Ella Wilkins
University of Melbourne(AU)Victorian Clinical Genetics Services(AU)Murdoch Children's Research Institute(AU)
Publications by Year
Research Areas
Acute Myeloid Leukemia Research, Genomics and Rare Diseases, Myeloproliferative Neoplasms: Diagnosis and Treatment, Renal and related cancers, BRCA gene mutations in cancer
Most-Cited Works
- → Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia(2011)596 cited
- → Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20(2009)547 cited
- → RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML(2020)151 cited
- → Clinical impact of genomic testing in patients with suspected monogenic kidney disease(2020)119 cited
- → Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome(2009)90 cited
- → Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patients(2007)84 cited