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2005 1
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2010 1
2014 1
2015 1
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2019 1
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Page 1
Clinical implications of conflicting variant interpretations in the cancer genetics clinic.
Zukin E, Culver JO, Liu Y, Yang Y, Ricker CN, Hodan R, Sturgeon D, Kingham K, Chun NM, Rowe-Teeter C, Singh K, Zell JA, Ladabaum U, McDonnell KJ, Ford JM, Parmigiani G, Braun D, Kurian AW, Gruber SB, Idos GE. Zukin E, et al. Among authors: chun nm. Genet Med. 2023 Jul;25(7):100837. doi: 10.1016/j.gim.2023.100837. Epub 2023 Apr 11. Genet Med. 2023. PMID: 37057674
Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients.
Culver JO, Ricker CN, Bonner J, Kidd J, Sturgeon D, Hodan R, Kingham K, Lowstuter K, Chun NM, Lebensohn AP, Rowe-Teeter C, Levonian P, Partynski K, Lara-Otero K, Hong C, Morales Pichardo J, Mills MA, Brown K, Lerman C, Ladabaum U, McDonnell KJ, Ford JM, Gruber SB, Kurian AW, Idos GE. Culver JO, et al. Among authors: chun nm. Cancer. 2021 Apr 15;127(8):1275-1285. doi: 10.1002/cncr.33357. Epub 2020 Dec 15. Cancer. 2021. PMID: 33320347 Free PMC article.
Patient communication of cancer genetic test results in a diverse population.
Ricker CN, Koff RB, Qu C, Culver J, Sturgeon D, Kingham KE, Lowstuter K, Chun NM, Rowe-Teeter C, Lebensohn A, Levonian P, Partynski K, Lara-Otero K, Hong C, Petrovchich IM, Mills MA, Hartman AR, Allen B, Ladabaum U, McDonnell K, Ford JM, Gruber SB, Kurian AW, Idos GE. Ricker CN, et al. Among authors: chun nm. Transl Behav Med. 2018 Jan 29;8(1):85-94. doi: 10.1093/tbm/ibx010. Transl Behav Med. 2018. PMID: 29385580 Free PMC article.
Parent decision-making around the genetic testing of children for germline TP53 mutations.
Alderfer MA, Zelley K, Lindell RB, Novokmet A, Mai PL, Garber JE, Nathan D, Scollon S, Chun NM, Patenaude AF, Ford JM, Plon SE, Schiffman JD, Diller LR, Savage SA, Malkin D, Ford CA, Nichols KE. Alderfer MA, et al. Among authors: chun nm. Cancer. 2015 Jan 15;121(2):286-93. doi: 10.1002/cncr.29027. Epub 2014 Sep 15. Cancer. 2015. PMID: 25223899 Free article.
Performance of BRCA1/2 mutation prediction models in Asian Americans.
Kurian AW, Gong GD, Chun NM, Mills MA, Staton AD, Kingham KE, Crawford BB, Lee R, Chan S, Donlon SS, Ridge Y, Panabaker K, West DW, Whittemore AS, Ford JM. Kurian AW, et al. Among authors: chun nm. J Clin Oncol. 2008 Oct 10;26(29):4752-8. doi: 10.1200/JCO.2008.16.8310. Epub 2008 Sep 8. J Clin Oncol. 2008. PMID: 18779604 Free PMC article.
Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk.
Idos GE, Kurian AW, Ricker C, Sturgeon D, Culver JO, Kingham KE, Koff R, Chun NM, Rowe-Teeter C, Lebensohn AP, Levonian P, Lowstuter K, Partynski K, Hong C, Mills MA, Petrovchich I, Ma CS, Hartman AR, Allen B, Wenstrup RJ, Lancaster JM, Brown K, Kidd J, Evans B, Mukherjee B, McDonnell KJ, Ladabaum U, Ford JM, Gruber SB. Idos GE, et al. Among authors: chun nm. JCO Precis Oncol. 2019 Mar 28;3:PO.18.00217. doi: 10.1200/PO.18.00217. eCollection 2019 Mar. JCO Precis Oncol. 2019. PMID: 34322651 Free PMC article.
Ductal lavage of fluid-yielding and non-fluid-yielding ducts in BRCA1 and BRCA2 mutation carriers and other women at high inherited breast cancer risk.
Kurian AW, Mills MA, Jaffee M, Sigal BM, Chun NM, Kingham KE, Collins LC, Nowels KW, Plevritis SK, Garber JE, Ford JM, Hartman AR. Kurian AW, et al. Among authors: chun nm. Cancer Epidemiol Biomarkers Prev. 2005 May;14(5):1082-9. doi: 10.1158/1055-9965.EPI-04-0776. Cancer Epidemiol Biomarkers Prev. 2005. PMID: 15894656