Publications by authors named "Nicole Millis"

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"Jumping too far ahead": Australian healthcare professional, scientist, and policy maker perspectives on using genomics in newborn screening.
Joanne Scarfe, Alexis Turner, Christian Meagher, Michelle A Farrar, Kaustuv Bhattacharya, Nicole Millis

Eur J Hum Genet· October 2025

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'Integrating Ethics and Equity with Economics and Effectiveness for newborn screening in the genomic age: A qualitative study protocol of stakeholder perspectives.
Didu S Kariyawasam, Joanne Scarfe, Christian Meagher, Michelle A Farrar, Kaustav Bhattacharya, Nicole Millis

PLoS One· March 2024

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Informing a national rare disease registry strategy in Australia: a mixed methods study.
Rasa Ruseckaite, Marisa Caruso, Chethana Mudunna, Falak Helwani, Nicole Millis

BMC Health Serv Res· October 2023

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Current state of rare disease registries and databases in Australia: a scoping review.
Rasa Ruseckaite, Chethana Mudunna, Marisa Caruso, Falak Helwani, Nicole Millis

Orphanet J Rare Dis· July 2023

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View from inside: Patient advocacy in guiding policy development for metabolic disorders.
Nicole Millis

J Inherit Metab Dis· September 2022

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The involvement of rare disease patient organisations in therapeutic innovation across rare paediatric neurological conditions: a narrative review.
Christina Q Nguyen, Kristine Alba-Concepcion, Elizabeth E Palmer, Jackie L Scully, Nicole Millis

Orphanet J Rare Dis· April 2022

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Rare diseases research and policy in Australia: On the journey to equitable care.
Kaustuv Bhattacharya, Nicole Millis, Adam Jaffe, Yvonne Zurynski

J Paediatr Child Health· June 2021

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Protecting the rare during a rare pandemic.
Gareth S Baynam, Carol Wicking, Kaustuv Bhattacharya, Nicole Millis

Med J Aust· July 2020

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Rare disease registries: a call to action.
Paul Lacaze, Nicole Millis, Megan Fookes, Yvonne Zurynski, Adam Jaffe

Intern Med J· September 2017

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