Evidence map›Paper›PMID 39845416›Full record

ArticleiScience2025

Germline predisposition in multiple myeloma.

Fernanda Martins Rodrigues, Jagoda Jasielec, Melody Perpich, Aelin Kim, Luke Moma, Yize Li, Erik Storrs, Michael C Wendl, Reyka G Jayasinghe, Mark Fiala and 7 more

Abstract read
In one paragraph

Article in iScience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. The Genetic and Molecular Analyses of Rare Candidate GermlineInternational journal of molecular sciences · 2026
    Article
  5. Multiple myeloma risk linked to DNA damage response genes.Journal of hematology & oncology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Fernanda Martins RodriguesDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jagoda JasielecSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Melody PerpichSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Aelin KimSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Luke MomaSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Yize LiDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Erik StorrsDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michael C WendlDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Reyka G JayasingheDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Mark FialaDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Andrew StefkaSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Benjamin DermanSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Andrzej J JakubowiakSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.
John F DiPersioDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Ravi VijDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lucy A GodleyDivision of Hematology/Oncology, Department of Medicine, Northwestern University, Chicago, IL 60611, USA.
Li DingDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

Funding

Pathogenic Variant Discovery Across a Broad Spectrum of Human DiseasesR01HG009711 · NHGRI · WASHINGTON UNIVERSITY · PI CHEN, FENG, DING, LI · 2017 to 2020
$2.2M
Deep Discovery and Clinical Interpretation of Germline and Somatic Cancer DriversU24CA211006 · NCI · WASHINGTON UNIVERSITY · PI DING, LI, GOVINDAN, RAMASWAMY · 2016 to 2020
$1.8M
NCI NIH HHS U24 CA211006NHGRI NIH HHS R01 HG009711
6 · The paper itself

Abstract

We present a study of rare germline predisposition variants in 954 unrelated individuals with multiple myeloma (MM) and 82 MM families. Using a candidate gene approach, we identified such variants across all age groups in 9.1% of sporadic and 18% of familial cases. Implicated genes included genes suggested in other MM risk studies as potential risk genes (

Indexed as

CancerGeneticsMolecular biology

Identifiers

PMID39845416
PMCPMC11750583

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.