Treffer 1 - 20 von 741 für Suche 'Prieur, Mary G.', Suchdauer: 2,36s Treffer weiter einschränken
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    Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus von Li, Qiyuan, Andrulis, Irene L., Arndt, Volker, Arver, Brita, Bandera, Elisa V., Barkardottir, Rosa B., Barrowdale, Daniel, Beckmann, Matthias W., Benitez, Javier, Bisogna, Maria, Bogdanova, Natalia, Bonanni, Bernardo, Børresen-Dale, Anne-Lise, Brauch, Hiltrud, Bruinsma, Fiona, Buhari, Shaik Ahmad, Burwinkel, Barbara, Campbell, Ian, Chang-Claude, Jenny, Chiquette, Jocelyne, Choi, Ji-Yeob, Czene, Kamila, Diez, Orland, Doherty, Jennifer A., Domchek, Susan M., Dörk, Thilo, Dumont, Martine, Figueroa, Jonine, Flyger, Henrik, Fostira, Florentia, Foulkes, William D., Friedman, Eitan, Frost, Debra, Gambino, Gaetana, Ganz, Patricia A., Garber, Judy, Gentry-Maharaj, Aleksandra, Ghoussaini, Maya, Giles, Graham G., Glasspool, Rosalind, Goldgar, David E., González-Neira, Anna, Goodman, Marc T., Guénel, Pascal, Haiman, Christopher A., Hallberg, Emily, Hartman, Mikael, Healey, Sue, Heitz, Florian, Høgdall, Estrid, Hogervorst, Frans B. L., Huzarski, Tomasz, Imyanitov, Evgeny N., John, Esther M., Kapuscinski, Miroslav, Karlan, Beth Y., Knight, Julia A., Konstantopoulou, Irene, Kosma, Veli-Matti, Kupryjanczyk, Jolanta, de la Hoya, Miguel, Lambrechts, Diether, De Leeneer, Kim, Li, Jingmei, Lubinski, Jan, Margolin, Sara, McGuffog, Lesley, McNeish, Iain, Meindl, Alfons, Mulligan, Anna Marie, Ness, Roberta B., Neuhausen, Susan L., Odunsi, Kunle, Olah, Edith, Orr, Nick, Osorio, Ana, Park, Sue Kyung, Poole, Elizabeth M., Rantala, Johanna, Risch, Harvey A., Sangrajrang, Suleeporn, Schildkraut, Joellen M., Schmidt, Marjanka K., Shu, Xiao-Ou, Sieh, Weiva, Singer, Christian F., Sinilnikova, Olga M., Slager, Susan, Southey, Melissa C., Stenmark-Askmalm, Marie, Tihomirova, Laima, Tung, Nadine, van Doorn, Helena C., Van't Veer, Laura J., Wentzensen, Nicolas, Wildiers, Hans, Zheng, Wei, Simard, Jacques, Pharoah, Paul D., Chenevix-Trench, Georgia

    Veröffentlicht in NATURE COMMUNICATIONS

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    Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Dennis, Joe, Tyrer, Jonathan P., McGuffog, Lesley, Bolla, Manjeet K., Adank, Muriel A., Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Baynes, Caroline, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Brenner, Hermann, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Collée, J. Margriet, Czene, Kamila, Devilee, Peter, Dwek, Miriam, Evans, D. Gareth, Flyger, Henrik, Fostira, Florentia, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gehrig, Andrea, Giles, Graham G., Goldgar, David E., Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hulick, Peter J., Hunter, David J., Jager, Agnes, Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Kiiski, Johanna I., Kraft, Peter, Kurian, Allison W., Lambrechts, Diether, Lesueur, Fabienne, Lindstrom, Tricia, Mannermaa, Arto, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, O’Brien, Katie M., Olsson, Håkan, Ottini, Laura, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Polley, Eric C., Pujana, Miquel Angel, Punie, Kevin, Rashid, Muhammad U., Rennert, Gad, Saloustros, Emmanouil, Santella, Regina, Scheuner, Maren T., Schmidt, Gunnar, Scott, Christopher, Swerdlow, Anthony, Tamimi, Rulla M., Taylor, Jack A., Thull, Darcy L., Tung, Nadine, Vachon, Celine M., Vega, Ana, Wang, Qin, Wendt, Camilla, Yang, Xiaohong R., Ziogas, Argyrios, Park, Sue K., Thomassen, Mads, Simard, Jacques, Chenevix-Trench, Georgia

    Veröffentlicht in Nature communications

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    Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer von Ferreira, Manuel A., Andrulis, Irene L., Anton-Culver, Hoda, Aronson, Kristan J., Barnes, Daniel R., Beckmann, Matthias W., Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V., Bojesen, Stig E., Bolla, Manjeet K., Brauch, Hiltrud, Campa, Daniele, Campbell, Ian, Canzian, Federico, Carter, Jonathan, Castelao, Jose E., Chang-Claude, Jenny, Couch, Fergus J., Cox, Angela, Cross, Simon S., de la Hoya, Miguel, Dennis, Joe, Devilee, Peter, Dörk, Thilo, Ejlertsen, Bent, Engel, Christoph, Eriksson, Mikael, Fletcher, Olivia, Flyger, Henrik, Frost, Debra, Gabrielson, Marike, Gapstur, Susan M., Garber, Judy, García-Sáenz, José A., Giles, Graham G., Glendon, Gord, Godwin, Andrew K., González-Neira, Anna, Gronwald, Jacek, Guénel, Pascal, Hall, Per, Hamann, Ute, He, Wei, Hulick, Peter J., Humphreys, Keith, Isaacs, Claudine, Jakimovska, Milena, Jakubowska, Anna, James, Paul A., John, Esther M., Johnson, Nichola, Karlan, Beth Y., Khusnutdinova, Elza, Kiiski, Johanna I., Jones, Michael E., Konstantopoulou, Irene, Laitman, Yael, Lambrechts, Diether, Lazaro, Conxi, Lindström, Sara, Manoochehri, Mehdi, Margolin, Sara, McGuffog, Lesley, Michailidou, Kyriaki, Montagna, Marco, Moreno, Fernando, Moserle, Lidia, Nevelsteen, Ines, Nussbaum, Robert L., Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Osorio, Ana, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peixoto, Ana, Peterlongo, Paolo, Poppe, Bruce, Presneau, Nadege, Risch, Harvey A., Saloustros, Emmanouil, Sanden, Kristin, Simard, Jacques, Singer, Christian F., Soucy, Penny, Spinelli, John J., Spurdle, Amanda B., Taylor, Jack A., Thöne, Kathrin, Toland, Amanda E., Tung, Nadine, Vachon, Celine M., van Asperen, Christi J., van Rensburg, Elizabeth J., Weitzel, Jeffrey N., Winqvist, Robert, Yannoukakos, Drakoulis, Zheng, Wei, Beesley, Jonathan

    Veröffentlicht in NATURE COMMUNICATIONS

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    Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes von Fachal, Laura, Kar, Siddhartha, Moradi Marjaneh, Mahdi, Alonso, M. Rosario, Anton-Culver, Hoda, Arason, Adalgeir, Arun, Banu K., Auer, Paul L., Barrowdale, Daniel, Białkowska, Katarzyna, Bolla, Manjeet K., Brooks-Wilson, Angela, Caldés, Trinidad, Campbell, Ian, Carter, Brian D., Christiansen, Hans, Collée, J. Margriet, Couch, Fergus J., Cox, Angela, Cross, Simon S., de la Hoya, Miguel, Ding, Yuan Chun, Dite, Gillian S., Domchek, Susan M., Dwek, Miriam, Eriksson, Mikael, Evans, D. Gareth, Floris, Giuseppe, Gambino, Gaetana, Gapstur, Susan M., García-Sáenz, José A., Gaudet, Mia M., Giles, Graham G., Glendon, Gord, Goldgar, David E., Greene, Mark H., Grip, Mervi, Guénel, Pascal, Håkansson, Niclas, Hall, Per, Harrington, Patricia A., Heyworth, Jane, Hogervorst, Frans B. L., Howell, Anthony, Huang, Guanmengqian, Hulick, Peter J., Jakimovska, Milena, Jakubowska, Anna, Janavicius, Ramunas, Johnson, Nichola, Kaaks, Rudolf, Kapoor, Pooja Middha, Ko, Yon-Dschun, Konstantopoulou, Irene, Laitman, Yael, Lee, Eunjung, Lindblom, Annika, Lo, Wing-Yee, Lophatananon, Artitaya, Manoukian, Siranoush, Margolin, Sara, Martinez, Maria Elena, Mayes, Rebecca, McLean, Catriona, Mebirouk, Noura, Miller, Austin, Moreno, Fernando, Mulligan, Anna Marie, Narod, Steven A., Nassir, Rami, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Osorio, Ana, Pankratz, V. Shane, Park, Sue K., Parsons, Michael T., Paul, James, Pedersen, Inge Sokilde, Prokofyeva, Darya, Ramus, Susan J., Rantala, Johanna, Risch, Harvey A., Saloustros, Emmanouil, Schoemaker, Minouk J., Scott, Rodney J., Shah, Mitul, Shen, Chen-Yang, Smichkoska, Snezhana, Tamimi, Rulla M., Thomassen, Mads, Toland, Amanda E., Tollenaar, Rob A. E. M., Troester, Melissa A., Vachon, Celine M., van Asperen, Christi J., Vega, Ana, Viel, Alessandra, Wildiers, Hans, Zhang, Yan

    Veröffentlicht in Nature genetics

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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.

    Veröffentlicht in Genetics in medicine

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    Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers von Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Shane Pankratz, V., Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, Meijers-Heijboer, Hanne E. J., Van Roozendaal, Cees E., Perez-Segura, Pedro, Jakubowska, Anna, Huzarski, Tomasz, Blecharz, Paweł, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., D’Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine, Narod, Steven, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary-Beth, Tung, Nadine, Hansen, Thomas v. O., Benitez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley, Porteous, Mary, Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Wappenschmidt, Barbara, Laitman, Yael, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gold, Bert

    Veröffentlicht in HUMAN GENETICS

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Dennis, Joe, Tyrer, Jonathan P., McGuffog, Lesley, Bolla, Manjeet K., Adank, Muriel A., Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Baynes, Caroline, Becher, Heiko, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Brenner, Hermann, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Collée, J. Margriet, Czene, Kamila, Devilee, Peter, Dwek, Miriam, Evans, D. Gareth, Flyger, Henrik, Fostira, Florentia, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gehrig, Andrea, Giles, Graham G., Goldgar, David E., Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hulick, Peter J., Hunter, David J., Jager, Agnes, Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Kiiski, Johanna I., Kraft, Peter, Lambrechts, Diether, Lesueur, Fabienne, Lindstrom, Tricia, Mannermaa, Arto, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, O’Brien, Katie M., Olsson, Håkan, Ottini, Laura, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Polley, Eric C., Pujana, Miquel Angel, Punie, Kevin, Rashid, Muhammad U., Rennert, Gad, Saloustros, Emmanouil, Santella, Regina, Scheuner, Maren T., Schmidt, Gunnar, Scott, Christopher, Swerdlow, Anthony, Tamimi, Rulla M., Taylor, Jack A., Thull, Darcy L., Tung, Nadine, Vachon, Celine M., Vega, Ana, Wang, Qin, Wendt, Camilla, Yang, Xiaohong R., Ziogas, Argyrios, Park, Sue K., Thomassen, Mads, Simard, Jacques, Chenevix-Trench, Georgia

    Veröffentlicht in NATURE COMMUNICATIONS

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    Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers von Blanco, Ignacio, Kuchenbaecker, Karoline, Cuadras, Daniel, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka Ruiz, Librado, Pablo, Sánchez-Gracia, Alejandro, Rozas, Julio, Bonifaci, Núria, McGuffog, Lesley, Pankratz, Vernon S, Islam, Abul, Mateo, Francesca, Berenguer, Antoni, Petit, Anna, Català, Isabel, Brunet, Joan, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Arun, Banu K, Toland, Amanda E, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Greene, Mark H, Mai, Phuong L, Nussbaum, Robert L, Andrulis, Irene L, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Timothy R, Barkardottir, Rosa B, Jakubowska, Anna, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Claes, Kathleen, Van Maerken, Tom, Díez, Orland, Hansen, Thomas V, Jønson, Lars, Gerdes, Anne-Marie, Ejlertsen, Bent, de la Hoya, Miguel, Caldés, Trinidad, Dunning, Alison M, Oliver, Clare, Fineberg, Elena, Cook, Margaret, Peock, Susan, McCann, Emma, Murray, Alex, Jacobs, Chris, Pichert, Gabriella, Lalloo, Fiona, Chu, Carol, Dorkins, Huw, Paterson, Joan, Ong, Kai-Ren, Teixeira, Manuel R, Hogervorst, Frans B L, van der Hout, Annemarie H, Seynaeve, Caroline, van der Luijt, Rob B, Ligtenberg, Marjolijn J L, Devilee, Peter, Wijnen, Juul T, Rookus, Matti A, Meijers-Heijboer, Hanne E J, Blok, Marinus J, van den Ouweland, Ans M W, Aalfs, Cora M, Rodriguez, Gustavo C, Phillips, Kelly-Anne A, Piedmonte, Marion, Nerenstone, Stacy R, Bae-Jump, Victoria L, O'Malley, David M, Ratner, Elena S, Schmutzler, Rita K, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg J, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda

    Veröffentlicht in PloS one

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    Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer von Gaudet, Mia M, Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, Segrè, Ayellet V, McGee, Kate, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M, Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, Frenay, Marc, GEMO Study Collaborators, Hogervorst, Frans B L, Rookus, Matti A, Collée, J Margriet, Hoogerbrugge, Nicoline, van Roozendaal, Kees E P, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V, Caldés, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Peterlongo, Paolo, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Rennert, Gad, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, D'Andrea, Emma, Friedman, Eitan, Laitman, Yael, Borg, Ake, Beattie, Mary, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Hopper, John L, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Overeem Hansen, Thomas V, Nielsen, Finn C, Greene, Mark H, Greene, Mark I, Mai, Phuong L, Osorio, Ana, Durán, Mercedes, Andres, Raquel, Benítez, Javier, Weitzel, Jeffrey N, Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Walker, Lisa

    Veröffentlicht in PLoS genetics

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