Similar articles for PMID: 19246480

Year	Number of Results
1998	1
2001	1
2003	3
2004	3
2005	1
2006	5
2007	6
2008	4
2009	2
2010	5
2011	4
2012	4
2013	6
2014	7
2015	5
2016	4
2017	13
2018	13
2019	10
2020	5
2021	1
2024	0

1

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.

2

All-cause mortality and survival in adults with 22q11.2 deletion syndrome.

Van L, Heung T, Graffi J, Ng E, Malecki S, Van Mil S, Boot E, Corral M, Chow EWC, Hodgkinson KA, Silversides C, Bassett AS. Van L, et al. Genet Med. 2019 Oct;21(10):2328-2335. doi: 10.1038/s41436-019-0509-y. Epub 2019 Apr 5. Genet Med. 2019. PMID: 30948858 Free PMC article.

3

Impact of a 22q11.2 Microdeletion on Adult All-Cause Mortality in Tetralogy of Fallot Patients.

van Mil S, Heung T, Malecki S, Van L, Chang J, Breetvelt E, Wald R, Oechslin E, Silversides C, Bassett AS. van Mil S, et al. Can J Cardiol. 2020 Jul;36(7):1091-1097. doi: 10.1016/j.cjca.2020.04.019. Epub 2020 Apr 26. Can J Cardiol. 2020. PMID: 32348848

4

22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.

van Engelen K, Topf A, Keavney BD, Goodship JA, van der Velde ET, Baars MJ, Snijder S, Moorman AF, Postma AV, Mulder BJ. van Engelen K, et al. Heart. 2010 Apr;96(8):621-4. doi: 10.1136/hrt.2009.182642. Heart. 2010. PMID: 20357389

5

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. 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.

6

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.

7

The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis.

Homans JF, de Reuver S, Heung T, Silversides CK, Oechslin EN, Houben ML, McDonald-McGinn DM, Kruyt MC, Castelein RM, Bassett AS. Homans JF, et al. Spine J. 2020 Jun;20(6):956-963. doi: 10.1016/j.spinee.2020.01.006. Epub 2020 Jan 18. Spine J. 2020. PMID: 31958577 Free PMC article.

8

Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers.

Shetty M, Srikanth A, Kadandale J, Hegde S. Shetty M, et al. Cytogenet Genome Res. 2016;148(4):249-55. doi: 10.1159/000446162. Epub 2016 Jun 15. Cytogenet Genome Res. 2016. PMID: 27300488

9

Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.

Huber J, Peres VC, de Castro AL, dos Santos TJ, da Fontoura Beltrão L, de Baumont AC, Cossio SL, Dalberto TP, Riegel M, Cañedo AD, Schaan BD, Pellanda LC. Huber J, et al. Pediatr Cardiol. 2014 Dec;35(8):1356-62. doi: 10.1007/s00246-014-0936-0. Epub 2014 Jun 1. Pediatr Cardiol. 2014. PMID: 24880467

10

Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications.

Butcher NJ, Kiehl TR, Hazrati LN, Chow EW, Rogaeva E, Lang AE, Bassett AS. Butcher NJ, et al. JAMA Neurol. 2013 Nov;70(11):1359-66. doi: 10.1001/jamaneurol.2013.3646. JAMA Neurol. 2013. PMID: 24018986 Free PMC article.

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