Hooper SR - Search Results

1

Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.

Allen TM, Hersh J, Schoch K, Curtiss K, Hooper SR, Shashi V. Allen TM, et al. Among authors: hooper sr. J Intellect Disabil Res. 2014 Jan;58(1):31-47. doi: 10.1111/jir.12054. Epub 2013 Jun 7. J Intellect Disabil Res. 2014. PMID: 23742203 Free PMC article.

2

Behavioural equivalents of anxiety in children with fragile X syndrome: parent and teacher report.

Sullivan K, Hooper S, Hatton D. Sullivan K, et al. J Intellect Disabil Res. 2007 Jan;51(Pt 1):54-65. doi: 10.1111/j.1365-2788.2006.00899.x. J Intellect Disabil Res. 2007. PMID: 17181603

3

Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.

Shashi V, Keshavan M, Kaczorowski J, Schoch K, Lewandowski KE, McConkie-Rosell A, Hooper SR, Kwapil TR. Shashi V, et al. Among authors: hooper sr. J Genet Couns. 2010 Oct;19(5):535-44. doi: 10.1007/s10897-010-9309-x. Epub 2010 Aug 3. J Genet Couns. 2010. PMID: 20680421 Free PMC article.

4

Discordance in Diagnoses and Treatment of Psychiatric Disorders in Children and Adolescents with 22q11.2 Deletion Syndrome.

Young AS, Shashi V, Schoch K, Kwapil T, Hooper SR. Young AS, et al. Among authors: hooper sr. Asian J Psychiatr. 2011 Jun 1;4(2):119-124. doi: 10.1016/j.ajp.2011.03.002. Asian J Psychiatr. 2011. PMID: 21743818 Free PMC article.

5

Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions.

Shashi V, Veerapandiyan A, Schoch K, Kwapil T, Keshavan M, Ip E, Hooper S. Shashi V, et al. J Intellect Disabil Res. 2012 Sep;56(9):865-78. doi: 10.1111/j.1365-2788.2011.01477.x. Epub 2011 Aug 31. J Intellect Disabil Res. 2012. PMID: 21883601

6

Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.

Schoch K, Harrell W, Hooper SR, Ip EH, Saldana S, Kwapil TR, Shashi V. Schoch K, et al. Among authors: hooper sr. J Learn Disabil. 2014 Mar-Apr;47(2):153-66. doi: 10.1177/0022219412443556. Epub 2012 May 9. J Learn Disabil. 2014. PMID: 22572413 Free PMC article.

7

Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study.

Shashi V, Veerapandiyan A, Keshavan MS, Zapadka M, Schoch K, Kwapil TR, Hooper SR, Stanley JA. Shashi V, et al. Among authors: hooper sr. Biol Psychiatry. 2012 Oct 15;72(8):684-91. doi: 10.1016/j.biopsych.2012.04.023. Epub 2012 May 25. Biol Psychiatry. 2012. PMID: 22633947 Free PMC article.

8

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.

Shashi V, Francis A, Hooper SR, Kranz PG, Zapadka M, Schoch K, Ip E, Tandon N, Howard TD, Keshavan MS. Shashi V, et al. Among authors: hooper sr. Eur J Hum Genet. 2012 Oct;20(10):1051-7. doi: 10.1038/ejhg.2012.138. Epub 2012 Jun 27. Eur J Hum Genet. 2012. PMID: 22763378 Free PMC article.

9

Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome.

Das Chakraborty R, Bernal AJ, Schoch K, Howard TD, Ip EH, Hooper SR, Keshavan MS, Jirtle RL, Shashi V. Das Chakraborty R, et al. Among authors: hooper sr. Transl Psychiatry. 2012 Apr 24;2(4):e105. doi: 10.1038/tp.2012.31. Transl Psychiatry. 2012. PMID: 22832905 Free PMC article.

10

Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.

Faux D, Schoch K, Eubanks S, Hooper SR, Shashi V. Faux D, et al. Among authors: hooper sr. J Genet Couns. 2012 Dec;21(6):835-44. doi: 10.1007/s10897-012-9535-5. Epub 2012 Aug 31. J Genet Couns. 2012. PMID: 22936417 Free PMC article.

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