Blue GM - Search Results

1

Management of People With a Fontan Circulation: a Cardiac Society of Australia and New Zealand Position statement.

Zentner D, Celermajer DS, Gentles T, d'Udekem Y, Ayer J, Blue GM, Bridgman C, Burchill L, Cheung M, Cordina R, Culnane E, Davis A, du Plessis K, Eagleson K, Finucane K, Frank B, Greenway S, Grigg L, Hardikar W, Hornung T, Hynson J, Iyengar AJ, James P, Justo R, Kalman J, Kasparian N, Le B, Marshall K, Mathew J, McGiffin D, McGuire M, Monagle P, Moore B, Neilsen J, O'Connor B, O'Donnell C, Pflaumer A, Rice K, Sholler G, Skinner JR, Sood S, Ward J, Weintraub R, Wilson T, Wilson W, Winlaw D, Wood A. Zentner D, et al. Among authors: blue gm. Heart Lung Circ. 2020 Jan;29(1):5-39. doi: 10.1016/j.hlc.2019.09.010. Epub 2019 Nov 15. Heart Lung Circ. 2020. PMID: 31735685 Free article. Review.

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

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

5

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.

6

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

7

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.

8

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.

9

The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease.

Blue GM, Humphreys D, Szot J, Major J, Chapman G, Bosman A, Kirk EP, Sholler GF, Harvey RP, Dunwoodie SL, Winlaw DS. Blue GM, et al. Int J Cardiol. 2017 Mar 1;230:155-163. doi: 10.1016/j.ijcard.2016.12.024. Epub 2016 Dec 13. Int J Cardiol. 2017. PMID: 27989580

10

Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.

Blue GM, Kirk EP, Giannoulatou E, Sholler GF, Dunwoodie SL, Harvey RP, Winlaw DS. Blue GM, et al. J Am Coll Cardiol. 2017 Feb 21;69(7):859-870. doi: 10.1016/j.jacc.2016.11.060. J Am Coll Cardiol. 2017. PMID: 28209227 Free article. Review.

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