1U01HG007437-01/HG/NHGRI NIH HHS/United States[Grants and Funding] - Search Results

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Year	Number of Results
2015	3
2016	1
2024	0

Page 1

Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup.

Overby CL, Heale B, Aronson S, Cherry JM, Dwight S, Milosavljevic A, Nelson T, Niehaus A, Weaver MA, Ramos EM, Williams MS. Overby CL, et al. Clin Pharmacol Ther. 2016 Feb;99(2):157-60. doi: 10.1002/cpt.270. Epub 2015 Nov 9. Clin Pharmacol Ther. 2016. PMID: 26418054 Free PMC article.

High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting.

Lee K, Berg JS, Milko L, Crooks K, Lu M, Bizon C, Owen P, Wilhelmsen KC, Weck KE, Evans JP, Garg S. Lee K, et al. Am J Ophthalmol. 2015 Aug;160(2):354-363.e9. doi: 10.1016/j.ajo.2015.04.026. Epub 2015 Apr 22. Am J Ophthalmol. 2015. PMID: 25910913 Free PMC article.

GenomeConnect: matchmaking between patients, clinical laboratories, and researchers to improve genomic knowledge.

Kirkpatrick BE, Riggs ER, Azzariti DR, Miller VR, Ledbetter DH, Miller DT, Rehm H, Martin CL, Faucett WA; ClinGen Resource. Kirkpatrick BE, et al. Hum Mutat. 2015 Oct;36(10):974-8. doi: 10.1002/humu.22838. Epub 2015 Aug 6. Hum Mutat. 2015. PMID: 26178529 Free PMC article.

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