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Nijmegen Breakage Syndrome mutations and risk of breast cancer.
Bogdanova N, Feshchenko S, Schürmann P, Waltes R, Wieland B, Hillemanns P, Rogov YI, Dammann O, Bremer M, Karstens JH, Sohn C, Varon R, Dörk T. Bogdanova N, et al. Among authors: schurmann p. Int J Cancer. 2008 Feb 15;122(4):802-6. doi: 10.1002/ijc.23168. Int J Cancer. 2008. PMID: 17957789 Free article.
NBS1 variant I171V and breast cancer risk.
Bogdanova N, Schürmann P, Waltes R, Feshchenko S, Zalutsky IV, Bremer M, Dörk T. Bogdanova N, et al. Among authors: schurmann p. Breast Cancer Res Treat. 2008 Nov;112(1):75-9. doi: 10.1007/s10549-007-9820-4. Epub 2007 Nov 30. Breast Cancer Res Treat. 2008. PMID: 18049891
Apoptosis gene polymorphisms and risk of prostate cancer: a hospital-based study of German patients treated with brachytherapy.
Meyer A, Coinac I, Bogdanova N, Dubrowinskaja N, Turmanov N, Haubold S, Schürmann P, Imkamp F, von Klot C, Merseburger AS, Machtens S, Bremer M, Hillemanns P, Kuczyk MA, Karstens JH, Serth J, Dörk T. Meyer A, et al. Among authors: schurmann p. Urol Oncol. 2013 Jan;31(1):74-81. doi: 10.1016/j.urolonc.2010.09.011. Epub 2011 Mar 10. Urol Oncol. 2013. PMID: 21396839
Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC).
Hein R, Maranian M, Hopper JL, Kapuscinski MK, Southey MC, Park DJ, Schmidt MK, Broeks A, Hogervorst FB, Bueno-de-Mesquita HB, Muir KR, Lophatananon A, Rattanamongkongul S, Puttawibul P, Fasching PA, Hein A, Ekici AB, Beckmann MW, Fletcher O, Johnson N, dos Santos Silva I, Peto J, Sawyer E, Tomlinson I, Kerin M, Miller N, Marmee F, Schneeweiss A, Sohn C, Burwinkel B, Guénel P, Cordina-Duverger E, Menegaux F, Truong T, Bojesen SE, Nordestgaard BG, Flyger H, Milne RL, Perez JI, Zamora MP, Benítez J, Anton-Culver H, Ziogas A, Bernstein L, Clarke CA, Brenner H, Müller H, Arndt V, Stegmaier C, Rahman N, Seal S, Turnbull C, Renwick A, Meindl A, Schott S, Bartram CR, Schmutzler RK, Brauch H, Hamann U, Ko YD; GENICA Network; Wang-Gohrke S, Dörk T, Schürmann P, Karstens JH, Hillemanns P, Nevanlinna H, Heikkinen T, Aittomäki K, Blomqvist C, Bogdanova NV, Zalutsky IV, Antonenkova NN, Bermisheva M, Prokovieva D, Farahtdinova A, Khusnutdinova E, Lindblom A, Margolin S, Mannermaa A, Kataja V, Kosma VM, Hartikainen J, Chen X, Beesley J; Kconfab Investigators; AOCS Group; Lambrechts D, Zhao H, Neven P, Wildiers H, Nickels S, Flesch-Janys D, Radice P, Peterlongo P, Manoukian S, Barile M, Co… See abstract for full author list ➔ Hein R, et al. Among authors: schurmann p. PLoS One. 2012;7(8):e42380. doi: 10.1371/journal.pone.0042380. Epub 2012 Aug 7. PLoS One. 2012. PMID: 22879957 Free PMC article.
CYP2B6*6 is associated with increased breast cancer risk.
Justenhoven C, Pentimalli D, Rabstein S, Harth V, Lotz A, Pesch B, Brüning T, Dörk T, Schürmann P, Bogdanova N, Park-Simon TW, Couch FJ, Olson JE, Fasching PA, Beckmann MW, Häberle L, Ekici A, Hall P, Czene K, Liu J, Li J, Baisch C, Hamann U, Ko YD, Brauch H. Justenhoven C, et al. Among authors: schurmann p. Int J Cancer. 2014 Jan 15;134(2):426-30. doi: 10.1002/ijc.28356. Epub 2013 Jul 30. Int J Cancer. 2014. PMID: 23824676 Free PMC article.
Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer.
Kohlhase S, Bogdanova NV, Schürmann P, Bermisheva M, Khusnutdinova E, Antonenkova N, Park-Simon TW, Hillemanns P, Meyer A, Christiansen H, Schindler D, Dörk T. Kohlhase S, et al. Among authors: schurmann p. PLoS One. 2014 Jan 21;9(1):e85334. doi: 10.1371/journal.pone.0085334. eCollection 2014. PLoS One. 2014. PMID: 24465539 Free PMC article.
Candidate gene variants of the immune system and sudden infant death syndrome.
Fard D, Läer K, Rothämel T, Schürmann P, Arnold M, Cohen M, Vennemann M, Pfeiffer H, Bajanowski T, Pfeufer A, Dörk T, Klintschar M. Fard D, et al. Among authors: schurmann p. Int J Legal Med. 2016 Jul;130(4):1025-1033. doi: 10.1007/s00414-016-1347-y. Epub 2016 Mar 14. Int J Legal Med. 2016. PMID: 26975745
184 results