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Neuromuscular Disorders : NMD|April 26, 2011
Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutationsYoshiaki Saito, Hirofumi Komaki, Ayako Hattori, et al.NPJ Regenerative Medicine|March 12, 2019
Variable outcomes of human heart attack recapitulated in genetically diverse miceEkaterina Salimova, Kristen J Nowak, Ana C Estrada, et al.International Journal of Radiation Oncology, Biology, Physics|July 13, 2000
Beam intensity modulation using tissue compensators or dynamic multileaf collimation in three-dimensional conformal radiotherapy of primary cancers of the oropharynx and larynx, including the elective neckE B van Dieren, P J Nowak, O B Wijers, et al.Frontiers in Public Health|March 28, 2019
Genomic Testing for Human Health and Disease Across the Life Cycle: Applications and Ethical, Legal, and Social ChallengesGemma A Bilkey, Belinda L Burns, Emily P Coles, et al.Frontiers in Public Health|March 28, 2019
Healthcare System Priorities for Successful Integration of Genomics: An Australian FocusBelinda L Burns, Gemma A Bilkey, Emily P Coles, et al.Genes, Chromosomes & Cancer|June 9, 2005
Identification of consistent novel submegabase deletions in low-grade oligodendrogliomas using array-based comparative genomic hybridizationMichael R Rossi, Daniel Gaile, Jeffrey Laduca, et al.Mutation Research|January 2, 2007
aCGH local copy number aberrations associated with overall copy number genomic instability in colorectal cancer: coordinate involvement of the regions including BCR and ABLJeremy D Bartos, Daniel P Gaile, Devin E McQuaid, et al.Human Molecular Genetics|December 25, 2007
Recurrent 16p11.2 microdeletions in autismRavinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, et al.European Journal of Neurology|May 20, 2026
Evaluation of Sustained Disease Control With Nipocalimab Versus Placebo in the Phase 3 Vivacity-MG3 StudyTuan Vu, Said R Beydoun, Richard J Nowak, et al.Journal of Paediatrics and Child Health|August 13, 2021
Pilot study of universal screening of children and child-parent cascade testing for familial hypercholesterolaemia in AustraliaAndrew C Martin, Amanda J Hooper, Richard Norman, et al.Pageof 93