Publications by authors named "Corrina Cliffe"

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Consultation informs strategies for improving the use of functional evidence in variant classification.
Rehan M Villani, Bronwyn Terrill, Emma Tudini, Maddison E McKenzie, Corrina C Cliffe

Am J Hum Genet· June 2025

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Consultation informs strategies to improve functional evidence use in variant classification.
Rehan M Villani, Bronwyn Terrill, Emma Tudini, Maddison E McKenzie, Corrina C Cliffe

medRxiv· December 2024

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Nationwide, Couple-Based Genetic Carrier Screening.
Edwin P Kirk, Martin B Delatycki, Alison D Archibald, Erin Tutty, Jade Caruana, Corrina C Cliffe

N Engl J Med· November 2024

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Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.
Kerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, Carey-Anne Evans, Emily O'Heir, Corrina Cliffe, Simon Cliffe

Genet Med· May 2024

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The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.
Alison D Archibald, Belinda J McClaren, Jade Caruana, Erin Tutty, Emily A King, Corrina C Cliffe

J Pers Med· October 2022

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Clinically Responsive Genomic Analysis Pipelines: Elements to Improve Detection Rate and Efficiency.
Samantha Leigh Sundercombe, Marina Berbic, Carey-Anne Evans, Corrina Cliffe, George Elakis

J Mol Diagn· July 2021

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Antenatal haemoglobinopathy screening - Experiences of a large Australian Centre.
Sylvia Ai, Corrina Cliffe, Giselle Kidson-Gerber

Obstet Med· June 2021

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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.

JAMA· June 2020

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