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JMIR Bioinformatics and Biotechnology|June 27, 2024
It Is in Our DNA: Bringing Electronic Health Records and Genomic Data Together for Precision MedicineAlan J Robertson, Andrew J Mallett, Zornitza Stark, et al.
Human Genomics|November 19, 2024
Analysis of public perceptions on the use of artificial intelligence in genomic medicineJack E Harrison, Fiona Lynch, Zornitza Stark, et al.
BMC Medical Ethics|May 28, 2026
Automating genomic reanalysis: perspectives of people living with, or impacted by, a genetic, rare or undiagnosed conditionFiona Lynch, Emily King, Savio Nona, et al.
The Medical Journal of Australia|January 14, 2026
Genomic Newborn Screening: Commodity or Public Good?Christopher Gyngell, Sebastian Lunke, Danya Vears, et al.
Seminars in Pediatric Neurology|July 3, 2018
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere SyndromeIan R Woodcock, Manoj P Menezes, Lee Coleman, et al.
American Journal of Medical Genetics. Part A|May 15, 2015
Copy number variants including RAS pathway genes-How much RASopathy is in the phenotype?Christina Lissewski, Sarina G Kant, Zornitza Stark, et al.
Pediatrics|August 26, 2015
Metronidazole Toxicity in Cockayne Syndrome: A Case SeriesBrian T Wilson, Andrew Strong, Sean O'Kelly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 22, 2019
Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomesDeborah Schofield, Luke Rynehart, Rupendra Shresthra, et al.
Pediatrics|January 3, 2019
Rapid Challenges: Ethics and Genomic Neonatal Intensive CareChristopher Gyngell, Ainsley J Newson, Dominic Wilkinson, et al.
Biology of Reproduction|July 31, 2022
Genomic testing in premature ovarian insufficiency: proceed with cautionElena J Tucker, Tiong Y Tan, Zornitza Stark, et al.
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