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A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

artículo científico publicado en 2011

Accuracy of self-reported nevus and pigmentation phenotype compared with clinical assessment in a population-based study of young Australian adults

artículo científico publicado en 2015

Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

scholarly article by Anne E. Cust published in June 2018

Common sequence variants on 20q11.22 confer melanoma susceptibility

artículo científico publicado en 2008

Early-life sun exposure and risk of melanoma before age 40 years

article

FRAMe: Familial Risk Assessment of Melanoma-a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanoma

artículo científico publicado en 2020

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

scientific journal article

MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study

artículo científico publicado en 2013

MC1R genotypes and risk of melanoma before age 40 years: a population-based case-control-family study

artículo científico publicado en 2012

Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK

article

Population-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family Study

artículo científico publicado en 2009

Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom

artículo científico publicado en 2014

Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanoma

artículo científico publicado en 2011

Sunscreen Use and Melanoma Risk Among Young Australian Adults

artículo científico publicado en 2018