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References from Pathogenic germ line variants in a prospective multicenter cohort of patients with multiple myeloma. Local targets link to admitted publications; unresolved targets remain external evidence.
Unresolved reference
2023 · External reference
Germline variants in targeted tumor sequencing using matched normal DNA
10.1001/jamaoncol.2015.5208 · 2016 · External reference
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol
10.1093/annonc/mdw018 · 2016 · External reference
Germline analysis from tumor–germline sequencing dyads to identify clinically actionable secondary findings
10.1158/1078-0432.ccr-16-0015 · 2016 · External reference
Patterns of hematologic malignancies and solid tumors among 37,838 first-degree relatives of 13,896 patients with multiple myeloma in Sweden
10.1002/ijc.24514 · 2009 · External reference
Multiple myeloma and family history of lymphohaematopoietic cancers: results from the International Multiple Myeloma Consortium
10.1111/bjh.14199 · 2016 · External reference
Familial monoclonal gammopathy of undetermined significance and multiple myeloma: epidemiology, risk factors, and biological characteristics
10.1182/blood-2011-11-387324 · 2012 · External reference
Inherited genetic susceptibility to multiple myeloma
10.1038/leu.2013.344 · 2014 · External reference
Characterization of rare germline variants in familial multiple myeloma
10.1038/s41408-021-00422-6 · 2021 · External reference
Comparison of universal genetic testing vs guideline-directed targeted testing for patients with hereditary cancer syndrome
10.1001/jamaoncol.2020.6252 · 2021 · External reference
Identification of germline cancer predisposition variants during clinical ctDNA testing
10.1038/s41598-021-93084-0 · 2021 · External reference
Yield and utility of germline testing following tumor sequencing in patients with cancer
10.1001/jamanetworkopen.2020.19452 · 2020 · External reference
NCCN guidelines insights: genetic/familial high-risk assessment: breast, ovarian, and pancreatic, version 1.2020
10.6004/jnccn.2020.0017 · 2020 · External reference
NCCN guidelines® insights: genetic/familial high-risk assessment: colorectal, version 1.2021
2021 · External reference
Confirmed pathogenic germline variants in cancer predisposition genes incidentally detected in somatic genomic profiling of multiple myeloma patients
10.1182/blood-2023-190878 · 2023 · External reference
Pathogenic germline variants in multiple myeloma
10.1182/blood-2021-151495 · 2021 · External reference