Bearden CE - Search Results

1

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.

Simon TJ, Bearden CE, Mc-Ginn DM, Zackai E. Simon TJ, et al. Among authors: bearden ce. Cortex. 2005 Apr;41(2):145-55. doi: 10.1016/s0010-9452(08)70889-x. Cortex. 2005. PMID: 15714897 Free PMC article. Clinical Trial.

2

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

Bearden CE, Woodin MF, Wang PP, Moss E, McDonald-McGinn D, Zackai E, Emannuel B, Cannon TD. Bearden CE, et al. J Clin Exp Neuropsychol. 2001 Aug;23(4):447-64. doi: 10.1076/jcen.23.4.447.1228. J Clin Exp Neuropsychol. 2001. PMID: 11780945

3

Williams syndrome cognitive profile also characterizes Velocardiofacial/DiGeorge syndrome.

Bearden CE, Wang PP, Simon TJ. Bearden CE, et al. Am J Med Genet. 2002 Aug 8;114(6):689-92. doi: 10.1002/ajmg.10539. Am J Med Genet. 2002. PMID: 12210289 No abstract available.

4

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

Bearden CE, Jawad AF, Lynch DR, Sokol S, Kanes SJ, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Am J Psychiatry. 2004 Sep;161(9):1700-2. doi: 10.1176/appi.ajp.161.9.1700. Am J Psychiatry. 2004. PMID: 15337663

5

Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms.

Bearden CE, van Erp TG, Monterosso JR, Simon TJ, Glahn DC, Saleh PA, Hill NM, McDonald-McGinn DM, Zackai E, Emanuel BS, Cannon TD. Bearden CE, et al. Neurocase. 2004 Jun;10(3):198-206. doi: 10.1080/13554790490495519. Neurocase. 2004. PMID: 15788257

6

Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.

Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Child Neuropsychol. 2005 Feb;11(1):109-17. doi: 10.1080/09297040590911239. Child Neuropsychol. 2005. PMID: 15846854 Free PMC article.

7

A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.

Simon TJ, Bish JP, Bearden CE, Ding L, Ferrante S, Nguyen V, Gee JC, McDonald-McGinn DM, Zackai EH, Emanuel BS. Simon TJ, et al. Among authors: bearden ce. Dev Psychopathol. 2005 Summer;17(3):753-84. doi: 10.1017/S0954579405050364. Dev Psychopathol. 2005. PMID: 16262991 Free PMC article. Review.

8

Mapping cortical thickness in children with 22q11.2 deletions.

Bearden CE, van Erp TG, Dutton RA, Tran H, Zimmermann L, Sun D, Geaga JA, Simon TJ, Glahn DC, Cannon TD, Emanuel BS, Toga AW, Thompson PM. Bearden CE, et al. Cereb Cortex. 2007 Aug;17(8):1889-98. doi: 10.1093/cercor/bhl097. Epub 2006 Oct 20. Cereb Cortex. 2007. PMID: 17056649 Free PMC article.

9

Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.

Bearden CE, van Erp TG, Dutton RA, Lee AD, Simon TJ, Cannon TD, Emanuel BS, McDonald-McGinn D, Zackai EH, Thompson PM. Bearden CE, et al. Cereb Cortex. 2009 Jan;19(1):115-26. doi: 10.1093/cercor/bhn064. Epub 2008 May 14. Cereb Cortex. 2009. PMID: 18483006 Free PMC article.

10

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.

Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, Olesen C, Skovby F, Werge TM, Templin L, Busa T, Philip N, Swillen A, Vermeesch JR, Devriendt K, Schneider M, Dahoun S, Eliez S, Schoch K, Hooper SR, Shashi V, Samanich J, Marion R, van Amelsvoort T, Boot E, Klaassen P, Duijff SN, Vorstman J, Yuen T, Silversides C, Chow E, Bassett A, Frisch A, Weizman A, Gothelf D, Niarchou M, van den Bree M, Owen MJ, Suñer DH, Andreo JR, Armando M, Vicari S, Digilio MC, Auton A, Kates WR, Wang T, Shprintzen RJ, Emanuel BS, Morrow BE. Delio M, et al. Among authors: bearden ce. Am J Hum Genet. 2013 Mar 7;92(3):439-47. doi: 10.1016/j.ajhg.2013.01.018. Epub 2013 Feb 28. Am J Hum Genet. 2013. PMID: 23453669 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

437 results

Search Page

Filters