Sebastian Lunke

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 21

Top Venues

European journal of human genetics : EJHG

Journal of personalized medicine

Clinical and translational science

Clinical epigenetics

Monash University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Monash University

Australia

PHD :: Medicine

Publications

Andreas Halman, Sebastian Lunke, Simon Sadedin, Claire Moore, Rachel Conyers
Benchmarking pharmacogenomics genotyping tools: Performance analysis on short-read sequencing samples and depth-dependent evaluation. Clinical and translational science 17 (8) (2024)
Stephanie Best, Zoe Fehlberg, Christopher Richards, Michael C J Quinn, Sebastian Lunke, Amanda B Spurdle, Karin S Kassahn, Chirag Patel, Danya F Vears, Ilias Goranitis, Fiona Lynch, Alan Robertson, Emma Tudini, John Chrisodoulou, Hamish S Scott, Julie McGaughran, Zornitza Stark
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European journal of human genetics : EJHG (2024)
Erin Tutty, Alison D Archibald, Lilian Downie, Clara L Gaff, Sebastian Lunke, Danya F Vears, Zornitza Stark, Stephanie Best
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework. European journal of human genetics : EJHG (2024)
Andreas Halman, Sebastian Lunke, Simon Sadedin, Claire Moore, Rachel Conyers
Benchmarking pharmacogenomics genotyping tools: Performance analysis on short-read sequencing samples and depth-dependent evaluation. Clinical and translational science 17 (8) (2024)
Ari E Horton, Sebastian Lunke, Simon Sadedin, Andrew Paul Fennell, Zornitza Stark
Elusive variants in autosomal recessive disease: how can we improve timely diagnosis? European journal of human genetics : EJHG (2023)
Sebastian Lunke, Sophie E Bouffler, Chirag V Patel, Sarah A Sandaradura, Meredith Wilson, Jason Pinner, Matthew F Hunter, Christopher P Barnett, Mathew Wallis, Benjamin Kamien, Tiong Yang Tan, Mary-Louise Freckmann, Belinda Chong, Dean Phelan, David Francis, Karin S Kassahn, Thuong T Ha, Song Gao, Peer Arts, Matilda R Jackson, Hamish S Scott, Stefanie Eggers, Simone Rowley, Kirsten Boggs, Ana Rakonjac, Gemma R Brett, Michelle G de Silva, Amanda Springer, Michelle Ward, Kirsty Stallard, Cas Simons, Thomas Conway, Andreas Halman, Nicole J Van Bergen, Tim Sikora, Liana N Semcesen, David A Stroud, Alison G Compton, David R Thorburn, Katrina M Bell, Simon Sadedin, Kathryn N North, John Chrisodoulou, Zornitza Stark
Integrated multi-omics for rapid rare disease diagnosis on a national scale. Nature medicine (2023)
Ari E Horton, Sebastian Lunke, Simon Sadedin, Andrew Paul Fennell, Zornitza Stark
Elusive variants in autosomal recessive disease: how can we improve timely diagnosis? European journal of human genetics : EJHG (2023)
Ari E Horton, Sebastian Lunke, Simon Sadedin, Andrew Paul Fennell, Zornitza Stark
Elusive variants in autosomal recessive disease: how can we improve timely diagnosis? European journal of human genetics : EJHG (2023)
Nicole J Van Bergen, Daniella Helena Hock, Lucy Spencer, Sean Massey, Tegan Stait, Zornitza Stark, Sebastian Lunke, Ain Roesley, Heidi Peters, Joy Yaplito Lee, Anna Le Fevre, Oliver Heath, Cristina Mignone, Joseph Yuan-Mou Yang, Monique M Ryan, Colleen D'Arcy, Margot Nash, Sile Smith, Nikeisha J Caruana, David R Thorburn, David Arthur Stroud, Susan M White, John Chrisodoulou, Natasha J Brown
Biallelic Variants in PYROXD2 Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial Function. International journal of molecular sciences 23 (2) (2022)
Alison D Archibald, Belinda J McClaren, Jade Caruana, Erin Tutty, Emily A King, Jane L Halliday, Stephanie Best, Anaita Kanga-Parabia, Bruce H Bennetts, Corrina C Cliffe, Evanthia Olympia Madelli, Gladys Ho, Jan Liebelt, Janet C Long, Jeffrey Braithwaite, Jillian Kennedy, R John H Massie, Jon D Emery, Julie McGaughran, Justine E Marum, Kirsten Boggs, Kristine Barlow-Stewart, Leslie Burnett, Lisa Dive, Lucinda Freeman, Mark R Davis, Martin J Downes, Mathew Wallis, Monica M Ferrie, Nicholas Pachter, Paul A Scuffham, Rachael Casella, Richard J N Allcock, Royston Ong, Samantha Edwards, Sarah Righetti, Sebastian Lunke, Sharon Lewis, Susan P Walker, Tiffany F Boughtwood, Tristan Hardy, Ainsley Janelle Newson, Edwin P Kirk, Nigel G Laing, Martin B Delatycki, null The Mackenzie's Mission Study Team
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation. Journal of personalized medicine 12 (11) (2022)
Alison D Archibald, Belinda J McClaren, Jade Caruana, Erin Tutty, Emily A King, Jane L Halliday, Stephanie Best, Anaita Kanga-Parabia, Bruce H Bennetts, Corrina C Cliffe, Evanthia Olympia Madelli, Gladys Ho, Jan Liebelt, Janet C Long, Jeffrey Braithwaite, Jillian Kennedy, R John H Massie, Jon D Emery, Julie McGaughran, Justine E Marum, Kirsten Boggs, Kristine Barlow-Stewart, Leslie Burnett, Lisa Dive, Lucinda Freeman, Mark R Davis, Martin J Downes, Mathew Wallis, Monica M Ferrie, Nicholas Pachter, Paul A Scuffham, Rachael Casella, Richard J N Allcock, Royston Ong, Samantha Edwards, Sarah Righetti, Sebastian Lunke, Sharon Lewis, Susan P Walker, Tiffany F Boughtwood, Tristan Hardy, Ainsley Janelle Newson, Edwin P Kirk, Nigel G Laing, Martin B Delatycki, null The Mackenzie's Mission Study Team
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation. Journal of personalized medicine 12 (11) (2022)
David I Francis, Zornitza Stark, Ingrid E Scheffer, Tiong Yang Tan, Krithika Murali, Lyndon Gallacher, David J Amor, Himanshu Goel, Lilian Downie, Chloe A Stutterd, Emma I Krzesinski, Anand Vasudevan, Ralph Oertel, Vida Petrovic, Amber Boys, Vivian Wei, Trent Burgess, Karen Dun, Karen L Oliver, Anne Baxter, Anna Hackett, Samantha Ayres, Sebastian Lunke, Paul Kalitsis, Meaghan Wall
Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability. European journal of human genetics : EJHG (2022)
Alison D Archibald, Belinda J McClaren, Jade Caruana, Erin Tutty, Emily A King, Jane L Halliday, Stephanie Best, Anaita Kanga-Parabia, Bruce H Bennetts, Corrina C Cliffe, Evanthia Olympia Madelli, Gladys Ho, Jan Liebelt, Janet C Long, Jeffrey Braithwaite, Jillian Kennedy, R John H Massie, Jon D Emery, Julie McGaughran, Justine E Marum, Kirsten Boggs, Kristine Barlow-Stewart, Leslie Burnett, Lisa Dive, Lucinda Freeman, Mark R Davis, Martin J Downes, Mathew Wallis, Monica M Ferrie, Nicholas Pachter, Paul A Scuffham, Rachael Casella, Richard J N Allcock, Royston Ong, Samantha Edwards, Sarah Righetti, Sebastian Lunke, Sharon Lewis, Susan P Walker, Tiffany F Boughtwood, Tristan Hardy, Ainsley Janelle Newson, Edwin P Kirk, Nigel G Laing, Martin B Delatycki, null The Mackenzie's Mission Study Team
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation. Journal of personalized medicine 12 (11) (2022)
Ari E Horton, Kai Mun Hong, Dinusha Pandithan, Meredith Allen, Caroline Killick, Stacy K Goergen, Amanda Springer, Dean Phelan, Melanie Marty, Rebecca Halligan, Joy Lee, James Pitt, Belinda Chong, John Chrisodoulou, Sebastian Lunke, Zornitza Stark, Michael Collingwood Fahey
Ethylmalonic encephalopathy masquerading as meningococcemia. Cold Spring Harbor molecular case studies 8 (2) (2022)
Sebastian Lunke, Scott Maxwell, Ishant Khurana, Harikrishnan Kaipananickal, Jun Okabe, Keith Al-Hasani, Assam El-Osta
Epigenetic evidence of an Ac/Dc axis by VPA and SAHA. Clinical epigenetics 13 (1) (2021)
Lilian Downie, Jane Halliday, Rachel Burt, Sebastian Lunke, Elly Lynch, Melissa Martyn, Zeffie Poulakis, Clara Gaff, Valerie Sung, Melissa Wake, Matthew F Hunter, Kerryn Saunders, Elizabeth Rose, Sharon Lewis, Anna Jarmolowicz, Dean Phelan, Heidi L Rehm, null null, David J Amor
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study. European journal of human genetics : EJHG 28 (5) (2019)
Tiong Yang Tan, Sebastian Lunke, Belinda Chong, Dean Phelan, Miriam Fanjul-Fernandez, Justine E Marum, Vanessa Siva Kumar, Zornitza Stark, Alison Yeung, Natasha J Brown, Chloe Stutterd, Martin B Delatycki, Simon Sadedin, Melissa Martyn, Ilias Goranitis, Natalie Thorne, Clara L Gaff, Susan M White
A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European journal of human genetics : EJHG 27 (12) (2019)
Lauren S Akesson, Stefanie Eggers, Clare J Love, Belinda Chong, Emma I Krzesinski, Natasha J Brown, Tiong Y Tan, Christopher M Richmond, David R Thorburn, John Chrisodoulou, Matthew F Hunter, Sebastian Lunke, Zornitza Stark
Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing. European journal of human genetics : EJHG 27 (12) (2019)
Zornitza Stark, Amy Nisselle, Belinda J McClaren, Fiona Lynch, Stephanie Best, Janet C Long, Melissa Martyn, Chirag Patel, Luregn J Schlapbach, Christopher Barnett, Christiane Theda, Jason Pinner, Marcel E Dinger, Sebastian Lunke, Clara L Gaff
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care. European journal of human genetics : EJHG 27 (10) (2019)
Oliver James Dillon, Sebastian Lunke, Zornitza Stark, Alison Yeung, Natalie Thorne, null null, Clara Gaff, Susan M White, Tiong Yang Tan
Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. European journal of human genetics : EJHG 26 (5) (2018)
Sebastian Lunke, Belinda Lee, Sevastjan Kranz, Peter Gibbs, Paul Waring, Michael Christie
Intratumorous heterogeneity for RAS mutations in a treatment-naïve colorectal tumour. Journal of clinical pathology 70 (8) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sebastian Lunke