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S

Sebastian Lunke

university of melbourne

38H-index
156Paper Count
4.9KCitation Count
Published Papers 81
Publication Date
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Scaling up genomic newborn screening: implementation lessons from the BabyScreen+ study
errEuropean Journal of Human Genetics
IF4.6
err2026-07-23
err0
errOAAI
errNathasha Kugenthiran; Erin Tutty; Anaita Kanga-Parabia; Jade Caruana; Katrina Scarff; Nitzan Lang; Lilian Downie; Sebastian Lunke; Alison D. Archibald; Zornitza Stark; Stephanie Best
errShare
errSave
Australian parents’ perspectives on extended genomic screening: what information to return and when?
errEuropean Journal of Human Genetics
IF4.6
err2026-06-27
err0
errOAAI
errFiona Lynch; Christopher Gyngell; Stephanie Best; Clara Gaff; Lilian Downie; Alison Archibald; Ilias Goranitis; Julian Savulescu; Sebastian Lunke; Zornitza Stark; Danya F. Vears
errShare
errSave
Automated reanalysis of genomic data for rare disease diagnostics at scale
errNature Medicine
IF50
err2026-06-24
err0
errOAAI
errMatthew J. Welland; K. D. Ahlquist; Paul De Fazio; Christina Austin-Tse; Lynn Pais; Laura Wedd; Samantha Bryen; Rocio Rius; Michael Franklin; Caitlin Morrison; Giles Hall; Laura Gauthier; Alex Bloemendal; David I. Francis; Andrew J. Mallett; Amali Mallawaarachchi; Paul J. Lockhart; Richard Leventer; Ingrid E. Scheffer; Katherine B. Howell; Karin S. Kassahn; Hamish S. Scott; Julie McGaughran; John Christodoulou; David R. Thorburn; Bryony A. Thompson; Chirag V. Patel; Greg Smith; Anne O’Donnell-Luria; Simon Sadedin; Heidi L. Rehm; Sebastian Lunke; Jeremiah Wander; Kaitlin E. Samocha; Cas Simons; Daniel G. MacArthur; Zornitza Stark
errShare
errSave
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity
errEpilepsia Open
IF2.9
err2026-05-04
err0
errOAAI
errTrupti Jadhav; Sophie E. Bouffler; Emily Innes; Michael Fahey; Matthew Hunter; Kavitha Kothur; Sebastian Lunke; Matthew Lynch; Emma Macdonald-Laurs; Elizabeth Emma Palmer; Chirag Patel; Jason Pinner; Kate Riney; Rani Sachdev; Sarah A. Sandaradura; Ingrid E. Scheffer; Zornitza Stark; Katherine B. Howell
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errSave
Mainstreaming genomic testing for mitochondrial disease in Australia
errEuropean Journal of Human Genetics
IF4.6
err2026-02-26
err0
errOAAI
errMegan Ball; Naomi Baker; Sze Chern Lim; Sarah Casauria; Sebastian Lunke; Alison G. Compton; David R. Thorburn; John Christodoulou; Zornitza Stark
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errSave
Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ study
errEuropean Journal of Human Genetics
IF4.6
err2026-02-24
err0
errOAAI
errErin Tutty; Anaita Kanga-Parabia; Nathasha Kugenthiran; Jade Caruana; Lilian Downie; Clara Gaff; Nitzan Lang; Sebastian Lunke; Katrina Scarff; Zornitza Stark; Stephanie Best; Alison D. Archibald
errShare
errSave
Genomic Newborn Screening: Commodity or Public Good?
errMedical Journal of Australia
IF8.5
err2026-01-14
err0
errOAAI
errChristopher Gyngell; Sebastian Lunke; Danya Vears; Zornitza L. Stark
errShare
errSave
Piloting an Interpretive External Quality Assurance Model for Genomic Testing for Childhood Syndromes and Intellectual Disability
errthe journal of molecular diagnostics
IF0
err2025-12-18
err0
errOAAI
errBen Lundie; Sze Yee Chai; Alicia B. Byrne; Dimitar Azmanov; John Christodoulou; Matilda A. Haas; Karin S. Kassahn; Sebastian Lunke; Ami Stott; Bryony A. Thompson; Tony Badrick; Bruce Bennetts
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errSave
Increased yield of genetic diagnoses in inherited heart diseases using expanded genome and RNA-splicing analyses
errGenetics in Medicine
IF6.2
err2025-10-29
err0
errOAAI
errYuchen Chang; Emma M. Rath; Magdalena Soka; Emma S. Singer; Gunjan Trivedi; Charlotte Burns; Rachel Austin; Tiffany Boughtwood; Jaye S. Brown; Sarah Casauria; Belinda Chong; Jasmina Cvetkovska; Sally L. Dunwoodie; Sebastian Lunke; Tessa Mattiske; Julie McGaughran; Sarah-Jane Pantaleo; Michael C.J. Quinn; Chris Semsarian; Ivan Macciocca; Jodie Ingles; Diane Fatkin; Eleni Giannoulatou; Richard D. Bagnall
errShare
errSave
Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study
errNature Medicine
IF50
err2025-10-09
err0
errOAAI
errSebastian Lunke; Lilian Downie; Jade Caruana; Nathasha Kugenthiran; Paul De Fazio; Sebastian Hollizeck; Sophie E. Bouffler; David J. Amor; Alison D. Archibald; Yvonne Bombard; John Christodoulou; Marc Clausen; Wendy Fagan; Clara Gaff; Ronda F. Greaves; Christopher Gyngell; Anaita Kanga-Parabia; Nitzan Lang; Crystle Lee; Fiona Lynch; Anthony Marty; Melanie Marty; Candice McGregor; Jessica Riseley; Simon Sadedin; Katrina Scarff; Michelle da Cunha Torres; Erin Tutty; Ching Vang; Meaghan Wall; Ee Ming Wong; Alison Yeung; Ilias Goranitis; Stephanie Best; Danya F. Vears; Zornitza Stark
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errSave
Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
erramerican journal of human genetics
IF0
err2025-05-28
err0
errOAAI
errRiccarda Peters; Stephanie Best; Fiona Lynch; Danya F. Vears; Lilian Downie; Alison D. Archibald; Sebastian Lunke; Zornitza Stark; Ilias Goranitis
errShare
errSave
Utility of ultrarapid genomic testing for management of malignant pediatric arrhythmia
errHeart Rhythm
IF5.7
err2025-05-22
err0
PREAI
errYuji Doi; Andreas Pflaumer; Ivan Macciocca; Vanessa Connell; Sebastain Lunke; Zornitza Stark; Andrew Davis
errShare
errSave
Nationwide, Couple-Based Genetic Carrier Screening
errOBSTETRICAL & GYNECOLOGICAL SURVEY
IF3.6
err2025-05-01
err0
PREAI
errKirk, E. P.; Delatycki, M. B.; Archibald, A. D.; Tutty, E.; Caruana, J.; Halliday, J. L.; Lewis, S.; Mcclaren, B. J.; Newson, A. J.; Dive, L.; Best, S.; Long, J. C.; Braithwaite, J.; Downes, M. J.; Scuffham, P. A.; Massie, J.; Barlow-Stewart, K.; Kulkarni, A.; Ruscigno, A.; Kanga-Parabia, A.; Rodrigues, B.; Bennetts, B. H.; Ebzery, C.; Hunt, C.; Cliffe, C. C.; Lee, C.; Azmanov, D.; King, E. A.; Madelli, E. O.; Zhang, F.; Ho, G.; Danos, I.; Liebelt, J.; Fletcher, J.; Kennedy, J.; Beilby, J.; Emery, J. D.; Mcgaughran, J.; Marum, J. E.; Scarff, K.; Fisk, K.; Harrison, K.; Boggs, K.; Giameos, L.; Fitzgerald, L.; Thomas, L.; Burnett, L.; Freeman, L.; Harris, M.; Berbic, M.; Davis, M. R.; Cifuentes Ochoa, M.; Wallis, M.; Wall, M.; Chow, M. T. M.; Ferrie, M. M.; Pachter, N.; Quayum, N.; Lang, N.; Pandy, P. Kasi; Casella, R.; Allcock, R. J. N.; Ong, R.; Edwards, S.; Sundercombe, S.; Jelenich, S.; Righetti, S.; Lunke, S.; Kaur, S.; Stock-Myer, S.; Eggers, S.; Walker, S. P.; Theodorou, T.; Catchpool, T.; Clinch, T.; Roscioli, T.; Hardy, T.; Zhu, Y.; Fehlberg, Z.; Boughtwood, T. F.; Laing, N. G.
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errSave
Guidelines for reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy
errPathology
IF3
err2025-03-26
err0
PREAI
errEdwin Kirk; Linda Mundy; Eric Lee; Ben Lundie; Nigel Laing; Alison D. Archibald; Ainsley J. Newson; Kym Mina; Kevin Carpenter; Kate Neas; Richard King; Monica Ferrie; Sebastian Lunke; Tiffany Boughtwood; Martin B. Delatycki; Jon Emery; Helen Mountain; Lisa Hui; Lisa Dive; Michelle A. Farrar; John Massie
errShare
errSave
The Intersection Between Genetic Reproductive Carrier Screening and Genomic Newborn Screening: Implications for Clinical Practice
errPRENATAL DIAGNOSIS
IF2.7
err2025-03-08
err0
errOAAI
errLilian Downie; Sebastian Lunke; Zornitza Stark
errShare
errSave
Critically unwell infants and children with mitochondrial disorders diagnosed by ultrarapid genomic sequencing
errGENETICS IN MEDICINE
IF6.2
err2025-01-01
err0
PREAI
errBall, Megan; Bouffer, Sophie E.; Barnett, Christopher B.; Freckmann, Mary-Louise; Hunter, Matthew F.; Kamien, Benjamin; Kassahn, Karin S.; Lunke, Sebastian; Patel, Chirag, V; Pinner, Jason; Roscioli, Tony; Sandaradura, Sarah A.; Scott, Hamish S.; Tan, Tiong Y.; Wallis, Mathew; Compton, Alison G.; Thorburn, David R.; Stark, Zornitza; Christodoulou, John
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errSave
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns
errEPIGENOMICS
IF2.6
err2024-10-04
err1
errOAAI
errAlshawsh, Mohammed; Wake, Melissa; Gecz, Jozef; Corbett, Mark; Saffery, Richard; Pitt, James; Greaves, Ronda; Williams, Katrina; Field, Michael; Cheong, Jeanie; Bui, Minh; Arora, Sheena; Sadedin, Simon; Lunke, Sebastian; Wall, Meg; Amor, David J.; Godler, David E.
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errSave
Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023
errHUMAN GENOMICS
IF4.3
err2024-08-17
err2
errOAAI
errMallawaarachchi, Amali; Biros, Erik; Harris, Trudie; Bennetts, Bruce; Boughtwood, Tiffany; Elliott, Justine; Fowles, Lindsay; Gardos, Robert; Garza, Denisse; Goranitis, Ilias; Haas, Matilda; Huntley, Vanessa; Jefferis, Julia; Kassahn, Karin; Leaver, Anna; Lundie, Ben; Lunke, Sebastian; O'Connor, Caitlin; Pratt, Greg; Quinlan, Catherine; Shearman, Dianne; Soraru, Jacqueline; Sundaram, Madhivanan; Tchan, Michel; Valente, Giulia; White, Julie; Wilkins, Ella; Alexander, Steve I.; Amir, Noa; Best, Stephanie; Gul, Hossai; Jayasinghe, Kushani; McCarthy, Hugh; Patel, Chirag; Stark, Zornitza; Mallett, Andrew J.
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errSave
Benchmarking pharmacogenomics genotyping tools: Performance analysis on short-read sequencing samples and depth-dependent evaluation
errCTS-CLINICAL AND TRANSLATIONAL SCIENCE
IF2.8
err2024-08-09
err1
errOAAI
errHalman, Andreas; Lunke, Sebastian; Sadedin, Simon; Moore, Claire; Conyers, Rachel
errShare
errSave
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-06-21
err1
errOAAI
errTutty, Erin; Archibald, Alison D.; Downie, Lilian; Gaff, Clara; Lunke, Sebastian; Vears, Danya F.; Stark, Zornitza; Best, Stephanie
errShare
errSave

Research Directions

No research directions
Co-authors
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