Rosalie R. Kenyon

SA Pathology, Frome Road
Adelaide, SA, Australia

Last Updated: 09/26/2026

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Found 11 publications

Semi-automated genomic newborn screening highlights complexities in reporting.

Semi-automated genomic newborn screening highlights complexities in reporting.

Journal: NPJ genomic medicine

Published: August 08, 2025

Impact of ASXL1 at diagnosis in patients with CML receiving frontline potent TKIs: high risk of kinase domain mutations.

Impact of ASXL1 at diagnosis in patients with CML receiving frontline potent TKIs: high risk of kinase domain mutations.

Journal: Blood

Published: June 06, 2025

Enhanced Detection of Splice-Altering Variants in Hematologic Malignancies Using Targeted RNA-Sequencing Data.

Enhanced Detection of Splice-Altering Variants in Hematologic Malignancies Using Targeted RNA-Sequencing Data.

Journal: The Journal of molecular diagnostics : JMD

Published: February 25, 2025

Trace element and δ13C values of the banana prawn Penaeus merguiensis reveal the importance of catchment-derived resources across both estuarine and nearshore habitats.

Trace element and δ13C values of the banana prawn Penaeus merguiensis reveal the importance of catchment-derived resources across both estuarine and nearshore habitats.

Journal: Marine environmental research

Published: August 05, 2024

Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion.

Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion.

Journal: Blood advances

Published: December 04, 2023

Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services.

Extending the new era of genomic testing into pregnancy management: A proposed model for Australian prenatal services.

Journal: The Australian & New Zealand journal of obstetrics & gynaecology

Published: November 12, 2023

Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention.

Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention.

Journal: Haematologica

Published: October 06, 2022

RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia.

RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia.

Journal: The Journal of molecular diagnostics : JMD

Published: December 05, 2021

Enhanced expression of transferrin receptor 1 contributes to oncogenic signalling by sphingosine kinase 1.

Enhanced expression of transferrin receptor 1 contributes to oncogenic signalling by sphingosine kinase 1.

Journal: Oncogene

Published: May 28, 2013

Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans.

Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans.

Journal: Nature communications

Published: September 20, 2012

Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia.

Genome-wide gene expression profiling identifies overlap with malignant adrenocortical tumours and novel mechanisms of inefficient steroidogenesis in familial ACTH-independent macronodular adrenal hyperplasia.

Journal: Endocrine-related cancer

Published: March 03, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026