Wheeler AC - Search Results

1

Food and Non-Food-Related Behavior across Settings in Children with Prader-Willi Syndrome.

Gantz MG, Andrews SM, Wheeler AC. Gantz MG, et al. Among authors: wheeler ac. Genes (Basel). 2020 Feb 17;11(2):204. doi: 10.3390/genes11020204. Genes (Basel). 2020. PMID: 32079283 Free PMC article.

2

"Just tell me what's going on": The views of parents of children with genetic conditions regarding the research use of their child's electronic health record.

Andrews SM, Raspa M, Edwards A, Moultrie R, Turner-Brown L, Wagner L, Alvarez Rivas A, Frisch MK, Wheeler AC. Andrews SM, et al. Among authors: wheeler ac. J Am Med Inform Assoc. 2020 Mar 1;27(3):429-436. doi: 10.1093/jamia/ocz208. J Am Med Inform Assoc. 2020. PMID: 31913479 Free PMC article.

3

Preferences for the research use of electronic health records among young adults with fragile X syndrome or autism spectrum disorder.

Wagner L, Frisch M, Turner-Brown L, Andrews S, Edwards A, Moultrie R, Alvarez Rivas A, Wheeler A, Raspa M. Wagner L, et al. Disabil Health J. 2020 Oct;13(4):100927. doi: 10.1016/j.dhjo.2020.100927. Epub 2020 Apr 8. Disabil Health J. 2020. PMID: 32360031 Free PMC article.

4

Ethical, Legal, and Social Issues Related to the Inclusion of Individuals With Intellectual Disabilities in Electronic Health Record Research: Scoping Review.

Raspa M, Moultrie R, Wagner L, Edwards A, Andrews S, Frisch MK, Turner-Brown L, Wheeler A. Raspa M, et al. J Med Internet Res. 2020 May 21;22(5):e16734. doi: 10.2196/16734. J Med Internet Res. 2020. PMID: 32436848 Free PMC article. Review.

5

Preferences for Accessing Electronic Health Records for Research Purposes: Views of Parents Who Have a Child With a Known or Suspected Genetic Condition.

Raspa M, Paquin RS, Brown DS, Andrews S, Edwards A, Moultrie R, Wagner L, Frisch M, Turner-Brown L, Wheeler AC. Raspa M, et al. Among authors: wheeler ac. Value Health. 2020 Dec;23(12):1639-1652. doi: 10.1016/j.jval.2020.06.016. Epub 2020 Oct 26. Value Health. 2020. PMID: 33248520 Free PMC article.

6

Age of diagnosis for children with chromosome 15q syndromes.

Wheeler AC, Gantz MG, Cope H, Strong TV, Bohonowych JE, Moore A, Vogel-Farley V. Wheeler AC, et al. J Neurodev Disord. 2023 Nov 7;15(1):37. doi: 10.1186/s11689-023-09504-x. J Neurodev Disord. 2023. PMID: 37936142 Free PMC article.

7

Autism Symptoms Across Adulthood in Men with Fragile X Syndrome: A Cross-Sectional Analysis.

Hartley SL, Wheeler AC, Mailick MR, Raspa M, Mihaila I, Bishop E, Bailey DB. Hartley SL, et al. Among authors: wheeler ac. J Autism Dev Disord. 2015 Nov;45(11):3668-79. doi: 10.1007/s10803-015-2513-7. J Autism Dev Disord. 2015. PMID: 26123010 Free PMC article.

8

Family Communication and Cascade Testing for Fragile X Syndrome.

Raspa M, Edwards A, Wheeler AC, Bishop E, Bailey DB Jr. Raspa M, et al. Among authors: wheeler ac. J Genet Couns. 2016 Oct;25(5):1075-84. doi: 10.1007/s10897-016-9940-2. Epub 2016 Mar 9. J Genet Couns. 2016. PMID: 26961978

9

Mobile technology use and skills among individuals with fragile X syndrome: implications for healthcare decision making.

Raspa M, Fitzgerald T, Furberg RD, Wylie A, Moultrie R, DeRamus M, Wheeler AC, McCormack L. Raspa M, et al. Among authors: wheeler ac. J Intellect Disabil Res. 2018 Oct;62(10):821-832. doi: 10.1111/jir.12537. Epub 2018 Aug 13. J Intellect Disabil Res. 2018. PMID: 30105880 Free PMC article.

10

A Description of the Educational Setting Among Individuals With Fragile X Syndrome.

Nash R, Riley C, Paramsothy P, Gilbertson K, Raspa M, Wheeler A, Dziuban EJ, Peacock G. Nash R, et al. Am J Intellect Dev Disabil. 2019 Jan;124(1):57-76. doi: 10.1352/1944-7558-124.1.57. Am J Intellect Dev Disabil. 2019. PMID: 30715925 Free PMC article.

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