Editorial: Public Health Genomics

por Lacaze, Paul, Baynam, Gareth
Publicado 2019

Changes to the Employers' Use of Genetic Information and Non-discrimination for Health Insurance in the USA: Implications for Australians

por Bilkey, Gemma A., Baynam, Gareth, Molster, Caron
Publicado 2018

mEDUrare: Supporting Integrated Care for Rare Diseases by Better Connecting Health and Education Through Policy

por Saggu, Harleen, Jones, Caleb, Lewis, Amber, Baynam, Gareth
Publicado 2021

Personalised analytics for rare disease diagnostics

por Anderson, Denise, Baynam, Gareth, Blackwell, Jenefer M., Lassmann, Timo
Publicado 2019

Incidental inequity

por Nowak, Kristen J., Bauskis, Alicia, Dawkins, Hugh J., Baynam, Gareth
Publicado 2018

Childhood rare diseases and the UN convention on the rights of the child

por Matthews, Lisa, Chin, Vaughan, Taliangis, Marisa, Samanek, Amanda, Baynam, Gareth
Publicado 2021

Editorial: Congenital anomalies: State of the art and the new paradigms for a precision public health approach

por Khoshnood, Babak, Baynam, Gareth, Loane, Maria, Rissmann, Anke, Botto, Lorenzo
Publicado 2022

Surfacing undiagnosed disease: consideration, counting and coding

por Baxter, Megan F., Hansen, Michele, Gration, Dylan, Groza, Tudor, Baynam, Gareth
Publicado 2023

A brief history of MECP2 duplication syndrome: 20-years of clinical understanding

por Ta, Daniel, Downs, Jenny, Baynam, Gareth, Wilson, Andrew, Richmond, Peter, Leonard, Helen
Publicado 2022

Medical Comorbidities in MECP2 Duplication Syndrome: Results from the International MECP2 Duplication Database

por Ta, Daniel, Downs, Jenny, Baynam, Gareth, Wilson, Andrew, Richmond, Peter, Leonard, Helen
Publicado 2022

The risk of major structural birth defects associated with seasonal influenza vaccination during pregnancy: A population‐based cohort study

por Sarna, Mohinder, Pereira, Gavin F., Foo, Damien, Baynam, Gareth S., Regan, Annette K.
Publicado 2022

3D facial analysis for rare disease diagnosis and treatment monitoring: Proof-Of-Concept plan for hereditary angioedema

por Jamuar, Saumya, Palmer, Richard, Dawkins, Hugh, Lee, Dae-Wook, Helmholz, Petra, Baynam, Gareth
Publicado 2023

Editorial: Precision Public Health

por Weeramanthri, Tarun Stephen, Dawkins, Hugh J. S., Baynam, Gareth, Bellgard, Matthew, Gudes, Ori, Semmens, James Bernard
Publicado 2018

SMART Work Design: Accelerating the Diagnosis of Rare Diseases in the Western Australian Undiagnosed Diseases Program

por Hay, Georgia J., Klonek, Florian E., Thomas, Cati S., Bauskis, Alicia, Baynam, Gareth, Parker, Sharon K.
Publicado 2020

Association between craniofacial anomalies, intellectual disability and autism spectrum disorder: Western Australian population-based study

por Junaid, Mohammed, Slack-Smith, Linda, Wong, Kingsley, Bourke, Jenny, Baynam, Gareth, Calache, Hanny, Leonard, Helen
Publicado 2022

Optimizing Precision Medicine for Public Health

por Bilkey, Gemma A., Burns, Belinda L., Coles, Emily P., Mahede, Trinity, Baynam, Gareth, Nowak, Kristen J.
Publicado 2019

Development of an International Database for a Rare Genetic Disorder: The MECP2 Duplication Database (MDBase)

por Ta, Daniel, Downs, Jenny, Baynam, Gareth, Wilson, Andrew, Richmond, Peter, Schmidt, Aron, Decker, Amelia, Leonard, Helen
Publicado 2022

Patterns, trends, and factors influencing hospitalizations for craniosynostosis in Western Australia. A population-based study

por Junaid, Mohammed, Slack-Smith, Linda, Wong, Kingsley, Hewitt, Timothy, Bourke, Jenny, Baynam, Gareth, Calache, Hanny, Leonard, Helen
Publicado 2023

Correction: Dispelling myths about rare disease registry system development

por Bellgard, Matthew, Beroud, Christophe, Parkinson, Kay, Harris, Tess, Ayme, Segolene, Baynam, Gareth, Weeramanthri, Tarun, Dawkins, Hugh, Hunter, Adam
Publicado 2014

Dispelling myths about rare disease registry system development

por Bellgard, Matthew, Beroud, Christophe, Parkinson, Kay, Harris, Tess, Ayme, Segolene, Baynam, Gareth, Weeramanthri, Tarun, Dawkins, Hugh, Hunter, Adam
Publicado 2013