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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2015 | 5 |
2016 | 3 |
2024 | 0 |
Search Results
6 results
Results by year
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Page 1
Building the foundation for genomics in precision medicine.
Nature. 2015 Oct 15;526(7573):336-42. doi: 10.1038/nature15816.
Nature. 2015.
PMID: 26469044
Free PMC article.
Review.
Are physicians prepared for whole genome sequencing? a qualitative analysis.
Christensen KD, Vassy JL, Jamal L, Lehmann LS, Slashinski MJ, Perry DL, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Murray MF, Green RC, McGuire AL; MedSeq Project Team.
Christensen KD, et al.
Clin Genet. 2016 Feb;89(2):228-34. doi: 10.1111/cge.12626. Epub 2015 Jul 7.
Clin Genet. 2016.
PMID: 26080898
Free PMC article.
Item in Clipboard
Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning Individualized Genetic Research Results in Pediatric Rare Disease Research, a Qualitative Interview Study.
Cacioppo CN, Chandler AE, Towne MC, Beggs AH, Holm IA.
Cacioppo CN, et al.
PLoS One. 2016 Apr 15;11(4):e0153597. doi: 10.1371/journal.pone.0153597. eCollection 2016.
PLoS One. 2016.
PMID: 27082877
Free PMC article.
Item in Clipboard
Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndrome.
Thaker VV, Esteves KM, Towne MC, Brownstein CA, James PM, Crowley L, Hirschhorn JN, Elsea SH, Beggs AH, Picker J, Agrawal PB.
Thaker VV, et al.
J Clin Endocrinol Metab. 2015 May;100(5):1723-30. doi: 10.1210/jc.2014-4215. Epub 2015 Mar 17.
J Clin Endocrinol Metab. 2015.
PMID: 25781356
Free PMC article.
Item in Clipboard
Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations.
Wolf SM, Branum R, Koenig BA, Petersen GM, Berry SA, Beskow LM, Daly MB, Fernandez CV, Green RC, LeRoy BS, Lindor NM, O'Rourke PP, Breitkopf CR, Rothstein MA, Van Ness B, Wilfond BS.
Wolf SM, et al.
J Law Med Ethics. 2015 Fall;43(3):440-63. doi: 10.1111/jlme.12288.
J Law Med Ethics. 2015.
PMID: 26479555
Free PMC article.
Item in Clipboard
Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentations.
Brownstein CA, Beggs AH, Rodan L, Shi J, Towne MC, Pelletier R, Cao S, Rosenberg PA, Urion DK, Picker J, Tan WH, Agrawal PB.
Brownstein CA, et al.
Neurogenetics. 2016 Jan;17(1):11-6. doi: 10.1007/s10048-015-0460-2. Epub 2015 Sep 22.
Neurogenetics. 2016.
PMID: 26395884
Free PMC article.
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