The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias

被引：4

作者：

Baughn, Linda B. ^{[1
]}

Li, Zhuo ^{[2
]}

Pearce, Kathryn ^{[1
]}

Vachon, Celine M. ^{[3
]}

Polley, Mei-Yin ^{[3
]}

Keats, Jonathan ^{[4
]}

Elhaik, Eran ^{[5
]}

Baird, Michael ^{[6
]}

Therneau, Terry ^{[3
]}

Cerhan, James R. ^{[3
]}

Bergsagel, P. Leif ^{[7
]}

Dispenzieri, Angela ^{[8
]}

Rajkumar, S. Vincent ^{[8
]}

Asmann, Yan W. ^{[2
]}

Kumar, Shaji ^{[8
]}

机构：

[1] Mayo Clin, Dept Lab Med & Pathol, Div Lab Genet, Rochester, MN USA

[2] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Jacksonville, FL 32224 USA

[3] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN USA

[4] Translat Genom Res Inst TGen, Integrated Canc Genom, Phoenix, AZ USA

[5] Lund Univ, Dept Biol, Lund, Sweden

[6] DNA Diagnost Ctr, Fairfield, OH USA

[7] Mayo Clin, Dept Internal Med, Div Hematol, Scottsdale, AZ USA

[8] Mayo Clin, Div Hematol, Dept Internal Med, Rochester, MN USA

来源：

BLOOD CANCER JOURNAL | 2020年 / 10卷 / 03期

基金：

美国国家卫生研究院;

关键词：

UNDETERMINED SIGNIFICANCE MGUS; MULTIPLE-MYELOMA; MONOCLONAL GAMMOPATHY; CYCLIN D1; RACIAL DISPARITIES; DYSREGULATION; POLYMORPHISM; PREVALENCE; AMERICAN;

D O I：

10.1038/s41408-020-0294-5

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

引用

页数：4

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