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Miriam Fine

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies
2015 · Maya Lewinsohn, Anna L. Brown, et al. · Blood · 217
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 · 152
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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
2019 · Michael T. Parsons, Emma Tudini, et al. · Human Mutation · 145
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Detection of t(2;5) in Anaplastic Large Cell Lymphoma
1999 · Kimberley A. Cataldo, Syed M. Jalal, et al. · The American Journal of Surgical Pathology · 107
Myeloperoxidase Immunoreactivity in Adult Acute Lymphoblastic Leukemia
2001 · Daniel A. Arber, David S. Snyder, et al. · American Journal of Clinical Pathology · 49
Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan anemia patient
2017 · Parvathy Venugopal, Sarah Moore, et al. · Haematologica · 33
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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia
2019 · Jesse J.C. Cheah, Anna L. Brown, et al. · Haematologica · 21
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 20
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Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics
2020 · for the ICCon Audit Study Collaborative Group, B. Meiser, et al. · Familial Cancer · 17
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Telomerase activity and proliferation index in aggressive mature B-cell lymphoma: comparison to germinal center phenotypic markers
2003 · Katharine C Chiu, Miriam Fine, et al. · Human Pathology · 13
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
An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families
2019 · Parvathy Venugopal, Jesse JC Cheah, et al. · Blood · 5
Expanded Phenotypic and Genetic Heterogeneity in the Clinical Spectrum of FPD-AML: Lymphoid Malignancies and Skin Disorders Are Common Features in Carriers of Germline RUNX1 Mutations
2016 · Anna L Brown, Christopher N Hahn, et al. · Blood · 4
Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice
2021 · for the ICCon Audit Study Collaborative Group, Bettina Meiser, et al. · Hereditary Cancer in Clinical Practice · 1
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Implications of Revertant Somatic Mosaicism in Bone Marrow Failure Syndromes
2019 · Parvathy Venugopal, Milena Babic, et al. · Experimental Hematology · 1
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease
2025 · Dimuthu Alankarage, Iryna Leshchynska, et al. · Human Genetics and Genomics Advances
An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated With Haematological Malignancy Development in Ddx41 Mutated Families
2019 · Jesse Cheah, Anna Brown, et al. · Experimental Hematology
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Familial clustering of haematological malignancies: harbingers of wider germline cancer susceptibility
2017 · Hamish S. Scott, Anna L. Brown, et al. · Pathology
Works count: 22
Citation count: 793
H-index: 10
I10-index: 10
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