Author

Matthew Regan

Observed name: Matt Regan

Institution: Monash Health

Observed institutions: Monash Medical Centre, Monash Children’s Hospital, Monash Health, Monash University

OpenAlex ID: A5111400614

Meeting the challenges of implementing rapid genomic testing in acute pediatric care

2018 · Zornitza Stark, Sebastian Lunke, et al. · Genetics in Medicine · 158

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

2021 · Adam M. Bournazos, Lisa G. Riley, et al. · Genetics in Medicine · 97

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

2020 · Natalie B. Tan, Rachel Stapleton, et al. · Molecular Genetics & Genomic Medicine · 83

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

2023 · Alicia B. Byrne, Peer Arts, et al. · Nature Medicine · 66

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

2020 · Alison Yeung, Natalie B. Tan, et al. · Genetics in Medicine · 37

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

2024 · Kerith-Rae Dias, Rupendra Shrestha, et al. · Genetics in Medicine · 10

A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship

2024 · Rachel Austin, Jaye S. Brown, et al. · Genetics in Medicine Open · 9

Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort study

2021 · Lisa Hui, Cecilia Pynaker, et al. · BMC Pediatrics · 5

Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study

2025 · Jacqui McCoy, Cecilia Pynaker, et al. · Genetics in Medicine Open · 2

Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnoses

2025 · Mahalia S. B. Frank, Melissa K. Bennett, et al. · Human Genomics · 1

Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: a retrospective population-based cohort study

2024 · Cecilia Pynaker, Jacqui McCoy, et al. · BMC Pediatrics · 1

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

2023 · Alicia B. Byrne, Peer Arts, et al. · Nature Medicine · 1

Genetic mosaicism in dermatology: Clinical utility of genetic testing of skin lesions

2019 · Brent J Doolan, Aaron J Robinson, et al. · Australasian Journal of Dermatology · 1

Scaling up Genomics

2026 · Kushani Jayasinghe, Rigan Tytherleigh, et al. · Clinical Journal of the American Society of Nephrology

Rapid genomic testing in acute paediatric care: Is it worth the trouble?

2018 · Zornitza Stark, Sebastian Lunke, et al. · Pathology

Works count: 16

Citation count: 568

H-index: 8

I10-index: 7