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001     153045
005     20240229123038.0
024 7 _ |a 10.1038/s41375-019-0703-6
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024 7 _ |a pmid:31913320
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024 7 _ |a 0887-6924
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024 7 _ |a 1476-5551
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037 _ _ |a DKFZ-2020-00127
041 _ _ |a eng
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100 1 _ |a Pertesi, Maroulio
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245 _ _ |a Genetic predisposition for multiple myeloma.
260 _ _ |a London
|c 2020
|b Springer Nature
336 7 _ |a article
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500 _ _ |a 2020 Mar;34(3):697-708
520 _ _ |a Multiple myeloma (MM) is the second most common blood malignancy. Epidemiological family studies going back to the 1920s have provided evidence for familial aggregation, suggesting a subset of cases have an inherited genetic background. Recently, studies aimed at explaining this phenomenon have begun to provide direct evidence for genetic predisposition to MM. Genome-wide association studies have identified common risk alleles at 24 independent loci. Sequencing studies of familial cases and kindreds have begun to identify promising candidate genes where variants with strong effects on MM risk might reside. Finally, functional studies are starting to give insight into how identified risk alleles promote the development of MM. Here, we review recent findings in MM predisposition field, and highlight open questions and future directions.
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700 1 _ |a Went, Molly
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700 1 _ |a Hansson, Markus
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700 1 _ |a Hemminki, Kari
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700 1 _ |a Houlston, Richard S
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700 1 _ |a Nilsson, Björn
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773 _ _ |a 10.1038/s41375-019-0703-6
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910 1 _ |a Deutsches Krebsforschungszentrum
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