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Article

Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes.

Human molecular genetics - 9 Jun 2021

Waller Rosalie Griffin, Klein Robert J, Vijai Joseph, McKay James D, Clay-Gilmour Alyssa, Wei Xiaomu, Madsen Michael J, Sborov Douglas W, Curtin Karen, Slager Susan L, Offit Kenneth, Vachon Celine M, Lipkin Steven M, Dumontet Charles, Camp Nicola J

Abstract excerpt

Inherited genetic risk factors play a role in multiple myeloma (MM), yet considerable missing heritability exists. Rare risk variants at genome-wide association study (GWAS) loci are a new avenue to explore. Pleiotropy between lymphoid neoplasms (LNs) has been suggested in family history and genetic studies, but no studies have interrogated sequencing for pleiotropic genes or rare risk variants. Sequencing...

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Identifiers

PMID: 33751038
DOI: 10.1093/hmg/ddab066
PMCID: PMC8188404

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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