Sherr EH - Search Results

1

Agenesis of the corpus callosum in California 1983-2003: a population-based study.

Glass HC, Shaw GM, Ma C, Sherr EH. Glass HC, et al. Among authors: sherr eh. Am J Med Genet A. 2008 Oct 1;146A(19):2495-500. doi: 10.1002/ajmg.a.32418. Am J Med Genet A. 2008. PMID: 18642362 Free PMC article.

2

Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations.

Hetts SW, Sherr EH, Chao S, Gobuty S, Barkovich AJ. Hetts SW, et al. Among authors: sherr eh. AJR Am J Roentgenol. 2006 Nov;187(5):1343-8. doi: 10.2214/AJR.05.0146. AJR Am J Roentgenol. 2006. PMID: 17056927

3

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.

Paul LK, Brown WS, Adolphs R, Tyszka JM, Richards LJ, Mukherjee P, Sherr EH. Paul LK, et al. Among authors: sherr eh. Nat Rev Neurosci. 2007 Apr;8(4):287-99. doi: 10.1038/nrn2107. Nat Rev Neurosci. 2007. PMID: 17375041 Free article. Review.

4

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. Li J, et al. Among authors: sherr eh. Am J Med Genet A. 2007 Aug 15;143A(16):1900-5. doi: 10.1002/ajmg.a.31855. Am J Med Genet A. 2007. PMID: 17632789

5

Clinical Reasoning: An encephalopathic 3-day-old infant.

Gelfand AA, Sznewajs A, Glass HC, Jelin AC, Sherr EH. Gelfand AA, et al. Among authors: sherr eh. Neurology. 2011 Jul 5;77(1):e1-5. doi: 10.1212/WNL.0b013e3182231407. Neurology. 2011. PMID: 21727263 Free PMC article. No abstract available.

6

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. Osbun N, et al. Among authors: sherr eh. Am J Med Genet A. 2011 Aug;155A(8):1865-76. doi: 10.1002/ajmg.a.34081. Epub 2011 Jul 7. Am J Med Genet A. 2011. PMID: 21739582 Free PMC article.

7

VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.

Slavotinek AM, Chao R, Vacik T, Yahyavi M, Abouzeid H, Bardakjian T, Schneider A, Shaw G, Sherr EH, Lemke G, Youssef M, Schorderet DF. Slavotinek AM, et al. Among authors: sherr eh. Hum Mutat. 2012 Feb;33(2):364-8. doi: 10.1002/humu.21658. Epub 2011 Dec 27. Hum Mutat. 2012. PMID: 22095910 Free PMC article.

8

Processing speed delays contribute to executive function deficits in individuals with agenesis of the corpus callosum.

Marco EJ, Harrell KM, Brown WS, Hill SS, Jeremy RJ, Kramer JH, Sherr EH, Paul LK. Marco EJ, et al. Among authors: sherr eh. J Int Neuropsychol Soc. 2012 May;18(3):521-9. doi: 10.1017/S1355617712000045. Epub 2012 Mar 6. J Int Neuropsychol Soc. 2012. PMID: 22390821 Free PMC article.

9

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. Hinkley LB, et al. Among authors: sherr eh. PLoS One. 2012;7(8):e39804. doi: 10.1371/journal.pone.0039804. Epub 2012 Aug 3. PLoS One. 2012. PMID: 22870191 Free PMC article. Clinical Trial.

10

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. Lau YC, et al. Among authors: sherr eh. J Autism Dev Disord. 2013 May;43(5):1106-18. doi: 10.1007/s10803-012-1653-2. J Autism Dev Disord. 2013. PMID: 23054201 Free PMC article.

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