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

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

S. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale, A. Lee, M. Thomassen, A. Gerdes, T. Kruse, U. Jensen, A. Skytte, M. Caligo, A. Liljegren, A. Lindblom, H. Olsson, U. Kristoffersson, M. Stenmark-Askmalm, B. Melin, S. Domchek, K. Nathanson, T. Rebbeck, A. Jakubowska, J. Lubinski, K. Jaworska, K. Durda, E. Złowocka, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, A. Toloczko-Grabarek, A. Osorio, J. Benitez, M. Duran, M. Tejada, U. Hamann, M. Rookus, van Leeuwen, Flora E, C. Aalfs, Meijers-Heijboer, Hanne E J, van Asperen, Christi J, van Roozendaal, K E P, N. Hoogerbrugge, J. Collée, M. Kriege, van der Luijt, Rob B, S. Peock, D. Frost, S. Ellis, R. Platte, E. Fineberg, D. Evans, F. Lalloo, C. Jacobs, R. Eeles, J. Adlard, R. Davidson, D. Eccles, T. Cole, J. Cook, J. Paterson, F. Douglas, C. Brewer, S. Hodgson, P. Morrison, L. Walker, M. Porteous, M. Kennedy, H. Pathak, A. Godwin, D. Stoppa-Lyonnet, V. Caux-Moncoutier, A. Pauw, M. Gauthier-Villars, S. Mazoyer, M. Léoné, A. Calender, C. Lasset, V. Bonadona, A. Hardouin, P. Berthet, Y. Bignon, N. Uhrhammer, L. Faivre, C. Loustalot, S. Buys, M. Daly, A. Miron, M. Terry, W. Chung, E. John, M. Southey, D. Goldgar, C. Singer, M. Tea, G. Pfeiler, A. Fink-Retter, Hansen, Thomas V O, B. Ejlertsen, O. Johannsson, K. Offit, T. Kirchhoff, M. Gaudet, J. Vijai, M. Robson, M. Piedmonte, K. Phillips, L. van Le, J. Hoffman, A. Ewart Toland, M. Montagna, S. Tognazzo, E. Imyanitov, C. Issacs, R. Janavicius, C. Lazaro, I. Blanco, E. Tornero, M. Navarro, K. Moysich, B. Karlan, J. Gross, E. Olah, T. Vaszko, S. Teo, P. Ganz, M. Beattie, C. Dorfling, van Rensburg, Elizabeth J, O. Diez, A. Kwong, R. Schmutzler, B. Wappenschmidt, C. Engel, A. Meindl, N. Ditsch, N. Arnold, S. Heidemann, D. Niederacher, S. Preisler-Adams, D. Gadzicki, R. Varon-Mateeva, H. Deissler, A. Gehrig, C. Sutter, K. Kast, B. Fiebig, D. Schäfer, T. Caldes, de la Hoya, Miguel, H. Nevanlinna, K. Aittomäki, M. Plante, A. Spurdle, S. Neuhausen, Y. Ding, X. Wang, N. Lindor, Z. Fredericksen, V. Pankratz, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, B. Bonanni, L. Bernard, R. Dolcetti, L. Papi, L. Ottini, P. Radice, M. Greene, P. Mai, I. Andrulis, G. Glendon, H. Ozcelik, Pharoah, Paul D P, S. Gayther, J. Simard, D. Easton, F. Couch, and G. Chenevix-Trench. Human mutation, 33 (4): 690–702 (2012)

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.

Dieter Niederacher

Volker Niederacher

Dieter Deußen

Letalitätsanalyse pädiatrischer Schädel-HirnverletzungenD. Deußen. Uni Frankfurt Main, (2006)

Hans Dieter Burkert

Heiliger Geist im Neuen Testament unter besonderer Berücksichtigung des Corpus Paulinum: eine kategoriegeleitete UntersuchungH. Burkert. Uni Bochum, (2009)

Dieter Pohlmann

Other publications of authors with the same name

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)Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2A. Mulligan, F. Couch, D. Barrowdale, S. Domchek, D. Eccles, H. Nevanlinna, S. Ramus, M. Robson, M. Sherman, A. Spurdle and 172 other author(s). Breast cancer research : BCR, 13 (6): R110 (2011)RAD51 135G--C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studiesA. Antoniou, O. Sinilnikova, J. Simard, M. Léoné, M. Dumont, S. Neuhausen, J. Struewing, D. Stoppa-Lyonnet, L. Barjhoux, D. Hughes and 69 other author(s). American journal of human genetics, 81 (6): 1186–1200 (2007)Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersS. Ramus, A. Antoniou, K. Kuchenbaecker, P. Soucy, J. Beesley, X. Chen, L. McGuffog, O. Sinilnikova, S. Healey, D. Barrowdale and 176 other author(s). Human mutation, 33 (4): 690–702 (2012)Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk predictionA. Antoniou, J. Beesley, L. McGuffog, O. Sinilnikova, S. Healey, S. Neuhausen, Y. Ding, T. Rebbeck, J. Weitzel, H. Lynch and 168 other author(s). Cancer research, 70 (23): 9742–9754 (2010)Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical managementS. Heidemann, C. Fischer, C. Engel, B. Fischer, L. Harder, B. Schlegelberger, D. Niederacher, T. Goecke, S. Doelken, N. Dikow and 4 other author(s). Breast cancer research and treatment, 134 (3): 1229–1239 (2012)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersD. Cox, J. Simard, D. Sinnett, Y. Hamdi, P. Soucy, M. Ouimet, L. Barjhoux, C. Verny-Pierre, L. McGuffog, S. Healey and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersA. Antoniou, C. Kartsonaki, O. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel and 169 other author(s). Human molecular genetics, 20 (16): 3304–3321 (2011)Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activityS. Tchatchou, A. Riedel, S. Lyer, J. Schmutzhard, O. Strobel-Freidekind, S. Gronert-Sum, C. Mietag, M. D'Amato, B. Schlehe, K. Hemminki and 17 other author(s). Human mutation, 31 (1): 60–66 (2010)Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer riskR. Yang, B. Chen, K. Hemminki, B. Wappenschmidt, C. Engel, C. Sutter, N. Ditsch, Weber, Bernhard H F, D. Niederacher, N. Arnold and 4 other author(s). Breast cancer research and treatment, 118 (2): 407–413 (2009)

BibSonomy

Disambiguation of "Niederacher, Dieter"

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

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

Please choose a person to relate this publication to

Dieter Niederacher

Volker Niederacher

Dieter Deußen

Hans Dieter Burkert

Dieter Pohlmann

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Niederacher, Dieter"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

Please choose a person to relate this publication to

Dieter Niederacher

Volker Niederacher

Dieter Deußen

Hans Dieter Burkert

Dieter Pohlmann

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

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers