Preoperative Diagnosis of Lynch Syndrome With DNA Mismatch Repair Immunohistochemistry on a Diagnostic Biopsy
Warrier, S. K, Trainer, A. H, Lynch, A. C, Mitchell, C, Hiscock, R, Sawyer, S, Boussioutas, A, Heriot, A. G
Published in Diseases of the colon & rectum (01.12.2011)
Published in Diseases of the colon & rectum (01.12.2011)
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Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
de Vries, B B A, White, S M, Knight, S J L, Regan, R, Homfray, T, Young, I D, Super, M, McKeown, C, Splitt, M, Quarrell, O W J, Trainer, A H, Niermeijer, M F, Malcolm, S, Flint, J, Hurst, J A, Winter, R M
Published in Journal of medical genetics (01.03.2001)
Published in Journal of medical genetics (01.03.2001)
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Tumour morphology predicts PALB2 germline mutation status
TEO, Z. L, PROVENZANO, E, SHACKLETON, K, CICCIARELLI, L, CONFAB, K, BUYS, S. S, ANDRULIS, I. L, MULLIGAN, A. M, GLENDON, G, JOHN, E. M, TERRY, M. B, DALY, M, DITE, G. S, ODEFREY, F. A, NGUYEN-DUMONT, T, GILES, G. G, DOWTY, J. G, WINSHIP, I, GOLDGAR, D. E, HOPPER, J. L, SOUTHEY, M. C, PARK, D. J, APICELLA, C, SAWYER, S. D, JAMES, P. A, MITCHELL, G, TRAINER, A. H, LINDEMAN, G. J
Published in British journal of cancer (09.07.2013)
Published in British journal of cancer (09.07.2013)
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Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same
Huq, A. J., Walsh, M., Rajagopalan, B., Finlay, M., Trainer, A. H., Bonnet, F., Sevenet, N., Winship, I. M.
Published in Familial cancer (01.10.2018)
Published in Familial cancer (01.10.2018)
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Consumer and clinician perspectives on personalising breast cancer prevention information
Keogh, L.A., Steel, E., Weideman, P., Butow, P., Collins, I.M., Emery, J.D., Mann, G.B., Bickerstaffe, A., Trainer, A.H., Hopper, L.J., Phillips, K.A.
Published in Breast (Edinburgh) (01.02.2019)
Published in Breast (Edinburgh) (01.02.2019)
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Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics
Meiser, B., Kaur, R., Kirk, J., Morrow, A., Peate, M., Wong, W. K. T., McPike, E., Cops, E., Dowson, C., Austin, R., Fine, M., Thrupp, L., Ward, R., Macrae, F., Hiller, J. E., Trainer, A. H., Mitchell, G.
Published in Familial cancer (01.10.2020)
Published in Familial cancer (01.10.2020)
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Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome
Vega, H, Trainer, A H, Gordillo, M, Crosier, M, Kayserili, H, Skovby, F, Uzielli, M L Giovannucci, Schnur, R E, Manouvrier, S, Blair, E, Hurst, J A, Forzano, F, Meins, M, Simola, K O J, Raas-Rothschild, A, Hennekam, R C M, Jabs, E Wang
Published in Journal of medical genetics (01.01.2010)
Published in Journal of medical genetics (01.01.2010)
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Rothmund–Thomson Syndrome with Myelodysplasia
Narayan, S., Fleming, C., Trainer, A. H., Craig, J. A.
Published in Pediatric dermatology (01.05.2001)
Published in Pediatric dermatology (01.05.2001)
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A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation
Ghaffari, S R, Boyd, E, Tolmie, J L, Crow, Y J, Trainer, A H, Connor, J M
Published in Journal of medical genetics (01.03.1998)
Published in Journal of medical genetics (01.03.1998)
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Chromosome 22q11 microdeletions in tetralogy of Fallot
Trainer, A H, Morrison, N, Dunlop, A, Wilson, N, Tolmie, J
Published in Archives of disease in childhood (01.01.1996)
Published in Archives of disease in childhood (01.01.1996)
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Mitotic Checkpoint Inactivation Fosters Transformation in Cells Lacking the Breast Cancer Susceptibility Gene, Brca2
Lee, Hyunsook, Trainer, Alison H, Friedman, Lori S, Thistlethwaite, Fiona C, Evans, Martin J, Ponder, Bruce A.J, Venkitaraman, Ashok R
Published in Molecular cell (01.07.1999)
Published in Molecular cell (01.07.1999)
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Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same: Fam Cancer
Huq, A. J., Walsh, M., Rajagopalan, B., Finlay, M., Trainer, A. H., Bonnet, Fabrice, Sevenet, N., Winship, I. M.
Published in Familial cancer (01.10.2018)
Published in Familial cancer (01.10.2018)
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Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients
Thompson, ER, Boyle, SE, Johnson, J, Ryland, GL, Sawyer, S, Choong, DY, Chenevix-Trench, G, Trainer, AH, Lindeman, GJ, Mitchell, G, James, PA, Campbell, IG
Published in Hereditary cancer in clinical practice (12.04.2012)
Published in Hereditary cancer in clinical practice (12.04.2012)
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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Rebbeck, Timothy R., Hamann, Ute, Olah, Edith, Solano, Angela R., Teo, Soo‐Hwang, Chan, TL, Couch, Fergus J., Palmero, Edenir Inêz, Park, Sue Kyung, Parsons, Michael T., Leslie, Goska, Aalfs, Cora M., Adlard, Julian, Agata, Simona, Aittomäki, Kristiina, Andrulis, Irene L., Barkardottir, Rosa B., Benitez, Javier, Blanco, Amie M., Bonadona, Valérie, Bonanni, Bernardo, Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B.M., Cook, Jackie, Davidson, Rosemarie, Leeneer, Kim, Domchek, Susan M., Dorfling, Cecilia M., Velazquez, Carolina, Easton, Douglas F., Feliubadaló, Lidia, Ferrer, Sandra Fert, Foretova, Lenka, Galvão, Henrique C. R., Garber, Judy, Gesta, Paul, Giannini, Giuseppe, Gutierrez‐Barrera, Angelica, Hogervorst, Frans B.L., Imyanitov, Evgeny N., Izquierdo, Angel, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, John, Esther M., Vijai, Joseph, Karlan, Beth Y., Kast, Karin, Investigators, KConFab, Korach, Jacob, Laitman, Yael, Lasset, Christine, Lázaro, Conxi, Lee, Annette, Lee, Min Hyuk, Lester, Jenny, Liljegren, Annelie, Machackova, Eva, Mari, Véronique, Meijers‐Heijboer, Hanne E.J., Miller, Austin, Montagna, Marco, Mulligan, Anna Marie, Ngeow, Joanne, Nielsen, Henriette Roed, Nussbaum, Robert L., Offit, Kenneth, Öfverholm, Anna, Osorio, Ana, Papp, Janos, Pedersen, Inge Sokilde, Peruga, Nina, Peterlongo, Paolo, Radice, Paolo, Robson, Mark, Rodriguez, Gustavo C., Rudaitis, Vilius, Schmidt, Ane Y., Senter, Leigha, Singer, Christian F., Skytte, Anne‐Bine, Sobol, Hagay, Teixeira, Manuel R., Tischkowitz, Marc, Toland, Amanda Ewart, Topka, Sabine, Trainer, Alison H, Varesco, Liliana, Varon‐Mateeva, Raymonda, Vega, Ana, Wachenfeldt, Anna, Wang‐Gohrke, Shan, Weber, Bernhard H. F., Yannoukakos, Drakoulis, Zorn, Kristin K., Chenevix‐Trench, Georgia, Spurdle, Amanda B., Nathanson, Katherine L.
Published in Human mutation (01.05.2018)
Published in Human mutation (01.05.2018)
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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Barnes, Daniel R., Rookus, Matti A., Dennis, Joe, Mavaddat, Nasim, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arun, Banu K., Barkardottir, Rosa B., Barrowdale, Daniel, Benitez, Javier, Białkowska, Katarzyna, Blok, Marinus J., Bonanni, Bernardo, Bozsik, Aniko, Buys, Saundra S., Caldés, Trinidad, Campbell, Ian, Christensen, Lise Lotte, Colas, Chrystelle, Berthet, Pascaline, Faivre, Laurence, Giraud, Sophie, Lasset, Christine, Mebirouk, Noura, Adlard, Julian, Antoniou, Antonis, Brennan, Paul, Brewer, Carole, Cook, Jackie, Easton, Douglas, Eeles, Ros, Hanson, Helen, Izatt, Louise, Ong, Kai-ren, O’Shaughnessy-Kirwan, Aoife, Daly, Mary B., Davidson, Rosemarie, Ding, Yuan Chun, Dorfling, Cecilia M., Engel, Christoph, Evans, D. Gareth, Friedlander, Michael, Friedman, Eitan, Ganz, Patricia A., Gerdes, Anne-Marie, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K., Gschwantler-Kaulich, Daphne, Hamann, Ute, Hu, Chunling, Hulick, Peter J., Hogervorst, Frans, Koudijs, Marco, Kruse, Torben A., Lazaro, Conxi, Lester, Jenny, Mai, Phuong L., Mari, Véronique, Meijers-Heijboer, Hanne E.J., Meindl, Alfons, Mensenkamp, Arjen R., Montagna, Marco, Mukherjee, Semanti, Mulligan, Anna Marie, Nevanlinna, Heli, Niederacher, Dieter, Olopade, Olufunmilayo I., Ott, Claus-Eric, Papi, Laura, Park, Sue K., Peissel, Bernard, Pfeiler, Georg, Phillips, Kelly-Anne, Prajzendanc, Karolina, Pujana, Miquel Angel, Ramus, Susan J., Rantala, Johanna, Rennert, Gad, Risch, Harvey A., Schuster, Hélène, Senter, Leigha, Side, Lucy E., Slavin, Thomas P., Soucy, Penny, Sutter, Christian, Thull, Darcy L., Toland, Amanda E., Tung, Nadine, van Engelen, Klaartje, van Rensburg, Elizabeth J., Wang-Gohrke, Shan, Wappenschmidt, Barbara, Yang, Xin, Zimbalatti, Dario, Offit, Kenneth, Couch, Fergus J., Schmutzler, Rita K., Antoniou, Antonis C.
Published in Genetics in medicine (01.10.2020)
Published in Genetics in medicine (01.10.2020)
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Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
Leslie, Goska, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Arnold, Norbert, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barwell, Julian, Belotti, Muriel, Berthet, Pascaline, Boonen, Susanne E, Borg, Åke, Brennan, Paul, Brewer, Carole, Bucalo, Agostino, Buys, Saundra S, Campbell, Ian, Cassingham, Hayley, Christensen, Lise Lotte, Claes, Kathleen B M, Coppa, Anna, Damante, Giuseppe, Davidson, Rosemarie, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesús, Ding, Yuan Chun, Domchek, Susan M, Donaldson, Alan, Eason, Jacqueline, Eeles, Ros, Evans, D Gareth, Feliubadaló, Lidia, Gehrig, Andrea, Giraud, Sophie, Godwin, Andrew K, Gregory, Helen, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hentschel, Julia, Horvath, Judit, Izquierdo, Angel, Jensen, Uffe Birk, John, Esther M, Kruse, Torben A, Lautrup, Charlotte, Lesueur, Fabienne, Manoukian, Siranoush, Meindl, Alfons, Monteiro, Alvaro N, Morrison, Patrick J, Muranen, Taru A, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Palli, Domenico, Parsons, Michael T, Pedersen, Inge Sokilde, Perez-Segura, Pedro, Petersen, Annabeth H, Pinto, Pedro, Pottinger, Caroline, Ramser, Juliane, Rantala, Johanna, Robson, Mark, Rogers, Mark T, Sánchez de Abajo, Ana María, Shah, Payal D, Sharif, Saba, Side, Lucy E, Steele, Linda, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teulé, Alex, Thull, Darcy L, Tischkowitz, Marc, Toland, Amanda E, Tommasi, Stefania, Toss, Angela, Trainer, Alison H, van Asperen, Christi J, Venturelli, Marta, Vijai, Joseph, Walker, Lisa, Wang-Gohrke, Shan, Whaite, Anna, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Chenevix-Trench, Georgia, Ottini, Laura
Published in JNCI : Journal of the National Cancer Institute (01.01.2022)
Published in JNCI : Journal of the National Cancer Institute (01.01.2022)
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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness
Patel, Vivek L, Busch, Evan L, Friebel, Tara M, Leslie, Goska, McGuffog, Lesley, Agnarsson, Bjarni A, Ahmed, Munaza, Azzollini, Jacopo, Barkardottir, Rosa B, Barnes, Daniel R, Barroso, Alicia, Belotti, Muriel, Bertelsen, Birgitte, Bonanni, Bernardo, Brunet, Joan, Caldés, Trinidad, Campbell, Ian G, Carnevali, Ileana, Chan, Tsun L, Collaborators, Embrace, Cook, Jackie, Damante, Giuseppe, Dennis, Joe, Domchek, Susan M, Donaldson, Alan, Ejlertsen, Bent, Engel, Christoph, Faivre, Laurence, Faust, Ulrike, Feliubadaló, Lídia, Gauthier-Villars, Marion, Géczi, Lajos, Gesta, Paul, Giannini, Giuseppe, Glendon, Gord, Godwin, Andrew K, Gutierrez-Barrera, Angelica M, Hamann, Ute, Honisch, Ellen, Izatt, Louise, Jager, Agnes, Johannsson, Oskar Th, Joseph, Vijai, Kang, Eunyoung, Kiiski, Johanna I, Kim, Sung-Won, Ko, Kwang-Pil, Kramer, Gero, Krogh, Lotte, Kwong, Ava, Larsen, Mirjam, Lasset, Christine, Lazaro, Conxi, Lemke, Johannes, Lesueur, Fabienne, Llovet, Patricia, Lopez-Fernández, Adria, Matricardi, Laura, Mebirouk, Noura, Montagna, Marco, Moserle, Lidia, Navratilova, Marie, Olah, Edith, Ong, Kai-Ren, Osorio, Ana, Ott, Claus-Eric, Petersen, Annabeth Høgh, Porteous, Mary E, Radice, Paolo, Rantala, Johanna, Rookus, Matti A, Rossing, Caroline M, Saule, Claire, Scarpitta, Rosa, Shah, Payal D, Skytte, Anne-Bine, Snape, Katie, Solano, Angela R, Soucy, Penny, Southey, Melissa C, Spurdle, Amanda B, Steele, Linda, Tan, Yen Y, Teo, Soo Hwang, Tischkowitz, Marc, Toland, Amanda E, Torres, Diana, Toss, Angela, van der Baan, Frederieke H, van Hest, Liselotte P, Viel, Alessandra, Villa, Roberta, von Wachenfeldt, Anna, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Yadav, Siddhartha, Yannoukakos, Drakoulis, Zorn, Kristin K, Pomerantz, Mark M, Nielsen, Henriette Roed
Published in Cancer research (Chicago, Ill.) (01.02.2020)
Published in Cancer research (Chicago, Ill.) (01.02.2020)
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