A Systematic Genetic Assessment of 1,433 Sequence Variants of Unknown Clinical Significance in the BRCA1 and BRCA2 Breast Cancer–Predisposition Genes von Easton, Douglas F., Deffenbaugh, Amie M., Pruss, Dmitry, Frye, Cynthia, Wenstrup, Richard J., Allen-Brady, Kristina, Tavtigian, Sean V., Monteiro, Alvaro N.A., Iversen, Edwin S., Couch, Fergus J., Goldgar, David E.

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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer von Hall, Michael J., Reid, Julia E., Burbidge, Lynn A., Pruss, Dmitry, Deffenbaugh, Amie M., Frye, Cynthia, Wenstrup, Richard J., Ward, Brian E., Scholl, Thomas A., Noll, Walter W.

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Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2 von Goldgar, David E., Easton, Douglas F., Deffenbaugh, Amie M., Monteiro, Alvaro N.A., Tavtigian, Sean V., Couch, Fergus J.

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Clinical Characteristics of Individuals With Germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 Individuals von Frank, T. S.

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Prediction of MLH1 and MSH2 Mutations in Lynch Syndrome von Balmaña, Judith, Stockwell, David H, Steyerberg, Ewout W, Stoffel, Elena M, Deffenbaugh, Amie M, Reid, Julia E, Ward, Brian, Scholl, Thomas, Hendrickson, Brant, Tazelaar, John, Burbidge, Lynn Anne, Syngal, Sapna

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Functional assays for classification of BRCA2 variants of uncertain significance von Farrugia, Daniel J, Agarwal, Mukesh K, Pankratz, Vernon S, Deffenbaugh, Amie M, Pruss, Dmitry, Frye, Cynthia, Wadum, Linda, Johnson, Kiley, Mentlick, Jennifer, Tavtigian, Sean V, Goldgar, David E, Couch, Fergus J

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Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance von CHENEVIX-TRENCH, Georgia, HEALEY, Sue, SCHOLL, Tom, BEKESSY, Anna, MARSH, Anna, LOVELOCK, Paul, WONG, Ming, TESORIERO, Andrea, RENARD, Helene, SOUTHEY, Melissa, HOPPER, John L, YANNOUKAKOS, Koulis, LAKBANI, Sunil, BROWN, Melissa, EASTON, Douglas, TAVTIGIAN, Sean V, GOLDGAR, David, SPURDLE, Amanda B, WARING, Paul, CUMMINGS, Margaret, BRINKWORTH, Ross, DEFFENBAUGH, Amie M, BURBIDGE, Lynn Anne, PRUSS, Dmitry, JUDKINS, Thad

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BRCA1/2 Genetic Testing in the Community Setting von CHEN, Wendy Y, GARBER, Judy E, HIGHAM, Suzanne, SCHNEIDER, Katherine A, DAVIS, Katie B, DEFFENBAUGH, Amie M, FRANK, Thomas S, GELMAN, Rebecca S, LI, Frederick P

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Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations von JUDKINS, Thaddeus, HENDRICKSON, Brant C, DEFFENBAUGH, Amie M, ELIASON, Kristilyn, LECLAIR, Benoit, NORTON, Michael J, WARD, Brian E, PRUSS, Dmitri, SCHOLL, Thomas

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Identification of germline 185delAG BRCA1 mutations in non‐Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado von Mullineaux, Lisa G., Castellano, Teresa M., Shaw, Jeffrey, Axell, Lisen, Wood, Marie E., Diab, Sami, Klein, Catherine, Sitarik, Mark, Deffenbaugh, Amie M., Graw, Sharon L.

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Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BR... von Judkins, T, Hendrickson, B C, Deffenbaugh, A M, Scholl, T

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A Multi-Exonic BRCA1 Deletion Identified in Multiple Families through Single Nucleotide Polymorphism Haplotype Pair Analysis and Gene Amplification with Widely Dispersed Primer Set... von Ward, Benjamin D., Hendrickson, Brant C., Judkins, Thaddeus, Deffenbaugh, Amie M., Leclair, Benoît, Ward, Brian E., Scholl, Thomas

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Clinical characteristics of individuals with germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 individuals von FRANK, Thomas S, DEFFENBAUGH, Amie M, CRITCHFIELD, Gregory C, REID, Julia E, HULICK, Mark, WARD, Brian E, LINGENFELTER, Beth, GUMPPER, Kathi L, SCHOLL, Thomas, TAVTIGIAN, Sean V, PRUSS, Dmitry R

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Hereditary susceptibility to breast cancer : Significance of age of onset in family history and contribution of BRCA1 and BRCA2 von FRANK, T. S, DEFFENBAUGH, A. M, HULICK, M, GUMPPER, K

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Frequency of germline and somatic BRCA1 mutations in ovarian cancer von BERCHUCK, A, HERON, K.-A, FRANK, T. S, CARNEY, M. E, LANCASTER, J. M, FRASER, E. G, VINSON, V. L, DEFFENBAUGH, A. M, MIRON, A, MARKS, J. R, FUTREAL, P. A

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Characterization of common BRCA1 and BRCA2 variants von Deffenbaugh, Amie M, Frank, Thomas S, Hoffman, Michael, Cannon-Albright, Lisa, Neuhausen, Susan L

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Hereditary susceptibility to breast cancer: Significance of age of onset in family history and contribution of BRCA1 and BRCA2 von Frank, Thomas S., Deffenbaugh, Amie M., Hulick, Mark, Gumpper, Kathryn

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Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia von Offit, Kenneth, Levran, Orna, Mullaney, Brian, Mah, Katherine, Nafa, Khedoudja, Batish, Sat Dev, Diotti, Raffaella, Schneider, Hildegard, Deffenbaugh, Amie, Scholl, Thomas, Proud, Virginia K., Robson, Mark, Norton, Larry, Ellis, Nathan, Hanenberg, Helmut, Auerbach, Arleen D.

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Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia von Wagner, John E., Tolar, Jakub, Levran, Orna, Scholl, Thomas, Deffenbaugh, Amie, Satagopan, Jaya, Ben-Porat, Leah, Mah, Katherine, Batish, Sat Dev, Kutler, David I., MacMillan, Margaret L., Hanenberg, Helmut, Auerbach, Arleen D.

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BRCA2 mutations and use thereof von Scholl, Thomas M, Ward, Brian E, Deffenbaugh, Amie, Burbidge, Lynn Anne, Noll, Walter W

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