Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control von Janavičius, Ramūnas

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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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Polygenic risk modeling for prediction of epithelial ovarian cancer risk von Dareng, Eileen O, Tyrer, Jonathan P, Barnes, Daniel R, Jones, Michelle R, Yang, Xin, Aben, Katja K H, Adank, Muriel A, Agata, Simona, Andrulis, Irene L, Anton-Culver, Hoda, Antonenkova, Natalia N, Aravantinos, Gerasimos, Arun, Banu K, Augustinsson, Annelie, Balmaña, Judith, Bandera, Elisa V, Barkardottir, Rosa B, Barrowdale, Daniel, Beckmann, Matthias W, Beeghly-Fadiel, Alicia, Benitez, Javier, Bermisheva, Marina, Bernardini, Marcus Q, Bjorge, Line, Black, Amanda, Bogdanova, Natalia V, Bonanni, Bernardo, Borg, Ake, Brenton, James D, Budzilowska, Agnieszka, Butzow, Ralf, Buys, Saundra S, Cai, Hui, Caligo, Maria A, Campbell, Ian, Cannioto, Rikki, Cassingham, Hayley, Chang-Claude, Jenny, Chanock, Stephen J, Chen, Kexin, Chiew, Yoke-Eng, Chung, Wendy K, Claes, Kathleen B M, Colonna, Sarah, Cook, Linda S, Couch, Fergus J, Daly, Mary B, Dao, Fanny, Davies, Eleanor, de la Hoya, Miguel, de Putter, Robin, Dennis, Joe, DePersia, Allison, Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Doherty, Jennifer A, Domchek, Susan M, Dörk, Thilo, du Bois, Andreas, Dürst, Matthias, Eccles, Diana M, Eliassen, Heather A, Engel, Christoph, Evans, Gareth D, Fasching, Peter A, Flanagan, James M, Fortner, Renée T, Machackova, Eva, Friedman, Eitan, Ganz, Patricia A, Garber, Judy, Gensini, Francesca, Giles, Graham G, Glendon, Gord, Godwin, Andrew K, Goodman, Marc T, Greene, Mark H, Gronwald, Jacek, Hahnen, Eric, Haiman, Christopher A, Håkansson, Niclas, Hamann, Ute, Hansen, Thomas V O, Harris, Holly R, Hartman, Mikael, Heitz, Florian, Hildebrandt, Michelle A T, Høgdall, Estrid, Høgdall, Claus K, Hopper, John L, Huang, Ruea-Yea, Huff, Chad, Hulick, Peter J, Huntsman, David G, Imyanitov, Evgeny N, Isaacs, Claudine, Jakubowska, Anna, James, Paul A, Janavicius, Ramunas

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Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer von Rump, Andreas, Benet-Pages, Anna, Schubert, Steffen, Kuhlmann, Jan Dominik, Janavičius, Ramūnas, Macháčková, Eva, Foretová, Lenka, Kleibl, Zdenek, Lhota, Filip, Zemankova, Petra, Betcheva-Krajcir, Elitza, Mackenroth, Luisa, Hackmann, Karl, Lehmann, Janin, Nissen, Anke, DiDonato, Nataliya, Opitz, Romy, Thiele, Holger, Kast, Karin, Wimberger, Pauline, Holinski-Feder, Elke, Emmert, Steffen, Schröck, Evelin, Klink, Barbara

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The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA... von Lakeman, Inge M. M., Vos, Juliën A. M., Barnes, Daniel R., Adlard, Julian, Andrulis, Irene L., Arason, Adalgeir, Arnold, Norbert, Arun, Banu K., Balmaña, Judith, Barrowdale, Daniel, Benitez, Javier, Borg, Ake, Caldés, Trinidad, Caligo, Maria A., Chung, Wendy K., Claes, Kathleen B. M., Collée, J. Margriet, Couch, Fergus J., Daly, Mary B., Dennis, Joe, Dhawan, Mallika, Domchek, Susan M., Eeles, Ros, Engel, Christoph, Evans, D. Gareth, Feliubadaló, Lidia, Foretova, Lenka, Friedman, Eitan, Frost, Debra, Ganz, Patricia A., Gayther, Simon A., Gerdes, Anne-Marie, Godwin, Andrew K., Goldgar, David E., Hahnen, Eric, Hake, Christopher R., Hamann, Ute, Hogervorst, Frans B. L., Hooning, Maartje J., Hopper, John L., Hulick, Peter J., Imyanitov, Evgeny N., Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, James, Paul A., Janavicius, Ramunas, Jensen, Uffe Birk, Jiao, Yue, John, Esther M., Karlan, Beth Y., Kets, Carolien M., Kwong, Ava, Legrand, Clémentine, Leslie, Goska, Lesueur, Fabienne, Loud, Jennifer T., Manoukian, Siranoush, McGuffog, Lesley, Miller, Austin, Gomes, Denise Molina, Montagna, Marco, Mouret-Fourme, Emmanuelle, Neuhausen, Susan L., Nevanlinna, Heli, Yie, Joanne Ngeow Yuen, Olah, Edith, Olopade, Olufunmilayo I., Park, Sue K., Parsons, Michael T., Peterlongo, Paolo, Radice, Paolo, Rantala, Johanna, Rennert, Gad, Schmutzler, Rita K., Sharma, Priyanka, Simard, Jacques, Singer, Christian F., Stadler, Zsofia, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel R., Teo, Soo Hwang, Teulé, Alex, Thomassen, Mads, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Tung, Nadine, Vega, Ana, Wappenschmidt, Barbara, Devilee, Peter, van Asperen, Christi J., Bernstein, Jonine L., Offit, Kenneth, Easton, Douglas F., Rookus, Matti A., Chenevix-Trench, Georgia, Schmidt, Marjanka K.

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Comprehensive BRCA1 and BRCA2 mutational profile in Lithuania von Janavičius, Ramūnas, Rudaitis, Vilius, Mickys, Ugnius, Elsakov, Pavel, Griškevičius, Laimonas

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Genetic counselling legislation and practice in cancer in EU Member States von McCrary, J Matt, Van Valckenborgh, Els, Poirel, Hélène A, de Putter, Robin, van Rooij, Jeroen, Horgan, Denis, Dierks, Marie-Luise, Antonova, Olga, Brunet, Joan, Chirita-Emandi, Adela, Colas, Chrystelle, Dalmas, Miriam, Ehrencrona, Hans, Grima, Claire, Janavičius, Ramūnas, Klink, Barbara, Koczok, Katalin, Krajc, Mateja, Lace, Baiba, Leitsalu, Liis, Mistrik, Martin, Paneque, Milena, Primorac, Dragan, Roetzer, Katharina M, Ronez, Joelle, Slámová, Lucie, Spanou, Elena, Stamatopoulos, Kostas, Stoklosa, Tomasz, Strang-Karlsson, Sonja, Szakszon, Katalin, Szczałuba, Krzysztof, Turner, Jacqueline, van Dooren, Marieke F, van Zelst-Stams, Wendy A G, Vassallo, Loredana-Maria, Wadt, Karin A W, Žigman, Tamara, Ripperger, Tim, Genuardi, Maurizio, Van den Bulcke, Marc, Bergmann, Anke Katharina

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Overlapping Phenotype of Cardiomyopathy in a Patient with Double Mutation: A Case Report von Glaveckaitė, Sigita, Mikštienė, Violeta, Preikšaitienė, Eglė, Norvilas, Rimvydas, Janavičius, Ramūnas, Valevičienė, Nomeda Rima

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Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk von Dareng, Eileen O, Tyrer, Jonathan P, Barnes, Daniel R, Jones, Michelle R, Yang, Xin, Aben, Katja K H, Adank, Muriel A, Agata, Simona, Andrulis, Irene L, Anton-Culver, Hoda, Antonenkova, Natalia N, Aravantinos, Gerasimos, Arun, Banu K, Augustinsson, Annelie, Balmaña, Judith, Bandera, Elisa V, Barkardottir, Rosa B, Barrowdale, Daniel, Beckmann, Matthias W, Beeghly-Fadiel, Alicia, Benitez, Javier, Bermisheva, Marina, Bernardini, Marcus Q, Bjorge, Line, Black, Amanda, Bogdanova, Natalia V, Bonanni, Bernardo, Borg, Ake, Brenton, James D, Budzilowska, Agnieszka, Butzow, Ralf, Buys, Saundra S, Cai, Hui, Caligo, Maria A, Campbell, Ian, Cannioto, Rikki, Cassingham, Hayley, Chang-Claude, Jenny, Chanock, Stephen J, Chen, Kexin, Chiew, Yoke-Eng, Chung, Wendy K, Claes, Kathleen B M, Colonna, Sarah, Cook, Linda S, Couch, Fergus J, Daly, Mary B, Dao, Fanny, Davies, Eleanor, de la Hoya, Miguel, de Putter, Robin, Dennis, Joe, DePersia, Allison, Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Doherty, Jennifer A, Domchek, Susan M, Dörk, Thilo, du Bois, Andreas, Dürst, Matthias, Eccles, Diana M, Eliassen, Heather A, Engel, Christoph, Evans, Gareth D, Fasching, Peter A, Flanagan, James M, Fortner, Renée T, Machackova, Eva, Friedman, Eitan, Ganz, Patricia A, Garber, Judy, Gensini, Francesca, Giles, Graham G, Glendon, Gord, Godwin, Andrew K, Goodman, Marc T, Greene, Mark H, Gronwald, Jacek, Hahnen, Eric, Haiman, Christopher A, Håkansson, Niclas, Hamann, Ute, Hansen, Thomas V O, Harris, Holly R, Hartman, Mikael, Heitz, Florian, Hildebrandt, Michelle A T, Høgdall, Estrid, Høgdall, Claus K, Hopper, John L, Huang, Ruea-Yea, Huff, Chad, Hulick, Peter J, Huntsman, David G, Imyanitov, Evgeny N, Isaacs, Claudine, Jakubowska, Anna, James, Paul A, Janavicius, Ramunas

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Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania von JANAVICIUS, Ramunas, PEPALYTE, Ingrida, KUCINSKAS, Vaidutis

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BRCA1 testing in Lithuania von Janavicius, Ramunas

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Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation von Janavičius, Ramūnas, Rudaitis, Vilius, Feng, Bing-Jian, Ozolina, Silvija, Griškevičius, Laimonas, Goldgar, David, Tihomirova, Laima

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Extremely low risk of pheochromocytomas in complete VHL gene deletion cases von Janavičius, Ramūnas, Adomaitis, Robertas, Jankevičius, Feliksas, Griškevičius, Laimonas

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Multiple endocrine neoplasia type 1: a case report and review of the literature von Šileikis, Audrius, Kildušis, Edvinas, Janavičius, Ramūnas, Strupas, Kęstutis

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Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers von Janavicius, Ramunas, Elsakov, Pavel

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Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses von Zhang, Haoyu, Ahearn, Thomas U., Beesley, Jonathan, Jiang, Xia, Anton-Culver, Hoda, Aronson, Kristan J., Beckmann, Matthias W., Benitez, Javier, Bialkowska, Katarzyna, Blanco, Ana, Blomqvist, Carl, Borg, Ake, Briceno, Ignacio, Brucker, Sara Y., Burwinkel, Barbara, Buys, Saundra S., Byers, Helen, Caldés, Trinidad, Chang-Claude, Jenny, Clarke, Christine L., Cox, Angela, Cross, Simon S., Czene, Kamila, Domchek, Susan M., Ekici, Arif B., Figueroa, Jonine, Foretova, Lenka, Fostira, Florentia, Garber, Judy, Gaudet, Mia M., Goldgar, David E., Häberle, Lothar, Hake, Christopher R., Hamann, Ute, Hillemanns, Peter, Holleczek, Bernd, Hollestelle, Antoinette, Hooning, Maartje J., Hoover, Robert N., Imyanitov, Evgeny N., Isaacs, Claudine, Jager, Agnes, Janavicius, Ramunas, Kaaks, Rudolf, Keeman, Renske, Konstantopoulou, Irene, Lazarova, Emilija, Lejbkowicz, Flavio, Leslie, Goska, Lindblom, Annika, Lissowska, Jolanta, Loud, Jennifer T., Mannermaa, Arto, Matricardi, Laura, Meindl, Alfons, Menon, Usha, Muranen, Taru A., Newman, William G., Nikitina-Zake, Liene, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Orr, Nick, Park-Simon, Tjoung-Won, Parsons, Michael T., Phillips, Kelly-Anne, Rack, Brigitte, Rennert, Hedy S., Risch, Harvey A., Rookus, Matti A., Rübner, Matthias, Rüdiger, Thomas, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Schöttker, Ben, Sherman, Mark E., Shu, Xiao-Ou, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony J., Szabo, Csilla I., Taylor, Jack A., Terry, MaryBeth, Thull, Darcy L., Toland, Amanda E., Tollenaar, Rob A. E. M., Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Untch, Michael, Vachon, Celine M., van der Kolk, Lizet E., van Veen, Elke M., Vega, Ana, Wappenschmidt, Barbara, Weitzel, Jeffrey N., Winqvist, Robert, Yannoukakos, Drakoulis, Pharoah, Paul D. P., García-Closas, Montserrat

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Apparently “BRCA‐Related” Breast and Ovarian Cancer Patient With Germline TP53 Mutation von Janavičius, Ramūnas, Andrėkutė, Kristina, Mickys, Ugnius, Rudaitis, Vilius, Brasiūnienė, Birutė, Griškevičius, Laimonas

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Abstract LB-044: Germline mutations in patients with hereditary breast and ovarian cancer establish ERCC2 as a cancer susceptibility gene von Schrock, Evelin, Benet-Pagès, Anna, Schubert, Steffen, Janavicius, Ramūnas, Hackmann, Karl, Betcheva-Krajcir, Elitza, Mackenroth, Luisa, Lehmann, Janin, Nissen, AM, Altmueller, Janine, Thiele, Holger, Di Donato, Nataliya, Klink, Barbara, Kuhlmann, Jan D., Tzschach, Andreas, Kast, Karin, Wimberger, Pauline, Holinski-Feder, Elke, Meindl, Alfons, Emmert, Steffen, Rump, Andreas

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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer von Kar, Siddhartha, Jiang, Xia, Finucane, Hilary, McGuffog, Lesley, Adams, Marcia, Agata, Simona, Allen, Jamie, Bernstein, Leslie, Bobolis, Kristie, Bogdanova, Natalia V, Bozsik, Aniko, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Bressac-de Paillerets, Brigitte, Brinton, Louise, Cai, Qiuyin, Caligo, Maria A, Castelao, J Esteban, Castera, Laurent, Chanock, Stephen J, Christiansen, Hans, Diez, Orland, Domchek, Susan M, dos-Santos-Silva, Isabel, Eeles, Ros, Ehrencrona, Hans, Eilber, Ursula, Ekici, Arif B, Engel, Christoph, Flyger, Henrik, Ganz, Patricia A, Garber, Judy, Gerdes, Anne-Marie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, González-Neira, Anna, Goodfellow, Paul, Greene, Mark H, Alnæs, Grethe I Grenaker, Haeberle, Lothar, Hankinson, Susan, Hodgson, Shirley, Hu, Chunling, Hunter, David J, Jensen, Uffe Birk, Jones, Michael, Kabisch, Maria, Kerin, Michael J, Khan, Sofia, Knight, Julia A, Lecarpentier, Julie, Lilyquist, Jenna, Lincoln, Anne, Lindblom, Annika, Luccarini, Craig, MacInnis, Robert J, Maishman, Tom, Miller, Nicola, Nadesan, Sue, Neuhausen, Susan L, Nevelsteen, Ines, Nordestgaard, Børge G, Olopade, Olufunmilayo I, Peixoto, Ana, Peto, Julian, Prokofieva, Darya, Radice, Paolo, Rahman, Nazneen, Rennert, Gad, Romero, Atocha, Sanders, Joyce, Schmidt, Daniel F, Schoemaker, Minouk J, Schwentner, Lukas, Sheng, Xin, Sukiennicki, Grzegorz, Surowy, Harald, Sutter, Christian, Swerdlow, Anthony, Tan, Yen Y, Tibiletti, Maria Grazia, Tihomirova, Laima, Tong, Ling, Truong, Thérèse, Tyrer, Jonathan, van Rensburg, Elizabeth J, Weinberg, Clarice R, Whittemore, Alice S, Winqvist, Robert, Wolk, Alicja, Yang, Xiaohong R, Zheng, Wei, Ottini, Laura, Thomassen, Mads, Schmutzler, Rita K, Couch, Fergus J, García-Closas, Montserrat, Simard, Jacques

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Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants von Li, Shuai, Silvestri, Valentina, Leslie, Goska, Rebbeck, Timothy R, Neuhausen, Susan L, Hopper, John L, Nielsen, Henriette Roed, Lee, Andrew, Yang, Xin, McGuffog, Lesley, Parsons, Michael T, Andrulis, Irene L, Arnold, Norbert, Belotti, Muriel, Borg, Åke, Buecher, Bruno, Buys, Saundra S, Caputo, Sandrine M, Chung, Wendy K, Colas, Chrystelle, Colonna, Sarah V, Cook, Jackie, Daly, Mary B, de la Hoya, Miguel, de Pauw, Antoine, Delhomelle, Hélène, Eason, Jacqueline, Engel, Christoph, Evans, D Gareth, Faust, Ulrike, Fehm, Tanja N, Fostira, Florentia, Fountzilas, George, Frone, Megan, Garcia-Barberan, Vanesa, Garre, Pilar, Gauthier-Villars, Marion, Gehrig, Andrea, Glendon, Gord, Goldgar, David E, Golmard, Lisa, Greene, Mark H, Hahnen, Eric, Hamann, Ute, Hanson, Helen, Hassan, Tiara, Hentschel, Julia, Horvath, Judit, Izatt, Louise, Janavicius, Ramunas, Jiao, Yue, John, Esther M, Karlan, Beth Y, Kim, Sung-Won, Konstantopoulou, Irene, Kwong, Ava, Laugé, Anthony, Lee, Jong Won, Lesueur, Fabienne, Mebirouk, Noura, Meindl, Alfons, Mouret-Fourme, Emmanuelle, Musgrave, Hannah, Ngeow Yuen Yie, Joanne, Niederacher, Dieter, Park, Sue K, Pedersen, Inge Sokilde, Ramser, Juliane, Ramus, Susan J, Rantala, Johanna, Rashid, Muhammad U, Reichl, Florian, Ritter, Julia, Rump, Andreas, Santamariña, Marta, Saule, Claire, Schmidt, Gunnar, Schmutzler, Rita K, Senter, Leigha, Shariff, Saba, Singer, Christian F, Southey, Melissa C, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen, Teo, Soo Hwang, Terry, Mary Beth, Thomassen, Mads, Tischkowitz, Marc, Toland, Amanda E, Torres, Diana, Vega, Ana, Wagner, Sebastian A, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Weber, Bernhard H F, Yannoukakos, Drakoulis, Spurdle, Amanda B, Easton, Douglas F, Chenevix-Trench, Georgia

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