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Melanocortin 1 receptor (MC1R) polymorphisms’ influence on size and dermoscopic features of nevi

Pigment cell and melanoma research, 2018-01, Vol.31 (1), p.39-50

2018

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Melanocortin‐1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium‐to‐giant congenital melanocytic nevi

Pigment cell and melanoma research, 2020-09, Vol.33 (5), p.685-694

2020

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Benefits of total body photography and digital dermatoscopy (“two-step method of digital follow-up”) in the early diagnosis of melanoma in patients at high risk for melanoma

Journal of the American Academy of Dermatology, 2012-07, Vol.67 (1), p.e17-e27

2012

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The MC1R melanoma risk variant p.R160W is associated with Parkinson disease

Annals of neurology, 2015-05, Vol.77 (5), p.889-894

2015

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Novel P397S MAPT variant associated with late onset and slow progressive frontotemporal dementia

Annals of clinical and translational neurology, 2019-08, Vol.6 (8), p.1559-1565

2019

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IRF4 rs12203592 functional variant and melanoma survival

International journal of cancer, 2017-04, Vol.140 (8), p.1845-1849

2017

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TERT gene amplification is associated with poor outcome in acral lentiginous melanoma

Journal of the American Academy of Dermatology, 2014-10, Vol.71 (4), p.839-841

2014

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Clinical, Epidemiological, and Molecular Heterogeneity in Acral Melanoma

Journal of investigative dermatology, 2018-02, Vol.138 (2), p.254-255

2018

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Monitoring of Donor‐Derived Cell‐Free DNA by Short Tandem Repeats: Concentration of Total Cell‐Free DNA and Fragment Size for Acute Rejection Risk Assessment in Liver Transplantation

Liver transplantation, 2022-02, Vol.28 (2), p.257-268

2022

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Common genetic variants associated with melanoma risk or naevus count in patients with wildtype MC1R melanoma

British journal of dermatology (1951), 2022-11, Vol.187 (5), p.753-764

2022

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Correlation among Dermoscopy, Confocal Reflectance Microscopy, and Histologic Features of Melanoma and Basal Cell Carcinoma Collision Tumor

Dermatologic surgery, 2011-02, Vol.37 (2), p.275-279

2011

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Update in genetic susceptibility in melanoma

Annals of translational medicine, 2015-09, Vol.3 (15), p.210-210

2015

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Oncogenic properties via MAPK signaling of the SOX5‐RAF1 fusion gene identified in a wild‐type NRAS/BRAF giant congenital nevus

Pigment cell and melanoma research, 2022-07, Vol.35 (4), p.450-460

2022

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Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: Implications for genetic counseling

Journal of the American Academy of Dermatology, 2014-11, Vol.71 (5), p.888-895

2014

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Influence of germline genetic variants on dermoscopic features of melanoma

Pigment cell and melanoma research, 2021-05, Vol.34 (3), p.618-628

2021

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Transcriptomic and Genetic Associations between Alzheimer’s Disease, Parkinson’s Disease, and Cancer

Cancers, 2021-06, Vol.13 (12), p.2990

2021

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AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy

Journal of investigative dermatology, 2017-06, Vol.137 (6), p.1297-1310

2017

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Association Between Confocal Morphologic Classification and Clinical Phenotypes of Multiple Primary and Familial Melanomas

JAMA dermatology (Chicago, Ill.), 2016-10, Vol.152 (10), p.1099

2016

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Inherited functional variants of the lymphocyte receptor CD5 influence melanoma survival

International journal of cancer, 2016-09, Vol.139 (6), p.1297-1302

2016

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A novel approach for the non-invasive diagnosis of pulmonary nodules using low-depth whole-genome sequencing of cell-free DNA

Translational lung cancer research, 2022-10, Vol.11 (10), p.2094-2110

2022

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Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome

Frontiers in aging neuroscience, 2023-01, Vol.14, p.1073258-1073258

2023

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Implementation of an open-source robotic platform for SARS-CoV-2 testing by real-time RT-PCR

PloS one, 2021-07, Vol.16 (7), p.e0252509-e0252509

2021

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Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

European journal of human genetics : EJHG, 2018-08, Vol.26 (8), p.1188-1193

2018

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Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma

Genetics in medicine, 2016-07, Vol.18 (7), p.727-736

2016

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A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk

Journal of Alzheimer's disease, 2017-01, Vol.56 (3), p.1065

2017

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Melanocortin 1 receptor (MC1R) polymorphisms’ influence on size and dermoscopic features of nevi

Melanocortin‐1 receptor (MC1R) genotypes do not correlate with size in two cohorts of medium‐to‐giant congenital melanocytic nevi

Benefits of total body photography and digital dermatoscopy (“two-step method of digital follow-up”) in the early diagnosis of melanoma in patients at high risk for melanoma

The MC1R melanoma risk variant p.R160W is associated with Parkinson disease

Novel P397S MAPT variant associated with late onset and slow progressive frontotemporal dementia

IRF4 rs12203592 functional variant and melanoma survival

TERT gene amplification is associated with poor outcome in acral lentiginous melanoma

Clinical, Epidemiological, and Molecular Heterogeneity in Acral Melanoma

Monitoring of Donor‐Derived Cell‐Free DNA by Short Tandem Repeats: Concentration of Total Cell‐Free DNA and Fragment Size for Acute Rejection Risk Assessment in Liver Transplantation

Common genetic variants associated with melanoma risk or naevus count in patients with wildtype MC1R melanoma

Correlation among Dermoscopy, Confocal Reflectance Microscopy, and Histologic Features of Melanoma and Basal Cell Carcinoma Collision Tumor

Update in genetic susceptibility in melanoma

Oncogenic properties via MAPK signaling of the SOX5‐RAF1 fusion gene identified in a wild‐type NRAS/BRAF giant congenital nevus

Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: Implications for genetic counseling

Influence of germline genetic variants on dermoscopic features of melanoma

Transcriptomic and Genetic Associations between Alzheimer’s Disease, Parkinson’s Disease, and Cancer

AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy

Association Between Confocal Morphologic Classification and Clinical Phenotypes of Multiple Primary and Familial Melanomas

Inherited functional variants of the lymphocyte receptor CD5 influence melanoma survival

A novel approach for the non-invasive diagnosis of pulmonary nodules using low-depth whole-genome sequencing of cell-free DNA

Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome

Implementation of an open-source robotic platform for SARS-CoV-2 testing by real-time RT-PCR

Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q

Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma

A Common Variant in the MC1R Gene (p.V92M) is associated with Alzheimer's Disease Risk

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