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Deficiencies in mismatch DNA repair: providing the soil for large-to-giant congenital melanocytic naevus development

British journal of dermatology (1951), 2023-01, Vol.188 (1), p.5-5

Stark, Mitchell S

2023

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Challenging the Lymph Node Progression Model of Melanoma

Journal of investigative dermatology, 2024-06

2024

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Large-Giant Congenital Melanocytic Nevi: Moving Beyond NRAS Mutations

Journal of investigative dermatology, 2019-04, Vol.139 (4), p.756-759

Stark, Mitchell S.

2019

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Characterization of the Melanoma miRNAome by Deep Sequencing

PloS one, 2010-03, Vol.5 (3), p.e9685-e9685

2010

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One step closer to improving melanoma diagnosis and prognosis with liquid biopsies

British journal of dermatology (1951), 2023-08, Vol.189 (3), p.255-259

2023

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Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays

Cancer research (Chicago, Ill.), 2007-03, Vol.67 (6), p.2632-2642

2007

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The Skin Molecular Ecosystem Holds the Key to Nevogenesis and Melanomagenesis

Journal of investigative dermatology, 2024-03, Vol.144 (3), p.456-465

2024

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An Integrated Microfluidic‐SERS Platform Enables Sensitive Phenotyping of Serum Extracellular Vesicles in Early Stage Melanomas

Advanced functional materials, 2022-01, Vol.32 (3), p.n/a

2022

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In Vivo Melanoma Cell Morphology and Tumor Aggressiveness: The Promise of Reflectance Confocal Microscopy in Reducing Unnecessary Excisions

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.2053-2054

2022

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BRAF variant allele fraction—A predictor of response to targeted therapy?

Journal of the European Academy of Dermatology and Venereology, 2023-10, Vol.37 (10), p.1945-1946

2023

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Spatial Randomness in the Distribution of Acquired Melanocytic Nevi of the Back in a Population-Based Sample

Journal of investigative dermatology, 2023-06, Vol.143 (6), p.1108-1111.e3

2023

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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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Distinct HOX Gene Family DNA Methylation Profiles in Histologically Normal Skin Dependent on Dermoscopic Pattern of Adjacent Nevi

Journal of investigative dermatology, 2023-09, Vol.143 (9), p.1830-1834.e6

2023

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Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma

PloS one, 2011-10, Vol.6 (10), p.e26121-e26121

2011

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A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

American journal of human genetics, 2008-02, Vol.82 (2), p.424-431

2008

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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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Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi

Journal of investigative dermatology, 2022-07, Vol.142 (7), p.1893-1902.e7

2022

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POT1 and multiple primary melanomas: the dermatological phenotype

Journal of medical genetics, 2024-09, Vol.61 (9), p.891-894

2024

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Defining the Molecular Genetics of Dermoscopic Naevus Patterns

Dermatology (Basel), 2019-01, Vol.235 (1), p.19-34

2019

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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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GOLM1 : expanding our understanding of melanoma susceptibility

Journal of medical genetics, 2023-09, Vol.60 (9), p.835-837

2023

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Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair

Journal of investigative dermatology, 2020-10, Vol.140 (10), p.2093-2096.e2

2020

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Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor

Pigment cell and melanoma research, 2011-06, Vol.24 (3), p.525-537

2011

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Deficiencies in mismatch DNA repair: providing the soil for large-to-giant congenital melanocytic naevus development

Challenging the Lymph Node Progression Model of Melanoma

Large-Giant Congenital Melanocytic Nevi: Moving Beyond NRAS Mutations

Characterization of the Melanoma miRNAome by Deep Sequencing

One step closer to improving melanoma diagnosis and prognosis with liquid biopsies

Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays

The Skin Molecular Ecosystem Holds the Key to Nevogenesis and Melanomagenesis

An Integrated Microfluidic‐SERS Platform Enables Sensitive Phenotyping of Serum Extracellular Vesicles in Early Stage Melanomas

In Vivo Melanoma Cell Morphology and Tumor Aggressiveness: The Promise of Reflectance Confocal Microscopy in Reducing Unnecessary Excisions

POT1 loss-of-function variants predispose to familial melanoma

BRAF variant allele fraction—A predictor of response to targeted therapy?

Spatial Randomness in the Distribution of Acquired Melanocytic Nevi of the Back in a Population-Based Sample

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

Distinct HOX Gene Family DNA Methylation Profiles in Histologically Normal Skin Dependent on Dermoscopic Pattern of Adjacent Nevi

Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma

A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color

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

Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing

Genome-Scale DNA Methylation Analysis Identifies Repeat Element Alterations that Modulate the Genomic Stability of Melanocytic Nevi

POT1 and multiple primary melanomas: the dermatological phenotype

Defining the Molecular Genetics of Dermoscopic Naevus Patterns

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

GOLM1 : expanding our understanding of melanoma susceptibility

Mutation Signatures in Melanocytic Nevi Reveal Characteristics of Defective DNA Repair

Melanoma cell invasiveness is regulated by miR-211 suppression of the BRN2 transcription factor

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