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Items: 1 to 20 of 104

1.

Runs of homozygosity and parental relatedness.

Rosenberg NA, Pemberton TJ, Li JZ, Belmont JW.

Genet Med. 2013 Sep;15(9):753-4. doi: 10.1038/gim.2013.108. No abstract available.

PMID:
24008258
2.

Response to Rosenberg et al.

Rehder CW, David KL, Hirsch B, Toriello HV, Wilson CM, Kearney HM.

Genet Med. 2013 Sep;15(9):754. doi: 10.1038/gim.2013.107. No abstract available.

PMID:
24008259
3.

American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.

Rehder CW, David KL, Hirsch B, Toriello HV, Wilson CM, Kearney HM.

Genet Med. 2013 Feb;15(2):150-2. doi: 10.1038/gim.2012.169. Epub 2013 Jan 17.

PMID:
23328890
4.

Personalized medicine: Bring clinical standards to human-genetics research.

Lyon GJ.

Nature. 2012 Feb 15;482(7385):300-1. doi: 10.1038/482300a. No abstract available.

PMID:
22337032
5.

Don't just invite us to the table: authentic community engagement.

Terry SF.

Genet Test Mol Biomarkers. 2013 Jun;17(6):443-5. doi: 10.1089/gtmb.2013.1545. No abstract available.

PMID:
23721344
6.

ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.

Hickey SE, Curry CJ, Toriello HV.

Genet Med. 2013 Feb;15(2):153-6. doi: 10.1038/gim.2012.165. Epub 2013 Jan 3.

PMID:
23288205
7.

The importance of patient engagement.

Williams JK, Daack-Hirsch S, Driessnack M, Downing NR, Simon C.

Genet Test Mol Biomarkers. 2013 Sep;17(9):649. doi: 10.1089/gtmb.2013.0346. Epub 2013 Aug 13. No abstract available.

8.

Regulation: The FDA is overcautious on consumer genomics.

Green RC, Farahany NA.

Nature. 2014 Jan 16;505(7483):286-7. No abstract available.

PMID:
24436984
9.

Putting DNA to the test.

[No authors listed]

Nature. 2009 Oct 8;461(7265):697-8. doi: 10.1038/461697b. No abstract available.

PMID:
19812626
10.

Genomic test validation for incidental findings.

Park JY, Fortina P, Kricka LJ.

Clin Chem. 2014 Feb;60(2):292-3. doi: 10.1373/clinchem.2013.210609. Epub 2013 Jul 1. No abstract available.

11.

Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness.

Grote L, Myers M, Lovell A, Saal H, Sund KL.

Am J Med Genet A. 2014 Jan;164A(1):87-98. doi: 10.1002/ajmg.a.36206. Epub 2013 Nov 15.

PMID:
24243712
12.

Genetics research: Clinical standards not practical in the lab.

Lindpaintner K.

Nature. 2012 Mar 7;483(7388):158. doi: 10.1038/483158c. No abstract available.

PMID:
22398544
13.

Ethical issues: from genome to therapy.

Magnus D.

Novartis Found Symp. 2000;229:122-5; discussion 125-30. No abstract available.

PMID:
11084937
14.

Variability in laboratory reporting practices for regions of homozygosity indicating parental relatedness as identified by SNP microarray testing.

Grote L, Myers M, Lovell A, Saal H, Lipscomb Sund K.

Genet Med. 2012 Dec;14(12):971-6. doi: 10.1038/gim.2012.83. Epub 2012 Jul 12.

PMID:
22791212
15.

Point-counterpoint. Ethics and genomic incidental findings.

McGuire AL, Joffe S, Koenig BA, Biesecker BB, McCullough LB, Blumenthal-Barby JS, Caulfield T, Terry SF, Green RC.

Science. 2013 May 31;340(6136):1047-8. doi: 10.1126/science.1240156. Epub 2013 May 16. No abstract available.

16.

Genetics and managed care: Policy statement of the American College of Medical Genetics.

Williams MS.

Genet Med. 2001 Nov-Dec;3(6):430-5. No abstract available.

PMID:
11715009
17.

When is a medical finding "incidental"?

Evans JP.

Genet Med. 2013 Jul;15(7):515-6. doi: 10.1038/gim.2013.74. Epub 2013 May 30. No abstract available.

PMID:
23722872
18.

Genomics, genetic epidemiology, and genomic medicine.

Lazaridis KN, Petersen GM.

Clin Gastroenterol Hepatol. 2005 Apr;3(4):320-8. Review.

PMID:
15822036
19.

Incidental swimming with millstones.

Kingsmore SF.

Sci Transl Med. 2013 Jul 17;5(194):194ed10. doi: 10.1126/scitranslmed.3006900. No abstract available.

20.

American College of Medical Genetics position statement on gene patents and accessibility of gene testing.

[No authors listed]

Genet Med. 1999 Jul-Aug;1(5):237. No abstract available.

PMID:
11256680

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