Sebastian Lunke

Affiliations
  • Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
  • Australian Genomics Health Alliance, Melbourne, VIC, Australia.
  • Department of Clinical Pathology, University of Melbourne, Melbourne, VIC, Australia.
ORCID: http://orcid.org/0000-0002-7168-0723

Publications (60)

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
Avec: 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 Christodoulou , Matthew F Hunter , Sebastian Lunke , Zornitza Stark

Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review.

Molecular genetics & genomic medicine
Avec: Natalie B Tan , Rachel Stapleton , Zornitza Stark , Martin B Delatycki , Alison Yeung , Matthew F Hunter , David J Amor , Natasha J Brown , Chloe A Stutterd , George McGillivray , Patrick Yap , Matthew Regan , Belinda Chong , Miriam Fanjul Fernandez , Justine Marum , Dean Phelan , Lynn S Pais , Susan M White , Sebastian Lunke , Tiong Y Tan

Severe NAD(P)HX Dehydratase (NAXD) Neurometabolic Syndrome May Present in Adulthood after Mild Head Trauma.

International journal of molecular sciences
Avec: Nicole J Van Bergen , Karen Gunanayagam , Adam M Bournazos , Adhish S Walvekar , Marc O Warmoes , Liana N Semcesen , Sebastian Lunke , Shobhana Bommireddipalli , Tim Sikora , Myrto Patraskaki , Dean L Jones , Denisse Garza , Dale Sebire , Samuel Gooley , Catriona A McLean , Parm Naidoo , Mugil Rajasekaran , David A Stroud , Carole L Linster , Mathew Wallis , Sandra T Cooper , John Christodoulou

POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.

American journal of human genetics
Avec: Kelly Smallwood , Kristin E N Watt , Satoru Ide , Kristina Baltrunaite , Chad Brunswick , Katherine Inskeep , Corrine Capannari , Margaret P Adam , Amber Begtrup , Debora R Bertola , Laurie Demmer , Erin Demo , Orrin Devinsky , Emily R Gallagher , Maria J Guillen Sacoto , Robert Jech , Boris Keren , Jennifer Kussmann , Roger Ladda , Lisa A Lansdon , Sebastian Lunke , Anne Mardy , Kirsty McWalters , Richard Person , Laura Raiti , Noriko Saitoh , Carol J Saunders , Rhonda Schnur , Matej Skorvanek , Susan L Sell , Anne Slavotinek , Bonnie R Sullivan , Zornitza Stark , Joseph D Symonds , Tara Wenger , Sacha Weber , Sandra Whalen , Susan M White , Juliane Winkelmann , Michael Zech , Shimriet Zeidler , Kazuhiro Maeshima , Rolf W Stottmann , Paul A Trainor , K Nicole Weaver

Integrated multi-omics for rapid rare disease diagnosis on a national scale.

Nature medicine
Avec: 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 Y Tan , Mary-Louise Freckmann , Belinda Chong , Dean Phelan , David Francis , Karin S Kassahn , Thuong 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 Christodoulou , Zornitza Stark

Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Kerith-Rae Dias , Rupendra Shrestha , Deborah Schofield , Carey-Anne Evans , Emily O'Heir , Ying Zhu , Futao Zhang , Krystle Standen , Ben Weisburd , Sarah L Stenton , Alba Sanchis-Juan , Harrison Brand , Michael E Talkowski , Alan Ma , Sondy Ghedia , Meredith Wilson , Sarah A Sandaradura , Janine Smith , Benjamin Kamien , Anne Turner , Madhura Bakshi , Lesley C Adès , David Mowat , Matthew Regan , George McGillivray , Ravi Savarirayan , Susan M White , Tiong Yang Tan , Zornitza Stark , Natasha J Brown , Luis A Pérez-Jurado , Emma Krzesinski , Matthew F Hunter , Lauren Akesson , Andrew Paul Fennell , Alison Yeung , Tiffany Boughtwood , Lisa J Ewans , Jennifer Kerkhof , Christopher Lucas , Louise Carey , Hugh French , Melissa Rapadas , Igor Stevanovski , Ira W Deveson , Corrina Cliffe , George Elakis , Edwin P Kirk , Tracy Dudding-Byth , Janice Fletcher , Rebecca Walsh , Mark A Corbett , Thessa Kroes , Jozef Gecz , Cliff Meldrum , Simon Cliffe , Meg Wall , Sebastian Lunke , Kathryn North , David J Amor , Michael Field , Bekim Sadikovic , Michael F Buckley , Anne O'Donnell-Luria , Tony Roscioli

Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.

BMJ open
Avec: Sebastian Lunke , Sophie E Bouffler , Lilian Downie , Jade Caruana , David J Amor , Alison Archibald , Yvonne Bombard , John Christodoulou , Marc Clausen , Paul De Fazio , Ronda F Greaves , Sebastian Hollizeck , Anaita Kanga-Parabia , Nitzan Lang , Fiona Lynch , Riccarda Peters , Simon Sadedin , Erin Tutty , Stefanie Eggers , Crystle Lee , Meaghan Wall , Alison Yeung , Clara Gaff , Christopher Gyngell , Danya F Vears , Stephanie Best , Ilias Goranitis , Zornitza Stark

Benchmarking pharmacogenomics genotyping tools: Performance analysis on short-read sequencing samples and depth-dependent evaluation.

Clinical and translational science
Avec: Andreas Halman , Sebastian Lunke , Simon Sadedin , Claire Moore , Rachel Conyers

Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services.

European journal of human genetics : EJHG
Avec: 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 Christodoulou , Hamish Scott , Julie McGaughran , Zornitza Stark

Critically unwell infants and children with mitochondrial disorders diagnosed by ultra-rapid genomic sequencing.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Megan Ball , Sophie E Bouffler , Christopher B Barnett , Mary-Louise Freckmann , Matthew F Hunter , Benjamin Kamien , Karin S Kassahn , Sebastian Lunke , Chirag V Patel , Jason Pinner , Tony Roscioli , Sarah A Sandaradura , Hamish S Scott , Tiong Y Tan , Mathew Wallis , Alison G Compton , David R Thorburn , Zornitza Stark , John Christodoulou

Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype.

Nature communications
Avec: Marija Kojic , Tomasz Gawda , Monika Gaik , Alexander Begg , Anna Salerno-Kochan , Nyoman D Kurniawan , Alun Jones , Katarzyna Drożdżyk , Anna Kościelniak , Andrzej Chramiec-Głąbik , Soroor Hediyeh-Zadeh , Maria Kasherman , Woo Jun Shim , Enakshi Sinniah , Laura A Genovesi , Rannvá K Abrahamsen , Christina D Fenger , Camilla G Madsen , Julie S Cohen , Ali Fatemi , Zornitza Stark , Sebastian Lunke , Joy Lee , Jonas K Hansen , Martin F Boxill , Boris Keren , Isabelle Marey , Margarita S Saenz , Kathleen Brown , Suzanne A Alexander , Sergey Mureev , Alina Batzilla , Melissa J Davis , Michael Piper , Mikael Bodén , Thomas H J Burne , Nathan J Palpant , Rikke S Møller , Sebastian Glatt , Brandon J Wainwright

ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients.

The Journal of experimental medicine
Avec: Katja Apelt , Susan M White , Hyun Suk Kim , Jung-Eun Yeo , Angela Kragten , Annelotte P Wondergem , Martin A Rooimans , Román González-Prieto , Wouter W Wiegant , Sebastian Lunke , Daniel Flanagan , Sarah Pantaleo , Catherine Quinlan , Winita Hardikar , Haico van Attikum , Alfred C O Vertegaal , Brian T Wilson , Rob M F Wolthuis , Orlando D Schärer , Martijn S Luijsterburg

Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level.

NPJ genomic medicine
Avec: Stephanie Best , Helen Brown , Sebastian Lunke , Chirag Patel , Jason Pinner , Christopher P Barnett , Meredith Wilson , Sarah A Sandaradura , Belinda McClaren , Gemma R Brett , Jeffrey Braithwaite , Zornitza Stark

Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Zornitza Stark , Deborah Schofield , Melissa Martyn , Luke Rynehart , Rupendra Shrestha , Khurshid Alam , Sebastian Lunke , Tiong Y Tan , Clara L Gaff , Susan M White

A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.

Journal of genetic counseling
Avec: Melissa Martyn , Anaita Kanga-Parabia , Elly Lynch , Paul A James , Ivan Macciocca , Alison H Trainer , Jane Halliday , Louise Keogh , Janney Wale , Ingrid Winship , Michael Bogwitz , Giulia Valente , Maie Walsh , Lilian Downie , David Amor , Mathew Wallis , Fiona Cunningham , Matthew Burgess , Natasha J Brown , Anna Jarmolowicz , Sebastian Lunke , Ilias Goranitis , Auteur inconnu , Clara L Gaff

Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function.

Human mutation
Avec: Atteeq U Rehman , Maryam Najafi , Marios Kambouris , Lihadh Al-Gazali , Periklis Makrythanasis , Abolfazl Rad , Reza Maroofian , Anna Rajab , Zornitza Stark , Jill V Hunter , Zeineb Bakey , Mari J Tokita , Weimin He , Francesco Vetrini , Andrea Petersen , Federico A Santoni , Hanan Hamamy , Kaman Wu , Fatma Al-Jasmi , Martin Helmstädter , Sebastian J Arnold , Fan Xia , Christopher Richmond , Pengfei Liu , Ehsan Ghayoor Karimiani , GholamReza Karami Madani , Sebastian Lunke , Hatem El-Shanti , Christine M Eng , Stylianos E Antonarakis , Jozef Hertecant , Magdalena Walkiewicz , Yaping Yang , Miriam Schmidts

Whole exome sequencing reveals a de novo missense variant in

Clinical case reports
Avec: Simranpreet Kaur , Nicole J Van Bergen , Wendy Anne Gold , Stefanie Eggers , Sebastian Lunke , Susan M White , Carolyn Ellaway , John Christodoulou

A cost-effectiveness analysis of genomic sequencing in a prospective versus historical cohort of complex pediatric patients.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Alison Yeung , Natalie B Tan , Tiong Y Tan , Zornitza Stark , Natasha Brown , Matthew F Hunter , Martin Delatycki , Chloe Stutterd , Ravi Savarirayan , George Mcgillivray , Rachel Stapleton , Smitha Kumble , Lilian Downie , Matthew Regan , Sebastian Lunke , Belinda Chong , Dean Phelan , Gemma R Brett , Anna Jarmolowicz , Yael Prawer , Giulia Valente , Yana Smagarinsky , Melissa Martyn , Callum McEwan , Ilias Goranitis , Clara Gaff , Susan M White

Ethylmalonic encephalopathy masquerading as meningococcemia.

Cold Spring Harbor molecular case studies
Avec: Ari Horton , Kai Mun Hong , Dinusha Pandithan , Meredith Allen , Caroline Killick , Stacy Goergen , Amanda Springer , Dean Phelan , Melanie Marty , Rebecca Halligan , Joy Lee , James Pitt , Belinda Chong , John Christodoulou , Sebastian Lunke , Zornitza Stark , Michael Fahey

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review.

JAMA neurology
Avec: Sarah U Morton , John Christodoulou , Gregory Costain , Francesco Muntoni , Emma Wakeling , Monica H Wojcik , Courtney E French , Anna Szuto , James J Dowling , Ronald D Cohn , F Lucy Raymond , Basil T Darras , David A Williams , Sebastian Lunke , Zornitza Stark , David H Rowitch , Pankaj B Agrawal

Australian public perspectives on genomic newborn screening: which conditions should be included?

Human genomics
Avec: Fiona Lynch , Stephanie Best , Clara Gaff , Lilian Downie , Alison D Archibald , Christopher Gyngell , Ilias Goranitis , Riccarda Peters , Julian Savulescu , Sebastian Lunke , Zornitza Stark , Danya F Vears

Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol.

BMJ open
Avec: Sophie E Bouffler , Ling Lee , Fiona Lynch , Melissa Martyn , Elly Lynch , Ivan Macciocca , Lisette Curnow , Giulia McCorkell , Sebastian Lunke , Belinda Chong , Justine E Marum , Martin Delatycki , Lilian Downie , Ilias Goranitis , Danya F Vears , Stephanie Best , Marc Clausen , Yvonne Bombard , Zornitza Stark , Clara L Gaff

Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.

Epigenomics
Avec: Mohammed Alshawsh , Melissa Wake , Jozef Gecz , Mark Corbett , Richard Saffery , James Pitt , Ronda Greaves , Katrina Williams , Michael Field , Jeanie Cheong , Minh Bui , Sheena Arora , Simon Sadedin , Sebastian Lunke , Meg Wall , David J Amor , David E Godler

Rapid Identification of Biallelic

Molecular syndromology
Avec: Christopher M Richmond , Sally Campbell , Hee W Foo , Sebastian Lunke , Zornitza Stark , Amanda Moody , Elizabeth Bannister , Anthea Greenway , Natasha Brown

Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate.

Human mutation
Avec: Lauren S Akesson , Adam Bournazos , Andrew Fennell , Emma I Krzesinski , Kenneth Tan , Amanda Springer , Katherine Rose , Ilias Goranitis , David Francis , Crystle Lee , Fathimath Faiz , Mark R Davis , John Christodoulou , Sebastian Lunke , Zornitza Stark , Matthew F Hunter , Sandra T Cooper

Missense variants in TAF1 and developmental phenotypes: challenges of determining pathogenicity.

Human mutation
Avec: Hanyin Cheng , Simona Capponi , Emma Wakeling , Elaine Marchi , Quan Li , Mengge Zhao , Chunhua Weng , Piatek G Stefan , Helena Ahlfors , Robert Kleyner , Alan Rope , Aimé Lumaka , Prosper Lukusa , Koenraad Devriendt , Joris Vermeesch , Jennifer E Posey , Elizabeth E Palmer , Lucinda Murray , Eyby Leon , Jullianne Diaz , Lisa Worgan , Amalia Mallawaarachchi , Julie Vogt , Sonja A de Munnik , Lauren Dreyer , Gareth Baynam , Lisa Ewans , Zornitza Stark , Sebastian Lunke , Ana R Gonçalves , Gabriela Soares , Jorge Oliveira , Emily Fassi , Marcia Willing , Jeff L Waugh , Laurence Faivre , Jean-Baptiste Riviere , Sebastien Moutton , Shehla Mohammed , Katelyn Payne , Laurence Walsh , Amber Begtrup , Maria J Guillen Sacoto , Ganka Douglas , Nora Alexander , Michael F Buckley , Paul R Mark , Lesley C Adès , Sarah A Sandaradura , James R Lupski , Tony Roscioli , Pankaj B Agrawal , Antonie D Kline , Auteur inconnu , Kai Wang , H T Marc Timmers , Gholson J Lyon

Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Adam M Bournazos , Lisa G Riley , Shobhana Bommireddipalli , Lesley Ades , Lauren S Akesson , Mohammad Al-Shinnag , Stephen I Alexander , Alison D Archibald , Shanti Balasubramaniam , Yemima Berman , Victoria Beshay , Kirsten Boggs , Jasmina Bojadzieva , Natasha J Brown , Samantha J Bryen , Michael F Buckley , Belinda Chong , Mark R Davis , Ruebena Dawes , Martin Delatycki , Liz Donaldson , Lilian Downie , Caitlin Edwards , Matthew Edwards , Amanda Engel , Lisa J Ewans , Fathimath Faiz , Andrew Fennell , Michael Field , Mary-Louise Freckmann , Lyndon Gallacher , Russell Gear , Himanshu Goel , Shuxiang Goh , Linda Goodwin , Bernadette Hanna , James Harraway , Megan Higgins , Gladys Ho , Bruce K Hopper , Ari E Horton , Matthew F Hunter , Aamira J Huq , Sarah Josephi-Taylor , Himanshu Joshi , Edwin Kirk , Emma Krzesinski , Kishore R Kumar , Frances Lemckert , Richard J Leventer , Suzanna E Lindsey-Temple , Sebastian Lunke , Alan Ma , Steven Macaskill , Amali Mallawaarachchi , Melanie Marty , Justine E Marum , Hugh J McCarthy , Manoj P Menezes , Alison McLean , Di Milnes , Shekeeb Mohammad , David Mowat , Aram Niaz , Elizabeth E Palmer , Chirag Patel , Shilpan G Patel , Dean Phelan , Jason R Pinner , Sulekha Rajagopalan , Matthew Regan , Jonathan Rodgers , Miriam Rodrigues , Richard H Roxburgh , Rani Sachdev , Tony Roscioli , Ruvishani Samarasekera , Sarah A Sandaradura , Elena Savva , Tim Schindler , Margit Shah , Ingrid B Sinnerbrink , Janine M Smith , Richard J Smith , Amanda Springer , Zornitza Stark , Samuel P Strom , Carolyn M Sue , Kenneth Tan , Tiong Y Tan , Esther Tantsis , Michel C Tchan , Bryony A Thompson , Alison H Trainer , Karin van Spaendonck-Zwarts , Rebecca Walsh , Linda Warwick , Stephanie White , Susan M White , Mark G Williams , Meredith J Wilson , Wui Kwan Wong , Dale C Wright , Patrick Yap , Alison Yeung , Helen Young , Kristi J Jones , Bruce Bennetts , Sandra T Cooper , Auteur inconnu

Clinical impact of genomic testing in patients with suspected monogenic kidney disease.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Kushani Jayasinghe , Zornitza Stark , Peter G Kerr , Clara Gaff , Melissa Martyn , John Whitlam , Belinda Creighton , Elizabeth Donaldson , Matthew Hunter , Anna Jarmolowicz , Lilian Johnstone , Emma Krzesinski , Sebastian Lunke , Elly Lynch , Kathleen Nicholls , Chirag Patel , Yael Prawer , Jessica Ryan , Emily J See , Andrew Talbot , Alison Trainer , Rigan Tytherleigh , Giulia Valente , Mathew Wallis , Louise Wardrop , Kirsty H West , Susan M White , Ella Wilkins , Andrew J Mallett , Catherine Quinlan

Clinical Utility of Real-Time Targeted Molecular Profiling in the Clinical Management of Ovarian Cancer: The ALLOCATE Study.

JCO precision oncology
Avec: Olga Kondrashova , Gwo-Yaw Ho , George Au-Yeung , Leakhena Leas , Tiffany Boughtwood , Kathryn Alsop , Giada Zapparoli , Alexander Dobrovic , Yi-An Ko , Arthur L Hsu , Clare J Love , Sebastian Lunke , Matthew J Wakefield , Orla McNally , Michael Quinn , Sumitra Ananda , Deborah Neesham , Anne Hamilton , Marisa Grossi , Alison Freimund , Yada Kanjanapan , Danny Rischin , Nadia Traficante , David Bowtell , Clare L Scott , Michael Christie , Graham R Taylor , Linda Mileshkin , Paul M Waring , Auteur inconnu

The role of exome sequencing in childhood interstitial or diffuse lung disease.

Orphanet journal of rare diseases
Avec: Suzanna E L Temple , Gladys Ho , Bruce Bennetts , Kirsten Boggs , Nada Vidic , David Mowat , John Christodoulou , André Schultz , Thet Gayagay , Tony Roscioli , Ying Zhu , Sebastian Lunke , David Armstrong , Joanne Harrison , Nitin Kapur , Tim McDonald , Hiran Selvadurai , Andrew Tai , Zornitza Stark , Adam Jaffe

Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation.

International journal of neonatal screening
Avec: Fiona Lynch , Stephanie Best , Clara Gaff , Lilian Downie , Alison D Archibald , Christopher Gyngell , Ilias Goranitis , Riccarda Peters , Julian Savulescu , Sebastian Lunke , Zornitza Stark , Danya F Vears

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
Avec: Erin Tutty , Alison D Archibald , Lilian Downie , Clara Gaff , Sebastian Lunke , Danya F Vears , Zornitza Stark , Stephanie Best

Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023.

Human genomics
Avec: Amali Mallawaarachchi , Erik Biros , Trudie Harris , Bruce Bennetts , Tiffany Boughtwood , Justine Elliott , Lindsay Fowles , Robert Gardos , Denisse Garza , Ilias Goranitis , Matilda Haas , Vanessa Huntley , Julia Jefferis , Karin Kassahn , Anna Leaver , Ben Lundie , Sebastian Lunke , Caitlin O'Connor , Greg Pratt , Catherine Quinlan , Dianne Shearman , Jacqueline Soraru , Madhivanan Sundaram , Michel Tchan , Giulia Valente , Julie White , Ella Wilkins , Steve I Alexander , Noa Amir , Stephanie Best , Hossai Gul , Kushani Jayasinghe , Hugh McCarthy , Chirag Patel , Zornitza Stark , Andrew J Mallett

Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature.

Clinical genetics
Avec: B Schönewolf-Greulich , A-M Bisgaard , R S Møller , M Dunø , K Brøndum-Nielsen , S Kaur , N J Van Bergen , S Lunke , S Eggers , C Jespersgaard , J Christodoulou , Z Tümer

Parental experiences of ultrarapid genomic testing for their critically unwell infants and children.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Gemma R Brett , Melissa Martyn , Fiona Lynch , Michelle G de Silva , Samantha Ayres , Lyndon Gallacher , Kirsten Boggs , Anne Baxendale , Sarah Schenscher , Sarah King-Smith , Lindsay Fowles , Amanda Springer , Sebastian Lunke , Anand Vasudevan , Emma Krzesinski , Jason Pinner , Sarah A Sandaradura , Christopher Barnett , Chirag Patel , Meredith Wilson , Zornitza Stark

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System.

JAMA
Avec: Auteur inconnu , Sebastian Lunke , Stefanie Eggers , Meredith Wilson , Chirag Patel , Christopher P Barnett , Jason Pinner , Sarah A Sandaradura , Michael F Buckley , Emma I Krzesinski , Michelle G de Silva , Gemma R Brett , Kirsten Boggs , David Mowat , Edwin P Kirk , Lesley C Adès , Lauren S Akesson , David J Amor , Samantha Ayres , Anne Baxendale , Sarah Borrie , Alessandra Bray , Natasha J Brown , Cheng Yee Chan , Belinda Chong , Corrina Cliffe , Martin B Delatycki , Matthew Edwards , George Elakis , Michael C Fahey , Andrew Fennell , Lindsay Fowles , Lyndon Gallacher , Megan Higgins , Katherine B Howell , Lauren Hunt , Matthew F Hunter , Kristi J Jones , Sarah King , Smitha Kumble , Sarah Lang , Maelle Le Moing , Alan Ma , Dean Phelan , Michael C J Quinn , Anna Richards , Christopher M Richmond , Jessica Riseley , Jonathan Rodgers , Rani Sachdev , Simon Sadedin , Luregn J Schlapbach , Janine Smith , Amanda Springer , Natalie B Tan , Tiong Y Tan , Suzanna L Temple , Christiane Theda , Anand Vasudevan , Susan M White , Alison Yeung , Ying Zhu , Melissa Martyn , Stephanie Best , Tony Roscioli , John Christodoulou , Zornitza Stark

The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.

Journal of the neurological sciences
Avec: Dhamidhu Eratne , Amy Schneider , Ella Lynch , Melissa Martyn , Dennis Velakoulis , Michael Fahey , Patrick Kwan , Richard Leventer , Haloom Rafehi , Belinda Chong , Zornitza Stark , Sebastian Lunke , Dean G Phelan , Melanie O'Keefe , Kirby Siemering , Kirsty West , Adrienne Sexton , Anna Jarmolowicz , Jessica A Taylor , Joshua Schultz , Rebecca Purvis , Eloise Uebergang , Heather Chalinor , Belinda Creighton , Nikki Gelfand , Tamar Saks , Yael Prawer , Yana Smagarinsky , Tianxin Pan , Ilias Goranitis , Zanfina Ademi , Clara Gaff , Aamira Huq , Maie Walsh , Paul A James , Emma I Krzesinski , Mathew Wallis , Chloe A Stutterd , Melanie Bahlo , Martin B Delatycki , Samuel F Berkovic

Paediatric genomic testing: Navigating medicare rebatable genomic testing.

Journal of paediatrics and child health
Avec: Rani Sachdev , Mike Field , Gareth S Baynam , John Beilby , Maria Berarducci , Yemima Berman , Tiffany Boughtwood , Marie B Cusack , Vanessa Fitzgerald , Jeffery Fletcher , Mary-Louise Freckmann , Natalie Grainger , Edwin Kirk , Ben Lundie , Sebastian Lunke , Lesley McGregor , David Mowat , Gayathri Parasivam , Vanessa Tyrell , Mathew Wallis , Susan M White , Alan S L Ma

Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution.

American journal of human genetics
Avec: Zornitza Stark , Rebecca E Foulger , Eleanor Williams , Bryony A Thompson , Chirag Patel , Sebastian Lunke , Catherine Snow , Ivone U S Leong , Arina Puzriakova , Louise C Daugherty , Sarah Leigh , Christopher Boustred , Olivia Niblock , Antonio Rueda-Martin , Oleg Gerasimenko , Kevin Savage , William Bellamy , Victor San Kho Lin , Roman Valls , Lavinia Gordon , Helen K Brittain , Ellen R A Thomas , Ana Lisa Taylor Tavares , Meriel McEntagart , Susan M White , Tiong Y Tan , Alison Yeung , Lilian Downie , Ivan Macciocca , Elena Savva , Crystle Lee , Ain Roesley , Paul De Fazio , Jane Deller , Zandra C Deans , Sue L Hill , Mark J Caulfield , Kathryn N North , Richard H Scott , Augusto Rendon , Oliver Hofmann , Ellen M McDonagh

Biallelic Variants in

International journal of molecular sciences
Avec: Nicole J Van Bergen , Daniella H 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 A Stroud , Susan M White , John Christodoulou , Natasha J Brown

Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Ilias Goranitis , You Wu , Sebastian Lunke , Susan M White , Tiong Y Tan , Alison Yeung , Matthew F Hunter , Melissa Martyn , Clara Gaff , Zornitza Stark

Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease.

Human molecular genetics
Avec: Sumudu S C Amarasekera , Daniella H Hock , Nicole J Lake , Sarah E Calvo , Sabine W Grønborg , Emma I Krzesinski , David J Amor , Michael C Fahey , Cas Simons , Flemming Wibrand , Vamsi K Mootha , Monkol Lek , Sebastian Lunke , Zornitza Stark , Elsebet Østergaard , John Christodoulou , David R Thorburn , David A Stroud , Alison G Compton

The cost of proband and trio exome and genome analysis in rare disease: a micro-costing study.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Dylan A Mordaunt , Francisco Santos Gonzalez , Sebastian Lunke , Stefanie Eggers , Simon Sadedin , Belinda Chong , Kim Dalziel , Zornitza Stark , Ilias Goranitis

Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.

American journal of human genetics
Avec: Emma Tudini , James Andrews , David M Lawrence , Sarah L King-Smith , Naomi Baker , Leanne Baxter , John Beilby , Bruce Bennetts , Victoria Beshay , Michael Black , Tiffany F Boughtwood , Kristian Brion , Pak Leng Cheong , Michael Christie , John Christodoulou , Belinda Chong , Kathy Cox , Mark R Davis , Lucas Dejong , Marcel E Dinger , Kenneth D Doig , Evelyn Douglas , Andrew Dubowsky , Melissa Ellul , Andrew Fellowes , Katrina Fisk , Cristina Fortuno , Kathryn Friend , Renee L Gallagher , Song Gao , Emma Hackett , Johanna Hadler , Michael Hipwell , Gladys Ho , Georgina Hollway , Amanda J Hooper , Karin S Kassahn , Rahul Krishnaraj , Chiyan Lau , Huong Le , Huei San Leong , Ben Lundie , Sebastian Lunke , Anthony Marty , Mary McPhillips , Lan T Nguyen , Katia Nones , Kristen Palmer , John V Pearson , Michael C J Quinn , Lesley H Rawlings , Simon Sadedin , Louisa Sanchez , Andreas W Schreiber , Emanouil Sigalas , Aygul Simsek , Julien Soubrier , Zornitza Stark , Bryony A Thompson , James U , Cassandra G Vakulin , Amanda V Wells , Cheryl A Wise , Rick Woods , Andrew Ziolkowski , Marie-Jo Brion , Hamish S Scott , Natalie P Thorne , Amanda B Spurdle , Auteur inconnu

Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability.

European journal of human genetics : EJHG
Avec: 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

The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.

Journal of personalized medicine
Avec: 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 O Madelli , Gladys Ho , Jan Liebelt , Janet C Long , Jeffrey Braithwaite , Jillian Kennedy , John 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 J Newson , Edwin P Kirk , Nigel G Laing , Martin B Delatycki , The Mackenzie's Mission Study Team

Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Lilian Downie , Jane Halliday , Sharon Lewis , Sebastian Lunke , Elly Lynch , Melissa Martyn , Clara Gaff , Anna Jarmolowicz , David J Amor

Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

European journal of human genetics : EJHG
Avec: 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 , Auteur inconnu , David J Amor

The expanding LARS2 phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy.

Human mutation
Avec: Lisa G Riley , Joëlle Rudinger-Thirion , Magali Frugier , Meredith Wilson , Melissa Luig , Thushari Indika Alahakoon , Cheng Yee Nixon , Edwin P Kirk , Tony Roscioli , Sebastian Lunke , Zornitza Stark , Klaas J Wierenga , Sirish Palle , Maie Walsh , Emily Higgs , Susan Arbuckle , Shalini Thirukeswaran , Alison G Compton , David R Thorburn , John Christodoulou

Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Zornitza Stark , Deborah Schofield , Melissa Martyn , Luke Rynehart , Rupendra Shrestha , Khurshid Alam , Sebastian Lunke , Tiong Y Tan , 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
Avec: 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

Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.

European journal of human genetics : EJHG
Avec: Zornitza Stark , Amy Nisselle , Belinda 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

Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders.

American journal of human genetics
Avec: Jacob R Stolz , Kendall M Foote , Hermine E Veenstra-Knol , Rolph Pfundt , Sanne W Ten Broeke , Nicole de Leeuw , Laura Roht , Sander Pajusalu , Reelika Part , Ionella Rebane , Katrin Õunap , Zornitza Stark , Edwin P Kirk , John A Lawson , Sebastian Lunke , John Christodoulou , Raymond J Louie , R Curtis Rogers , Jessica M Davis , A Micheil Innes , Xing-Chang Wei , Boris Keren , Cyril Mignot , Robert Roger Lebel , Steven M Sperber , Ai Sakonju , Nienke Dosa , Daniela Q C M Barge-Schaapveld , Cacha M P C D Peeters-Scholte , Claudia A L Ruivenkamp , Bregje W van Bon , Joanna Kennedy , Karen J Low , Sian Ellard , Lewis Pang , Joseph J Junewick , Paul R Mark , Gemma L Carvill , Geoffrey T Swanson

Clinical and laboratory reporting impact of ACMG-AMP and modified ClinGen variant classification frameworks in MYH7-related cardiomyopathy.

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Christopher M Richmond , Paul A James , Sarah-Jane Pantaleo , Belinda Chong , Sebastian Lunke , Tiong Y Tan , Ivan Macciocca

Epigenetic evidence of an Ac/Dc axis by VPA and SAHA.

Clinical epigenetics
Avec: Sebastian Lunke , Scott Maxwell , Ishant Khurana , Harikrishnan K N , Jun Okabe , Keith Al-Hasani , Assam El-Osta

MSH2-deficient prostate tumours have a distinct immune response and clinical outcome compared to MSH2-deficient colorectal or endometrial cancer.

Prostate cancer and prostatic diseases
Avec: Patrick McCoy , Stefano Mangiola , Geoff Macintyre , Ryan Hutchinson , Ben Tran , Bernard Pope , Peter Georgeson , Matthew K H Hong , Natalie Kurganovs , Sebastian Lunke , Michael J Clarkson , Marek Cmero , Michael Kerger , Ryan Stuchbery , Ken Chow , Izhak Haviv , Andrew Ryan , Anthony J Costello , Niall M Corcoran , Christopher M Hovens

Distinct diagnostic trajectories in NBAS-associated acute liver failure highlights the need for timely functional studies.

JIMD reports
Avec: Lauren S Akesson , Rocio Rius , Natasha J Brown , Jeremy Rosenbaum , Sarah Donoghue , Michael Stormon , Charmaine Chai , Esmeralda Bordador , Yiran Guo , Hakon Hakonarson , Alison G Compton , David R Thorburn , Sumudu Amarasekera , Justine Marum , Alisha Monaco , Crystle Lee , Belinda Chong , Sebastian Lunke , Zornitza Stark , John Christodoulou

Gene selection for genomic newborn screening: Moving toward consensus?

Genetics in medicine : official journal of the American College of Medical Genetics
Avec: Lilian Downie , Sophie E Bouffler , David J Amor , John Christodoulou , Alison Yeung , Ari E Horton , Ivan Macciocca , Alison D Archibald , Meghan Wall , Jade Caruana , Sebastian Lunke , Zornitza Stark

Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.

American journal of human genetics
Avec: Zornitza Stark , Tiffany Boughtwood , Matilda Haas , Jeffrey Braithwaite , Clara L Gaff , Ilias Goranitis , Amanda B Spurdle , David P Hansen , Oliver Hofmann , Nigel Laing , Sylvia Metcalfe , Ainsley J Newson , Hamish S Scott , Natalie Thorne , Robyn L Ward , Marcel E Dinger , Stephanie Best , Janet C Long , Sean M Grimmond , John Pearson , Nicola Waddell , Christopher P Barnett , Matthew Cook , Michael Field , David Fielding , Stephen B Fox , Jozef Gecz , Adam Jaffe , Richard J Leventer , Paul J Lockhart , Sebastian Lunke , Andrew J Mallett , Julie McGaughran , Linda Mileshkin , Katia Nones , Tony Roscioli , Ingrid E Scheffer , Christopher Semsarian , Cas Simons , David M Thomas , David R Thorburn , Richard Tothill , Deborah White , Sally Dunwoodie , Peter T Simpson , Peta Phillips , Marie-Jo Brion , Keri Finlay , Michael Cj Quinn , Tessa Mattiske , Emma Tudini , Kirsten Boggs , Sean Murray , Kathy Wells , John Cannings , Andrew H Sinclair , John Christodoulou , Kathryn N North

Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study.

The Lancet. Neurology
Avec: Alissa M D'Gama , Sarah Mulhern , Beth R Sheidley , Fadil Boodhoo , Sarah Buts , Natalie J Chandler , Joanna Cobb , Meredith Curtis , Edward J Higginbotham , Jonathon Holland , Tayyaba Khan , Julia Koh , Nicole S Y Liang , Lyndsey McRae , Sarah E Nesbitt , Brandon T Oby , Ben Paternoster , Alistair Patton , Graham Rose , Elizabeth Scotchman , Rozalia Valentine , Kimberly N Wiltrout , Auteur inconnu , Auteur inconnu , Robin Z Hayeems , Puneet Jain , Sebastian Lunke , Christian R Marshall , Shira Rockowitz , Neil J Sebire , Zornitza Stark , Susan M White , Lyn S Chitty , J Helen Cross , Ingrid E Scheffer , Vann Chau , Gregory Costain , Annapurna Poduri , Katherine B Howell , Amy McTague

Réseau de co-auteurs

Zornitza Stark 45 collaborations
John Christodoulou 20 collaborations
Susan M White 17 collaborations
Belinda Chong 14 collaborations
Ilias Goranitis 14 collaborations
Melissa Martyn 14 collaborations
Lilian Downie 13 collaborations
Tiong Y Tan 12 collaborations
Stephanie Best 12 collaborations
Matthew F Hunter 11 collaborations
Alison Yeung 10 collaborations
David J Amor 10 collaborations
Clara Gaff 10 collaborations
Natasha J Brown 9 collaborations
Chirag Patel 9 collaborations
None None 9 collaborations
David R Thorburn 8 collaborations
Dean Phelan 8 collaborations
Mathew Wallis 8 collaborations
Sarah A Sandaradura 8 collaborations
Simon Sadedin 8 collaborations
Tony Roscioli 8 collaborations
Kirsten Boggs 7 collaborations
Fiona Lynch 7 collaborations
Clara L Gaff 7 collaborations
Stefanie Eggers 6 collaborations
Emma I Krzesinski 6 collaborations
Meredith Wilson 6 collaborations
Jason Pinner 6 collaborations
Amanda Springer 6 collaborations
Danya F Vears 6 collaborations
Anna Jarmolowicz 6 collaborations
Alison D Archibald 6 collaborations
Lauren S Akesson 5 collaborations
Martin B Delatycki 5 collaborations
Sophie E Bouffler 5 collaborations
Gemma R Brett 5 collaborations
Alison G Compton 5 collaborations
David Mowat 5 collaborations
Tiffany Boughtwood 5 collaborations
Edwin P Kirk 5 collaborations
Elly Lynch 5 collaborations
Ivan Macciocca 5 collaborations
Christopher M Richmond 4 collaborations
Matthew Regan 4 collaborations
Nicole J Van Bergen 4 collaborations
David A Stroud 4 collaborations
Christopher P Barnett 4 collaborations
Mary-Louise Freckmann 4 collaborations
Karin S Kassahn 4 collaborations
Hamish S Scott 4 collaborations
Emma Krzesinski 4 collaborations
Michael Field 4 collaborations
Michael F Buckley 4 collaborations
Crystle Lee 4 collaborations
Giulia Valente 4 collaborations
Justine E Marum 4 collaborations
Mark R Davis 4 collaborations
Lyndon Gallacher 4 collaborations
Gladys Ho 4 collaborations
Bruce Bennetts 4 collaborations
Natalie B Tan 3 collaborations
Chloe A Stutterd 3 collaborations
Sandra T Cooper 3 collaborations
Boris Keren 3 collaborations
Benjamin Kamien 3 collaborations
Michelle G de Silva 3 collaborations
Cas Simons 3 collaborations
Kathryn N North 3 collaborations
Rupendra Shrestha 3 collaborations
Deborah Schofield 3 collaborations
Ying Zhu 3 collaborations
Alan Ma 3 collaborations
Lesley C Adès 3 collaborations
Tiong Yang Tan 3 collaborations
Jozef Gecz 3 collaborations
Jade Caruana 3 collaborations
Anaita Kanga-Parabia 3 collaborations
Riccarda Peters 3 collaborations
Erin Tutty 3 collaborations
Christopher Gyngell 3 collaborations
Michael C J Quinn 3 collaborations
Amanda B Spurdle 3 collaborations
Emma Tudini 3 collaborations
Julie McGaughran 3 collaborations
Catherine Quinlan 3 collaborations
Jeffrey Braithwaite 3 collaborations
Paul A James 3 collaborations
Jane Halliday 3 collaborations
Maie Walsh 3 collaborations
Martin Delatycki 3 collaborations
Yael Prawer 3 collaborations
Andrew Fennell 3 collaborations
Rani Sachdev 3 collaborations
Bryony A Thompson 3 collaborations
Andrew J Mallett 3 collaborations
Lindsay Fowles 3 collaborations
Ben Lundie 3 collaborations
Samantha Ayres 3 collaborations
Anand Vasudevan 3 collaborations
Marcel E Dinger 3 collaborations
Ingrid E Scheffer 3 collaborations
Janet C Long 3 collaborations
Sharon Lewis 3 collaborations
Clare J Love 2 collaborations
Rachel Stapleton 2 collaborations
George McGillivray 2 collaborations
Patrick Yap 2 collaborations
Justine Marum 2 collaborations
Adam M Bournazos 2 collaborations
Liana N Semcesen 2 collaborations
Shobhana Bommireddipalli 2 collaborations
Tim Sikora 2 collaborations
Denisse Garza 2 collaborations
Amber Begtrup 2 collaborations
Maria J Guillen Sacoto 2 collaborations
Chirag V Patel 2 collaborations
David Francis 2 collaborations
Song Gao 2 collaborations
Andreas Halman 2 collaborations
Janine Smith 2 collaborations
Ravi Savarirayan 2 collaborations
Lisa J Ewans 2 collaborations
Corrina Cliffe 2 collaborations
George Elakis 2 collaborations
Rebecca Walsh 2 collaborations
Meg Wall 2 collaborations
Yvonne Bombard 2 collaborations
Marc Clausen 2 collaborations
Paul De Fazio 2 collaborations
Meaghan Wall 2 collaborations
Joy Lee 2 collaborations
Belinda McClaren 2 collaborations
Luke Rynehart 2 collaborations
Khurshid Alam 2 collaborations
Alison H Trainer 2 collaborations
Natasha Brown 2 collaborations
Chloe Stutterd 2 collaborations
Smitha Kumble 2 collaborations
Yana Smagarinsky 2 collaborations
Melanie Marty 2 collaborations
James Pitt 2 collaborations
Michael Fahey 2 collaborations
Gregory Costain 2 collaborations
Emma Wakeling 2 collaborations
Pankaj B Agrawal 2 collaborations
Julian Savulescu 2 collaborations
Melissa Wake 2 collaborations
Kenneth Tan 2 collaborations
Fathimath Faiz 2 collaborations
Elizabeth E Palmer 2 collaborations
Paul R Mark 2 collaborations
Lisa G Riley 2 collaborations
Yemima Berman 2 collaborations
Victoria Beshay 2 collaborations
Matthew Edwards 2 collaborations
Himanshu Goel 2 collaborations
Megan Higgins 2 collaborations
Ari E Horton 2 collaborations
Edwin Kirk 2 collaborations
Richard J Leventer 2 collaborations
Amali Mallawaarachchi 2 collaborations
Jonathan Rodgers 2 collaborations
Elena Savva 2 collaborations
Kristi J Jones 2 collaborations
Kushani Jayasinghe 2 collaborations
Belinda Creighton 2 collaborations
Ella Wilkins 2 collaborations
Michael Christie 2 collaborations
Linda Mileshkin 2 collaborations
Adam Jaffe 2 collaborations
Matilda Haas 2 collaborations
Anne Baxendale 2 collaborations
Christopher Barnett 2 collaborations
Michael C Fahey 2 collaborations
Katherine B Howell 2 collaborations
Luregn J Schlapbach 2 collaborations
Christiane Theda 2 collaborations
John Beilby 2 collaborations
Ain Roesley 2 collaborations
Oliver Hofmann 2 collaborations
Daniella H Hock 2 collaborations
Tiffany F Boughtwood 2 collaborations
Katia Nones 2 collaborations
Marie-Jo Brion 2 collaborations
Ainsley J Newson 2 collaborations
Natalie Thorne 2 collaborations
Miriam Fanjul Fernandez 1 collaboration
Lynn S Pais 1 collaboration
Karen Gunanayagam 1 collaboration
Adhish S Walvekar 1 collaboration
Marc O Warmoes 1 collaboration
Myrto Patraskaki 1 collaboration
Dean L Jones 1 collaboration
Dale Sebire 1 collaboration
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Kelly Smallwood 1 collaboration
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Fan Xia 1 collaboration
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