Unusual suspects in hereditary melanoma: POT1, POLE, BAP1-Reference-Cited by-同舟云学术

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Unusual suspects in hereditary melanoma: POT1, POLE, BAP1

Published:2022-12 Issue:12 Volume:38 Page:1204-1207
ISSN:0168-9525
Container-title:Trends in Genetics
language:en
Short-container-title:Trends in Genetics

Author:

Maas Ellie J.^ORCID,Betz-Stablein Brigid,Aoude Lauren G.,Soyer H. Peter,McInerney-Leo Aideen M.

Publisher

Elsevier BV

Subject

Genetics

Reference15 articles.

1. Skin Cancer in Australia;Australian Institute of Health and Welfare,2016

2. Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors;Gandini;Eur. J. Cancer,2005

3. Update in genetic susceptibility in melanoma;Miriam Potrony;Ann. Transl. Med.,2015

4. Germline p16 mutations in familial melanoma;Hussussian;Nat. Genet.,1994

5. POT1 loss-of-function variants predispose to familial melanoma;Robles-Espinoza;Nat. Genet.,2014

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Malignant Melanoma: An Overview, New Perspectives, and Vitamin D Signaling;Cancers;2024-06-18

2. POT1 and multiple primary melanomas: the dermatological phenotype;Journal of Medical Genetics;2024-05-08

3. Genetic testing for familial melanoma;Italian Journal of Dermatology and Venereology;2024-02

4. MITF E318K: A rare homozygous case with multiple primary melanoma;Pigment Cell & Melanoma Research;2023-08-27

5. GOLM1: expanding our understanding of melanoma susceptibility;Journal of Medical Genetics;2023-07-24

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