Author of the publication

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

F. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis, M. Gaudet, E. Dicks, M. Kosel, S. Healey, O. Sinilnikova, A. Lee, F. Bacot, D. Vincent, Hogervorst, Frans B L, S. Peock, D. Stoppa-Lyonnet, A. Jakubowska, P. Radice, R. Schmutzler, S. Domchek, M. Piedmonte, C. Singer, E. Friedman, M. Thomassen, Hansen, Thomas V O, S. Neuhausen, C. Szabo, I. Blanco, M. Greene, B. Karlan, J. Garber, C. Phelan, J. Weitzel, M. Montagna, E. Olah, I. Andrulis, A. Godwin, D. Yannoukakos, D. Goldgar, T. Caldes, H. Nevanlinna, A. Osorio, M. Terry, M. Daly, van Rensburg, Elizabeth J, U. Hamann, S. Ramus, A. Toland, M. Caligo, O. Olopade, N. Tung, K. Claes, M. Beattie, M. Southey, E. Imyanitov, M. Tischkowitz, R. Janavicius, E. John, A. Kwong, O. Diez, J. Balmaña, R. Barkardottir, B. Arun, G. Rennert, S. Teo, P. Ganz, I. Campbell, van der Hout, Annemarie H, van Deurzen, Carolien H M, C. Seynaeve, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Gille, Johannes J P, Ausems, Margreet G E M, M. Blok, Ligtenberg, Marjolijn J L, M. Rookus, P. Devilee, S. Verhoef, van Os, Theo A M, J. Wijnen, D. Frost, S. Ellis, E. Fineberg, R. Platte, D. Evans, L. Izatt, R. Eeles, J. Adlard, D. Eccles, J. Cook, C. Brewer, F. Douglas, S. Hodgson, P. Morrison, L. Side, A. Donaldson, C. Houghton, M. Rogers, H. Dorkins, J. Eason, H. Gregory, E. McCann, A. Murray, A. Calender, A. Hardouin, P. Berthet, C. Delnatte, C. Nogues, C. Lasset, C. Houdayer, D. Leroux, E. Rouleau, F. Prieur, F. Damiola, H. Sobol, I. Coupier, L. Venat-Bouvet, L. Castera, M. Gauthier-Villars, M. Léoné, P. Pujol, S. Mazoyer, Y. Bignon, E. Złowocka-Perłowska, J. Gronwald, J. Lubinski, K. Durda, K. Jaworska, T. Huzarski, A. Spurdle, A. Viel, B. Peissel, B. Bonanni, G. Melloni, L. Ottini, L. Papi, L. Varesco, M. Tibiletti, P. Peterlongo, S. Volorio, S. Manoukian, V. Pensotti, N. Arnold, C. Engel, H. Deissler, D. Gadzicki, A. Gehrig, K. Kast, K. Rhiem, A. Meindl, D. Niederacher, N. Ditsch, H. Plendl, S. Preisler-Adams, S. Engert, C. Sutter, R. Varon-Mateeva, B. Wappenschmidt, Weber, Bernhard H F, B. Arver, M. Stenmark-Askmalm, N. Loman, R. Rosenquist, Z. Einbeigi, K. Nathanson, T. Rebbeck, S. Blank, D. Cohn, G. Rodriguez, L. Small, M. Friedlander, V. Bae-Jump, A. Fink-Retter, C. Rappaport, D. Gschwantler-Kaulich, G. Pfeiler, M. Tea, N. Lindor, B. Kaufman, S. Shimon Paluch, Y. Laitman, A. Skytte, A. Gerdes, I. Pedersen, S. Moeller, T. Kruse, U. Jensen, J. Vijai, K. Sarrel, M. Robson, N. Kauff, A. Mulligan, G. Glendon, H. Ozcelik, B. Ejlertsen, F. Nielsen, L. Jønson, M. Andersen, Y. Ding, L. Steele, L. Foretova, A. Teulé, C. Lazaro, J. Brunet, M. Pujana, P. Mai, J. Loud, C. Walsh, J. Lester, S. Orsulic, S. Narod, J. Herzog, S. Sand, S. Tognazzo, S. Agata, T. Vaszko, J. Weaver, A. Stavropoulou, S. Buys, A. Romero, de la Hoya, Miguel, K. Aittomäki, T. Muranen, M. Duran, W. Chung, A. Lasa, C. Dorfling, A. Miron, J. Benitez, L. Senter, D. Huo, S. Chan, A. Sokolenko, J. Chiquette, L. Tihomirova, T. Friebel, B. Agnarsson, K. Lu, F. Lejbkowicz, P. James, P. Hall, A. Dunning, D. Tessier, J. Cunningham, S. Slager, C. Wang, S. Hart, K. Stevens, J. Simard, T. Pastinen, V. Pankratz, K. Offit, D. Easton, G. Chenevix-Trench, and A. Antoniou. PLoS genetics, 9 (3): e1003212 (2013)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

Daniel Vincent Grimm

Vincent Herrmann

Vincent Fochtman

Vincent Feyen

Vincent Wroblewsky

Other publications of authors with the same name

RMTP2: Validating the Interval Timed Extension for SDL with an Industrial-Size Multicast Protocol.B. Parreaux, D. Vincent, and G. Babonneau. SDL Forum, volume 2708 of Lecture Notes in Computer Science, page 218-233. Springer, (2003)Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer riskF. Couch, X. Wang, L. McGuffog, A. Lee, C. Olswold, K. Kuchenbaecker, P. Soucy, Z. Fredericksen, D. Barrowdale, J. Dennis and 252 other author(s). PLoS genetics, 9 (3): e1003212 (2013)A Formal Approach for Software Maintenance.U. Waqar, F. Khendek, and D. Vincent. ICSM, page 608-617. IEEE Computer Society, (2002)Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancersJ. French, M. Ghoussaini, S. Edwards, K. Meyer, K. Michailidou, S. Ahmed, S. Khan, M. Maranian, M. O'Reilly, K. Hillman and 201 other author(s). American journal of human genetics, 92 (4): 489–503 (2013)Work in progress - A survey of popular game creation platforms used for computing education.K. Doss, V. Juarez, D. Vincent, P. Doerschuk, and J. Liu. FIE, page 1. IEEE Computer Society, (2011)Enriching SDL Specifications with MSCs.F. Khendek, and D. Vincent. SAM, page 305-319. VERIMAG, IRISA, SDL Forum, (2000)Introducing programming concepts through video game creation.P. Doerschuk, V. Juarez, J. Liu, D. Vincent, K. Doss, and J. Mann. FIE, page 523-529. IEEE Computer Society, (2013)From MSC and UML to SDL.S. Bourduas, F. Khendek, and D. Vincent. COMPSAC, page 153-158. IEEE Computer Society, (2002)Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancerS. Bojesen, K. Pooley, S. Johnatty, J. Beesley, K. Michailidou, J. Tyrer, S. Edwards, H. Pickett, H. Shen, C. Smart and 427 other author(s). Nature genetics, 45 (4): 371-84, 384e1-2 (2013)Classification of metal transfer mode using neural networks.D. Vincent, J. McCardle, and R. Stroud. ICNN, page 522-525. IEEE, (1995)

BibSonomy

Disambiguation of "Vincent, Daniel"

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Daniel Vincent Grimm

Vincent Herrmann

Vincent Fochtman

Vincent Feyen

Vincent Wroblewsky

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Vincent, Daniel"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

Please choose a person to relate this publication to

Daniel Vincent Grimm

Vincent Herrmann

Vincent Fochtman

Vincent Feyen

Vincent Wroblewsky

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
community post
history of this post
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk