Scherer SW - Search Results

1

A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.

Zarrei M, Merico D, Kellam B, Engchuan W, Scriver T, Jokhan R, Wilson MD, Parr J, Lemire EG, Stavropoulos DJ, Scherer SW. Zarrei M, et al. Among authors: scherer sw. Am J Med Genet A. 2017 May;173(5):1287-1293. doi: 10.1002/ajmg.a.38176. Epub 2017 Apr 3. Am J Med Genet A. 2017. PMID: 28371330

2

Genetic analysis of patients with the Saethre-Chotzen phenotype.

Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I. Chun K, et al. Among authors: scherer sw. Am J Med Genet. 2002 Jun 15;110(2):136-43. doi: 10.1002/ajmg.10400. Am J Med Genet. 2002. PMID: 12116251

3

Recent segmental and gene duplications in the mouse genome.

Cheung J, Wilson MD, Zhang J, Khaja R, MacDonald JR, Heng HH, Koop BF, Scherer SW. Cheung J, et al. Among authors: scherer sw. Genome Biol. 2003;4(8):R47. doi: 10.1186/gb-2003-4-8-r47. Epub 2003 Jul 9. Genome Biol. 2003. PMID: 12914656 Free PMC article.

4

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW. Zeesman S, et al. Among authors: scherer sw. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. Am J Med Genet A. 2006. PMID: 16470794

5

Comparative analysis of the paired immunoglobulin-like receptor (PILR) locus in six mammalian genomes: duplication, conversion, and the birth of new genes.

Wilson MD, Cheung J, Martindale DW, Scherer SW, Koop BF. Wilson MD, et al. Among authors: scherer sw. Physiol Genomics. 2006 Nov 27;27(3):201-18. doi: 10.1152/physiolgenomics.00284.2005. Epub 2006 Aug 22. Physiol Genomics. 2006. PMID: 16926269 Free article.

6

Contribution of SHANK3 mutations to autism spectrum disorder.

Moessner R, Marshall CR, Sutcliffe JS, Skaug J, Pinto D, Vincent J, Zwaigenbaum L, Fernandez B, Roberts W, Szatmari P, Scherer SW. Moessner R, et al. Among authors: scherer sw. Am J Hum Genet. 2007 Dec;81(6):1289-97. doi: 10.1086/522590. Epub 2007 Oct 16. Am J Hum Genet. 2007. PMID: 17999366 Free PMC article.

7

The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptoms.

Tam E, Young EJ, Morris CA, Marshall CR, Loo W, Scherer SW, Mervis CB, Osborne LR. Tam E, et al. Among authors: scherer sw. Am J Med Genet A. 2008 Jul 15;146A(14):1797-806. doi: 10.1002/ajmg.a.32360. Am J Med Genet A. 2008. PMID: 18553513 Free PMC article.

8

Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Liu XQ, Paterson AD, Szatmari P; Autism Genome Project Consortium. Liu XQ, et al. Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16. Biol Psychiatry. 2008. PMID: 18632090 Free PMC article.

9

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.

Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW. Fernandez BA, et al. Among authors: scherer sw. J Med Genet. 2010 Mar;47(3):195-203. doi: 10.1136/jmg.2009.069369. Epub 2009 Sep 15. J Med Genet. 2010. PMID: 19755429

10

Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndrome.

Horike S, Ferreira JC, Meguro-Horike M, Choufani S, Smith AC, Shuman C, Meschino W, Chitayat D, Zackai E, Scherer SW, Weksberg R. Horike S, et al. Among authors: scherer sw. Am J Med Genet A. 2009 Nov;149A(11):2415-23. doi: 10.1002/ajmg.a.33065. Am J Med Genet A. 2009. PMID: 19876907

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