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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1990 2
1991 1
1992 1
1993 2
1994 2
1995 3
1996 1
1997 1
1998 1
1999 2
2000 2
2001 2
2003 3
2004 5
2005 3
2006 2
2007 3
2008 5
2009 6
2010 7
2011 5
2012 3
2015 1
2016 1
2017 1
2021 1
2023 0

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60 results

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Page 1
Familial non-BRCA1/BRCA2-associated breast cancer.
Eccles DM, Pichert G. Eccles DM, et al. Among authors: pichert g. Lancet Oncol. 2005 Sep;6(9):705-11. doi: 10.1016/S1470-2045(05)70318-1. Lancet Oncol. 2005. PMID: 16129371 Review.
Cancer genetics in oncology practice.
Olopade OI, Pichert G. Olopade OI, et al. Among authors: pichert g. Ann Oncol. 2001 Jul;12(7):895-908. doi: 10.1023/a:1011176107455. Ann Oncol. 2001. PMID: 11521793 Free article. Review.
Genetic Testing for Rare Cancer: The Wider Issues.
Jacobs C, Pichert G. Jacobs C, et al. Among authors: pichert g. Recent Results Cancer Res. 2016;205:213-26. doi: 10.1007/978-3-319-29998-3_12. Recent Results Cancer Res. 2016. PMID: 27075356
Risk reducing mastectomy: outcomes in 10 European centres.
Evans DG, Baildam AD, Anderson E, Brain A, Shenton A, Vasen HF, Eccles D, Lucassen A, Pichert G, Hamed H, Moller P, Maehle L, Morrison PJ, Stoppat-Lyonnet D, Gregory H, Smyth E, Niederacher D, Nestle-Krämling C, Campbell J, Hopwood P, Lalloo F, Howell A. Evans DG, et al. Among authors: pichert g. J Med Genet. 2009 Apr;46(4):254-8. doi: 10.1136/jmg.2008.062232. Epub 2008 Nov 7. J Med Genet. 2009. PMID: 18996907
Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1.
Goudie DR, D'Alessandro M, Merriman B, Lee H, Szeverényi I, Avery S, O'Connor BD, Nelson SF, Coats SE, Stewart A, Christie L, Pichert G, Friedel J, Hayes I, Burrows N, Whittaker S, Gerdes AM, Broesby-Olsen S, Ferguson-Smith MA, Verma C, Lunny DP, Reversade B, Lane EB. Goudie DR, et al. Among authors: pichert g. Nat Genet. 2011 Feb 27;43(4):365-9. doi: 10.1038/ng.780. Nat Genet. 2011. PMID: 21358634
Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriers.
Finkelman BS, Rubinstein WS, Friedman S, Friebel TM, Dubitsky S, Schonberger NS, Shoretz R, Singer CF, Blum JL, Tung N, Olopade OI, Weitzel JN, Lynch HT, Snyder C, Garber JE, Schildkraut J, Daly MB, Isaacs C, Pichert G, Neuhausen SL, Couch FJ, van't Veer L, Eeles R, Bancroft E, Evans DG, Ganz PA, Tomlinson GE, Narod SA, Matloff E, Domchek S, Rebbeck TR. Finkelman BS, et al. Among authors: pichert g. J Clin Oncol. 2012 Apr 20;30(12):1321-8. doi: 10.1200/JCO.2011.37.8133. Epub 2012 Mar 19. J Clin Oncol. 2012. PMID: 22430266 Free PMC article.
60 results