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Items: 15

1.

Consent process for US-based family reference DNA samples.

Katsanis SH, Snyder L, Arnholt K, Mundorff AZ.

Forensic Sci Int Genet. 2018 Jan;32:71-79. doi: 10.1016/j.fsigen.2017.10.011. Epub 2017 Oct 29.

PMID:
29107870
2.

Perceptions of Personalized Medicine in an Academic Health System: Educational Findings.

Vorderstrasse A, Katsanis SH, Minear MA, Yang N, Rakhra-Burris T, Reeves JW, Cook-Deegan R, Ginsburg GS, Ann Simmons L.

J Contemp Med Educ. 2015;3(1):14-19.

3.

Perspectives on genetic and genomic technologies in an academic medical center: the duke experience.

Katsanis SH, Minear MA, Vorderstrasse A, Yang N, Reeves JW, Rakhra-Burris T, Cook-Deegan R, Ginsburg GS, Simmons LA.

J Pers Med. 2015 Apr 3;5(2):67-82. doi: 10.3390/jpm5020067.

4.

Preliminary perspectives on DNA collection in anti-human trafficking efforts.

Katsanis SH, Kim J, Minear MA, Chandrasekharan S, Wagner JK.

Recent Adv DNA Gene Seq. 2014;8(2):78-90.

PMID:
25687341
5.

Educating future providers of personalized medicine.

Katsanis SH, Dungan JR, Gilliss CL, Ginsburg GA.

N C Med J. 2013 Nov-Dec;74(6):491-2. No abstract available.

6.

Brave New World of human-rights DNA collection.

Kim J, Katsanis SH.

Trends Genet. 2013 Jun;29(6):329-32. doi: 10.1016/j.tig.2013.04.002. Review.

PMID:
23706944
7.

Molecular genetic testing and the future of clinical genomics.

Katsanis SH, Katsanis N.

Nat Rev Genet. 2013 Jun;14(6):415-26. doi: 10.1038/nrg3493. Review.

8.

Personal DNA testing in college classrooms: perspectives of students and professors.

Daley LA, Wagner JK, Himmel TL, McPartland KA, Katsanis SH, Shriver MD, Royal CD.

Genet Test Mol Biomarkers. 2013 Jun;17(6):446-52. doi: 10.1089/gtmb.2012.0404. Epub 2013 Mar 28.

PMID:
23537214
9.

Treacher Collins Syndrome.

Katsanis SH, Jabs EW.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2004 Jul 20 [updated 2012 Aug 30].

10.

Characterization of the standard and recommended CODIS markers.

Katsanis SH, Wagner JK.

J Forensic Sci. 2013 Jan;58 Suppl 1:S169-72. doi: 10.1111/j.1556-4029.2012.02253.x. Epub 2012 Aug 24.

PMID:
22925064
11.

Policy implications for familial searching.

Kim J, Mammo D, Siegel MB, Katsanis SH.

Investig Genet. 2011 Nov 1;2:22. doi: 10.1186/2041-2223-2-22.

12.

A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exon.

Macaya D, Katsanis SH, Hefferon TW, Audlin S, Mendelsohn NJ, Roggenbuck J, Cutting GR.

Am J Med Genet A. 2009 Aug;149A(8):1624-7. doi: 10.1002/ajmg.a.32834.

PMID:
19572402
13.

Carrier screening for cystic fibrosis in US genetic testing laboratories: a survey of laboratory directors.

Kaufman DJ, Katsanis SH, Javitt GH, Murphy JA, Scott JA, Hudson KL.

Clin Genet. 2008 Oct;74(4):367-73. doi: 10.1111/j.1399-0004.2008.01070.x. Epub 2008 Aug 12.

PMID:
18700896
14.

Public health. A case study of personalized medicine.

Katsanis SH, Javitt G, Hudson K.

Science. 2008 Apr 4;320(5872):53-4. doi: 10.1126/science.1156604. No abstract available. Erratum in: Science.2008 Apr 18;320(5874):316.

PMID:
18388277
15.

Oversight of US genetic testing laboratories.

Hudson KL, Murphy JA, Kaufman DJ, Javitt GH, Katsanis SH, Scott J.

Nat Biotechnol. 2006 Sep;24(9):1083-90. No abstract available.

PMID:
16964214

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