Ms Ella Wilkins
Honorary (Fellow)
Department of Paediatrics
10 Scholarly works
0 Projects
HIGHLIGHTS
2025
Journal article
Cracking the code: an integrated electronic medical record approach to early diagnosis of genetic kidney disease in children with microscopic haematuria
DOI: 10.1007/s00467-025-06702-82024
Journal article
Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023
DOI: 10.1186/s40246-024-00656-y2024
Journal article
Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years
DOI: 10.1016/j.ekir.2024.04.0682022
Journal article
The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome
DOI: 10.1002/ajmg.a.629502016
Journal article
“It wasn't a disaster or anything”: Parents’ experiences of their child's uncertain chromosomal microarray result
DOI: 10.1002/ajmg.a.378382012
Journal article
Closing the case of APOE in multiple sclerosis: No association with disease risk in over 29 000 subjects
DOI: 10.1136/jmedgenet-2012-1011752012
Journal article
A DNA resequencing array for genes involved in Parkinson's disease
DOI: 10.1016/j.parkreldis.2011.12.012
RECENT SCHOLARLY WORKS
2011
Journal article
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
DOI: 10.1038/ng.9132011
Journal article
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips
DOI: 10.1186/1471-2105-12-682009
Journal article
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
DOI: 10.1038/ng.396