Christopher P Barnett (Christopher Barnett)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Intellectual Disability

Extracellular Matrix

Top Venues

American journal of medical genetics. Part A

The Australian & New Zealand journal of obstetrics & gynaecology

Science translational medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Alice Rogers, Lucas De Jong, Wendy Waters, Lesley H Rawlings, Keryn Simons, Song Gao, Julien Soubrier, Rosalie Kenyon, Ming Lin, Rob King, David M Lawrence, Peter Muller, Shannon Leblanc, Lesley McGregor, Suzanne C E H Sallevelt, Jan Liebelt, Tristan S E Hardy, Janice M Fletcher, Hamish S Scott, Abhi Kulkarni, Christopher P Barnett, Karin S Kassahn
Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services. The Australian & New Zealand journal of obstetrics & gynaecology (2024)
Alicia B Byrne, Pascal Brouillard, Drew L Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A Secker, Anna Oszmiana, Milena Babic, Kelly L Betterman, Peter J Brautigan, Melissa White, Sandra G Piltz, Paul Q Thomas, Christopher N Hahn, Matthias Rath, Ute Felbor, G Christoph Korenke, Christopher L Smith, Kathleen H Wood, Sarah E Sheppard, Denise M Adams, Ariana Kariminejad, Raphaël Helaers, Laurence M Boon, Nicole Revencu, Lynette Moore, Christopher P Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S Scott, Natasha L Harvey
Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema. Science translational medicine 14 (634) (2022)
Alice P Rogers, Kathryn Friend, Lesley Rawlings, Christopher P Barnett
A de novo missense variant in MED13 in a patient with global developmental delay, marked facial dysmorphism, macroglossia, short stature, and macrocephaly. American journal of medical genetics. Part A 185 (8) (2021)
Shannon LeBlanc, Dildeepa Naveen, Eric Haan, Christopher P Barnett, Lesley Rawlings, Tony Roscioli, Nicola Poplawski
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer risk. American journal of medical genetics. Part A 182 (7) (2020)
Eleanor G Ludington, Sui Yu, Ha Ae Bae, Christopher P Barnett
Novel de novo 2q14.3 deletion disrupting CNTNAP5 in a girl with intellectual impairment, thin corpus callosum, and microcephaly. American journal of medical genetics. Part A 182 (7) (2020)