Blue GM - Search Results

1

ConanVarvar: a versatile tool for the detection of large syndromic copy number variation from whole-genome sequencing data.

Gudkov M, Thibaut L, Khushi M, Blue GM, Winlaw DS, Dunwoodie SL, Giannoulatou E. Gudkov M, et al. Among authors: blue gm. BMC Bioinformatics. 2023 Feb 15;24(1):49. doi: 10.1186/s12859-023-05154-x. BMC Bioinformatics. 2023. PMID: 36792982 Free PMC article.

2

The negative impact of Alagille syndrome on survival of infants with pulmonary atresia.

Blue GM, Mah JM, Cole AD, Lal V, Wilson MJ, Chard RB, Sholler GF, Hawker RE, Sherwood MC, Winlaw DS. Blue GM, et al. J Thorac Cardiovasc Surg. 2007 Apr;133(4):1094-6. doi: 10.1016/j.jtcvs.2006.12.009. J Thorac Cardiovasc Surg. 2007. PMID: 17382662 Free article. No abstract available.

3

GATA4 mutations in 357 unrelated patients with congenital heart malformation.

Butler TL, Esposito G, Blue GM, Cole AD, Costa MW, Waddell LB, Walizada G, Sholler GF, Kirk EP, Feneley M, Harvey RP, Winlaw DS. Butler TL, et al. Among authors: blue gm. Genet Test Mol Biomarkers. 2010 Dec;14(6):797-802. doi: 10.1089/gtmb.2010.0028. Epub 2010 Sep 27. Genet Test Mol Biomarkers. 2010. PMID: 20874241

4

Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4.

Moradi Marjaneh M, Kirk EP, Posch MG, Ozcelik C, Berger F, Hetzer R, Otway R, Butler TL, Blue GM, Griffiths LR, Fatkin D, Martinson JJ, Winlaw DS, Feneley MP, Harvey RP. Moradi Marjaneh M, et al. Among authors: blue gm. PLoS One. 2011;6(6):e20711. doi: 10.1371/journal.pone.0020711. Epub 2011 Jun 6. PLoS One. 2011. PMID: 21673957 Free PMC article.

5

Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart.

Esposito G, Butler TL, Blue GM, Cole AD, Sholler GF, Kirk EP, Grossfeld P, Perryman BM, Harvey RP, Winlaw DS. Esposito G, et al. Among authors: blue gm. Am J Med Genet A. 2011 Oct;155A(10):2416-21. doi: 10.1002/ajmg.a.34187. Am J Med Genet A. 2011. PMID: 22043484

6

Congenital heart disease: current knowledge about causes and inheritance.

Blue GM, Kirk EP, Sholler GF, Harvey RP, Winlaw DS. Blue GM, et al. Med J Aust. 2012 Aug 6;197(3):155-9. doi: 10.5694/mja12.10811. Med J Aust. 2012. PMID: 22860792 Review.

7

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.

Soemedi R, Wilson IJ, Bentham J, Darlay R, Töpf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, Mamasoula C, Rahman TJ, Hall D, Rauch A, Devriendt K, Gewillig M, O' Sullivan J, Winlaw DS, Bu'Lock F, Brook JD, Bhattacharya S, Lathrop M, Santibanez-Koref M, Cordell HJ, Goodship JA, Keavney BD. Soemedi R, et al. Among authors: blue gm. Am J Hum Genet. 2012 Sep 7;91(3):489-501. doi: 10.1016/j.ajhg.2012.08.003. Epub 2012 Aug 30. Am J Hum Genet. 2012. PMID: 22939634 Free PMC article.

8

Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning.

Blue GM, Kasparian NA, Sholler GF, Kirk EP, Winlaw DS. Blue GM, et al. Int J Cardiol. 2015 Jan 15;178:124-30. doi: 10.1016/j.ijcard.2014.10.119. Epub 2014 Oct 22. Int J Cardiol. 2015. PMID: 25464235

9

Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.

Blue GM, Kirk EP, Giannoulatou E, Dunwoodie SL, Ho JW, Hilton DC, White SM, Sholler GF, Harvey RP, Winlaw DS. Blue GM, et al. J Am Coll Cardiol. 2014 Dec 16;64(23):2498-506. doi: 10.1016/j.jacc.2014.09.048. J Am Coll Cardiol. 2014. PMID: 25500235 Free article.

10

Bioengineering and Stem Cell Technology in the Treatment of Congenital Heart Disease.

Bosman A, Edel MJ, Blue G, Dilley RJ, Harvey RP, Winlaw DS. Bosman A, et al. J Clin Med. 2015 Apr 22;4(4):768-81. doi: 10.3390/jcm4040768. J Clin Med. 2015. PMID: 26239354 Free PMC article. Review.

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