Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
42400230
TITLE
Genome-Wide Association Study of Nevus Count Reveals Opposing Effects of Genetic Loci Near IRF4 and MC1R on Flat Versus Raised Nevus Count in the Brisbane Twin Nevus Study: A Cross-Sectional Analysis.
ABSTRACT
Germline genetic variation can influence the number of nevi on the skin. However, nevi can be classified in many ways (e.g., by shape, size or evolution); little is known of how genetics influences the density of different nevus morphologies on the body. Here, we explore how germline genetics influences the density of flat, raised and atypical nevi, and identify which classification correlates most with genetic risk of melanoma. We estimate heritability and perform genome-wide association analysis of flat, raised, and atypical nevus count within the Brisbane Twin Nevus Study (N = 3862). We compare the effect estimates of genetic loci associated with each morphology. We also assess how well each morphology correlates with the genetic risk of melanoma using a polygenic risk score of melanoma. Heritability estimates revealed both unique and shared genetic effects between morphologies. We identified two loci near IRF4 and MC1R showing opposing effects on flat and raised nevus counts. Variation in raised nevus count showed the strongest correlation with melanoma risk using polygenic risk scores. Although some genetic effects are shared between nevus morphologies, they appear to be genetically distinct phenotypes. Given the opposing effects of IRF4 and MC1R on flat and raised nevus counts, future studies of nevus count should consider, where possible, analysing each nevus morphology separately as well as combined.
© 2026 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
DATE PUBLISHED
2026 Jul
HISTORY
PUBSTATUS PUBSTATUSDATE
revised 2026/05/11
received 2026/02/19
accepted 2026/05/26
medline 2026/07/04 06:32
pubmed 2026/07/04 06:31
entrez 2026/07/04 02:13
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Ingold N Ingold Nathan N School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, University of Queensland, Brisbane, Queensland, Australia.
Zhu G Zhu Gu G QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Duffy DL Duffy David L DL QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Mothershaw A Mothershaw Adam A Frazer Institute, Dermatology Research Centre, University of Queensland, Brisbane, Queensland, Australia.
Martin NG Martin Nicholas G NG QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
MacGregor S MacGregor Stuart S School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, University of Queensland, Brisbane, Queensland, Australia.
Law MH Law Matthew H MH School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, University of Queensland, Brisbane, Queensland, Australia.
INVESTIGATORS
JOURNAL
VOLUME: 39
ISSUE: 4
TITLE: Pigment cell & melanoma research
ISOABBREVIATION: Pigment Cell Melanoma Res
YEAR: 2026
MONTH: Jul
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1755-148X
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Pigment Cell Melanoma Res
COUNTRY: England
ISSNLINKING: 1755-1471
NLMUNIQUEID: 101318927
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Twin Study
COMMENTS AND CORRECTIONS
GRANTS
GRANTID AGENCY COUNTRY
1150144 National Health and Medical Research Council
496682 National Health and Medical Research Council
HD50735 NIH HHS United States
GENERAL NOTE
KEYWORDS
KEYWORD
IRF4
MC1R
genome-wide association study
heritability
moles
naevi
nevi
nevus morphology
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Humans
Genome-Wide Association Study
Interferon Regulatory Factors genetics
Interferon Regulatory Factor-4 genetics
Genetic Loci genetics
Receptor, Melanocortin, Type 1 genetics
Genetic Predisposition to Disease genetics
Female genetics
Cross-Sectional Studies genetics
Skin Neoplasms pathology
Nevus pathology
Male pathology
Genetic Risk Score pathology
Melanoma pathology
Polymorphism, Single Nucleotide genetics
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
REGISTRYNUMBER NAMEOFSUBSTANCE
0 Interferon Regulatory Factors
0 Interferon Regulatory Factor-4
0 Receptor, Melanocortin, Type 1
OTHER ID's