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- Study Description
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Important Links and Information
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Request access via Authorized Access
- Instructions for requestors
- Data Use Certification (DUC) Agreement
- Talking Glossary of Genetic Terms
This goal of this project is to perform systematic analyses of germline genetic alterations in sporadic and familial multiple myeloma (MM) to discover candidate genes from these exome data. In this proposal, we will build on our prior work and pre-existing genomic data to prioritize, identify and validate novel candidate genes conferring susceptibility to MM.
- Study Design:
- Case Set
- Study Type:
- Case Set
- Total number of consented subjects: 2280
- Subject Sample Telemetry Report (SSTR)
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Request access via Authorized Access
- Authorized Access
- Publicly Available Data
- Link to other NCBI resources related to this study
- Study Inclusion/Exclusion Criteria
The inclusion criteria is anyone with MM, but the preferred criteria are:
- Age of Onset <65, Caucasian AND/OR
- Family History of MM in FDR, SDR or a family history of lymphoma in FDR/SDR
- Availability of 500ng of sequencing quality DNA
- Institutional certification for data sharing in dbGAP
- Availability of core variables
- Core variables are age, gender, age at diagnosis, ethnicity
- Selected Publications
- Diseases/Traits Related to Study (MeSH terms)
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- Primary Phenotype: Multiple Myeloma
- Authorized Data Access Requests
- Study Attribution
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Principal Investigator
- Vijai Joseph, PhD. Memorial Sloan Kettering Cancer Center, New York, NY, USA.
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Funding Source for Vijai Joseph
- R21CA209533. National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
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Sequencing Center
- Center for Inherited Disease Research (CIDR). Johns Hopkins University, Baltimore, MD, USA.
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Funding Source for CIDR Sequencing
- HHSN268201700006I, NIH contract "High throughput genotyping for studying the genetic contributions to human disease". National Institutes of Health, Bethesda, MD, USA.
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Principal Investigator