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Australian and New Zealand Journal of Public Health|February 5, 2015
Differences in grass pollen allergen exposure across AustraliaPaul J Beggs, Constance H Katelaris, Danielle Medek, et al.
American Journal of Human Genetics|June 6, 2023
Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq ProjectRobert C Green, Nidhi Shah, Casie A Genetti, et al.
Aerobiologia|April 13, 2016
Regional and seasonal variation in airborne grass pollen levels between cities of Australia and New ZealandDanielle E Medek, Paul J Beggs, Bircan Erbas, et al.
Human Mutation|March 21, 2012
Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemiaHanna T Gazda, Milena Preti, Mee Rie Sheen, et al.
European Journal of Sport Science|July 2, 2025
'We're All (Cauliflower) Ears': A Delphi Study Including Staff and Players to Co-Construct Sports Science and Medicine (Performance and Wellbeing) Research Priorities for Premiership RugbyBen Jones, Omar Heyward, Matt Cross, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|January 25, 2023
Adverse events following first and second dose COVID-19 vaccination in England, October 2020 to September 2021: a national vaccine surveillance platform self-controlled case series studyRuby Sm Tsang, Mark Joy, Rachel Byford, et al.
JMIR Formative Research|July 5, 2022
Methodological Issues in Using a Common Data Model of COVID-19 Vaccine Uptake and Important Adverse Events of Interest: Feasibility Study of Data and Connectivity COVID-19 Vaccines Pharmacovigilance in the United KingdomGayathri Delanerolle, Robert Williams, Ana Stipancic, et al.
Thorax|January 28, 2021
Assessing the impact of the 13 valent pneumococcal vaccine on childhood empyema in AustraliaRoxanne Strachan, Nusrat Homaira, Sean Beggs, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
NPJ Genomic Medicine|July 14, 2020
Children's rare disease cohorts: an integrative research and clinical genomics initiativeShira Rockowitz, Nicholas LeCompte, Mary Carmack, et al.
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