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Corrina C. Cliffe

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
2020 · Australian Genomics Health Alliance Acute Care Flagship, Sebastian Lunke, et al. · JAMA · 245
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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 · 102
Nationwide, Couple-Based Genetic Carrier Screening
2024 · Edwin P. Kirk, Martin B. Delatycki, et al. · New England Journal of Medicine · 84
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The Australian Reproductive Genetic Carrier Screening Project (Mackenzie’s Mission): Design and Implementation
2022 · Alison D. Archibald, Belinda J. McClaren, et al. · Journal of Personalized Medicine · 71
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Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation
2022 · Emma Tudini, James Andrews, et al. · The American Journal of Human Genetics · 33
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Consultation informs strategies for improving the use of functional evidence in variant classification
2025 · Rehan M. Villani, Bronwyn Terrill, et al. · The American Journal of Human Genetics · 15
Clinically Responsive Genomic Analysis Pipelines
2021 · Samantha Leigh Sundercombe, Marina Berbic, et al. · Journal of Molecular Diagnostics · 12
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 · 11
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Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
2020 · Sebastian Lunke, Stefanie Eggers, et al. · Obstetrical & Gynecological Survey · 8
Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education
2026 · Amy Nisselle, Douglas Liddicoat, et al. · The American Journal of Human Genetics · 3
Antenatal haemoglobinopathy screening – Experiences of a large Australian Centre
2020 · Sylvia Ai, Corrina Cliffe, et al. · Obstetric Medicine · 1
Indications and outcomes of rapid turn around time whole exome sequencing studies
2020 · Michael F. Buckley, George Elakis, et al. · Pathology · 1
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P171 – 1509 Malnutrition in young adults with epilepsy and neurodisabilities
2013 · C Cliffe, KB Das, et al. · European Journal of Paediatric Neurology · 1
Laboratory Considerations for Reproductive Genetic Carrier Screening
2026 · Corrina C. Cliffe, Richard J.N. Allcock, et al. · Journal of Molecular Diagnostics
Processed pseudogenes and the potential impact on genomic analysis
2026 · Chloe La Spina, Corrina Cliffe, et al. · Pathology
P456: Community co-designed workshops build confidence in the use of functional evidence for variant classification
2026 · Rehan Villani, Bronwyn Terrill, et al. · Genetics in Medicine Open
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Community co-designed workshops build confidence in use of functional evidence for variant classification
2025 · Rehan Marie Villani, Bronwyn Terrill, et al. · medRxiv
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Nationwide, Couple-Based Genetic Carrier Screening
2025 · E. P. Kirk, M. B. Delatycki, et al. · Obstetrical & Gynecological Survey
Nationwide, Couple-Based Genetic Carrier Screening
2025 · EP Kirk, MB Delatycki, et al. · Obstetric Anesthesia Digest
Emerging technologies in the investigation of DNA methylation profiles
2024 · Krystle Standen, Michael Buckley, et al. · Pathology
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Delivering high throughput urgent exome sequencing at a diagnostic laboratory
2022 · Samantha Sundercombe, Corrina Cliffe, et al. · Pathology
The design and post-implementation review of an algorithm for antenatal haemoglobinopathy screening
2022 · Corrina Cliffe, Sylvia Ai, et al. · Pathology
Haemoglobinopathy screening in pregnancy
2018 · Sylvia Ai, Corrina Cliffe, et al. · Pathology
The validation of a diagnostic exome sequencing service for the investigation of monogenic disorders
2018 · C. Cliffe, G. Elakis, et al. · Pathology
Works count: 24
Citation count: 587
H-index: 8
I10-index: 8
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