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Items: 16

1.

Vaccine adverse events in a safety net healthcare system and a managed care organization.

Narwaney KJ, Breslin K, Ross CA, Shoup JA, Wain KF, Weintraub ES, McNeil MM, Hambidge SJ.

Vaccine. 2017 Mar 1;35(9):1335-1340. doi: 10.1016/j.vaccine.2017.01.017. Epub 2017 Feb 6.

PMID:
28185740
2.

Integration of data from a safety net health care system into the Vaccine Safety Datalink.

Hambidge SJ, Ross C, Shoup JA, Wain K, Narwaney K, Breslin K, Weintraub ES, McNeil MM.

Vaccine. 2017 Mar 1;35(9):1329-1334. doi: 10.1016/j.vaccine.2017.01.027. Epub 2017 Feb 1.

PMID:
28161424
3.

Screening for and Diagnosis of Depression Among Adolescents in a Large Health Maintenance Organization.

Lewandowski RE, O'Connor B, Bertagnolli A, Beck A, Tinoco A, Gardner WP, Jelinek-Berents CX, Newton DA, Wain KF, Boggs JM, Brace NE, deSa P, Scholle SH, Hoagwood K, Horwitz SM.

Psychiatr Serv. 2016 Jun 1;67(6):636-41. doi: 10.1176/appi.ps.201400465. Epub 2016 Feb 14.

PMID:
26876655
4.

ClinGen--the Clinical Genome Resource.

Rehm HL, Berg JS, Brooks LD, Bustamante CD, Evans JP, Landrum MJ, Ledbetter DH, Maglott DR, Martin CL, Nussbaum RL, Plon SE, Ramos EM, Sherry ST, Watson MS; ClinGen..

N Engl J Med. 2015 Jun 4;372(23):2235-42. doi: 10.1056/NEJMsr1406261. Epub 2015 May 27. No abstract available.

5.

The utilization of counseling skills by the laboratory genetic counselor.

Goodenberger ML, Thomas BC, Wain KE.

J Genet Couns. 2015 Feb;24(1):6-17. doi: 10.1007/s10897-014-9749-9. Epub 2014 Aug 20.

PMID:
25138081
6.

Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review.

Wain KE, Ellingson MS, McDonald J, Gammon A, Roberts M, Pichurin P, Winship I, Riegert-Johnson DL, Weitzel JN, Lindor NM.

Genet Med. 2014 Aug;16(8):588-93. doi: 10.1038/gim.2014.5. Epub 2014 Feb 13.

7.

Looking back and moving forward: an historical perspective from laboratory genetic counselors.

Zetzsche LH, Kotzer KE, Wain KE.

J Genet Couns. 2014 Jun;23(3):363-70. doi: 10.1007/s10897-013-9670-7. Epub 2013 Nov 12.

PMID:
24217982
8.

Towards a Universal Clinical Genomics Database: the 2012 International Standards for Cytogenomic Arrays Consortium Meeting.

Riggs ER, Wain KE, Riethmaier D, Savage M, Smith-Packard B, Kaminsky EB, Rehm HL, Martin CL, Ledbetter DH, Faucett WA.

Hum Mutat. 2013 Jun;34(6):915-9. doi: 10.1002/humu.22306. Epub 2013 Apr 2.

9.

Chromosomal microarray impacts clinical management.

Riggs ER, Wain KE, Riethmaier D, Smith-Packard B, Faucett WA, Hoppman N, Thorland EC, Patel VC, Miller DT.

Clin Genet. 2014 Feb;85(2):147-53. doi: 10.1111/cge.12107. Epub 2013 Feb 21.

PMID:
23347240
10.

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype.

Hoppman-Chaney N, Wain K, Seger PR, Superneau DW, Hodge JC.

Clin Genet. 2013 Apr;83(4):345-51. doi: 10.1111/j.1399-0004.2012.01925.x. Epub 2012 Aug 7.

PMID:
22775350
11.

Hereditary hemorrhagic telangiectasia and risks for adverse pregnancy outcomes.

Wain K, Swanson K, Watson W, Jeavons E, Weaver A, Lindor N.

Am J Med Genet A. 2012 Aug;158A(8):2009-14. doi: 10.1002/ajmg.a.35458. Epub 2012 Jun 18.

PMID:
22711524
12.

The laboratory-clinician team: a professional call to action to improve communication and collaboration for optimal patient care in chromosomal microarray testing.

Wain KE, Riggs E, Hanson K, Savage M, Riethmaier D, Muirhead A, Mitchell E, Packard BS, Faucett WA.

J Genet Couns. 2012 Oct;21(5):631-7. doi: 10.1007/s10897-012-9507-9. Epub 2012 May 18.

13.

Towards an evidence-based process for the clinical interpretation of copy number variation.

Riggs ER, Church DM, Hanson K, Horner VL, Kaminsky EB, Kuhn RM, Wain KE, Williams ES, Aradhya S, Kearney HM, Ledbetter DH, South ST, Thorland EC, Martin CL.

Clin Genet. 2012 May;81(5):403-12. doi: 10.1111/j.1399-0004.2011.01818.x. Epub 2011 Dec 13. Review.

14.

Living at risk: the sibling's perspective of early-onset Alzheimer's disease.

Wain KE, Uhlmann WR, Heidebrink J, Roberts JS.

J Genet Couns. 2009 Jun;18(3):239-51. doi: 10.1007/s10897-008-9206-8. Epub 2009 Jan 9.

PMID:
19132519
15.

First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies.

Northup JK, Wain KE, Hawkins JC, Matalon R, Velagaleti GV.

Am J Med Genet A. 2008 Oct 1;146A(19):2578-82. doi: 10.1002/ajmg.a.32486. No abstract available.

PMID:
18792973
16.

Sex differences in outcome after implantable cardioverter defibrillator implantation in nonischemic cardiomyopathy.

Albert CM, Quigg R, Saba S, Estes NA 3rd, Shaechter A, Subacius H, Howard A, Levine J, Kadish A; DEFINITE Investigators..

Am Heart J. 2008 Aug;156(2):367-72. doi: 10.1016/j.ahj.2008.02.026.

PMID:
18657670

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