Neuropeptide modulation of lymphatic smooth muscle tone in the canine forelimb

por Dobbins, David E.
Publicado 1992

Receptor mechanisms of PAF mediated lymphatic constriction in the canine forelimb

por Dobbins, D. E.
Publicado 1992

CanVar: A resource for sharing germline variation in cancer patients

por Chubb, Daniel, Broderick, Peter, Dobbins, Sara E., Houlston, Richard S.
Publicado 2016

Mutational processes contributing to the development of multiple myeloma

por Hoang, Phuc H., Cornish, Alex J., Dobbins, Sara E., Kaiser, Martin, Houlston, Richard S.
Publicado 2019

Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes

por Dobbins, Sara E., Broderick, Peter, Chubb, Daniel, Kinnersley, Ben, Sherborne, Amy L., Houlston, Richard S.
Publicado 2016

Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms

por Hoang, Phuc H., Dobbins, Sara E., Cornish, Alex J., Chubb, Daniel, Law, Philip J., Kaiser, Martin, Houlston, Richard S.
Publicado 2018

The TERT variant rs2736100 is associated with colorectal cancer risk

por Kinnersley, B, Migliorini, G, Broderick, P, Whiffin, N, Dobbins, S E, Casey, G, Hopper, J, Sieber, O, Lipton, L, Kerr, D J, Dunlop, M G, Tomlinson, I PM, Houlston, R S
Publicado 2012

Search for rare protein altering variants influencing susceptibility to multiple myeloma

por Scales, Matthew, Chubb, Daniel, Dobbins, Sara E., Johnson, David C., Li, Ni, Sternberg, Michael J., Weinhold, Neils, Stein, Caleb, Jackson, Graham, Davies, Faith E., Walker, Brian A., Wardell, Christopher P., Houlston, Richard S., Morgan, Gareth J.
Publicado 2017

Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer

por Chubb, Daniel, Broderick, Peter, Dobbins, Sara E., Frampton, Matthew, Kinnersley, Ben, Penegar, Steven, Price, Amy, Ma, Yussanne P., Sherborne, Amy L., Palles, Claire, Timofeeva, Maria N., Bishop, D. Timothy, Dunlop, Malcolm G., Tomlinson, Ian, Houlston, Richard S.
Publicado 2016

Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort

por Grigoriadis, Dionysios, Sackey, Ege, Riches, Katie, van Zanten, Malou, Brice, Glen, England, Ruth, Mills, Mike, Dobbins, Sara E., Lee, Li Ling, Jeffery, Steve, Dong, Liang, Savage, David B., Mortimer, Peter S., Keeley, Vaughan, Pittman, Alan, Gordon, Kristiana, Ostergaard, Pia
Publicado 2022

Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism

por Li, Ni, Johnson, David C., Weinhold, Niels, Kimber, Scott, Dobbins, Sara E., Mitchell, Jonathan S., Kinnersley, Ben, Sud, Amit, Law, Philip J., Orlando, Giulia, Scales, Matthew, Wardell, Christopher P., Försti, Asta, Hoang, Phuc H., Went, Molly, Holroyd, Amy, Hariri, Fadi, Pastinen, Tomi, Meissner, Tobias, Goldschmidt, Hartmut, Hemminki, Kari, Morgan, Gareth J., Kaiser, Martin, Houlston, Richard S.
Publicado 2017

TCF12 is mutated in anaplastic oligodendroglioma

por Labreche, Karim, Simeonova, Iva, Kamoun, Aurélie, Gleize, Vincent, Chubb, Daniel, Letouzé, Eric, Riazalhosseini, Yasser, Dobbins, Sara E., Elarouci, Nabila, Ducray, Francois, de Reyniès, Aurélien, Zelenika, Diana, Wardell, Christopher P., Frampton, Mathew, Saulnier, Olivier, Pastinen, Tomi, Hallout, Sabrina, Figarella-Branger, Dominique, Dehais, Caroline, Idbaih, Ahmed, Mokhtari, Karima, Delattre, Jean-Yves, Huillard, Emmanuelle, Mark Lathrop, G., Sanson, Marc, Houlston, Richard S.
Publicado 2015

Correspondence: SEMA4A variation and risk of colorectal cancer

por Kinnersley, Ben, Chubb, Daniel, Dobbins, Sara E., Frampton, Matthew, Buch, Stephan, Timofeeva, Maria N., Castellví-Bel, Sergi, Farrington, Susan M., Forsti, Asta, Hampe, Jochen, Hemminki, Kari, Hofstra, Robert M. W., Northwood, Emma, Palles, Claire, Pinheiro, Manuela, Ruiz-Ponte, Clara, Schafmayer, Clemens, Teixeira, Manuel R., Westers, Helga, van Wezel, Tom, Timothy Bishop, D., Tomlinson, Ian, Dunlop, Malcolm G., Houlston, Richard S.
Publicado 2016

Genome-wide association analysis identifies a meningioma risk locus at 11p15.5

por Claus, Elizabeth B, Cornish, Alex J, Broderick, Peter, Schildkraut, Joellen M, Dobbins, Sara E, Holroyd, Amy, Calvocoressi, Lisa, Lu, Lingeng, Hansen, Helen M, Smirnov, Ivan, Walsh, Kyle M, Schramm, Johannes, Hoffmann, Per, Nöthen, Markus M, Jöckel, Karl-Heinz, Swerdlow, Anthony, Larsen, Signe Benzon, Johansen, Christoffer, Simon, Matthias, Bondy, Melissa, Wrensch, Margaret, Houlston, Richard S, Wiemels, Joseph L
Publicado 2018

Common variation at 10p12.31 near MLLT10 influences meningioma risk

por Dobbins, Sara E, Broderick, Peter, Melin, Beatrice, Feychting, Maria, Johansen, Christoffer, Andersson, Ulrika, Brännström, Thomas, Schramm, Johannes, Olver, Bianca, Lloyd, Amy, Ma, Yussanne P, Hosking, Fay J, Lönn, Stefan, Ahlbom, Anders, Henriksson, Roger, Schoemaker, Minouk J, Hepworth, Sarah J, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Eisele, Lewin, Kosteljanetz, Michael, Muir, Kenneth, Swerdlow, Anthony, Simon, Matthias, Houlston, Richard S
Publicado 2011

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

por Broderick, Peter, Chubb, Daniel, Johnson, David C, Weinhold, Niels, Försti, Asta, Lloyd, Amy, Olver, Bianca, Ma, Yussanne, Dobbins, Sara E, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Childs, J. Anthony, Ross, Fiona M, Jackson, Graham H, Neben, Kai, Jauch, Anna, Hoffmann, Per, Mühleisen, Thomas W, Nöthen, Markus M, Moebus, Susanne, Tomlinson, Ian P, Goldschmidt, Hartmut, Hemminki, Kari, Morgan, Gareth J, Houlston, Richard S
Publicado 2011

The CCND1 870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

por Weinhold, Niels, Johnson, David C, Chubb, Daniel, Chen, Bowang, Försti, Asta, Hosking, Fay J, Broderick, Peter, Ma, Yussanne P, Dobbins, Sara E, Hose, Dirk, Walker, Brian A, Davies, Faith E, Kaiser, Martin F, Li, Ni L, Gregory, Walter A, Jackson, Graham H, Witzens-Harig, Mathias, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Jauch, Anna, Goldschmidt, Hartmut, Houlston, Richard S, Morgan, Gareth J, Hemminki, Kari
Publicado 2013

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1

por Vijayakrishnan, J, Kumar, R, Henrion, M Y R, Moorman, A V, Rachakonda, P S, Hosen, I, da Silva Filho, M I, Holroyd, A, Dobbins, S E, Koehler, R, Thomsen, H, Irving, J A, Allan, J M, Lightfoot, T, Roman, E, Kinsey, S E, Sheridan, E, Thompson, P D, Hoffmann, P, Nöthen, M M, Heilmann-Heimbach, S, Jöckel, K H, Greaves, M, Harrison, C J, Bartram, C R, Schrappe, M, Stanulla, M, Hemminki, K, Houlston, R S
Publicado 2017

Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

por Chubb, Daniel, Weinhold, Niels, Broderick, Peter, Chen, Bowang, Johnson, David C, Försti, Asta, Vijayakrishnan, Jayaram, Migliorini, Gabriele, Dobbins, Sara E, Holroyd, Amy, Hose, Dirk, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Jackson, Graham H, Irving, Julie A, Pratt, Guy, Fegan, Chris, Fenton, James AL, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Straka, Christian, Einsele, Hermann, Langer, Christian, Dörner, Elisabeth, Allan, James M, Jauch, Anna, Morgan, Gareth J, Hemminki, Kari, Houlston, Richard S, Goldschmidt, Hartmut
Publicado 2013

A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer

por Al-Tassan, Nada A., Whiffin, Nicola, Hosking, Fay J., Palles, Claire, Farrington, Susan M., Dobbins, Sara E., Harris, Rebecca, Gorman, Maggie, Tenesa, Albert, Meyer, Brian F., Wakil, Salma M., Kinnersley, Ben, Campbell, Harry, Martin, Lynn, Smith, Christopher G., Idziaszczyk, Shelley, Barclay, Ella, Maughan, Timothy S., Kaplan, Richard, Kerr, Rachel, Kerr, David, Buchannan, Daniel D., Ko Win, Aung, Hopper, John, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Dunlop, Malcolm G., Tomlinson, Ian P., Cheadle, Jeremy P., Houlston, Richard S.
Publicado 2015