The genomic landscape of pediatric myelodysplastic syndromes
Myelodysplastic syndromes (MDS) are uncommon in children and have poor prognosis. Here, the authors interrogate the genomic landscape of MDS, confirming adult and paediatric MDS are separate diseases with disparate mechanisms, and highlighting that SAMD9/SAMD9L mutations represent a new class of MDS...
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2017-11-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-017-01590-5 |
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doaj-d4725852501c4cd68e3d57d74d9225b12021-05-11T07:44:40ZengNature Publishing GroupNature Communications2041-17232017-11-018111010.1038/s41467-017-01590-5The genomic landscape of pediatric myelodysplastic syndromesJason R. Schwartz0Jing Ma1Tamara Lamprecht2Michael Walsh3Shuoguo Wang4Victoria Bryant5Guangchun Song6Gang Wu7John Easton8Chimene Kesserwan9Kim E. Nichols10Charles G. Mullighan11Raul C. Ribeiro12Jeffery M. Klco13Department of Oncology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Computational Biology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Computational Biology, St. Jude Children’s Research HospitalDepartment of Computational Biology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalDepartment of Oncology, St. Jude Children’s Research HospitalDepartment of Pathology, St. Jude Children’s Research HospitalMyelodysplastic syndromes (MDS) are uncommon in children and have poor prognosis. Here, the authors interrogate the genomic landscape of MDS, confirming adult and paediatric MDS are separate diseases with disparate mechanisms, and highlighting that SAMD9/SAMD9L mutations represent a new class of MDS predisposition.https://doi.org/10.1038/s41467-017-01590-5 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jason R. Schwartz Jing Ma Tamara Lamprecht Michael Walsh Shuoguo Wang Victoria Bryant Guangchun Song Gang Wu John Easton Chimene Kesserwan Kim E. Nichols Charles G. Mullighan Raul C. Ribeiro Jeffery M. Klco |
spellingShingle |
Jason R. Schwartz Jing Ma Tamara Lamprecht Michael Walsh Shuoguo Wang Victoria Bryant Guangchun Song Gang Wu John Easton Chimene Kesserwan Kim E. Nichols Charles G. Mullighan Raul C. Ribeiro Jeffery M. Klco The genomic landscape of pediatric myelodysplastic syndromes Nature Communications |
author_facet |
Jason R. Schwartz Jing Ma Tamara Lamprecht Michael Walsh Shuoguo Wang Victoria Bryant Guangchun Song Gang Wu John Easton Chimene Kesserwan Kim E. Nichols Charles G. Mullighan Raul C. Ribeiro Jeffery M. Klco |
author_sort |
Jason R. Schwartz |
title |
The genomic landscape of pediatric myelodysplastic syndromes |
title_short |
The genomic landscape of pediatric myelodysplastic syndromes |
title_full |
The genomic landscape of pediatric myelodysplastic syndromes |
title_fullStr |
The genomic landscape of pediatric myelodysplastic syndromes |
title_full_unstemmed |
The genomic landscape of pediatric myelodysplastic syndromes |
title_sort |
genomic landscape of pediatric myelodysplastic syndromes |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2017-11-01 |
description |
Myelodysplastic syndromes (MDS) are uncommon in children and have poor prognosis. Here, the authors interrogate the genomic landscape of MDS, confirming adult and paediatric MDS are separate diseases with disparate mechanisms, and highlighting that SAMD9/SAMD9L mutations represent a new class of MDS predisposition. |
url |
https://doi.org/10.1038/s41467-017-01590-5 |
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