Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

MyelomA Genetics International Consortium.

Leukemia & lymphoma - 1 May 2012

Morgan Gareth, Johnsen Hans Erik, Goldschmidt Hartmut, Palumbo Antonio, Cavo Michele, Sonneveld Pieter, Miguel Jesus San, Chim Char Sang, Browne Paul, Einsele Hermann, Waage Anders, Turesson Ingemar, Spencer Andrew, Hajek Roman, Ludwig Heinz, Hemminki Kari, Houlston Richard

Abstract excerpt

While the etiology of multiple myeloma (MM) is largely unknown, evidence for an inherited genetic susceptibility is provided by the two-fold increased risk of the disease seen in first-degree relatives of cases of MM. It is likely that part of this heritable risk is a consequence of the co-inheritance of low-risk genetic variants. The accumulated experience to date in identifying risk variants for other tumors...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic Predisposition to Disease
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple Myeloma

Source

Identifiers

PMID: 22080755
DOI: 10.3109/10428194.2011.639881

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MyelomA Genetics International Consortium.PMID 22080755Read ↗

Genetic predisposition for multiple myeloma.Semantic proximity Read ↗

Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).Semantic proximity Read ↗

FaMMily Affairs: Dissecting inherited contributions to multiple myeloma risk.Semantic proximity Read ↗

Inherited genetic susceptibility to multiple myeloma.Semantic proximity Read ↗

Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance.Semantic proximity Read ↗

Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.Semantic proximity Read ↗

Identification of novel genetic loci for risk of multiple myeloma by functional annotationSemantic proximity Read ↗

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.Semantic proximity Read ↗

A polygenic risk score for multiple myeloma risk prediction.Semantic proximity Read ↗

Epidemiology, genetics and treatment of multiple myeloma and precursor diseases.Semantic proximity Read ↗

A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry.Semantic proximity Read ↗

Multiple Myeloma Risk and Outcomes Are Associated with Pathogenic Germline Variants in DNA Repair Genes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.