Bassett AS - Search Results

1

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, Scherer SW. Costain G, et al. Among authors: bassett as. J Neurodev Disord. 2019 Feb 7;11(1):3. doi: 10.1186/s11689-019-9263-3. J Neurodev Disord. 2019. PMID: 30732576 Free PMC article.

2

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.

Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW. Bassett AS, et al. Hum Mol Genet. 2008 Dec 15;17(24):4045-53. doi: 10.1093/hmg/ddn307. Epub 2008 Sep 20. Hum Mol Genet. 2008. PMID: 18806272 Free PMC article.

3

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Bassett AS, Scherer SW, Brzustowicz LM. Bassett AS, et al. Am J Psychiatry. 2010 Aug;167(8):899-914. doi: 10.1176/appi.ajp.2009.09071016. Epub 2010 May 3. Am J Psychiatry. 2010. PMID: 20439386 Free PMC article. Review.

4

13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.

Costain G, Silversides CK, Marshall CR, Shago M, Costain N, Bassett AS. Costain G, et al. Among authors: bassett as. Int J Cardiol. 2011 Jan 21;146(2):134-9. doi: 10.1016/j.ijcard.2010.05.070. Epub 2010 Jul 3. Int J Cardiol. 2011. PMID: 20598760 Free PMC article. Review.

5

Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report.

Costain G, Ho A, Crawley AP, Mikulis DJ, Brzustowicz LM, Chow EW, Bassett AS. Costain G, et al. Among authors: bassett as. Schizophr Res. 2010 Sep;122(1-3):81-4. doi: 10.1016/j.schres.2010.06.014. Epub 2010 Jul 16. Schizophr Res. 2010. PMID: 20638248 Free PMC article.

6

Clinically detectable copy number variations in a Canadian catchment population of schizophrenia.

Bassett AS, Costain G, Fung WL, Russell KJ, Pierce L, Kapadia R, Carter RF, Chow EW, Forsythe PJ. Bassett AS, et al. J Psychiatr Res. 2010 Nov;44(15):1005-9. doi: 10.1016/j.jpsychires.2010.06.013. J Psychiatr Res. 2010. PMID: 20643418 Free PMC article.

7

Practical guidelines for managing patients with 22q11.2 deletion syndrome.

Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.

8

Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions.

Costain G, Chow EW, Silversides CK, Bassett AS. Costain G, et al. Among authors: bassett as. J Med Genet. 2011 Dec;48(12):819-24. doi: 10.1136/jmedgenet-2011-100440. Epub 2011 Nov 2. J Med Genet. 2011. PMID: 22051516 Free article.

9

Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome.

Costain G, Chow EW, Ray PN, Bassett AS. Costain G, et al. Among authors: bassett as. J Intellect Disabil Res. 2012 Jun;56(6):641-51. doi: 10.1111/j.1365-2788.2011.01510.x. Epub 2011 Dec 6. J Intellect Disabil Res. 2012. PMID: 22142442 Free PMC article.

10

Functional outcomes of adults with 22q11.2 deletion syndrome.

Butcher NJ, Chow EW, Costain G, Karas D, Ho A, Bassett AS. Butcher NJ, et al. Among authors: bassett as. Genet Med. 2012 Oct;14(10):836-43. doi: 10.1038/gim.2012.66. Epub 2012 Jun 28. Genet Med. 2012. PMID: 22744446 Free PMC article.

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