Pinner, Jason
UNSW Sydney · Sydney Children's Hospital
7 papers on CoChatORCID 0000-0002-8323-1802
Most cited papers
- Verified
Effects of Breast Milk on the Severity and Outcome of Neonatal Abstinence Syndrome Among Infants of Drug-Dependent Mothers
Abdel-Latif, M. E., Pinner, J., Clews, S., Cooke, F., Lui, K., & Oei, J. (2006) · Pediatrics
Prenatal Substance Exposure EffectsInfant Nutrition and Health
Cited by 266
- 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
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
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
Oliver, K. L., Trivisano, M., Mandelstam, S. A., De Dominicis, A., Francis, D. I., Green, T. E., Muir, A. M., Chowdhary, A., Hertzberg, C., Goldhahn, K., et al. (2023) · Epilepsia
Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders
Cited by 23
- Verified
The impact of non‐invasive prenatal testing on anxiety in women considered at high or low risk for aneuploidy after combined first trimester screening
Richmond, Z., Fleischer, R., Chopra, M., Pinner, J., D'Souza, M., Fridgant, Y., & Hyett, J. (2017) · Prenatal Diagnosis
Prenatal Screening and DiagnosticsMaternal Mental Health During Pregnancy and Postpartum
Cited by 14
- Verified
De novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
Dias, K.-R., Carlston, C. M., Blok, L. E. R., De Hayr, L., Nawaz, U., Evans, C.-A., Bayrak-Toydemir, P., Htun, S., Zhu, Y., Ma, A., et al. (2022) · Genetics in Medicine
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 13
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free