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Items: 1 to 50 of 56

1.

Primary Care Providers' Preferences and Concerns Regarding Specific Visual Displays for Returning Hemoglobin A1c Test Results to Patients.

Zikmund-Fisher BJ, Solomon JB, Scherer AM, Exe NL, Tarini BA, Fagerlin A, Witteman HO.

Med Decis Making. 2019 Oct;39(7):796-804. doi: 10.1177/0272989X19873625. Epub 2019 Sep 26.

PMID:
31556795
2.

Vaccine administration error rates at a large academic medical center and its affiliated clinics - Familiarity matters.

Reed L, Tarini BA, Andreae MC.

Vaccine. 2019 Aug 23;37(36):5390-5396. doi: 10.1016/j.vaccine.2019.07.027. Epub 2019 Jul 23.

PMID:
31350155
3.

Systems Integration: The Next Frontier in Newborn-Screening Timeliness.

Simon NJ, Atkins A, Yusuf C, Tarini BA.

J Public Health Manag Pract. 2019 Feb 14. doi: 10.1097/PHH.0000000000000968. [Epub ahead of print]

PMID:
30789598
4.

Misclassification of VLCAD carriers due to variable confirmatory testing after a positive NBS result.

Atkins AE, Tarini BA, Phillips EK, Calhoun ARUL.

J Community Genet. 2019 Oct;10(4):447-451. doi: 10.1007/s12687-019-00409-8. Epub 2019 Feb 5.

5.

An Assessment of Public Preferences for Newborn Screening Using Best-Worst Scaling.

Tarini BA, Simon NJ, Payne K, Gebremariam A, Rose A, Prosser LA.

J Pediatr. 2018 Oct;201:62-68.e1. doi: 10.1016/j.jpeds.2018.05.035. Epub 2018 Jul 16.

PMID:
30025667
6.

Newborn Screening Collection and Delivery Processes in Michigan Birthing Hospitals: Strategies to Improve Timeliness.

Cochran AL, Tarini BA, Kleyn M, Zayas-Cabán G.

Matern Child Health J. 2018 Oct;22(10):1436-1443. doi: 10.1007/s10995-018-2524-z.

PMID:
29616441
7.

Family History Collection Practices: National Survey of Pediatric Primary Care Providers.

Tarini BA, Gornick MC, Zikmund-Fisher BJ, Saal HM, Edmondson L, Uhlmann WR.

Clin Pediatr (Phila). 2018 May;57(5):537-546. doi: 10.1177/0009922817733693. Epub 2017 Oct 16.

PMID:
29034736
8.

Adolescent bariatric surgery: a systematic review of recommendation documents.

Childerhose JE, Alsamawi A, Mehta T, Smith JE, Woolford S, Tarini BA.

Surg Obes Relat Dis. 2017 Oct;13(10):1768-1779. doi: 10.1016/j.soard.2017.08.008. Epub 2017 Aug 12. Review.

PMID:
28958402
9.

Graphics help patients distinguish between urgent and non-urgent deviations in laboratory test results.

Zikmund-Fisher BJ, Scherer AM, Witteman HO, Solomon JB, Exe NL, Tarini BA, Fagerlin A.

J Am Med Inform Assoc. 2017 May 1;24(3):520-528. doi: 10.1093/jamia/ocw169.

10.

Biobank participant support of newborn screening for disorders with variable treatment and intervention options.

Bunnell ME, Tarini BA, Petros M, Goldenberg AJ, Arjunan A, Wicklund C.

J Community Genet. 2016 Oct;7(4):291-302. Epub 2016 Sep 1.

11.

A Quality Improvement Collaborative to Improve Pediatric Primary Care Genetic Services.

Rinke ML, Driscoll A, Mikat-Stevens N, Healy J, Colantuoni E, Elias AF, Pletcher BA, Gubernick RS, Larson I, Chung WK, Tarini BA.

Pediatrics. 2016 Feb;137(2):e20143874. doi: 10.1542/peds.2014-3874. Epub 2016 Jan 28.

12.

Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study.

Tarini BA, Zikmund-Fisher BJ, Saal HM, Edmondson L, Uhlmann WR.

J Pediatr. 2015 Dec;167(6):1404-8.e1. doi: 10.1016/j.jpeds.2015.08.065. Epub 2015 Oct 23.

PMID:
26477869
13.

Effect of "Pink Eye" Label on Parents' Intent to Use Antibiotics and Perceived Contagiousness.

Scherer LD, Finan C, Simancek D, Finkelstein JI, Tarini BA.

Clin Pediatr (Phila). 2016 Jun;55(6):543-8. doi: 10.1177/0009922815601983. Epub 2015 Aug 20.

PMID:
26294761
14.

Understanding Outcomes in Adolescent Bariatric Surgery.

Childerhose JE, Tarini BA.

Pediatrics. 2015 Aug;136(2):e312-4. doi: 10.1542/peds.2015-0867. No abstract available.

15.

Framing optional genetic testing in the context of mandatory newborn screening tests.

Lillie SE, Tarini BA, Janz NK, Zikmund-Fisher BJ.

BMC Med Inform Decis Mak. 2015 Jun 27;15:50. doi: 10.1186/s12911-015-0173-3.

16.

Parent and public interest in whole-genome sequencing.

Dodson DS, Goldenberg AJ, Davis MM, Singer DC, Tarini BA.

Public Health Genomics. 2015;18(3):151-9. doi: 10.1159/000375115. Epub 2015 Mar 6.

17.

Primary-care providers' perceived barriers to integration of genetics services: a systematic review of the literature.

Mikat-Stevens NA, Larson IA, Tarini BA.

Genet Med. 2015 Mar;17(3):169-76. doi: 10.1038/gim.2014.101. Epub 2014 Sep 11. Review.

PMID:
25210938
18.

Primary care providers' experiences notifying parents of cystic fibrosis newborn screening results.

Finan C, Nasr SZ, Rothwell E, Tarini BA.

Clin Pediatr (Phila). 2015 Jan;54(1):67-75. doi: 10.1177/0009922814545619. Epub 2014 Aug 6.

19.

The value of time in assessing the effectiveness of newborn screening for congenital adrenal hyperplasia.

Tarini BA.

JAMA Pediatr. 2014 Jun;168(6):515-6. doi: 10.1001/jamapediatrics.2014.246. No abstract available.

PMID:
24733500
20.

Effects of undergoing multiplex genetic susceptibility testing on parent attitudes towards testing their children.

Madeo AC, Tercyak KP, Tarini BA, McBride CM.

Ann Behav Med. 2014 Jun;47(3):388-94. doi: 10.1007/s12160-013-9553-z.

21.

Family history in primary care pediatrics.

Tarini BA, McInerney JD.

Pediatrics. 2013 Dec;132(Suppl 3):S203-10. doi: 10.1542/peds.2013-1032D.

22.

Genetic services and attitudes in primary care pediatrics.

Rinke ML, Mikat-Stevens N, Saul R, Driscoll A, Healy J, Tarini BA.

Am J Med Genet A. 2014 Feb;164A(2):449-55. doi: 10.1002/ajmg.a.36339. Epub 2013 Nov 19.

PMID:
24254914
23.

Screening practices for identifying type 2 diabetes in adolescents.

Lee JM, Eason A, Nelson C, Kazzi NG, Cowan AE, Tarini BA.

J Adolesc Health. 2014 Feb;54(2):139-43. doi: 10.1016/j.jadohealth.2013.07.003. Epub 2013 Aug 20.

24.

Personalized medicine in primary care: the need for relevance.

Tarini BA, Saul RA.

Per Med. 2013 Aug;10(6):515-517. doi: 10.2217/pme.13.52. No abstract available.

PMID:
29776187
25.

Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.

Wade CH, Tarini BA, Wilfond BS.

Annu Rev Genomics Hum Genet. 2013;14:535-55. doi: 10.1146/annurev-genom-091212-153425. Epub 2013 Jul 15. Review.

26.

The perils of SNP microarray testing: uncovering unexpected consanguinity.

Tarini BA, Konczal LL, Goldenberg AJ, Goldman EB, McCandless SE.

Pediatr Neurol. 2013 Jul;49(1):50-3. doi: 10.1016/j.pediatrneurol.2013.03.008.

27.

Parents' interest in whole-genome sequencing of newborns.

Goldenberg AJ, Dodson DS, Davis MM, Tarini BA.

Genet Med. 2014 Jan;16(1):78-84. doi: 10.1038/gim.2013.76. Epub 2013 Jun 6.

28.

Effects of hypothetical type 2 diabetes genetic testing on parents' efforts to prevent diabetes in children.

Tarini BA, Herman WH, Lee JM.

Clin Pediatr (Phila). 2013 Sep;52(9):821-8. doi: 10.1177/0009922813488644. Epub 2013 May 14.

29.
30.

Influence of "GERD" label on parents' decision to medicate infants.

Scherer LD, Zikmund-Fisher BJ, Fagerlin A, Tarini BA.

Pediatrics. 2013 May;131(5):839-45. doi: 10.1542/peds.2012-3070. Epub 2013 Apr 1.

31.

A risk score for identifying overweight adolescents with dysglycemia in primary care settings.

Lee JM, Gebremariam A, Woolford SJ, Tarini BA, Valerio MA, Bashir S, Eason AJ, Choi PY, Gurney JG.

J Pediatr Endocrinol Metab. 2013;26(5-6):477-88. doi: 10.1515/jpem-2012-0259.

32.

Anticipating the arrival of low-penetrance genetic testing to primary care medicine.

Tarini BA, Exe N, Zikmund-Fisher BJ.

J Community Genet. 2013 Apr;4(2):285-8. doi: 10.1007/s12687-013-0139-z. Epub 2013 Feb 12.

33.

Blindness in Walnut Grove: how did Mary Ingalls lose her sight?

Allexan SS, Byington CL, Finkelstein JI, Tarini BA.

Pediatrics. 2013 Mar;131(3):404-6. doi: 10.1542/peds.2012-1438. Epub 2013 Feb 4. No abstract available.

34.

Ethical issues in neonatal and pediatric clinical trials.

Laventhal N, Tarini BA, Lantos J.

Pediatr Clin North Am. 2012 Oct;59(5):1205-20. doi: 10.1016/j.pcl.2012.07.007. Epub 2012 Aug 26. Review.

35.

Ethical issues with newborn screening in the genomics era.

Tarini BA, Goldenberg AJ.

Annu Rev Genomics Hum Genet. 2012;13:381-93. doi: 10.1146/annurev-genom-090711-163741. Epub 2012 May 1. Review.

36.

Decision analysis, economic evaluation, and newborn screening: challenges and opportunities.

Prosser LA, Grosse SD, Kemper AR, Tarini BA, Perrin JM.

Genet Med. 2013;14(8):703-712. doi: 10.1038/gim.2012.24. Epub 2012 Apr 5.

37.

Communicating with parents about newborn screening: the skill of eliciting unspoken emotions.

Tarini BA.

Arch Pediatr Adolesc Med. 2012 Jan;166(1):95-6. doi: 10.1001/archpediatrics.2011.767. No abstract available.

38.

A policy impact analysis of the mandatory NCAA sickle cell trait screening program.

Tarini BA, Brooks MA, Bundy DG.

Health Serv Res. 2012 Feb;47(1 Pt 2):446-61. doi: 10.1111/j.1475-6773.2011.01357.x. Epub 2011 Dec 8.

39.

False-positive newborn screening result and future health care use in a state Medicaid cohort.

Tarini BA, Clark SJ, Pilli S, Dombkowski KJ, Korzeniewski SJ, Gebremariam A, Eisenhandler J, Grigorescu V.

Pediatrics. 2011 Oct;128(4):715-22. doi: 10.1542/peds.2010-2448. Epub 2011 Sep 19.

40.

Commentary: Children and predictive genomic testing: disease prevention, research protection, and our future.

Tarini BA, Tercyak KP, Wilfond BS.

J Pediatr Psychol. 2011 Nov-Dec;36(10):1113-21. doi: 10.1093/jpepsy/jsr040. Epub 2011 Aug 4.

41.

Storage and use of residual newborn screening blood spots: a public policy emergency.

Tarini BA.

Genet Med. 2011 Jul;13(7):619-20. doi: 10.1097/GIM.0b013e31822176df. No abstract available.

42.

Genetic testing and youth sports.

Brooks MA, Tarini BA.

JAMA. 2011 Mar 9;305(10):1033-4. doi: 10.1001/jama.2011.286. No abstract available.

PMID:
21386082
43.

Parents' interest in predictive genetic testing for their children when a disease has no treatment.

Tarini BA, Singer D, Clark SJ, Davis MM.

Pediatrics. 2009 Sep;124(3):e432-8. doi: 10.1542/peds.2008-2389. Epub 2009 Aug 24.

PMID:
19706561
44.

Afraid in the hospital: parental concern for errors during a child's hospitalization.

Tarini BA, Lozano P, Christakis DA.

J Hosp Med. 2009 Nov;4(9):521-7. doi: 10.1002/jhm.508.

45.

Not without my permission: parents' willingness to permit use of newborn screening samples for research.

Tarini BA, Goldenberg A, Singer D, Clark SJ, Butchart A, Davis MM.

Public Health Genomics. 2010;13(3):125-30. doi: 10.1159/000228724. Epub 2009 Jul 11.

PMID:
19602864
46.

Neonatal sepsis: looking beyond the blood culture: evaluation of a study of universal primer polymerase chain reaction for identification of neonatal sepsis.

Decamp LR, Dempsey AF, Tarini BA.

Arch Pediatr Adolesc Med. 2009 Jan;163(1):12-4. doi: 10.1001/archpediatrics.2008.515. Review. No abstract available. Erratum in: Arch Pediatr Adolesc Med. 2009 Jan;163(1):348.

PMID:
19124697
47.

Parents' concern about their own and their children's genetic disease risk: potential effects of family history vs genetic test results.

Tarini BA, Singer D, Clark SJ, Davis MM.

Arch Pediatr Adolesc Med. 2008 Nov;162(11):1079-83. doi: 10.1001/archpedi.162.11.1079.

PMID:
18981357
48.

Waiving informed consent in newborn screening research: balancing social value and respect.

Tarini BA, Burke W, Scott CR, Wilfond BS.

Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):23-30. doi: 10.1002/ajmg.c.30164.

PMID:
18200521
49.

Toward family-centered inpatient medical care: the role of parents as participants in medical decisions.

Tarini BA, Christakis DA, Lozano P.

J Pediatr. 2007 Dec;151(6):690-5, 695.e1. Epub 2007 Sep 17.

PMID:
18035155
50.

The current revolution in newborn screening: new technology, old controversies.

Tarini BA.

Arch Pediatr Adolesc Med. 2007 Aug;161(8):767-72. Review.

PMID:
17679658

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