Sherr EH - Search Results

1

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. Sherr EH, et al. Neurology. 2005 Nov 8;65(9):1496-8. doi: 10.1212/01.wnl.0000183066.09239.b6. Neurology. 2005. PMID: 16275846

2

Periventricular heterotopia associated with chromosome 5p anomalies.

Sheen VL, Wheless JW, Bodell A, Braverman E, Cotter PD, Rauen KA, Glenn O, Weisiger K, Packman S, Walsh CA, Sherr EH. Sheen VL, et al. Among authors: sherr eh. Neurology. 2003 Mar 25;60(6):1033-6. doi: 10.1212/01.wnl.0000052689.03214.61. Neurology. 2003. PMID: 12654978

3

Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome.

Slavotinek A, Li C, Sherr EH, Chudley AE. Slavotinek A, et al. Among authors: sherr eh. Am J Med Genet A. 2006 Sep 15;140(18):1909-14. doi: 10.1002/ajmg.a.31399. Am J Med Genet A. 2006. PMID: 16894541

4

ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.

Marco EJ, Abidi FE, Bristow J, Dean WB, Cotter P, Jeremy RJ, Schwartz CE, Sherr EH. Marco EJ, et al. Among authors: sherr eh. J Med Genet. 2008 Feb;45(2):100-5. doi: 10.1136/jmg.2007.052324. Epub 2007 Sep 24. J Med Genet. 2008. PMID: 17893116

5

Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus.

Tang PH, Bartha AI, Norton ME, Barkovich AJ, Sherr EH, Glenn OA. Tang PH, et al. Among authors: sherr eh. AJNR Am J Neuroradiol. 2009 Feb;30(2):257-63. doi: 10.3174/ajnr.A1331. Epub 2008 Nov 6. AJNR Am J Neuroradiol. 2009. PMID: 18988682 Free PMC article.

6

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. Wahl M, et al. Among authors: sherr eh. AJNR Am J Neuroradiol. 2009 Feb;30(2):282-9. doi: 10.3174/ajnr.A1361. Epub 2008 Nov 11. AJNR Am J Neuroradiol. 2009. PMID: 19001538 Free PMC article.

7

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. Nakata Y, et al. Among authors: sherr eh. AJNR Am J Neuroradiol. 2009 Jun;30(6):1142-8. doi: 10.3174/ajnr.A1527. Epub 2009 Feb 26. AJNR Am J Neuroradiol. 2009. PMID: 19246528 Free PMC article.

8

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families.

Hanna RM, Marsh SE, Swistun D, Al-Gazali L, Zaki MS, Abdel-Salam GM, Al-Tawari A, Bastaki L, Kayserili H, Rajab A, Boglárka B, Dietrich RB, Dobyns WB, Truwit CL, Sattar S, Chuang NA, Sherr EH, Gleeson JG. Hanna RM, et al. Among authors: sherr eh. Neurology. 2011 Jan 25;76(4):373-82. doi: 10.1212/WNL.0b013e318208f492. Neurology. 2011. PMID: 21263138 Free PMC article.

9

ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.

Marco EJ, Abidi FE, Bristow J, Dean WB, Cotter P, Jeremy RJ, Schwartz CE, Sherr EH. Marco EJ, et al. Among authors: sherr eh. BMJ Case Rep. 2009;2009:bcr06.2009.1999. doi: 10.1136/bcr.06.2009.1999. Epub 2009 Jul 2. BMJ Case Rep. 2009. PMID: 21731583 Free PMC article.

10

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.

Hanson E, Bernier R, Porche K, Jackson FI, Goin-Kochel RP, Snyder LG, Snow AV, Wallace AS, Campe KL, Zhang Y, Chen Q, D'Angelo D, Moreno-De-Luca A, Orr PT, Boomer KB, Evans DW, Kanne S, Berry L, Miller FK, Olson J, Sherr E, Martin CL, Ledbetter DH, Spiro JE, Chung WK; Simons Variation in Individuals Project Consortium. Hanson E, et al. Biol Psychiatry. 2015 May 1;77(9):785-93. doi: 10.1016/j.biopsych.2014.04.021. Epub 2014 Jun 16. Biol Psychiatry. 2015. PMID: 25064419 Free PMC article.

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