Author

Julia Dobbins

Observed institutions: South Australia Pathology, University of South Australia, Centre for Cancer Biology

ORCID: 0000-0001-5833-2655

Observed ORCID: 0000-0001-5833-2655

OpenAlex ID: A5014761965

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

2020 · Anna L. Brown, Peer Arts, et al. · Blood Advances · 153

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

2023 · Alicia B. Byrne, Peer Arts, et al. · Nature Medicine · 66

The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

2021 · Claire C. Homan, Sarah L. King-Smith, et al. · Haematologica · 52

Titin-related familial dilated cardiomyopathy: factors associated with disease onset

2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 20

A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship

2024 · Rachel Austin, Jaye S. Brown, et al. · Genetics in Medicine Open · 9

Australian Familial Haematological Cancer Study - Findings from 15 Years of Aggregated Clinical, Genomic and Transcriptomic Data

2019 · Christopher N Hahn, Milena Babic, et al. · Blood · 2

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death

2023 · Alicia B. Byrne, Peer Arts, et al. · Nature Medicine · 1

Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility

2019 · Anna L Brown, Milena Babic, et al. · Blood · 1

Durvalumab and Acalabrutinib for Relapsed/Refractory (r/r) High-Grade B-Cell Lymphoma: MoST15, Open Label Phase II Sub-Study of the Molecular Screening and Therapeutics in Leukaemia and Lymphoma (MoST-LLy) Framework

2024 · Danielle N Blunt, Rosemary Harrup, et al. · Blood

Development of a Data Portal for Aggregation and Analysis of Genomics Data in Familial Platelet Disorder With Predisposition to Myeloid Malignancy – the Runx1.db

2019 · Claire Homan, Mark Armstrong, et al. · Experimental Hematology

014 The diagnostic odyssey for fabry disease: ten years experience in testing

2018 · Julia Dobbins, Maria Fuller, et al. · Journal of Neurology Neurosurgery & Psychiatry

112 Blood spot testing for late onset pompe disease

2018 · Julia Dobbins, Tim Pyragius, et al. · Journal of Neurology Neurosurgery & Psychiatry

Works count: 12

Citation count: 304

H-index: 5

I10-index: 4