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Relationship of Chromosome Arm 10q Variants to Occurrence of Multiple Primary Melanoma in the Population-Based Genes, Environment, and Melanoma (GEM) Study.

作者信息

Miles Jonathan A, Orlow Irene, Kanetsky Peter A, Luo Li, Cust Anne E, Armstrong Bruce K, Kricker Anne, Anton-Culver Hoda, Gruber Stephen B, Gallagher Richard P, Zanetti Roberto, Rosso Stefano, Sacchetto Lidia, Dwyer Terence, Gibbs David C, Busam Klaus J, Mavinkurve Vikram, Ollila David W, Begg Colin B, Berwick Marianne, Thomas Nancy E

机构信息

Department of Dermatology, University of North Carolina, Chapel Hill, North Carolina, USA.

Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

出版信息

J Invest Dermatol. 2019 Jun;139(6):1410-1412. doi: 10.1016/j.jid.2018.11.030. Epub 2018 Dec 17.

DOI:10.1016/j.jid.2018.11.030
PMID:30571972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6535117/
Abstract
摘要

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Relationship of Chromosome Arm 10q Variants to Occurrence of Multiple Primary Melanoma in the Population-Based Genes, Environment, and Melanoma (GEM) Study.在基于人群的基因、环境与黑色素瘤（GEM）研究中，染色体臂10q变异与多发性原发性黑色素瘤发生的关系。
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本文引用的文献

1
Improvement of Genetic Testing for Cutaneous Melanoma in Countries With Low to Moderate Incidence: The Rule of 2 vs the Rule of 3.在发病率低至中等的国家中改善皮肤黑色素瘤的基因检测：2法则与3法则
JAMA Dermatol. 2017 Nov 1;153(11):1122-1129. doi: 10.1001/jamadermatol.2017.2926.
2
Vitamin D receptor polymorphisms and survival in patients with cutaneous melanoma: a population-based study.维生素D受体基因多态性与皮肤黑色素瘤患者的生存率：一项基于人群的研究。
Carcinogenesis. 2016 Jan;37(1):30-8. doi: 10.1093/carcin/bgv157. Epub 2015 Oct 31.
3
Inherited variation at MC1R and histological characteristics of primary melanoma.黑素皮质素受体1（MC1R）的遗传变异与原发性黑色素瘤的组织学特征
PLoS One. 2015 Mar 19;10(3):e0119920. doi: 10.1371/journal.pone.0119920. eCollection 2015.
4
Variants associated with susceptibility to pancreatic cancer and melanoma do not reciprocally affect risk.与胰腺癌和黑色素瘤易感性相关的变异不会相互影响风险。
Cancer Epidemiol Biomarkers Prev. 2014 Jun;23(6):1121-4. doi: 10.1158/1055-9965.EPI-13-0627. Epub 2014 Mar 18.
5
Survival for patients with single and multiple primary melanomas: the genes, environment, and melanoma study.单发和多发黑色素瘤患者的生存：基因、环境与黑色素瘤研究。
JAMA Dermatol. 2013 Aug;149(8):921-7. doi: 10.1001/jamadermatol.2013.4581.
6
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.一项针对犹他州高危家系的全基因组关联分析发现了 10q 染色体臂上的一个新的黑色素瘤风险变异。
Hum Genet. 2012 Jan;131(1):77-85. doi: 10.1007/s00439-011-1048-z. Epub 2011 Jun 26.
7
Quantifying and correcting for the winner's curse in genetic association studies.在基因关联研究中对胜者之咒进行量化与校正。
Genet Epidemiol. 2009 Jul;33(5):453-62. doi: 10.1002/gepi.20398.
8
A design for cancer case-control studies using only incident cases: experience with the GEM study of melanoma.一种仅使用新发病例的癌症病例对照研究设计：黑色素瘤GEM研究的经验
Int J Epidemiol. 2006 Jun;35(3):756-64. doi: 10.1093/ije/dyl044. Epub 2006 Mar 23.
9
Polymorphisms in nucleotide excision repair genes and risk of multiple primary melanoma: the Genes Environment and Melanoma Study.核苷酸切除修复基因多态性与多发性原发性黑色素瘤风险：基因、环境与黑色素瘤研究
Carcinogenesis. 2006 Mar;27(3):610-8. doi: 10.1093/carcin/bgi252. Epub 2005 Oct 29.
10
Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.基于人群样本的CDKN2A突变携带者患黑色素瘤的终生风险。
J Natl Cancer Inst. 2005 Oct 19;97(20):1507-15. doi: 10.1093/jnci/dji312.