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Items: 1 to 20 of 101

1.

Incidental swimming with millstones.

Kingsmore SF.

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

2.

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.

3.

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.

4.

Incidentalomas in genomics and radiology.

Solomon BD.

N Engl J Med. 2014 Mar 13;370(11):988-90. doi: 10.1056/NEJMp1310471. No abstract available.

PMID:
24620864
6.

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
7.

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
8.

Genetics. New company pushes the envelope on pre-conception testing.

Couzin-Frankel J.

Science. 2012 Oct 19;338(6105):315-6. doi: 10.1126/science.338.6105.315. No abstract available.

PMID:
23087222
9.

Next-generation sequencing applied to rare diseases genomics.

Danielsson K, Mun LJ, Lordemann A, Mao J, Lin CH.

Expert Rev Mol Diagn. 2014 May;14(4):469-87. doi: 10.1586/14737159.2014.904749. Epub 2014 Apr 4. Review.

PMID:
24702023
10.

Have we asked too much of consent?

Koenig BA.

Hastings Cent Rep. 2014 Jul-Aug;44(4):33-4. doi: 10.1002/hast.329. No abstract available.

11.

Taxonomizing, sizing, and overcoming the incidentalome.

Kohane IS, Hsing M, Kong SW.

Genet Med. 2012 Apr;14(4):399-404. doi: 10.1038/gim.2011.68. Epub 2012 Feb 9.

12.

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.

Wolf SM, Annas GJ, Elias S.

Science. 2013 May 31;340(6136):1049-50. doi: 10.1126/science.1239119. Epub 2013 May 16. No abstract available.

13.

DNA donor rights affirmed.

Hayden EC.

Nature. 2012 Mar 21;483(7390):387. doi: 10.1038/483387a. No abstract available.

PMID:
22437587
14.

Call for prudence in whole-genome testing.

van El CG, Dondorp WJ, de Wert GM, Cornel MC.

Science. 2013 Aug 30;341(6149):958-9. doi: 10.1126/science.341.6149.958-b. No abstract available.

PMID:
23990543
15.

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
16.

[Rare diseases are common].

Has C, Giehl K.

Hautarzt. 2014 Jun;65(6):488-9. doi: 10.1007/s00105-013-2709-8. German. No abstract available.

PMID:
24898502
17.

'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.

Daack-Hirsch S, Driessnack M, Hanish A, Johnson VA, Shah LL, Simon CM, Williams JK.

Clin Genet. 2013 Jul;84(1):11-8. doi: 10.1111/cge.12167. Epub 2013 May 3.

18.

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
19.

Next Generation Diagnostics for Rare Neurological Diseases: The Future is Here.

Innes AM, Boycott KM.

Can J Neurol Sci. 2014 May;41(3):299-300. No abstract available.

PMID:
24718813
20.

Three-year experience of a CAP/ACMG methods-based external proficiency testing program for laboratories offering DNA sequencing for rare inherited disorders.

Richards CS, Palomaki GE, Lacbawan FL, Lyon E, Feldman GL; CAP/ACMG Biochemical and Molecular Genetics Resource Committee.

Genet Med. 2014 Jan;16(1):25-32. doi: 10.1038/gim.2013.65. Epub 2013 May 23.

PMID:
23703682
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