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Results: 1 to 20 of 72

1.

Communicating new knowledge on previously reported genetic variants.

Aronson SJ, Clark EH, Varugheese M, Baxter S, Babb LJ, Rehm HL.

Genet Med. 2012 Apr 5. doi: 10.1038/gim.2012.19. [Epub ahead of print]

PMID:
22481129
[PubMed - as supplied by publisher]
Free PMC Article
2.

Internet and information technology use in treatment of diabetes.

Kaufman N.

Int J Clin Pract Suppl. 2010 Feb;(166):41-6. doi: 10.1111/j.1742-1241.2009.02277.x. Review.

PMID:
20377663
[PubMed - indexed for MEDLINE]
3.

Clinical application of high throughput molecular screening techniques for pharmacogenomics.

Wiita AP, Schrijver I.

Pharmgenomics Pers Med. 2011;4:109-21. doi: 10.2147/PGPM.S15302. Epub 2011 Sep 8.

PMID:
23226057
[PubMed]
Free PMC Article
4.

[Development of antituberculous drugs: current status and future prospects].

Tomioka H, Namba K.

Kekkaku. 2006 Dec;81(12):753-74. Review. Japanese.

PMID:
17240921
[PubMed - indexed for MEDLINE]
5.

Whole genome sequencing for lung cancer.

Daniels M, Goh F, Wright CM, Sriram KB, Relan V, Clarke BE, Duhig EE, Bowman RV, Yang IA, Fong KM.

J Thorac Dis. 2012 Apr 1;4(2):155-63. doi: 10.3978/j.issn.2072-1439.2012.02.01.

PMID:
22833821
[PubMed]
Free PMC Article
6.

GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.

DE LA Vega FM, Bustamante CD, Leal SM.

Pac Symp Biocomput. 2011:74-5.

PMID:
21121034
[PubMed - as supplied by publisher]
Free PMC Article
7.

FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets.

Pope BJ, Nguyen-Dumont T, Odefrey F, Hammet F, Bell R, Tao K, Tavtigian SV, Goldgar DE, Lonie A, Southey MC, Park DJ.

BMC Bioinformatics. 2013 Feb 25;14:65. doi: 10.1186/1471-2105-14-65.

PMID:
23441864
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Usability of a novel clinician interface for genetic results.

Neri PM, Pollard SE, Volk LA, Newmark LP, Varugheese M, Baxter S, Aronson SJ, Rehm HL, Bates DW.

J Biomed Inform. 2012 Oct;45(5):950-7. doi: 10.1016/j.jbi.2012.03.007. Epub 2012 Apr 12.

PMID:
22521718
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Guidelines, editors, pharma and the biological paradigm shift.

Singh AR, Singh SA.

Mens Sana Monogr. 2007 Jan;5(1):27-30. doi: 10.4103/0973-1229.32176.

PMID:
22058616
[PubMed]
Free PMC Article
10.

Ethics and genetic selection in purebred dogs.

Meyers-Wallen VN.

Reprod Domest Anim. 2003 Feb;38(1):73-6.

PMID:
12535334
[PubMed - indexed for MEDLINE]
11.

Clinical assessment incorporating a personal genome.

Ashley EA, Butte AJ, Wheeler MT, Chen R, Klein TE, Dewey FE, Dudley JT, Ormond KE, Pavlovic A, Morgan AA, Pushkarev D, Neff NF, Hudgins L, Gong L, Hodges LM, Berlin DS, Thorn CF, Sangkuhl K, Hebert JM, Woon M, Sagreiya H, Whaley R, Knowles JW, Chou MF, Thakuria JV, Rosenbaum AM, Zaranek AW, Church GM, Greely HT, Quake SR, Altman RB.

Lancet. 2010 May 1;375(9725):1525-35. doi: 10.1016/S0140-6736(10)60452-7.

PMID:
20435227
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Updating Systematic Reviews.

Shojania KG, Sampson M, Ansari MT, Ji J, Garritty C, Rader T, Moher D.

Rockville (MD): Agency for Healthcare Research and Quality (US); 2007 Sep.

PMID:
20734512
[PubMed]
Books & Documents
13.

Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling.

O'Daniel JM, Lee K.

Cancer J. 2012 Jul-Aug;18(4):287-92. doi: 10.1097/PPO.0b013e318262467e. Review.

PMID:
22846728
[PubMed - indexed for MEDLINE]
14.

Interpretation of genetic testing: variants of unknown significance.

Fogel BL.

Continuum (Minneap Minn). 2011 Apr;17(2 Neurogenetics):347-52. doi: 10.1212/01.CON.0000396975.87637.86.

PMID:
22810825
[PubMed]
Free PMC Article
15.

New directions in laboratory-clinician communications.

Zinder O.

Clin Chim Acta. 1998 Dec;278(2):83-94.

PMID:
10023816
[PubMed - indexed for MEDLINE]
16.

Massively parallel sequencing: the next big thing in genetic medicine.

Tucker T, Marra M, Friedman JM.

Am J Hum Genet. 2009 Aug;85(2):142-54. doi: 10.1016/j.ajhg.2009.06.022. Review.

PMID:
19679224
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

[Health technology assessment report: Computer-assisted Pap test for cervical cancer screening].

Della Palma P, Moresco L, Giorgi Rossi P.

Epidemiol Prev. 2012 Sep-Oct;36(5 Suppl 3):e1-43. Italian.

PMID:
23139174
[PubMed - indexed for MEDLINE]
18.

Cystic fibrosis testing in a referral laboratory: results and lessons from a six-year period.

Ridge PG, Miller C, Bayrak-Toydemir P, Best DH, Mao R, Swensen JJ, Lyon E, Voelkerding KV.

J Clin Bioinforma. 2013 Jan 23;3(1):3. doi: 10.1186/2043-9113-3-3.

PMID:
23343000
[PubMed]
Free PMC Article
19.

The role of technology in the clinical laboratory of the future.

Wilkinson DS.

Clin Lab Manage Rev. 1997 Sep-Oct;11(5):322-30.

PMID:
10175175
[PubMed - indexed for MEDLINE]
20.

Downsizing genomic medicine: approaching the ethical complexity of whole-genome sequencing by starting small.

Sharp RR.

Genet Med. 2011 Mar;13(3):191-4. doi: 10.1097/GIM.0b013e31820f603f.

PMID:
21311340
[PubMed - indexed for MEDLINE]

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