Dean Phelan
University of Melbourne
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Publication
Featured researches published by Dean Phelan.
JAMA Pediatrics | 2017
Tiong Yang Tan; Oliver James Dillon; Zornitza Stark; Deborah Schofield; Khurshid Alam; Rupendra Shrestha; Belinda Chong; Dean Phelan; Gemma R. Brett; Emma Creed; Anna Jarmolowicz; Patrick Yap; Maie Walsh; Lilian Downie; David J. Amor; Ravi Savarirayan; George McGillivray; Alison Yeung; Heidi Peters; Susan J. Robertson; Aaron J Robinson; Ivan Macciocca; Simon Sadedin; Katrina M. Bell; Alicia Oshlack; Peter Georgeson; Natalie P. Thorne; Clara Gaff; Susan M. White
Importance Optimal use of whole-exome sequencing (WES) in the pediatric setting requires an understanding of who should be considered for testing and when it should be performed to maximize clinical utility and cost-effectiveness. Objectives To investigate the impact of WES in sequencing-naive children suspected of having a monogenic disorder and evaluate its cost-effectiveness if WES had been available at different time points in their diagnostic trajectory. Design, Setting, and Participants This prospective study was part of the Melbourne Genomics Health Alliance demonstration project. At the ambulatory outpatient clinics of the Victorian Clinical Genetics Services at the Royal Children’s Hospital, Melbourne, Australia, children older than 2 years suspected of having a monogenic disorder were prospectively recruited from May 1 through November 30, 2015, by clinical geneticists after referral from general and subspecialist pediatricians. All children had nondiagnostic microarrays and no prior single-gene or panel sequencing. Exposures All children underwent singleton WES with targeted phenotype-driven analysis. Main Outcomes and Measures The study examined the clinical utility of a molecular diagnosis and the cost-effectiveness of alternative diagnostic trajectories, depending on timing of WES. Results Of 61 children originally assessed, 44 (21 [48%] male and 23 [52%] female) aged 2 to 18 years (mean age at initial presentation, 28 months; range, 0-121 months) were recruited, and a diagnosis was achieved in 23 (52%) by singleton WES. The diagnoses were unexpected in 8 of 23 (35%), and clinical management was altered in 6 of 23 (26%). The mean duration of the diagnostic odyssey was 6 years, with each child having a mean of 19 tests and 4 clinical genetics and 4 nongenetics specialist consultations, and 26 (59%) underwent a procedure while under general anesthetic for diagnostic purposes. Economic analyses of the diagnostic trajectory identified that WES performed at initial tertiary presentation resulted in an incremental cost savings of A
Journal of Cardiovascular Electrophysiology | 2011
Lucas Eastaugh; Paul A. James; Dean Phelan; Andrew M. Davis
9020 (US
European Heart Journal | 2016
Dean Phelan; David John Anderson; Sara E. Howden; Raymond C.B. Wong; Peter Hickey; Kate Pope; Gabrielle R. Wilson; Alice Pébay; Andrew M. Davis; Steven Petrou; Andrew G. Elefanty; Edouard G. Stanley; Paul A. James; Ivan Macciocca; Melanie Bahlo; Micheal M H Cheung; David J. Amor; David A. Elliott; Paul J. Lockhart
6838) per additional diagnosis (95% CI, A
Annals of clinical and translational neurology | 2017
Maie Walsh; Katrina M. Bell; Belinda Chong; Emma Creed; Gemma R. Brett; Kate Pope; Natalie P. Thorne; Simon Sadedin; Peter Georgeson; Dean Phelan; Timothy Day; J. Taylor; Adrienne C. Sexton; Paul J. Lockhart; Lynette Kiers; Michael Fahey; Ivan Macciocca; Clara Gaff; Alicia Oshlack; Eppie M. Yiu; Paul A. James; Zornitza Stark; Monique M. Ryan
4304-A
Genetics in Medicine | 2018
Zornitza Stark; Sebastian Lunke; Gemma R. Brett; Natalie B. Tan; Rachel Stapleton; Smitha Kumble; Alison Yeung; Dean Phelan; Belinda Chong; Miriam Fanjul‐Fernández; Justine Marum; Matthew Hunter; Anna Jarmolowicz; Yael Prawer; Jessica R. Riseley; Matthew Regan; Justine Elliott; Melissa Martyn; Stephanie Best; Tiong Yang Tan; Clara Gaff; Susan M. White
15 404 [US
OA Genetics | 2013
Dean Phelan; Gabrielle R. Wilson; Paul A. James; Paul J. Lockhart
3263-US
Nature Communications | 2018
David John Anderson; David I. Kaplan; Katrina M. Bell; Katerina Koutsis; John M. Haynes; Richard J. Mills; Dean Phelan; Elizabeth Qian; Ana Rita Leitoguinho; Deevina Arasaratnam; Tanya Labonne; Elizabeth S. Ng; Richard P. Davis; Simona Casini; Robert Passier; James E. Hudson; Enzo R. Porrello; Mauro W. Costa; Arash Rafii; Clare L. Curl; Lea M.D. Delbridge; Richard P. Harvey; Alicia Oshlack; Michael M. Cheung; Christine L. Mummery; Stephen Petrou; Andrew G. Elefanty; Edouard G. Stanley; David A. Elliott
11 678]) compared with the standard diagnostic pathway. Even if WES were performed at the first genetics appointment, there would be an incremental cost savings of A
Human Mutation | 2018
Alexander J. Abrams; Flavia Fontanesi; Natalie B. L. Tan; Elena Buglo; Ion J. Campeanu; Adriana P. Rebelo; Andrew J. Kornberg; Dean Phelan; Zornitza Stark; Stephan Züchner
5461 (US
Seminars in Pediatric Neurology | 2017
Ian R. Woodcock; Manoj P. Menezes; Lee Coleman; Joy Yaplito-Lee; Heidi Peters; Susan M. White; Rachel Stapleton; Dean Phelan; Belinda Chong; Sebastian Lunke; Zornitza Stark; James Pitt; Monique M. Ryan; C. F. Robertson; Eppie M. Yiu
4140) (95% CI, A
Molecular Therapy | 2015
Marguerite V. Evans-Galea; Sze HweeOng; Dongcheng Zhang; Matthew Burton; Chou H. Sim; Dean Phelan; Sarah E. M. Stephenson; Gabrielle R. Wilson; Donald F. Newgreen; Paul J. Lockhart; Martin B. Delatycki
1433-A