerd, Barlera, Simona, Tognoni, Gianni, Franzosi, Maria Grazia, Linksted, Pamela, Green, Fiona R., Rasheed, Asif, Zaidi, Moazzam, Shah, Nabi, Samuel, Maria, Mallick, Nadeem H., Azhar, Muhammad, Zaman, Khan S., Samad, Abdus, Ishaq, Mohammad, Gardezi, Ali R., Frossard, Philippe M., Spector, Tim, Peltonen, Leena, Nieminen, Markku S., Sinisalo, Juha, Salomaa, Veikko, Ripatti, Samuli, Bennett, Derrick, Leander, Karin, Gigante, Bruna, de Faire, Ulf, Pietri, Silvia, Gori, Francesca, Marchioli, Roberto, Sivapalaratnam, Suthesh, Kastelein, John J. P., Trip, Mieke D., Theodoraki, Eirini V., Dedoussis, George V., Engert, Jamie C., Yusuf, Salim, Anand, Sonia S.
Published in Nature genetics (01.04.2011)
Published in Nature genetics (01.04.2011)
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Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
STRAWBRIDGE, Rona J, DUPUIS, Josée, NICA, Alexandra, WHEELER, Eleanor, HAN CHEN, VOIGHT, Benjamin F, TANEERA, Jalal, KANONI, Stavroula, PEDEN, John F, TURRINI, Fabiola, GUSTAFSSON, Stefan, ZABENA, Carina, PROKOPENKO, Inga, ALMGREN, Peter, BARKER, David J. P, BARNES, Daniel, DENNISON, Elaine M, ERIKSSON, Johan G, ERIKSSON, Per, EURY, Elodie, FOLKERSEN, Lasse, FOX, Caroline S, FRAYLING, Timothy M, BARKER, Adam, GOEL, Anuj, GU, Harvest F, HORIKOSHI, Momoko, ISOMAA, Bo, JACKSON, Anne U, JAMESON, Karen A, KAJANTIE, Eero, KERR-CONTE, Julie, KUULASMAA, Teemu, KUUSISTO, Johanna, AHLQVIST, Emma, LOOS, Ruth J. F, JIAN'AN LUAN, MAKRILAKIS, Konstantinos, MANNING, Alisa K, MARTINEZ-LARRAD, Maria Teresa, NARISU, Narisu, MANNILA, Maria Nastase, OHRVIK, John, OSMOND, Clive, PASCOE, Laura, RYBIN, Denis, PAYNE, Felicity, SAYER, Avan A, SENNBLAD, Bengt, SILVEIRA, Angela, STANCAKOVA, Alena, STIRRUPS, Kathy, SWIFT, Amy J, SYVÄNEN, Ann-Christine, PETRIE, John R, TRAVERS, Mary E, BOUATIA-NAJI, Nabila, DIMAS, Antigone S
Published in Diabetes (New York, N.Y.) (01.10.2011)
Published in Diabetes (New York, N.Y.) (01.10.2011)
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Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
Broadbent, Helen M., Peden, John F., Lorkowski, Stefan, Goel, Anuj, Ongen, Halit, Green, Fiona, Clarke, Robert, Collins, Rory, Franzosi, Maria Grazia, Tognoni, Gianni, Seedorf, Udo, Rust, Stephan, Eriksson, Per, Hamsten, Anders, Farrall, Martin, Watkins, Hugh
Published in Human molecular genetics (15.03.2008)
Published in Human molecular genetics (15.03.2008)
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Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease
Elliott, Paul, Chambers, John C, Zhang, Weihua, Clarke, Robert, Hopewell, Jemma C, Peden, John F, Erdmann, Jeanette, Braund, Peter, Engert, James C, Bennett, Derrick, Coin, Lachlan, Ashby, Deborah, Tzoulaki, Ioanna, Brown, Ian J, Mt-Isa, Shahrul, McCarthy, Mark I, Peltonen, Leena, Freimer, Nelson B, Farrall, Martin, Ruokonen, Aimo, Hamsten, Anders, Lim, Noha, Froguel, Philippe, Waterworth, Dawn M, Vollenweider, Peter, Waeber, Gerard, Jarvelin, Marjo-Riitta, Mooser, Vincent, Scott, James, Hall, Alistair S, Schunkert, Heribert, Anand, Sonia S, Collins, Rory, Samani, Nilesh J, Watkins, Hugh, Kooner, Jaspal S
Published in JAMA : the journal of the American Medical Association (01.07.2009)
Published in JAMA : the journal of the American Medical Association (01.07.2009)
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An in silico evaluation of Tn916 as a tool for generalized mutagenesis in Haemophilus influenzae Rd
Hosking, Sarah L, Deadman, Mary E, Moxon, E. Richard, Peden, John F, Saunders, Nigel J, High, Nicola J
Published in Microbiology (Society for General Microbiology) (01.09.1998)
Published in Microbiology (Society for General Microbiology) (01.09.1998)
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HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis
FEEHALLY, John, FARRALL, Martin, PADMANABHAN, Sandosh, VYSE, Timothy J, ZAWADZKA, Anna, REES, Andrew J, LATHROP, Mark, RATCLIFFET, Peter J, BOLAND, Anne, GALE, Daniel P, GUT, Ivo, HEATH, Simon, KUMAR, Ashish, PEDEN, John F, MAXWELL, Patrick H, MORRIS, David L
Published in Journal of the American Society of Nephrology (01.10.2010)
Published in Journal of the American Society of Nephrology (01.10.2010)
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Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
SMITH, Nicholas L, CHEN, Ming-Huei, DE MAAT, Moniek P. M, RUMLEY, Ann, XIAOXIAO KONG, QIONG YANG, WILLIAMS, Frances M. K, VITART, Veronique, CAMPBELL, Harry, MÄLARSTIG, Anders, WIGGINS, Kerri L, VAN DUIJN, Cornelia M, DEHGHAN, Abbas, MCARDLE, Wendy L, PANKOW, James S, JOHNSON, Andrew D, SILVEIRA, Angela, MCKNIGHT, Barbara, UITTERLINDEN, Andre G, ALEKSIC, Nena, MEIGS, James B, PETERS, Annette, KOENIG, Wolfgang, STRACHAN, David P, CUSHMAN, Mary, KATHIRESAN, Sekar, ROTTER, Jerome I, BOVILL, Edwin G, HOFMAN, Albert, BOERWINKLE, Eric, TOFLER, Geoffrey H, PEDEN, John F, PSATY, Bruce M, LEEBEEK, Frank, BASU, Saonli, FOLSOM, Aaron R, LARSON, Martin G, SPECTOR, Timothy D, WRIGHT, Alan F, WILSON, James F, HAMSTEN, Anders, LUMLEY, Thomas, WITTEMAN, Jacqueline C. M, WEIHONG TANG, O'DONNELL, Christopher J, SORANZO, Nicole, HAYWARD, Caroline, RUDAN, Igor, SABATER-LLEAL, Maria, BIS, Joshua C
Published in Circulation (New York, N.Y.) (30.03.2010)
Published in Circulation (New York, N.Y.) (30.03.2010)
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