Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk von Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J., Dennis, Joe, Alonso, M. Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K., Castelao, Jose E., Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A., Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I., Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P., van der Kolk, Lizet E., Wahlström, Cecilia, Wang, Qin, Perry, John R. B., Benitez, Javier, Schmidt, Marjanka K., Schmutzler, Rita K., Pharoah, Paul D. P., Droit, Arnaud, Dunning, Alison M., Kvist, Anders, Devilee, Peter, Easton, Douglas F., Simard, Jacques

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Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk von McGuffog, Lesley, Lee, Andrew J, Kuchenbaecker, Karoline, Gaudet, Mia M, Kosel, Matthew L, Healey, Sue C, Bacot, François, Jakubowska, Anna, Schmutzler, Rita Katharina, Piedmonte, Marion R, Singer, Christian Fridolin, Friedman, Eitan A, Neuhausen, Susan L, Greene, Mark H, Andrulis, Irene L. L, Godwin, Andrew K, Yannoukakos, Drakoulis, Caldes, Trinidad, Osorio, Ana, Terry, Mary Beth Eth, Daly, Mary Beryl, van Rensburg, Elizabeth J, Tung, Nadine M, Claes, Kathleen B. M, Imyanitov, Evgeny N, Kwong, Ava, Balmaña Gelpí, Judith, Arun, Banu K, Teo, Soo, Campbell, Ian, Seynaeve, Caroline M, Ligtenberg, Marjolijn J. L, Rookus, Matti A, Devilee, Peter P, Verhoef, Senno, van Os, Theo A. M, Fineberg, Elena, Eccles, Diana M, Cook, Jacqueline A, Donaldson, Alan, Rogers, Mark T, McCann, Emma, Berthet, Pascaline, Delnatte, Capucine, Prieur, Fabienne, Sobol, H, Coupier, I, Gauthier-Villars, M, Léoné, M, Mazoyer, S, Złowocka-Perłowska, E, Lubinski, J, Ottini, L, Papi, L, Gehrig, A, Niederacher, D, Ditsch, N, Preisler-Adams, S, Varon-Mateeva, R, Wappenschmidt, B, Weber, B.H.F, Arver, B, Stenmark-Askmalm, M, Rosenquist, R, Einbeigi, Z, Nathanson, K.L, Rebbeck, T.R, Rodriguez, G.C, Friedlander, M, Bae-Jump, V.L, Lindor, N.M, Kaufman, B, Laitman, Y, Pedersen, I.S, Jensen, U.B, Sarrel, K, Mulligan, A.M, Glendon, G, Ozcelik, H, Andersen, M.K, Ding, Y.C, Teule, Alex, Lazaro Garcia, Conxi, Brunet, Joan, Pujana, Miquel Ángel, Loud, J.T, Walsh, C, Herzog, J, Tognazzo, S, Agata, S, Weaver, J, Aittomäki, K, Muranen, T.A, Miron, A, Benitez, J, Senter, L, Huo, D, Hart, S, Easton, D.F, Chenevix-Trench, G

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SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma von Bayley, Jean-Pierre, Dr, Kunst, Henricus PM, MD, Cascon, Alberto, PhD, Sampietro, Maria Lourdes, PhD, Gaal, José, MD, Korpershoek, Esther, BSc, Hinojar-Gutierrez, Adolfo, MD, Timmers, Henri JLM, MD, Hoefsloot, Lies H, PhD, Hermsen, Mario A, PhD, Suárez, Carlos, Prof, Hussain, A Karim, Ing, Vriends, Annette HJT, MD, Hes, Frederik J, MD, Jansen, Jeroen C, MD, Tops, Carli M, PhD, Corssmit, Eleonora P, MD, de Knijff, Peter, Prof, Lenders, Jacques WM, Prof, Cremers, Cor WRJ, Prof, Devilee, Peter, Prof, Dinjens, Winand NM, PhD, de Krijger, Ronald R, MD, Robledo, Mercedes, PhD

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SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma von Hao, Huai-Xiang, Khalimonchuk, Oleh, Schraders, Margit, Dephoure, Noah, Bayley, Jean-Pierre, Kunst, Henricus, Devilee, Peter, Cremers, Cor W.R.J, Schiffman, Joshua D, Bentz, Brandon G, Gygi, Steven P, Winge, Dennis R, Kremer, Hannie, Rutter, Jared

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Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2 von Boonen, Rick A. C. M., Rodrigue, Amélie, Stoepker, Chantal, Wiegant, Wouter W., Vroling, Bas, Sharma, Milan, Rother, Magdalena B., Celosse, Nandi, Vreeswijk, Maaike P. G., Couch, Fergus, Simard, Jacques, Devilee, Peter, Masson, Jean-Yves, van Attikum, Haico

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Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype von Lakhani, Sunil R, Reis-Filho, Jorge S, Fulford, Laura, Penault-Llorca, Frederique, van der Vijver, Marc, Parry, Suzanne, Bishop, Timothy, Benitez, Javier, Rivas, Carmen, Bignon, Yves-Jean, Chang-Claude, Jenny, Hamann, Ute, Cornelisse, Cees J, Devilee, Peter, Beckmann, Matthias W, Nestle-Krämling, Carolin, Daly, Peter A, Haites, Neva, Varley, Jenny, Lalloo, Fiona, Evans, Gareth, Maugard, Christine, Meijers-Heijboer, Hanne, Klijn, Jan G M, Olah, Edith, Gusterson, Barry A, Pilotti, Silvana, Radice, Paolo, Scherneck, Siegfried, Sobol, Hagay, Jacquemier, Jocelyne, Wagner, Teresa, Peto, Julian, Stratton, Michael R, McGuffog, Lesley, Easton, Douglas F

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The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency von Bayley, Jean-Pierre, Devilee, Peter, Taschner, Peter E M

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Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk von Easton, Douglas F, Pharoah, Paul D.P, Antoniou, Antonis C, Tischkowitz, Marc, Tavtigian, Sean V, Nathanson, Katherine L, Devilee, Peter, Meindl, Alfons, Couch, Fergus J, Southey, Melissa, Goldgar, David E, Evans, D. Gareth R, Chenevix-Trench, Georgia, Rahman, Nazneen, Robson, Mark, Domchek, Susan M, Foulkes, William D

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The functional impact of variants of uncertain significance in BRCA2 von Mesman, Romy L. S., Calléja, Fabienne M. G. R., Hendriks, Giel, Morolli, Bruno, Misovic, Branislav, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.

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Akkermansia muciniphila and Helicobacter typhlonius modulate intestinal tumor development in mice von Dingemanse, Celia, Belzer, Clara, van Hijum, Sacha A F T, Günthel, Marie, Salvatori, Daniela, den Dunnen, Johan T, Kuijper, Ed J, Devilee, Peter, de Vos, Willem M, van Ommen, GertJan B, Robanus-Maandag, Els C

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Personalized early detection and prevention of breast cancer: ENVISION consensus statement von Pashayan, Nora, Antoniou, Antonis C., Ivanus, Urska, Esserman, Laura J., Easton, Douglas F., French, David, Sroczynski, Gaby, Hall, Per, Cuzick, Jack, Evans, D. Gareth, Simard, Jacques, Garcia-Closas, Montserrat, Schmutzler, Rita, Wegwarth, Odette, Pharoah, Paul, Moorthie, Sowmiya, De Montgolfier, Sandrine, Baron, Camille, Herceg, Zdenko, Turnbull, Clare, Balleyguier, Corinne, Rossi, Paolo Giorgi, Wesseling, Jelle, Ritchie, David, Tischkowitz, Marc, Broeders, Mireille, Reisel, Dan, Metspalu, Andres, Callender, Thomas, de Koning, Harry, Devilee, Peter, Delaloge, Suzette, Schmidt, Marjanka K., Widschwendter, Martin

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Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk von Boonen, Rick A C M, Wiegant, Wouter W, Celosse, Nandi, Vroling, Bas, Heijl, Stephan, Kote-Jarai, Zsofia, Mijuskovic, Martina, Cristea, Simona, Solleveld-Westerink, Nienke, van Wezel, Tom, Beerenwinkel, Niko, Eeles, Rosalind, Devilee, Peter, Vreeswijk, Maaike P G, Marra, Giancarlo, van Attikum, Haico

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PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients von Giardiello, Daniele, Hooning, Maartje J, Hauptmann, Michael, Keeman, Renske, Heemskerk-Gerritsen, B A M, Becher, Heiko, Blomqvist, Carl, Bojesen, Stig E, Bolla, Manjeet K, Camp, Nicola J, Czene, Kamila, Devilee, Peter, Eccles, Diana M, Fasching, Peter A, Figueroa, Jonine D, Flyger, Henrik, García-Closas, Montserrat, Haiman, Christopher A, Hamann, Ute, Hopper, John L, Jakubowska, Anna, Leeuwen, Floor E, Lindblom, Annika, Lubiński, Jan, Margolin, Sara, Martinez, Maria Elena, Nevanlinna, Heli, Nevelsteen, Ines, Pelders, Saskia, Pharoah, Paul D P, Siesling, Sabine, Southey, Melissa C, van der Hout, Annemieke H, van Hest, Liselotte P, Chang-Claude, Jenny, Hall, Per, Easton, Douglas F, Steyerberg, Ewout W, Schmidt, Marjanka K

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Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease von Morgan, Neil V, Morris, Mark R, Cangul, Hakan, Gleeson, Diane, Straatman-Iwanowska, Anna, Davies, Nicholas, Keenan, Stephen, Pasha, Shanaz, Rahman, Fatimah, Gentle, Dean, Vreeswijk, Maaike P G, Devilee, Peter, Knowles, Margaret A, Ceylaner, Serdar, Trembath, Richard C, Dalence, Carlos, Kismet, Erol, Köseoğlu, Vedat, Rossbach, Hans-Christoph, Gissen, Paul, Tannahill, David, Maher, Eamonn R

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Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients von Giardiello, Daniele, Hooning, Maartje J, Hauptmann, Michael, Keeman, Renske, Heemskerk-Gerritsen, B A M, Becher, Heiko, Blomqvist, Carl, Bojesen, Stig E, Bolla, Manjeet K, Camp, Nicola J, Czene, Kamila, Devilee, Peter, Eccles, Diana M, Fasching, Peter A, Figueroa, Jonine D, Flyger, Henrik, García-Closas, Montserrat, Haiman, Christopher A, Hamann, Ute, Hopper, John L, Jakubowska, Anna, Leeuwen, Floor E, Lindblom, Annika, Lubiński, Jan, Margolin, Sara, Martinez, Maria Elena, Nevanlinna, Heli, Nevelsteen, Ines, Pelders, Saskia, Pharoah, Paul D P, Siesling, Sabine, Southey, Melissa C, van der Hout, Annemieke H, van Hest, Liselotte P, Chang-Claude, Jenny, Hall, Per, Easton, Douglas F, Steyerberg, Ewout W, Schmidt, Marjanka K

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants von 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.

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What do we use: Platelet-rich plasma or platelet-leukocyte gel? von Everts, Peter A.M., van Zundert, André, Schönberger, Jacques P.A.M., Devilee, Roger J.J., Knape, Johannes T.A.

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Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma von Bayley, Jean-Pierre, van Minderhout, Ivonne, Weiss, Marjan M, Jansen, Jeroen C, Oomen, Peter H N, Menko, Fred H, Pasini, Barbara, Ferrando, Barbara, Wong, Nora, Alpert, Lesley C, Williams, Rosie, Blair, Edward, Devilee, Peter, Taschner, Peter E M

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Pathology of Ovarian Cancers in BRCA1 and BRCA2 Carriers von LAKHANI, Sunil R, MANEK, Sanjiv, MEIJERS-HEIJBOER, Hanne, RADICE, Paolo, PILOTTI, Silvana, NEVANLINNA, Heli, BUTZOW, Ralf, SOBOL, Hagay, JACQUEMIER, Jocylyne, LYONET, Dominique Stoppa, NEUHAUSEN, Susan L, WEBER, Barbara, PENAULT-LLORCA, Frederique, WAGNER, Teresa, WINQVIST, Robert, BIGNON, Yves-Jean, MONTI, Franco, SCHMITT, Fernando, LENOIR, Gilbert, SEITZ, Susanne, HAMMAN, Ute, PHAROAH, Paul, LANE, Geoff, FLANAGAN, Adrienne, PONDER, Bruce, BISHOP, D. Timothy, EASTON, Douglas F, ARNOUT, Laurent, MERRETT, Samantha, MCGUFFOG, Lesley, STEELE, Dawn, DEVILEE, Peter, KLIJN, Jan G. M

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The MDM2 Promoter SNP285C/309G Haplotype Diminishes Sp1 Transcription Factor Binding and Reduces Risk for Breast and Ovarian Cancer in Caucasians von Knappskog, Stian, Bjørnslett, Merete, Myklebust, Line M., Huijts, Petra E.A., Vreeswijk, Maaike P., Edvardsen, Hege, Guo, Yongli, Zhang, Xuemei, Yang, Ming, Ylisaukko-oja, Sanna K., Alhopuro, Pia, Arola, Johanna, Tollenaar, Rob A.E.M., van Asperen, Christi J., Seynaeve, Caroline, Staalesen, Vidar, Chrisanthar, Ranjan, Løkkevik, Erik, Salvesen, Helga B., Evans, D. Gareth, Newman, William G., Lin, Dongxin, Aaltonen, Lauri A., Børresen-Dale, Anne-Lise, Tell, Grethe S., Stoltenberg, Camilla, Romundstad, Pål, Hveem, Kristian, Lillehaug, Johan R., Vatten, Lars, Devilee, Peter, Dørum, Anne, Lønning, Per E.

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