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Results: 1 to 20 of 26

Cited In for PubMed (Select 20407217)

1.

Interest in genomic SNP testing for prostate cancer risk: a pilot survey.

Hall MJ, Ruth KJ, Chen DY, Gross LM, Giri VN.

Hered Cancer Clin Pract. 2015 Apr 8;13(1):11. doi: 10.1186/s13053-015-0032-3. eCollection 2015.

2.

Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes.

Hamilton JG, Hutson SP, Frohnmayer AE, Han PK, Peters JA, Carr AG, Alter BP.

J Genet Couns. 2014 Dec 27. [Epub ahead of print]

PMID:
25540896
3.

Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding.

Haga SB, Mills R, Pollak KI, Rehder C, Buchanan AH, Lipkus IM, Crow JH, Datto M.

Genome Med. 2014 Jul 31;6(7):58. doi: 10.1186/s13073-014-0058-6. eCollection 2014.

4.

Prevalence and correlates of receiving and sharing high-penetrance cancer genetic test results: findings from the Health Information National Trends Survey.

Taber JM, Chang CQ, Lam TK, Gillanders EM, Hamilton JG, Schully SD.

Public Health Genomics. 2015;18(2):67-77. doi: 10.1159/000368745.

PMID:
25427996
5.

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients.

Scollon S, Bergstrom K, Kerstein RA, Wang T, Hilsenbeck SG, Ramamurthy U, Gibbs RA, Eng CM, Chintagumpala MM, Berg SL, McCullough LB, McGuire AL, Plon SE, Parsons DW.

Genome Med. 2014 Sep 17;6(9):69. doi: 10.1186/s13073-014-0069-3. eCollection 2014.

6.

To worry or not to worry: breast cancer genetic counseling communication with low-income Latina immigrants.

Joseph G, Guerra C.

J Community Genet. 2015 Jan;6(1):63-76. doi: 10.1007/s12687-014-0202-4. Epub 2014 Aug 23.

7.

Striking a balance in communicating pharmacogenetic test results: promoting comprehension and minimizing adverse psychological and behavioral response.

Haga SB, Mills R, Bosworth H.

Patient Educ Couns. 2014 Oct;97(1):10-5. doi: 10.1016/j.pec.2014.06.007. Epub 2014 Jun 21.

PMID:
24985359
8.

Information-seeking and sharing behavior following genomic testing for diabetes risk.

Mills R, Powell J, Barry W, Haga SB.

J Genet Couns. 2015 Feb;24(1):58-66. doi: 10.1007/s10897-014-9736-1. Epub 2014 Jun 14.

PMID:
24927802
9.
10.

Genetic testing of children for predisposition to mood disorders: anticipating the clinical issues.

Erickson JA, Kuzmich L, Ormond KE, Gordon E, Christman MF, Cho MK, Levinson DF.

J Genet Couns. 2014 Aug;23(4):566-77. doi: 10.1007/s10897-014-9710-y. Epub 2014 Mar 22.

11.

In their own words: treating very young BRCA1/2 mutation-positive women with care and caution.

Hoskins LM, Werner-Lin A, Greene MH.

PLoS One. 2014 Feb 28;9(2):e87696. doi: 10.1371/journal.pone.0087696. eCollection 2014.

12.

Impact of delivery models on understanding genomic risk for type 2 diabetes.

Haga SB, Barry WT, Mills R, Svetkey L, Suchindran S, Willard HF, Ginsburg GS.

Public Health Genomics. 2014;17(2):95-104. doi: 10.1159/000358413. Epub 2014 Feb 27.

13.

Genomics education for the public: perspectives of genomic researchers and ELSI advisors.

Dressler LG, Jones SS, Markey JM, Byerly KW, Roberts MC.

Genet Test Mol Biomarkers. 2014 Mar;18(3):131-40. doi: 10.1089/gtmb.2013.0366. Epub 2014 Feb 4.

14.

Participants' recall and understanding of genomic research and large-scale data sharing.

Robinson JO, Slashinski MJ, Wang T, Hilsenbeck SG, McGuire AL.

J Empir Res Hum Res Ethics. 2013 Oct;8(4):42-52. doi: 10.1525/jer.2013.8.4.42.

15.

Concerns about unintended negative consequences of informing the public about multifactorial risks may be premature for young adult smokers.

Waters EA, Kincaid C, Kaufman AR, Stock ML, Peterson LM, Muscanell NL, Guadagno RE.

Br J Health Psychol. 2014 Nov;19(4):720-36. doi: 10.1111/bjhp.12069. Epub 2013 Oct 1.

16.

Delivering pharmacogenetic testing in a primary care setting.

Mills R, Voora D, Peyser B, Haga SB.

Pharmgenomics Pers Med. 2013 Sep 18;6:105-12. doi: 10.2147/PGPM.S50598. eCollection 2013.

17.

Translational Genomic Research: Protocol Development and Initial Outcomes following SNP Testing for Colon Cancer Risk.

Nusbaum R, Leventhal KG, Hooker GW, Peshkin BN, Butrick M, Salehizadeh Y, Tuong W, Eggly S, Mathew J, Goerlitz D, Shields PG, Schwartz MD, Graves KD.

Transl Behav Med. 2013 Mar 1;3(1):17-29. Epub 2012 Jun 10.

18.

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.

Hurle B, Citrin T, Jenkins JF, Kaphingst KA, Lamb N, Roseman JE, Bonham VL.

Genet Med. 2013 Aug;15(8):658-63. doi: 10.1038/gim.2013.14. Epub 2013 Feb 28.

19.

Incorporating genomics into breast and prostate cancer screening: assessing the implications.

Chowdhury S, Dent T, Pashayan N, Hall A, Lyratzopoulos G, Hallowell N, Hall P, Pharoah P, Burton H.

Genet Med. 2013 Jun;15(6):423-32. doi: 10.1038/gim.2012.167. Epub 2013 Feb 14. Review.

20.

Public knowledge of and attitudes toward genetics and genetic testing.

Haga SB, Barry WT, Mills R, Ginsburg GS, Svetkey L, Sullivan J, Willard HF.

Genet Test Mol Biomarkers. 2013 Apr;17(4):327-35. doi: 10.1089/gtmb.2012.0350. Epub 2013 Feb 13.

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