Molecular tumor profiling: translating genomic insights into clinical advances

por Trainer, Alison H
Publicado 2004

Exploring Implementation of Personal Breast Cancer Risk Assessments

por Sierra, Maria A., Wheeler, Jack C. W., Devereux, Lisa, Trainer, Alison H., Keogh, Louise
Publicado 2021

A cost-effectiveness model of genetic testing and periodical clinical screening for the evaluation of families with dilated cardiomyopathy

por Catchpool, Max, Ramchand, Jay, Martyn, Melissa, Hare, David L., James, Paul A., Trainer, Alison H., Knight, Josh, Goranitis, Ilias
Publicado 2019

The Clinical and Psychosocial Outcomes for Women Who Received Unexpected Clinically Actionable Germline Information Identified through Research: An Exploratory Sequential Mixed-Met...

por Forrest, Laura E., Forbes Shepherd, Rowan, Tutty, Erin, Pearce, Angela, Campbell, Ian, Devereux, Lisa, Trainer, Alison H., James, Paul A., Young, Mary-Anne
Publicado 2022

Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer

por Thompson, Ella R., Rowley, Simone M., Sawyer, Sarah, kConFab, Eccles, Diana M., Trainer, Alison H., Mitchell, Gillian, James, Paul A., Campbell, Ian G.
Publicado 2013

Germline whole exome sequencing of a family with appendiceal mucinous tumours presenting with pseudomyxoma peritonei

por Lung, Mei Sim, Mitchell, Catherine A., Doyle, Maria A., Lynch, Andrew C., Gorringe, Kylie L., Bowtell, David D. L., Campbell, Ian G., Trainer, Alison H.
Publicado 2020

Development of a person-centred digital platform for the long-term support of people living with an adult-onset genetic disease predisposition: a mixed-methods study protocol

por Best, Stephanie, Al Mahmud, Abdullah, Tyagi, Shivani, Wheeler, Jack C W, Forkan, Abdur Rahim Mohammad, Lewis, Alexandra, Shuakat, Nadeem, Kaul, Rohit, Ward, Aisha, Wickramasinghe, Nilmini, Jayaraman, Prem Prakash, Trainer, Alison H
Publicado 2023

Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context

por Thompson, Ella R., Gorringe, Kylie L., Rowley, Simone M., Li, Na, McInerny, Simone, Wong-Brown, Michelle W., Devereux, Lisa, Li, Jason, Trainer, Alison H., Mitchell, Gillian, Scott, Rodney J., James, Paul A., Campbell, Ian G.
Publicado 2015

Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs

por Li, Na, Rowley, Simone M., Thompson, Ella R., McInerny, Simone, Devereux, Lisa, Amarasinghe, Kaushalya C., Zethoven, Magnus, Lupat, Richard, Goode, David, Li, Jason, Trainer, Alison H., Gorringe, Kylie L., James, Paul A., Campbell, Ian G.
Publicado 2018

The iPrevent Online Breast Cancer Risk Assessment and Risk Management Tool: Usability and Acceptability Testing

por Lo, Louisa L, Collins, Ian M, Bressel, Mathias, Butow, Phyllis, Emery, Jon, Keogh, Louise, Weideman, Prue, Steel, Emma, Hopper, John L, Trainer, Alison H, Mann, Gregory B, Bickerstaffe, Adrian, Antoniou, Antonis C, Cuzick, Jack, Phillips, Kelly-Anne
Publicado 2018

Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice

por Meiser, Bettina, Kaur, Rajneesh, Morrow, April, Peate, Michelle, Wong, W. K. Tim, McPike, Emily, Cops, Elisa, Nichols, Cassandra, Austin, Rachel, Fine, Miriam, Thrupp, Letitia, Ward, Robyn, Macrae, Finlay, Hiller, Janet E., Trainer, Alison H., Mitchell, Gillian
Publicado 2021

The predicted impact and cost‐effectiveness of systematic testing of people with incident colorectal cancer for Lynch syndrome

por Kang, Yoon‐Jung, Killen, James, Caruana, Michael, Simms, Kate, Taylor, Natalie, Frayling, Ian M, Snowsill, Tristan, Huxley, Nicola, Coupe, Veerle MH, Hughes, Suzanne, Freeman, Victoria, Boussioutas, Alex, Trainer, Alison H, Ward, Robyn L, Mitchell, Gillian, Macrae, Finlay A, Canfell, Karen
Publicado 2019

Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles

por Thompson, Ella R., Doyle, Maria A., Ryland, Georgina L., Rowley, Simone M., Choong, David Y. H., Tothill, Richard W., Thorne, Heather, Barnes, Daniel R., Li, Jason, Ellul, Jason, Philip, Gayle K., Antill, Yoland C., James, Paul A., Trainer, Alison H., Mitchell, Gillian, Campbell, Ian G.
Publicado 2012

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls

por Thompson, Ella R., Gorringe, Kylie L., Rowley, Simone M., Wong-Brown, Michelle W., McInerny, Simone, Li, Na, Trainer, Alison H., Devereux, Lisa, Doyle, Maria A., Li, Jason, Lupat, Richard, Delatycki, Martin B., Mitchell, Gillian, James, Paul A., Scott, Rodney J., Campbell, Ian G.
Publicado 2015

Genome-wide association study identifies a novel variant in RAD51B associated with male breast cancer risk

por Orr, Nick, Lemnrau, Alina, Cooke, Rosie, Fletcher, Olivia, Tomczyk, Katarzyna, Jones, Michael, Johnson, Nichola, Lord, Christopher J, Mitsopoulos, Costas, Zvelebil, Marketa, McDade, Simon S, Buck, Gemma, Blancher, Christine, Consortium, KConFab, Trainer, Alison H, James, Paul A, Bojesen, Stig E, Bokmand, Susanne, Nevanlinna, Heli, Mattson, Johanna, Friedman, Eitan, Laitman, Yael, Palli, Domenico, Masala, Giovanna, Zanna, Ines, Ottini, Laura, Giannini, Giuseppe, Hollestelle, Antoinette, van den Ouweland, Ans M.W., Novaković, Srdjan, Krajc, Mateja, Gago-Dominguez, Manuela, Castelao, Jose Esteban, Olsson, Håkan, Hedenfalk, Ingrid, Easton, Douglas F, Pharoah, Paul DP, Dunning, Alison M, Bishop, D Timothy, Neuhausen, Susan L, Steele, Linda, Houlston, Richard S, Garcia-Closas, Montserrat, Ashworth, Alan, Swerdlow, Anthony J
Publicado 2012

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

por Southey, Melissa C, Park, Daniel J, Nguyen-Dumont, Tu, Campbell, Ian, Thompson, Ella, Trainer, Alison H, Chenevix-Trench, Georgia, Simard, Jacques, Dumont, Martine, Soucy, Penny, Thomassen, Mads, Jønson, Lars, Pedersen, Inge S, Hansen, Thomas VO, Nevanlinna, Heli, Khan, Sofia, Sinilnikova, Olga, Mazoyer, Sylvie, Lesueur, Fabienne, Damiola, Francesca, Schmutzler, Rita, Meindl, Alfons, Hahnen, Eric, Dufault, Michael R, Chris Chan, TL, Kwong, Ava, Barkardóttir, Rosa, Radice, Paolo, Peterlongo, Paolo, Devilee, Peter, Hilbers, Florentine, Benitez, Javier, Kvist, Anders, Törngren, Therese, Easton, Douglas, Hunter, David, Lindstrom, Sara, Kraft, Peter, Zheng, Wei, Gao, Yu-Tang, Long, Jirong, Ramus, Susan, Feng, Bing-Jian, Weitzel, Jeffrey N, Nathanson, Katherine, Offit, Kenneth, Joseph, Vijai, Robson, Mark, Schrader, Kasmintan, Wang, San Ming, Kim, Yeong C, Lynch, Henry, Snyder, Carrie, Tavtigian, Sean, Neuhausen, Susan, Couch, Fergus J, Goldgar, David E
Publicado 2013

The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study

por Davidson, Aimee L., Dressel, Uwe, Norris, Sarah, Canson, Daffodil M., Glubb, Dylan M., Fortuno, Cristina, Hollway, Georgina E., Parsons, Michael T., Vidgen, Miranda E., Holmes, Oliver, Koufariotis, Lambros T., Lakis, Vanessa, Leonard, Conrad, Wood, Scott, Xu, Qinying, McCart Reed, Amy E., Pickett, Hilda A., Al-Shinnag, Mohammad K., Austin, Rachel L., Burke, Jo, Cops, Elisa J., Nichols, Cassandra B., Goodwin, Annabel, Harris, Marion T., Higgins, Megan J., Ip, Emilia L., Kiraly-Borri, Catherine, Lau, Chiyan, Mansour, Julia L., Millward, Michael W., Monnik, Melissa J., Pachter, Nicholas S., Ragunathan, Abiramy, Susman, Rachel D., Townshend, Sharron L., Trainer, Alison H., Troth, Simon L., Tucker, Katherine M., Wallis, Mathew J., Walsh, Maie, Williams, Rachel A., Winship, Ingrid M., Newell, Felicity, Tudini, Emma, Pearson, John V., Poplawski, Nicola K., Mar Fan, Helen G., James, Paul A., Spurdle, Amanda B., Waddell, Nicola, Ward, Robyn L.
Publicado 2023

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015

por Thompson, Ella R., Wong-Brown, Michelle, Rowley, Simone M., Dooley, Susan, Lil, Na, Hipwell, Michael, McInerny, Simone, Meldrum, Cliff, Devereux, Lisa, Mossman, David, Trainer, Alison H., Millar, Briar-Rose, Mitchell, Gillian, Smith, Cate, James, Paul A., Campbell, Ian G., Scott, Rodney J., Klonowska, Katarzyna, Jakubowska, Anna, Maksimenko, Jelena, Irmejs, Arvids, Nakazawa-Miklasevica, Miki, Melbarde-Gorkusa, Inga, Trofimovics, Genadijs, Gardovskis, Janis, Miklasevics, Edvins, Tęcza, Karolina, Pamuła-Piłat, Jolanta, Łanuszewska, Joanna, Grzybowska, Ewa, Miklasevics, Edvins, Szwiec, M., Tomiczek-Szwiec, J., Gełej, M., Cybulski, C., Huzarski, T., Kilar, E., Oczko-Wojciechowska, Małgorzata, Świerniak, Michał, Krajewska, Jolanta, Kowalska, Małgorzata, Tyszkiewicz, Tomasz, Pawlaczek, Agnieszka, Jarząb, Michał, Kowal, Monika, Rusinek, Dagmara, Zebracka-Gala, Jadwiga, Czarniecka, Agnieszka, Jarzab, Barbara, Plawski, Andrzej, Borun, Paweł, Szczepinska, Joanna, Siolek, Monika, Kozak-Klonowska, Beata, Kaczmarek, Katarzyna, Muszyńska, Magdalena, Marciniak, Wojciech, Sukiennicki, Grzegorz, Lener, Marcin, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Gromowski, Tomasz, Huzarski, Tomasz, Byrski, Tomasz, Gronwald, Jacek, Oszurek, Oleg, Cybulski, Cezary, Dębniak, Tadeusz, Morawski, Antoni, Jakubowska, Anna, Lubiński, Jan, Sukiennicki, Grzegorz, Muszyńska, Magdalena, Marciniak, Wojciech, Kaczmarek, Katarzyna, Lener, Marcin, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Gromowski, Tomasz, Huzarski, Tomasz, Byrski, Tomasz, Gronwald, Jacek, Oszurek, Oleg, Cybulski, Cezary, Dębniak, Tadeusz, Morawski, Antoni, Jakubowska, Anna, Lubiński, Jan, Post, Michał
Publicado 2017

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

por Barnes, Daniel R, Silvestri, Valentina, Leslie, Goska, McGuffog, Lesley, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L, Arason, Adalgeir, Arnold, Norbert, Auber, Bernd, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barrowdale, Daniel, Barwell, Julian, Belotti, Muriel, Benitez, Javier, Berthet, Pascaline, Boonen, Susanne E, Borg, Åke, Bozsik, Aniko, Brady, Angela F, Brennan, Paul, Brewer, Carole, Brunet, Joan, Bucalo, Agostino, Buys, Saundra S, Caldés, Trinidad, Caligo, Maria A, Campbell, Ian, Cassingham, Hayley, Christensen, Lise Lotte, Cini, Giulia, Claes, Kathleen B M, Cook, Jackie, Coppa, Anna, Cortesi, Laura, Damante, Giuseppe, Darder, Esther, Davidson, Rosemarie, de la Hoya, Miguel, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesús, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M, Donaldson, Alan, Eason, Jacqueline, Eeles, Ros, Engel, Christoph, Evans, D Gareth, Feliubadaló, Lidia, Fostira, Florentia, Frone, Megan, Frost, Debra, Gallagher, David, Gehrig, Andrea, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Greene, Mark H, Gregory, Helen, Gross, Eva, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hanson, Helen, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Izquierdo, Angel, James, Paul A, Janavicius, Ramunas, Jensen, Uffe Birk, Johannsson, Oskar Th, John, Esther M, Kramer, Gero, Kroeldrup, Lone, Kruse, Torben A, Lautrup, Charlotte, Lazaro, Conxi, Lesueur, Fabienne, Lopez-Fernández, Adria, Mai, Phuong L, Manoukian, Siranoush, Matrai, Zoltan, Matricardi, Laura, Maxwell, Kara N, Mebirouk, Noura, Meindl, Alfons, Montagna, Marco, Monteiro, Alvaro N, Morrison, Patrick J, Muranen, Taru A, Murray, Alex, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nguyen-Dumont, Tu, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Palli, Domenico, Parsons, Michael T, Pedersen, Inge Sokilde, Peissel, Bernard, Perez-Segura, Pedro, Peterlongo, Paolo, Petersen, Annabeth H, Pinto, Pedro, Porteous, Mary E, Pottinger, Caroline, Pujana, Miquel Angel, Radice, Paolo, Ramser, Juliane, Rantala, Johanna, Robson, Mark, Rogers, Mark T, Rønlund, Karina, Rump, Andreas, Sánchez de Abajo, Ana María, Shah, Payal D, Sharif, Saba, Side, Lucy E, Singer, Christian F, Stadler, Zsofia, Steele, Linda, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel R, Teulé, Alex, Thull, Darcy L, Tischkowitz, Marc, Toland, Amanda E, Tommasi, Stefania, Toss, Angela, Trainer, Alison H, Tripathi, Vishakha, Valentini, Virginia, van Asperen, Christi J, Venturelli, Marta, Viel, Alessandra, Vijai, Joseph, Walker, Lisa, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Whaite, Anna, Zanna, Ines, Offit, Kenneth, Thomassen, Mads, Couch, Fergus J, Schmutzler, Rita K, Simard, Jacques, Easton, Douglas F, Chenevix-Trench, Georgia, Antoniou, Antonis C, Ottini, Laura
Publicado 2021

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

por Hakkaart, Christopher, Pearson, John F., Marquart, Louise, Dennis, Joe, Wiggins, George A. R., Barnes, Daniel R., Robinson, Bridget A., Mace, Peter D., Aittomäki, Kristiina, Andrulis, Irene L., Arun, Banu K., Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B., Belhadj, Sami, Berger, Lieke, Blok, Marinus J., Boonen, Susanne E., Borde, Julika, Bradbury, Angela R., Brunet, Joan, Buys, Saundra S., Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B. M., Collonge-Rame, Marie-Agnès, Cook, Jackie, Cosgrove, Casey, Couch, Fergus J., Daly, Mary B., Dandiker, Sita, Davidson, Rosemarie, de la Hoya, Miguel, de Putter, Robin, Delnatte, Capucine, Dhawan, Mallika, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Donaldson, Alan, Eason, Jacqueline, Easton, Douglas F., Ehrencrona, Hans, Engel, Christoph, Evans, D. Gareth, Faust, Ulrike, Feliubadaló, Lidia, Fostira, Florentia, Friedman, Eitan, Frone, Megan, Frost, Debra, Garber, Judy, Gayther, Simon A., Gehrig, Andrea, Gesta, Paul, Godwin, Andrew K., Goldgar, David E., Greene, Mark H., Hahnen, Eric, Hake, Christopher R., Hamann, Ute, Hansen, Thomas V. O., Hauke, Jan, Hentschel, Julia, Herold, Natalie, Honisch, Ellen, Hulick, Peter J., Imyanitov, Evgeny N., Isaacs, Claudine, Izatt, Louise, Izquierdo, Angel, Jakubowska, Anna, James, Paul A., Janavicius, Ramunas, John, Esther M., Joseph, Vijai, Karlan, Beth Y., Kemp, Zoe, Kirk, Judy, Konstantopoulou, Irene, Koudijs, Marco, Kwong, Ava, Laitman, Yael, Lalloo, Fiona, Lasset, Christine, Lautrup, Charlotte, Lazaro, Conxi, Legrand, Clémentine, Leslie, Goska, Lesueur, Fabienne, Mai, Phuong L., Manoukian, Siranoush, Mari, Véronique, Martens, John W. M., McGuffog, Lesley, Mebirouk, Noura, Meindl, Alfons, Miller, Austin, Montagna, Marco, Moserle, Lidia, Mouret-Fourme, Emmanuelle, Musgrave, Hannah, Nambot, Sophie, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Yie, Joanne Ngeow Yuen, Nguyen-Dumont, Tu, Nikitina-Zake, Liene, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Osorio, Ana, Ott, Claus-Eric, Park, Sue K., Parsons, Michael T., Pedersen, Inge Sokilde, Peixoto, Ana, Perez-Segura, Pedro, Peterlongo, Paolo, Pocza, Timea, Radice, Paolo, Ramser, Juliane, Rantala, Johanna, Rodriguez, Gustavo C., Rønlund, Karina, Rosenberg, Efraim H., Rossing, Maria, Schmutzler, Rita K., Shah, Payal D., Sharif, Saba, Sharma, Priyanka, Side, Lucy E., Simard, Jacques, Singer, Christian F., Snape, Katie, Steinemann, Doris, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel R., Teo, Soo Hwang, Thomassen, Mads, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Trainer, Alison H., Tripathi, Vishakha, Tung, Nadine, van Engelen, Klaartje, van Rensburg, Elizabeth J., Vega, Ana, Viel, Alessandra, Walker, Lisa, Weitzel, Jeffrey N., Wevers, Marike R., Chenevix-Trench, Georgia, Spurdle, Amanda B., Antoniou, Antonis C., Walker, Logan C.
Publicado 2022