Lisa K. Anderson
Herston, QLD 4029, Australia
Last Updated: 09/26/2026
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Found 22 publications
Capacity building to address antimicrobial resistance in remote Australia: The inaugural HOT NORTH Antimicrobial Academy.
Journal: Infection, disease & health
Published: January 22, 2024
Concurrent nonavalent human papillomavirus (HPV) vaccination and immune stimulation with imiquimod to treat recalcitrant HPV-associated high grade vaginal intra-epithelial neoplasia.
Journal: Gynecologic oncology reports
Published: October 14, 2023
Minimizing Sample Failure Rates for Challenging Clinical Tumor Samples.
Journal: The Journal of molecular diagnostics : JMD
Published: August 11, 2022
Squamous cell carcinoma differentiation at progression as a resistance mechanism in metastatic non-small cell lung carcinoma harbouring a targetable mutation.
Journal: Pathology
Published: October 22, 2021
Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesis.
Journal: Human molecular genetics
Published: March 23, 2021
Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis.
Journal: Annals of the rheumatic diseases
Published: November 04, 2020
Normal human enthesis harbours conventional CD4+ and CD8+ T cells with regulatory features and inducible IL-17A and TNF expression.
Journal: Annals of the rheumatic diseases
Published: March 11, 2020
Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome.
Journal: Molecular genetics & genomic medicine
Published: September 15, 2019
A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 20, 2019
Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort.
Journal: Pediatric diabetes
Published: February 19, 2018
Point mutation in p14ARF -specific exon 1β of CDKN2A causing familial melanoma and astrocytoma.
Journal: The British journal of dermatology
Published: December 27, 2017
Last Updated: 09/26/2026