Bassett AS - Search Results

1

Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.

Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams SG, Keavney BD, Thiruvahindrapuram B, Scherer SW, Bassett AS. Reuter MS, et al. Among authors: bassett as. Circ Genom Precis Med. 2021 Aug;14(4):e003410. doi: 10.1161/CIRCGEN.121.003410. Epub 2021 Jul 30. Circ Genom Precis Med. 2021. PMID: 34328347 Free PMC article. Clinical Trial.

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

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.

7

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.

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

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.

Silversides CK, Lionel AC, Costain G, Merico D, Migita O, Liu B, Yuen T, Rickaby J, Thiruvahindrapuram B, Marshall CR, Scherer SW, Bassett AS. Silversides CK, et al. Among authors: bassett as. PLoS Genet. 2012;8(8):e1002843. doi: 10.1371/journal.pgen.1002843. Epub 2012 Aug 9. PLoS Genet. 2012. PMID: 22912587 Free PMC article.

10

1q21.1 Microduplication expression in adults.

Dolcetti A, Silversides CK, Marshall CR, Lionel AC, Stavropoulos DJ, Scherer SW, Bassett AS. Dolcetti A, et al. Among authors: bassett as. Genet Med. 2013 Apr;15(4):282-9. doi: 10.1038/gim.2012.129. Epub 2012 Sep 27. Genet Med. 2013. PMID: 23018752 Free PMC article. Review.

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