Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 17

1.

Aberrant white matter microstructure in children with 16p11.2 deletions.

Owen JP, Chang YS, Pojman NJ, Bukshpun P, Wakahiro ML, Marco EJ, Berman JI, Spiro JE, Chung WK, Buckner RL, Roberts TP, Nagarajan SS, Sherr EH, Mukherjee P; Simons VIP Consortium.

J Neurosci. 2014 Apr 30;34(18):6214-23. doi: 10.1523/JNEUROSCI.4495-13.2014.

PMID:
24790192
[PubMed - indexed for MEDLINE]
2.

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

Sajan SA, Fernandez L, Nieh SE, Rider E, Bukshpun P, Wakahiro M, Christian SL, Rivière JB, Sullivan CT, Sudi J, Herriges MJ, Paciorkowski AR, Barkovich AJ, Glessner JT, Millen KJ, Hakonarson H, Dobyns WB, Sherr EH.

PLoS Genet. 2013;9(10):e1003823. doi: 10.1371/journal.pgen.1003823. Epub 2013 Oct 3.

PMID:
24098143
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Resting-state networks and the functional connectome of the human brain in agenesis of the corpus callosum.

Owen JP, Li YO, Yang FG, Shetty C, Bukshpun P, Vora S, Wakahiro M, Hinkley LB, Nagarajan SS, Sherr EH, Mukherjee P.

Brain Connect. 2013;3(6):547-62. doi: 10.1089/brain.2013.0175. Epub 2013 Nov 16.

PMID:
24063289
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Test-retest reliability of computational network measurements derived from the structural connectome of the human brain.

Owen JP, Ziv E, Bukshpun P, Pojman N, Wakahiro M, Berman JI, Roberts TP, Friedman EJ, Sherr EH, Mukherjee P.

Brain Connect. 2013;3(2):160-76. doi: 10.1089/brain.2012.0121. Erratum in: Brain Connect. 2013;3(3):316.

PMID:
23350832
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

The structural connectome of the human brain in agenesis of the corpus callosum.

Owen JP, Li YO, Ziv E, Strominger Z, Gold J, Bukhpun P, Wakahiro M, Friedman EJ, Sherr EH, Mukherjee P.

Neuroimage. 2013 Apr 15;70:340-55. doi: 10.1016/j.neuroimage.2012.12.031. Epub 2012 Dec 23.

PMID:
23268782
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

Zufferey F, Sherr EH, Beckmann ND, Hanson E, Maillard AM, Hippolyte L, Macé A, Ferrari C, Kutalik Z, Andrieux J, Aylward E, Barker M, Bernier R, Bouquillon S, Conus P, Delobel B, Faucett WA, Goin-Kochel RP, Grant E, Harewood L, Hunter JV, Lebon S, Ledbetter DH, Martin CL, Männik K, Martinet D, Mukherjee P, Ramocki MB, Spence SJ, Steinman KJ, Tjernagel J, Spiro JE, Reymond A, Beckmann JS, Chung WK, Jacquemont S; Simons VIP Consortium; 16p11.2 European Consortium.

J Med Genet. 2012 Oct;49(10):660-8. doi: 10.1136/jmedgenet-2012-101203. Erratum in: J Med Genet. 2014 Jul;51(7):478.

PMID:
23054248
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Autism traits in individuals with agenesis of the corpus callosum.

Lau YC, Hinkley LB, Bukshpun P, Strominger ZA, Wakahiro ML, Baron-Cohen S, Allison C, Auyeung B, Jeremy RJ, Nagarajan SS, Sherr EH, Marco EJ.

J Autism Dev Disord. 2013 May;43(5):1106-18. doi: 10.1007/s10803-012-1653-2.

PMID:
23054201
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

The role of corpus callosum development in functional connectivity and cognitive processing.

Hinkley LB, Marco EJ, Findlay AM, Honma S, Jeremy RJ, Strominger Z, Bukshpun P, Wakahiro M, Brown WS, Paul LK, Barkovich AJ, Mukherjee P, Nagarajan SS, Sherr EH.

PLoS One. 2012;7(8):e39804. doi: 10.1371/journal.pone.0039804. Epub 2012 Aug 3.

PMID:
22870191
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.

Simons Vip Consortium.

Neuron. 2012 Mar 22;73(6):1063-7. doi: 10.1016/j.neuron.2012.02.014. Epub 2012 Mar 21.

PMID:
22445335
[PubMed - indexed for MEDLINE]
Free Article
10.

Laterality of brain and ocular lesions in Aicardi syndrome.

Cabrera MT, Winn BJ, Porco T, Strominger Z, Barkovich AJ, Hoyt CS, Wakahiro M, Sherr EH.

Pediatr Neurol. 2011 Sep;45(3):149-54. doi: 10.1016/j.pediatrneurol.2011.04.007.

PMID:
21824560
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

Osbun N, Li J, O'Driscoll MC, Strominger Z, Wakahiro M, Rider E, Bukshpun P, Boland E, Spurrell CH, Schackwitz W, Pennacchio LA, Dobyns WB, Black GC, Sherr EH.

Am J Med Genet A. 2011 Aug;155A(8):1865-76. doi: 10.1002/ajmg.a.34081. Epub 2011 Jul 7.

PMID:
21739582
[PubMed - indexed for MEDLINE]
12.

Diffusion tensor imaging of Aicardi syndrome.

Wahl M, Strominger ZA, Wakahiro M, Jeremy RJ, Mukherjee P, Sherr EH.

Pediatr Neurol. 2010 Aug;43(2):87-91. doi: 10.1016/j.pediatrneurol.2010.03.005.

PMID:
20610117
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Diffusion abnormalities and reduced volume of the ventral cingulum bundle in agenesis of the corpus callosum: a 3T imaging study.

Nakata Y, Barkovich AJ, Wahl M, Strominger Z, Jeremy RJ, Wakahiro M, Mukherjee P, Sherr EH.

AJNR Am J Neuroradiol. 2009 Jun;30(6):1142-8. doi: 10.3174/ajnr.A1527. Epub 2009 Feb 26.

PMID:
19246528
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Variability of homotopic and heterotopic callosal connectivity in partial agenesis of the corpus callosum: a 3T diffusion tensor imaging and Q-ball tractography study.

Wahl M, Strominger Z, Jeremy RJ, Barkovich AJ, Wakahiro M, Sherr EH, Mukherjee P.

AJNR Am J Neuroradiol. 2009 Feb;30(2):282-9. doi: 10.3174/ajnr.A1361. Epub 2008 Nov 11.

PMID:
19001538
[PubMed - indexed for MEDLINE]
Free Article
15.

Agenesis of the corpus callosum, optic coloboma, intractable seizures, craniofacial and skeletal dysmorphisms: an autosomal recessive disorder similar to Temtamy syndrome.

Li J, Shivakumar S, Wakahiro M, Mukherjee P, Barkovich AJ, Slavotinek A, Sherr EH.

Am J Med Genet A. 2007 Aug 15;143A(16):1900-5.

PMID:
17632789
[PubMed - indexed for MEDLINE]
16.

Online support groups for Parkinson's patients: a pilot study of effectiveness.

Lieberman MA, Winzelberg A, Golant M, Wakahiro M, DiMinno M, Aminoff M, Christine C.

Soc Work Health Care. 2005;42(2):23-38.

PMID:
16390834
[PubMed - indexed for MEDLINE]
17.

Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.

Sherr EH, Owen R, Albertson DG, Pinkel D, Cotter PD, Slavotinek AM, Hetts SW, Jeremy RJ, Schilmoeller G, Schilmoeller K, Wakahiro M, Barkovich AJ.

Neurology. 2005 Nov 8;65(9):1496-8.

PMID:
16275846
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk