Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF. (Q40510567)

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20 March 2020

title

Genetic susceptibility to cutaneous melanoma in southern Switzerland: role of CDKN2A, MC1R and MITF (English)

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20 March 2020

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15

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Miriam Potrony

2

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20 March 2020

Celia Badenas

14

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20 March 2020

author name string

C Mangas

1

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C Mainetti

3

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E Bianchi

4

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P Carrozza Merlani

5

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A Mancarella Eberhardt

6

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E Maspoli-Postizzi

7

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G Marazza

8

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A Marcollo-Pini

9

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F Pelloni

10

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C Sessa

11

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B Simona

12

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J A Puig-Butillé

13

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language of work or name

English

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publication date

31 August 2016

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British Journal of Dermatology

20 March 2020

published in

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volume

175

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issue

5

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page(s)

1030-1037

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Selection criteria for genetic assessment of patients with familial melanoma

20 March 2020

cites work

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Malignant melanoma in the 21st century: the emerging molecular landscape

21 January 2018

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Role of the CDKN2A locus in patients with multiple primary melanomas

21 January 2018

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Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents

21 January 2018

1 reference

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

21 January 2018

1 reference

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants

21 January 2018

1 reference

Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia

21 January 2018

1 reference

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

21 January 2018

1 reference

POT1 loss-of-function variants predispose to familial melanoma

21 January 2018

1 reference

Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden

21 January 2018

1 reference

Novel MC1R variants in Ligurian melanoma patients and controls.

21 January 2018

1 reference

MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis

21 January 2018

1 reference

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

21 January 2018

1 reference

BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs

21 January 2018

1 reference

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

21 January 2018

1 reference

Prevalence of MITF p.E318K in Patients With Melanoma Independent of the Presence of CDKN2A Causative Mutations

21 January 2018

1 reference

Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study

21 January 2018

1 reference

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

21 January 2018

1 reference

Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population.

21 January 2018

1 reference

A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.

21 January 2018

1 reference

Classifying variants of CDKN2A using computational and laboratory studies

21 January 2018

1 reference

Genetic testing in familial melanoma: uptake and implications.

21 January 2018

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Freckles and solar lentigines have different risk factors in Caucasian women

21 January 2018

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Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development

21 January 2018

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Cutaneous phenotype andMC1R variants as modifying factors for the development of melanoma inCDKN2A G101W mutation carriers from 4 countries

21 January 2018

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The A148T Variant of the CDKN2A Gene Is Not Associated with Melanoma Risk in the French and Italian Populations

21 January 2018

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21 January 2018

Identifiers

DOI

10.1111/BJD.14897

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20 March 2020

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