Barnett, Christopher
Women's and Children's Hospital · Women's and Children's Health Network · The University of Adelaide
6 papers on CoChatORCID 0000-0003-1717-3824
Most cited papers
- Verified
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, H. A. F., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., et al. (2017) · Nature Genetics
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 559
- Verified
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Australian Genomics Health Alliance Acute Care Flagship, Lunke, S., Eggers, S., Wilson, M., Patel, C., Barnett, C. P., Pinner, J., Sandaradura, S. A., Buckley, M. F., Krzesinski, E. I., et al. (2020) · JAMA
Genomics and Rare DiseasesMetabolism and Genetic Disorders
Cited by 239
- Verified
Parental experiences of ultrarapid genomic testing for their critically unwell infants and children
Brett, G. R., Martyn, M., Lynch, F., de Silva, M. G., Ayres, S., Gallacher, L., Boggs, K., Baxendale, A., Schenscher, S., King-Smith, S., et al. (2020) · Genetics in Medicine
Genomics and Rare DiseasesEthics and Legal Issues in Pediatric Healthcare
Cited by 47
- Verified
Spliceosome Malfunction Causes Neurodevelopmental Disorders with Overlapping Features
Li, D., Wang, Q., Bayat, A., Battig, M. R., Zhou, Y., Bosch, D. G. M., van Haaften, G., Granger, L., Petersen, A. K., Pérez-Jurado, L. A., et al. (2024) · Journal of Clinical Investigation
Genetics and Neurodevelopmental DisordersRNA Research and Splicing
Cited by 46
- Verified
Attitudes of Australian health professionals towards rapid genomic testing in neonatal and paediatric intensive care.
Stark, Z., Nisselle, A., McClaren, B., Lynch, F., Best, S., Long, J. C., Martyn, M., Patel, C., Schlapbach, L. J., Barnett, C., et al. (2019) · European Journal of Human Genetics
Genomics and Rare DiseasesMetabolism and Genetic Disorders
Cited by 43
- Verified
Circular RNAs accumulate in ageing human placental tissue and in stillbirth, leading to DNA damage and cellular senescence
Arthurs, A. L., Jackson, M. R., McCullough, D., Scott, H. S., Barnett, C. P., Webb, S. T., Smith, M. D., Jankovic-Karasoulos, T., Dekker, G. A., & Roberts, C. T. (2024) · American Journal of Obstetrics and Gynecology
Circular RNAs in diseasesTelomeres, Telomerase, and Senescence
Cited by 6
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