Robinson LS - Search Results

1

Use of panel tests in place of single gene tests in the cancer genetics clinic.

Yorczyk A, Robinson LS, Ross TS. Yorczyk A, et al. Among authors: robinson ls. Clin Genet. 2015 Sep;88(3):278-82. doi: 10.1111/cge.12488. Epub 2014 Oct 16. Clin Genet. 2015. PMID: 25318351

2

An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.

Pritzlaff M, Yorczyk A, Robinson LS, Pirzadeh-Miller S, Lin T, Euhus D, Ross TS. Pritzlaff M, et al. Among authors: robinson ls. J Genet Couns. 2014 Dec;23(6):1034-44. doi: 10.1007/s10897-014-9732-5. Epub 2014 Jun 12. J Genet Couns. 2014. PMID: 24916850 Free PMC article.

3

Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Foley SB, Rios JJ, Mgbemena VE, Robinson LS, Hampel HL, Toland AE, Durham L, Ross TS. Foley SB, et al. Among authors: robinson ls. EBioMedicine. 2015 Jan;2(1):74-81. doi: 10.1016/j.ebiom.2014.12.003. EBioMedicine. 2015. PMID: 26023681 Free PMC article.

4

Prediction of Cancer Prevention: From Mammogram Screening to Identification of BRCA1/2 Mutation Carriers in Underserved Populations.

Robinson LS, Hendrix A, Xie XJ, Yan J, Pirzadeh-Miller S, Pritzlaff M, Read P, Pass S, Euhus D, Ross TS. Robinson LS, et al. EBioMedicine. 2015 Oct 21;2(11):1827-33. doi: 10.1016/j.ebiom.2015.10.022. eCollection 2015 Nov. EBioMedicine. 2015. PMID: 26870808 Free PMC article.

5

Genetic Counseling Assistants: an Integral Piece of the Evolving Genetic Counseling Service Delivery Model.

Pirzadeh-Miller S, Robinson LS, Read P, Ross TS. Pirzadeh-Miller S, et al. Among authors: robinson ls. J Genet Couns. 2017 Aug;26(4):716-727. doi: 10.1007/s10897-016-0039-6. Epub 2016 Nov 10. J Genet Couns. 2017. PMID: 27832509

6

Genetic predisposition syndromes and their management.

Euhus DM, Robinson L. Euhus DM, et al. Surg Clin North Am. 2013 Apr;93(2):341-62. doi: 10.1016/j.suc.2013.01.005. Epub 2013 Feb 11. Surg Clin North Am. 2013. PMID: 23464690 Review.

7

Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO.

Euhus DM, Smith KC, Robinson L, Stucky A, Olopade OI, Cummings S, Garber JE, Chittenden A, Mills GB, Rieger P, Esserman L, Crawford B, Hughes KS, Roche CA, Ganz PA, Seldon J, Fabian CJ, Klemp J, Tomlinson G. Euhus DM, et al. J Natl Cancer Inst. 2002 Jun 5;94(11):844-51. doi: 10.1093/jnci/94.11.844. J Natl Cancer Inst. 2002. PMID: 12048272

8

Screening for Lynch Syndrome by Immunohistochemistry of Mismatch Repair Proteins: Significance of Indeterminate Result and Correlation With Mutational Studies.

Sarode VR, Robinson L. Sarode VR, et al. Arch Pathol Lab Med. 2019 Oct;143(10):1225-1233. doi: 10.5858/arpa.2018-0201-OA. Epub 2019 Mar 27. Arch Pathol Lab Med. 2019. PMID: 30917047 Free article.

9

The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndrome.

Lewis CM, Bu D, Sarode V, Robinson L, Wilson KS, Viscusi RK, Eng C, Euhus DM. Lewis CM, et al. Breast Cancer Res Treat. 2012 Dec;136(3):911-8. doi: 10.1007/s10549-012-2322-z. Epub 2012 Nov 7. Breast Cancer Res Treat. 2012. PMID: 23132533

10

Optimizing efficiency and skill utilization: Analysis of genetic counselors' attitudes regarding delegation in a clinical setting.

Read P, Yashar BM, Robinson L, Marvin M. Read P, et al. J Genet Couns. 2020 Feb;29(1):67-77. doi: 10.1002/jgc4.1181. Epub 2019 Nov 13. J Genet Couns. 2020. PMID: 31721370 Free article.

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