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Coronavirus (COVID-19)

Mar 27 2020
Many people in our community are feeling worried about COVID-19, our team is here to support you. Please visit our dedicated COVID-19 informati...

Team Harley - City2Surf 2017

Jun 27 2017
Mum Danielle puts it beautifully: "Why we started Team Harley: To raise awareness for Congenital Heart Disease in memory of our amazing...

Halor's story

Jun 23 2017
One of our patients, Halor, was featured on The Children's Hospital at Westmead's Facebook page this week:     ...

Kids Heart Research Publications - 2013


Early outcomes from a new regional programme for the surgical management of hypoplastic left heart syndrome.
ANZ Journal of Surgery, Feb-2013
Orr Y, Leclair K, Jacobe S, Badawi N, Nicholson IA, Chard RB, Sholler GF, Winlaw DS. 

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Human Molecular Genetics, Apr-2013
Cordell HJ, Topf A, Mamasoula C, Postma AV, Bentham J, Zelenika D, Heath S, Blue G, Cosgrove C, Granados-Riveron J, Darlay R, Soemedi R, Wilson IJ, Ayers KL, Rahman TJ, Hall D, Mulder BJM, Zwinderman AH, van Engelen K, Brook JD, Setchfield K, Bu'lock FA, Thornborough C, O'sullivan J, Stuart AG, Parsons J, Bhattacharya S, Winlaw D, Mital S, Gewillig M, Breckpot J, Devriendt K, Moorman AFM, Rauch A, Lathrop GM, Keavney BD, Goodship JA.

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Nature Genetics, May-2013
Cordell HJ, Bentham J, Töpf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, Hall D, van Engelen K, Moorman AFM, Zwinderman AH, Barnett P, Koopmann TT, Adriaens ME, Varro A, George AL, Remedios dos C, Bishopric NH, Bezzina CR, O'Sullivan J, Gewillig M, Bu'Lock FA, Winlaw DS, Bhattacharya S, Devriendt K, Brook JD, Mulder BJM, Mital S, Postma AV, Lathrop GM, Farrall M, Goodship JA, Keavney BD.

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls.
Circulation: Cardiovascular Genetics, Jul-2013
Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, T?pf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, Riveron JG, Setchfield K, Brook JD, Bu'Lock FA, Thorborough C, Rahman TJ, Doza JP, Tan HL, O'Sullivan J, Stuart AG, Blue G, Winlaw D, Postma AV, Mulder BJ, Zqinderman AH, van Engelen K, Moorman AF, Rauch A, Gewilig M, Brechpot J, devriendt K, Lathrop GM, Farrall M, Goodship JA, Cordell HJ, Brody LC, Keavney BD.

A novel class of anticancer compounds targets the actin cytoskeleton in tumor cells
Cancer Research, Aug-2013
Stehn JR, Haass NK, McCluskey A, Bonello T, Desouza M, Kottyan G, Treutlein H, Zeng J, Nascimento PRBB, Sequeira VB, Butler TL, Allanson M, Fath T, Hill TA, Schevzov G, Palmer SJ, Hardeman EC, Winlaw DS, Reeve VE, Dixon I, Weninger W, Cripe TP, Gunning PW.

Parents' perceptions of genetics services for congenital heart disease: the role of demographic, clinical, and psychological factors in determining service attendance.
Genetics in Medicine, Nov-2013
Kasparian NA, Fidock B, Sholler GF, Camphausen C, Murphy DN, Cooper SG, Kaul R, Jones O, Winlaw DS, Kirk EPE. 

The Australian and New Zealand Fontan Registry: description and initial results from the first population based Fontan registry.
Journal of Internal Medicine, Nov-2013
Iyengar AJ, Winlaw DS, Galati JC, Gentles TL, Weintraub RG, Justo RN, Wheaton GR, Bullock A, Clermajer DS, d'Udekem Y.



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