Hayes I - Search Results

1

Community detection of long QT syndrome with a clinical registry: an alternative to ECG screening programs?

Earle N, Crawford J, Smith W, Hayes I, Shelling A, Hood M, Stiles M, Maxwell F, Heaven D, Love DR, Skinner JR. Earle N, et al. Among authors: hayes i. Heart Rhythm. 2013 Feb;10(2):233-8. doi: 10.1016/j.hrthm.2012.10.043. Epub 2012 Nov 1. Heart Rhythm. 2013. PMID: 23123674

2

Array comparative genomic hybridisation: a new tool in the diagnostic genetic armoury.

Marquis-Nicholson R, Aftimos S, Hayes I, George A, Love DR. Marquis-Nicholson R, et al. Among authors: hayes i. N Z Med J. 2010 Jul 16;123(1318):50-61. N Z Med J. 2010. PMID: 20651866 Review.

3

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.

Skinner JR, Crawford J, Smith W, Aitken A, Heaven D, Evans CA, Hayes I, Neas KR, Stables S, Koelmeyer T, Denmark L, Vuletic J, Maxwell F, White K, Yang T, Roden DM, Leren TP, Shelling A, Love DR; Cardiac Inherited Disease Group New Zealand. Skinner JR, et al. Among authors: hayes i. Heart Rhythm. 2011 Mar;8(3):412-9. doi: 10.1016/j.hrthm.2010.11.016. Epub 2010 Nov 9. Heart Rhythm. 2011. PMID: 21070882

4

Chromosome microarray analysis in a clinical environment: new perspective and new challenge.

George A, Marquis-Nicholson R, Zhang LT, Love JM, Ashton F, Aftimos S, Hayes I, Williams LC, Love DR. George A, et al. Among authors: hayes i. Br J Biomed Sci. 2011;68(2):100-8. doi: 10.1080/09674845.2011.11730334. Br J Biomed Sci. 2011. PMID: 21706924 Review.

5

Recurrent Transmission of a 17q12 Microdeletion and a Variable Clinical Spectrum.

George AM, Love DR, Hayes I, Tsang B. George AM, et al. Among authors: hayes i. Mol Syndromol. 2012 Jan;2(2):72-75. doi: 10.1159/000335344. Epub 2011 Dec 31. Mol Syndromol. 2012. PMID: 22511894 Free PMC article.

6

Inheritance of a Ring Chromosome 21 in a Couple Undergoing In Vitro Fertilization (IVF): A Case Report.

Mazzaschi RL, Love DR, Hayes I, George A. Mazzaschi RL, et al. Among authors: hayes i. Case Rep Genet. 2011;2011:158086. doi: 10.1155/2011/158086. Epub 2011 Jul 31. Case Rep Genet. 2011. PMID: 23074672 Free PMC article.

7

A rare chromosome 3 imbalance and its clinical implications.

Sims K, Mazzaschi RL, Payne E, Hayes I, Love DR, George AM. Sims K, et al. Among authors: hayes i. Case Rep Pediatr. 2012;2012:846564. doi: 10.1155/2012/846564. Epub 2012 Oct 11. Case Rep Pediatr. 2012. PMID: 23097735 Free PMC article.

8

Array comparative genomic hybridization identifies a heterozygous deletion of the entire KCNJ2 gene as a cause of sudden cardiac death.

Marquis-Nicholson R, Prosser DO, Love JM, Zhang L, Hayes I, George AM, Crawford JR, Skinner JR, Love DR. Marquis-Nicholson R, et al. Among authors: hayes i. Circ Cardiovasc Genet. 2014 Feb;7(1):17-22. doi: 10.1161/CIRCGENETICS.113.000415. Epub 2014 Jan 6. Circ Cardiovasc Genet. 2014. PMID: 24395924

9

12q14 Microdeletions: Additional Case Series with Confirmation of a Macrocephaly Region.

Mc Cormack A, Sharpe C, Gregersen N, Smith W, Hayes I, George AM, Love DR. Mc Cormack A, et al. Among authors: hayes i. Case Rep Genet. 2015;2015:192071. doi: 10.1155/2015/192071. Epub 2015 Jul 22. Case Rep Genet. 2015. PMID: 26266063 Free PMC article.

10

Detection of sudden death syndromes in New Zealand.

Earle N, Crawford J, Gibson K, Love D, Hayes I, Neas K, Stiles M, Graham M, Donoghue T, Aitken A, Skinner J. Earle N, et al. Among authors: hayes i. N Z Med J. 2016 Nov 18;129(1445):67-74. N Z Med J. 2016. PMID: 27857240

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