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

Year Number of Results
1998 1
1999 1
2000 1
2002 3
2003 1
2004 2
2005 5
2006 3
2007 1
2008 1
2009 1
2023 0
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19 results
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Page 1
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE. Easton DF, et al. Among authors: deffenbaugh am. Am J Hum Genet. 2007 Nov;81(5):873-83. doi: 10.1086/521032. Epub 2007 Sep 6. Am J Hum Genet. 2007. PMID: 17924331 Free PMC article.
Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.
Leegte B, van der Hout AH, Deffenbaugh AM, Bakker MK, Mulder IM, ten Berge A, Leenders EP, Wesseling J, de Hullu J, Hoogerbrugge N, Ligtenberg MJ, Ardern-Jones A, Bancroft E, Salmon A, Barwell J, Eeles R, Oosterwijk JC. Leegte B, et al. Among authors: deffenbaugh am. J Med Genet. 2005 Mar;42(3):e20. doi: 10.1136/jmg.2004.027243. J Med Genet. 2005. PMID: 15744030 Free PMC article. Review. No abstract available.
BRCA1/2 genetic testing in the community setting.
Chen WY, Garber JE, Higham S, Schneider KA, Davis KB, Deffenbaugh AM, Frank TS, Gelman RS, Li FP. Chen WY, et al. Among authors: deffenbaugh am. J Clin Oncol. 2002 Nov 15;20(22):4485-92. doi: 10.1200/JCO.2002.08.147. J Clin Oncol. 2002. PMID: 12431973
Characterization of common BRCA1 and BRCA2 variants.
Deffenbaugh AM, Frank TS, Hoffman M, Cannon-Albright L, Neuhausen SL. Deffenbaugh AM, et al. Genet Test. 2002 Summer;6(2):119-21. doi: 10.1089/10906570260199375. Genet Test. 2002. PMID: 12215251
Functional assays for classification of BRCA2 variants of uncertain significance.
Farrugia DJ, Agarwal MK, Pankratz VS, Deffenbaugh AM, Pruss D, Frye C, Wadum L, Johnson K, Mentlick J, Tavtigian SV, Goldgar DE, Couch FJ. Farrugia DJ, et al. Among authors: deffenbaugh am. Cancer Res. 2008 May 1;68(9):3523-31. doi: 10.1158/0008-5472.CAN-07-1587. Cancer Res. 2008. PMID: 18451181 Free PMC article.
Prediction of MLH1 and MSH2 mutations in Lynch syndrome.
Balmaña J, Stockwell DH, Steyerberg EW, Stoffel EM, Deffenbaugh AM, Reid JE, Ward B, Scholl T, Hendrickson B, Tazelaar J, Burbidge LA, Syngal S. Balmaña J, et al. Among authors: deffenbaugh am. JAMA. 2006 Sep 27;296(12):1469-78. doi: 10.1001/jama.296.12.1469. JAMA. 2006. PMID: 17003395
19 results