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Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants

PloS one, 2020-09, Vol.15 (9), p.e0238529-e0238529

2020

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Skin Pigmentation Genetics for the Clinic

Dermatology (Basel), 2017-01, Vol.233 (1), p.1-15

2017

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The NR4A2 nuclear receptor is recruited to novel nuclear foci in response to UV irradiation and participates in nucleotide excision repair

PloS one, 2013-11, Vol.8 (11), p.e78075

2013

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MicroRNA expression profiling of cutaneous squamous cell carcinomas and precursor lesions

Skin health and disease, 2024-06, Vol.4 (3), p.e360-n/a

2024

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Genetic variation in IRF4 expression modulates growth characteristics, tyrosinase expression and interferon‐gamma response in melanocytic cells

Pigment cell and melanoma research, 2018-01, Vol.31 (1), p.51-63

2018

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Acquired melanocytic naevus phenotypes and MC1R genotypes in Han Chinese: a cross-sectional study

PeerJ (San Francisco, CA), 2017-12, Vol.5, p.e4168-e4168, Article e4168

2017

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Whole-Exome Sequencing of Acquired Nevi Identifies Mechanisms for Development and Maintenance of Benign Neoplasms

Journal of investigative dermatology, 2018-07, Vol.138 (7), p.1636-1644

2018

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Assessing the genetic risk of nodular melanoma using a candidate gene approach

British journal of dermatology (1951), 2024-01, Vol.190 (2), p.199-206

2024

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Abstract 5861: BOP1 expression contributes to the proliferative/invasive phenotype in melanoma

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.5861-5861

2020

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MITF E318K: A rare homozygous case with multiple primary melanoma

Pigment cell and melanoma research, 2024-01, Vol.37 (1), p.68-73

2024

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Abstract 5376: Whole-exome sequencing of acquired nevi identifies novel mechanisms for development and maintenance of benign neoplasms

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.5376-5376

2018

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Phenotypic Characterization of Nevus and Tumor Patterns in MITF E318K Mutation Carrier Melanoma Patients

Journal of investigative dermatology, 2014-01, Vol.134 (1), p.141-149

2014

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Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls

Journal of investigative dermatology, 2020-02, Vol.140 (2), p.498-501.e17

2020

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The MC1R r allele does not increase melanoma risk in MITF E318K carriers

British journal of dermatology (1951), 2023-05, Vol.188 (6), p.770-776

2023

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Genome-Wide Association Study Suggests the Variant rs7551288A within the DHCR24 Gene Is Associated with Poor Overall Survival in Melanoma Patients

Cancers, 2022-05, Vol.14 (10), p.2410

2022

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BRAFV600E mutation status of involuting and stable nevi in dabrafenib therapy with or without trametinib

JAMA dermatology (Chicago, Ill.), 2014-10, Vol.150 (10), p.1079

2014

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Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

Pigment cell and melanoma research, 2014-07, Vol.27 (4), p.552-564

2014

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Abstract 5588: Nevus count and dermoscopic pattern associated with MC1R RHC-variant alleles in a case-control study of melanoma

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.5588-5588

2015

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Patients’ and doctors’ preferences for disclosing dermatology results

Australasian journal of dermatology, 2017-11, Vol.58 (4), p.e282-e283

2017

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BRAF wild-type melanoma in situ arising in a BRAF V600E mutant dysplastic nevus

JAMA dermatology (Chicago, Ill.), 2015-04, Vol.151 (4), p.417

2015

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IRF4 rs12203592T/T genotype is associated with nodular melanoma

Melanoma research, 2019-08, Vol.29 (4), p.445-446

2019

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Genetic variation in IRF 4 expression modulates growth characteristics, tyrosinase expression and interferon‐gamma response in melanocytic cells

Pigment cell and melanoma research, 2018-01, Vol.31 (1), p.51-63

2018

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GSTP1 does not modify MC1R effects on melanoma risk

Experimental dermatology, 2017-08, Vol.26 (8), p.730-733

2017

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Dermoscopy, reflectance confocal microscopy and histopathology of a melanoma in situ from an individual homozygous for GSTP 1105 V al/ MC 1 R 92 M et

Australasian journal of dermatology, 2016-02, Vol.57 (1), p.64-67

2016

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Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants

Skin Pigmentation Genetics for the Clinic

The NR4A2 nuclear receptor is recruited to novel nuclear foci in response to UV irradiation and participates in nucleotide excision repair

MicroRNA expression profiling of cutaneous squamous cell carcinomas and precursor lesions

Genetic variation in IRF4 expression modulates growth characteristics, tyrosinase expression and interferon‐gamma response in melanocytic cells

Acquired melanocytic naevus phenotypes and MC1R genotypes in Han Chinese: a cross-sectional study

Whole-Exome Sequencing of Acquired Nevi Identifies Mechanisms for Development and Maintenance of Benign Neoplasms

Assessing the genetic risk of nodular melanoma using a candidate gene approach

ERK hyperactivation serves as a unified mechanism of escape in intrinsic and acquired CDK4/6 inhibitor resistance in acral lentiginous melanoma

Abstract 5861: BOP1 expression contributes to the proliferative/invasive phenotype in melanoma

MITF E318K: A rare homozygous case with multiple primary melanoma

Abstract 5376: Whole-exome sequencing of acquired nevi identifies novel mechanisms for development and maintenance of benign neoplasms

Phenotypic Characterization of Nevus and Tumor Patterns in MITF E318K Mutation Carrier Melanoma Patients

Genes Determining Nevus Count and Dermoscopic Appearance in Australian Melanoma Cases and Controls

The MC1R r allele does not increase melanoma risk in MITF E318K carriers

Genome-Wide Association Study Suggests the Variant rs7551288A within the DHCR24 Gene Is Associated with Poor Overall Survival in Melanoma Patients

BRAFV600E mutation status of involuting and stable nevi in dabrafenib therapy with or without trametinib

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

Abstract 5588: Nevus count and dermoscopic pattern associated with MC1R RHC-variant alleles in a case-control study of melanoma

Patients’ and doctors’ preferences for disclosing dermatology results

BRAF wild-type melanoma in situ arising in a BRAF V600E mutant dysplastic nevus

IRF4 rs12203592T/T genotype is associated with nodular melanoma

Genetic variation in IRF 4 expression modulates growth characteristics, tyrosinase expression and interferon‐gamma response in melanocytic cells

GSTP1 does not modify MC1R effects on melanoma risk

Dermoscopy, reflectance confocal microscopy and histopathology of a melanoma in situ from an individual homozygous for GSTP 1105 V al/ MC 1 R 92 M et

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