J. Elliott

发表

Meeting the challenges of implementing rapid genomic testing in acute pediatric care

Melbourne Genomics Health Alliance, Natalie B Tan, D. Phelan, 2018, Genetics in Medicine.

Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

C. Dissanayake, D. Francis, D. Amor, 2018, Scientific Reports.

Receiving Genomic Sequencing Results through the Victorian Undiagnosed Disease Program: Exploring Parental Experiences

Michal Chalk, L. Gallacher, J. Elliott, 2022, Journal of personalized medicine.

Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests

M. Pertile, M. Delatycki, D. Francis, 2017, Genetics in Medicine.

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

S. A. Vera, V. Faundes, Alexandra Ure, 2019, Journal of Neurodevelopmental Disorders.

The Acute Management of Intracerebral Hemorrhage: A Clinical Review

Martin R. Smith, J. Elliott, 2010, Anesthesia and analgesia.

Performance of a cell‐free DNA prenatal screening test, choice of prenatal procedure, and chromosome conditions identified during pregnancy after low‐risk cell‐free DNA screening

M. Pertile, M. Delatycki, A. Archibald, 2023, Prenatal diagnosis.

Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria’s Undiagnosed Diseases Program

D. MacArthur, N. Brown, A. O’Donnell-Luria, 2021, Journal of Medical Genetics.

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

S. A. Vera, V. Faundes, Alexandra Ure, 2019, Journal of Neurodevelopmental Disorders.

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

V. Faundes, K. Cornish, M. Field, 2019, Molecular Autism.

Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X

C. Dissanayake, D. Francis, D. Amor, 2018, Scientific Reports.

Experiences of receiving an increased chance of sex chromosome aneuploidy result from non‐invasive prenatal testing in Australia: “A more complicated scenario than what I had ever realized”

A. Archibald, Melody Menezes, J. Elliott, 2022, Journal of genetic counseling.

UK families with children with rare chromosome disorders: Changing experiences of diagnosis and counselling (2003‐2013)

B. Searle, A. Szczepura, M. Hultén, 2018, Clinical genetics.

Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests

M. Pertile, M. Delatycki, D. Francis, 2017, Genetics in Medicine.

Meeting the challenges of implementing rapid genomic testing in acute pediatric care

Natalie B Tan, D. Phelan, Z. Stark, 2018, Genetics in Medicine.