Wills, Christopher, Watts, Katie, Houseman, Amy, Maughan, Timothy S., Fisher, David, Al-Tassan, Nada A., Houlston, Richard S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458
2025.
Relationship between inherited genetic variation and survival from colorectal cancer stratified by tumour location.
Scientific Reports
15
, 2423.
10.1038/s41598-024-77870-0
|
|
|
Chen, Zhishan, Guo, Xingyi, Tao, Ran, Huyghe, Jeroen R., Law, Philip J., Fernandez-Rozadilla, Ceres, Ping, Jie, Jia, Guochong, Long, Jirong, Li, Chao, Shen, Quanhu, Xie, Yuhan, Timofeeva, Maria N., Thomas, Minta, Schmit, Stephanie L., Díez-Obrero, Virginia, Devall, Matthew, Moratalla-Navarro, Ferran, Fernandez-Tajes, Juan, Palles, Claire, Sherwood, Kitty, Briggs, Sarah E. W., Svinti, Victoria, Donnelly, Kevin, Farrington, Susan M., Blackmur, James, Vaughan-Shaw, Peter G., Shu, Xiao-Ou, Lu, Yingchang, Broderick, Peter, Studd, James, Harrison, Tabitha A., Conti, David V., Schumacher, Fredrick R., Melas, Marilena, Rennert, Gad, Obón-Santacana, Mireia, Martín-Sánchez, Vicente, Oh, Jae Hwan, Kim, Jeongseon, Jee, Sun Ha, Jung, Keum Ji, Kweon, Sun-Seog, Shin, Min-Ho, Shin, Aesun, Ahn, Yoon-Ok, Kim, Dong-Hyun, Oze, Isao, Wen, Wanqing, Matsuo, Keitaro, Matsuda, Koichi, Tanikawa, Chizu, Ren, Zefang, Gao, Yu-Tang, Jia, Wei-Hua, Hopper, John L., Jenkins, Mark A., Win, Aung Ko, Pai, Rish K., Figueiredo, Jane C., Haile, Robert W., Gallinger, Steven, Woods, Michael O., Newcomb, Polly A., Duggan, David, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Kaplan, Richard, Kerr, Rachel, Kerr, David, Kirac, Iva, Böhm, Jan, Mecklin, Jukka-Pekka, Jousilahti, Pekka, Knekt, Paul, Aaltonen, Lauri A., Rissanen, Harri, Pukkala, Eero, Eriksson, Johan G., Cajuso, Tatiana, Hänninen, Ulrika, Kondelin, Johanna, Palin, Kimmo, Tanskanen, Tomas, Renkonen-Sinisalo, Laura, Männistö, Satu, Albanes, Demetrius, Weinstein, Stephanie J., Ruiz-Narvaez, Edward, Palmer, Julie R., Buchanan, Daniel D., Platz, Elizabeth A., Visvanathan, Kala, Ulrich, Cornelia M., Siegel, Erin, Brezina, Stefanie, Gsur, Andrea, Campbell, Peter T., Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann, Slattery, Martha L., Potter, John D., Tsilidis, Kostas K., Schulze, Matthias B., Gunter, Marc J., Murphy, Neil, Castells, Antoni, Castellví-Bel, Sergi, Moreira, Leticia, Arndt, Volker, Shcherbina, Anna, Bishop, D. Timothy, Giles, Graham G., Southey, Melissa C., Idos, Gregory E., McDonnell, Kevin J., Abu-Ful, Zomoroda, Greenson, Joel K., Shulman, Katerina, Lejbkowicz, Flavio, Offit, Kenneth, Su, Yu-Ru, Steinfelder, Robert, Keku, Temitope O., van Guelpen, Bethany, Hudson, Thomas J., Hampel, Heather, Pearlman, Rachel, Berndt, Sonja I., Hayes, Richard B., Martinez, Marie Elena, Thomas, Sushma S., Pharoah, Paul D. P., Larsson, Susanna C., Yen, Yun, Lenz, Heinz-Josef, White, Emily, Li, Li, Doheny, Kimberly F., Pugh, Elizabeth, Shelford, Tameka, Chan, Andrew T., Cruz-Correa, Marcia, Lindblom, Annika, Hunter, David J., Joshi, Amit D., Schafmayer, Clemens, Scacheri, Peter C., Kundaje, Anshul, Schoen, Robert E., Hampe, Jochen, Stadler, Zsofia K., Vodicka, Pavel, Vodickova, Ludmila, Vymetalkova, Veronika, Edlund, Christopher K., Gauderman, W. James, Shibata, David, Toland, Amanda, Markowitz, Sanford, Kim, Andre, Chanock, Stephen J., van Duijnhoven, Franzel, Feskens, Edith J. M., Sakoda, Lori C., Gago-Dominguez, Manuela, Wolk, Alicja, Pardini, Barbara, FitzGerald, Liesel M., Lee, Soo Chin, Ogino, Shuji, Bien, Stephanie A., Kooperberg, Charles, Li, Christopher I., Lin, Yi, Prentice, Ross, Qu, Conghui, Bézieau, Stéphane, Yamaji, Taiki, Sawada, Norie, Iwasaki, Motoki, Le Marchand, Loic, Wu, Anna H., Qu, Chenxu, McNeil, Caroline E., Coetzee, Gerhard, Hayward, Caroline, Deary, Ian J., Harris, Sarah E., Theodoratou, Evropi, Reid, Stuart, Walker, Marion, Ooi, Li Yin, Lau, Ken S., Zhao, Hongyu, Hsu, Li, Cai, Qiuyin, Dunlop, Malcolm G., Gruber, Stephen B., Houlston, Richard S., Moreno, Victor, Casey, Graham, Peters, Ulrike, Tomlinson, Ian and Zheng, Wei
2024.
Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes.
Nature Communications
15
(1)
, 3557.
10.1038/s41467-024-47399-x
|
|
|
Paller, Channing J., Tukachinsky, Hanna, Maertens, Alexandra, Decker, Brennan, Sampson, Julian R., Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458 and Antonarakis, Emmanuel S.
2024.
Pan-cancer interrogation of MUTYH variants reveals biallelic inactivation and defective base excision repair across a spectrum of solid tumors.
JCO Precision Oncology
8
(8)
10.1200/PO.23.00251
|
|
|
Wills, Christopher, Watts, Katie, Maughan, Timothy S., Fisher, David, Al-Tassan, Nada A., Houlston, Richard S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458
2023.
Germline variation in RASAL2 may predict survival in patients with RAS-activated colorectal cancer.
Genes Chromosomes and Cancer
62
(6)
, pp. 332-341.
10.1002/gcc.23133
|
|
|
Wills, Christopher, Houseman, Amy, Watts, Katie, Maughan, Timothy S., Fisher, David, Houlston, Richard S., West, Hannah D. ORCID: https://orcid.org/0000-0002-6104-6534, Escott Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2023.
Relationship between 233 colorectal cancer risk loci and survival in 1,926 patients with advanced disease.
BJC Reports
1
, 2.
10.1038/s44276-023-00003-z
|
|
|
Fernandez-Rozadilla, Ceres, Timofeeva, Maria, Chen, Zhishan, Law, Philip, Thomas, Minta, Schmit, Stephanie, Díez-Obrero, Virginia, Hsu, Li, Fernandez-Tajes, Juan, Palles, Claire, Sherwood, Kitty, Briggs, Sarah, Svinti, Victoria, Donnelly, Kevin, Farrington, Susan, Blackmur, James, Vaughan-Shaw, Peter, Shu, Xiao-ou, Long, Jirong, Cai, Qiuyin, Guo, Xingyi, Lu, Yingchang, Broderick, Peter, Studd, James, Huyghe, Jeroen, Harrison, Tabitha, Conti, David, Dampier, Christopher, Devall, Mathew, Schumacher, Fredrick, Melas, Marilena, Rennert, Gad, Obón-Santacana, Mireia, Martín-Sánchez, Vicente, Moratalla-Navarro, Ferran, Oh, Jae Hwan, Kim, Jeongseon, Jee, Sun Ha, Jung, Keum Ji, Kweon, Sun-Seog, Shin, Min-Ho, Shin, Aesun, Ahn, Yoon-Ok, Kim, Dong-Hyun, Oze, Isao, Wen, Wanqing, Matsuo, Keitaro, Matsuda, Koichi, Tanikawa, Chizu, Ren, Zefang, Gao, Yu-Tang, Jia, Wei-Hua, Hopper, John, Jenkins, Mark, Win, Aung Ko, Pai, Rish, Figueiredo, Jane, Haile, Robert, Gallinger, Steven, Woods, Michael, Newcomb, Polly, Duggan, David, Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458, Kaplan, Richard, Maughan, Timothy, Kerr, Rachel, Kerr, David, Kirac, Iva, Böhm, Jan, Mecklin, Lukka-Pekka, Jousilahti, Pekka, Knekt, Paul, Aaltonen, Lauri, Rissanen, Harri, Pukkala, Eero, Eriksson, Johan, Cajuso, Tatiana, Hänninen, Ulrika, Kondelin, Johanna, Palin, Kimmo, Tanskanen, Tomas, Renkonen-Sinisalo, Laura, Zanke, Brent, Männistö, Satu, Albanes, Demetrius, Weinstein, Stephanie, Ruiz-Narvaez, Edward, Palmer, Julie, Buchanan, Daniel, Platz, Elizabeth, Visvanathan, Kala, Ulrich, Cornelia, Siegel, Erin, Brezina, Stefanie, Gsur, Andrea, Campbell, Peter, Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann, Slattery, Martha, Potter, John, Tsilidis, Konstantinos, Schulze, Matthias, Gunter, Marc, Murphy, Neil, Castells, Antoni, Castellví-Bel, Sergi, Moreira, Leticia, Arndt, Volker, Shcherbina, Anna, Stern, Mariana, Pardamean, Bens, Bishop, Timothy, Giles, Graham, Southey, Melissa, Idos, Gregory, McDonnell, Kevin, Abu-Ful, Zomoroda, Greenson, Joel, Shulman, Katerina, Lejbkowicz, Flavio, Offit, Kenneth, Su, Yu-Ru, Steinfelder, Robert, Keku, Temitope, van Guelpen, Bethany, Hudson, Thomas, Hampel, Heather, Pearlman, Rachel, Berndt, Sonja, Hayes, Richard, Martinez, Marie Elena, Thomas, Sushma, Corley, Douglas, Pharoah, Paul, Larsson, Susanna, Yen, Yun, Lenz, Heinz-Josef, White, Emily, Li, Li, Doheny, Kimberly, Pugh, Elizabeth, Shelford, Tameka, Chan, Andrew, Cruz-Correa, Marcia, Lindblom, Annika, Hunter, David, Joshi, Amit, Schafmayer, Clemens, Scacheri, Peter, Kundaje, Anshul, Nickerson, Deborah, Schoen, Robert, Hampe, Jochen, Stadler, Zsofia, Vodicka, Pavel, Vodickova, Ludmila, Vymetalkova, Veronika, Papadopoulos, Nickolas, Edlund, Chistopher, Gauderman, William, Thomas, Duncan, Shibata, David, Toland, Amanda, Markowitz, Sanford, Kim, Andre, Chanock, Stephen, van Duijnhoven, Franzel, Feskens, Edith, Sakoda, Lori, Gago-Dominguez, Manuela, Wolk, Alicja, Naccarati, Alessio, Pardini, Barbara, FitzGerald, Liesel, Lee, Soo Chin, Ogino, Shuji, Bien, Stephanie, Kooperberg, Charles, Li, Christopher, Lin, Yi, Prentice, Ross, Qu, Conghui, Bézieau, Stéphane, Tangen, Catherine, Mardis, Elaine, Yamaji, Taiki, Sawada, Norie, Iwasaki, Motoki, Haiman, Christopher, Le Marchand, Loic, Wu, Anna, Qu, Chenxu, McNeil, Caroline, Coetzee, Gerhard, Hayward, Caroline, Deary, Ian, Harris, Sarah, Theodoratou, Evropi, Reid, Stuart, Walker, Marion, Ooi, Li Yin, Moreno, Victor, Casey, Graham, Gruber, Stephen, Tomlinson, Ian, Zheng, Wei, Dunlop, Malcolm, Houlston, Richard and Peters, Ulrike
2023.
Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.
Nature Genetics
55
, 519–520.
10.1038/s41588-023-01334-w
|
|
|
Fernandez-Rozadilla, Ceres, Timofeeva, Maria, Chen, Zhishan, Law, Philip, Thomas, Minta, Schmit, Stephanie, Díez-Obrero, Virginia, Hsu, Li, Fernandez-Tajes, Juan, Palles, Claire, Sherwood, Kitty, Briggs, Sarah, Svinti, Victoria, Donnelly, Kevin, Farrington, Susan, Blackmur, James, Vaughan-Shaw, Peter, Shu, Xiao-ou, Long, Jirong, Cai, Qiuyin, Guo, Xingyi, Lu, Yingchang, Broderick, Peter, Studd, James, Huyghe, Jeroen, Harrison, Tabitha, Conti, David, Dampier, Christopher, Devall, Mathew, Schumacher, Fredrick, Melas, Marilena, Rennert, Gad, Obón-Santacana, Mireia, Martin-Sanchez, Vicente, Moratalla-Navarro, Ferran, Hwan Oh, Jae, Kim, Jeongseon, Jee, Sun Ha, Jung, Keum Ji, Kweon, Sun-Seog, Shin, Min-Ho, Shin, Aesun, Ahn, Yoon-Ok, Kim, Dong-Hyun, Oze, Isao, Wen, Wanqing, Matsuo, Keitaro, Matsuda, Koichi, Tanikawa, Chizu, Ren, Zefang, Gao, Yu-Tang, Jia, Wei-Hua, Hopper, John, Jenkins, Mark, Win, Aung Ko, Pai, Rish, Figueiredo, Jane, Haile, Robert, Gallinger, Steven, Woods, Michael, Newcomb, Polly, Duggan, David, Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458, Kaplan, Richard, Maughan, Timothy, Kerr, Rachel, Kerr, David, Kirac, Iva, Bohm, Jan, Mecklin, Lukka-Pekka, Jousilahti, Pekka, Knekt, Paul, Aaltonen, Lauri, Rissanen, Harri, Pukkala, Eero, Eriksson, Johan, Cajuso, Tatiana, Hanninen, Ulrika, Kondelin, Johanna, Palin, Kimmo, Tanskanen, Tomas, Renkonen-Sinisalo, Laura, Zanke, Brent, Männistö, Satu, Albanes, Demetrius, Weinstein, Stephanie, Ruiz-Narvaez, Edward, Palmer, Julie, Buchanan, Daniel, Platz, Elizabeth, Visvanathan, Kala, Ulrich, Cornelia, Siegel, Erin, Brezina, Stefanie, Gsur, Andrea, Campbell, Peter, Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann and Slattery, Martha
2022.
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and East Asian ancestries.
Nature Genetics
10.1038/s41588-022-01222-9
|
|
|
Watts, Katie, Wills, Christopher, Madi, Ayman, Palles, Claire, Maughan, Timothy S., Kaplan, Richard, Al-Tassan, Nada A., Kerr, Rachel, Kerr, David J., Houlston, Richard S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2022.
Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand-foot syndrome.
International Journal of Cancer
151
(6)
, pp. 957-966.
10.1002/ijc.34046
|
|
|
Wills, Christopher, He, Yazhou, Summers, Matthew G., Lin, Yi, Phipps, Amanda I., Watts, Katie, Law, Philip J., Al-Tassan, Nada A., Maughan, Timothy S., Kaplan, Richard, Houlston, Richard S., Peters, Ulrike, Newcomb, Polly A., Chan, Andrew T., Buchanan, Daniel D., Gallinger, Steve, Marchand, Loic L., Pai, Rish K., Shi, Qian, Alberts, Steven R., Gray, Victoria, West, Hannah D. ORCID: https://orcid.org/0000-0002-6104-6534, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dunlop, Malcolm G. and Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458
2021.
Genome-wide search for determinants of survival in 1,926 patients with advanced colorectal cancer with follow-up in over 22,000 patients.
European Journal Of Cancer
159
, pp. 247-258.
10.1016/j.ejca.2021.09.047
Item availability restricted. |
|
|
Watts, Katie, Wills, Christopher, Madi, Ayman, Palles, Claire, Maughan, Timothy S., Kaplan, Richard, Al-Tassan, Nada A., Kerr, Rachel, Kerr, David, Gray, Victoria, West, Hannah ORCID: https://orcid.org/0000-0002-6104-6534, Houlston, Richard S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2021.
Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer.
International Journal of Cancer
149
(9)
, pp. 1713-1722.
10.1002/ijc.33739
|
|
|
Culliford, Richard, Cornish, Alex J., Law, Philip J., Farrington, Susan M., Palin, Kimmo, Jenkins, Mark A., Casey, Graham, Hoffmeister, Michael, Brenner, Hermann, Chang-Claude, Jenny, Kirac, Iva, Maughan, Tim, Brezina, Stefanie, Gsur, Andrea, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Aaltonen, Lauri A., Dunlop, Malcom G. and Soulston, Richard S.
2021.
Lack of an association between gallstone disease and bilirubin levels with risk of colorectal cancer: A Mendelian randomisation analysis.
British Journal of Cancer
124
, pp. 1169-1174.
10.1038/s41416-020-01211-x
|
|
|
Cornish, Alex J., Law, Philip J., Timofeeva, Maria, Palin, Kimmo, Farrington, Susan M., Palles, Claire, Jenkins, Mark A., Casey, Graham, Brenner, Hermann, Chang-Claude, Jenny, Hoffmeister, Michael, Kirac, Iva, Maughan, Tim, Brezina, Stefanie, Gsur, Andrea, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Aaltonen, Lauri A., Tomlinson, Ian, Dunlop, Malcolm G. and Houlston, Richard S.
2020.
Modifiable pathways for colorectal cancer: a mendelian randomisation analysis.
Lancet Gastroenterology and Hepatology
5
(1)
, pp. 55-62.
10.1016/S2468-1253(19)30294-8
|
|
|
Summers, Matthew G. ORCID: https://orcid.org/0000-0001-6387-124X, Maughan, Timothy S., Kaplan, Richard, Law, Philip J., Houlston, Richard S., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2020.
Comprehensive analysis of colorectal cancer-risk loci and survival outcome: a prognostic role for CDH1 variants.
European Journal Of Cancer
124
, pp. 56-63.
10.1016/j.ejca.2019.09.024
|
|
|
Gray, Victoria, Briggs, Sarah, Palles, Claire, Jaegar, Emma, Iveson, Timothy, Kerr, Rachel, Saunders, Mark P., Paul, James, Harkin, Andrea, McQueen, John, Summers, Matthew G., Johnstone, Elaine, Wang, Haitao, Gatcombe, Laura, Maughan, Timothy S., Kaplan, Richard, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Al-Tassan, Nada A., Meyer, Brian F., Wakil, Salma M., Houlston, Richard S., Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Tomlinson, Ian and Church, David N.
2019.
Pattern recognition receptor polymorphisms as predictors of oxaliplatin benefit in colorectal cancer.
JNCI: Journal of the National Cancer Institute
111
(8)
, pp. 828-836.
10.1093/jnci/djy215
|
|
|
Law, Philip J., Timofeeva, Maria, Fernandez-Rozadilla, Ceres, Broderick, Peter, Studd, James, Fernandez-Tajes, Juan, Farrington, Susan, Svinti, Victoria, Palles, Claire, Orlando, Giulia, Sud, Amit, Holroyd, Amy, Penegar, Steven, Theodoratou, Evropi, Vaughan-Shaw, Peter, Campbell, Harry, Zgaga, Lina, Hayward, Caroline, Campbell, Archie, Harris, Sarah, Deary, Ian J., Starr, John, Gatcombe, Laura, Pinna, Maria, Briggs, Sarah, Martin, Lynn, Jaeger, Emma, Sharma-Oates, Archana, East, James, Leedham, Simon, Arnold, Roland, Johnstone, Elaine, Wang, Haitao, Kerr, David, Kerr, Rachel, Maughan, Tim, Kaplan, Richard, Al-Tassan, Nada, Palin, Kimmo, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Buchanan, Daniel D., Win, Aung-Ko, Hopper, John, Jenkins, Mark E., Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steven, Duggan, David, Casey, Graham, Hoffmann, Per, Nöthen, Markus M., Jöckel, Karl-Heinz, Easton, Douglas F., Pharoah, Paul D. P., Peto, Julian, Canzian, Federico, Swerdlow, Anthony, Eeles, Rosalind A., Kote-Jarai, Zsofia, Muir, Kenneth, Pashayan, Nora, Harkin, Andrea, Allan, Karen, McQueen, John, Paul, James, Iveson, Timothy, Saunders, Mark, Butterbach, Katja, Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann, Kirac, Iva, Matošević, Petar, Hofer, Philipp, Brezina, Stefanie, Gsur, Andrea, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Aaltonen, Lauri A., Tomlinson, Ian, Houlston, Richard S. and Dunlop, Malcolm G.
2019.
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
Nature Communications
10
, 2154.
10.1038/s41467-019-09775-w
|
|
|
West, Hannah ORCID: https://orcid.org/0000-0002-6104-6534, Coffey, Michelle, Wagner, Michael J., McLeod, Howard L., Colley, James P., Adams, Richard A. ORCID: https://orcid.org/0000-0003-3915-7243, Fleck, Oliver, Maughan, Timothy S., Fisher, David, Kaplan, Richard S., Harris, Rebecca and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2018.
Role for nucleotide excision repair gene variants in oxaliplatin-induced peripheral neuropathy.
JCO Precision Oncology
2
, pp. 1-18.
10.1200/PO.18.00090
|
|
|
Madi, A., Fisher, D., Maughan, T. S., Colley, J. P., Meade, A. M., Maynard, J., Humphreys, V., Wasan, H., Adams, R. A. ORCID: https://orcid.org/0000-0003-3915-7243, Idziaszczyk, S., Harris, R., Kaplan, R. S. and Cheadle, J. P. ORCID: https://orcid.org/0000-0001-9453-8458
2018.
Common and rare DPYD variants are predictive for 5FU/capecitabine (5FU) toxicity: The MRC COIN and COIN-B trials.
Presented at: 43rd ESMO Congress 2018,
Munich, Germany,
19-23 October 2018.
Annals of Oncology.
, vol.29
(Supple)
Oxford University Press,
VIII22.
10.1093/annonc/mdy269.072
|
|
Madi, Ayman, Fisher, David, Maughan, Timothy S., Colley, James P., Meade, Angela M., Maynard, Julie, Humphreys, Vikki, Wasan, Harpreet, Adams, Richard A. ORCID: https://orcid.org/0000-0003-3915-7243, Idziaszczyk, Shelley, Harris, Rebecca, Kaplan, Richard S. and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2018.
Pharmacogenetic analyses of 2,183 patients with advanced colorectal cancer; Potential role for common dihydropyrimidine dehydrogenase variants in toxicity to chemotherapy.
European Journal of Cancer
102
, pp. 31-39.
10.1016/j.ejca.2018.07.009
|
|
|
Tanskanen, Tomas, van den Berg, Linda, Välimäki, Niko, Aavikko, Mervi, Ness-Jensen, Eivind, Hveem, Kristian, Wettergren, Yvonne, Bexe Lindskog, Elinor, Tõnisson, Neeme, Metspalu, Andres, Silander, Kaisa, Orlando, Giulia, Law, Philip J., Tuupanen, Sari, Gylfe, Alexandra E., Hänninen, Ulrika A., Cajuso, Tatiana, Kondelin, Johanna, Sarin, Antti-Pekka, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Järvinen, Heikki, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Tenesa, Albert, Farrington, Susan M., Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Tim S., Kaplan, Richard, Kerr, Rachel, Kerr, David, Buchanan, Daniel D., Win, Aung K., Hopper, John, Jenkins, Mark A., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fredrick R., Casey, Graham, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Dunlop, Malcolm G., Tomlinson, Ian P., Houlston, Richard S., Palin, Kimmo and Aaltonen, Lauri A.
2018.
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.
International Journal of Cancer
142
(3)
, pp. 540-546.
10.1002/ijc.31076
|
|
|
May-Wilson, Sebastian, Sud, Amit, Law, Philip J., Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Farrington, Susan M., Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy S., Fisher, David, Kerr, Rachel, Kerr, David, Passarelli, Michael N., Figueiredo, Jane C., Buchanan, Daniel D., Win, Aung K., Hopper, John L., Jenkins, Mark A., Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steven, Conti, David, Schumacher, Fred, Casey, Graham, Aaltonen, Lauri A., Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Tomlinson, Ian P., Dunlop, Malcolm G. and Houlston, Richard S.
2017.
Pro-inflammatory fatty acid profile and colorectal cancer risk: a Mendelian randomisation analysis.
European Journal of Cancer
84
, pp. 228-238.
10.1016/j.ejca.2017.07.034
|
|
Summers, Matthew ORCID: https://orcid.org/0000-0001-6387-124X, Smith, Chris, Maughan, Timothy, Kaplan, Rick, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2017.
BRAF and NRAS locus-specific variants have different outcomes on survival to colorectal cancer.
Clinical Cancer Research
23
(11)
, pp. 2742-2749.
10.1158/1078-0432.CCR-16-1541
|
|
|
Rodriguez-Broadbent, Henry, Law, Philip J., Sud, Amit, Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Ripatti, Samuli, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Palotie, Aarno, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Farrington, Susan M., Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy S., Kaplan, Richard, Kerr, Rachel, Kerr, David, Passarelli, Michael N., Figueiredo, Jane C., Buchanan, Daniel D., Win, Aung K., Hopper, John L., Jenkins, Mark A., Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steven, Conti, David, Schumacher, Fred, Casey, Graham, Aaltonen, Lauri A., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Tomlinson, Ian P., Dunlop, Malcolm G. and Houlston, Richard S.
2017.
Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.
International Journal of Cancer
140
(12)
, pp. 2701-2708.
10.1002/ijc.30709
|
|
|
Madi, Ayman, Fisher, David, Maughan, Timothy S., Colley, James P., Meade, Angela M., Tejpar, Sabine, Vam den Bosch, Ben, Maynard, Julie, Humphreys, Vikki, Wasan, Harpreet, Adams, Richard A. ORCID: https://orcid.org/0000-0003-3915-7243, Idziaszczyk, Shelley, Harris, Rebecca, Kaplan, Richard S. and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2017.
Comprehensive pharmacogenetic profiling of the epidermal growth factor receptor pathway for biomarkers of response to, and toxicity from, cetuximab.
Journal of Medical Genetics
54
(8)
, pp. 567-571.
10.1136/jmedgenet-2016-104317
|
|
|
Seligmann, J.F., Fisher, D., Smith, C. G., Richman, S.D., Elliott, F., Brown, S., Adams, Richard ORCID: https://orcid.org/0000-0003-3915-7243, Maughan, T., Quirke, P., Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458, Seymour, M. and Middleton, G.
2017.
Investigating the poor outcomes of BRAF-mutant advanced colorectal cancer: Analysis from 2530 patients in randomised clinical trials.
Annals of Oncology
28
(3)
, pp. 562-568.
10.1093/annonc/mdw645
|
|
|
Jarvis, David, Mitchell, Jonathan S., Law, Philip J., Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hanninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Kaprio, Jaakko, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Jarvinen, Heikki, Renkonen-Sinisalo, Laura, Lepisto, Anna, Bohm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Farrington, Susan M., Mimofeeva, Maria N., Meyer, Brian ., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy, Kaplan, Richard, Kerr, Rachel, Buchanan, Daniel D., Win, Aung K., Hopper, John L., Jenkins, Mark A., Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Taipale, Jussi, Aaltonen, Lauri A., Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458, Dunlop, Malcolm G., Tomlinson, Ian P. and Houlston, Richard S.
2016.
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.
British Journal of Cancer
115
, pp. 266-272.
10.1038/bjc.2016.188
|
|
|
Orlando, Giulia, Law, Philip J., Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti-Pekka, Kaprio, Jaakko, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Ripatti, Samuli, Palotie, Aarno, Järvinen, Heikki, Renkonen-Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka-Pekka, Al-Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Tenesa, Albert, Farrington, Susan, Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy Stanley, Kaplan, Richard, Kerr, Rachel, Kerr, David, Buchanan, Daniel D., Ko Win, Aung, Hopper, John, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Taipale, Jussi, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Dunlop, Malcolm G., Tomlinson, Ian P., Aaltonen, Lauri A. and Houlston, Richard S.
2016.
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.
Human Molecular Genetics
25
(11)
, pp. 2349-2359.
10.1093/hmg/ddw087
|
|
|
Phipps, Amanda I., Passarelli, Michael N., Chan, Andrew T., Harrison, Tabitha A., Jeon, Jihyoun, Hutter, Carolyn M., Berndt, Sonja I., Brenner, Hermann, Caan, Bette J., Campbell, Peter T., Chang-Claude, Jenny, Chanock, Stephen J., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Curtis, Keith R., Duggan, David, Fisher, David, Fuchs, Charles S., Gala, Manish, Giovannucci, Edward L., Hayes, Richard B., Hoffmeister, Michael, Hsu, Li, Jacobs, Eric J., Jansen, Lina, Kaplan, Richard, Kap, Elisabeth J., Maughan, Timothy S., Potter, John D., Schoen, Robert E., Seminara, Daniela, Slattery, Martha L., West, Hannah, White, Emily, Peters, Ulrike and Newcomb, Polly A.
2016.
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.
Carcinogenesis
37
(1)
, pp. 87-95.
10.1093/carcin/bgv161
|
|
Cheng, Timothy H. T., Thompson, Deborah, Painter, Jodie, O?Mara, Tracy, Gorman, Maggie, Martin, Lynn, Palles, Claire, Jones, Angela, Buchanan, Daniel D., Ko Win, Aung, Hopper, John, Jenkins, Mark, Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steve, Conti, David, Schumacher, Fred, Casey, Graham, Giles, Graham G, Pharoah, Paul, Peto, Julian, Cox, Angela, Swerdlow, Anthony, Couch, Fergus, Cunningham, Julie M., Goode, Ellen L., Winham, Stacey J., Lambrechts, Diether, Fasching, Peter, Burwinkel, Barbara, Brenner, Hermann, Brauch, Hiltrud, Chang-Claude, Jenny, Salvesen, Helga B., Kristensen, Vessela, Darabi, Hatef, Li, Jingmei, Liu, Tao, Lindblom, Annika, Hall, Per, de Polanco, Magdalena Echeverry, Sans, Monica, Carracedo, Angel, Castellvi-Bel, Sergi, Rojas-Martinez, Augusto, Aguiar Jnr, Samuel, Teixeira, Manuel R., Dunning, Alison M., Dennis, Joe, Otton, Geoffrey, Proietto, Tony, Holliday, Elizabeth, Attia, John, Ashton, Katie, Scott, Rodney J., McEvoy, Mark, Dowdy, Sean C., Fridley, Brooke L., Werner, Henrica M. J., Trovik, Jone, Njolstad, Tormund S., Tham, Emma, Mints, Miriam, Runnebaum, Ingo, Hillemanns, Peter, Dörk, Thilo, Amant, Frederic, Schrauwen, Stefanie, Hein, Alexander, Beckmann, Matthias W., Ekici, Arif, Czene, Kamila, Meindl, Alfons, Bolla, Manjeet K., Michailidou, Kyriaki, Tyrer, Jonathan P., Wang, Qin, Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Annibali, Daniela, Depreeuw, Jeroen, Al-Tassan, Nada A., Harris, Rebecca, Meyer, Brian F., Whiffin, Nicola, Hosking, Fay J, Kinnersley, Ben, Farrington, Susan M., Timofeeva, Maria, Tenesa, Albert, Campbell, Harry, Haile, Robert W., Hodgson, Shirley, Carvajal-Carmona, Luis, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Easton, Douglas, Dunlop, Malcolm, Houlston, Richard, Spurdle, Amanda and Tomlinson, Ian
2015.
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Scientific Reports
5
, 17369.
10.1038/srep17369
|
|
Smith, Christopher G., Fisher, David, Harris, Rebecca, Maughan, Timothy S., Phipps, Amanda I., Richman, Susan, Seymour, Matthew, Tomlinson, Ian, Rosmarin, Dan, Kerr, David, Chan, Andrew T., Peters, Ulrike, Newcombe, Polly A., Idziaszczyk, Shelley, West, Hannah, Meade, Angela, Kaplan, Richard and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2015.
Analyses of 7,635 patients with colorectal cancer using independent training and validation cohorts show that rs9929218 in CDH1 is a prognostic marker of survival.
Clinical Cancer Research
21
(15)
, pp. 3453-3461.
10.1158/1078-0432.CCR-14-3136
|
|
|
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 Alexis, Barclay, Ella, Maughan, Timothy Stanley, 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 Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Houlston, Richard S.
2015.
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
Scientific Reports
5
, 10442.
10.1038/srep10442
|
|
|
Venderbosch, Sabine, Nagtegaal, Iris D., Maughan, Tim S., Smith, Christopher G., Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Fisher, David, Kaplan, Richard, Quirke, Philip, Seymour, Matthew T., Richman, Susan D., Meijer, Gerrit A., Ylstra, Bauke, Heideman, Danielle A. M., de Haan, Anton F. J., Punt, Cornelius J. A. and Koopman, Miriam
2014.
Mismatch repair status and BRAF mutation status in metastatic colorectal cancer patients: a pooled analysis of the CAIRO, CAIRO2, COIN, and FOCUS studies.
Clinical Cancer Research
20
(20)
, pp. 5322-5330.
10.1158/1078-0432.CCR-14-0332
|
|
|
Smith, Christopher G., West, Hannah, Harris, Rebecca, Idziaszczyk, Shelley, Maughan, Timothy S., Kaplan, Richard, Richman, Susan, Quirke, Philip, Seymour, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Steinke, Verena, Propping, Peter, Hes, Frederik J., Wijnen, Juul and Cheadle, Jeremy ORCID: https://orcid.org/0000-0001-9453-8458
2014.
Response.
Journal of the National Cancer Institute
106
(5)
, dju087.
10.1093/jnci/dju087
|
|
Smith, Chris, Fisher, D., Claes, B., Maughan, T. S., Idziaszczyk, Shelley, Peuteman, G., Harris, Rebecca, James, Michelle D., Meade, A., Jasani, Bharat, Adams, Richard A. ORCID: https://orcid.org/0000-0003-3915-7243, Kenny, S., Kaplan, R., Lambrechts, D. and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2013.
Somatic profiling of the epidermal growth factor receptor pathway in tumors from patients with advanced colorectal cancer treated with chemotherapy ± cetuximab.
Clinical Cancer Research
19
(15)
, pp. 4104-4113.
10.1158/1078-0432.CCR-12-2581
|
|
Smith, Chris, West, Hannah, Harris, Rebecca, Idziaszczyk, Shelley Alexis, Maughan, Timothy Stanley, Kaplan, Richard, Richman, Susan, Quirke, Philip, Seymour, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Steinke, Verena, Propping, Peter, Hes, Frederik J., Wijnen, Juul and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2013.
Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis.
Journal of the National Cancer Institute
105
(16)
, pp. 1249-1253.
10.1093/jnci/djt183
|
|
Smith, Chris, Naven, Marc ORCID: https://orcid.org/0000-0002-6339-3257, Harris, Rebecca, Colley, James, West, Hannah, Li, Ning, Liu, Yuan, Adams, Richard ORCID: https://orcid.org/0000-0003-3915-7243, Maughan, Timothy S., Nichols, Laura, Kaplan, Richard, Wagner, Michael J., McLeod, Howard L. and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2013.
Exome resequencing identifies potential tumor-suppressor genes that predispose to colorectal cancer.
Human Mutation
34
(7)
, pp. 1026-1034.
10.1002/humu.22333
|
|
Dunlop, Malcolm G., Dobbins, Sara E., Farrington, Susan Mary, Jones, Angela M., Palles, Claire, Whiffin, Nicola, Tenesa, Albert, Spain, Sarah, Broderick, Peter, Ooi, Li-Yin, Domingo, Enric, Smillie, Claire, Henrion, Marc, Frampton, Matthew, Martin, Lynn, Grimes, Graeme, Gorman, Maggie, Semple, Colin, Ma, Yusanne P., Barclay, Ella, Prendergast, James, Cazier, Jean-Baptiste, Olver, Bianca, Penegar, Steven, Lubbe, Steven, Chander, Ian, Carvajal-Carmona, Luis G., Ballereau, Stephane, Lloyd, Amy, Vijayakrishnan, Jayaram, Zgaga, Lina, Rudan, Igor, Theodoratou, Evropi, Thomas, Huw, Maher, Eamonn, Evans, Gareth, Walker, Lisa, Halliday, Dorothy, Lucassen, Anneke, Paterson, Joan, Hodgson, Shirley, Homfray, Tessa, Side, Lucy, Izatt, Louise, Donaldson, Alan, Tomkins, Susan, Morrison, Patrick, Brewer, Carole, Henderson, Alex, Davidson, Rosemarie, Murday, Victoria, Cook, Jaqueline, Haites, Neva, Bishop, Timothy, Sheridan, Eamonn, Green, Andrew, Marks, Christopher, Carpenter, Sue, Broughton, Mary, Greenhalge, Lynn, Suri, Mohnish, Starr, John M., Deary, Ian, Kirac, Iva, Kovacevi, Dujo, Aaltonen, Lauri A., Renkonen-Sinisalo, Laura, Mecklin, Jukka-Pekka, Matsuda, Koichi, Nakamura, Yusuke, Okada, Yukinori, Gallinger, Steven, Duggan, David J., Conti, David, Newcomb, Polly, Hopper, John, Jenkins, Mark A., Schumacher, Fredrick, Casey, Graham, Easton, Douglas, Shah, Mitul, Pharoah, Paul, Lindblom, Annika, Liu, Tao, Edler, David, Lenander, Claes, Dalén, Johan, Hjern, Fredrik, Lundqvist, Nils, Lindforss, Ulrik, Påhlman, Lars, Smedh, Kennet, Törnqvist, Anders, Holm, Jörn, Janson, Martin, Andersson, Magnus, Ekelund, Susanne, Olsson, Louise, Smith, Chris, West, Hannah, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, MacDonald, Graham, Samuel, Leslie M., Ahmad, Athar, Corrie, Philippa, Jodrell, Duncan, Palmer, Cheryl, Wilson, Charles, O'Hagan, Julie, Smith, David, McDermott, Ray, Walshe, Janice, Cassidy, James, McDonald, Alec, Mohammed, Nazia, White, Jeff, Yosef, Hosney, Breathnach, Oscar, Grogan, Liam, Thomas, Robert, Eatock, Martin, Henry, Paul, Houston, Russell, Johnston, Patrick, Wilson, Richard, Geh, Ian, Danwata, Falalu, Hindley, Andrew, Susnerwala, Shabbir, Bradley, Chris, Conn, Andrew, Raine, Anne, Twelves, Chris, Falk, Stephen, Hopkins, Kirstin, Tahir, Saad, Dhadda, Amandeep, Maraveyas, Anthony, Sgouros, Joseph, Teo, Mark, Ahmad, Rizvana, Cleator, Susan, Creak, Antonia, Lowdell, Charles, Riddle, Philippa, Benstead, Kim, Farrugia, David, Reed, Nicholas, Shepherd, Stephen, Levine, Edward, Mullamitha, Saifee, Saunders, Mark, Valle, Juan, Wilson, Gregory, Jones, Adam, Weaver, Andrew, Clark, Peter I., Haylock, Brain, Iqbal, Mussawar I., Myint, Arthur S., Smith, David, Beesley, Sharon, Sevitt, Timothy, Nicoll, Jonathan, Daniel, Francis, Ford, Victoria, Talbot, Toby, Butt, Mohammad, Hamid, Abdel, Mack, Paul, Roy, Raj, Osborne, Richard, McKinna, Fiona, Alsab, Heidar, Basu, Devyanee, Murray, Phillip, Sizer, Bruce, Azam, Faisal A., Neupane, Rekha, Waterston, Ashita, Glaholm, John, Blesing, Claire, Lowndes, Sarah, Medisetti, Aruna, Gaya, Andrew, Leslie, Martin, Maisey, Nicholas, Ross, Paul, Dunn, Grainne, Al-Salihi, Omar, Wasan, Harpreet S., Palmer, Cheryl, Tan, Li Tee, Dent, Jo, Hofmann, Uschi, Joffe, Johnathan K., Sherwin, Elizabeth, Soomal, Rabinder, Chakrabarti, Amitabha, Joseph, Shibu, Van der Voet, Johannes, Wadd, Nicholas J., Wilson, David, Anjarwalia, Salim, Hall, Julia, Hughes, Rob, Polychronis, Andrew, Scarffe, John H., Hill, Mark, James, Rodger D., Shah, Riyaz, Summers, Jeffrey, Hartley, Andrew, Carney, Desmond, McCaffrey, John, Bystricky, Brano, O'Reilly, Seamus, Gupta, Rajnish, Al-Mishlab, Talib, Gidden, Fiona, O'Hara, Richard, Stewart, Jill, Ashford, Richard, Glynne-Jones, Robert, Harrison, Mark, Mawdsley, Suzannah, Barlow, Hilary, Tighe, Mary, Walther, Julie, Neal, Janet, Rees, Charlotte, Bridgewater, John, Karp, Stephen, McGovern, Ursula, Atherton, Philip J., El-deeb, Hany, Macmillan, Craig, Patel, Kinnari, Bessell, Eric Michael, Dickinson, Peter D., Potter, Vanessa, Jephcott, Catherine, McAdam, Karen, Wrigley, Jessica, Osborne, Richard, Muthuramalingam, Sethupathi, O'Callaghan, Anne, Bridgewater, John, Melcher, Lucinda, Braconi, Chiara, Geh, Ju Ian, Palmer, Dan, Narayana, Priya, Steven, Neil, Gaya, Andres, Maisey, Nicholas, Rudman, Sarah, Chakraborti, Prabir, Kelly, Kay, Macgregor, Carol, Whillis, David, Freebairn, Alice, Gildersleve, James, Sharif, Sahid, Astras, George, Hickish, Tamas, Beech, Darren, Ellis, Richard, Kulkarni, Rajendra, Shankland, K., Begent, Richard, Mayer, Astrid, Meyer, Timothy, Strauss, Sandra, Hall, Viriginia, Raj, Sanjay, Chau, Ian, Cunningham, David, Birtle, Alison, Biswas, Ashoke, Susnerwala, Shabbir, Wise, Marcus, Cummins, Sebastian, Essapen, Sharadah, Middleton, Gary, Topham, Claire, Langley, Ruth, McKinna, Fiona, Webb, Andrew, Wilkins, Marie, Iveson, Timothy John, Dhadda, Amandeep, Hamid, Abdel, Askill, Colin, Wagstaff, John, Azzabi, Ashraf, Bateman, Adrian, Prejbisz, Jan, Tsang, David, Ali, Nasim, Jones, Amanda, O'Neill, Paul, Cottrill, Christopher, Propper, David, Lofts, Fiona Jane, Kennedy, James, Anthoney, David A., Cooper, Rachel, Crellin, Adrian, Melcher, Alan, Seymour, Matthew, Baughan, Christopher, Alexander, Emma, Cleator, Susan, Crown, John, Fennelly, David, Adab, Fawzi, Giridharan, Selvaraj, Pedley, Ian, Wright, Kathryn, Bliss, Peter, Cogill, Geoffrey, Lo, Nangi, Toy, Elizabeth, Bridgewater, John, Hochhauser, Daniel, Ledermann, Jonathan, Brewster, A. E., Maughan, Timothy Stanley, Mort, Diana, Mukherjee, Somnath, Dobrowsky, Werner, Calvert, Paula, Leonard, Gregory, Ahmad, Rizvana, Ford, Hugo, Moody, Anne Margeret, Goriah, Sonia, Wilkins, Margeret, Clive, Sally, Dawson, Lesley, McLean, Catriona, Phillips, Hamish Andrew, Gopi, Kakumudi, Tomlinson, Marjorie, Clenton, Susan, Furniss, Debra, Hornbuckle, Joanne, Pledge, Simon, Wadsley, Jonathan, Abbas, Mohammed, Marshall, Ernest, Harper-Wynne, Catherine, Barnes, Anne, Kumar, Satish, Vigneswaran, Vallipuram, Farrugia, David, Webb, Andrew, Gollins, Simon, Falk, Stephen, Genton, M., Sparrow, Geoff, Bale, Catherine, Fuller, C., Mullard, Anna, Stuart, Nicholas, Williams, Rachel, Keane, Maccon, Maughan, Tim, Seymour, Matthew, Wilson, Richard, Wasan, Harpreet, Adams, Richard Alexander ORCID: https://orcid.org/0000-0003-3915-7243, Madi, Ayman, Cassidy, James, Kennedy, James, Hodgkinson, Elizabeth, Rogers, Penny, Pope, Malcolm, Kaplan, Rick, Meade, Angela, Parmar, Mahesh, Kenny, Sarah, Fisher, David, Harper, Lynda, Mitchell, Jena, Nichols, Laura, Sydes, Benjamin, Clement, Louise, Kay, Edward, Courtney, Cheryl, Gallagher, Madalena, Murphy, Claire, Thompson, Lindsay, Beall, Sarah, Hassan, Sharma, Gracie, Richard, Griffiths, Gareth O., Mason, Malcolm David ORCID: https://orcid.org/0000-0003-1505-2869, Parker, Chris, Rudd, Robin, Johnson, Patrick, Whelan, Jeremy, Northover, John, Brown, Julia, Aapro, Matti, Stout, Ronald, Midgley, Rachel, Kerr, David J., Campbell, Harry, Tomlinson, Ian P. and Houlston, Richard S.
2012.
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk [Letter].
Nature Genetics
44
(7)
, pp. 770-776.
10.1038/ng.2293
|
|
Houlston, Richard S., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Maughan, Timothy Stanley
2012.
COGENT (COlorectal cancer GENeTics) revisited.
Mutagenesis
27
(2)
, pp. 143-151.
10.1093/mutage/ger059
|
|
Maughan, Timothyn S., Adams, Richard A. ORCID: https://orcid.org/0000-0003-3915-7243, Smith, Chris, Meade, Angela M., Seymour, Matthew T., Wilson, Richard H., Idziaszczyk, Shelley A., Harris, Rebecca, Fisher, David, Kenny, Sarah L., Kay, Edward, Mitchell, Jenna K., Madi, Ayman, Jasani, Bharat, James, Michelle D., Bridgewater, John, Kennedy, M. John, Claes, Bart, Lambrechts, Diether, Kaplan, Richard and Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458
2011.
Addition of cetuximab to oxaliplatin-based first-line combination chemotherapy for treatment of advanced colorectal cancer: results of the randomised phase 3 MRC COIN trial.
The Lancet
377
(9783)
, pp. 2103-2114.
10.1016/S0140-6736(11)60613-2
|
|
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 Peter ORCID: https://orcid.org/0000-0001-9453-8458, 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. and Tomlinson, Ian P. M.
2011.
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13.
Human Molecular Genetics
21
(4)
, pp. 934-946.
10.1093/hmg/ddr523
|
|
Tomlinson, Ian P. M., Carvajal-Carmona, Luis G., Dobbins, Sara E., Tenesa, Albert, Jones, Angela M., Howarth, Kimberley, Palles, Claire, Broderick, Peter, Jaeger, Emma E. M., Farrington, Susan, Lewis, Annabelle, Prendergast, James G. D., Pittman, Alan M., Theodoratou, Evropi, Olver, Bianca, Walker, Marion, Penegar, Steven, Barclay, Ella, Whiffin, Nicola, Martin, Lynn, Ballereau, Stephane, Lloyd, Amy, Gorman, Maggie, Lubbe, Steven, Howie, Bryan, Marchini, Jonathan, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Castells, Antoni, Carracedo, Angel, Castellvi-Bel, Sergi, Duggan, David, Conti, David, Cazier, Jean-Baptiste, Campbell, Harry, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Gallinger, Steven, Newcomb, Polly, Hopper, John, Jenkins, Mark A., Aaltonen, Lauri A., Kerr, David J., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Pharoah, Paul, Casey, Graham, Houlston, Richard S. and Dunlop, Malcolm G.
2011.
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
PLoS Genetics
7
(6)
, e1002105.
10.1371/journal.pgen.1002105
|
|
|
Houlston, Richard S, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Dobbins, Sara E., Tenesa, Albert, Jones, Angela M., Howarth, Kimberley, Spain, Sarah L., Broderick, Peter, Domingo, Enric, Farrington, Susan, Prendergast, James G. D., Pittman, Alan M., Theodoratou, Evi, Smith, Chris, Olver, Bianca, Walther, Axel, Barnetson, Rebecca A., Churchman, Michael, Jaeger, Emma E. M., Penegar, Steven, Barclay, Ella, Martin, Lynn, Gorman, Maggie, Mager, Rachel, Johnstone, Elaine, Midgley, Rachel, Niittymäki, Iina, Tuupanen, Sari, Colley, James, Idziaszczyk, Shelley Alexis, Thomas, Huw J. W., Lucassen, Anneke M., Evans, D. Gareth R., Maher, Eamonn R., Maughan, Timothy Stanley, Dimas, Antigone, Dermitzakis, Emmanouil, Cazier, Jean-Baptiste, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Carvajal-Carmona, Luis G., Campbell, Harry, Dunlop, Malcolm G. and Tomlinson, Ian P. M.
2010.
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 [Letter].
Nature Genetics
42
(11)
, pp. 973-977.
10.1038/ng.670
|
|
Idziaszczyk, Shelley Alexis, Wilson, C. H., Smith, Chris, Adams, D. J. and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2010.
Analysis of the frequency of GNAS codon 201 mutations in advanced colorectal cancer [Letter].
Cancer Genetics and Cytogenetics
202
(1)
, pp. 67-69.
10.1016/j.cancergencyto.2010.04.023
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2010.
MUTYH-associated polyposis.
Rodriguez-Bigas, Miguel A., Cutait, Raul, Lynch, Patrick M., Tomlinson, Ian and Vasen, Hans F. A., eds.
Hereditary Colorectal Cancer,
M.D. Anderson Solid Tumor Oncology Series,
vol. 5.
New York:
Springer,
pp. 133-146.
|
|
Dallosso, Anthony Richard, Jones, Siân, Azzopardi, Duncan, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Al-Tassan, Nada A., Williams, Geraint Trefor ORCID: https://orcid.org/0000-0003-3768-9940, Idziaszczyk, Shelley Alexis, Davies, D. Rhodri, Milewski, Peter, Williams, Sally, Beynon, John, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2009.
The APC Variant p.Glu1317Gln predisposes to colorectal adenomas by a novel mechanism of relaxing the target for tumorigenic somatic APC mutations.
Human Mutation
30
(10)
, pp. 1412-1418.
10.1002/humu.21089
|
|
Bonnet, Cleo, Aldred, Mark, Von Ruhland, Christopher John, Harris, Rebecca, Sandford, Richard and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2009.
Defects in cell polarity underlie TSC and ADPKD-associated cystogenesis.
Human Molecular Genetics
18
(12)
, pp. 2166-2176.
10.1093/hmg/ddp149
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2009.
MUTYH-associated colorectal polyposis and cancer.
Schwab, Manfred, ed.
Encyclopedia of Cancer. 2nd ed,
Springer,
|
|
Tee, Andrew ORCID: https://orcid.org/0000-0002-5577-4631, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2009.
Tuberous sclerosis complex.
Schwab, Manfred, ed.
Encyclopedia of Cancer. 2nd ed,
Springer,
|
|
| University of Wales 2008. Screening methods and sequences relating thereto. US7393940B2. [Patent]. |
|
Azzopardi, Duncan, Dallosso, Anthony Richard, Eliason, Kristilyn, Hendrickson, Brant C., Jones, Natalie, Rawstorne, Edward Charles, Colley, James, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Frye, Cynthia, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Wenstrup, Richard, Scholl, Thomas and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2008.
Multiple rare nonsynonymous variants in the 'adenomatous polyposis coli' gene predispose to colorectal adenomas.
Cancer Research
68
(2)
, pp. 358-363.
10.1158/0008-5472.CAN-07-5733
|
|
Dallosso, Anthony Richard, Dolwani, Sunil ORCID: https://orcid.org/0000-0002-3113-5472, Jones, N., Jones, Sian, Colley, James, Maynard, Julie Helen, Idziaszczyk, Shelley Alexis, Humphreys, Vikki, Arnold, J., Donaldson, A., Eccles, D., Ellis, A., Evans, D. G., Frayling, Ian, Hes, F. J., Houlston, R S, Maher, E R, Nielsen, M, Parry, S, Tyler, E, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2008.
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3.
Gut
57
(9)
, pp. 1252-1255.
10.1136/gut.2007.145748
|
|
Payne, Y., Williams, M., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Stott, N. C. H., Rowlands, M., Shickle, D., West, G., Meredith, Linda, Goodchild, M., Harper, Peter Stanley and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286
2008.
Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales The South Wales Cystic Fibrosis Carrier Screening Research Team.
Clinical Genetics
51
(3)
, pp. 153-163.
10.1111/j.1399-0004.1997.tb02445.x
|
|
Goorden, Susanna M. I., van Woerden, Geeske M., van der Weerd, Louise, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Elgersma, Ype
2007.
Cognitive deficits inTsc1+/-mice in the absence of cerebral lesions and seizures.
Annals of Neurology
62
(6)
, pp. 648-655.
10.1002/ana.21317
|
|
Dolwani, Sunil ORCID: https://orcid.org/0000-0002-3113-5472, Williams, Geraint Trefor ORCID: https://orcid.org/0000-0003-3768-9940, West, K.P., Newman, J., Stock, D., Williams, A.P., Best, J., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2007.
Analysis of inherited MYH (MUTYH) mutations in British Asian patients with colorectal cancer [Letter].
Gut
56
(4)
, p. 593.
10.1136/gut.2006.094532
|
|
Wilson, Catherine Helen, Bonnet, Cleo, Guy, Carol, Idziaszczyk, Shelley Alexis, Colley, James, Humphreys, Vikki, Maynard, Julie Helen, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2006.
Tsc1 Haploinsufficiency without Mammalian Target of Rapamycin Activation Is Sufficient for Renal Cyst Formation in Tsc1+/- Mice.
Cancer Research
66
(16)
, pp. 7934-8.
10.1158/0008-5472.CAN-06-1740
|
|
Wilson, Catherine Helen, Idziaszczyk, Shelley Alexis, Colley, James, Humphreys, Vikki, Guy, Carol, Maynard, Julie Helen, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2005.
Induction of renal tumorigenesis with elevated levels of somatic loss of heterozygosity in Tsc1+/- mice on a Blm-deficient background.
Cancer Research
65
(22)
, pp. 10179-10182.
10.1158/0008-5472.CAN-05-2688
|
|
Colley, James, Jones, Sian, Dallosso, Anthony R., Maynard, Julie Helen, Humphreys, Vikki, Dolwani, Sunil ORCID: https://orcid.org/0000-0002-3113-5472, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2005.
Rapid recognition of aberrant dHPLC elution profiles using the Transgenomic NavigatorTM software.
Human Mutation
26
(2)
, p. 165.
10.1002/humu.9354
|
|
Wilson, Catherine Helen, Idziaszczyk, Shelley Alexis, Parry, Lee ORCID: https://orcid.org/0000-0002-4467-9196, Guy, Carol, Griffiths, David Francis Rees, Lazda, Edgar Janis, Bayne, Rosemary A. L., Smith, Andrew J. H., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2005.
A mouse model of tuberous sclerosis 1 showing background specific early post-natal mortality and metastatic renal cell carcinoma.
Human Molecular Genetics
14
(13)
, pp. 1839-1850.
10.1093/hmg/ddi190
|
|
Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Jones, Sian, Dolwani, Sunil ORCID: https://orcid.org/0000-0002-3113-5472 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2005.
MutYH (MYH) and colorectal cancer.
Biochemical Society Transactions
33
(4)
, pp. 679-683.
10.1042/BST0330679
|
|
Bai, Haibo, Jones, Sian, Guan, Xin, Wilson, Teresa M., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Lu, A-Lien
2005.
Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis.
Nucleic Acids Research
33
(2)
, pp. 597-604.
10.1093/nar/gki209
|
|
Fleischmann, Christina, Peto, Julian, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Shah, Bindiya, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Houlston, Richard S.
2004.
Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer.
International Journal of Cancer
109
(4)
, pp. 554-558.
10.1002/ijc.20020
|
|
Jones, Sian, Lambert, S., Williams, Geraint Trevor ORCID: https://orcid.org/0000-0003-3768-9940, Best, J. M., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2004.
Increased frequency of the k-ras G12C mutation in MYH polyposis colorectal adenomas.
British Journal of Cancer
90
(8)
, pp. 1591-1593.
10.1038/sj.bjc.6601747
|
|
|
Al-Tassan, Nada, Eisen, Tim, Maynard, Julie Helen, Bridle, Helen, Shah, Bindiya, Fleischmann, Christina, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Houlston, Richard S.
2004.
Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma.
Human Genetics
114
(2)
, pp. 207-210.
10.1007/s00439-003-1033-2
|
|
Kwiatkowski, D.J., Reeve, M. P., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2003.
Molecular genetics.
Curatolo, Paolo, ed.
Tuberous Sclerosis Complex: From Basic Science to Clinical Phenotypes,
International Review of Child Neurology (Mac Keith Press),
Cambridge:
Cambridge University Press,
pp. 228-263.
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2003.
Exposing the MYtH about base excision repair and human inherited disease.
Human Molecular Genetics
12
(s2)
, R159-R165.
10.1093/hmg/ddg259
|
|
Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Dolwani, Sunil ORCID: https://orcid.org/0000-0002-3113-5472, Jones, Sian, Eccles, Diana, Ellis, Anthony, Evans, D. Gareth, Frayling, Ian Martin, Jordan, Sheila, Maher, Eamonn R., Mak, Tony, Maynard, Julie Helen, Pigatto, Francesca, Shaw, Joan and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2003.
Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH.
The Lancet
362
(9377)
, pp. 39-41.
10.1016/S0140-6736(03)13805-6
|
|
Gill, Hefin, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Maynard, Julie Helen, Fleming, Nick, Whatley, Sharon D., Cranston, T, Thompson, E M, Leonard, H, Davis, M, Christodoulou, J, Skjeldal, O, Hanefeld, F, Kerr, A, Tandy, A, Ravine, D. and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286
2003.
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome.
Journal of Medical Genetics
40
(5)
, pp. 380-384.
10.1136/jmg.40.5.380
|
|
Emmerson, Paul, Maynard, Julie Helen, Jones, Sian, Butler, Rachel, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2003.
Characterizing mutations in samples with low-level mosaicism by collection and analysis of DHPLC fractionated heteroduplexes.
Human Mutation
21
(2)
, pp. 112-115.
10.1002/humu.10159
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, J.
2003.
Tuberous sclerosis: genetics.
Cooper, David Neil, ed.
Encyclopedia of the Human Genome,
London:
Nature Publishing Group,
pp. 650-656.
|
|
Jones, Sian, Emmerson, Paul, Maynard, Julie Helen, Best, Jacqueline M., Jordan, Sheila, Williams, Geraint Trefor ORCID: https://orcid.org/0000-0003-3768-9940, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2002.
Biallelic germline mutations in MYH predispose to multiple colorectal ademona and somatic G:C to T:A mutations.
Human Molecular Genetics
11
(23)
, pp. 2961-2967.
10.1093/hmg/11.23.2961
|
|
Al-Tassan, Nada ORCID: https://orcid.org/0000-0001-9453-8458, Chmiel, Nikolas H., Maynard, Julie Helen, Fleming, Nick, Livingston, Alison L., Williams, Geraint Trefor ORCID: https://orcid.org/0000-0003-3768-9940, Hodges, Angela Kaye, Davies, D.Rhodri, David, Sheila S., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2002.
Inherited variants of MYH associated with somatic G:C to T:A mutations in colorectal tumors.
Nature Genetics
30
(2)
, pp. 227-32.
10.1038/ng828
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Krawczak, Michael, Thomas, Meinir W, Hodges, Angela Kaye, Al-Tassan, Nada, Fleming, Nick and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2002.
Different combinations of biallelic APC mutation confer different growth advantages in colorectal tumours.
Cancer Research
62
, pp. 363-366.
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Krawczak, Michael, Thomas, Meinir W., Hodges, Angela Kaye, Al-Tassan, Nada, Fleming, Nick and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2002.
Different combinations of biallelic APC mutation confer different growth advantages in colorectal tumours.
Cancer Research
62
(2)
, pp. 363-366.
|
|
Antonarakis, Emmanuel S., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2002.
Temperature modulation of DHPLC analysis for detection of coexisting constitutional and mosaic sequence variants in TSC2.
Journal of Biochemical and Biophysical Methods
51
(2)
, pp. 161-164.
10.1016/S0165-022X(02)00011-8
|
|
Hodges, Angela K., Li, Shaowei, Maynard, Julie Helen, Parry, Lee ORCID: https://orcid.org/0000-0002-4467-9196, Braverman, Richard, DeClue, Jeffrey E., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2001.
Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberin.
Human Molecular Genetics
10
(25)
, pp. 2899-9205.
10.1093/hmg/10.25.2899
|
|
Parry, Lee ORCID: https://orcid.org/0000-0002-4467-9196, Maynard, Julie Helen, Patel, A., Clifford, S. C., Morrissey, C., Maher, E. R., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
2001.
Analysis of the TSC1 and TSC2 genes in sporadic renal cell carcinomas.
British Journal of Cancer
85
, pp. 1226-1230.
10.1054/bjoc.2001.2072
|
|
Soucek, Thomas, Rosner, Margit, Miloloza, Angelina, Kubista, Marion, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Hengstschläger, Markus
2001.
Tuberous sclerosis causing mutants of the TSC2 gene product affect proliferation and p27 expression.
Oncogene
20
(35)
, pp. 4904-4909.
|
|
Jones, Alistair C., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2001.
Low level mosaicism detectable by DHPLC but not by direct sequencing.
Human Mutation
17
(3)
, pp. 233-234.
10.1002/humu.8
|
|
Fleming, Nick, Maynard, Julie H., Tzitzis, Loukas, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2001.
LD-PCR coupled to long-read direct sequencing: an approach for mutation detection in genes with compact genomic structures.
Journal of Biochemical and Biophysical Methods
47
(1-2)
, pp. 131-136.
10.1016/S0165-022X(00)00159-7
|
|
Benvenuto, Giovanna, Li, Shaowei, Brown, Samantha J., Braverman, Richard, Vass, William C., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Halley, Dicky J. J., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Wienecke, Ralf and DeClue, Jeffrey E.
2000.
The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitination.
Oncogene
19
(54)
, pp. 6306-6316.
10.1038/sj.onc.1204009
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Dobbie, Lorraine, Idziaszczyk, Shelley, Hodges, Angela Kaye, Smith, Andrew J.H., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Young, Janet
2000.
Genomic organization and comparative analysis of the mouse tuberous sclerosis 1 (Tsc1) locus.
Mammalian Genome
11
(12)
, pp. 1135-1138.
10.1007/s003350010203
|
|
Lamlum, Hanan, Al-Tassan, Nada A., Jaeger, Emma, Frayling, Ian Martin, Sieber, Oliver, Bin Reza, Faisal, Eckert, Maria, Rowan, Andrew, Barclay, Ella, Atkin, Wendy, Williams, Christopher, Gilbert, John, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Bell, Jennie, Houlston, Richard, Bodmer, Walter, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Tomlinson, Ian
2000.
Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q.
Human Molecular Genetics
9
(15)
, pp. 2215-2221.
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Reeve, Mary Pat, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Kwiatkowski, David J.
2000.
Molecular genetic advances in tuberous sclerosis.
Human Genetics
107
(2)
, pp. 97-114.
10.1007/s004390000348
|
|
Jones, Alistair C., Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Cohen, David and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2000.
Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosis.
Human Genetics
106
(6)
, pp. 663-668.
10.1007/s004390000316
|
|
Parry, Lee ORCID: https://orcid.org/0000-0002-4467-9196, Maynard, Julie Helen, Patel, Amit, Hodges, Angela, von Deimling, Andreas, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
2000.
Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours.
Human Genetics
107
(4)
, pp. 350-356.
10.1007/s004390000390
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Gill, Harinder, Fleming, Nick, Maynard, Julie Helen, Kerr, Alison, Leonard, Helen, Krawczak, Michael, Cooper, David Neil ORCID: https://orcid.org/0000-0002-8943-8484, Lynch, Sally, Thomas, Nicholas Stuart Tudor, Hughes, Helen, Hulten, Maj, Ravine, David, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286
2000.
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.
Human Molecular Genetics
9
(7)
, pp. 1119-1129.
10.1093/hmg/9.7.1119
|
|
Jones, Alistair C., Austin, Jehannine, Hansen, Nancy, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Oefner, Peter J., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379
1999.
Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis.
Clinical Chemistry
45
(8)
, pp. 1133-1140.
|
|
Jones, Alistair C., Shyamsundar, Magitha M., Thomas, Meinir W., Maynard, Julie Helen, Idziaszczyk, Shelley, Tomkins, Susan, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
1999.
Comprehensive mutation analysis of TSC1 and TSC2 - and phenotypic correlations in 150 families with tuberous sclerosis.
American Journal of Human Genetics
64
(5)
, pp. 1305-1315.
10.1086/302381
|
|
van Slegtenhorst, M., Nellist, M., Nagelkerken, B., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Snell, Russell, van den Ouweland, Ans, Reuser, Arnold, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Halley, D. and van der Sluijs, Peter
1998.
Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products.
Human Molecular Genetics
7
(6)
, pp. 1053-1057.
10.1093/hmg/7.6.1053
|
|
Jones, Alistair C., Daniells, Claire E., Snell, Russell G., Tachataki, Maria, Idziaszczyk, Shelley Alexis, Krawczak, Michael, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
1997.
Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosis.
Human Molecular Genetics
6
(12)
, pp. 2155-2161.
10.1093/hmg/6.12.2155
|
|
Sampson, Julian R. ORCID: https://orcid.org/0000-0002-2902-2348, Maheshwar, Magitha M., Aspinwall, Richard, Thompson, Peter, Cheadle, Jeremy P ORCID: https://orcid.org/0000-0001-9453-8458, Ravine, David, Roy, Sushmita, Haan, Eric, Bernstein, Jay and Harris, Peter C.
1997.
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene.
American Journal of Human Genetics
61
(4)
, pp. 843-851.
10.1086/514888
|
|
Maheshwar, Magitha M., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Jones, Alistair C., Myring, Jenny, Fryer, Alan E., Harris, Peter C. and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
1997.
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosis.
Human Molecular Genetics
6
(11)
, pp. 1991-1996.
10.1093/hmg/6.11.1991
|
|
Kobayashi, Toshiyuki, Urakami, Shinji, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Aspinwall, Richard, Harris, Peter, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348 and Hino, Okio
1997.
Identification of a leader exon and a core promoter for the rat tuberous sclerosis 2 (Tsc2) gene and structural comparison with the human homolog.
Mammalian Genome
8
(8)
, pp. 554-558.
10.1007/s003359900502
|
|
van Slegtenhorst, Marjon, de Hoogt, Ronald, Hermans, Caroline, Nellist, Mark, Janssen, Bart, Verhoef, Senno, Lindhout, Dick, van den Ouwenland, Ans, Halley, Dicky, Young, Janet, Burley, Mariwyn, Jeremiah, Steve, Woodward, Karen, Nahmias, Joseph, Fox, Margaret, Ekong, Rosemary, Osborne, John, Wolfe, Jonathan, Povey, Sue, Snell, Russell G., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Jones, Alistair C., Tachataki, Maria, Ravine, David, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Reeve, Mary Pat, Richardson, Paul, Wilmer, Friederike, Munro, Cheryl, Hawkins, Trevor L., Sepp, Tiina, Ali, Johari B. M., Ward, Susannah, Green, Andrew J., Yates, John R. W., Kwiatkowska, Jolanta, Henske, Elizabeth P., Short, M. Priscilla, Haines, Jonathan H., Jowziak, Sergiusz and Kwiatkowski, David J.
1997.
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
Science
277
(5327)
, pp. 805-808.
10.1126/science.277.5327.805
|
|
Aspinwall, Richard, Rothwell, Dominic G., Roldan- Arjona, Teresa, Anselmino, Catherine, Ward, Christopher J., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348, Lindahl, Thomas, Harris, Peter C. and Hickson, Ian D.
1997.
Cloning and characterization of a functional human homolog of Escherichia coli endonuclease III.
Proceedings of the National Academy of Sciences of the United States of America
94
(1)
, pp. 109-114.
|
|
Maheshwar, Magitha M., Sandford, Richard, Nellist, Mark, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Sgotto, Barbara, Vaudin, Mark and Sampson, Julian Roy ORCID: https://orcid.org/0000-0002-2902-2348
1996.
Comparative analysis and genomic structure of the tuberous sclerosis 2 (TSC2) gene in human and pufferfish.
Human Molecular Genetics
5
(1)
, pp. 131-137.
10.1093/hmg/5.1.131
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Meredith, Alison L., Millar-Jones, Lynne and Goodchild, Mary C.
1995.
Two CF patients, one homozygous for the 621 + 1G>T splice mutation, the other homozygous for the 1898 + 1G>A splice mutation [Letter].
Journal of Medical Genetics
32
(2)
, p. 158.
10.1136/jmg.32.2.158
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Shaw, D. J.
1995.
The cystic fibrosis gene: cloning and characterisation.
Shaw, D. J., ed.
Molecular genetics of human inherited disease,
Chichester:
Wiley,
pp. 41-68.
|
|
Schwarz, Martin J., Malone, Geraldine M., Haworth, Andrea, Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Meredith, Alison Linda, Gardner, Anne, Sawyer, I. Hilary, Connarty, Margaret, Dennis, Nick, Seller, Anneke, Harris, Ann, Taylor, Rohan, Dear, Simon, Middleton-Price, Helen, McMahon, Cathie, Mayall, Ed, McMahon, Rob, Barton, David E., Giles, Martin, Lindley, Victoria, Plaha, Davinder S., Price, Susan, Sharif, Abid, Cross, Gareth S., Dalton, Ann, Taylor, Graham, Wallace, Andrew, Tassabehji, Mayada, Whittaker, Joanne L., Butler, Rachel, Curtis, Ann, Pinkett, Ros, Gilfillan, Annette J., Brock, David J. H., Higgins, G. Scott, Lanyon, George, Miedzybrodzka, Zosia, Davidson, Mark, Graham, Colin A. and Hill, Alison J. M.
1995.
Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories.
Human Mutation
6
(4)
, pp. 326-333.
10.1002/humu.1380060406
|
|
James, C, Houlihan, G. D., Snell, Russell G., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458 and Harper, Peter Stanley
1994.
Late-onset Huntington's Disease: a clinical and molecular study.
Age and Ageing
23
(6)
, pp. 445-448.
10.1093/ageing/23.6.445
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Belloni, Elena, Ferrari, Maurizio, Millar-Jones, Lynne and Meredith, Alison Linda
1994.
A novel mutation (M1V) in the translation initiation codon of the cystic fibrosis transmembrane conductance regulator gene, in three CF chromosomes of Italian origin.
Human Molecular Genetics
3
(8)
, pp. 1431-1432.
10.1093/hmg/3.8.1431
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458
1994.
Population variation of common cystic fibrosis mutations.
Human Mutation
4
(3)
, pp. 167-177.
10.1002/humu.1380040302
|
|
Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, AI-Jader, Layla N. and Meredith, Alison L.
1993.
Two novel frame-shift mutations: 977 insA in exon 6B, and 4016 insT in exon 21, of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Human Molecular Genetics
2
(3)
, pp. 317-319.
10.1093/hmg/2.3.317
|
|
MacMillan, J. C., Snell, R. G., Tyler, A., Houlihan, G. D., Fenton, I., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Lazarou, L. P., Shaw, J. D. and Harper, Peter Stanley
1993.
Molecular analysis and clinical correlations of the Huntington's disease mutation.
The Lancet
342
(8877)
, pp. 954-958.
10.1016/0140-6736(93)92002-B
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Goodchild, Mary C. and Meredith, Alison L.
1993.
Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5% of CF chromosomes in Wales.
Human Molecular Genetics
2
(10)
, pp. 1551-1556.
10.1093/hmg/2.10.1551
|
|
Snell, Russell G., MacMillan, John C., Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Fenton, Iain, Lazarou, Lazarus P., Davies, Peter, MacDonald, Marcy E., Gusella, James F., Harper, Peter Stanley and Shaw, Duncan J.
1993.
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
Nature Genetics
4
(4)
, pp. 393-397.
10.1038/ng0893-393
|
|
Cheadle, Jeremy Peter ORCID: https://orcid.org/0000-0001-9453-8458, Al-Jader, Layla N. and Meredith, Alison L.
1993.
A novel nonsense mutation, W846XI (amber termination), in exon 14a of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Human Molecular Genetics
2
(7)
, pp. 1067-1068.
10.1093/hmg/2.7.1067
|
|
al-Jader, Layla N., Meredith, Alison L., Ryley, Henry Charles, Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Maguire, S., Owen, G., Goodchild, M. C. and Harper, Peter Stanley
1992.
Severity of chest disease in cystic fibrosis patients in relation to their genotypes.
Journal of Medical Genetics
29
(12)
, pp. 883-887.
10.1136/jmg.29.12.883
|
|
Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, Myring, J., al-Jader, Layla and Meredith, L.
1992.
Mutation analysis of 184 cystic fibrosis families in Wales.
Journal of Medical Genetics
29
(9)
, pp. 642-646.
10.1136/jmg.29.9.642
|
|
Cheadle, Jeremy P. ORCID: https://orcid.org/0000-0001-9453-8458, al-Jader, Layla N., Goodchild, M> and Meredith, Alison L.
1992.
Mild pulmonary disease in a cystic fibrosis child homozygous for R553X.
Journal of Medical Genetics
29
(8)
, p. 597.
10.1136/jmg.29.8.597
|
|



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