Bassett AS - Search Results

1

Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot.

Reuter MS, Jobling R, Chaturvedi RR, Manshaei R, Costain G, Heung T, Curtis M, Hosseini SM, Liston E, Lowther C, Oechslin E, Sticht H, Thiruvahindrapuram B, Mil SV, Wald RM, Walker S, Marshall CR, Silversides CK, Scherer SW, Kim RH, Bassett AS. Reuter MS, et al. Among authors: bassett as. Genet Med. 2019 Apr;21(4):1001-1007. doi: 10.1038/s41436-018-0260-9. Epub 2018 Sep 20. Genet Med. 2019. PMID: 30232381 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

Premature death in adults with 22q11.2 deletion syndrome.

Bassett AS, Chow EW, Husted J, Hodgkinson KA, Oechslin E, Harris L, Silversides C. Bassett AS, et al. J Med Genet. 2009 May;46(5):324-30. doi: 10.1136/jmg.2008.063800. Epub 2009 Feb 25. J Med Genet. 2009. PMID: 19246480 Free PMC article.

4

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.

5

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.

6

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.

7

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.

8

Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot.

Piran S, Bassett AS, Grewal J, Swaby JA, Morel C, Oechslin EN, Redington AN, Liu PP, Silversides CK. Piran S, et al. Among authors: bassett as. Am Heart J. 2011 Jan;161(1):131-7. doi: 10.1016/j.ahj.2010.09.015. Am Heart J. 2011. PMID: 21167345 Free PMC article.

9

Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome.

Swaby JA, Silversides CK, Bekeschus SC, Piran S, Oechslin EN, Chow EW, Bassett AS. Swaby JA, et al. Among authors: bassett as. Am J Cardiol. 2011 Feb 1;107(3):466-71. doi: 10.1016/j.amjcard.2010.09.045. Am J Cardiol. 2011. PMID: 21257016 Free PMC article.

10

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.

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