Bleyl SB - Search Results

1

Experience with Integrating Diagnostic Decision Support Software with Electronic Health Records: Benefits versus Risks of Information Sharing.

Segal MM, Rahm AK, Hulse NC, Wood G, Williams JL, Feldman L, Moore GJ, Gehrum D, Yefko M, Mayernick S, Gildersleeve R, Sunderland MC, Bleyl SB, Haug P, Williams MS. Segal MM, et al. Among authors: bleyl sb. EGEMS (Wash DC). 2017 Dec 6;5(1):23. doi: 10.5334/egems.244. EGEMS (Wash DC). 2017. PMID: 29930964 Free PMC article.

2

Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelines.

Khalifa A, Mason CC, Garvin JH, Williams MS, Del Fiol G, Jackson BR, Bleyl SB, Alterovitz G, Huff SM. Khalifa A, et al. Among authors: bleyl sb. J Am Med Inform Assoc. 2021 Nov 25;28(12):2617-2625. doi: 10.1093/jamia/ocab201. J Am Med Inform Assoc. 2021. PMID: 34569596 Free PMC article.

3

A qualitative study of prevalent laboratory information systems and data communication patterns for genetic test reporting.

Khalifa A, Mason CC, Garvin JH, Williams MS, Del Fiol G, Jackson BR, Bleyl SB, Huff SM. Khalifa A, et al. Among authors: bleyl sb. Genet Med. 2021 Nov;23(11):2171-2177. doi: 10.1038/s41436-021-01251-5. Epub 2021 Jul 6. Genet Med. 2021. PMID: 34230635 Free article.

4

A qualitative investigation of biomedical informatics interoperability standards for genetic test reporting: benefits, challenges, and motivations from the testing laboratory's perspective.

Khalifa A, Mason CC, Garvin JH, Williams MS, Del Fiol G, Jackson BR, Bleyl SB, Huff SM. Khalifa A, et al. Among authors: bleyl sb. Genet Med. 2021 Nov;23(11):2178-2185. doi: 10.1038/s41436-021-01301-y. Epub 2021 Aug 25. Genet Med. 2021. PMID: 34429527 Free article.

5

Global implementation of genomic medicine: We are not alone.

Manolio TA, Abramowicz M, Al-Mulla F, Anderson W, Balling R, Berger AC, Bleyl S, Chakravarti A, Chantratita W, Chisholm RL, Dissanayake VH, Dunn M, Dzau VJ, Han BG, Hubbard T, Kolbe A, Korf B, Kubo M, Lasko P, Leego E, Mahasirimongkol S, Majumdar PP, Matthijs G, McLeod HL, Metspalu A, Meulien P, Miyano S, Naparstek Y, O'Rourke PP, Patrinos GP, Rehm HL, Relling MV, Rennert G, Rodriguez LL, Roden DM, Shuldiner AR, Sinha S, Tan P, Ulfendahl M, Ward R, Williams MS, Wong JE, Green ED, Ginsburg GS. Manolio TA, et al. Sci Transl Med. 2015 Jun 3;7(290):290ps13. doi: 10.1126/scitranslmed.aab0194. Sci Transl Med. 2015. PMID: 26041702 Free PMC article. Review.

6

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals.

Bleyl SB, Mumford BR, Brown-Harrison MC, Pagotto LT, Carey JC, Pysher TJ, Ward K, Chin TK. Bleyl SB, et al. Am J Med Genet. 1997 Oct 31;72(3):257-65. Am J Med Genet. 1997. PMID: 9332651

7

Familial total anomalous pulmonary venous return: a large Utah-Idaho family.

Bleyl S, Ruttenberg HD, Carey JC, Ward K. Bleyl S, et al. Am J Med Genet. 1994 Oct 1;52(4):462-6. doi: 10.1002/ajmg.1320520412. Am J Med Genet. 1994. PMID: 7747759

8

A rapid gene sequencing panel strategy to facilitate precision neonatal medicine.

Brunelli L, Mao R, Jenkins SM, Bleyl SB, Dames SA, Miller CE, Ostrander B, Tvrdik T, Andrews S, Flores J, Patel S, Gudgeon JM, Schaefer S. Brunelli L, et al. Among authors: bleyl sb. Am J Med Genet A. 2017 Jul;173(7):1979-1982. doi: 10.1002/ajmg.a.38259. Epub 2017 May 12. Am J Med Genet A. 2017. PMID: 28497657 No abstract available.

9

Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndrome.

Carlston CM, Bleyl SB, Andrews A, Meyers L, Brown S, Bayrak-Toydemir P, Bale JF, Botto LD. Carlston CM, et al. Among authors: bleyl sb. Am J Med Genet A. 2019 May;179(5):792-796. doi: 10.1002/ajmg.a.61091. Epub 2019 Feb 17. Am J Med Genet A. 2019. PMID: 30773818

10

Clinical utility of a next generation sequencing panel assay for Marfan and Marfan-like syndromes featuring aortopathy.

Wooderchak-Donahue W, VanSant-Webb C, Tvrdik T, Plant P, Lewis T, Stocks J, Raney JA, Meyers L, Berg A, Rope AF, Yetman AT, Bleyl SB, Mesley R, Bull DA, Collins RT, Ojeda MM, Roberts A, Lacro R, Woerner A, Stoler J, Bayrak-Toydemir P. Wooderchak-Donahue W, et al. Among authors: bleyl sb. Am J Med Genet A. 2015 Aug;167A(8):1747-57. doi: 10.1002/ajmg.a.37085. Epub 2015 May 5. Am J Med Genet A. 2015. PMID: 25944730

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

48 results

Search Page