Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

por Klein, Christopher J., Botuyan, Maria-Victoria, Wu, Yanhong, Ward, Christopher J., Nicholson, Garth A., Hammans, Simon, Hojo, Kaori, Yamanishi, Hiromitch, Karpf, Adam R., Wallace, Douglas C., Simon, Mariella, Lander, Cecilie, Boardman, Lisa A., Cunningham, Julie M., Smith, Glenn E., Litchy, William J., Boes, Benjamin, Atkinson, Elizabeth J., Middha, Sumit, Dyck, P. James, Parisi, Joseph E., Mer, Georges, Smith, David I., Dyck, Peter J.
Publicado 2011

TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer

por Chien, Jeremy, Sicotte, Hugues, Fan, Jian-Bing, Humphray, Sean, Cunningham, Julie M., Kalli, Kimberly R., Oberg, Ann L., Hart, Steven N., Li, Ying, Davila, Jaime I., Baheti, Saurabh, Wang, Chen, Dietmann, Sabine, Atkinson, Elizabeth J., Asmann, Yan W., Bell, Debra A., Ota, Takayo, Tarabishy, Yaman, Kuang, Rui, Bibikova, Marina, Cheetham, R. Keira, Grocock, Russell J., Swisher, Elizabeth M., Peden, John, Bentley, David, Kocher, Jean-Pierre A., Kaufmann, Scott H., Hartmann, Lynn C., Shridhar, Viji, Goode, Ellen L.
Publicado 2015

SARS-CoV-2 Infections Among Children in the Biospecimens from Respiratory Virus-Exposed Kids (BRAVE Kids) Study

por Hurst, Jillian H., Heston, Sarah M., Chambers, Hailey N., Cunningham, Hannah M., Price, Meghan J., Suarez, Liliana, Crew, Carter G., Bose, Shree, Aquino, Jhoanna N., Carr, Stuart T., Griffin, S. Michelle, Smith, Stephanie H., Jenkins, Kirsten, Pfeiffer, Trevor S., Rodriguez, Javier, DeMarco, C. Todd, De Naeyer, Nicole A., Gurley, Thaddeus C., Louzao, Raul, Cunningham, Coleen K., Steinbach, William J., Denny, Thomas N., Lugo, Debra J., Moody, M. Anthony, Permar, Sallie R., Rotta, Alexandre T., Turner, Nicholas A., Walter, Emmanuel B., Woods, Christopher W., Kelly, Matthew S.
Publicado 2020

Understanding and responding to COVID-19 in Wales: protocol for a privacy-protecting data platform for enhanced epidemiology and evaluation of interventions

por Lyons, Jane, Akbari, Ashley, Torabi, Fatemeh, Davies, Gareth I, North, Laura, Griffiths, Rowena, Bailey, Rowena, Hollinghurst, Joseph, Fry, Richard, Turner, Samantha L, Thompson, Daniel, Rafferty, James, Mizen, Amy, Orton, Chris, Thompson, Simon, Au-Yeung, Lee, Cross, Lynsey, Gravenor, Mike B, Brophy, Sinead, Lucini, Biagio, John, Ann, Szakmany, Tamas, Davies, Jan, Davies, Chris, Thomas, Daniel Rh, Williams, Christopher, Emmerson, Chris, Cottrell, Simon, Connor, Thomas R, Taylor, Chris, Pugh, Richard J, Diggle, Peter, John, Gareth, Scourfield, Simon, Hunt, Joe, Cunningham, Anne M, Helliwell, Kathryn, Lyons, Ronan
Publicado 2020

Severe Acute Respiratory Syndrome Coronavirus 2 Infections Among Children in the Biospecimens from Respiratory Virus-Exposed Kids (BRAVE Kids) Study

por Hurst, Jillian H, Heston, Sarah M, Chambers, Hailey N, Cunningham, Hannah M, Price, Meghan J, Suarez, Lilianna, Crew, Carter G, Bose, Shree, Aquino, Jhoanna N, Carr, Stuart T, Griffin, S Michelle, Smith, Stephanie H, Jenkins, Kirsten, Pfeiffer, Trevor S, Rodriguez, Javier, DeMarco, C Todd, De Naeyer, Nicole A, Gurley, Thaddeus C, Louzao, Raul, Zhao, Congwen, Cunningham, Coleen K, Steinbach, William J, Denny, Thomas N, Lugo, Debra J, Moody, M Anthony, Permar, Sallie R, Rotta, Alexandre T, Turner, Nicholas A, Walter, Emmanuel B, Woods, Christopher W, Kelly, Matthew S
Publicado 2020

Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22

por Cicek, Mine S., Cunningham, Julie M., Fridley, Brooke L., Serie, Daniel J., Bamlet, William R., Diergaarde, Brenda, Haile, Robert W., Le Marchand, Loic, Krontiris, Theodore G., Younghusband, H. Banfield, Gallinger, Steven, Newcomb, Polly A., Hopper, John L., Jenkins, Mark A., Casey, Graham, Schumacher, Fredrick, Chen, Zhu, DeRycke, Melissa S., Templeton, Allyson S., Winship, Ingrid, Green, Roger C., Green, Jane S., Macrae, Finlay A., Parry, Susan, Young, Graeme P., Young, Joanne P., Buchanan, Daniel, Thomas, Duncan C., Bishop, D. Timothy, Lindor, Noralane M., Thibodeau, Stephen N., Potter, John D., Goode, Ellen L.
Publicado 2012

Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22

por Cicek, Mine S., Cunningham, Julie M., Fridley, Brooke L., Serie, Daniel J., Bamlet, William R., Diergaarde, Brenda, Haile, Robert W., Le Marchand, Loic, Krontiris, Theodore G., Younghusband, H. Banfield, Gallinger, Steven, Newcomb, Polly A., Hopper, John L., Jenkins, Mark A., Casey, Graham, Schumacher, Fredrick, Chen, Zhu, DeRycke, Melissa S., Templeton, Allyson S., Winship, Ingrid, Green, Roger C., Green, Jane S., Macrae, Finlay A., Parry, Susan, Young, Graeme P., Young, Joanne P., Buchanan, Daniel, Thomas, Duncan C., Bishop, D. Timothy, Lindor, Noralane M., Thibodeau, Stephen N., Potter, John D., Goode, Ellen L.
Publicado 2012

Molecular Subclasses of Clear Cell Ovarian Carcinoma and Their Impact on Disease Behavior and Outcomes

por Bolton, Kelly L., Chen, Denise, Corona de la Fuente, Rosario, Fu, Zhuxuan, Murali, Rajmohan, Köbel, Martin, Tazi, Yanis, Cunningham, Julie M., Chan, Irenaeus C.C., Wiley, Brian J., Moukarzel, Lea A., Winham, Stacey J., Armasu, Sebastian M., Lester, Jenny, Elishaev, Esther, Laslavic, Angela, Kennedy, Catherine J., Piskorz, Anna, Sekowska, Magdalena, Brand, Alison H., Chiew, Yoke-Eng, Pharoah, Paul, Elias, Kevin M., Drapkin, Ronny, Churchman, Michael, Gourley, Charlie, DeFazio, Anna, Karlan, Beth, Brenton, James D., Weigelt, Britta, Anglesio, Michael S., Huntsman, David, Gayther, Simon, Konner, Jason, Modugno, Francesmary, Lawrenson, Kate, Goode, Ellen L., Papaemmanuil, Elli
Publicado 2022

Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

por Muranen, Taru A., Khan, Sofia, Fagerholm, Rainer, Aittomäki, Kristiina, Cunningham, Julie M., Dennis, Joe, Leslie, Goska, McGuffog, Lesley, Parsons, Michael T., Simard, Jacques, Slager, Susan, Soucy, Penny, Easton, Douglas F., Tischkowitz, Marc, Spurdle, Amanda B., Schmutzler, Rita K., Wappenschmidt, Barbara, Hahnen, Eric, Hooning, Maartje J., Singer, Christian F., Wagner, Gabriel, Thomassen, Mads, Pedersen, Inge Sokilde, Domchek, Susan M., Nathanson, Katherine L., Lazaro, Conxi, Rossing, Caroline Maria, Andrulis, Irene L., Teixeira, Manuel R., James, Paul, Garber, Judy, Weitzel, Jeffrey N., Jakubowska, Anna, Yannoukakos, Drakoulis, John, Esther M., Southey, Melissa C., Schmidt, Marjanka K., Antoniou, Antonis C., Chenevix-Trench, Georgia, Blomqvist, Carl, Nevanlinna, Heli
Publicado 2020

Inherited Variants in Regulatory T Cell Genes and Outcome of Ovarian Cancer

por Goode, Ellen L., DeRycke, Melissa, Kalli, Kimberly R., Oberg, Ann L., Cunningham, Julie M., Maurer, Matthew J., Fridley, Brooke L., Armasu, Sebastian M., Serie, Daniel J., Ramar, Priya, Goergen, Krista, Vierkant, Robert A., Rider, David N., Sicotte, Hugues, Wang, Chen, Winterhoff, Boris, Phelan, Catherine M., Schildkraut, Joellen M., Weber, Rachel P., Iversen, Ed, Berchuck, Andrew, Sutphen, Rebecca, Birrer, Michael J., Hampras, Shalaka, Preus, Leah, Gayther, Simon A., Ramus, Susan J., Wentzensen, Nicolas, Yang, Hannah P., Garcia-Closas, Montserrat, Song, Honglin, Tyrer, Jonathan, Pharoah, Paul P. D., Konecny, Gottfried, Sellers, Thomas A., Ness, Roberta B., Sucheston, Lara E., Odunsi, Kunle, Hartmann, Lynn C., Moysich, Kirsten B., Knutson, Keith L.
Publicado 2013

Germline whole exome sequencing and large-scale replication identifies FANCM as a likely high grade serous ovarian cancer susceptibility gene

por Dicks, Ed, Song, Honglin, Ramus, Susan J., Oudenhove, Elke Van, Tyrer, Jonathan P., Intermaggio, Maria P., Kar, Siddhartha, Harrington, Patricia, Bowtell, David D., Group, AOCS Study, Cicek, Mine S., Cunningham, Julie M., Fridley, Brooke L., Alsop, Jennifer, Jimenez-Linan, Mercedes, Piskorz, Anna, Goranova, Teodora, Kent, Emma, Siddiqui, Nadeem, Paul, James, Crawford, Robin, Poblete, Samantha, Lele, Shashi, Sucheston-Campbell, Lara, Moysich, Kirsten B., Sieh, Weiva, McGuire, Valerie, Lester, Jenny, Odunsi, Kunle, Whittemore, Alice S., Bogdanova, Natalia, Dürst, Matthias, Hillemanns, Peter, Karlan, Beth Y., Gentry-Maharaj, Aleksandra, Menon, Usha, Tischkowitz, Marc, Levine, Douglas, Brenton, James D., Dörk, Thilo, Goode, Ellen L., Gayther, Simon A., Pharoah, D.P. Paul
Publicado 2017

Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

por Lindström, Sara, Thompson, Deborah J., Paterson, Andrew D., Li, Jingmei, Gierach, Gretchen L., Scott, Christopher, Stone, Jennifer, Douglas, Julie A., dos-Santos-Silva, Isabel, Fernandez-Navarro, Pablo, Verghase, Jajini, Smith, Paula, Brown, Judith, Luben, Robert, Wareham, Nicholas J., Loos, Ruth J.F., Heit, John A., Pankratz, V. Shane, Norman, Aaron, Goode, Ellen L., Cunningham, Julie M., deAndrade, Mariza, Vierkant, Robert A., Czene, Kamila, Fasching, Peter A., Baglietto, Laura, Southey, Melissa C., Giles, Graham G., Shah, Kaanan P., Chan, Heang-Ping, Helvie, Mark A., Beck, Andrew H., Knoblauch, Nicholas W., Hazra, Aditi, Hunter, David J., Kraft, Peter, Pollan, Marina, Figueroa, Jonine D., Couch, Fergus J., Hopper, John L., Hall, Per, Easton, Douglas F., Boyd, Norman F., Vachon, Celine M., Tamimi, Rulla M.
Publicado 2014

Validating genetic risk associations for ovarian cancer through the International Ovarian Cancer Association Consortium

por Pearce, C L, Near, A M, Van Den Berg, D J, Ramus, S J, Gentry-Maharaj, A, Menon, U, Gayther, S A, Anderson, A R, Edlund, C K, Wu, A H, Chen, X, Beesley, J, Webb, P M, Holt, S K, Chen, C, Doherty, J A, Rossing, M A, Whittemore, A S, McGuire, V, DiCioccio, R A, Goodman, M T, Lurie, G, Carney, M E, Wilkens, L R, Ness, R B, Moysich, K B, Edwards, R, Jennison, E, Kjaer, S K, Hogdall, E, Hogdall, C K, Goode, E L, Sellers, T A, Vierkant, R A, Cunningham, J M, Schildkraut, J M, Berchuck, A, Moorman, P G, Iversen, E S, Cramer, D W, Terry, K L, Vitonis, A F, Titus-Ernstoff, L, Song, H, Pharoah, P D P, Spurdle, A B, Anton-Culver, H, Ziogas, A, Brewster, W, Galitovskiy, V, Chenevix-Trench, G
Publicado 2009

Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility “Hot-Spot”

por Johnatty, Sharon E., Beesley, Jonathan, Chen, Xiaoqing, Macgregor, Stuart, Duffy, David L., Spurdle, Amanda B., deFazio, Anna, Gava, Natalie, Webb, Penelope M., Rossing, Mary Anne, Doherty, Jennifer Anne, Goodman, Marc T., Lurie, Galina, Thompson, Pamela J., Wilkens, Lynne R., Ness, Roberta B., Moysich, Kirsten B., Chang-Claude, Jenny, Wang-Gohrke, Shan, Cramer, Daniel W., Terry, Kathryn L., Hankinson, Susan E., Tworoger, Shelley S., Garcia-Closas, Montserrat, Yang, Hannah, Lissowska, Jolanta, Chanock, Stephen J., Pharoah, Paul D., Song, Honglin, Whitemore, Alice S., Pearce, Celeste L., Stram, Daniel O., Wu, Anna H., Pike, Malcolm C., Gayther, Simon A., Ramus, Susan J., Menon, Usha, Gentry-Maharaj, Aleksandra, Anton-Culver, Hoda, Ziogas, Argyrios, Hogdall, Estrid, Kjaer, Susanne K., Hogdall, Claus, Berchuck, Andrew, Schildkraut, Joellen M., Iversen, Edwin S., Moorman, Patricia G., Phelan, Catherine M., Sellers, Thomas A., Cunningham, Julie M., Vierkant, Robert A., Rider, David N., Goode, Ellen L., Haviv, Izhak, Chenevix-Trench, Georgia
Publicado 2010

A targeted genetic association study of epithelial ovarian cancer susceptibility

por Earp, Madalene, Winham, Stacey J., Larson, Nicholas, Permuth, Jennifer B., Sicotte, Hugues, Chien, Jeremy, Anton-Culver, Hoda, Bandera, Elisa V., Berchuck, Andrew, Cook, Linda S., Cramer, Daniel, Doherty, Jennifer A., Goodman, Marc T., Levine, Douglas A., Monteiro, Alvaro N.A., Ness, Roberta B., Pearce, Celeste L., Rossing, Mary Anne, Tworoger, Shelley S., Wentzensen, Nicolas, Bisogna, Maria, Brinton, Louise, Brooks-Wilson, Angela, Carney, Michael E., Cunningham, Julie M., Edwards, Robert P., Fogarty, Zachary C., Iversen, Edwin S., Kraft, Peter, Larson, Melissa C., Le, Nhu D., Lin, Hui-Yi, Lissowska, Jolanta, Modugno, Francesmary, Moysich, Kirsten B., Olson, Sara H., Pike, Malcolm C., Poole, Elizabeth M., Rider, David N., Terry, Kathryn L., Thompson, Pamela J., van den Berg, David, Vierkant, Robert A., Vitonis, Allison F., Wilkens, Lynne R., Wu, Anna H., Yang, Hannah P., Ziogas, Argyrios, Phelan, Catherine M., Schildkraut, Joellen M., Chen, Yian Ann, Sellers, Thomas A., Fridley, Brooke L., Goode, Ellen L.
Publicado 2016

Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci

por Glubb, Dylan M., Johnatty, Sharon E., Quinn, Michael C.J., O’Mara, Tracy A., Tyrer, Jonathan P., Gao, Bo, Fasching, Peter A., Beckmann, Matthias W., Lambrechts, Diether, Vergote, Ignace, Velez Edwards, Digna R., Beeghly-Fadiel, Alicia, Benitez, Javier, Garcia, Maria J., Goodman, Marc T., Thompson, Pamela J., Dörk, Thilo, Dürst, Matthias, Modungo, Francesmary, Moysich, Kirsten, Heitz, Florian, du Bois, Andreas, Pfisterer, Jacobus, Hillemanns, Peter, Karlan, Beth Y., Lester, Jenny, Goode, Ellen L., Cunningham, Julie M., Winham, Stacey J., Larson, Melissa C., McCauley, Bryan M., Kjær, Susanne Krüger, Jensen, Allan, Schildkraut, Joellen M., Berchuck, Andrew, Cramer, Daniel W., Terry, Kathryn L., Salvesen, Helga B., Bjorge, Line, Webb, Penny M., Grant, Peter, Pejovic, Tanja, Moffitt, Melissa, Hogdall, Claus K., Hogdall, Estrid, Paul, James, Glasspool, Rosalind, Bernardini, Marcus, Tone, Alicia, Huntsman, David, Woo, Michelle, Group, AOCS, deFazio, Anna, Kennedy, Catherine J., Pharoah, Paul D.P., MacGregor, Stuart, Chenevix-Trench, Georgia
Publicado 2017

Polymorphisms in Stromal Genes and Susceptibility to Serous Epithelial Ovarian Cancer: A Report from the Ovarian Cancer Association Consortium

por Amankwah, Ernest K., Wang, Qinggang, Schildkraut, Joellen M., Tsai, Ya-Yu, Ramus, Susan J., Fridley, Brooke L., Beesley, Jonathan, Johnatty, Sharon E., Webb, Penelope M., Chenevix-Trench, Georgia, Dale, Laura C., Lambrechts, Diether, Amant, Frederic, Despierre, Evelyn, Vergote, Ignace, Gayther, Simon A., Gentry-Maharaj, Aleksandra, Menon, Usha, Chang-Claude, Jenny, Wang-Gohrke, Shan, Anton-Culver, Hoda, Ziogas, Argyrios, Dörk, Thilo, Dürst, Matthias, Antonenkova, Natalia, Bogdanova, Natalia, Brown, Robert, Flanagan, James M., Kaye, Stanley B., Paul, James, Bützow, Ralf, Nevanlinna, Heli, Campbell, Ian, Eccles, Diana M., Karlan, Beth Y., Gross, Jenny, Walsh, Christine, Pharoah, Paul D. P., Song, Honglin, Krüger Kjær, Susanne, Høgdall, Estrid, Høgdall, Claus, Lundvall, Lene, Nedergaard, Lotte, Kiemeney, Lambertus A. L. M., Massuger, Leon F. A. G., van Altena, Anne M., Vermeulen, Sita H. H. M., Le, Nhu D., Brooks-Wilson, Angela, Cook, Linda S., Phelan, Catherine M., Cunningham, Julie M., Vachon, Celine M., Vierkant, Robert A., Iversen, Edwin S., Berchuck, Andrew, Goode, Ellen L., Sellers, Thomas A., Kelemen, Linda E.
Publicado 2011

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32

por Conde, Lucia, Halperin, Eran, Akers, Nicholas K., Brown, Kevin M., Smedby, Karin E., Rothman, Nathaniel, Nieters, Alexandra, Slager, Susan L., Brooks-Wilson, Angela, Agana, Luz, Riby, Jacques, Liu, Jianjun, Adami, Hans-Olov, Darabi, Hatef, Hjalgrim, Henrik, Low, Hui-Qi, Humphreys, Keith, Melbye, Mads, Chang, Ellen T., Glimelius, Bengt, Cozen, Wendy, Davis, Scott, Hartge, Patricia, Morton, Lindsay M., Schenk, Maryjean, Wang, Sophia S., Armstrong, Bruce, Kricker, Anne, Milliken, Sam, Purdue, Mark P., Vajdic, Claire M., Boyle, Peter, Lan, Qing, Zahm, Shelia H., Zhang, Yawei, Zheng, Tongzhang, Becker, Nikolaus, Benavente, Yolanda, Boffetta, Paolo, Brennan, Paul, Butterbach, Katja, Cocco, Pierluigi, Foretova, Lenka, Maynadié, Marc, de Sanjosé, Silvia, Staines, Anthony, Spinelli, John J., Achenbach, Sara J., Call, Timothy G., Camp, Nicola J., Caporaso, Neil E., Cerhan, James R., Cunningham, Julie M., Goldin, Lynn R, Hanson, Curtis A., Kay, Neil E., Lanasa, Mark C., Leis, Jose F., Marti, Gerald E., Rabe, Kari G., Rassenti, Laura Z., Spector, Logan G., Strom, Sara S., Vachon, Celine M., Weinberg, J. Brice, Holly, Elizabeth A., Chanock, Stephen, Smith, Martyn T., Bracci, Paige M., Skibola, Christine F.
Publicado 2010

Genetic overlap between endometriosis and endometrial cancer: evidence from cross‐disease genetic correlation and GWAS meta‐analyses

por Painter, Jodie N., O'Mara, Tracy A., Morris, Andrew P., Cheng, Timothy H. T., Gorman, Maggie, Martin, Lynn, Hodson, Shirley, Jones, Angela, Martin, Nicholas G., Gordon, Scott, Henders, Anjali K., Attia, John, McEvoy, Mark, Holliday, Elizabeth G., Scott, Rodney J., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Rübner, Matthias, Hall, Per, Czene, Kamila, Dörk, Thilo, Dürst, Matthias, Hillemanns, Peter, Runnebaum, Ingo, Lambrechts, Diether, Amant, Frederic, Annibali, Daniela, Depreeuw, Jeroen, Vanderstichele, Adriaan, Goode, Ellen L., Cunningham, Julie M., Dowdy, Sean C., Winham, Stacey J., Trovik, Jone, Hoivik, Erling, Werner, Henrica M. J., Krakstad, Camilla, Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Tham, Emma, Mints, Miriam, Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Pharoah, Paul D. P., Dunning, Alison M., Dennis, Joe, Bolla, Manjeet K., Michailidou, Kyriaki, Wang, Qin, Tyrer, Jonathan P., Hopper, John L., Peto, Julian, Swerdlow, Anthony J., Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Chang‐Claude, Jenny, Couch, Fergus J., Giles, Graham G., Kristensen, Vessela N., Cox, Angela, Zondervan, Krina T., Nyholt, Dale R., MacGregor, Stuart, Montgomery, Grant W., Tomlinson, Ian, Easton, Douglas F., Thompson, Deborah J., Spurdle, Amanda B.
Publicado 2018

Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

por Carvajal-Carmona, Luis G., O’Mara, Tracy A., Painter, Jodie N., Lose, Felicity A., Dennis, Joe, Michailidou, Kyriaki, Tyrer, Jonathan P., Ahmed, Shahana, Ferguson, Kaltin, Healey, Catherine S., Pooley, Karen, Beesley, Jonathan, Cheng, Timothy, Jones, Angela, Howarth, Kimberley, Martin, Lynn, Gorman, Maggie, Hodgson, Shirley, Wentzensen, Nicholas, Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Renner, Stefan P., Dörk, Thilo, Hillemanns, Peter, Dürst, Matthias, Runnebaum, Ingo, Lambrechts, Diether, Coenegrachts, Lieve, Schrauwen, Stefanie, Amant, Frederic, Winterhoff, Boris, Dowdy, Sean C., Goode, Ellen L., Teoman, Attila, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Werner, Henrica M. J., Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Wersäll, Ofra, Mints, Miriam, Tham, Emma, Hall, Per, Czene, Kamila, Liu, Jianjun, Li, Jingmei, Hopper, John L., Southey, Melissa C., Ekici, Arif B., Ruebner, Matthias, Johnson, Nichola, Peto, Julian, Burwinkel, Barbara, Marme, Frederik, Brenner, Hermann, Dieffenbach, Aida K., Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Depreeuw, Jeroen, Moisse, Matthieu, Chang-Claude, Jenny, Rudolph, Anja, Couch, Fergus J., Olson, Janet E., Giles, Graham G., Bruinsma, Fiona, Cunningham, Julie M., Fridley, Brooke L., Børresen-Dale, Anne-Lise, Kristensen, Vessela N., Cox, Angela, Swerdlow, Anthony J., Orr, Nicholas, Bolla, Manjeet K., Wang, Qin, Weber, Rachel Palmieri, Chen, Zhihua, Shah, Mitul, Pharoah, Paul D. P., Dunning, Alison M., Tomlinson, Ian, Easton, Douglas F., Spurdle, Amanda B., Thompson, Deborah J.
Publicado 2014