Shashi V - Search Results

1

Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.

Hart SJ, Schoch K, Shashi V, Callanan N. Hart SJ, et al. Among authors: shashi v. J Genet Couns. 2016 Feb;25(1):6-17. doi: 10.1007/s10897-015-9910-0. Epub 2015 Nov 18. J Genet Couns. 2016. PMID: 26578232

2

Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

Lewandowski KE, Shashi V, Berry PM, Kwapil TR. Lewandowski KE, et al. Among authors: shashi v. Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):27-36. doi: 10.1002/ajmg.b.30379. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17034021

3

Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.

Shashi V, Kwapil TR, Kaczorowski J, Berry MN, Santos CS, Howard TD, Goradia D, Prasad K, Vaibhav D, Rajarethinam R, Spence E, Keshavan MS. Shashi V, et al. Psychiatry Res. 2010 Jan 30;181(1):1-8. doi: 10.1016/j.pscychresns.2009.07.003. Psychiatry Res. 2010. PMID: 19962860 Free PMC article.

4

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Shashi V, Howard TD, Keshavan MS, Kaczorowski J, Berry MN, Schoch K, Spence EJ, Kwapil TR. Shashi V, et al. Psychiatry Res. 2010 Jul 30;178(2):433-6. doi: 10.1016/j.psychres.2010.04.048. Epub 2010 May 20. Psychiatry Res. 2010. PMID: 20488547 Free PMC article.

5

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. 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.

6

Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.

Veerapandiyan A, Chinn IK, Schoch K, Maloney KA, Shashi V. Veerapandiyan A, et al. Among authors: shashi v. Eur J Med Genet. 2011 Jan-Feb;54(1):63-6. doi: 10.1016/j.ejmg.2010.09.004. Epub 2010 Sep 29. Eur J Med Genet. 2011. PMID: 20887823

7

Pseudometabolic presentation of dystrophinopathy due to a missense mutation.

Veerapandiyan A, Shashi V, Jiang YH, Gallentine WB, Schoch K, Smith EC. Veerapandiyan A, et al. Among authors: shashi v. Muscle Nerve. 2010 Dec;42(6):975-9. doi: 10.1002/mus.21823. Muscle Nerve. 2010. PMID: 21104870 Free PMC article.

8

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: shashi v. 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.

9

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.

Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Veerapandiyan A, et al. Among authors: shashi v. Am J Med Genet A. 2011 Sep;155A(9):2186-95. doi: 10.1002/ajmg.a.34226. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834039

10

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

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