Publication:
Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

Simple item page
dc.contributor.authorPertesi, Maroulio
dc.contributor.authorVallee, Maxime
dc.contributor.authorWei, Xiaomu
dc.contributor.authorRevuelta, Maria V
dc.contributor.authorGalia, Perrine
dc.contributor.authorDemangel, Delphine
dc.contributor.authorOliver, Javier
dc.contributor.authorFoll, Matthieu
dc.contributor.authorChen, Siwei
dc.contributor.authorPerrial, Emeline
dc.contributor.authorGarderet, Laurent
dc.contributor.authorCorre, Jill
dc.contributor.authorLeleu, Xavier
dc.contributor.authorBoyle, Eileen M
dc.contributor.authorDecaux, Olivier
dc.contributor.authorRodon, Philippe
dc.contributor.authorKolb, Brigitte
dc.contributor.authorSlama, Borhane
dc.contributor.authorMineur, Philippe
dc.contributor.authorVoog, Eric
dc.contributor.authorLe Bris, Catherine
dc.contributor.authorFontan, Jean
dc.contributor.authorMaigre, Michel
dc.contributor.authorBeaumont, Marie
dc.contributor.authorAzais, Isabelle
dc.contributor.authorSobol, Hagay
dc.contributor.authorVignon, Marguerite
dc.contributor.authorRoyer, Bruno
dc.contributor.authorPerrot, Aurore
dc.contributor.authorFuzibet, Jean-Gabriel
dc.contributor.authorDorvaux, VEronique
dc.contributor.authorAnglaret, Bruno
dc.contributor.authorCony-Makhoul, Pascale
dc.contributor.authorBerthou, Christian
dc.contributor.authorDesquesnes, Florence
dc.contributor.authorPegourie, Brigitte
dc.contributor.authorLeyvraz, Serge
dc.contributor.authorMosser, Laurent
dc.contributor.authorFrenkiel, Nicole
dc.contributor.authorAugeul-Meunier, Karine
dc.contributor.authorLeduc, Isabelle
dc.contributor.authorLeyronnas, Cecile
dc.contributor.authorVoillat, Laurent
dc.contributor.authorCasassus, Philippe
dc.contributor.authorMathiot, Claire
dc.contributor.authorCheron, Nathalie
dc.contributor.authorPaubelle, Etienne
dc.contributor.authorMoreau, Philippe
dc.contributor.authorBignon, Yves-Jean
dc.contributor.authorJoly, Bertrand
dc.contributor.authorBourquard, Pascal
dc.contributor.authorCaillot, Denis
dc.contributor.authorNaman, Herve
dc.contributor.authorRigaudeau, Sophie
dc.contributor.authorMarit, Gerald
dc.contributor.authorMacro, Margaret
dc.contributor.authorLambrecht, Isabelle
dc.contributor.authorCliquennois, Manuel
dc.contributor.authorVincent, Laure
dc.contributor.authorHelias, Philippe
dc.contributor.authorAvet-Loiseau, Herve
dc.contributor.authorMoreno, Victor
dc.contributor.authorReis, Rui Manuel
dc.contributor.authorVarkonyi, Judit
dc.contributor.authorKruszewski, Marcin
dc.contributor.authorVangsted, Annette Juul
dc.contributor.authorJurczyszyn, Artur
dc.contributor.authorZaucha, Jan Maciej
dc.contributor.authorSainz, Juan
dc.contributor.authorKrawczyk-Kulis, Malgorzata
dc.contributor.authorWątek, Marzena
dc.contributor.authorPelosini, Matteo
dc.contributor.authorIskierka-Jażdżewska, Elzbieta
dc.contributor.authorGrząśko, Norbert
dc.contributor.authorMartinez-Lopez, Joaquin
dc.contributor.authorJerez, Andres
dc.contributor.authorCampa, Daniele
dc.contributor.authorBuda, Gabriele
dc.contributor.authorLesueur, Fabienne
dc.contributor.authorDudziński, Marek
dc.contributor.authorGarcia-Sanz, Ramon
dc.contributor.authorNagler, Arnon
dc.contributor.authorRymko, Marcin
dc.contributor.authorJamroziak, Krzysztof
dc.contributor.authorButrym, Aleksandra
dc.contributor.authorCanzian, Federico
dc.contributor.authorObazee, Ofure
dc.contributor.authorNilsson, Björn
dc.contributor.authorKlein, Robert J
dc.contributor.authorLipkin, Steven M
dc.contributor.authorMcKay, James D
dc.contributor.authorDumontet, Charles
dc.contributor.funderFrench National Cancer Institute (INCA)
dc.contributor.funderFondation Française pour la Recherche contre le Myélome et les Gammapathies (FFMRG)
dc.contributor.funderIntergroupe Francophone du Myélome (IFM)
dc.date.accessioned2023-01-25T13:32:35Z
dc.date.available2023-01-25T13:32:35Z
dc.date.issued2019-02-08
dc.description.abstractMultiple myeloma (MM) is the third most common hematological malignancy, after Non-Hodgkin Lymphoma and Leukemia. MM is generally preceded by Monoclonal Gammopathy of Undetermined Significance (MGUS), and epidemiological studies have identified older age, male gender, family history, and MGUS as risk factors for developing MM.
dc.description.versionSi
dc.identifier.citationPertesi M, Vallée M, Wei X, Revuelta MV, Galia P, Demangel D, et al. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma. Leukemia. 2019 Sep;33(9):2324-2330
dc.identifier.doi10.1038/s41375-019-0452-6
dc.identifier.essn1476-5551
dc.identifier.pmcPMC6756025
dc.identifier.pmid30967618
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756025/pdf
dc.identifier.unpaywallURLhttps://www.nature.com/articles/s41375-019-0452-6.pdf
dc.identifier.urihttp://hdl.handle.net/10668/13806
dc.issue.number9
dc.journal.titleLeukemia
dc.journal.titleabbreviationLeukemia
dc.language.isoen
dc.organizationCentro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica-GENYO
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Regional de Málaga
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.page.number2324-2330
dc.provenanceRealizada la curación de contenido 17/02/2025
dc.publisherSpringer Nature
dc.pubmedtypeLetter
dc.pubmedtypeResearch Support, N.I.H., Extramural
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDNCI R01 NCI CA167824
dc.relation.publisherversionhttps://www.nature.com/articles/s41375-019-0452-6
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectMieloma
dc.subjectExoma
dc.subjectFemale
dc.subjectGermline mutation
dc.subject.decsComplejo multienzimático de ribonucleasas del exosoma
dc.subject.decsExoma
dc.subject.decsFemenino
dc.subject.decsHumanos
dc.subject.decsLinaje
dc.subject.decsMieloma múltiple
dc.subject.decsMutación de línea germinal
dc.subject.decsPredisposición genética a la enfermedad
dc.subject.decsSecuenciación del exoma
dc.subject.meshExome
dc.subject.meshExosome multienzyme ribonuclease complex
dc.subject.meshFemale
dc.subject.meshGenetic predisposition to disease
dc.subject.meshGerm-line mutation
dc.subject.meshHumans
dc.subject.meshMultiple myeloma
dc.subject.meshPedigree
dc.subject.meshExome sequencing
dc.titleExome sequencing identifies germline variants in DIS3 in familial multiple myeloma.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number33
dspace.entity.typePublication

Files

Original bundle

Now showing 1 - 2 of 2
Thumbnail Image
Name:
PMC6756025.pdf
Size:
1.36 MB
Format:
Adobe Portable Document Format
Download
Thumbnail Image
Name:
Pertesi_ExomeSequencing_MaterialSuplementario.pdf
Size:
715.74 KB
Format:
Adobe Portable Document Format
Download

Collections

SAS - Hospital Regional Universitario de Málaga
Centro Pfizer-Andalucía de Genómica e Investigación Oncológica (GENYO)
Instituto de Investigación Biomédica de Málaga - Plataforma Bionand (IBIMA)
SAS - Hospital Universitario Virgen de la Victoria

© 2023 – Repositorio Institucional de Salud de Andalucía - Fundación Pública Andaluza Progreso y Salud - Consejería de Salud y Consumo de la Junta de Andalucía