Saam J - Search Results

1

Mutation profile differences in younger and older patients with advanced breast cancer using circulating tumor DNA (ctDNA).

Clifton K, Luo J, Tao Y, Saam J, Rich T, Roshal A, Frith A, Rigden C, Ademuyiwa F, Weilbaecher K, Hernandez-Aya L, Peterson LL, Bagegni N, Suresh R, Bose R, Opyrchal M, Wildes TM, Ma C. Clifton K, et al. Among authors: saam j. Breast Cancer Res Treat. 2021 Feb;185(3):639-646. doi: 10.1007/s10549-020-06019-0. Epub 2020 Nov 20. Breast Cancer Res Treat. 2021. PMID: 33219484

2

Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counseling.

Calip GS, Kidd J, Bernhisel R, Cox HC, Saam J, Rauscher GH, Lancaster JM, Hoskins KF. Calip GS, et al. Among authors: saam j. Breast Cancer Res Treat. 2021 Jan;185(1):195-204. doi: 10.1007/s10549-020-05922-w. Epub 2020 Sep 11. Breast Cancer Res Treat. 2021. PMID: 32918117 Free PMC article.

3

Identification of KRAS^G12C Mutations in Circulating Tumor DNA in Patients With Cancer.

Thein KZ, Biter AB, Banks KC, Duda AW, Saam J, Roszik J, Janku F, Skoulidis F, Heymach JV, Kopetz S, Meric-Bernstam F, Hong DS. Thein KZ, et al. Among authors: saam j. JCO Precis Oncol. 2022 Jul;6:e2100547. doi: 10.1200/PO.21.00547. JCO Precis Oncol. 2022. PMID: 35862868 Free PMC article.

4

Multigene assessment of genetic risk for women for two or more breast cancers.

Weitzel JN, Kidd J, Bernhisel R, Shehayeb S, Frankel P, Blazer KR, Turco D, Nehoray B, McGreevy K, Svirsky K, Brown K, Gardiner A, Daly M, Hughes E, Cummings S, Saam J, Slavin TP. Weitzel JN, et al. Among authors: saam j. Breast Cancer Res Treat. 2021 Aug;188(3):759-768. doi: 10.1007/s10549-021-06201-y. Epub 2021 Apr 7. Breast Cancer Res Treat. 2021. PMID: 33826040 Free PMC article.

5

Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer.

Fernandes PH, Saam J, Peterson J, Hughes E, Kaldate R, Cummings S, Theisen A, Chen S, Trost J, Roa BB. Fernandes PH, et al. Among authors: saam j. Cancer. 2014 Apr 1;120(7):963-7. doi: 10.1002/cncr.28504. Epub 2014 Jan 10. Cancer. 2014. PMID: 24415441 Free article.

6

Cell-Free Circulating Tumor DNA Improves Standard Genotyping of Non-Small-Cell Lung Cancer and Increases Detection of Targetable Alterations in a Selected Hispanic Cohort.

Zatarain-Barrón ZL, Cardona AF, Díaz-García D, Trejo Rosales R, Rojas L, Cruz-Rico G, Nagy R, Cabrera L, Vargas C, Saam J, Barrón F, Arrieta O. Zatarain-Barrón ZL, et al. Among authors: saam j. Oncology. 2021;99(8):539-546. doi: 10.1159/000514648. Epub 2021 Apr 26. Oncology. 2021. PMID: 33902046

7

Therapeutic Actionability of Circulating Cell-Free DNA Alterations in Carcinoma of Unknown Primary.

Kato S, Weipert C, Gumas S, Okamura R, Lee S, Sicklick JK, Saam J, Kurzrock R. Kato S, et al. Among authors: saam j. JCO Precis Oncol. 2021 Nov 3;5:PO.21.00011. doi: 10.1200/PO.21.00011. eCollection 2021. JCO Precis Oncol. 2021. PMID: 34778692 Free PMC article.

8

A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.

Buys SS, Sandbach JF, Gammon A, Patel G, Kidd J, Brown KL, Sharma L, Saam J, Lancaster J, Daly MB. Buys SS, et al. Among authors: saam j. Cancer. 2017 May 15;123(10):1721-1730. doi: 10.1002/cncr.30498. Epub 2017 Jan 13. Cancer. 2017. PMID: 28085182 Free article.

9

Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories.

Saam J, Arnell C, Theisen A, Moyes K, Marino I, Roundy KM, Wenstrup RJ. Saam J, et al. Oncology. 2015;89(5):288-93. doi: 10.1159/000437307. Epub 2015 Aug 28. Oncology. 2015. PMID: 26315041 Free article.

10

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes.

Eggington JM, Bowles KR, Moyes K, Manley S, Esterling L, Sizemore S, Rosenthal E, Theisen A, Saam J, Arnell C, Pruss D, Bennett J, Burbidge LA, Roa B, Wenstrup RJ. Eggington JM, et al. Among authors: saam j. Clin Genet. 2014 Sep;86(3):229-37. doi: 10.1111/cge.12315. Epub 2013 Dec 20. Clin Genet. 2014. PMID: 24304220

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