Shashi V - Search Results

1

Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.

Zhao Y, Diacou A, Johnston HR, Musfee FI, McDonald-McGinn DM, McGinn D, Crowley TB, Repetto GM, Swillen A, Breckpot J, Vermeesch JR, Kates WR, Digilio MC, Unolt M, Marino B, Pontillo M, Armando M, Di Fabio F, Vicari S, van den Bree M, Moss H, Owen MJ, Murphy KC, Murphy CM, Murphy D, Schoch K, Shashi V, Tassone F, Simon TJ, Shprintzen RJ, Campbell L, Philip N, Heine-Suñer D, García-Miñaúr S, Fernández L; International 22q11.2 Brain and Behavior Consortium; Bearden CE, Vingerhoets C, van Amelsvoort T, Eliez S, Schneider M, Vorstman JAS, Gothelf D, Zackai E, Agopian AJ, Gur RE, Bassett AS, Emanuel BS, Goldmuntz E, Mitchell LE, Wang T, Morrow BE. Zhao Y, et al. Among authors: shashi v. Am J Hum Genet. 2020 Jan 2;106(1):26-40. doi: 10.1016/j.ajhg.2019.11.010. Epub 2019 Dec 20. Am J Hum Genet. 2020. PMID: 31870554 Free PMC article.

2

Choanal atresia in a patient with the deletion (9p) syndrome.

Shashi V, Golden WL, Fryburg JS. Shashi V, et al. Am J Med Genet. 1994 Jan 1;49(1):88-90. doi: 10.1002/ajmg.1320490116. Am J Med Genet. 1994. PMID: 8172257 Review.

3

Vasomotor instability in neonates with chromosome 22q11 deletion syndrome.

Shashi V, Berry MN, Hines MH. Shashi V, et al. Am J Med Genet A. 2003 Sep 1;121A(3):231-4. doi: 10.1002/ajmg.a.20219. Am J Med Genet A. 2003. PMID: 12923863

4

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.

Shashi V, Keshavan MS, Howard TD, Berry MN, Basehore MJ, Lewandowski E, Kwapil TR. Shashi V, et al. Clin Genet. 2006 Mar;69(3):234-8. doi: 10.1111/j.1399-0004.2006.00569.x. Clin Genet. 2006. PMID: 16542388

5

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.

6

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.

7

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

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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